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Encoded by eukaryotic nuclear DNA in plants and animals and by viral DNA in certain viruses whose genome is based on DNA, miRNAs function via base-pairing with complementary sequences within mRNA molecules. As a result, these mRNA strands are silenced because they can no longer be translated into proteins by ribosomes, and such complexes are often actively disassembled by the cell ('target degradation'). 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N-acetylgalactosaminyltransferase ( EC 2.4.1.41 ) is an enzyme that catalyzes the chemical reaction UDP-N-acetyl-D-galactosamine + polypeptide UDP + N-acetyl-D-galactosaminyl-polypeptide Thus, the two substrates of this enzyme are UDP-N-acetyl-D-galactosamine and polypeptide, whereas its two products are UDP and N-acetyl-D-galactosaminyl-polypeptide. This enzyme belongs to the family of glycosyltransferases, specifically the hexosyltransferases. This enzyme participates in o-glycan biosynthesis and glycan structures - biosynthesis 1. It has 2 cofactors : manganese, and calcium."], "t": []}], "preferred_name": "Polypeptide N-acetylgalactosaminyltransferases", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10063:SF2", "l": "RAL GTPASE-ACTIVATING PROTEIN SUBUNIT ALPHA-2", "d": [], "t": []}], "preferred_name": "RAL GTPASE-ACTIVATING PROTEIN SUBUNIT ALPHA-2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR46812", "l": "CARBOXYMETHYLENEBUTENOLIDASE HOMOLOG", "d": [], "t": []}], "preferred_name": "CARBOXYMETHYLENEBUTENOLIDASE HOMOLOG", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR14047:SF11", "l": "P ANTIGEN FAMILY MEMBER 4", "d": [], "t": []}], "preferred_name": "P ANTIGEN FAMILY MEMBER 4", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24399:SF34", "l": "ZINC FINGER AND BTB DOMAIN-CONTAINING PROTEIN 39", "d": [], "t": []}], "preferred_name": "ZINC FINGER AND BTB DOMAIN-CONTAINING PROTEIN 39", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24035", "l": "MULTIPLE EPIDERMAL GROWTH FACTOR-LIKE DOMAINS PROTEIN", "d": [], "t": []}], "preferred_name": "MULTIPLE EPIDERMAL GROWTH FACTOR-LIKE DOMAINS PROTEIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10110:SF90", "l": "SODIUM_HYDROGEN EXCHANGER 3", "d": [], "t": []}], "preferred_name": "SODIUM_HYDROGEN EXCHANGER 3", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12113:SF11", "l": "DICKKOPF-RELATED PROTEIN 1", "d": [], "t": []}], "preferred_name": "DICKKOPF-RELATED PROTEIN 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR47218", "l": "C-TYPE LECTIN DOMAIN FAMILY 7 MEMBER A", "d": [], "t": []}], "preferred_name": "C-TYPE LECTIN DOMAIN FAMILY 7 MEMBER A", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR22997:SF6", "l": "PIH1 DOMAIN-CONTAINING PROTEIN 2", "d": [], "t": []}], "preferred_name": "PIH1 DOMAIN-CONTAINING PROTEIN 2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR13544", "l": "SELENOPROTEIN T", "d": [], "t": []}], "preferred_name": "SELENOPROTEIN T", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24403:SF58", "l": "ZINC FINGER PROTEIN 462", "d": [], "t": []}], "preferred_name": "ZINC FINGER PROTEIN 462", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR31564:SF0", "l": "ANAPHASE-PROMOTING COMPLEX SUBUNIT 16", "d": [], "t": []}], "preferred_name": "ANAPHASE-PROMOTING COMPLEX SUBUNIT 16", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:19", "l": "Protocadherins", "d": ["The protocadherin (PCDH) gene family encodes proteins with an ectodomain comprising six or seven cadherin repeats with high sequence conservation within the family and weaker homology to the cadherin repeats of members of the major cadherin family. Further, protocadherins have a single transmembrane domain and a distinct, protocadherin-specific, cytoplasmic domain. Protocadherins can be further subdivided into clustered and non-clustered protocadherins on the basis of particular genomic organizations."], "t": []}], "preferred_name": "Protocadherins", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12768:SF5", "l": "BECLIN-2", "d": [], "t": []}], "preferred_name": "BECLIN-2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10662:SF12", "l": "NUCLEAR RNA EXPORT FACTOR 3", "d": [], "t": []}], "preferred_name": "NUCLEAR RNA EXPORT FACTOR 3", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12965:SF0", "l": "VACUOLAR PROTEIN SORTING-ASSOCIATED PROTEIN 54", "d": [], "t": []}], "preferred_name": "VACUOLAR PROTEIN SORTING-ASSOCIATED PROTEIN 54", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR28630:SF3", "l": "PEROXIREDOXIN-LIKE 2C", "d": [], "t": []}], "preferred_name": "PEROXIREDOXIN-LIKE 2C", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:1662", "l": "Inhibin subunits", "d": [], "t": []}], "preferred_name": "Inhibin subunits", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24300:SF409", "l": "CYTOCHROME P450 2A13", "d": [], "t": []}], "preferred_name": "CYTOCHROME P450 2A13", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR21072", "l": "GPI TRANSAMIDASE COMPONENT PIG-S", "d": [], "t": []}], "preferred_name": "GPI TRANSAMIDASE COMPONENT PIG-S", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11039:SF39", "l": "NEBULIN-RELATED-ANCHORING PROTEIN", "d": [], "t": []}], "preferred_name": "NEBULIN-RELATED-ANCHORING PROTEIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10857:SF6", "l": "COPINE-7", "d": [], "t": []}], "preferred_name": "COPINE-7", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24061:SF517", "l": "TASTE RECEPTOR TYPE 1 MEMBER 2", "d": [], "t": []}], "preferred_name": "TASTE RECEPTOR TYPE 1 MEMBER 2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24068:SF429", "l": "UBIQUITIN-CONJUGATING ENZYME E2 E2", "d": [], "t": []}], "preferred_name": "UBIQUITIN-CONJUGATING ENZYME E2 E2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR48018:SF147", "l": "OLFACTORY RECEPTOR 5M3", "d": [], "t": []}], "preferred_name": "OLFACTORY RECEPTOR 5M3", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24155", "l": "OSTEOCLAST-STIMULATING FACTOR 1", "d": [], "t": []}], "preferred_name": "OSTEOCLAST-STIMULATING FACTOR 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR21013:SF10", "l": "ATP SYNTHASE MITOCHONDRIAL F1 COMPLEX ASSEMBLY FACTOR 2", "d": [], "t": []}], "preferred_name": "ATP SYNTHASE MITOCHONDRIAL F1 COMPLEX ASSEMBLY FACTOR 2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:1051", "l": "Nucleoporins", "d": ["The nucleoporins are a family of proteins which are the constituent building blocks of the nuclear pore complex (NPC). The nuclear pore complex is a massive structure that extends across the nuclear envelope, forming a gateway that regulates the flow of macromolecules between the cell nucleus and the cytoplasm. Nuclear pores in turn allow the transport of water-soluble molecules across the nuclear envelope. Nucleoporins, a family of around 30 proteins, are the main components of the nuclear pore complex in eukaryotic cells. Nucleoporin 62 is the most abundant member of this family. Nucleoporins are able to transport molecules across the nuclear envelope at a very high rate. A single NPC is able to transport 60,000 protein molecules across the nuclear envelope every minute."], "t": []}], "preferred_name": "Nucleoporins", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11829:SF156", "l": "FORKHEAD BOX PROTEIN E3", "d": [], "t": []}], "preferred_name": "FORKHEAD BOX PROTEIN E3", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR21101:SF13", "l": "RESISTIN-LIKE BETA", "d": [], "t": []}], "preferred_name": "RESISTIN-LIKE BETA", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24061:SF5", "l": "G-PROTEIN COUPLED RECEPTOR FAMILY C GROUP 6 MEMBER A", "d": [], "t": []}], "preferred_name": "G-PROTEIN COUPLED RECEPTOR FAMILY C GROUP 6 MEMBER A", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:431", "l": "Exostosin glycosyltransferase family", "d": [], "t": []}], "preferred_name": 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"PANTHER.FAMILY:PTHR12192:SF26", "l": "GLUTATHIONE-SPECIFIC GAMMA-GLUTAMYLCYCLOTRANSFERASE 1", "d": [], "t": []}], "preferred_name": "GLUTATHIONE-SPECIFIC GAMMA-GLUTAMYLCYCLOTRANSFERASE 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR14454:SF6", "l": "GRB2-ASSOCIATED AND REGULATOR OF MAPK PROTEIN 1", "d": [], "t": []}], "preferred_name": "GRB2-ASSOCIATED AND REGULATOR OF MAPK PROTEIN 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11309:SF34", "l": "FRIZZLED-2", "d": [], "t": []}], "preferred_name": "FRIZZLED-2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR15955", "l": "RWD DOMAIN CONTAINING PROTEIN 2", "d": [], "t": []}], "preferred_name": "RWD DOMAIN CONTAINING PROTEIN 2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR23113:SF220", "l": "RAL GUANINE NUCLEOTIDE DISSOCIATION 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"preferred_name": "PROTEIN EFR3 HOMOLOG B", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR13869:SF3", "l": "SODIUM CHANNEL SUBUNIT BETA-2", "d": [], "t": []}], "preferred_name": "SODIUM CHANNEL SUBUNIT BETA-2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:1643", "l": "TNK family tyrosine kinases", "d": [], "t": []}], "preferred_name": "TNK family tyrosine kinases", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR46199:SF3", "l": "RAC GTPASE-ACTIVATING PROTEIN 1", "d": [], "t": []}], "preferred_name": "RAC GTPASE-ACTIVATING PROTEIN 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR23266:SF357", "l": "IMMUNOGLOBULIN HEAVY VARIABLE 3-11-RELATED", "d": [], "t": []}], "preferred_name": "IMMUNOGLOBULIN HEAVY VARIABLE 3-11-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR22957:SF686", "l": "GROWTH HORMONE-REGULATED TBC PROTEIN 1", "d": [], "t": []}], "preferred_name": "GROWTH HORMONE-REGULATED TBC PROTEIN 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24206:SF103", "l": "LIM DOMAIN-CONTAINING PROTEIN 2", "d": [], "t": []}], "preferred_name": "LIM DOMAIN-CONTAINING PROTEIN 2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR13798", "l": "RNA BINDING MOTIF RBM PROTEIN -RELATED", "d": [], "t": []}], "preferred_name": "RNA BINDING MOTIF RBM PROTEIN -RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR14949:SF27", "l": "EPIDERMAL GROWTH FACTOR-LIKE PROTEIN 8", "d": [], "t": []}], "preferred_name": "EPIDERMAL GROWTH FACTOR-LIKE PROTEIN 8", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR13117:SF5", "l": "PROTEIN 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In spite of the large variety of these proteins, however, the vast majority typically function as interaction modules that bind DNA, RNA, proteins, or other small, useful molecules, and variations in structure serve primarily to alter the binding specificity of a particular protein. Since their original discovery and the elucidation of their structure, these interaction modules have proven ubiquitous in the biological world. In addition, zinc fingers have become extremely useful in various therapeutic and research capacities. 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"PANTHER.FAMILY:PTHR10231:SF36", "l": "UDP-N-ACETYLGLUCOSAMINE TRANSPORTER", "d": [], "t": []}], "preferred_name": "UDP-N-ACETYLGLUCOSAMINE TRANSPORTER", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR14297:SF8", "l": "ENDOPLASMIC RETICULUM MEMBRANE ADAPTER PROTEIN XK", "d": [], "t": []}], "preferred_name": "ENDOPLASMIC RETICULUM MEMBRANE ADAPTER PROTEIN XK", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24416:SF370", "l": "HIGH AFFINITY NERVE GROWTH FACTOR RECEPTOR", "d": [], "t": []}], "preferred_name": "HIGH AFFINITY NERVE GROWTH FACTOR RECEPTOR", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR16228:SF22", "l": "SOLUTE CARRIER FAMILY 41 MEMBER 3", "d": [], "t": []}], "preferred_name": "SOLUTE CARRIER FAMILY 41 MEMBER 3", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24351:SF43", "l": 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"TUMOR NECROSIS FACTOR ALPHA-INDUCED PROTEIN 8", "d": [], "t": []}], "preferred_name": "TUMOR NECROSIS FACTOR ALPHA-INDUCED PROTEIN 8", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10502", "l": "ANNEXIN", "d": [], "t": []}], "preferred_name": "ANNEXIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR45653:SF6", "l": "DEDICATOR OF CYTOKINESIS PROTEIN 2", "d": [], "t": []}], "preferred_name": "DEDICATOR OF CYTOKINESIS PROTEIN 2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR23266:SF241", "l": "IMMUNOGLOBULIN HEAVY VARIABLE 3-30-RELATED", "d": [], "t": []}], "preferred_name": "IMMUNOGLOBULIN HEAVY VARIABLE 3-30-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR21141:SF5", "l": "LARGE RIBOSOMAL SUBUNIT PROTEIN P2", "d": [], "t": []}], "preferred_name": "LARGE RIBOSOMAL SUBUNIT 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"PANTHER.FAMILY:PTHR21043", "l": "IOJAP SUPERFAMILY ORTHOLOG", "d": [], "t": []}], "preferred_name": "IOJAP SUPERFAMILY ORTHOLOG", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR15146", "l": "INTEGRAL MEMBRANE PROTEIN GPR137", "d": [], "t": []}], "preferred_name": "INTEGRAL MEMBRANE PROTEIN GPR137", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR14097", "l": "OXIDOREDUCTASE HTATIP2", "d": [], "t": []}], "preferred_name": "OXIDOREDUCTASE HTATIP2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12669", "l": "EUKARYOTIC TRANSLATION INITIATION FACTOR 4E-BINDING PROTEIN", "d": [], "t": []}], "preferred_name": "EUKARYOTIC TRANSLATION INITIATION FACTOR 4E-BINDING PROTEIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24332", "l": "HOMEOBOX PROTEIN CDX", "d": [], "t": []}], "preferred_name": "HOMEOBOX PROTEIN CDX", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:1857", "l": "Tim17 family", "d": [], "t": []}], "preferred_name": "Tim17 family", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR46436", "l": "CENTROSOMAL PROTEIN OF 76 KDA", "d": [], "t": []}], "preferred_name": "CENTROSOMAL PROTEIN OF 76 KDA", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR21547:SF0", "l": "CLUSTERIN-ASSOCIATED PROTEIN 1", "d": [], "t": []}], "preferred_name": "CLUSTERIN-ASSOCIATED PROTEIN 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR23243:SF3", "l": "SUPRABASIN", "d": [], "t": []}], "preferred_name": "SUPRABASIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR44281:SF4", "l": "SPINDLE ASSEMBLY ABNORMAL PROTEIN 6 HOMOLOG", "d": [], "t": []}], 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Deficiencies are associated with several peroxisomal disorders. Numerous peroxin proteins serve several functions including the recognition of cytoplasmic proteins that contain peroxisomal targeting signals (PTS) that tag them for transport by peroxisomal proteins to the peroxisome."], "t": []}], "preferred_name": "Peroxins", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR45822", "l": "FREE FATTY ACID RECEPTOR 2-RELATED", "d": [], "t": []}], "preferred_name": "FREE FATTY ACID RECEPTOR 2-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR46257:SF4", "l": "TYROSINE-PROTEIN PHOSPHATASE NON-RECEPTOR TYPE 6", "d": [], "t": []}], "preferred_name": "TYROSINE-PROTEIN PHOSPHATASE NON-RECEPTOR TYPE 6", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24291:SF193", "l": "CYTOCHROME P450 4V2", "d": [], "t": []}], "preferred_name": "CYTOCHROME P450 4V2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, 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For example, each human cell has about 1.8 meters of DNA, (~6 ft) but wound on the histones it has about 90 micrometers (0.09�mm) of chromatin, which, when duplicated and condensed during mitosis, result in about 120 micrometers of chromosomes."], "t": []}], "preferred_name": "Histones", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:992", "l": "Histone deacetylases, class IIA", "d": [], "t": []}], "preferred_name": "Histone deacetylases, class IIA", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12035:SF127", "l": "SIALIC ACID-BINDING IG-LIKE LECTIN 11", "d": [], "t": []}], "preferred_name": "SIALIC ACID-BINDING IG-LIKE LECTIN 11", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24320:SF275", "l": "RETINOL DEHYDROGENASE 12", "d": [], "t": []}], "preferred_name": "RETINOL DEHYDROGENASE 12", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11792:SF19", "l": "ARRESTIN-C", "d": [], "t": []}], "preferred_name": "ARRESTIN-C", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11782:SF31", "l": "ECTONUCLEOSIDE TRIPHOSPHATE DIPHOSPHOHYDROLASE 8", "d": [], "t": []}], "preferred_name": "ECTONUCLEOSIDE TRIPHOSPHATE DIPHOSPHOHYDROLASE 8", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR28653:SF1", "l": "ATPASE SWSAP1", "d": [], "t": []}], "preferred_name": "ATPASE SWSAP1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24241:SF132", "l": "NEUROPEPTIDE FF RECEPTOR 2", "d": [], "t": []}], "preferred_name": "NEUROPEPTIDE FF RECEPTOR 2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR21008:SF0", "l": "S-ADENOSYLMETHIONINE SENSOR UPSTREAM OF MTORC1", "d": [], "t": []}], "preferred_name": "S-ADENOSYLMETHIONINE SENSOR UPSTREAM OF MTORC1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:1713", "l": "MicroRNA MIR130 family", "d": ["In molecular biology, miR-130 microRNA precursor is a small non-coding RNA that regulates gene expression. This microRNA has been identified in mouse (MI0000156, MI0000408), and in human (MI0000448, MI0000748). miR-130 appears to be vertebrate-specific miRNA and has now been predicted or experimentally confirmed in a range of vertebrate species (MIPF0000034). Mature microRNAs are processed from the precursor stem-loop by the Dicer enzyme. In this case, the mature sequence is excised from the 3' arm of the hairpin. It has been found that miR-130 is upregulated in a type of cancer called hepatocellular carcinoma. It has been shown that miR-130a is expressed in the hematopoietic stem/progenitor cell compartment but not in mature blood cells."], "t": []}], "preferred_name": "MicroRNA MIR130 family", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR23267:SF402", "l": "IMMUNOGLOBULIN KAPPA VARIABLE 1-39-RELATED", "d": [], "t": []}], "preferred_name": "IMMUNOGLOBULIN KAPPA VARIABLE 1-39-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR23267:SF499", "l": "IMMUNOGLOBULIN KAPPA VARIABLE 2-28-RELATED", "d": [], "t": []}], "preferred_name": "IMMUNOGLOBULIN KAPPA VARIABLE 2-28-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR26451:SF819", "l": "OLFACTORY RECEPTOR 12D3", "d": [], "t": []}], "preferred_name": "OLFACTORY RECEPTOR 12D3", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR43355", "l": "FLAVIN REDUCTASE (NADPH)", "d": [], "t": []}], "preferred_name": "FLAVIN REDUCTASE (NADPH)", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR48018:SF137", "l": "OLFACTORY RECEPTOR 8D4", "d": [], "t": []}], "preferred_name": "OLFACTORY RECEPTOR 8D4", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR46403:SF1", "l": "TP53-REGULATED INHIBITOR OF APOPTOSIS 1", "d": [], "t": []}], "preferred_name": "TP53-REGULATED INHIBITOR OF APOPTOSIS 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24381:SF153", "l": "ZINC FINGER PROTEIN 778", "d": [], "t": []}], "preferred_name": "ZINC FINGER PROTEIN 778", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR23245:SF25", "l": "TRNA WYBUTOSINE-SYNTHESIZING PROTEIN 2 HOMOLOG", "d": [], "t": []}], "preferred_name": "TRNA WYBUTOSINE-SYNTHESIZING PROTEIN 2 HOMOLOG", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR34914", "l": "LYMPHOCYTE EXPANSION MOLECULE", "d": [], "t": []}], "preferred_name": "LYMPHOCYTE EXPANSION MOLECULE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:1306", "l": "SIN3 histone deacetylase complex subunits", "d": ["Mammalian genomes encode two homologs of SIN3 (SIN3A/B), which associate individually with HDAC1 and HDAC2, RBBP4 and RBBP7, SDS3, and the SIN3-associated proteins SAP18 and SAP30 to form the core SIN3 complex. Different studies have identified additional interaction partners including MeCP2 (methyl-CpG-binding protein), RBP1 (RB-binding protein), BRMS1 (breast cancer metastasis suppressor), ING1/2 (inhibitor of growth), SAP25, SAP130, and SAP180, as well as the histone demethylase RBP2/KDM5A (Hayakawa and Nakayama, 2011 and Kadamb et al., 2013)."], "t": []}], "preferred_name": "SIN3 histone deacetylase complex subunits", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR21964:SF16", "l": "BREAST CANCER METASTASIS-SUPPRESSOR 1-LIKE PROTEIN", "d": [], "t": []}], "preferred_name": "BREAST CANCER METASTASIS-SUPPRESSOR 1-LIKE PROTEIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR28583", "l": "ACID AMIDASE", "d": [], "t": []}], "preferred_name": "ACID AMIDASE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR23317:SF78", "l": "DEDICATOR OF CYTOKINESIS PROTEIN 7", "d": [], "t": []}], "preferred_name": "DEDICATOR OF CYTOKINESIS PROTEIN 7", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24056:SF111", "l": "CYCLIN-DEPENDENT KINASE-LIKE 5", "d": [], "t": []}], "preferred_name": "CYCLIN-DEPENDENT KINASE-LIKE 5", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR15856", "l": "PHD FINGER PROTEIN 20-RELATED", "d": [], "t": []}], "preferred_name": "PHD FINGER PROTEIN 20-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR14716", "l": "CILIA- AND FLAGELLA-ASSOCIATED PROTEIN 69", "d": [], "t": []}], "preferred_name": "CILIA- AND FLAGELLA-ASSOCIATED PROTEIN 69", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10358", "l": "ENDOSULFINE", "d": [], "t": []}], "preferred_name": "ENDOSULFINE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10286", "l": "INORGANIC PYROPHOSPHATASE", "d": [], "t": []}], "preferred_name": "INORGANIC PYROPHOSPHATASE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR23268:SF95", "l": "T CELL RECEPTOR BETA VARIABLE 5-4", "d": [], "t": []}], "preferred_name": "T CELL RECEPTOR BETA VARIABLE 5-4", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR47695:SF5", "l": "DISABLED HOMOLOG 2", "d": [], "t": []}], "preferred_name": "DISABLED HOMOLOG 2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR22981:SF7", "l": "3-HYDROXYISOBUTYRATE DEHYDROGENASE, MITOCHONDRIAL", "d": [], "t": []}], "preferred_name": "3-HYDROXYISOBUTYRATE DEHYDROGENASE, MITOCHONDRIAL", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:613", "l": "Beaded filament structural proteins", "d": ["The beaded filament structural proteins are components of the cytoskeleton in the eye lens."], "t": []}], "preferred_name": "Beaded filament structural proteins", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR46789", "l": "FORKHEAD BOX PROTEIN R1", "d": [], "t": []}], "preferred_name": "FORKHEAD BOX PROTEIN R1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR21035", "l": "28S RIBOSOMAL PROTEIN S26, MITOCHONDRIAL", "d": [], "t": []}], "preferred_name": "28S RIBOSOMAL PROTEIN S26, MITOCHONDRIAL", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR43323", "l": "3-HYDROXY-3-METHYLGLUTARYL COENZYME A SYNTHASE", "d": [], "t": []}], "preferred_name": "3-HYDROXY-3-METHYLGLUTARYL COENZYME A SYNTHASE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR31195", "l": "GEO02494P1", "d": [], "t": []}], "preferred_name": "GEO02494P1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24384:SF131", "l": "ZINC FINGER PROTEIN 430", "d": [], "t": []}], "preferred_name": "ZINC FINGER PROTEIN 430", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR46260:SF1", "l": "KELCH DOMAIN-CONTAINING PROTEIN 8A", "d": [], "t": []}], "preferred_name": "KELCH DOMAIN-CONTAINING PROTEIN 8A", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:1354", "l": "Epidermal differentiation complex", "d": ["The epidermal differentiation complex ( EDC ) is a gene complex comprising over fifty genes encoding proteins involved in the terminal differentiation and cornification of keratinocytes, the primary cell type of the epidermis. In humans, the complex is located on a 1.9 Mbp stretch within chromosome 1q 21. The proteins encoded by EDC genes are closely related in terms of function, and evolutionarily they belong to three distinct gene families : the cornified envelope precursor family, the S100 protein family and the S100 fused type protein (SFTP) family. It has been hypothesized that the clustering of EDC genes occurred due to duplication events which were evolutionarily favored during the adaptation to terrestrial environments. EDC proteins have been involved in a variety of skin disorders including ichthyosis vulgaris, atopic dermatitis and psoriasis."], "t": []}], "preferred_name": "Epidermal differentiation complex", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12743:SF0", "l": "HOLOCYTOCHROME C-TYPE SYNTHASE", "d": [], "t": []}], "preferred_name": "HOLOCYTOCHROME C-TYPE SYNTHASE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10217", "l": "VOLTAGE AND LIGAND GATED POTASSIUM CHANNEL", "d": [], "t": []}], "preferred_name": "VOLTAGE AND LIGAND GATED POTASSIUM CHANNEL", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR14776:SF1", "l": "CADHERIN-LIKE AND PC-ESTERASE DOMAIN-CONTAINING PROTEIN 1", "d": [], "t": []}], "preferred_name": "CADHERIN-LIKE AND PC-ESTERASE DOMAIN-CONTAINING PROTEIN 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR43220:SF21", "l": "TRANSMEMBRANE PROTEIN 41A", "d": [], "t": []}], "preferred_name": "TRANSMEMBRANE PROTEIN 41A", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR47279", "l": "TRANSCRIPTION FACTOR SOX-30", "d": [], "t": []}], "preferred_name": "TRANSCRIPTION FACTOR SOX-30", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24377:SF143", "l": "ZINC FINGER PROTEIN 880", "d": [], "t": []}], "preferred_name": "ZINC FINGER PROTEIN 880", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11722:SF4", "l": "LARGE RIBOSOMAL SUBUNIT PROTEIN EL13", "d": [], "t": []}], "preferred_name": "LARGE RIBOSOMAL SUBUNIT PROTEIN EL13", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR15052:SF2", "l": "GENERAL TRANSCRIPTION FACTOR 3C POLYPEPTIDE 2", "d": [], "t": []}], "preferred_name": "GENERAL TRANSCRIPTION FACTOR 3C POLYPEPTIDE 2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24211", "l": "LIM DOMAIN-CONTAINING PROTEIN", "d": [], "t": []}], "preferred_name": "LIM DOMAIN-CONTAINING PROTEIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR16017", "l": "GASTRULATION DEFECTIVE PROTEIN 1-RELATED", "d": [], "t": []}], "preferred_name": "GASTRULATION DEFECTIVE PROTEIN 1-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR15528:SF12", "l": "PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR GAMMA COACTIVATOR 1-BETA", "d": [], "t": []}], "preferred_name": "PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR GAMMA COACTIVATOR 1-BETA", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR31690:SF4", "l": "FUCOSE MUTAROTASE", "d": [], "t": []}], "preferred_name": "FUCOSE MUTAROTASE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:1444", "l": "M28 metallopeptidases", "d": ["These genes encode zinc dependent metallopeptidases that require cocatalytic metal ions. 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{"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR23255:SF22", "l": "ACTIVIN RECEPTOR TYPE-1B", "d": [], "t": []}], "preferred_name": "ACTIVIN RECEPTOR TYPE-1B", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:461", "l": "Carboxylesterases", "d": ["In enzymology, a carboxylesterase or carboxylic-ester hydrolase ( EC 3.1.1.1 ) is an enzyme that catalyzes a chemical reaction of the form a carboxylic ester + H 2O an alcohol + a carboxylate Thus, the two substrates of this enzyme are carboxylic ester and H 2O, whereas its two products are alcohol and carboxylate."], "t": []}], "preferred_name": "Carboxylesterases", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR45716:SF6", "l": "SYNAPTOTAGMIN-LIKE PROTEIN 5", "d": [], "t": []}], "preferred_name": "SYNAPTOTAGMIN-LIKE PROTEIN 5", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12015:SF210", "l": "C-X-C MOTIF CHEMOKINE 9", "d": [], "t": []}], "preferred_name": "C-X-C MOTIF CHEMOKINE 9", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12247:SF20", "l": "POLYHOMEOTIC-LIKE PROTEIN 1", "d": [], "t": []}], "preferred_name": "POLYHOMEOTIC-LIKE PROTEIN 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR22710:SF2", "l": "X-RAY RADIATION RESISTANCE-ASSOCIATED PROTEIN 1", "d": [], "t": []}], "preferred_name": "X-RAY RADIATION RESISTANCE-ASSOCIATED PROTEIN 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12107:SF7", "l": "VOLTAGE-DEPENDENT CALCIUM CHANNEL GAMMA-4 SUBUNIT", "d": [], "t": []}], "preferred_name": "VOLTAGE-DEPENDENT CALCIUM CHANNEL GAMMA-4 SUBUNIT", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12241:SF91", "l": "TUBULIN POLYGLUTAMYLASE 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In humans, plasma kallikrein ( KLKB1 ) has no known homologue, while tissue kallikrein-related peptidases ( KLKs ) encode a family of fifteen closely related serine proteases. These genes are localised to chromosome 19q13, forming the largest contiguous cluster of proteases within the human genome. Kallikreins are responsible for the coordination of various physiological functions including blood pressure, semen liquefaction and skin desquamation."], "t": []}], "preferred_name": "Kallikreins", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR45620:SF2", "l": "CORTICOTROPIN-RELEASING FACTOR RECEPTOR 1", "d": [], "t": []}], "preferred_name": "CORTICOTROPIN-RELEASING FACTOR RECEPTOR 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12170:SF5", "l": "E3 UBIQUITIN-PROTEIN TRANSFERASE RMND5A", "d": [], "t": []}], "preferred_name": "E3 UBIQUITIN-PROTEIN TRANSFERASE RMND5A", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR15549", "l": "PAIRED IMMUNOGLOBULIN-LIKE TYPE 2 RECEPTOR", "d": [], "t": []}], "preferred_name": "PAIRED IMMUNOGLOBULIN-LIKE TYPE 2 RECEPTOR", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11267:SF98", "l": "T-BOX TRANSCRIPTION FACTOR TBX15", "d": [], "t": []}], "preferred_name": "T-BOX TRANSCRIPTION FACTOR TBX15", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR15813:SF10", "l": "SORTING NEXIN-24", "d": [], "t": []}], "preferred_name": "SORTING NEXIN-24", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR13088", "l": "FAS APOPTOTIC INHIBITORY MOLECULE FAIM", "d": [], "t": []}], "preferred_name": "FAS APOPTOTIC INHIBITORY MOLECULE FAIM", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR16055", "l": "INTEGRATOR COMPLEX SUBUNIT 10", "d": [], "t": []}], "preferred_name": "INTEGRATOR COMPLEX SUBUNIT 10", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR15854:SF4", "l": "PEROXYNITRITE ISOMERASE THAP4", "d": [], "t": []}], "preferred_name": "PEROXYNITRITE ISOMERASE THAP4", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11827:SF58", "l": "SOLUTE CARRIER FAMILY 12 MEMBER 2", "d": [], "t": []}], "preferred_name": "SOLUTE CARRIER FAMILY 12 MEMBER 2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR45690:SF19", "l": "NACHT, LRR AND PYD DOMAINS-CONTAINING PROTEIN 3", "d": [], "t": []}], "preferred_name": "NACHT, LRR AND PYD DOMAINS-CONTAINING PROTEIN 3", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10909:SF390", "l": "PEROXISOMAL ACYL-COENZYME A OXIDASE 3", "d": [], "t": []}], "preferred_name": "PEROXISOMAL ACYL-COENZYME A OXIDASE 3", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24376:SF69", "l": "ZINC FINGER PROTEIN 574", "d": [], "t": []}], "preferred_name": "ZINC FINGER PROTEIN 574", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR34994:SF1", "l": "PROTEIN FAM25A-RELATED", "d": [], "t": []}], "preferred_name": "PROTEIN FAM25A-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12066", "l": "TELOMERASE REVERSE TRANSCRIPTASE", "d": [], "t": []}], "preferred_name": "TELOMERASE REVERSE TRANSCRIPTASE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11875", "l": "TESTIS-SPECIFIC Y-ENCODED PROTEIN", "d": [], "t": []}], "preferred_name": "TESTIS-SPECIFIC Y-ENCODED PROTEIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR15496", "l": "GENERAL TRANSCRIPTION FACTOR 3C POLYPEPTIDE 4 FAMILY", "d": [], "t": []}], "preferred_name": "GENERAL TRANSCRIPTION FACTOR 3C POLYPEPTIDE 4 FAMILY", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR45624", "l": "MITOCHONDRIAL BASIC AMINO ACIDS TRANSPORTER-RELATED", "d": [], "t": []}], "preferred_name": "MITOCHONDRIAL BASIC AMINO ACIDS TRANSPORTER-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10424:SF78", "l": "ENDOGENOUS RETROVIRAL ENVELOPE PROTEIN HEMO", "d": [], "t": []}], "preferred_name": "ENDOGENOUS RETROVIRAL ENVELOPE PROTEIN HEMO", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:595", "l": "INO80 complex", "d": ["ATP-dependent nucleosome remodeling complex which slides mononucleosomes to a central position on a DNA template while tightly organizing nucleosomes within arrays. Functions in maintaining genome stability and removes H2AZ from nucleosomes. May play a largely repressive role in gene transcription, blocking H3K79 methylation and restricting transcription to gene units in euchromatin and away from silent regions, such as heterochromatin. Activates the expression of pluripotency factors by facilitating the recruitment of Mediator and Pol II at their promoters. Required for fork maintenance and progression in stalled replication forks. It is recruited to DNA damage sites and the ACTR8 subunit is required for this recruitment."], "t": []}], "preferred_name": "INO80 complex", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12305:SF81", "l": "PHOSPHATIDYLINOSITOL 3,4,5-TRISPHOSPHATE 3-PHOSPHATASE AND DUAL-SPECIFICITY PROTEIN PHOSPHATASE PTEN", "d": [], "t": []}], "preferred_name": "PHOSPHATIDYLINOSITOL 3,4,5-TRISPHOSPHATE 3-PHOSPHATASE AND DUAL-SPECIFICITY PROTEIN PHOSPHATASE PTEN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:1226", "l": "LY6/PLAUR domain containing", "d": [], "t": []}], "preferred_name": "LY6/PLAUR domain containing", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24113", "l": "RAN GTPASE-ACTIVATING PROTEIN 1", "d": [], "t": []}], "preferred_name": "RAN GTPASE-ACTIVATING PROTEIN 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR16083:SF11", "l": "LEUCINE-RICH REPEAT AND CALPONIN HOMOLOGY DOMAIN-CONTAINING PROTEIN 2", "d": [], "t": []}], "preferred_name": "LEUCINE-RICH REPEAT AND CALPONIN HOMOLOGY DOMAIN-CONTAINING PROTEIN 2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR31333", "l": "PWWP DOMAIN-CONTAINING DNA REPAIR FACTOR 3 FAMILY MEMBER", "d": [], "t": []}], "preferred_name": "PWWP DOMAIN-CONTAINING DNA REPAIR FACTOR 3 FAMILY MEMBER", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR48103:SF2", "l": "MIDASIN", "d": [], "t": []}], "preferred_name": "MIDASIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24355:SF15", "l": "G PROTEIN-COUPLED RECEPTOR KINASE 6", "d": [], "t": []}], "preferred_name": "G PROTEIN-COUPLED RECEPTOR KINASE 6", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR45711", "l": "CHLORIDE CHANNEL PROTEIN", "d": [], "t": []}], "preferred_name": "CHLORIDE CHANNEL PROTEIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12080:SF49", "l": "SIGNALING LYMPHOCYTIC ACTIVATION MOLECULE", "d": [], "t": []}], "preferred_name": "SIGNALING LYMPHOCYTIC ACTIVATION MOLECULE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10654:SF20", "l": "ENHANCER OF FILAMENTATION 1", "d": [], "t": []}], "preferred_name": "ENHANCER OF FILAMENTATION 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR45805:SF3", "l": "NUCLEAR RECEPTOR ROR-ALPHA", "d": [], "t": []}], "preferred_name": "NUCLEAR RECEPTOR ROR-ALPHA", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR17972", "l": "NUCLEOLAR RNA-ASSOCIATED PROTEIN", "d": [], "t": []}], "preferred_name": "NUCLEOLAR RNA-ASSOCIATED PROTEIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR48024:SF28", "l": "RNA-BINDING PROTEIN 38", "d": [], "t": []}], "preferred_name": "RNA-BINDING PROTEIN 38", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR22968:SF12", "l": "SERINE_THREONINE-PROTEIN KINASE D2", "d": [], "t": []}], "preferred_name": "SERINE_THREONINE-PROTEIN KINASE D2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR23288", "l": "OCCLUDIN AND RNA POLYMERASE II ELONGATION FACTOR ELL", "d": [], "t": []}], "preferred_name": "OCCLUDIN AND RNA POLYMERASE II ELONGATION FACTOR ELL", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR46568:SF1", "l": "ALKYLDIHYDROXYACETONEPHOSPHATE SYNTHASE, PEROXISOMAL", "d": [], "t": []}], "preferred_name": "ALKYLDIHYDROXYACETONEPHOSPHATE SYNTHASE, PEROXISOMAL", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10258:SF3", "l": "CALCIUM-ACTIVATED POTASSIUM CHANNEL SUBUNIT BETA-4", "d": [], "t": []}], "preferred_name": "CALCIUM-ACTIVATED POTASSIUM CHANNEL SUBUNIT BETA-4", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR28567:SF4", "l": "PROTEIN FAM53C", "d": [], "t": []}], "preferred_name": "PROTEIN FAM53C", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR43851", "l": "FAMILY NOT NAMED", "d": [], "t": []}], "preferred_name": "FAMILY NOT NAMED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:445", "l": "Oligosaccharyltransferase complex subunits", "d": ["Oligosaccharyltransferase or OST ( EC 2.4.1.119 ) is a membrane protein complex that transfers a 14- sugar oligosaccharide from dolichol to nascent protein. It is a type of glycosyltransferase. The sugar Glc 3Man 9GlcNAc 2 (where Glc= Glucose, Man= Mannose, and GlcNAc= N-acetylglucosamine ) is attached to an asparagine (Asn) residue in the sequence Asn-X- Ser or Asn-X- Thr where X is any amino acid except proline. This sequence is called a glycosylation sequon. The reaction catalyzed by OST is the central step in the N -linked glycosylation pathway."], "t": []}], "preferred_name": "Oligosaccharyltransferase complex subunits", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:2049", "l": "Tet methylcytosine dioxygenase family", "d": [], "t": []}], "preferred_name": "Tet methylcytosine dioxygenase family", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR34491:SF173", "l": "CENTRIOLIN", "d": [], "t": []}], "preferred_name": "CENTRIOLIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR16148", "l": "NF-KAPPA-B-REPRESSING FACTOR-RELATED", "d": [], "t": []}], "preferred_name": "NF-KAPPA-B-REPRESSING FACTOR-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11524:SF13", "l": "RIBOSOMAL PROTEIN UL30-LIKE", "d": [], "t": []}], "preferred_name": "RIBOSOMAL 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"4'-PHOSPHOPANTETHEINE PHOSPHATASE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR23147:SF80", "l": "RNA-BINDING PROTEIN 4B", "d": [], "t": []}], "preferred_name": "RNA-BINDING PROTEIN 4B", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12496:SF2", "l": "METHYLTRANSFERASE-LIKE PROTEIN 25B", "d": [], "t": []}], "preferred_name": "METHYLTRANSFERASE-LIKE PROTEIN 25B", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR16108:SF2", "l": "TRANSMEMBRANE PROTEIN 40", "d": [], "t": []}], "preferred_name": "TRANSMEMBRANE PROTEIN 40", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24652", "l": "LOW-DENSITY LIPOPROTEIN RECEPTOR CLASS A DOMAIN-CONTAINING PROTEIN 2", "d": [], "t": []}], "preferred_name": "LOW-DENSITY LIPOPROTEIN RECEPTOR CLASS A DOMAIN-CONTAINING PROTEIN 2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR23308", "l": "NUCLEAR INHIBITOR OF PROTEIN PHOSPHATASE-1", "d": [], "t": []}], "preferred_name": "NUCLEAR INHIBITOR OF PROTEIN PHOSPHATASE-1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR46232", "l": "SMARCE1 REGULATOR OF CHROMATIN", "d": [], "t": []}], "preferred_name": "SMARCE1 REGULATOR OF CHROMATIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR13680:SF42", "l": "CDGSH IRON-SULFUR DOMAIN-CONTAINING PROTEIN 1", "d": [], "t": []}], "preferred_name": "CDGSH IRON-SULFUR DOMAIN-CONTAINING PROTEIN 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR31179", "l": "RAB GTPASE-BINDING EFFECTOR PROTEIN", "d": [], "t": []}], "preferred_name": "RAB GTPASE-BINDING EFFECTOR PROTEIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR26453:SF50", "l": "OLFACTORY RECEPTOR 2A12", "d": [], "t": []}], "preferred_name": "OLFACTORY RECEPTOR 2A12", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR14248:SF32", "l": "CYCLIN-Y-LIKE PROTEIN 1", "d": [], "t": []}], "preferred_name": "CYCLIN-Y-LIKE PROTEIN 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10250:SF2", "l": "ARACHIDONATE 5-LIPOXYGENASE-ACTIVATING PROTEIN", "d": [], "t": []}], "preferred_name": "ARACHIDONATE 5-LIPOXYGENASE-ACTIVATING PROTEIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11318", "l": "GUANYLIN FAMILY MEMBER", "d": [], "t": []}], "preferred_name": "GUANYLIN FAMILY MEMBER", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR48002:SF112", "l": "OLFACTORY RECEPTOR 4Q3", "d": [], "t": []}], "preferred_name": "OLFACTORY RECEPTOR 4Q3", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12550", "l": "HEPATOMA-DERIVED GROWTH FACTOR-RELATED", "d": [], "t": []}], "preferred_name": "HEPATOMA-DERIVED GROWTH FACTOR-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11532:SF48", "l": "ADIPOCYTE ENHANCER-BINDING PROTEIN 1", "d": [], "t": []}], "preferred_name": "ADIPOCYTE ENHANCER-BINDING PROTEIN 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11707", "l": "L-ASPARAGINASE", "d": [], "t": []}], "preferred_name": "L-ASPARAGINASE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR31548:SF5", "l": "CLARIN-2", "d": [], "t": []}], "preferred_name": "CLARIN-2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR35347", "l": "COILED-COIL DOMAIN-CONTAINING PROTEIN 175", "d": [], "t": []}], "preferred_name": "COILED-COIL DOMAIN-CONTAINING PROTEIN 175", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24388:SF71", "l": "ZINC FINGER AND BTB DOMAIN-CONTAINING PROTEIN 38", "d": [], "t": []}], "preferred_name": "ZINC FINGER AND BTB DOMAIN-CONTAINING PROTEIN 38", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR48033:SF3", "l": "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN D0", "d": [], "t": []}], "preferred_name": "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN D0", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11437:SF4", "l": "RIBONUCLEASE K6", "d": [], "t": []}], "preferred_name": "RIBONUCLEASE K6", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:1338", "l": "Chromosomal passenger complex", "d": [], "t": []}], "preferred_name": "Chromosomal passenger complex", "taxa": []} {"type": 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Loss of functional miR-146 (and mir-145) could predispose an individual to suffer from chromosome 5q deletion syndrome. miR-146 has also been reported to be highly upregulated in osteoarthritis cartilage, and could be involved in its pathogenesis. mir-146 expression is associated with survival in triple negative breast cancer."], "t": []}], "preferred_name": "MicroRNA MIR146 family", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR15706:SF6", "l": "NEUTROPHIL CYTOSOL FACTOR 1-RELATED", "d": [], "t": []}], "preferred_name": "NEUTROPHIL CYTOSOL FACTOR 1-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR46252", "l": "BRORIN FAMILY MEMBER", "d": [], "t": []}], "preferred_name": "BRORIN FAMILY MEMBER", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR35255", "l": "TRANSMEMBRANE PROTEIN 71", "d": [], "t": []}], "preferred_name": "TRANSMEMBRANE PROTEIN 71", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12893", "l": "GOLGI REASSEMBLY STACKING PROTEIN GRASP", "d": [], "t": []}], "preferred_name": "GOLGI REASSEMBLY STACKING PROTEIN GRASP", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR21621:SF5", "l": "BETA-CITRYLGLUTAMATE SYNTHASE B", "d": [], "t": []}], "preferred_name": "BETA-CITRYLGLUTAMATE SYNTHASE B", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12876", "l": "N4BP1-RELATED", "d": [], "t": []}], "preferred_name": "N4BP1-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11394:SF27", "l": "TASTE RECEPTOR TYPE 2 MEMBER 20", "d": [], "t": []}], "preferred_name": "TASTE RECEPTOR TYPE 2 MEMBER 20", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR13110:SF15", "l": "U6 SNRNA-ASSOCIATED SM-LIKE PROTEIN LSM3", "d": [], "t": []}], "preferred_name": "U6 SNRNA-ASSOCIATED SM-LIKE PROTEIN LSM3", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24117", "l": "AGAP007537-PB", "d": [], "t": []}], "preferred_name": "AGAP007537-PB", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR47266:SF6", "l": "GYPSY RETROTRANSPOSON INTEGRASE-LIKE PROTEIN 1", "d": [], "t": []}], "preferred_name": "GYPSY RETROTRANSPOSON INTEGRASE-LIKE PROTEIN 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11960:SF3", "l": "EUKARYOTIC TRANSLATION INITIATION FACTOR 4E TYPE 1B", "d": [], "t": []}], "preferred_name": "EUKARYOTIC TRANSLATION INITIATION FACTOR 4E TYPE 1B", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:1752", "l": "IPT domain containing", "d": ["The IPT (Ig-like, plexins, transcription factors) domain has an immunoglobulin like fold. 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Lipocalins have been associated with many biological processes, among them immune response, pheromone transport, biological prostaglandin synthesis, retinoid binding, and cancer cell interactions."], "t": []}], "preferred_name": "Lipocalins", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24293:SF1", "l": "CHOLESTEROL 24-HYDROXYLASE", "d": [], "t": []}], "preferred_name": "CHOLESTEROL 24-HYDROXYLASE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR21636:SF2", "l": "PROTEIN DOK-7", "d": [], "t": []}], "preferred_name": "PROTEIN DOK-7", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR46462:SF1", "l": "HISTONE-LYSINE N-METHYLTRANSFERASE SETD5", "d": [], "t": []}], "preferred_name": "HISTONE-LYSINE N-METHYLTRANSFERASE SETD5", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:418", "l": "AT-rich interaction domain containing", "d": ["In molecular biology, the ARID domain (AT-rich interaction domain; also known as BRIGHT domain)) is a protein domain that binds to DNA. ARID domain-containing proteins are found in fungi and invertebrate and vertebrate metazoans. ARID-encoding genes are involved in a variety of biological processes including embryonic development, cell lineage gene regulation and cell cycle control. Although the specific roles of this domain and of ARID-containing proteins in transcriptional regulation are yet to be elucidated, they include both positive and negative transcriptional regulation and a likely involvement in the modification of chromatin structure. The basic structure of the ARID domain appears to be a series of six alpha-helices separated by beta-strands, loops, or turns, but the structured region may extend to an additional helix at either or both ends of the basic six. Based on primary sequence homology, they can be partitioned into three structural classes: Minimal ARID proteins that consist of a core domain formed by six alpha helices; ARID proteins that supplement the core domain with an N-terminal alpha-helix; and Extended-ARID proteins, which contain the core domain and additional alpha-helices at their N- and C-termini."], "t": []}], "preferred_name": "AT-rich interaction domain containing", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR14554:SF1", "l": "CHROMOSOME 11 OPEN READING FRAME 98", "d": [], "t": []}], "preferred_name": "CHROMOSOME 11 OPEN READING FRAME 98", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR46052:SF3", "l": "PHOSDUCIN", "d": [], "t": []}], "preferred_name": "PHOSDUCIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR37000", "l": "MUCIN-22", "d": [], "t": []}], 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Together with a number of accessory proteins, these ESCRT complexes enable a unique mode of membrane remodeling that results in membranes bending/budding away from the cytoplasm. These ESCRT components have been isolated and studied in a number of organisms including yeast and humans. The ESCRT machinery plays a vital role in a number of cellular processes including multivesicular body (MVB) biogenesis, cellular abscission, and viral budding. Multivesicular body (MVB) biogenesis is a process in which ubiquitin tagged proteins enter organelles called endosomes via the formation of vesicles. This process is essential for cells to destroy misfolded and damaged proteins. Without ESCRT machinery, these proteins can build up and lead to neurodegenerative disease. For example, abnormalities in ESCRT-III components can lead to neurological disorders such as hereditary spastic paraplegia (HSP). Cellular abscission, the process by which the membrane connecting two daughter cells is cleaved, is also mediated by ESCRT machinery. Without the ESCRT complexes, daughter cells could not separate and abnormal cells containing twice the amount of DNA would be generated. These cells would inevitably be destroyed through a process known as apoptosis. Lastly, viral budding, or the process by which specific types of viruses exit cells, may not occur in the absence of ESCRT machinery. 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Many FOX proteins are important to embryonic development. FOX proteins also have pioneering transcription activity by being able to bind condensed chromatin during cell differentiation processes. The defining feature of FOX proteins is the forkhead box, a sequence of 80 to 100 amino acids forming a motif that binds to DNA. This forkhead motif is also known as the winged helix due to the butterfly-like appearance of the loops in the protein structure of the domain. 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Proteins containing BIR are known as inhibitor of apoptosis proteins (IAPs), or BIR-containing proteins (BIRPs or BIRCs), and include BIRC1 (NAIP), BIRC2 (cIAP1), BIRC3 (cIAP2), BIRC4 (xIAP), BIRC5 (survivin) and BIRC6. BIR domains belong to the zinc-finger domain family and characteristically have a number of invariant amino acid residues, including 3 conserved cysteines and one conserved histidine, which coordinate a zinc ion. They are typically composed of 4-5 alpha helices and a three-stranded beta sheet."], "t": []}], "preferred_name": "Baculoviral IAP repeat containing", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR13493", "l": "ZINC FINGER CCHC DOMAIN-CONTAINING", "d": [], "t": []}], "preferred_name": "ZINC FINGER CCHC DOMAIN-CONTAINING", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24243:SF3", "l": "MOTILIN RECEPTOR", "d": [], "t": []}], "preferred_name": "MOTILIN RECEPTOR", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11132:SF238", "l": "SOLUTE CARRIER FAMILY 35 MEMBER C2", "d": [], "t": []}], "preferred_name": "SOLUTE CARRIER FAMILY 35 MEMBER C2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR28645", "l": "TRANSMEMBRANE PROTEIN 119", "d": [], "t": []}], "preferred_name": "TRANSMEMBRANE PROTEIN 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"preferred_name": "OLFACTORY RECEPTOR 6C68", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR46513:SF43", "l": "LOW-DENSITY LIPOPROTEIN RECEPTOR-RELATED PROTEIN 5-LIKE PROTEIN", "d": [], "t": []}], "preferred_name": "LOW-DENSITY LIPOPROTEIN RECEPTOR-RELATED PROTEIN 5-LIKE PROTEIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10527:SF17", "l": "TRANSPORTIN-2", "d": [], "t": []}], "preferred_name": "TRANSPORTIN-2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11505:SF217", "l": "LINE-1 RETROTRANSPOSABLE ELEMENT ORF1 PROTEIN", "d": [], "t": []}], "preferred_name": "LINE-1 RETROTRANSPOSABLE ELEMENT ORF1 PROTEIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR47387", "l": "NECTIN-2", "d": [], "t": []}], "preferred_name": "NECTIN-2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, 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"PANTHER.FAMILY:PTHR35355", "l": "PROTEIN FAM229A", "d": [], "t": []}], "preferred_name": "PROTEIN FAM229A", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR17388:SF2", "l": "SECRETOGRANIN-3", "d": [], "t": []}], "preferred_name": "SECRETOGRANIN-3", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11346:SF21", "l": "GRIFIN", "d": [], "t": []}], "preferred_name": "GRIFIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR21646:SF76", "l": "UBIQUITIN CARBOXYL-TERMINAL HYDROLASE 32", "d": [], "t": []}], "preferred_name": "UBIQUITIN CARBOXYL-TERMINAL HYDROLASE 32", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR31831:SF1", "l": "RIKEN CDNA 2010003K11 GENE", "d": [], "t": []}], "preferred_name": "RIKEN CDNA 2010003K11 GENE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR43128:SF10", "l": "L-LACTATE DEHYDROGENASE A CHAIN", "d": [], "t": []}], "preferred_name": "L-LACTATE DEHYDROGENASE A CHAIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR22798", "l": "MCT-1 PROTEIN", "d": [], "t": []}], "preferred_name": "MCT-1 PROTEIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR45618:SF20", "l": "BRAIN MITOCHONDRIAL CARRIER PROTEIN 1", "d": [], "t": []}], "preferred_name": "BRAIN MITOCHONDRIAL CARRIER PROTEIN 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR15116:SF14", "l": "DNA-BINDING PROTEIN SATB1", "d": [], "t": []}], "preferred_name": "DNA-BINDING PROTEIN SATB1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12533:SF11", "l": "NUCLEAR FACTOR OF ACTIVATED T-CELLS, CYTOPLASMIC 4", "d": [], "t": []}], "preferred_name": "NUCLEAR 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[]} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12831:SF0", "l": "GENERAL TRANSCRIPTION FACTOR IIH SUBUNIT 3", "d": [], "t": []}], "preferred_name": "GENERAL TRANSCRIPTION FACTOR IIH SUBUNIT 3", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR33724", "l": "INTRAFLAGELLAR TRANSPORT PROTEIN 43 HOMOLOG", "d": [], "t": []}], "preferred_name": "INTRAFLAGELLAR TRANSPORT PROTEIN 43 HOMOLOG", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12383", "l": "PROTEASE FAMILY S26 MITOCHONDRIAL INNER MEMBRANE PROTEASE-RELATED", "d": [], "t": []}], "preferred_name": "PROTEASE FAMILY S26 MITOCHONDRIAL INNER MEMBRANE PROTEASE-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11738:SF186", "l": "OSTEOCLAST-ASSOCIATED IMMUNOGLOBULIN-LIKE RECEPTOR", "d": [], "t": []}], "preferred_name": "OSTEOCLAST-ASSOCIATED 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{"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:1556", "l": "Retriever complex", "d": [], "t": []}], "preferred_name": "Retriever complex", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR46536", "l": "ARL14 EFFECTOR PROTEIN", "d": [], "t": []}], "preferred_name": "ARL14 EFFECTOR PROTEIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR23073:SF76", "l": "26S PROTEASOME REGULATORY SUBUNIT 10B", "d": [], "t": []}], "preferred_name": "26S PROTEASOME REGULATORY SUBUNIT 10B", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR48018:SF32", "l": "OLFACTORY RECEPTOR 5L1", "d": [], "t": []}], "preferred_name": "OLFACTORY RECEPTOR 5L1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR15708", "l": "ACTIN BUNDLING/MISSING IN METASTASIS-RELATED", "d": [], "t": []}], 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The main difference between tyrosine-specific phosphatases and dual-specificity phosphatases lies in the width of the latter enzymes' catalytic pocket: thus they can accommodate phosphorylated serine or threonine side chains as well as phosphorylated tyrosines."], "t": []}], "preferred_name": "Dual specificity phosphatases", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR15948", "l": "G-PROTEIN COUPLED RECEPTOR 89-RELATED", "d": [], "t": []}], "preferred_name": "G-PROTEIN COUPLED RECEPTOR 89-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR31743:SF1", "l": "SHORT TRANSIENT RECEPTOR POTENTIAL CHANNEL 4-ASSOCIATED PROTEIN", "d": [], "t": []}], "preferred_name": "SHORT TRANSIENT RECEPTOR POTENTIAL CHANNEL 4-ASSOCIATED PROTEIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR13817:SF17", "l": "MYOSIN-BINDING PROTEIN C, FAST-TYPE", 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"preferred_name": "FIBRONECTIN TYPE III DOMAIN-CONTAINING PROTEIN 3B", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR43826:SF3", "l": "GLUCOSE-6-PHOSPHATE EXCHANGER SLC37A4", "d": [], "t": []}], "preferred_name": "GLUCOSE-6-PHOSPHATE EXCHANGER SLC37A4", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11528:SF79", "l": "HEAT SHOCK PROTEIN HSP 90-BETA", "d": [], "t": []}], "preferred_name": "HEAT SHOCK PROTEIN HSP 90-BETA", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR31433", "l": "PX DOMAIN-CONTAINING PROTEIN 1", "d": [], "t": []}], "preferred_name": "PX DOMAIN-CONTAINING PROTEIN 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:3475", "l": "Glutathione peroxidase family", "d": ["Glutathione peroxidases are enzymes that catalyse the reduction of H2O2 or organic hydroperoxides to water or the 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MAP kinases are found in eukaryotes only, but they are fairly diverse and encountered in all animals, fungi and plants, and even in an array of unicellular eukaryotes."], "t": []}], "preferred_name": "Mitogen-activated protein kinases", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR34529:SF1", "l": "AP-1 COMPLEX-ASSOCIATED REGULATORY PROTEIN", "d": [], "t": []}], "preferred_name": "AP-1 COMPLEX-ASSOCIATED REGULATORY PROTEIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR23074:SF33", "l": "FIDGETIN-LIKE PROTEIN 2", "d": [], "t": []}], "preferred_name": "FIDGETIN-LIKE PROTEIN 2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR37866", "l": "PRE T-CELL ANTIGEN RECEPTOR ALPHA", "d": [], "t": []}], "preferred_name": "PRE T-CELL ANTIGEN RECEPTOR ALPHA", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR28680:SF1", "l": "CENTROMERE PROTEIN X", "d": [], "t": []}], "preferred_name": "CENTROMERE PROTEIN X", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR15544:SF0", "l": "TETRATRICOPEPTIDE REPEAT PROTEIN 33", "d": [], "t": []}], "preferred_name": "TETRATRICOPEPTIDE REPEAT PROTEIN 33", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR45706:SF7", "l": "TYROSINE-PROTEIN PHOSPHATASE NON-RECEPTOR TYPE 4", "d": [], "t": []}], "preferred_name": "TYROSINE-PROTEIN PHOSPHATASE NON-RECEPTOR TYPE 4", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR31488:SF6", "l": "C-MANNOSYLTRANSFERASE DPY19L2-RELATED", "d": [], "t": []}], "preferred_name": "C-MANNOSYLTRANSFERASE DPY19L2-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:249", "l": "Transient receptor potential cation channels", "d": ["Transient receptor potential channels (TRP channels) are a group of ion channels located mostly on the plasma membrane of numerous human and animal cell types. 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Many tannin -consuming animals secrete a tannin-binding protein ( mucin ) in their saliva. Tannin-binding capacity of salivary mucin is directly related to its proline content. Advantages in using salivary proline-rich proteins (PRPs) to inactivate tannins are: PRPs inactivate tannins to a greater extent than do dietary proteins; this results in reduced fecal nitrogen losses, PRPs contain non specific nitrogen and nonessential amino acids; this makes them more convenient for an animal to exploit rather than using up valuable dietary protein. An example of this class of protein is IB5, a human parotid salivary protein known to bind with polyphenols (binding responsible for the astringency mouth feel)."], "t": []}], "preferred_name": "Proline rich proteins", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:1455", "l": "Ferritin chains", "d": ["Ferritin is a universal intracellular protein that stores iron and releases it in a controlled fashion. 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Ferritin that is not combined with iron is called apoferritin."], "t": []}], "preferred_name": "Ferritin chains", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR31954", "l": "CILIA- AND FLAGELLA-ASSOCIATED PROTEIN 157", "d": [], "t": []}], "preferred_name": "CILIA- AND FLAGELLA-ASSOCIATED PROTEIN 157", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR22599:SF12", "l": "MOB KINASE ACTIVATOR 3C", "d": [], "t": []}], "preferred_name": "MOB KINASE ACTIVATOR 3C", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11157:SF118", "l": "ELONGATION OF VERY LONG CHAIN FATTY ACIDS PROTEIN 7", "d": [], "t": []}], "preferred_name": "ELONGATION OF VERY LONG CHAIN FATTY ACIDS PROTEIN 7", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12763:SF56", "l": "MITOCHONDRIAL IMPORT INNER MEMBRANE TRANSLOCASE SUBUNIT TIM14", "d": [], "t": []}], "preferred_name": "MITOCHONDRIAL IMPORT INNER MEMBRANE TRANSLOCASE SUBUNIT TIM14", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR45616:SF52", "l": "KERATIN, TYPE II CUTICULAR HB3", "d": [], "t": []}], "preferred_name": "KERATIN, TYPE II CUTICULAR HB3", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11972", "l": "NADPH OXIDASE", "d": [], "t": []}], "preferred_name": "NADPH OXIDASE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR19971:SF9", "l": "SIGNAL-REGULATORY PROTEIN BETA-2", "d": [], "t": []}], "preferred_name": "SIGNAL-REGULATORY PROTEIN BETA-2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12771:SF2", "l": "ELMO DOMAIN-CONTAINING PROTEIN 3", "d": [], "t": []}], "preferred_name": "ELMO DOMAIN-CONTAINING PROTEIN 3", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR15036:SF43", "l": "CONTACTIN-ASSOCIATED PROTEIN 1", "d": [], "t": []}], "preferred_name": "CONTACTIN-ASSOCIATED PROTEIN 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR22974:SF20", "l": "SERINE_THREONINE-PROTEIN KINASE TOUSLED-LIKE 2", "d": [], "t": []}], "preferred_name": "SERINE_THREONINE-PROTEIN KINASE TOUSLED-LIKE 2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:1736", "l": "MicroRNA MIR7 family", "d": [], "t": []}], "preferred_name": "MicroRNA MIR7 family", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR14402:SF8", "l": "RECEPTOR-TRANSPORTING PROTEIN 4", "d": [], "t": []}], "preferred_name": "RECEPTOR-TRANSPORTING PROTEIN 4", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR23232:SF69", "l": "ZINC FINGER PROTEIN 688", "d": [], "t": []}], "preferred_name": "ZINC FINGER PROTEIN 688", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24056:SF241", "l": "CYCLIN-DEPENDENT KINASE-LIKE 2", "d": [], "t": []}], "preferred_name": "CYCLIN-DEPENDENT KINASE-LIKE 2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11267:SF83", "l": "T-BOX TRANSCRIPTION FACTOR T", "d": [], "t": []}], "preferred_name": "T-BOX TRANSCRIPTION FACTOR T", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR19818:SF167", "l": "ZINC FINGER PROTEIN ZIC 4", "d": [], "t": []}], "preferred_name": "ZINC FINGER PROTEIN ZIC 4", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24253:SF64", "l": "PLASMA KALLIKREIN", "d": [], "t": []}], "preferred_name": "PLASMA KALLIKREIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR23210:SF23", "l": "ACTIVATING TRANSCRIPTION FACTOR 7-INTERACTING PROTEIN 2", "d": [], "t": []}], "preferred_name": "ACTIVATING TRANSCRIPTION FACTOR 7-INTERACTING PROTEIN 2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12011:SF216", "l": "ADHESION G-PROTEIN COUPLED RECEPTOR D1", "d": [], "t": []}], "preferred_name": "ADHESION G-PROTEIN COUPLED RECEPTOR D1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24404:SF41", "l": "ZINC FINGER PROTEIN 613", "d": [], "t": []}], "preferred_name": "ZINC FINGER PROTEIN 613", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:956", "l": "Prefoldin subunits", "d": ["Prefoldin is a family of proteins used in protein folding complexes. It is classified as a heterohexameric molecular chaperone in both archaea and eukarya, including humans. A prefoldin molecule works as a transfer protein in conjunction with a molecule of chaperonin to form a chaperone complex and correctly fold other nascent proteins. 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The presence of the proteins bound to a pre-mRNA molecule serves as a signal that the pre-mRNA is not yet fully processed and therefore not ready for export to the cytoplasm. Since most mature RNA is exported from the nucleus relatively quickly, most RNA-binding protein in the nucleus exist as heterogeneous ribonucleoprotein particles. After splicing has occurred, the proteins remain bound to spliced introns and target them for degradation. hnRNPs are also integral to the 40s subunit of the ribosome and therefore important for the translation of mRNA in the cytoplasm. However, hnRNPs also have their own nuclear localization sequences (NLS) and are therefore found mainly in the nucleus. Though it is known that a few hnRNPs shuttle between the cytoplasm and nucleus, immunofluorescence microscopy with hnRNP-specific antibodies shows nucleoplasmic localization of these proteins with little staining in the nucleolus or cytoplasm. This is likely because of its major role in binding to newly transcribed RNAs. High-resolution immunoelectron microscopy has shown that hnRNPs localize predominantly to the border regions of chromatin, where it has access to these nascent RNAs.The proteins involved in the hnRNP complexes are collectively known as heterogeneous ribonucleoproteins. They include protein K and polypyrimidine tract-binding protein (PTB), which is regulated by phosphorylation catalyzed by protein kinase A and is responsible for suppressing RNA splicing at a particular exon by blocking access of the spliceosome to the polypyrimidine tract. hnRNPs are also responsible for strengthening and inhibiting splice sites by making such sites more or less accessible to the spliceosome. 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vertebrate and invertebrate animals. 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It is the last enzyme in the respiratory electron transport chain of mitochondria (or bacteria) located in the mitochondrial (or bacterial) membrane. It receives an electron from each of four cytochrome c molecules, and transfers them to one oxygen molecule, converting molecular oxygen to two molecules of water. In the process, it binds four protons from the inner aqueous phase to make water, and in addition translocates four protons across the membrane, helping to establish a transmembrane difference of proton electrochemical potential that the ATP synthase then uses to synthesize ATP."], "t": []}], "preferred_name": "Mitochondrial complex IV: cytochrome c oxidase subunits", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:467", "l": "Phospholipases", "d": ["A phospholipase is an enzyme that hydrolyzes phospholipids into fatty acids and other lipophilic substances. There are four major classes, termed A, B, C and D, distinguished by the type of reaction which they catalyze: Phospholipase A Phospholipase A1 - cleaves the SN-1 acyl chain. Phospholipase A2 - cleaves the SN-2 acyl chain, releasing arachidonic acid. Phospholipase B - cleaves both SN-1 and SN-2 acyl chains ; this enzyme is also known as a lysophospholipase. Phospholipase C - cleaves before the phosphate, releasing diacylglycerol and a phosphate-containing head group. Phospholipase Cs play a central role in signal transduction, releasing the second messenger inositol triphosphate. Phospholipase D - cleaves after the phosphate, releasing phosphatidic acid and an alcohol. Types C and D are considered phosphodiesterases. Phospholipase A2 acts on the intact lecithin molecule and hydrolyses the fatty acid esterified to the second carbon atom. The resulting products are lysolecithin and a fatty acid. 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implicated in the regulation of neurotransmitter release at synapses. Specifically, they are thought to be involved in regulating the number of synaptic vesicles available for release via exocytosis at any one time. Synapsins are present in invertebrates and vertebrates and are somewhat homologous across evaluated vertebrates. Current studies suggest the following hypothesis for the role of synapsin: synapsins bind synaptic vesicles to components of the cytoskeleton which prevents them from migrating to the presynaptic membrane and releasing neurotransmitter. During an action potential, synapsins are phosphorylated by PKA (cAMP dependent protein kinase), releasing the synaptic vesicles and allowing them to move to the membrane and release their neurotransmitter. Gene knockout studies in mice (where the mouse is unable to produce synapsin) have had some surprising results. Mice lacking all three synapsins are prone to seizures, and experience learning defects. These results suggest that while synapsins are not essential for synaptic function, they do serve an important modulatory role. 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"CYSTATIN", "d": [], "t": []}], "preferred_name": "CYSTATIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12794", "l": "GEMIN2", "d": [], "t": []}], "preferred_name": "GEMIN2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24410:SF16", "l": "GALECTIN-3-BINDING PROTEIN", "d": [], "t": []}], "preferred_name": "GALECTIN-3-BINDING PROTEIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24393:SF56", "l": "ZINC FINGER PROTEIN 784", "d": [], "t": []}], "preferred_name": "ZINC FINGER PROTEIN 784", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11086", "l": "DEOXYCYTIDYLATE DEAMINASE-RELATED", "d": [], "t": []}], "preferred_name": "DEOXYCYTIDYLATE DEAMINASE-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24416:SF125", "l": "ANGIOPOIETIN-1 RECEPTOR", "d": [], "t": []}], "preferred_name": "ANGIOPOIETIN-1 RECEPTOR", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10046", "l": "ATP DEPENDENT LON PROTEASE FAMILY MEMBER", "d": [], "t": []}], "preferred_name": "ATP DEPENDENT LON PROTEASE FAMILY MEMBER", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR23158:SF54", "l": "TRANSPORT AND GOLGI ORGANIZATION PROTEIN 1 HOMOLOG", "d": [], "t": []}], "preferred_name": "TRANSPORT AND GOLGI ORGANIZATION PROTEIN 1 HOMOLOG", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR22691:SF1", "l": "CENTROSOMAL PROTEIN CCDC61", "d": [], "t": []}], "preferred_name": "CENTROSOMAL PROTEIN CCDC61", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:790", "l": "Adhesion G protein-coupled receptors", "d": ["Adhesion GPCRs are structurally identified on the basis of a large extracellular region, similar to the Class B GPCR, but which is linked to the 7TM region by a 'stalk' motif containing a GPCR proteolytic site. The N-terminus often shares structural homology with proteins such as lectins and immunoglobulins, leading to the term adhesion GPCR."], "t": []}], "preferred_name": "Adhesion G protein-coupled receptors", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11736:SF162", "l": "MELANOMA-ASSOCIATED ANTIGEN B4", "d": [], "t": []}], "preferred_name": "MELANOMA-ASSOCIATED ANTIGEN B4", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:1627", "l": "Axonemal dynein assembly factors", "d": ["This comprises a group of genes encoding cytoplasmic factors that are involved in axonemal dynein pre-assembly."], "t": []}], "preferred_name": "Axonemal dynein assembly factors", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR13149", "l": "VACUOLAR PROTEIN SORTING-ASSOCIATED PROTEIN VPS25", "d": [], "t": []}], "preferred_name": "VACUOLAR PROTEIN SORTING-ASSOCIATED PROTEIN VPS25", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10658:SF27", "l": "PHOSPHATIDYLINOSITOL TRANSFER PROTEIN BETA ISOFORM", "d": [], "t": []}], "preferred_name": "PHOSPHATIDYLINOSITOL TRANSFER PROTEIN BETA ISOFORM", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR23262:SF133", "l": "KERATIN-ASSOCIATED PROTEIN 9-6-RELATED", "d": [], "t": []}], "preferred_name": "KERATIN-ASSOCIATED PROTEIN 9-6-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR16477:SF2", "l": "COILED-COIL DOMAIN-CONTAINING PROTEIN 106", "d": [], "t": []}], "preferred_name": "COILED-COIL DOMAIN-CONTAINING PROTEIN 106", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:630", "l": "Leukocyte immunoglobulin like receptors", "d": ["The leukocyte immunoglobulin-like receptors (LILR) are a family of receptors possessing extracellular immunoglobulin domains. They are also known as CD85, ILTs and LIR, and can exert immunomodulatory effects on a wide range of immune cells. The human genes encoding these receptors are found in a gene cluster at chromosomal region 19q13.4."], "t": []}], "preferred_name": "Leukocyte immunoglobulin like receptors", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24329:SF567", "l": "RHOX HOMEOBOX FAMILY MEMBER 2-RELATED", "d": [], "t": []}], "preferred_name": "RHOX HOMEOBOX FAMILY MEMBER 2-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR31888", "l": "SMALL INTEGRAL MEMBRANE PROTEIN 19", "d": [], "t": []}], "preferred_name": "SMALL INTEGRAL MEMBRANE PROTEIN 19", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR23122:SF45", "l": "PROTEIN PALS2", "d": [], "t": []}], "preferred_name": "PROTEIN PALS2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR45616:SF31", "l": "KERATIN, TYPE II CYTOSKELETAL 73", "d": [], "t": []}], "preferred_name": "KERATIN, TYPE II CYTOSKELETAL 73", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR15975", "l": "CCR4-NOT TRANSCRIPTION COMPLEX SUBUNIT 11", "d": [], "t": []}], "preferred_name": "CCR4-NOT TRANSCRIPTION COMPLEX SUBUNIT 11", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11409:SF43", "l": "ADENOSINE DEAMINASE", "d": [], "t": []}], "preferred_name": "ADENOSINE DEAMINASE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR26452:SF701", "l": "OLFACTORY RECEPTOR 11L1", "d": [], "t": []}], "preferred_name": "OLFACTORY RECEPTOR 11L1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR22923:SF5", "l": "CEREBELLIN-1", "d": [], "t": []}], "preferred_name": "CEREBELLIN-1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR14166:SF15", "l": "SLIT-ROBO RHO GTPASE-ACTIVATING PROTEIN 1", "d": [], "t": []}], "preferred_name": "SLIT-ROBO RHO GTPASE-ACTIVATING PROTEIN 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR23008", "l": "CHROMOSOME 28 C10ORF62 HOMOLOG", "d": [], "t": []}], "preferred_name": "CHROMOSOME 28 C10ORF62 HOMOLOG", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11923", "l": "SCAVENGER RECEPTOR CLASS B TYPE-1 SR-B1", "d": [], "t": []}], "preferred_name": "SCAVENGER RECEPTOR CLASS B TYPE-1 SR-B1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR13034", "l": "DYNACTIN P62 SUBUNIT", "d": [], "t": []}], "preferred_name": "DYNACTIN P62 SUBUNIT", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR46258:SF3", "l": "VESICLE-TRAFFICKING PROTEIN SEC22A", "d": [], "t": []}], "preferred_name": "VESICLE-TRAFFICKING PROTEIN SEC22A", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10159:SF343", "l": "DUAL SPECIFICITY PROTEIN PHOSPHATASE 16", "d": [], "t": []}], "preferred_name": "DUAL SPECIFICITY PROTEIN PHOSPHATASE 16", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR15642:SF3", "l": "CYTOCHROME C OXIDASE ASSEMBLY FACTOR 3 HOMOLOG, MITOCHONDRIAL", "d": [], "t": []}], "preferred_name": "CYTOCHROME C OXIDASE ASSEMBLY FACTOR 3 HOMOLOG, MITOCHONDRIAL", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11955:SF62", "l": "CELLULAR RETINOIC ACID-BINDING PROTEIN 1", "d": [], "t": []}], "preferred_name": "CELLULAR RETINOIC ACID-BINDING PROTEIN 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR13292:SF0", "l": "AUTOPHAGY-RELATED PROTEIN 101", "d": [], "t": []}], "preferred_name": "AUTOPHAGY-RELATED PROTEIN 101", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR32017", "l": "SPINDLE AND KINETOCHORE-ASSOCIATED PROTEIN 2", "d": [], "t": []}], "preferred_name": "SPINDLE AND KINETOCHORE-ASSOCIATED PROTEIN 2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10630", "l": "MONOCYTE DIFFERENTIATION ANTIGEN CD14", "d": [], "t": []}], "preferred_name": "MONOCYTE DIFFERENTIATION ANTIGEN CD14", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:1218", "l": "LIM domain containing", "d": ["LIM domains are protein structural domains, composed of two contiguous zinc finger domains, separated by a two- amino acid residue hydrophobic linker. They are named after their initial discovery in the proteins L in11, I sl-1 & M ec-3. LIM-domain containing proteins have been shown to play roles in cytoskeletal organisation, organ development and oncogenesis. LIM-domains mediate protein:protein interactions that are critical to cellular processes. LIM domains have highly divergent sequences, apart from certain key residues. The sequence divergence allow a great many different binding sites to be grafted onto the same basic domain. The conserved residues are those involved in zinc binding or the hydrophobic core of the protein. The sequence signature of LIM domains is as follows: - 2-4 -- 13-19 --- 2-4 ----- 2-4 -- 13-20 -C- 2-4 - LIM domain organisation LIM domains frequently occur in multiples, as seen in proteins such as TES, LMO4, and can also be attached to other domains in order to confer a binding or targeting function upon them, such as LIM-kinase. The LIM superclass of genes have been classified into 14 classes: ABLIM, CRP, ENIGMA, EPLIN, LASP, LHX, LMO, LIMK, LMO7, MICAL, PXN, PINCH, TES, and ZYX. Six of these classes (i.e., ABLIM, MICAL, ENIGMA, ZYX, LHX, LM07) originated in the stem lineage of animals, and this expansion is thought to have made a major contribution to the origin of animal multicellularity. LIM domains are also found in various bacterial lineages where they are typically fused to a metallopeptidase domain. Some versions show fusions to an inactive P-loop NTPase at their N-terminus and a single transmembrane helix. These domain fusions suggest that the prokaryotic LIM domains are likely to regulate protein processing at the cell membrane. The domain architectural syntax is remarkable parallel to those of the prokaryotic versions of the B-box zinc finger and the AN1 zinc finger domains."], "t": []}], "preferred_name": "LIM domain containing", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR43503", "l": "MCG48959-RELATED", "d": [], "t": []}], "preferred_name": "MCG48959-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR15362:SF4", "l": "CDP-DIACYLGLYCEROL--INOSITOL 3-PHOSPHATIDYLTRANSFERASE", "d": [], "t": []}], "preferred_name": "CDP-DIACYLGLYCEROL--INOSITOL 3-PHOSPHATIDYLTRANSFERASE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR21396", "l": "39S RIBOSOMAL PROTEIN L43", "d": [], "t": []}], "preferred_name": "39S RIBOSOMAL PROTEIN L43", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10844", "l": "CAVEOLIN", "d": [], 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"biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR43270", "l": "BETA-ALA-HIS DIPEPTIDASE", "d": [], "t": []}], "preferred_name": "BETA-ALA-HIS DIPEPTIDASE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR15208:SF2", "l": "RECEPTOR-BINDING CANCER ANTIGEN EXPRESSED ON SISO CELLS", "d": [], "t": []}], "preferred_name": "RECEPTOR-BINDING CANCER ANTIGEN EXPRESSED ON SISO CELLS", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12098", "l": "E3 UBIQUITIN-PROTEIN LIGASE PELLINO-RELATED", "d": [], "t": []}], "preferred_name": "E3 UBIQUITIN-PROTEIN LIGASE PELLINO-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12019:SF24", "l": "LAMINA-ASSOCIATED POLYPEPTIDE 2, ISOFORM ALPHA", "d": [], "t": []}], "preferred_name": "LAMINA-ASSOCIATED POLYPEPTIDE 2, ISOFORM ALPHA", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR23083:SF475", "l": "TETRATRICOPEPTIDE REPEAT PROTEIN 7A", "d": [], "t": []}], "preferred_name": "TETRATRICOPEPTIDE REPEAT PROTEIN 7A", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR23267:SF437", "l": "IMMUNOGLOBULIN LAMBDA VARIABLE 2-8", "d": [], "t": []}], "preferred_name": "IMMUNOGLOBULIN LAMBDA VARIABLE 2-8", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11252:SF9", "l": "POLYRIBONUCLEOTIDE NUCLEOTIDYLTRANSFERASE 1, MITOCHONDRIAL", "d": [], "t": []}], "preferred_name": "POLYRIBONUCLEOTIDE NUCLEOTIDYLTRANSFERASE 1, MITOCHONDRIAL", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:895", "l": "MAP kinase phosphatases", "d": [], "t": []}], "preferred_name": "MAP kinase phosphatases", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12129:SF17", "l": "HEPARAN SULFATE 2-O-SULFOTRANSFERASE 1", "d": [], "t": []}], "preferred_name": "HEPARAN SULFATE 2-O-SULFOTRANSFERASE 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24271:SF51", "l": "GRANZYME M", "d": [], "t": []}], "preferred_name": "GRANZYME M", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:2176", "l": "Solute carrier family 25", "d": [], "t": []}], "preferred_name": "Solute carrier family 25", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR23280:SF18", "l": "BAND 4.1-LIKE PROTEIN 4B", "d": [], "t": []}], "preferred_name": "BAND 4.1-LIKE PROTEIN 4B", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR16193:SF0", "l": "TETRATRICOPEPTIDE REPEAT PROTEIN 27", "d": [], "t": []}], "preferred_name": "TETRATRICOPEPTIDE REPEAT PROTEIN 27", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR45682:SF1", "l": "DUAL SPECIFICITY PROTEIN PHOSPHATASE 3", "d": [], "t": []}], "preferred_name": "DUAL SPECIFICITY PROTEIN PHOSPHATASE 3", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR18921:SF2", "l": "THYROID RECEPTOR-INTERACTING PROTEIN 11", "d": [], "t": []}], "preferred_name": "THYROID RECEPTOR-INTERACTING PROTEIN 11", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR28453:SF1", "l": "PROTEIN SNORC", "d": [], "t": []}], "preferred_name": "PROTEIN SNORC", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12306", "l": "CELL DEATH ACTIVATOR CIDE", "d": [], "t": []}], "preferred_name": "CELL DEATH ACTIVATOR CIDE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:89", "l": "Zinc fingers RANBP2-type", "d": ["This group represents genes encoding proteins with the zinc finger domain found in RanBP2 proteins. Ran is an evolutionary conserved member of the Ras superfamily that regulates all receptor-mediated transport between the nucleus and the cytoplasm. Ran binding protein 2 (RanBP2) is a 358kDa nucleoporin located on the cytoplasmic side of the nuclear pore complex which plays a role in nuclear protein import . 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It is likely that they evolved to take on specialized roles in the particular tissues in which they are expressed: PIEZO1 is expressed mainly in non-neuronal cells, whereas PIEZO2 is expressed in sensory neurons and in some specialized mechanosensory structures."], "t": []}], "preferred_name": "Piezo type mechanosensitive ion channel components", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10822:SF12", "l": "GLYPICAN-5", "d": [], "t": []}], "preferred_name": "GLYPICAN-5", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24248:SF154", "l": "D(3) DOPAMINE RECEPTOR", "d": [], "t": []}], "preferred_name": "D(3) DOPAMINE RECEPTOR", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10763", "l": "CELL DIVISION CONTROL PROTEIN 6-RELATED", "d": [], "t": []}], "preferred_name": "CELL DIVISION CONTROL PROTEIN 6-RELATED", "taxa": []} {"type": 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"CHROMODOMAIN-HELICASE-DNA-BINDING PROTEIN 9", "d": [], "t": []}], "preferred_name": "CHROMODOMAIN-HELICASE-DNA-BINDING PROTEIN 9", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11097:SF9", "l": "EXOSOME COMPLEX COMPONENT RRP43", "d": [], "t": []}], "preferred_name": "EXOSOME COMPLEX COMPONENT RRP43", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR45879:SF4", "l": "CAMP-RESPONSIVE ELEMENT MODULATOR", "d": [], "t": []}], "preferred_name": "CAMP-RESPONSIVE ELEMENT MODULATOR", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR14522", "l": "EMO2-RELATED", "d": [], "t": []}], "preferred_name": "EMO2-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10694:SF43", "l": "LYSINE-SPECIFIC DEMETHYLASE 5C", "d": [], "t": []}], "preferred_name": "LYSINE-SPECIFIC DEMETHYLASE 5C", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10621:SF13", "l": "UV EXCISION REPAIR PROTEIN RAD23 HOMOLOG B", "d": [], "t": []}], "preferred_name": "UV EXCISION REPAIR PROTEIN RAD23 HOMOLOG B", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR14027", "l": "RNA POLYMERASE-ASSOCIATED PROTEIN CTR9", "d": [], "t": []}], "preferred_name": "RNA POLYMERASE-ASSOCIATED PROTEIN CTR9", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12731:SF1", "l": "TRANSLOCON-ASSOCIATED PROTEIN SUBUNIT DELTA", "d": [], "t": []}], "preferred_name": "TRANSLOCON-ASSOCIATED PROTEIN SUBUNIT DELTA", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12983", "l": "RING FINGER 10 FAMILY MEMBER", "d": [], "t": []}], "preferred_name": "RING FINGER 10 FAMILY MEMBER", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR44899", "l": "CAMK FAMILY PROTEIN KINASE", "d": [], "t": []}], "preferred_name": "CAMK FAMILY PROTEIN KINASE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12258:SF10", "l": "14 KDA PHOSPHOHISTIDINE PHOSPHATASE", "d": [], "t": []}], "preferred_name": "14 KDA PHOSPHOHISTIDINE PHOSPHATASE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR48051", "l": "FAMILY NOT NAMED", "d": [], "t": []}], "preferred_name": "FAMILY NOT NAMED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:1133", "l": "Arylamine N-acetyltransferases", "d": ["In enzymology, an arylamine N-acetyltransferase ( EC 2.3.1.5 ) is an enzyme that catalyzes the chemical reaction acetyl-CoA + an arylamine CoA + an N-acetylarylamine Thus, the two substrates of this enzyme are acetyl-CoA and arylamine, whereas its two products are CoA and N-acetylarylamine. This enzyme belongs to the family of transferases, specifically those acyltransferases transferring groups other than aminoacyl groups. The systematic name of this enzyme class is acetyl-CoA:arylamine N-acetyltransferase. Other names in common use include arylamine acetylase, beta-naphthylamine N-acetyltransferase, 4-aminobiphenyl N-acetyltransferase, acetyl CoA-arylamine N-acetyltransferase, 2-naphthylamine N-acetyltransferase, arylamine acetyltransferase, indoleamine N-acetyltransferase, N-acetyltransferase, p-aminosalicylate N-acetyltransferase, serotonin acetyltransferase, and serotonin N-acetyltransferase."], "t": []}], "preferred_name": "Arylamine N-acetyltransferases", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR46675", "l": "E3 UBIQUITIN-PROTEIN LIGASE RNF182", "d": [], "t": []}], "preferred_name": "E3 UBIQUITIN-PROTEIN LIGASE RNF182", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR13832", "l": "PROTEIN PHOSPHATASE 2C", "d": [], "t": []}], "preferred_name": "PROTEIN PHOSPHATASE 2C", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11523:SF26", 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"preferred_name": "TRNA-DIHYDROURIDINE SYNTHASE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR19890:SF10", "l": "FIBROBLAST GROWTH FACTOR RECEPTOR-LIKE 1", "d": [], "t": []}], "preferred_name": "FIBROBLAST GROWTH FACTOR RECEPTOR-LIKE 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24085:SF1", "l": "NUCLEAR RECEPTOR SUBFAMILY 4 GROUP A MEMBER 1", "d": [], "t": []}], "preferred_name": "NUCLEAR RECEPTOR SUBFAMILY 4 GROUP A MEMBER 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR15977", "l": "CILIA- AND FLAGELLA-ASSOCIATED PROTEIN 46", "d": [], "t": []}], "preferred_name": "CILIA- AND FLAGELLA-ASSOCIATED PROTEIN 46", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24278:SF37", "l": "TRANSMEMBRANE GAMMA-CARBOXYGLUTAMIC ACID PROTEIN 1", "d": [], "t": []}], "preferred_name": "TRANSMEMBRANE 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Although classed as peroxidases by the enzyme commission they are distinct from other heme peroxidases. Both use H2O2 as an oxidant as a first step; however, catalases specifically oxidize H2O2 in the next step, thereby generating two molecules of water and oxygen by consuming two molecules of H2O2, while peroxidases oxidize other organic and inorganic substrates. Catalases have a distinct fold and evolutionary origin from the animal heme peroxidase family. 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"biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12048", "l": "CCAAT-BINDING FACTOR-RELATED", "d": [], "t": []}], "preferred_name": "CCAAT-BINDING FACTOR-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24115:SF361", "l": "KINESIN-LIKE PROTEIN KIF1A", "d": [], "t": []}], "preferred_name": "KINESIN-LIKE PROTEIN KIF1A", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR28448:SF1", "l": "UPF0728 PROTEIN C10ORF53", "d": [], "t": []}], "preferred_name": "UPF0728 PROTEIN C10ORF53", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR23167:SF52", "l": "SMOOTHELIN", "d": [], "t": []}], "preferred_name": "SMOOTHELIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11711", "l": "ADP RIBOSYLATION FACTOR-RELATED", "d": [], "t": []}], "preferred_name": "ADP RIBOSYLATION FACTOR-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR42808:SF3", "l": "HYDROXYSTEROID DEHYDROGENASE-LIKE PROTEIN 2", "d": [], "t": []}], "preferred_name": "HYDROXYSTEROID DEHYDROGENASE-LIKE PROTEIN 2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24381:SF409", "l": "ZINC FINGER PROTEIN 641", "d": [], "t": []}], "preferred_name": "ZINC FINGER PROTEIN 641", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11461:SF199", "l": "SERPIN B11", "d": [], "t": []}], "preferred_name": "SERPIN B11", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24300:SF275", "l": "CYTOCHROME P450 2F1", "d": [], "t": []}], "preferred_name": "CYTOCHROME P450 2F1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR31922:SF2", "l": "TRANSMEMBRANE PROTEIN 215", "d": 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"biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24390:SF70", "l": "FEZ FAMILY ZINC FINGER PROTEIN 1", "d": [], "t": []}], "preferred_name": "FEZ FAMILY ZINC FINGER PROTEIN 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR13531:SF8", "l": "TRANSMEMBRANE PROTEIN 80", "d": [], "t": []}], "preferred_name": "TRANSMEMBRANE PROTEIN 80", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR35682:SF1", "l": "TRANSMEMBRANE PROTEIN 252", "d": [], "t": []}], "preferred_name": "TRANSMEMBRANE PROTEIN 252", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:1071", "l": "Acid phosphatases", "d": ["Acid phosphatase ( EC 3.1.3.2, acid phosphomonoesterase, phosphomonoesterase, glycerophosphatase, acid monophosphatase, acid phosphohydrolase, acid phosphomonoester hydrolase, uteroferrin, acid nucleoside diphosphate phosphatase, orthophosphoric-monoester phosphohydrolase (acid optimum) ) is a phosphatase, a type of enzyme, used to free attached phosphoryl groups from other molecules during digestion. It can be further classified as a phosphomonoesterase."], "t": []}], "preferred_name": "Acid phosphatases", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:348", "l": "Immunoglobulins", "d": ["Immunoglobulins (IG) or antibodies are antigen receptors of the B cells of the adaptive immune response, acquired by jawed vertebrates (or gnathostomata) more than 450 million years ago and found in all extant jawed vertebrate species from fishes to humans. IG are anchored in the membrane of a B cell as part of a signaling B cell receptor (BcR = membrane IG+CD79) or are secreted by plasmocytes. IG recognize antigens in their native (unprocessed) form. IG are made of two identical heavy (H) chains and two identical light (kappa or lambda) chains, encoded by genes located in three major loci: the IG heavy (IGH) locus at 14q32.33, IG kappa (IGK) locus at 2p11.2 and IG lambda (IGL) locus at 22q11.2. Genes outside of these major loci are orphons. There are four IG gene types, variable (V), diversity (D) (only for IGH), joining (J) and constant (C) genes which contribute to the IG chain synthesis. The variable domain at the N-terminal end of each IG chain results from a V-(D)-J rearrangement whereas the remaining of the chain, or constant region, is encoded by a C gene. The combinatorial and junctional diversity together with IG somatic hypermutations create a huge diversity of 1012 specific IG per individual, the limiting factor being only the number of B cells that an organism is genetically programmed to prod"], "t": []}], "preferred_name": "Immunoglobulins", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR15952:SF12", "l": "EXPORTIN-T", "d": [], "t": []}], "preferred_name": "EXPORTIN-T", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12141:SF3", "l": "ARFAPTIN-2", "d": [], "t": []}], "preferred_name": "ARFAPTIN-2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24073:SF941", "l": "RAS-RELATED PROTEIN RAB-20", "d": [], "t": []}], "preferred_name": "RAS-RELATED PROTEIN RAB-20", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR47898", "l": "KUNITZ-TYPE 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"biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11706:SF40", "l": "NATURAL RESISTANCE-ASSOCIATED MACROPHAGE PROTEIN 2", "d": [], "t": []}], "preferred_name": "NATURAL RESISTANCE-ASSOCIATED MACROPHAGE PROTEIN 2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR23105:SF38", "l": "NHP2-LIKE PROTEIN 1", "d": [], "t": []}], "preferred_name": "NHP2-LIKE PROTEIN 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR13914", "l": "PROLINE OXIDASE", "d": [], "t": []}], "preferred_name": "PROLINE OXIDASE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10484", "l": "HISTONE H4", "d": [], "t": []}], "preferred_name": "HISTONE H4", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11006:SF60", "l": "PROTEIN ARGININE N-METHYLTRANSFERASE 9", "d": [], "t": []}], "preferred_name": 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"PANTHER.FAMILY:PTHR24028:SF71", "l": "PROTOCADHERIN BETA-16", "d": [], "t": []}], "preferred_name": "PROTOCADHERIN BETA-16", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:1908", "l": "Endothelins", "d": [], "t": []}], "preferred_name": "Endothelins", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10353", "l": "GLYCOSYL HYDROLASE", "d": [], "t": []}], "preferred_name": "GLYCOSYL HYDROLASE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11109:SF11", "l": "GTP CYCLOHYDROLASE 1", "d": [], "t": []}], "preferred_name": "GTP CYCLOHYDROLASE 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11214:SF19", "l": "BETA-1,3-GALACTOSYLTRANSFERASE 2", "d": [], "t": []}], "preferred_name": "BETA-1,3-GALACTOSYLTRANSFERASE 2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR21663", "l": "HYPOTHETICAL HEAT DOMAIN-CONTAINING", "d": [], "t": []}], "preferred_name": "HYPOTHETICAL HEAT DOMAIN-CONTAINING", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR46123", "l": "MIX-TYPE HOMEOBOX GENE 1-RELATED", "d": [], "t": []}], "preferred_name": "MIX-TYPE HOMEOBOX GENE 1-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10424:SF68", "l": "ENDOGENOUS RETROVIRUS GROUP 3 MEMBER 1 ENV POLYPROTEIN", "d": [], "t": []}], "preferred_name": "ENDOGENOUS RETROVIRUS GROUP 3 MEMBER 1 ENV POLYPROTEIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10278:SF0", "l": "CORTICOTROPIN-RELEASING FACTOR-BINDING PROTEIN", "d": [], "t": []}], "preferred_name": "CORTICOTROPIN-RELEASING FACTOR-BINDING PROTEIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:1975", "l": "Mitochondrially encoded RNAs", "d": [], "t": []}], "preferred_name": "Mitochondrially encoded RNAs", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:438", "l": "Sialyltransferases", "d": ["Sialyltransferases are a subset of glycosyltransferases that catalyze the transfer of sialic acid (Sia) residues from an activated sugar donor (CMP-βNeu5Ac, CMP-βNeu5Gc, CMP-βKdn) to the hydroxyl group at the terminal non reducing position of Gal, GlcNAc, GalNAc or Sia monosaccharides of glycoconjugate acceptors (glycoproteins or glycolipids) leading to the formation of α2-3, α2-6 or α2-8 glycosidic linkages. Animal sialyltransferases are gathered in a unique group of the CAZy classification (GT#29). Within this group, four families are distinguished based on the glycosidic linkage formed and the monosaccharide acceptor (ST3Gal, ST6Gal, ST6GalNAc and ST8Sia)."], "t": []}], "preferred_name": "Sialyltransferases", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR28594", "l": "ATR-INTERACTING PROTEIN", "d": [], "t": []}], "preferred_name": "ATR-INTERACTING PROTEIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR14920", "l": "OSMOTIC AVOIDANCE ABNORMAL PROTEIN 1/WD REPEAT MEMBRANE PROTEIN", "d": [], "t": []}], "preferred_name": "OSMOTIC AVOIDANCE ABNORMAL PROTEIN 1/WD REPEAT MEMBRANE PROTEIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR38140:SF6", "l": "KERATIN-ASSOCIATED PROTEIN 19-1", "d": [], "t": []}], "preferred_name": "KERATIN-ASSOCIATED PROTEIN 19-1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR23055:SF75", "l": "CALAXIN", "d": [], "t": []}], "preferred_name": "CALAXIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11142:SF4", "l": "PSEUDOURIDYLATE SYNTHASE 1 HOMOLOG", "d": [], "t": []}], "preferred_name": "PSEUDOURIDYLATE SYNTHASE 1 HOMOLOG", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12918", "l": "CYSTEINE DIOXYGENASE", "d": [], "t": []}], "preferred_name": "CYSTEINE DIOXYGENASE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR15104", "l": "DIHYDROPTERIDINE REDUCTASE", "d": [], "t": []}], "preferred_name": "DIHYDROPTERIDINE REDUCTASE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR45732", "l": "ADP-RIBOSYLATION FACTOR-LIKE PROTEIN 8", "d": [], "t": []}], "preferred_name": "ADP-RIBOSYLATION FACTOR-LIKE PROTEIN 8", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR13145", "l": "SSM4 PROTEIN", "d": [], "t": []}], "preferred_name": "SSM4 PROTEIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR28052:SF1", "l": "UPF0545 PROTEIN C22ORF39", "d": [], "t": []}], "preferred_name": "UPF0545 PROTEIN C22ORF39", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR22793:SF6", "l": "MYOCARDIN-RELATED TRANSCRIPTION FACTOR A", "d": [], "t": []}], "preferred_name": "MYOCARDIN-RELATED TRANSCRIPTION FACTOR A", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11830:SF28", "l": "SMALL RIBOSOMAL SUBUNIT PROTEIN ES1", "d": [], "t": []}], "preferred_name": "SMALL RIBOSOMAL SUBUNIT PROTEIN ES1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:1938", "l": "H3 histones", "d": ["Histone H3 is one of the five main histone proteins involved in the structure of chromatin in eukaryotic cells. Featuring a main globular domain and a long N-terminal tail, H3 is involved with the structure of the nucleosomes of the 'beads on a string' structure. Histone proteins are highly post-translationally modified however Histone H3 is the most extensively modified of the five histones. The term 'Histone H3' alone is purposely ambiguous in that it does not distinguish between sequence variants or modification state. Histone H3 is an important protein in the emerging field of epigenetics, where its sequence variants and variable modification states are thought to play a role in the dynamic and long term regulation of genes."], "t": []}], "preferred_name": "H3 histones", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:153", "l": "Olfactory receptors, family 6", "d": [], "t": []}], "preferred_name": "Olfactory receptors, family 6", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR19256:SF65", "l": "T CELL RECEPTOR GAMMA CONSTANT 1-RELATED", "d": [], "t": []}], "preferred_name": "T CELL RECEPTOR GAMMA CONSTANT 1-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR22999:SF23", "l": "SORTING NEXIN-16", "d": [], "t": []}], "preferred_name": "SORTING NEXIN-16", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": 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"biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR45973:SF8", "l": "LEUCINE-RICH REPEAT-CONTAINING PROTEIN 49", "d": [], "t": []}], "preferred_name": "LEUCINE-RICH REPEAT-CONTAINING PROTEIN 49", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR42980", "l": "2-OXOISOVALERATE DEHYDROGENASE SUBUNIT BETA-RELATED", "d": [], "t": []}], "preferred_name": "2-OXOISOVALERATE DEHYDROGENASE SUBUNIT BETA-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR14418:SF5", "l": "CONDENSIN COMPLEX SUBUNIT 3", "d": [], "t": []}], "preferred_name": "CONDENSIN COMPLEX SUBUNIT 3", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR16056:SF18", "l": "REGULATOR OF MICROTUBULE DYNAMICS PROTEIN 3", "d": [], "t": []}], "preferred_name": "REGULATOR OF MICROTUBULE DYNAMICS PROTEIN 3", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR46843", "l": "BTB/POZ DOMAIN-CONTAINING PROTEIN 16", "d": [], "t": []}], "preferred_name": "BTB/POZ DOMAIN-CONTAINING PROTEIN 16", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24055:SF109", "l": "MITOGEN-ACTIVATED PROTEIN KINASE 11", "d": [], "t": []}], "preferred_name": "MITOGEN-ACTIVATED PROTEIN KINASE 11", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12277:SF69", "l": "PROTEIN ABHD12B", "d": [], "t": []}], "preferred_name": "PROTEIN ABHD12B", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR43448", "l": "PROTOHEME IX FARNESYLTRANSFERASE, MITOCHONDRIAL", "d": [], "t": []}], "preferred_name": "PROTOHEME IX FARNESYLTRANSFERASE, MITOCHONDRIAL", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR45677:SF8", "l": "CYSTEINE SULFINIC ACID DECARBOXYLASE", "d": [], "t": []}], "preferred_name": "CYSTEINE SULFINIC ACID DECARBOXYLASE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR21338", "l": "MITOCHONDRIAL RIBOSOMAL PROTEIN L41", "d": [], "t": []}], "preferred_name": "MITOCHONDRIAL RIBOSOMAL PROTEIN L41", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11668:SF204", "l": "SERINE_THREONINE-PROTEIN PHOSPHATASE PP1-GAMMA CATALYTIC SUBUNIT", "d": [], "t": []}], "preferred_name": "SERINE_THREONINE-PROTEIN PHOSPHATASE PP1-GAMMA CATALYTIC SUBUNIT", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10024:SF115", "l": "SYNAPTOTAGMIN-11", "d": [], "t": []}], "preferred_name": "SYNAPTOTAGMIN-11", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR48050:SF12", "l": "UDP-GLUCURONOSYLTRANSFERASE 1A3-RELATED", "d": [], "t": []}], "preferred_name": "UDP-GLUCURONOSYLTRANSFERASE 1A3-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR23211", "l": "TRANS-GOLGI NETWORK INTEGRAL MEMBRANE PROTEIN TGN38", "d": [], "t": []}], "preferred_name": "TRANS-GOLGI NETWORK INTEGRAL MEMBRANE PROTEIN TGN38", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR13622:SF8", "l": "THIAMIN PYROPHOSPHOKINASE 1", "d": [], "t": []}], "preferred_name": "THIAMIN PYROPHOSPHOKINASE 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR15223:SF1", "l": "NADH DEHYDROGENASE [UBIQUINONE] 1 BETA SUBCOMPLEX SUBUNIT 2, MITOCHONDRIAL", "d": [], "t": []}], "preferred_name": "NADH DEHYDROGENASE [UBIQUINONE] 1 BETA SUBCOMPLEX SUBUNIT 2, MITOCHONDRIAL", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:1324", "l": "STEAP family", "d": ["The STEAP proteins are essential transmembrane 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"t": []}], "preferred_name": "PROLARGIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11699:SF131", "l": "MITOCHONDRIAL 10-FORMYLTETRAHYDROFOLATE DEHYDROGENASE", "d": [], "t": []}], "preferred_name": "MITOCHONDRIAL 10-FORMYLTETRAHYDROFOLATE DEHYDROGENASE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR14972:SF7", "l": "PROTEIN FAM117A", "d": [], "t": []}], "preferred_name": "PROTEIN FAM117A", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24056:SF107", "l": "CYCLIN-DEPENDENT KINASE 11A-RELATED", "d": [], "t": []}], "preferred_name": "CYCLIN-DEPENDENT KINASE 11A-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR15225:SF4", "l": "N-MYC-INTERACTOR", "d": [], "t": []}], "preferred_name": "N-MYC-INTERACTOR", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR20275", "l": "NAD KINASE", "d": [], "t": []}], "preferred_name": "NAD KINASE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24118:SF72", "l": "ANKYRIN REPEAT AND SOCS BOX PROTEIN 16", "d": [], "t": []}], "preferred_name": "ANKYRIN REPEAT AND SOCS BOX PROTEIN 16", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:2179", "l": "Solute carrier family 28", "d": [], "t": []}], "preferred_name": "Solute carrier family 28", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12691:SF10", "l": "MEDIATOR OF RNA POLYMERASE II TRANSCRIPTION SUBUNIT 23", "d": [], "t": []}], "preferred_name": "MEDIATOR OF RNA POLYMERASE II TRANSCRIPTION SUBUNIT 23", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR43995:SF1", "l": "PRE-MRNA-PROCESSING FACTOR 19", "d": [], "t": []}], "preferred_name": "PRE-MRNA-PROCESSING FACTOR 19", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR28682:SF1", "l": "INHIBITORY SYNAPTIC FACTOR 2A", "d": [], "t": []}], "preferred_name": "INHIBITORY SYNAPTIC FACTOR 2A", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR26453:SF91", "l": "OLFACTORY RECEPTOR 2M4", "d": [], "t": []}], "preferred_name": "OLFACTORY RECEPTOR 2M4", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR31416:SF1", "l": "TRANSMEMBRANE PROTEIN 125", "d": [], "t": []}], "preferred_name": "TRANSMEMBRANE PROTEIN 125", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:1171", "l": "SCF complex", "d": ["Skp, Cullin, F-box containing complex (or SCF complex ) is a multi-protein E3 ubiquitin ligase complex catalyzing the ubiquitination of proteins destined for proteasomal degradation. It has important roles in the ubiquitination of proteins involved in the cell cycle and also marks various other cellular proteins for destruction. Core Components SCF contains three core subunits, and a number of less critical components: F-box protein ( e.g. Cdc4 ) â€' Contributes to the specificity of SCF by aggregating to target proteins independently of the complex and then binding to the Skp1 component, thus allowing the protein to be brought into proximity with the functional E2 protein. The F-box is also essential in regulating SCF activity during the course of the cell-cycle. SCF levels are thought to remain constant throughout the cell-cycle. Instead, F-box affinity for protein substrates is regulated through cdk/cyclin mediated phosphorylation of target proteins. Skp1 â€' Skp1 is a bridging protein and forms part of the horseshoe-shaped complex in tandem with cullin (cul1). Skp1 is essential in the recognition and binding of the F-box. Cullin ( CUL1 ) â€' CUL1 forms the major structural scaffold of the SCF complex and links the skp1 domain with the Rbx1 domain. RBX1 â€' Rbx1 contains a small zinc-binding domain called the RING Finger, to which the E2-ubiquitin conjugate binds, allowing the transferral of the ubiquitin to a lysine residue on the target protein. SCF and Cell Cycle Regulation Progression through the cell cycle in eukaryotes is regulated through synthesisdephosphorylation of cell-cycle-regulating proteins. Two ubiquitin ligases are crucial in the cell cycle. The anaphase-promoting complex or cyclosome ( APC/C ) controls the metaphase â€' anaphase transition when bound to its substrate-specific activating subunit Cdc20 : this complex ubiquitinylates the separase -inhibiting protein securin, paving the way for separase to break cohesin and thus separate the sister chromatids at the centromere. APC/C with another activating subunit, Cdh1, is active in G1 phase and controls levels of the mitosis-regulating B-type cyclins. SCF controls the transitions between G1/S and G2/M phases. Two F-box-protein-bound SCF complexes (SCF- Skp2 and SCF- β-TrCP ), are most well studied among over 70 F-box proteins identified in humans. SCF-Skp2 mainly ubiquitinates and degrades cyclin-dependent kinase inhibitors (CKIs) such as p27 and p21 as well as the G1-/S-specific cyclin E, in vivo and in vitro. Therefore, SCF-Skp2 promotes cell-cycle progression and cell growth. On the other hand, SCF-βTrCP promotes proteolysis of Emi1, an APC/C-Cdh1 inhibitor, and Wee1, a Cdk1 inhibitor, in early mitosis via phosphorylation at their degron (the amino acid motif DSGXXS, where X can be any amino acid) by kinases such as Polo-like kinase 1 (Plk1) and Cdk1â€'cyclin B. SCF-βTrCP and APC/C control each other to regulate timely progression through the cell cycle. Lists of substrates of SCF-Skp2 and -βTrCP are still growing. SCF and Plant Hormone Signaling In plants, the plant hormone auxin stimulates binding of SCF-TIR1 to the AUX/IAA repressor and then the degradation of the repressor, resulting in the activation of auxin-responsive genes. The TIR1 F-box protein acts as an auxin receptor and directly links reception of auxin to degradation of the Aux/IAA proteins. TIR1 (Transport Inhibitor Response 1) belongs to AFBs (Auxin Signaling F-box proteins). In plants, the plant hormone Jasmonate allows binding between SCF-COI1 to the JAZ transcription factor. 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"taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR46892:SF1", "l": "VISUAL SYSTEM HOMEOBOX 2", "d": [], "t": []}], "preferred_name": "VISUAL SYSTEM HOMEOBOX 2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR16048:SF3", "l": "E3 UBIQUITIN-PROTEIN LIGASE MSL2", "d": [], "t": []}], "preferred_name": "E3 UBIQUITIN-PROTEIN LIGASE MSL2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR28596:SF1", "l": "BBSOME-INTERACTING PROTEIN 1", "d": [], "t": []}], "preferred_name": "BBSOME-INTERACTING PROTEIN 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12195:SF4", "l": "CYTOPLASMIC FMR1-INTERACTING PROTEIN 1", "d": [], "t": []}], "preferred_name": "CYTOPLASMIC FMR1-INTERACTING PROTEIN 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11606:SF15", "l": "GLUTAMATE DEHYDROGENASE 2, MITOCHONDRIAL", "d": [], "t": []}], "preferred_name": "GLUTAMATE DEHYDROGENASE 2, MITOCHONDRIAL", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR22796:SF13", "l": "UP-REGULATOR OF CELL PROLIFERATION", "d": [], "t": []}], "preferred_name": "UP-REGULATOR OF CELL PROLIFERATION", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11105", "l": "CITRATE LYASE SUBUNIT BETA-RELATED", "d": [], "t": []}], "preferred_name": "CITRATE LYASE SUBUNIT BETA-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR48001:SF186", "l": "OLFACTORY RECEPTOR 1G1", "d": [], "t": []}], "preferred_name": "OLFACTORY RECEPTOR 1G1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:728", "l": "S ribosomal proteins", "d": [], "t": []}], "preferred_name": "S ribosomal proteins", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR23330", "l": "P300 TRANSCRIPTIONAL COFACTOR JMY-RELATED", "d": [], "t": []}], "preferred_name": "P300 TRANSCRIPTIONAL COFACTOR JMY-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR45971", "l": "PHOX (PX) DOMAIN-CONTAINING PROTEIN", "d": [], "t": []}], "preferred_name": "PHOX (PX) DOMAIN-CONTAINING PROTEIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR13630", "l": "GAMMA-SECRETASE-ACTIVATING PROTEIN", "d": [], "t": []}], "preferred_name": "GAMMA-SECRETASE-ACTIVATING PROTEIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24085:SF2", "l": "NUCLEAR RECEPTOR SUBFAMILY 4 GROUP A MEMBER 3", "d": [], "t": []}], "preferred_name": "NUCLEAR RECEPTOR SUBFAMILY 4 GROUP A MEMBER 3", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR22950:SF244", "l": "NEUTRAL AMINO ACID TRANSPORTER 9", "d": [], "t": []}], "preferred_name": "NEUTRAL AMINO ACID TRANSPORTER 9", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11010:SF11", "l": "THYMUS-SPECIFIC SERINE PROTEASE", "d": [], "t": []}], "preferred_name": "THYMUS-SPECIFIC SERINE PROTEASE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:1998", "l": "minichromosome maintenance 2-7 complex", "d": ["The eukaryotic minichromosome maintenance 2-7 complex is the core of the inactive MCM replication licensing complex and the catalytic core of the Cdc45-MCM-GINS replicative helicase."], "t": []}], "preferred_name": "minichromosome maintenance 2-7 complex", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR15593", "l": "PHOSPHATIDYLINOSITOL 3-KINASE REGULATORY SUBUNIT", "d": [], "t": []}], "preferred_name": 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This process is called RNA interference (RNAi) and it is found in many eukaryotes; it is a key process in defense against viral infections, as it is triggered by the presence of double-stranded RNA (dsRNA)."], "t": []}], "preferred_name": "RISC loading complex subunits", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR23131", "l": "ENDORIBONUCLEASE LACTB2", "d": [], "t": []}], "preferred_name": "ENDORIBONUCLEASE LACTB2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24356:SF150", "l": "MICROTUBULE-ASSOCIATED SERINE_THREONINE-PROTEIN KINASE 1", "d": [], "t": []}], "preferred_name": "MICROTUBULE-ASSOCIATED SERINE_THREONINE-PROTEIN KINASE 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:1970", "l": "CREB3 transcription factor family", "d": [], "t": []}], "preferred_name": "CREB3 transcription factor family", "taxa": []} {"type": 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PROTEIN 514", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR14383:SF2", "l": "DIFFERENTIALLY EXPRESSED IN FDCP 6 HOMOLOG", "d": [], "t": []}], "preferred_name": "DIFFERENTIALLY EXPRESSED IN FDCP 6 HOMOLOG", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR33559", "l": "PROTEASOME ASSEMBLY CHAPERONE 4", "d": [], "t": []}], "preferred_name": "PROTEASOME ASSEMBLY CHAPERONE 4", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR14241", "l": "INTERFERON-INDUCED PROTEIN 44", "d": [], "t": []}], "preferred_name": "INTERFERON-INDUCED PROTEIN 44", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR20870", "l": "BARDET-BIEDL SYNDROME 1 PROTEIN", "d": [], "t": []}], "preferred_name": "BARDET-BIEDL SYNDROME 1 PROTEIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR36863", "l": "SHIELDIN COMPLEX SUBUNIT 1", "d": [], "t": []}], "preferred_name": "SHIELDIN COMPLEX SUBUNIT 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR43884", "l": "ACYL-COA DEHYDROGENASE", "d": [], "t": []}], "preferred_name": "ACYL-COA DEHYDROGENASE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR16247", "l": "RIKEN CDNA 9430015G10 GENE", "d": [], "t": []}], "preferred_name": "RIKEN CDNA 9430015G10 GENE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24353:SF137", "l": "CAMP-DEPENDENT PROTEIN KINASE CATALYTIC SUBUNIT GAMMA", "d": [], "t": []}], "preferred_name": "CAMP-DEPENDENT PROTEIN KINASE CATALYTIC SUBUNIT GAMMA", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24241:SF83", "l": "G-PROTEIN COUPLED RECEPTOR 150-RELATED", "d": [], "t": []}], "preferred_name": "G-PROTEIN COUPLED RECEPTOR 150-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR21694:SF18", "l": "COILED-COIL DOMAIN-CONTAINING PROTEIN 63", "d": [], "t": []}], "preferred_name": "COILED-COIL DOMAIN-CONTAINING PROTEIN 63", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12933:SF0", "l": "U3 SMALL NUCLEOLAR RNA-ASSOCIATED PROTEIN 25 HOMOLOG", "d": [], "t": []}], "preferred_name": "U3 SMALL NUCLEOLAR RNA-ASSOCIATED PROTEIN 25 HOMOLOG", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR45819:SF3", "l": "ARF-GAP WITH GTPASE, ANK REPEAT AND PH DOMAIN-CONTAINING PROTEIN 2", "d": [], "t": []}], "preferred_name": "ARF-GAP WITH GTPASE, ANK REPEAT AND PH DOMAIN-CONTAINING PROTEIN 2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10969:SF14", "l": "MICROTUBULE-ASSOCIATED PROTEINS 1A_1B LIGHT CHAIN 3A", "d": [], "t": []}], "preferred_name": "MICROTUBULE-ASSOCIATED PROTEINS 1A_1B LIGHT CHAIN 3A", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:628", "l": "Latent transforming growth factor beta binding proteins", "d": [], "t": []}], "preferred_name": "Latent transforming growth factor beta binding proteins", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR45690:SF15", "l": "NACHT, LRR AND PYD DOMAINS-CONTAINING PROTEIN 14", "d": [], "t": []}], "preferred_name": "NACHT, LRR AND PYD DOMAINS-CONTAINING PROTEIN 14", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10104:SF18", "l": "STATHMIN-2", "d": [], "t": []}], "preferred_name": "STATHMIN-2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:1194", "l": "Mannosidases alpha class 2", "d": ["Glycoside hydrolases of family 38 are Class II α-mannosidases. They range in breadth of specificity from the Golgi α-mannosidase (2A1), which has a dual specificity for α-1,6 and α-1,3-linked mannoses, to the lysosomal mannosidases, which have either broad (2B1 cleaves α1,2, α1,3 and α1,6 linkages) or narrow specificities (2B2 is specific for α-1,6). There have been GH38 mannosidases identified in a number of different localizations, classed into subfamilies with different substrate specificities and biochemical properties, and, presumably, different physiological roles. The Golgi enzyme is identified as 2A1 (Class 2, A for Golgi, enzyme 1). Lysosomal GH38 mannosidases are indicated by 'B' (2B1, 2B2) and those likely existing in the cytoplasm by 'C'."], "t": []}], "preferred_name": "Mannosidases alpha class 2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR15592", "l": "MATRIN 3/NUCLEAR PROTEIN 220-RELATED", "d": [], "t": []}], "preferred_name": "MATRIN 3/NUCLEAR PROTEIN 220-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:407", "l": "Arachidonate lipoxygenases", "d": ["Lipoxygenases ( EC 1.13.11.- ) are a family of iron -containing enzymes that catalyse the dioxygenation of polyunsaturated fatty acids in lipids containing a cis,cis-1,4- pentadiene structure. It catalyses the following reaction: fatty acid + O 2 = fatty acid hydroperoxide Lipoxygenases are found in plants, animals and fungi. Products of lipoxygenases are involved in diverse cell functions."], "t": []}], "preferred_name": "Arachidonate lipoxygenases", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10438:SF230", "l": "THIOREDOXIN DOMAIN-CONTAINING PROTEIN 8", "d": [], "t": []}], "preferred_name": "THIOREDOXIN DOMAIN-CONTAINING PROTEIN 8", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR31545:SF2", "l": "SPEEDY PROTEIN C", "d": [], "t": []}], "preferred_name": "SPEEDY PROTEIN C", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR13980", "l": "CDC68 RELATED", "d": [], "t": []}], "preferred_name": "CDC68 RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR48043", "l": "EG:EG0003.4 PROTEIN-RELATED", "d": [], "t": []}], "preferred_name": "EG:EG0003.4 PROTEIN-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR43842:SF2", "l": "PROPIONYL-COA CARBOXYLASE BETA CHAIN, MITOCHONDRIAL", "d": [], "t": []}], "preferred_name": "PROPIONYL-COA CARBOXYLASE BETA CHAIN, MITOCHONDRIAL", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR13190:SF20", "l": "AUTOPHAGY-RELATED PROTEIN 2 HOMOLOG B", "d": [], "t": []}], "preferred_name": "AUTOPHAGY-RELATED PROTEIN 2 HOMOLOG B", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10806:SF28", "l": "SIGNAL PEPTIDASE COMPLEX CATALYTIC SUBUNIT SEC11B-RELATED", "d": [], "t": []}], "preferred_name": "SIGNAL PEPTIDASE COMPLEX CATALYTIC SUBUNIT SEC11B-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:2167", "l": "Solute carrier family 15", "d": [], "t": []}], "preferred_name": "Solute carrier family 15", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR14499:SF122", "l": "BTB_POZ DOMAIN-CONTAINING PROTEIN KCTD7", "d": [], "t": []}], "preferred_name": "BTB_POZ DOMAIN-CONTAINING PROTEIN KCTD7", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR45867:SF3", "l": "ACID PHOSPHATASE TYPE 7", "d": [], "t": []}], "preferred_name": "ACID PHOSPHATASE TYPE 7", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR14235:SF0", "l": "OSTEOCALCIN", "d": [], "t": []}], "preferred_name": "OSTEOCALCIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11500", "l": "BETA CASEIN", "d": [], "t": []}], "preferred_name": "BETA CASEIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR45849", "l": "FACT COMPLEX SUBUNIT SSRP1", "d": [], "t": []}], "preferred_name": "FACT COMPLEX SUBUNIT SSRP1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR16821:SF4", "l": "FRATAXIN, MITOCHONDRIAL", "d": [], "t": []}], "preferred_name": "FRATAXIN, MITOCHONDRIAL", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24044:SF467", "l": "DELTA AND NOTCH-LIKE EPIDERMAL GROWTH FACTOR-RELATED RECEPTOR", "d": [], "t": []}], "preferred_name": "DELTA AND NOTCH-LIKE EPIDERMAL GROWTH FACTOR-RELATED RECEPTOR", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10533:SF14", "l": "PEPTIDE YY-RELATED", "d": [], "t": []}], "preferred_name": "PEPTIDE YY-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR13195:SF0", "l": "PSEUDOURIDYLATE SYNTHASE TRUB2, MITOCHONDRIAL", "d": [], "t": []}], "preferred_name": "PSEUDOURIDYLATE SYNTHASE TRUB2, MITOCHONDRIAL", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:1842", "l": "NDRG family", "d": [], "t": []}], "preferred_name": "NDRG family", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR46769:SF1", "l": "FIBROCYSTIN", "d": [], "t": []}], "preferred_name": "FIBROCYSTIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR14166:SF6", "l": "SLIT-ROBO RHO GTPASE-ACTIVATING PROTEIN 2-RELATED", "d": [], "t": []}], "preferred_name": "SLIT-ROBO RHO GTPASE-ACTIVATING PROTEIN 2-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10218:SF130", "l": "GUANINE NUCLEOTIDE-BINDING PROTEIN SUBUNIT ALPHA-12", "d": [], "t": []}], "preferred_name": "GUANINE NUCLEOTIDE-BINDING PROTEIN SUBUNIT ALPHA-12", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11909:SF100", "l": "SERINE_THREONINE-PROTEIN KINASE VRK2", "d": [], "t": []}], "preferred_name": "SERINE_THREONINE-PROTEIN KINASE VRK2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11256:SF46", "l": "INDUCED MYELOID LEUKEMIA CELL DIFFERENTIATION PROTEIN MCL-1", "d": [], "t": []}], "preferred_name": "INDUCED MYELOID LEUKEMIA CELL DIFFERENTIATION PROTEIN MCL-1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR13650", "l": "SPATACSIN", "d": [], "t": []}], "preferred_name": "SPATACSIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR45161:SF1", "l": "CYTOSKELETON-ASSOCIATED PROTEIN 4", "d": [], "t": []}], "preferred_name": "CYTOSKELETON-ASSOCIATED PROTEIN 4", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR47335:SF1", "l": "UNCONVENTIONAL MYOSIN-XVI", "d": [], "t": []}], "preferred_name": "UNCONVENTIONAL MYOSIN-XVI", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10331:SF23", "l": "CENTROMERE PROTEIN J", "d": [], "t": []}], "preferred_name": "CENTROMERE PROTEIN J", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR46829:SF1", "l": "STERILE ALPHA MOTIF DOMAIN-CONTAINING PROTEIN 15", "d": [], "t": []}], "preferred_name": "STERILE ALPHA MOTIF DOMAIN-CONTAINING PROTEIN 15", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12157:SF15", "l": "REGULATING SYNAPTIC MEMBRANE EXOCYTOSIS PROTEIN 2", "d": [], "t": []}], "preferred_name": "REGULATING SYNAPTIC MEMBRANE EXOCYTOSIS PROTEIN 2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR38498", "l": "TRANSMEMBRANE PROTEIN 191B-RELATED", "d": [], "t": []}], "preferred_name": "TRANSMEMBRANE PROTEIN 191B-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10977:SF3", "l": "DIPHOSPHOMEVALONATE DECARBOXYLASE", "d": [], "t": []}], "preferred_name": "DIPHOSPHOMEVALONATE DECARBOXYLASE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10797:SF1", "l": "CCR4-NOT TRANSCRIPTION COMPLEX SUBUNIT 8", "d": [], "t": []}], "preferred_name": "CCR4-NOT TRANSCRIPTION COMPLEX SUBUNIT 8", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10869", "l": "PROLYL 4-HYDROXYLASE ALPHA SUBUNIT", "d": [], "t": []}], "preferred_name": "PROLYL 4-HYDROXYLASE ALPHA SUBUNIT", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:1928", "l": "Peptidase family A1", "d": ["Aspartic proteases are a catalytic type of protease enzymes that use an activated water molecule bound to one or more aspartate residues for catalysis of their peptide substrates. In general, they have two highly conserved aspartates in the active site and are optimally active at acidic pH. Nearly all known aspartyl proteases are inhibited by pepstatin.Aspartic endopeptidases EC 3.4.23. of vertebrate, fungal and retroviral origin have been characterised. More recently, aspartic endopeptidases associated with the processing of bacterial type 4 prepilin and archaean preflagellin have been described.Eukaryotic aspartic proteases include pepsins, cathepsins, and renins. They have a two-domain structure, arising from ancestral duplication. Retroviral and retrotransposon proteases (retroviral aspartyl proteases) are much smaller and appear to be homologous to a single domain of the eukaryotic aspartyl proteases. Each domain contributes a catalytic Asp residue, with an extended active site cleft localized between the two lobes of the molecule. One lobe has probably evolved from the other through a gene duplication event in the distant past. In modern-day enzymes, although the three-dimensional structures are very similar, the amino acid sequences are more divergent, except for the catalytic site motif, which is very conserved. The presence and position of disulfide bridges are other conserved features of aspartic peptidases."], "t": []}], "preferred_name": "Peptidase family A1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR16489", "l": "GH11727P", "d": [], "t": []}], "preferred_name": "GH11727P", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR16719", "l": "CYTOCHROME C OXIDASE COPPER CHAPERONE", "d": [], "t": []}], "preferred_name": "CYTOCHROME C OXIDASE COPPER CHAPERONE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR34924", "l": "UPF0573 PROTEIN C2ORF70", "d": [], "t": []}], "preferred_name": "UPF0573 PROTEIN C2ORF70", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10404:SF26", "l": "TRANSFERRIN RECEPTOR PROTEIN 1", "d": [], "t": []}], "preferred_name": "TRANSFERRIN RECEPTOR PROTEIN 1", "taxa": []} {"type": 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A typical example is FasR, which forms the DISC upon trimerization as a result of its ligand ( FasL ) binding. The DISC is composed of the death receptor, FADD, and caspase 8. It transduces a downstream signal cascade resulting in apoptosis. The Fas ligands, or cytotoxicity-dependent APO-1-associated proteins, physically associate with APO-1 (also known as the Fas receptor, or CD95), a tumor necrosis factor containing a functional death domain. This association leads to the formation of the DISC, thereby inducing apoptosis. The entire process is initiated when the cell registers the presence of CD95L, the cognate ligand for APO-1. Upon binding, the CAP proteins and procaspase-8 (composed of FLICE, MACH, and Mch5) bind to CD95 through death domain and death effector domain interactions. Procaspase-8 activation is thought to occur through a dimerization process with other procaspase-8 molecules, known as an induced proximity model. The CAP proteins associate only with the oligomerized version of APO-1 when forming the complex. The CAP1 are CAP2 proteins are also known as FADD/MORT1, an adaptor molecule with a death domain. CAP4 is also called FLICE, a cysteine protease with two death effector domains. CAP3 is the prodomain of FLICE generated during proteolytic activation. Once the DISC assembles, it allows APO-1 signaling to occur, which triggers cell death. In order to do this, downstream targets such as FLICE must be activated. In its inactive state, FLICE's two death domains are thought to bind together and prevent its activation. Once APO-1 aggregates within the cytosol, it recruits FADD, CAP3, and FLICE to the receptor, where FLICE is modified into several active subunits, which have the ability to cleave a variety of substrates. This proteolytic activity then results in a cascade of caspase activation, and ultimately cell death. This apoptotic activity is critical for tissue homeostasis and immune function. APO-1-mediated apoptosis can be inhibited by a variety of factors, including the viral caspase inhibitors CrmA and p35, as well as viral FLICE-inhibitory proteins known as v-FLIPs. When in the presence of APO-1, v-FLIPs preferentially bind and prevent procaspase-8 from being recruited; as such, apoptosis is stalled. Interestingly, humans have a homolog for v-FLIP known as c-FLIP, which occurs in two endogenous forms (c-FLIPL (long) and c-FLIPS (short)). These are similar in structure to procaspase-8, but lack the amino acids necessary for caspase-8 catalytic activity. It is thought that c-FLIP may be involved in modulating the immune system, as c-FLIPS is upregulated upon stimulation of the T cell receptor. Furthermore, as high expression of FLIP is known to promote tumor growth, these inhibitor molecules play a role in cancer proliferation. The DISC has been implicated as a possible drug development target for various cancers, including leukemia, glioma, and colon cancer. In glioma cells, the effects of TRAIL (tumor necrosis factor-related apoptosis-inducing ligand) have been shown to induce DISC-mediated apoptosis. Specifically, TRAIL works by activating two death receptors, DR4 and DR5; these bind to FADD, which then interacts with caspase-8 to assemble the DISC. Tumor cells show varying sensitivity to TRAIL modulated apoptosis, depending on the presence of the antiapoptotic FLIP proteins. Additionally, studies in leukemia have indicated that the histone deacetylase inhibitor LAQ824 increases apoptosis by decreasing the expression levels of the c-FLIPs. 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CCHHC-type zinc fingers form small compact structures that can sit entirely within the major groove of DNA (PMID: 18073212),(PMID: 24097990), (PMID: 25098749), (PMID: 26158299), (PMID: 14744132)."], "t": []}], "preferred_name": "Zinc fingers C2H2C-type", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11829:SF167", "l": "HEPATOCYTE NUCLEAR FACTOR 3-BETA", "d": [], "t": []}], "preferred_name": "HEPATOCYTE NUCLEAR FACTOR 3-BETA", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR42757:SF12", "l": "IGLON FAMILY MEMBER 5", "d": [], "t": []}], "preferred_name": "IGLON FAMILY MEMBER 5", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:2246", "l": "FERRY complex subunits", "d": ["The FERRY complex is proposed to function as a Rab5 effector to shuttle mRNA to the cell periphery for local translation."], "t": []}], "preferred_name": "FERRY complex subunits", 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Two GATA zinc fingers are found in GATA-family transcription factors. However, there are several proteins that only contain a single copy of the domain. It is also worth noting that many GATA-type Znfs (such as those found in the proteins GATAD2B and MTA1) have not been experimentally demonstrated to be DNA-binding domains. Furthermore, several GATA-type Znfs have been demonstrated to act as protein-recognition domains. 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In some species there is a single member of this family which gives the mature product mir-33. 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Their action results in the introduction of a trans double-bond between C2 (α) and C3 (β) of the acyl-CoA thioester substrate. Flavin adenine dinucleotide ( FAD ) is a required co-factor in addition to the presence of an active site glutamate in order for the enzyme to function. ACADs can be categorized into three distinct groups based on their specificity for short-, medium-, or long-chain fatty acid acyl-CoA substrates. While different dehydrogenases target fatty acids of varying chain length, all types of ACADs are mechanistically similar. Differences in the enzyme occur based on the location of the active site along the amino acid sequence. ACADs are an important class of enzymes in mammalian cells because of their role in metabolizing fatty acids present in ingested food materials. This enzyme's action represents the first step in fatty acid metabolism (the process of breaking long chains of fatty acids into acetyl CoA molecules). 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This family represents HAD Asp-based protein phosphatases."], "t": []}], "preferred_name": "HAD Asp-based protein phosphatases", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24393:SF69", "l": "HISTONE-LYSINE N-METHYLTRANSFERASE MECOM", "d": [], "t": []}], "preferred_name": "HISTONE-LYSINE N-METHYLTRANSFERASE MECOM", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11860:SF101", "l": "CMRF35-LIKE MOLECULE 1", "d": [], "t": []}], "preferred_name": "CMRF35-LIKE MOLECULE 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR43073:SF2", "l": "DIHYDROPYRIMIDINE DEHYDROGENASE [NADP(+)]", "d": [], "t": []}], "preferred_name": "DIHYDROPYRIMIDINE DEHYDROGENASE [NADP(+)]", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR35660:SF1", "l": "SERINE-RICH AND TRANSMEMBRANE DOMAIN-CONTAINING PROTEIN 1", "d": [], "t": []}], "preferred_name": "SERINE-RICH AND TRANSMEMBRANE DOMAIN-CONTAINING PROTEIN 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR18866:SF33", "l": "METHYLCROTONOYL-COA CARBOXYLASE SUBUNIT ALPHA, MITOCHONDRIAL-RELATED", "d": [], "t": []}], "preferred_name": "METHYLCROTONOYL-COA CARBOXYLASE SUBUNIT ALPHA, MITOCHONDRIAL-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR14429:SF5", "l": "AUTISM SUSCEPTIBILITY GENE 2 PROTEIN", "d": [], "t": []}], "preferred_name": "AUTISM SUSCEPTIBILITY GENE 2 PROTEIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR28588", "l": "HAUS AUGMIN-LIKE COMPLEX SUBUNIT 5", "d": [], "t": []}], "preferred_name": "HAUS AUGMIN-LIKE COMPLEX SUBUNIT 5", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR13194", "l": "COMPLEX I INTERMEDIATE-ASSOCIATED PROTEIN 30", "d": [], "t": []}], "preferred_name": "COMPLEX I INTERMEDIATE-ASSOCIATED PROTEIN 30", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR14087:SF7", "l": "THYMOCYTE NUCLEAR PROTEIN 1", "d": [], "t": []}], "preferred_name": "THYMOCYTE NUCLEAR PROTEIN 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR18914:SF23", "l": "CATENIN ALPHA-2", "d": [], "t": []}], "preferred_name": "CATENIN ALPHA-2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR14677:SF37", "l": "AN1-TYPE ZINC FINGER PROTEIN 1", "d": [], "t": []}], "preferred_name": "AN1-TYPE ZINC FINGER PROTEIN 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24093", "l": "CATION TRANSPORTING ATPASE", "d": [], "t": []}], "preferred_name": "CATION TRANSPORTING ATPASE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR15414", "l": "OS-9-RELATED", "d": [], "t": []}], "preferred_name": "OS-9-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR21588", "l": "COILED-COIL-HELIX-COILED-COIL-HELIX DOMAIN CONTAINING 6", "d": [], "t": []}], "preferred_name": "COILED-COIL-HELIX-COILED-COIL-HELIX DOMAIN CONTAINING 6", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR15692:SF8", "l": "MASTERMIND-LIKE PROTEIN 3", "d": [], "t": []}], "preferred_name": "MASTERMIND-LIKE PROTEIN 3", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR33517:SF4", "l": "SPERMATOGENESIS-ASSOCIATED PROTEIN 46", "d": [], "t": []}], "preferred_name": "SPERMATOGENESIS-ASSOCIATED PROTEIN 46", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR22774:SF15", "l": "BRIDGE-LIKE LIPID TRANSFER PROTEIN FAMILY MEMBER 3A", "d": [], "t": []}], "preferred_name": "BRIDGE-LIKE LIPID TRANSFER PROTEIN FAMILY MEMBER 3A", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:1280", "l": "Super elongation complex", "d": ["The super elongation complex (SEC) consists of the RNA polymerase II (Pol II) elongation factors eleven-nineteen Lys-rich leukaemia (ELL) proteins, positive transcription elongation factor b (P-TEFb) and several frequent mixed lineage leukaemia (MLL) translocation partners. It is one of the most active P-TEFb-containing complexes required for rapid transcriptional induction in the presence or absence of paused Pol II. The SEC was found to regulate the transcriptional elongation checkpoint control (TECC) stage of transcription, and misregulation of this stage is associated with cancer pathogenesis."], "t": []}], "preferred_name": "Super elongation complex", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR48041:SF90", "l": "ATP-BINDING CASSETTE SUB-FAMILY G MEMBER 1", "d": [], "t": []}], "preferred_name": "ATP-BINDING CASSETTE SUB-FAMILY G MEMBER 1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR33663:SF1", "l": "COILED-COIL DOMAIN-CONTAINING PROTEIN 177", "d": [], "t": []}], "preferred_name": "COILED-COIL DOMAIN-CONTAINING PROTEIN 177", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR46282", "l": "LEUCINE-RICH MELANOCYTE DIFFERENTIATION-ASSOCIATED PROTEIN", "d": [], "t": []}], "preferred_name": "LEUCINE-RICH MELANOCYTE DIFFERENTIATION-ASSOCIATED 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"HGNC.FAMILY:1046", "l": "Cellular communication network factors", "d": [], "t": []}], "preferred_name": "Cellular communication network factors", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR20902:SF0", "l": "TRAFFICKING PROTEIN PARTICLE COMPLEX SUBUNIT 5", "d": [], "t": []}], "preferred_name": "TRAFFICKING PROTEIN PARTICLE COMPLEX SUBUNIT 5", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR14958:SF22", "l": "BTB_POZ DOMAIN-CONTAINING PROTEIN KCTD2", "d": [], "t": []}], "preferred_name": "BTB_POZ DOMAIN-CONTAINING PROTEIN KCTD2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11492", "l": "NUCLEAR FACTOR I", "d": [], "t": []}], "preferred_name": "NUCLEAR FACTOR I", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24102:SF18", "l": "PHD FINGER PROTEIN 21B", "d": [], "t": []}], "preferred_name": "PHD FINGER PROTEIN 21B", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR13072", "l": "DYNACTIN 6", "d": [], "t": []}], "preferred_name": "DYNACTIN 6", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR46495:SF3", "l": "DUAL SPECIFICITY PROTEIN PHOSPHATASE 21", "d": [], "t": []}], "preferred_name": "DUAL SPECIFICITY PROTEIN PHOSPHATASE 21", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR12305:SF60", "l": "PHOSPHATIDYLINOSITOL 3,4,5-TRISPHOSPHATE 3-PHOSPHATASE TPTE2-RELATED", "d": [], "t": []}], "preferred_name": "PHOSPHATIDYLINOSITOL 3,4,5-TRISPHOSPHATE 3-PHOSPHATASE TPTE2-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:1225", "l": "UTPb subcomplex", "d": [], "t": []}], "preferred_name": "UTPb subcomplex", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR35156:SF1", "l": "TESTIS-EXPRESSED PROTEIN 52", "d": [], "t": []}], "preferred_name": "TESTIS-EXPRESSED PROTEIN 52", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR24314", "l": "NON-SPECIFIC LIPID TRANSFER PROTEIN-RELATED", "d": [], "t": []}], "preferred_name": "NON-SPECIFIC LIPID TRANSFER PROTEIN-RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR14795", "l": "HELICASE RELATED", "d": [], "t": []}], "preferred_name": "HELICASE RELATED", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR11732:SF294", "l": "ALDO-KETO REDUCTASE FAMILY 1 MEMBER B1", "d": [], "t": []}], "preferred_name": "ALDO-KETO REDUCTASE FAMILY 1 MEMBER B1", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR45852", "l": "SER/THR-PROTEIN KINASE RIO2", "d": [], "t": []}], "preferred_name": "SER/THR-PROTEIN KINASE RIO2", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR23159:SF14", "l": "TESTIS-SPECIFIC GENE 10 PROTEIN", "d": [], "t": []}], "preferred_name": "TESTIS-SPECIFIC GENE 10 PROTEIN", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:1420", "l": "WTAP complex", "d": [], "t": []}], "preferred_name": "WTAP complex", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10677:SF21", "l": "UBIQUILIN-4", "d": [], "t": []}], "preferred_name": "UBIQUILIN-4", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR14549", "l": "TRANSMEMBRANE PROTEIN 223", "d": [], "t": []}], "preferred_name": "TRANSMEMBRANE PROTEIN 223", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR16253", "l": "TETRATRICOPEPTIDE REPEAT PROTEIN 22", "d": [], "t": []}], "preferred_name": "TETRATRICOPEPTIDE REPEAT PROTEIN 22", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR45929", "l": "JAK PATHWAY SIGNAL TRANSDUCTION ADAPTOR MOLECULE", "d": [], "t": []}], "preferred_name": "JAK PATHWAY SIGNAL TRANSDUCTION ADAPTOR MOLECULE", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:1026", "l": "MutS homologs", "d": ["Mismatch repair contributes to the overall fidelity of DNA replication and is essential for combating the adverse effects of damage to the genome. It involves the correction of mismatched base pairs that have been missed by the proofreading element ( Klenow fragment ) of the DNA polymerase complex. The post-replicative Mismatch Repair System (MMRS) of Escherichia coli involves MutS (Mutator S), MutL and MutH proteins, and acts to correct point mutations or small insertion/deletion loops produced during DNA replication. MutS and MutL are involved in preventing recombination between partially homologous DNA sequences. The assembly of MMRS is initiated by MutS, which recognizes and binds to mispaired nucleotides and allows further action of MutL and MutH to eliminate a portion of newly synthesized DNA strand containing the mispaired base. MutS can also collaborate with methyltransferases in the repair of O(6)-methylguanine damage, which would otherwise pair with thymine during replication to create an O(6)mG:T mismatch. MutS exists as a dimer, where the two monomers have different conformations and form a heterodimer at the structural level. Only one monomer recognises the mismatch specifically and has ADP bound. Non-specific major groove DNA-binding domains from both monomers embrace the DNA in a clamp-like structure. Mismatch binding induces ATP uptake and a conformational change in the MutS protein, resulting in a clamp that translocates on DNA. MutS is a modular protein with a complex structure, and is composed of: N-terminal mismatch-recognition domain, which is similar in structure to tRNA endonuclease. Connector domain, which is similar in structure to Holliday junction resolvase ruvC. Core domain, which is composed of two separate subdomains that join together to form a helical bundle; from within the core domain, two helices act as levers that extend towards (but do not touch) the DNA. Clamp domain, which is inserted between the two subdomains of the core domain at the top of the lever helices; the clamp domain has a beta-sheet structure. ATPase domain (connected to the core domain), which has a classical Walker A motif. HTH (helix-turn-helix) domain, which is involved in dimer contacts. Homologues of MutS have been found in many species including eukaryotes (MSH 1, 2, 3, 4, 5, and 6 proteins), archaea and bacteria, and together these proteins have been grouped into the MutS family. Although many of these proteins have similar activities to the E. coli MutS, there is significant diversity of function among the MutS family members. This diversity is even seen within species, where many species encode multiple MutS homologues with distinct functions. Inter-species homologues may have arisen through frequent ancient horizontal gene transfer of MutS (and MutL) from bacteria to archaea and eukaryotes via endosymbiotic ancestors of mitochondria and chloroplasts. ."], "t": []}], "preferred_name": "MutS homologs", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "HGNC.FAMILY:3419", "l": "PEAK pseudokinase family", "d": ["The PEAK family of pseudokinase scaffolds are important regulators and integrators of cellular signaling and also play oncogenic roles in a variety of human cancers."], "t": []}], "preferred_name": "PEAK pseudokinase family", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR17573", "l": "UROPLAKIN II", "d": [], "t": []}], "preferred_name": "UROPLAKIN II", "taxa": []} {"type": "biolink:GeneFamily", "ic": null, "identifiers": [{"i": "PANTHER.FAMILY:PTHR10511:SF2", "l": "GRANULOCYTE COLONY-STIMULATING FACTOR", "d": [], "t": []}], "preferred_name": 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