# terms

id: GO:0141058
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the removal of a methyl group from a modified lysine residue of the histone H4 protein. This is a dioxygenase reaction that is dependent on Fe(II) and 2-oxoglutarate.","definition_xrefs":["PMID:17947579"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone demethylase activity","termid":"GO:0032452"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0032452"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140096"}],"interesting_parent_ids":["GO:0140096","GO:0003674","GO:0003824","GO:0032452"],"is_obsolete":false,"name":"histone H4 demethylase activity","termid":"GO:0141058"}


id: MONDO:0010619
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"X-linked hypophosphatemia (XLH) is a hereditary renal phosphate-wasting disorder characterized by hypophosphatemia, rickets and/or osteomalacia, and diminished growth.","definition_xrefs":["Orphanet:89936"],"direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked dominant disease","termid":"MONDO:0020604"},{"relation_name":"is_a","term_name":"X-linked hypophosphatemic rickets","termid":"MONDO:0020720"},{"relation_name":"is_a","term_name":"abnormal mineralization disorder","termid":"MONDO:0800096"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"X-linked dominant hypophosphatemic rickets","secondary_identifiers":["NANDO:1200779","MESH:D053098","ICD10CM:E83.3","NCIT:C85234","SCTID:82236004","UMLS:C0733682","MEDGEN:196551","NCIT:C123265","DOID:0050445","OMIM:307800","GARD:12943"],"synonyms":[{"name":"HPDR","type":"related"},{"name":"HYP","type":"related"},{"name":"X-linked dominant hypophosphatemic rickets","type":"exact"},{"name":"X-linked hereditary hypophosphatemic rickets","type":"exact"},{"name":"X-linked hypophosphatemia","type":"broad"},{"name":"X-linked hypophosphatemic rickets","type":"broad"},{"name":"XLH","type":"exact"},{"name":"XLHR","type":"related"},{"name":"hereditary hypophosphatemic rickets, X-linked","type":"exact"},{"name":"hypophophatemia, X-linked","type":"related"},{"name":"hypophophatemic vitamin D-resistant rickets","type":"related"},{"name":"hypophosphatemia, X-linked","type":"related"},{"name":"hypophosphatemia, vitamin D-resistant rickets","type":"exact"},{"name":"hypophosphatemic rickets X-linked dominant","type":"exact"},{"name":"hypophosphatemic rickets, X-linked","type":"exact"},{"name":"hypophosphatemic rickets, X-linked dominant","type":"related"},{"name":"hypophosphatemic rickets, X-linked dominant, X-linked dominant","type":"exact"},{"name":"hypophosphatemic vitamin D-resistant rickets","type":"related"},{"name":"rickets, vitamin D-resistant","type":"exact"},{"name":"vitamin D-resistant rickets, X-linked","type":"exact"}],"termid":"MONDO:0010619","xrefs":{"Monarch":{"xref_id":"0010619"}}}


id: PBO:0073034
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"secretin receptor","termid":"PBO:0073034"}


id: MONDO:0003932
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A glioma affecting the optic tract and occurring in childhood.","definition_xrefs":["NCIT:C7535"],"direct_ancestors":[{"relation_name":"is_a","term_name":"optic nerve glioma","termid":"MONDO:0003235"},{"relation_name":"is_a","term_name":"childhood neoplasm","termid":"MONDO:0021079"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"childhood optic nerve glioma","secondary_identifiers":["UMLS:C0278653","DOID:6576","MEDGEN:124487"],"synonyms":[{"name":"childhood optic tract glioma","type":"exact"},{"name":"childhood visual pathway glioma","type":"exact"},{"name":"glioma of childhood visual pathway","type":"exact"},{"name":"glioma of paediatric visual pathway","type":"exact"},{"name":"glioma of pediatric visual pathway","type":"exact"},{"name":"glioma of the childhood visual pathway","type":"exact"},{"name":"glioma of the paediatric visual pathway","type":"exact"},{"name":"glioma of the pediatric visual pathway","type":"exact"},{"name":"optic nerve glioma of childhood","type":"exact"},{"name":"paediatric optic nerve glioma","type":"exact"},{"name":"paediatric optic tract glioma","type":"exact"},{"name":"paediatric visual pathway glioma","type":"exact"},{"name":"pediatric optic nerve glioma","type":"exact"},{"name":"pediatric optic tract glioma","type":"exact"},{"name":"pediatric visual pathway glioma","type":"exact"},{"name":"visual pathway and hypothalamic glioma, childhood","type":"related"},{"name":"visual pathway glioma","type":"broad"}],"termid":"MONDO:0003932","xrefs":{"Monarch":{"xref_id":"0003932"}}}


id: GO:0098700
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The active transport of neurotransmitters into a synaptic vesicle. This import is fuelled by an electrochemical gradient across the vesicle membrane, established by the action of proton pumps.","definition_xrefs":["GOC:PARL","PMID:10099709","GOC:bf","GOC:pad","PMID:15217342"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neurotransmitter transport","termid":"GO:0006836"},{"relation_name":"is_a","term_name":"establishment of localization in cell","termid":"GO:0051649"},{"relation_name":"part_of","term_name":"synaptic vesicle cycle","termid":"GO:0099504"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0016192","GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"neurotransmitter loading into synaptic vesicle","synonyms":[{"name":"neurotransmitter import into synaptic vesicle","type":"exact"},{"name":"neurotransmitter uptake into synaptic vesicle","type":"exact"},{"name":"synaptic vesicle neurotransmitter loading","type":"exact"}],"termid":"GO:0098700"}


id: GO:0050403
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: trans-zeatin + UDP-D-glucose = O-beta-D-glucosyl-trans-zeatin + H+ + UDP.","definition_xrefs":["EC:2.4.1.203","RHEA:23224"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glucosyltransferase activity","termid":"GO:0035251"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016757","GO:0003674","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"trans-zeatin O-beta-D-glucosyltransferase activity","secondary_identifiers":["KEGG_REACTION:R02118","MetaCyc:RXN-4723"],"synonyms":[{"name":"UDP-glucose:trans-zeatin O-beta-D-glucosyltransferase activity","type":"related"},{"name":"UDPglucose:trans-zeatin O-beta-D-glucosyltransferase activity","type":"related"},{"name":"uridine diphosphoglucose-zeatin O-glucosyltransferase activity","type":"related"},{"name":"zeatin O-b-D-glucosyltransferase activity","type":"exact"},{"name":"zeatin O-beta-D-glucosyltransferase activity","type":"related"},{"name":"zeatin O-glucosyltransferase activity","type":"related"}],"termid":"GO:0050403"}


id: PBO:0091653
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycosyl hydrolase family 3","termid":"PBO:0091653"}


id: GO:0019284
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of L-methionine from S-adenosylmethionine.","definition_xrefs":["GOC:vw","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-methionine salvage","termid":"GO:0071267"},{"relation_name":"part_of","term_name":"S-adenosylmethionine cycle","termid":"GO:0033353"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"part_of","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006790","GO:0044281","GO:0008150","GO:0006520"],"is_obsolete":false,"name":"L-methionine salvage from S-adenosylmethionine","synonyms":[{"name":"L-methionine formation from S-adenosylmethionine","type":"exact"},{"name":"L-methionine synthesis from S-adenosylmethionine","type":"exact"}],"termid":"GO:0019284"}


id: PBO:0001886
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DASH complex subunit Dam1","termid":"PBO:0001886"}


id: PR:Q9UTA2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC25B8.18 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9UTA2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"redox protein fmp46, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC25B8.18","synonyms":[{"name":"Spom972h-SPAC25B8.18","type":"exact"}],"termid":"PR:Q9UTA2"}


id: PBO:0075590
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine peptidase inhibitor, Kunitz type 2","termid":"PBO:0075590"}


id: MONDO:0859338
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spermatogenic failure","termid":"MONDO:0004983"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"spermatogenic failure 78","secondary_identifiers":["DOID:0070577","OMIM:620170","MEDGEN:1824049","UMLS:C5774276"],"termid":"MONDO:0859338","xrefs":{"Monarch":{"xref_id":"0859338"}}}


id: MONDO:0020474
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cheirospondyloenchondromatosis is an extremely rare type of enchondromatosis of very early onset (from neonatal period to infancy) characterized by symmetrical multiple enchondromas with metacarpal and phalangeal involvement resulting in short hands and feet, platyspondyly, mild to moderate short stature and intellectual disability.","definition_xrefs":["Orphanet:99647"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with disorganized development of skeletal components (obsolete MONDO:0019708)","termid":"MONDO:0019708"},{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cheirospondyloenchondromatosis","secondary_identifiers":["GARD:19682","icd11.foundation:1707937102","MEDGEN:1390387","UMLS:C4510810","SCTID:725104005"],"synonyms":[{"name":"generalised enchondromatosis with platyspondyly","type":"exact"},{"name":"generalized enchondromatosis with platyspondyly","type":"exact"}],"termid":"MONDO:0020474","xrefs":{"Monarch":{"xref_id":"0020474"}}}


id: PBO:0034313
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_intracellular_endoparasite","termid":"PBO:0034313"}


id: PBO:0059409
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein S35","termid":"PBO:0059409"}


id: PBO:0046339
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ectonucleotide pyrophosphatase/phosphodiesterase 4","termid":"PBO:0046339"}


id: PBO:0082420
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Bifunctional triacylglycerol lipase and 1-acyl DHAP reductase; NADPH-dependent 1-acyl dihydroxyacetone phosphate reductase involved in phosphatidic acid biosynthesis; lipid droplet triacylglycerol lipase involved in mobilization of non-polar lipids; found in lipid particles, endoplasmic reticulum and mitochondrial outer membrane; forms NADPH-regulated channel in mitochondrial outer membrane; required for spore germination; role in cell wall biosynthesis; capable of metabolizing steroid hormones","termid":"PBO:0082420"}


id: GO:0071361
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an ethanol stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to ethanol","termid":"GO:0045471"},{"relation_name":"is_a","term_name":"cellular response to alcohol","termid":"GO:0097306"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to ethanol","termid":"GO:0071361"}


id: PBO:0053451
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long intergenic non-protein coding RNA 399","termid":"PBO:0053451"}


id: MONDO:0035037
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare genetic disorder of the visual organs (obsolete MONDO:0035037)","secondary_identifiers":["Orphanet:522504"],"termid":"MONDO:0035037","xrefs":{"Monarch":{"xref_id":"0035037"}}}


id: PBO:0061608
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear casein kinase and cyclin dependent kinase substrate 1 pseudogene 1","termid":"PBO:0061608"}


id: GO:0051462
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the regulated release of cortisol from a cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of glucocorticoid secretion","termid":"GO:2000849"},{"relation_name":"regulates","term_name":"cortisol secretion","termid":"GO:0043400"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0023052","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"regulation of cortisol secretion","termid":"GO:0051462"}


id: PBO:0078096
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trafficking protein particle complex subunit 4","termid":"PBO:0078096"}


id: PBO:0078122
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor alpha variable 8-4","termid":"PBO:0078122"}


id: PBO:0062856
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"otopetrin 1","termid":"PBO:0062856"}


id: MONDO:0009060
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cystic disease of lung","secondary_identifiers":["UMLS:C0555214","OMIM:219600","MESH:C563237","MEDGEN:640840"],"synonyms":[{"name":"cystic disease of lung","type":"exact"}],"termid":"MONDO:0009060","xrefs":{"Monarch":{"xref_id":"0009060"}}}


id: PBO:0039533
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ANKRD34C antisense RNA 1","termid":"PBO:0039533"}


id: GO:0021957
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Generation of a long process of a pyramidal cell, that carries efferent (outgoing) action potentials from the cell body in cerebral cortex layer V towards target cells in the gray matter of the spinal cord. This axonal process is a member of those that make up the corticospinal tract.","definition_xrefs":["GOC:jid","PMID:9878731","GO_REF:0000021","GOC:cls","GOC:dgh","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"central nervous system projection neuron axonogenesis","termid":"GO:0021952"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"corticospinal tract morphogenesis","synonyms":[{"name":"CST axonogenesis","type":"exact"},{"name":"corticospinal tract axonogenesis","type":"exact"}],"termid":"GO:0021957"}


id: GO:0046854
data:
  {"annotated_genes":["SJAG_03131","SJAG_03170","SJAG_04537","SJAG_00063","SJAG_02613","SJAG_05330","SJAG_01863","SJAG_00053","SJAG_00114","SJAG_04545","SJAG_01571","SJAG_00296","SJAG_04930","SJAG_02289"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90728,91352,92725,96199,110582,110709,117900],"is_not":false,"summary":null,"term":"GO:0046854"},{"annotations":[91350],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902635"},{"annotations":[89923,103860],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1902647"},{"annotations":[97094,61275,61384,62810,110618],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036092"},{"annotations":[116973],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1902648"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of phosphatidylinositol phosphate.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatidylinositol biosynthetic process","termid":"GO:0006661"}],"gene_count":14,"genes_by_uniquename":{"SJAG_00053":null,"SJAG_00063":null,"SJAG_00114":null,"SJAG_00296":null,"SJAG_01571":null,"SJAG_01863":null,"SJAG_02289":null,"SJAG_02613":null,"SJAG_03131":null,"SJAG_03170":null,"SJAG_04537":null,"SJAG_04545":null,"SJAG_04930":null,"SJAG_05330":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"phosphatidylinositol phosphate biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000108":null},"secondary_identifiers":["GO:0046837"],"synonyms":[{"name":"PIP biosynthesis","type":"exact"},{"name":"PtdInsP biosynthesis","type":"exact"},{"name":"phosphatidylinositol phosphate biosynthesis","type":"exact"},{"name":"phosphatidylinositol phosphate phosphorylation","type":"narrow"},{"name":"phosphatidylinositol phosphorylation","type":"related"},{"name":"phosphoinositide phosphorylation","type":"narrow"}],"termid":"GO:0046854","terms_by_termid":{"GO:0036092":null,"GO:0046854":null,"GO:1902635":null,"GO:1902647":null,"GO:1902648":null}}


id: GO:0051154
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of striated muscle cell differentiation.","definition_xrefs":["GOC:ai","CL:0000737"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of muscle cell differentiation","termid":"GO:0051148"},{"relation_name":"is_a","term_name":"regulation of striated muscle cell differentiation","termid":"GO:0051153"},{"relation_name":"negatively_regulates","term_name":"striated muscle cell differentiation","termid":"GO:0051146"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of striated muscle cell differentiation","synonyms":[{"name":"down regulation of striated muscle cell differentiation","type":"exact"},{"name":"down-regulation of striated muscle cell differentiation","type":"exact"},{"name":"downregulation of striated muscle cell differentiation","type":"exact"},{"name":"inhibition of striated muscle cell differentiation","type":"narrow"}],"termid":"GO:0051154"}


id: MONDO:0004026
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A small, benign growth that arises from the skin. It is characterized by the presence of fibrovascular tissue lined by epidermis. It may be sessile or pendulous and usually occurs in sites where there is friction.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reactive cutaneous fibrous lesion","termid":"MONDO:0006603"},{"relation_name":"is_a","term_name":"fibroepithelial polyp","termid":"MONDO:0060765"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"skin tag","secondary_identifiers":["SCTID:201091002","UMLS:C0037293","NCIT:C3374","DOID:6873","MEDGEN:11452"],"synonyms":[{"name":"acrochordon","type":"exact"},{"name":"cutaneous fibroepithelial polyp","type":"exact"},{"name":"cutaneous tag","type":"exact"},{"name":"fibroepithelial polyp","type":"related"},{"name":"fibroepithelial polyp of skin","type":"exact"},{"name":"fibroepithelial polyp of the skin","type":"exact"},{"name":"fibroma molle","type":"exact"},{"name":"soft fibroma","type":"exact"}],"termid":"MONDO:0004026","xrefs":{"Monarch":{"xref_id":"0004026"}}}


id: PBO:0055857
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LRP4 antisense RNA 1","termid":"PBO:0055857"}


id: GO:0090688
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The part of the cleavage furrow closest to the cell surface.","definition_xrefs":["PMID:27082518","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"cleavage furrow","termid":"GO:0032154"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005886","GO:0005575"],"is_obsolete":false,"name":"cleavage furrow rim","termid":"GO:0090688"}


id: GO:0018421
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of N-acetylglucosamine-1-phosphate to a serine residue in a protein.","definition_xrefs":["GOC:mah","PMID:9353330"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphotransferase activity, for other substituted phosphate groups","termid":"GO:0016780"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016780"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016780","GO:0016740","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"UDP-N-acetylglucosamine:serine-protein N-acetylglucosamine-1-phosphotransferase activity","termid":"GO:0018421"}


id: MONDO:0003173
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An astrocytoma that arises from the brain stem.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brain stem glioma","termid":"MONDO:0002911"},{"relation_name":"is_a","term_name":"brain astrocytoma","termid":"MONDO:0021631"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"brain stem astrocytic neoplasm","secondary_identifiers":["UMLS:C1332608","MEDGEN:231458","SCTID:107581000119103","NCIT:C7445","DOID:4860"],"synonyms":[{"name":"astrocytoma (excluding glioblastoma) of brainstem","type":"exact"},{"name":"brain stem astrocytoma","type":"exact"},{"name":"brainstem astrocytoma","type":"exact"},{"name":"brainstem astrocytoma (excluding glioblastoma)","type":"exact"}],"termid":"MONDO:0003173","xrefs":{"Monarch":{"xref_id":"0003173"}}}


id: FYPO:0006935
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which a cell has normal volume, dimensions and shape, and is viable, when subject to nitrogen starvation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"normal cell morphology during nitrogen starvation","termid":"FYPO:0002048"},{"relation_name":"is_a","term_name":"viable cell","termid":"FYPO:0000124"},{"relation_name":"is_a","term_name":"normal cell morphology during nitrogen starvation","termid":"FYPO:0002048"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000004","FYPO:0000257"],"is_obsolete":false,"name":"viable cell with normal cell morphology during nitrogen starvation","synonyms":[{"name":"small viable spherical cell during nitrogen starvation","type":"exact"},{"name":"viable cell with normal cell morphology during nitrogen depletion","type":"exact"},{"name":"viable cell with normal cell morphology during nitrogen deprivation","type":"exact"},{"name":"viable cell with normal cell shape and size during nitrogen starvation","type":"exact"},{"name":"viable cell with normal morphology during nitrogen starvation","type":"exact"},{"name":"viable orb during nitrogen starvation","type":"exact"},{"name":"viable round cells during nitrogen starvation","type":"related"},{"name":"viable rounded cell during nitrogen starvation","type":"related"},{"name":"viable rounded cells during nitrogen starvation","type":"related"},{"name":"viable spherical cell during nitrogen depletion","type":"exact"},{"name":"viable spherical cell during nitrogen deprivation","type":"exact"},{"name":"viable spherical cell during nitrogen starvation","type":"exact"},{"name":"viable spheroid cell during nitrogen depletion","type":"related"},{"name":"viable spheroid cell during nitrogen deprivation","type":"related"},{"name":"viable spheroid cell during nitrogen starvation","type":"related"}],"termid":"FYPO:0006935"}


id: GO:0005091
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"The binding activity of a molecule that brings together a guanyl-nucleotide exchange factor and one or more other proteins, permitting them to function in a coordinated way.","definition_xrefs":["GOC:mtg_MIT_16mar07","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-macromolecule adaptor activity","termid":"GO:0030674"},{"relation_name":"is_a","term_name":"GTPase regulator activity","termid":"GO:0030695"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0060090"},{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0030674"}],"interesting_parent_ids":["GO:0030674","GO:0060090","GO:0030234","GO:0003674","GO:0098772"],"is_obsolete":false,"name":"guanyl-nucleotide exchange factor adaptor activity","termid":"GO:0005091"}


id: PBO:0029584
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_RNA_catabolic_process_during_vegetative_growth","termid":"PBO:0029584"}


id: PBO:0001222
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rab subfamily","termid":"PBO:0001222"}


id: PBO:0083602
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame unlikely to encode a functional protein; identified by homology","termid":"PBO:0083602"}


id: GO:2001057
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving a reactive nitrogen species.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metabolic process","termid":"GO:0008152"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"reactive nitrogen species metabolic process","synonyms":[{"name":"RNS metabolic process","type":"exact"},{"name":"RNS metabolism","type":"exact"},{"name":"reactive nitrogen species metabolism","type":"exact"}],"termid":"GO:2001057"}


id: PBO:0058437
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5001","termid":"PBO:0058437"}


id: MONDO:0003956
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"spondyloarthropathy","termid":"MONDO:0005095"},{"relation_name":"is_a","term_name":"vertebral column disorder","termid":"MONDO:0000812"},{"relation_name":"is_a","term_name":"bone disorder","termid":"MONDO:0005381"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Baastrup syndrome","secondary_identifiers":["UMLS:C0158248","DOID:6643","MEDGEN:510482","SCTID:82304009","ICD9:721.5"],"synonyms":[{"name":"Baastrup syndrome","type":"exact"},{"name":"Baastrup's syndrome","type":"exact"},{"name":"kissing spine","type":"exact"}],"termid":"MONDO:0003956","xrefs":{"Monarch":{"xref_id":"0003956"}}}


id: GO:0140056
data:
  {"annotated_genes":["SJAG_04978","SJAG_00053","SJAG_04221","SJAG_01697","SJAG_03552","SJAG_04413","SJAG_03247","SJAG_03499","SJAG_01772","SJAG_01564","SJAG_01929","SJAG_01168","SJAG_00380","SJAG_03005","SJAG_04417","SJAG_01116","SJAG_00029","SJAG_02699","SJAG_01633","SJAG_03416","SJAG_01305","SJAG_02587","SJAG_05184","SJAG_01598","SJAG_03347","SJAG_03848","SJAG_03710","SJAG_04023","SJAG_04966","SJAG_03170","SJAG_01437","SJAG_01324","SJAG_00171","SJAG_02320","SJAG_02626","SJAG_04370","SJAG_03536","SJAG_00280"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[94132],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016240"},{"annotations":[89921,118114,101278,118382,117595,90994,103857,111114,96957],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061817"},{"annotations":[95055],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048211"},{"annotations":[90416,106988,107114,116058,105318],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990456"},{"annotations":[108885],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071562"},{"annotations":[106493,114647],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990854"},{"annotations":[93828],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140057"},{"annotations":[116993,109117,99015,112127,109270,99807,99707,100615,108145,117972],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048278"},{"annotations":[91841,116949,117651,117870,118273,89233,99747,90091],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006904"}]},"cv_name":"biological_process","definition":"The process by which an organelle membrane interacts with another membrane via molecular tethers that physically bridge the two membranes and attach them to each other.","definition_xrefs":["PMID:27875684"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane docking","termid":"GO:0022406"},{"relation_name":"is_a","term_name":"organelle localization","termid":"GO:0051640"}],"gene_count":38,"genes_by_uniquename":{"SJAG_00029":null,"SJAG_00053":null,"SJAG_00171":null,"SJAG_00280":null,"SJAG_00380":null,"SJAG_01116":null,"SJAG_01168":null,"SJAG_01305":null,"SJAG_01324":null,"SJAG_01437":null,"SJAG_01564":null,"SJAG_01598":null,"SJAG_01633":null,"SJAG_01697":null,"SJAG_01772":null,"SJAG_01929":null,"SJAG_02320":null,"SJAG_02587":null,"SJAG_02626":null,"SJAG_02699":null,"SJAG_03005":null,"SJAG_03170":null,"SJAG_03247":null,"SJAG_03347":null,"SJAG_03416":null,"SJAG_03499":null,"SJAG_03536":null,"SJAG_03552":null,"SJAG_03710":null,"SJAG_03848":null,"SJAG_04023":null,"SJAG_04221":null,"SJAG_04370":null,"SJAG_04413":null,"SJAG_04417":null,"SJAG_04966":null,"SJAG_04978":null,"SJAG_05184":null},"genotype_count":0,"in_subsets":["bp_goslim_japonicus"],"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"organelle localization by membrane tethering","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0140056","terms_by_termid":{"GO:0006904":null,"GO:0016240":null,"GO:0048211":null,"GO:0048278":null,"GO:0061817":null,"GO:0071562":null,"GO:0140057":null,"GO:1990456":null,"GO:1990854":null}}


id: GO:0150051
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The network of the Golgi apparatus structures located within the postsynapse.","definition_xrefs":["PMID:23838184","GOC:bc","GOC:aruk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Golgi apparatus","termid":"GO:0005794"},{"relation_name":"part_of","term_name":"postsynapse","termid":"GO:0098794"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005794"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005794","GO:0005737","GO:0005575"],"is_obsolete":false,"name":"postsynaptic Golgi apparatus","synonyms":[{"name":"Golgi outpost","type":"related"}],"termid":"GO:0150051"}


id: MONDO:0003780
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A broad classification of disorders that affect the cell-mediated aspect of the immune response. Circulating numbers of T lymphocytes are decreased or ineffective.","definition_xrefs":["NCIT:C27145"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immunodeficiency disease","termid":"MONDO:0021094"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"T-cell immunodeficiency","secondary_identifiers":["DOID:613","SCTID:402792003","UMLS:C1274233","MEDGEN:226894"],"synonyms":[{"name":"T lymphocyte deficiency","type":"related"},{"name":"T-cell immunodeficiency","type":"exact"},{"name":"T-lymphocyte deficiency (finding)","type":"exact"},{"name":"T-lymphocyte immunodeficiency","type":"exact"}],"termid":"MONDO:0003780","xrefs":{"Monarch":{"xref_id":"0003780"}}}


id: MONDO:0002771
data:
  {"annotated_genes":["SJAG_01836","SJAG_03855","SJAG_02194","SJAG_00566","SJAG_05979","SJAG_03125"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84594],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0800029"},{"annotations":[86092],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957261"},{"annotations":[86091],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957263"},{"annotations":[85860],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957294"},{"annotations":[85691],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013878"},{"annotations":[84819],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014612"},{"annotations":[86654],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030690"}]},"cv_name":"mondo","definition":"Chronic progressive interstitial lung disorder characterized by the replacement of the lung tissue by connective tissue, leading to progressive dyspnea, respiratory failure, or right heart failure. Causes include chronic inflammatory processes, exposure to environmental irritants, radiation therapy, autoimmune disorders, certain drugs, or it may be idiopathic (no identifiable cause).","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"interstitial lung disease","termid":"MONDO:0015925"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00566":null,"SJAG_01836":null,"SJAG_02194":null,"SJAG_03125":null,"SJAG_03855":null,"SJAG_05979":null},"genotype_count":0,"is_obsolete":false,"name":"pulmonary fibrosis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:3770","MEDGEN:11028","MESH:D011658","EFO:0009448","NCIT:C26869","SCTID:51615001","UMLS:C0034069"],"synonyms":[{"name":"fibrosis of lung","type":"exact"},{"name":"pulmonary interstitial fibrosis","type":"exact"}],"termid":"MONDO:0002771","terms_by_termid":{"MONDO:0013878":null,"MONDO:0014612":null,"MONDO:0030690":null,"MONDO:0800029":null,"MONDO:0957261":null,"MONDO:0957263":null,"MONDO:0957294":null},"xrefs":{"Monarch":{"xref_id":"0002771"}}}


id: PBO:0086774
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; SWAT-GFP and mCherry fusion proteins localize to the cell periphery and vacuole; YCL048W-A has a paralog, YDR524C-B, that arose from the whole genome duplication","termid":"PBO:0086774"}


id: MONDO:0019269
data:
  {"annotated_genes":["SJAG_02085","SJAG_02842","SJAG_02326","SJAG_01307"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84805,84806],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014010"},{"annotations":[85391,85392],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100221"}]},"cv_name":"mondo","definition":"Disorders of cornification that are characterized by visible scaling and/or hyperkeratosis of most or all of the skin. Inherited ichthyoses, defined as the generalized form of Mendelian disorders of cornification, affect most or all of the skin. This etiologically and phenotypically heterogenous group of conditions is caused by mutations in various different genes important for keratinocyte differentiation and epidermal barrier function. Acquired forms of ichthyosis can be observed with certain autoimmune, inflammatory, metabolic, endocrine, or infectious diseases or with malignancies.","definition_xrefs":["PMID:22739337"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epidermal disease","termid":"MONDO:0019268"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01307":null,"SJAG_02085":null,"SJAG_02326":null,"SJAG_02842":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"ichthyosis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:79354","MedDRA:10021198","HP:0008064","MESH:D007057","MEDGEN:7002","GARD:18985","NANDO:1200618","NCIT:C84776","DOID:1697","UMLS:C0020757"],"synonyms":[{"name":"DOC","type":"exact"},{"name":"disorder of cornification","type":"exact"},{"name":"fish scale disease","type":"exact"},{"name":"fish skin disease","type":"exact"},{"name":"ichthyoses","type":"exact"},{"name":"ichthyosis","type":"exact"},{"name":"ichthyosis (disease)","type":"exact"},{"name":"non-syndromic ichthyosis","type":"related"}],"termid":"MONDO:0019269","terms_by_termid":{"MONDO:0014010":null,"MONDO:0100221":null},"xrefs":{"Monarch":{"xref_id":"0019269"}}}


id: PBO:0015225
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CWg2 Partner","termid":"PBO:0015225"}


id: MONDO:0023196
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"frontonasal malformation cloacal exstrophy","synonyms":[{"name":"fronto nasal malformation cloacal exstrophy","type":"related"}],"termid":"MONDO:0023196","xrefs":{"Monarch":{"xref_id":"0023196"}}}


id: PBO:0046192
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ELMO domain containing 3","termid":"PBO:0046192"}


id: MONDO:0018864
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Kikuchi-Fujimoto disease (KFD) is a benign and self-limited disorder, characterized by regional cervical lymphadenopathy with tenderness, usually accompanied with mild fever and night sweats. Less frequent symptoms include weight loss, nausea, vomiting, sore throat.","definition_xrefs":["Orphanet:50918"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymphadenitis","termid":"MONDO:0002052"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"Kikuchi-Fujimoto disease","secondary_identifiers":["NCIT:C71719","UMLS:C0398367","MEDGEN:97979","MESH:D020042","SCTID:127217009","GARD:6834"],"synonyms":[{"name":"Kikuchi disease","type":"exact"},{"name":"Kikuchi necrotizing lymphadenitis","type":"related"},{"name":"Kikuchi's disease","type":"related"},{"name":"Kikuchi-Fujimoto's disease","type":"related"},{"name":"histiocytic necrotising lymphadenitis","type":"related"},{"name":"histiocytic necrotizing lymphadenitis","type":"exact"},{"name":"nosocomial Kikuchi's disease","type":"related"}],"termid":"MONDO:0018864","xrefs":{"Monarch":{"xref_id":"0018864"}}}


id: PBO:0071123
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 125","termid":"PBO:0071123"}


id: GO:0008810
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the endohydrolysis of (1->4)-beta-D-glucosidic linkages in cellulose, lichenin and cereal beta-D-glucans.","definition_xrefs":["EC:3.2.1.4"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, hydrolyzing O-glycosyl compounds","termid":"GO:0004553"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016798"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0016798","GO:0003824"],"is_obsolete":false,"name":"cellulase activity","secondary_identifiers":["MetaCyc:RXN-2043"],"synonyms":[{"name":"1,4-(1,3;1,4)-beta-D-glucan 4-glucanohydrolase activity","type":"related"},{"name":"9.5 cellulase activity","type":"related"},{"name":"alkali cellulase activity","type":"narrow"},{"name":"avicelase activity","type":"related"},{"name":"beta-1,4-endoglucan hydrolase activity","type":"broad"},{"name":"beta-1,4-glucanase activity","type":"broad"},{"name":"carboxymethyl cellulase activity","type":"narrow"},{"name":"celluase A","type":"related"},{"name":"celludextrinase activity","type":"related"},{"name":"cellulase A 3","type":"related"},{"name":"cellulosin AP","type":"related"},{"name":"endo-1,4-beta-D-glucanase activity","type":"broad"},{"name":"endo-1,4-beta-D-glucanohydrolase activity","type":"broad"},{"name":"endo-1,4-beta-glucanase activity","type":"broad"},{"name":"endoglucanase D","type":"related"},{"name":"endoglucanase activity","type":"broad"},{"name":"pancellase SS","type":"related"}],"termid":"GO:0008810"}


id: MONDO:0001857
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A brucellosis involving an infection caused by Brucella canis [NCBITaxon:36855] in dogs and humans. The disease has symptom fever, has symptom sweats, has symptom weakness, has symptom weight loss, has symptom headache, has symptom lymphadenopathy and has symptom splenomegaly.","definition_xrefs":["DOID:14019","PMID:1172954"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brucellosis","termid":"MONDO:0005683"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Brucella canis brucellosis","secondary_identifiers":["SCTID:428174001","UMLS:C0494040","ICD9:023.3","MEDGEN:635501"],"termid":"MONDO:0001857","xrefs":{"Monarch":{"xref_id":"0001857"}}}


id: PBO:0088325
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GATOR2-SEACAT complex/GATOR1-SEACIT GTPase complex ubiquitin-protein ligase E3 subunit Sea3","termid":"PBO:0088325"}


id: GO:1902217
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any apoptotic process in an erythrocyte.","definition_xrefs":["GOC:mtg_apoptosis","GOC:rl","GOC:TermGenie","GOC:BHF","PMID:14569084"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myeloid cell apoptotic process","termid":"GO:0033028"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"erythrocyte apoptotic process","synonyms":[{"name":"RBC apoptosis","type":"narrow"},{"name":"RBC apoptotic process","type":"exact"},{"name":"erythrocyte apoptosis","type":"narrow"},{"name":"red blood cell apoptosis","type":"narrow"},{"name":"red blood cell apoptotic process","type":"exact"}],"termid":"GO:1902217"}


id: PBO:0045304
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynamin binding protein","termid":"PBO:0045304"}


id: PBO:0068765
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 2","termid":"PBO:0068765"}


id: GO:0047122
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: A + H2O + quinaldate = AH(2) + kynurenate.","definition_xrefs":["RHEA:16697","EC:1.3.99.18"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-CH group of donors","termid":"GO:0016627"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"quinaldate 4-oxidoreductase activity","secondary_identifiers":["MetaCyc:1.3.99.18-RXN","KEGG_REACTION:R03687"],"synonyms":[{"name":"quinaldic acid 4-oxidoreductase activity","type":"related"},{"name":"quinoline-2-carboxylate:acceptor 4-oxidoreductase (hydroxylating)","type":"related"}],"termid":"GO:0047122"}


id: PBO:0051410
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin lambda variable 1-44","termid":"PBO:0051410"}


id: PBO:0088385
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FAD-dependent oxidoreductase involved in late endosome to Golgi transport","termid":"PBO:0088385"}


id: PBO:0039899
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rho guanine nucleotide exchange factor 3","termid":"PBO:0039899"}


id: GO:0033421
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A triplet codon-amino acid adaptor activity that recognizes a CCU codon.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"triplet codon-amino acid adaptor activity","termid":"GO:0030533"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003723"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0060090"}],"interesting_parent_ids":["GO:0003674","GO:0060090","GO:0005488","GO:0003723"],"is_obsolete":false,"name":"CCU codon-amino acid adaptor activity","synonyms":[{"name":"CCT codon-amino acid adaptor activity","type":"exact"},{"name":"proline tRNA","type":"related"}],"termid":"GO:0033421"}


id: MONDO:0032864
data:
  {"annotated_genes":["SJAG_04350"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86395],"is_not":false,"summary":null,"term":"MONDO:0032864"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04350":null},"genotype_count":0,"is_obsolete":false,"name":"intellectual developmental disorder with speech delay, autism, and dysmorphic facies","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5231456","MEDGEN:1684848","OMIM:618672"],"synonyms":[{"name":"IDDSADF","type":"related"},{"name":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, AUTISM, AND DYSMORPHIC FACIES","type":"related"}],"termid":"MONDO:0032864","terms_by_termid":{"MONDO:0032864":null},"xrefs":{"Monarch":{"xref_id":"0032864"}}}


id: PR:O94251
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pop7 gene.","definition_xrefs":["UniProtKB:O94251","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribonucleases P/MRP protein subunit POP7 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBP8B7.01c","synonyms":[{"name":"RNA-processing protein POP7 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-pop7","type":"exact"}],"termid":"PR:O94251"}


id: MOD:01976
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-serine residue to O3-(poly-3-hydroxybutyrate)-L-serine.","definition_xrefs":["PubMed:17659252","PubMed:20004640","RESID:AA0618"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-acylated residue","termid":"MOD:00671"},{"relation_name":"is_a","term_name":"modified L-serine residue","termid":"MOD:00916"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"O3-(poly-3-hydroxybutyrate)-L-serine","synonyms":[{"name":"(2S)-2-amino-3-[([(3R)-3-hydroxybutanoyl]oxy)-poly([(3R)-3-methyl-1-oxopropane-1,3-diyl]oxy)]propanoic acid","type":"exact"},{"name":"MOD_RES O3-poly(beta-hydroxybutyryl)lysine","type":"exact"},{"name":"O3-(poly-3-hydroxybutyrate)-L-serine","type":"exact"},{"name":"O3-poly(3-hydroxybutanoate)serine","type":"exact"},{"name":"O3-poly(3-hydroxybutanoic acid)serine","type":"exact"},{"name":"O3-poly(3-hydroxybutyrate)serine","type":"exact"},{"name":"O3-poly(3-hydroxybutyric acid)serine","type":"exact"},{"name":"O3-poly(beta-hydroxybutyrate)serine","type":"exact"},{"name":"O3-poly[(R)-3-hydroxybutyrate]serine","type":"exact"}],"termid":"MOD:01976"}


id: GO:0052633
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: cis-aconitate + H2O = isocitrate.","definition_xrefs":["GOC:pde","MetaCyc:ACONITATEHYDR-RXN","GOC:vw","EC:4.2.1.3"],"gene_count":0,"genotype_count":0,"name":"obsolete isocitrate hydro-lyase (cis-aconitate-forming) activity (obsolete GO:0052633)","synonyms":[{"name":"aconitate hydratase activity","type":"broad"},{"name":"cis-aconitase activity","type":"broad"},{"name":"citrate hydro-lyase activity","type":"broad"},{"name":"citrate(isocitrate) hydro-lyase (cis-aconitate-forming)","type":"broad"},{"name":"citrate(isocitrate) hydro-lyase activity","type":"broad"}],"termid":"GO:0052633"}


id: PBO:0017919
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schizosaccharomyces specific protein, double strand break localizing Dbl7","termid":"PBO:0017919"}


id: MONDO:0014495
data:
  {"annotated_genes":["SJAG_02623"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86223],"is_not":false,"summary":null,"term":"MONDO:0014495"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02623":null},"genotype_count":0,"is_obsolete":false,"name":"retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C4015242","OMIM:616108","Orphanet:436245","GARD:17730","MEDGEN:863679"],"synonyms":[{"name":"RDJCSS","type":"related"},{"name":"retinal dystrophy, juvenile cataracts, and short stature syndrome","type":"related"},{"name":"retinal dystrophy-juvenile cataract-short stature syndrome","type":"exact"}],"termid":"MONDO:0014495","terms_by_termid":{"MONDO:0014495":null},"xrefs":{"Monarch":{"xref_id":"0014495"}}}


id: PBO:0082563
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Chaperone for Replication Protein A complex (RPA); involved in nuclear import of RPA and its binding to ssDNA at replication forks; has a role in regulation of Ty1 transposition","termid":"PBO:0082563"}


id: GO:0052184
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The alteration by an organism of the levels of hormones or growth regulators in the symbiont organism. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation by organism of symbiont hormone or growth regulator levels (obsolete GO:0052184)","synonyms":[{"name":"modulation by organism of symbiont hormone or growth regulator levels","type":"exact"}],"termid":"GO:0052184"}


id: MONDO:0001967
data:
  {"annotated_genes":["SJAG_04950","SJAG_03077","SJAG_03051","SJAG_04148"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85352],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:8000015"},{"annotations":[86481],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030736"},{"annotations":[85167],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013689"},{"annotations":[85926],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054850"}]},"cv_name":"mondo","definition":"A congenital disorder characterized by the presence of extremely hypoplastic gonads preventing the development of secondary sex characteristics.","definition_xrefs":["NCIT:C61420"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypogonadism","termid":"MONDO:0002146"}],"gene_count":4,"genes_by_uniquename":{"SJAG_03051":null,"SJAG_03077":null,"SJAG_04148":null,"SJAG_04950":null},"genotype_count":0,"is_obsolete":false,"name":"gonadal dysgenesis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0018051","GARD:2538","ICD9:758.6","MEDGEN:9075","SCTID:205681004","DOID:14447","MESH:D006059"],"synonyms":[{"name":"gonadal dysgenesis syndrome","type":"exact"}],"termid":"MONDO:0001967","terms_by_termid":{"MONDO:0013689":null,"MONDO:0030736":null,"MONDO:0054850":null,"MONDO:8000015":null},"xrefs":{"Monarch":{"xref_id":"0001967"}}}


id: GO:0071572
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of histone H3 by the removal of an acetyl group from lysine at position 56 of the histone.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete histone H3-K56 deacetylation (obsolete GO:0071572)","termid":"GO:0071572"}


id: GO:0030555
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Specifies the site of a posttranscriptional modification in an RNA molecule by base pairing with a short sequence around the target residue.","definition_xrefs":["GOC:mah","PMID:12457565"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA binding","termid":"GO:0003723"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003723"}],"interesting_parent_ids":["GO:0003674","GO:0003723","GO:0005488"],"is_obsolete":false,"name":"RNA modification guide activity","termid":"GO:0030555"}


id: MONDO:0010458
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hypospadias","termid":"MONDO:0005345"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypospadias 4, X-linked","secondary_identifiers":["GARD:18187","UMLS:C3275458","OMIM:300856","MEDGEN:477089"],"synonyms":[{"name":"HYSP4","type":"related"},{"name":"hypospadias 4, X-linked, susceptibility to","type":"related"}],"termid":"MONDO:0010458","xrefs":{"Monarch":{"xref_id":"0010458"}}}


id: FYPO:0004350
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of RNA measured in a cell during a cellular response to methylglyoxal is normal (i.e. indistinguishable from wild type). Total RNA or a specific RNA, such as the mRNA transcribed from a gene of interest, may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal RNA level during vegetative growth","termid":"FYPO:0001317"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0000257","FYPO:0001312"],"is_obsolete":false,"name":"normal RNA level during cellular response to methylglyoxal","synonyms":[{"name":"normal RNA accumulation during cellular response to methylglyoxal","type":"related"},{"name":"normal RNA level during cellular response to methylglyoxal during mitotic cell cycle","type":"related"},{"name":"normal RNA level during cellular response to methylglyoxal during vegetative growth","type":"exact"},{"name":"normal mRNA level during cellular response to methylglyoxal","type":"narrow"},{"name":"normal transcript level during cellular response to methylglyoxal","type":"exact"}],"termid":"FYPO:0004350"}


id: PBO:0038950
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adipocyte associated pyruvate carboxylase interacting lncRNA","termid":"PBO:0038950"}


id: GO:0062058
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a transcription factor TFIIH holo complex.","definition_xrefs":["PMID:11259578"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex binding","termid":"GO:0044877"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"transcription factor TFIIH holo complex binding","termid":"GO:0062058"}


id: PBO:0078742
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TRMT2B antisense RNA 1","termid":"PBO:0078742"}


id: GO:0004619
data:
  {"annotated_genes":["SJAG_02009"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[94518],"is_not":false,"summary":null,"term":"GO:0004619"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: (2R)-2-phosphoglycerate = (2R)-3-phosphoglycerate.","definition_xrefs":["RHEA:15901"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular phosphotransferase activity","termid":"GO:0016868"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02009":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016853","GO:0003674"],"is_obsolete":false,"name":"phosphoglycerate mutase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-71654","Reactome:R-HSA-71445","KEGG_REACTION:R01516"],"synonyms":[{"name":"2,3-bisphosphoglycerate-dependent phosphoglycerate mutase activity","type":"narrow"},{"name":"2,3-bisphosphoglycerate-independent phosphoglycerate mutase activity","type":"narrow"},{"name":"D-phosphoglycerate 2,3-phosphomutase activity","type":"related"},{"name":"PGA mutase activity","type":"related"},{"name":"PGAM activity","type":"related"},{"name":"PGM","type":"exact"},{"name":"phosphoglycerate phosphomutase activity","type":"related"},{"name":"phosphoglyceromutase activity","type":"related"}],"termid":"GO:0004619","terms_by_termid":{"GO:0004619":null}}


id: PBO:0073067
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"syndecan 4 pseudogene","termid":"PBO:0073067"}


id: PBO:0070132
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 46 pseudogene","termid":"PBO:0070132"}


id: GO:0160112
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A structural network of microtubule inner proteins (MIPs) located inside the lumen of the B tubule of the axonemal microtubule doublet that helps stabilize the B tubule.","definition_xrefs":["PMID:37295417","GOC:krc","PMID:29430673"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"A axonemal microtubule","termid":"GO:0097649"},{"relation_name":"part_of","term_name":"axonemal microtubule doublet inner sheath","termid":"GO:0160110"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0015630"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0015630","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"axonemal B tubule inner sheath","termid":"GO:0160112"}


id: PBO:0066063
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rap guanine nucleotide exchange factor like 1","termid":"PBO:0066063"}


id: PBO:0055904
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat containing 27","termid":"PBO:0055904"}


id: PBO:0051742
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"integrator complex subunit 9","termid":"PBO:0051742"}


id: MONDO:0032617
data:
  {"annotated_genes":["SJAG_03782"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85774],"is_not":false,"summary":null,"term":"MONDO:0032617"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial complex I deficiency, nuclear type","termid":"MONDO:0100223"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03782":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005066"],"is_obsolete":false,"name":"mitochondrial complex 1 deficiency, nuclear type 11","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:16321","OMIM:618234","MEDGEN:1648356","DOID:0112089","UMLS:C4748769"],"synonyms":[{"name":"MC1DN11","type":"related"},{"name":"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 11","type":"related"}],"termid":"MONDO:0032617","terms_by_termid":{"MONDO:0032617":null},"xrefs":{"Monarch":{"xref_id":"0032617"}}}


id: PBO:0046044
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation initiation factor 3 subunit C","termid":"PBO:0046044"}


id: PBO:0052874
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin associated protein 6-3","termid":"PBO:0052874"}


id: FYECO:0000088
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which 2-oxoglutarate was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ 2-OG","synonyms":[{"name":"2-OG present","type":"exact"},{"name":"2-oxoglutarate added","type":"exact"},{"name":"2-oxoglutarate present","type":"exact"}],"termid":"FYECO:0000088"}


id: PBO:0030137
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_GTPase_activity","termid":"PBO:0030137"}


id: PBO:0055654
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long intergenic non-protein coding RNA 3094","termid":"PBO:0055654"}


id: PBO:0043729
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase subunit 6C pseudogene 8","termid":"PBO:0043729"}


id: PBO:0060118
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND6 pseudogene 19","termid":"PBO:0060118"}


id: GO:1900098
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of plasma cell differentiation.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of immune effector process","termid":"GO:0002697"},{"relation_name":"is_a","term_name":"regulation of B cell differentiation","termid":"GO:0045577"},{"relation_name":"is_a","term_name":"regulation of immune response","termid":"GO:0050776"},{"relation_name":"regulates","term_name":"plasma cell differentiation","termid":"GO:0002317"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of plasma cell differentiation","synonyms":[{"name":"regulation of plasma cell development","type":"related"}],"termid":"GO:1900098"}


id: GO:0140364
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A ribonucleoprotein granule located in the cytoplasm and the nucleus. GW-bodies minimally contain the Argonaute2 (Ago2) and TNRC6B proteins, together with specific target RNAs.","definition_xrefs":["PMID:16418578","PMID:26930655","PMID:29576456"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoplasmic ribonucleoprotein granule","termid":"GO:0036464"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005737","GO:0005575"],"is_obsolete":false,"name":"GW body","synonyms":[{"name":"GW-body","type":"exact"}],"termid":"GO:0140364"}


id: PATO:0001707
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A behavioral quality of a process inhering in a bearer by virtue of the bearer's exhibiting marked activity.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"behavioural activity","termid":"PATO:0002265"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"behavioural active","termid":"PATO:0001707"}


id: PBO:0064942
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protease associated domain containing 1","termid":"PBO:0064942"}


id: PBO:0017647
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cenp-W ortholog","termid":"PBO:0017647"}


id: GO:0051292
data:
  {"annotated_genes":["SJAG_01833"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[107231],"is_not":false,"summary":null,"term":"GO:0051292"}]},"cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a nuclear pore complex.","definition_xrefs":["GOC:ai","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear pore organization","termid":"GO:0006999"},{"relation_name":"is_a","term_name":"pore complex assembly","termid":"GO:0046931"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01833":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0065003"}],"interesting_parent_ids":["GO:0044085","GO:0008150","GO:0065003"],"is_obsolete":false,"name":"nuclear pore complex assembly","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"NPC assembly","type":"exact"},{"name":"nuclear pore assembly","type":"exact"},{"name":"nuclear pore biogenesis","type":"exact"},{"name":"nuclear pore biosynthesis","type":"exact"},{"name":"nuclear pore complex biogenesis","type":"exact"},{"name":"nuclear pore complex biosynthesis","type":"exact"},{"name":"nuclear pore complex formation","type":"exact"},{"name":"nuclear pore formation","type":"exact"}],"termid":"GO:0051292","terms_by_termid":{"GO:0051292":null}}


id: PBO:0004313
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autophagy associated protein Atg9","termid":"PBO:0004313"}


id: GO:0051378
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to serotonin (5-hydroxytryptamine), a monoamine neurotransmitter occurring in the peripheral and central nervous systems, also having hormonal properties.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cation binding","termid":"GO:0043169"},{"relation_name":"is_a","term_name":"amine binding","termid":"GO:0043176"},{"relation_name":"is_a","term_name":"organic cyclic compound binding","termid":"GO:0097159"},{"relation_name":"is_a","term_name":"heterocyclic compound binding","termid":"GO:1901363"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"serotonin binding","synonyms":[{"name":"5-hydroxytryptamine binding","type":"exact"}],"termid":"GO:0051378"}


id: MONDO:0017840
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The simple virilizing form of classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency (classical 21 OHD CAH) is characterized by genital ambiguity and virilization of the external genitalia in females, hypocortisolism and precocious pseudopuberty without salt-wasting.","definition_xrefs":["Orphanet:315311"],"direct_ancestors":[{"relation_name":"is_a","term_name":"classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency","termid":"MONDO:0008728"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002525"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0002525"],"is_obsolete":false,"name":"classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, simple virilizing form","secondary_identifiers":["MEDGEN:1826061","GARD:21399","UMLS:C5679895"],"synonyms":[{"name":"classic 21-OHD CAH, simple virilizing form","type":"exact"}],"termid":"MONDO:0017840","xrefs":{"Monarch":{"xref_id":"0017840"}}}


id: PBO:0040348
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP synthase membrane subunit f pseudogene 5","termid":"PBO:0040348"}


id: GO:0034900
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 3-(N-formyl)-formiminopyruvate + H2O = 3-formiminopyruvate + formate.","definition_xrefs":["UM-BBD_reactionID:r1399"],"gene_count":0,"genotype_count":0,"name":"obsolete 3-(N-formyl)-formiminopyruvate hydrolase activity (obsolete GO:0034900)","termid":"GO:0034900"}


id: GO:0002656
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of tolerance induction to nonself antigen.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of tolerance induction dependent upon immune response","termid":"GO:0002653"},{"relation_name":"is_a","term_name":"regulation of tolerance induction to nonself antigen","termid":"GO:0002655"},{"relation_name":"negatively_regulates","term_name":"tolerance induction to nonself antigen","termid":"GO:0002462"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of tolerance induction to nonself antigen","synonyms":[{"name":"down regulation of tolerance induction to nonself antigen","type":"exact"},{"name":"down-regulation of tolerance induction to nonself antigen","type":"exact"},{"name":"downregulation of tolerance induction to nonself antigen","type":"exact"},{"name":"inhibition of tolerance induction to nonself antigen","type":"narrow"}],"termid":"GO:0002656"}


id: GO:0033204
data:
  {"annotated_genes":["SJAG_01623","SJAG_03796"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[104038,118032],"is_not":false,"summary":null,"term":"GO:0033204"}]},"cv_name":"molecular_function","definition":"Binding to RNA subunit of ribonuclease P.","definition_xrefs":["PMID:11455963","GOC:pg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA binding","termid":"GO:0003723"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01623":null,"SJAG_03796":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003723"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003723","GO:0003674"],"is_obsolete":false,"name":"ribonuclease P RNA binding","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"RNase P RNA binding","type":"exact"}],"termid":"GO:0033204","terms_by_termid":{"GO:0033204":null}}


id: GO:1990038
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The periphery of a Lewy body. In Parkinson's disease, it contains spherical accumulations of filaments arranged in a loose, radiating array.","definition_xrefs":["NIF_Subcellular:sao5764355747"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"Lewy body","termid":"GO:0097413"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"Lewy body corona","synonyms":[{"name":"halo","type":"broad"}],"termid":"GO:1990038"}


id: MONDO:0004391
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A extraosseous chondrosarcoma that occurs in an adult.","definition_xrefs":["MONDO:design_pattern"],"gene_count":0,"genotype_count":0,"name":"obsolete adult extraosseous chondrosarcoma (obsolete MONDO:0004391)","secondary_identifiers":["DOID:7902"],"synonyms":[{"name":"extraosseous chondrosarcoma of adults","type":"exact"}],"termid":"MONDO:0004391","xrefs":{"Monarch":{"xref_id":"0004391"}}}


id: FYPO:0007859
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the nucleus divides into two or more fragments, each enclosed by nuclear envelope and containing a DNA mass, in a cell that does not form a mitotic spindle or undergo cytokinesis. In these cells, the nucleus does not elongate into a dumbbell shape, but instead the nuclear envelope takes on a ruffled aspect and then eventually pinches into two nuclear masses.","definition_xrefs":["PomBase:jh","PMID:20967237","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitosis","termid":"FYPO:0000337"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0001985","FYPO:0000337","FYPO:0005447","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"nuclear division in absence of mitotic spindle","synonyms":[{"name":"nuclear division in absence of mitotic spindle during mitotic cell cycle","type":"related"},{"name":"nuclear division in absence of mitotic spindle during vegetative growth","type":"exact"},{"name":"nuclear fission","type":"exact"},{"name":"nuclear fission in absence of mitotic spindle","type":"exact"},{"name":"rel syn DNA segregation in absence of mitotic spindle","type":"related"}],"termid":"FYPO:0007859"}


id: GO:0005104
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a fibroblast growth factor receptor (FGFR).","definition_xrefs":["GOC:ceb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"growth factor receptor binding","termid":"GO:0070851"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"fibroblast growth factor receptor binding","secondary_identifiers":["GO:0001521","GO:0005162"],"synonyms":[{"name":"FGF receptor binding","type":"exact"},{"name":"FGFR binding","type":"exact"},{"name":"FGFR ligand","type":"narrow"},{"name":"fibroblast growth factor","type":"broad"},{"name":"fibroblast growth factor receptor ligand","type":"narrow"}],"termid":"GO:0005104"}


id: PR:O14254
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An isocitrate dehydrogenase [NADP], mitochondrial that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR11822:SF0","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"isocitrate dehydrogenase [NADP], mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC6G10.08","secondary_identifiers":["UniProtKB:O14254"],"synonyms":[{"name":"IDH (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"IDP (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"NADP(+)-specific ICDH (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"SPAC6G10.08","type":"related"},{"name":"Spom972h-IDH2nadp","type":"exact"},{"name":"oxalosuccinate decarboxylase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14254"}


id: PBO:0057672
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1263","termid":"PBO:0057672"}


id: GO:0050033
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-rhamnono-1,4-lactone + H2O = L-rhamnonate + H+.","definition_xrefs":["EC:3.1.1.65","RHEA:10288"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxylic ester hydrolase activity","termid":"GO:0052689"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016788","GO:0003824","GO:0016787","GO:0003674"],"is_obsolete":false,"name":"L-rhamnono-1,4-lactonase activity","secondary_identifiers":["KEGG_REACTION:R03772","MetaCyc:L-RHAMNONO-14-LACTONASE-RXN"],"synonyms":[{"name":"L-rhamno-gamma-lactonase activity","type":"related"},{"name":"L-rhamnono-1,4-lactone lactonohydrolase activity","type":"related"},{"name":"L-rhamnono-gamma-lactonase activity","type":"related"}],"termid":"GO:0050033"}


id: FYPO:0007763
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of phosphatidate cytidylyltransferase activity is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased catalytic activity","termid":"FYPO:0000663"},{"relation_name":"is_a","term_name":"abnormal phosphatidate cytidylyltransferase activity","termid":"FYPO:0007762"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0000652","FYPO:0001985","FYPO:0000654","FYPO:0000661"],"is_obsolete":false,"name":"decreased phosphatidate cytidylyltransferase activity","synonyms":[{"name":"decreased CDP-diacylglycerol synthase activity","type":"exact"},{"name":"reduced CDP-diacylglycerol synthase activity","type":"exact"},{"name":"reduced phosphatidate cytidylyltransferase activity","type":"exact"}],"termid":"FYPO:0007763"}


id: PBO:0050250
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group nucleosomal binding domain 2 pseudogene 28","termid":"PBO:0050250"}


id: PBO:0086462
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative metal transporter involved in mitochondrial iron accumulation; MMT1 has a paralog, MMT2, that arose from the whole genome duplication","termid":"PBO:0086462"}


id: PBO:0061364
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleophosmin 1 pseudogene 24","termid":"PBO:0061364"}


id: GO:0070399
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of wall teichoic acid, which is a major component of the cell wall of Gram-positive bacteria and typically consists of a polymer of glycerol-phosphate or ribitol-phosphate to which are attached glycosyl and D-alanyl ester residues and which is covalently linked to peptidoglycan.","definition_xrefs":["GOC:add","PMID:14665680"],"direct_ancestors":[{"relation_name":"is_a","term_name":"wall teichoic acid metabolic process","termid":"GO:0070397"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"wall teichoic acid catabolic process","synonyms":[{"name":"wall teichoic acid breakdown","type":"exact"},{"name":"wall teichoic acid catabolism","type":"exact"},{"name":"wall teichoic acid degradation","type":"exact"}],"termid":"GO:0070399"}


id: PBO:0062184
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 4 subfamily N member 4","termid":"PBO:0062184"}


id: PBO:0047053
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 114 member A1","termid":"PBO:0047053"}


id: MONDO:0700176
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A lymphoma that occurs in cats. It is associated with exposure to feline leukemia virus and feline immunodeficiency virus.","definition_xrefs":["NCIT:C132193"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymphoma, non-human animal","termid":"MONDO:0700102"},{"relation_name":"is_a","term_name":"feline neoplasm","termid":"MONDO:0700175"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"feline lymphoma","secondary_identifiers":["OMIA:001733-9685"],"termid":"MONDO:0700176","xrefs":{"Monarch":{"xref_id":"0700176"}}}


id: MONDO:0014085
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any congenital hydrocephalus in which the cause of the disease is a mutation in the MPDZ gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital hydrocephalus","termid":"MONDO:0016349"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"hydrocephalus, nonsyndromic, autosomal recessive 2","secondary_identifiers":["UMLS:C3554691","MEDGEN:767605","OMIM:615219"],"synonyms":[{"name":"HYC2","type":"related"},{"name":"MPDZ congenital hydrocephalus","type":"exact"},{"name":"congenital hydrocephalus caused by mutation in MPDZ","type":"exact"},{"name":"hydrocephalus, congenital, 2, with or without brain or eye anomalies","type":"exact"},{"name":"hydrocephalus, nonsyndromic, autosomal recessive 2","type":"exact"},{"name":"hydrocephalus, nonsyndromic, autosomal recessive type 2","type":"exact"}],"termid":"MONDO:0014085","xrefs":{"Monarch":{"xref_id":"0014085"}}}


id: GO:1904820
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a peritoneum over time, from its formation to the mature structure.","definition_xrefs":["GO_REF:0000094","GOC:TermGenie","GOC:dph","PMID:15840053"],"direct_ancestors":[{"relation_name":"is_a","term_name":"serous membrane development","termid":"GO:1904817"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"peritoneum development","synonyms":[{"name":"peritonaeum development","type":"related"}],"termid":"GO:1904820"}


id: GO:0090033
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the frequency, rate or extent of the process in which a multicellular organism or a group of unicellular organisms grow in a threadlike, filamentous shape.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of filamentous growth","termid":"GO:0010570"},{"relation_name":"is_a","term_name":"positive regulation of growth","termid":"GO:0045927"},{"relation_name":"positively_regulates","term_name":"filamentous growth","termid":"GO:0030447"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of filamentous growth","termid":"GO:0090033"}


id: PBO:0076890
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis expressed 44","termid":"PBO:0076890"}


id: MONDO:0008911
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"histiocytoid cardiomyopathy","termid":"MONDO:0010771"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005267"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005267","MONDO:0005066"],"is_obsolete":false,"name":"cardiac lipidosis, familial","secondary_identifiers":["GARD:15148","OMIM:212080","MEDGEN:395234","UMLS:C1859332","MESH:C565884"],"synonyms":[{"name":"cardiac lipidosis, familial","type":"exact"}],"termid":"MONDO:0008911","xrefs":{"Monarch":{"xref_id":"0008911"}}}


id: GO:1990030
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Ramification of basket cell axon surrounding cell bodies, forming the characteristic pericellular baskets from which the cell class derives its name.","definition_xrefs":["NIF_Subcellular:sao413722576"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"axon","termid":"GO:0030424"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"pericellular basket","synonyms":[{"name":"peri cellular basket","type":"exact"},{"name":"peri-cellular basket","type":"exact"}],"termid":"GO:1990030"}


id: GO:0003998
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: an acyl phosphate + H2O = a carboxylate + phosphate.","definition_xrefs":["EC:3.6.1.7"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrophosphatase activity","termid":"GO:0016462"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016787","GO:0003674"],"is_obsolete":false,"name":"acylphosphatase activity","secondary_identifiers":["MetaCyc:ACYLPHOSPHATASE-RXN","RHEA:14965"],"synonyms":[{"name":"1,3-diphosphoglycerate phosphatase activity","type":"related"},{"name":"GP 1-3","type":"related"},{"name":"Ho 1-3","type":"related"},{"name":"acetic phosphatase activity","type":"related"},{"name":"acetylphosphatase activity","type":"related"},{"name":"acylphosphate phosphohydrolase activity","type":"related"}],"termid":"GO:0003998"}


id: FYPO:0005894
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to chromatin is normal (i.e. indistinguishable from wild type) during G1 phase of the mitotic cell cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to chromatin during vegetative growth","termid":"FYPO:0001509"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000138","FYPO:0001320","FYPO:0001312","FYPO:0000002"],"is_obsolete":false,"name":"normal protein localization to chromatin during mitotic G1 phase","synonyms":[{"name":"normal protein localisation to chromatin during mitotic G1 phase","type":"exact"},{"name":"normal protein localization to chromatin during G1 phase during vegetative growth","type":"exact"},{"name":"normal protein localization to chromatin during G1 phase of mitotic cell cycle","type":"exact"}],"termid":"FYPO:0005894"}


id: GO:1905570
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of ferrichrome biosynthetic process.","definition_xrefs":["GO_REF:0000058","PMID:654321","GOC:TermGenie","GOC:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of amide metabolic process","termid":"GO:0034250"},{"relation_name":"is_a","term_name":"positive regulation of siderophore biosynthetic process","termid":"GO:1900706"},{"relation_name":"is_a","term_name":"regulation of ferrichrome biosynthetic process","termid":"GO:1905568"},{"relation_name":"positively_regulates","term_name":"ferrichrome biosynthetic process","termid":"GO:0031169"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0019748"},{"rel_name":"regulates","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0019748","GO:0008150"],"is_obsolete":false,"name":"positive regulation of ferrichrome biosynthetic process","synonyms":[{"name":"activation of ferrichrome anabolism","type":"narrow"},{"name":"activation of ferrichrome biosynthesis","type":"narrow"},{"name":"activation of ferrichrome biosynthetic process","type":"narrow"},{"name":"activation of ferrichrome biosynthetic process, peptide formation","type":"narrow"},{"name":"activation of ferrichrome biosynthetic process, peptide modification","type":"narrow"},{"name":"activation of ferrichrome formation","type":"narrow"},{"name":"activation of ferrichrome synthesis","type":"narrow"},{"name":"positive regulation of ferrichrome anabolism","type":"exact"},{"name":"positive regulation of ferrichrome biosynthesis","type":"exact"},{"name":"positive regulation of ferrichrome biosynthetic process, peptide formation","type":"narrow"},{"name":"positive regulation of ferrichrome biosynthetic process, peptide modification","type":"narrow"},{"name":"positive regulation of ferrichrome formation","type":"exact"},{"name":"positive regulation of ferrichrome synthesis","type":"exact"},{"name":"up regulation of ferrichrome anabolism","type":"exact"},{"name":"up regulation of ferrichrome biosynthesis","type":"exact"},{"name":"up regulation of ferrichrome biosynthetic process","type":"exact"},{"name":"up regulation of ferrichrome biosynthetic process, peptide formation","type":"narrow"},{"name":"up regulation of ferrichrome biosynthetic process, peptide modification","type":"narrow"},{"name":"up regulation of ferrichrome formation","type":"exact"},{"name":"up regulation of ferrichrome synthesis","type":"exact"},{"name":"up-regulation of ferrichrome anabolism","type":"exact"},{"name":"up-regulation of ferrichrome biosynthesis","type":"exact"},{"name":"up-regulation of ferrichrome biosynthetic process","type":"exact"},{"name":"up-regulation of ferrichrome biosynthetic process, peptide formation","type":"narrow"},{"name":"up-regulation of ferrichrome biosynthetic process, peptide modification","type":"narrow"},{"name":"up-regulation of ferrichrome formation","type":"exact"},{"name":"up-regulation of ferrichrome synthesis","type":"exact"},{"name":"upregulation of ferrichrome anabolism","type":"exact"},{"name":"upregulation of ferrichrome biosynthesis","type":"exact"},{"name":"upregulation of ferrichrome biosynthetic process","type":"exact"},{"name":"upregulation of ferrichrome biosynthetic process, peptide formation","type":"narrow"},{"name":"upregulation of ferrichrome biosynthetic process, peptide modification","type":"narrow"},{"name":"upregulation of ferrichrome formation","type":"exact"},{"name":"upregulation of ferrichrome synthesis","type":"exact"}],"termid":"GO:1905570"}


id: MONDO:0018222
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete X-linked intellectual disability due to GRIA3 anomalies (obsolete MONDO:0018222)","secondary_identifiers":["Orphanet:364028"],"termid":"MONDO:0018222","xrefs":{"Monarch":{"xref_id":"0018222"}}}


id: GO:0035131
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process, occurring after embryonic development, by which the anatomical structures of the pelvic fin are generated and organized. The pelvic fins are bilaterally paired fins mounted in a ventral-lateral position on most fish. These fins are used primarily for lateral mobility and propulsion.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"post-embryonic appendage morphogenesis","termid":"GO:0035120"},{"relation_name":"is_a","term_name":"pelvic fin morphogenesis","termid":"GO:0035139"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"post-embryonic pelvic fin morphogenesis","termid":"GO:0035131"}


id: MONDO:0957382
data:
  {"annotated_genes":["SJAG_03641"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85875],"is_not":false,"summary":null,"term":"MONDO:0957382"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"fatal multiple mitochondrial dysfunctions syndrome","termid":"MONDO:0017338"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03641":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0002525"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004069","MONDO:0002525"],"is_obsolete":false,"name":"multiple mitochondrial dysfunctions syndrome 7","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1841222","UMLS:C5830586","OMIM:620423"],"termid":"MONDO:0957382","terms_by_termid":{"MONDO:0957382":null},"xrefs":{"Monarch":{"xref_id":"0957382"}}}


id: MONDO:0024414
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cellulitis","termid":"MONDO:0005230"},{"relation_name":"is_a","term_name":"anaerobic bacteria infectious disease","termid":"MONDO:0024389"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"anaerobic cellulitis","secondary_identifiers":["ICD9:682.9","MEDGEN:537100","ICD9:041.84","SCTID:238401006","UMLS:C0241828"],"synonyms":[{"name":"anaerobic cellulitis","type":"exact"}],"termid":"MONDO:0024414","xrefs":{"Monarch":{"xref_id":"0024414"}}}


id: PBO:0031394
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-growth_auxotrophic_for_arginine","termid":"PBO:0031394"}


id: PBO:0002118
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat protein Vps8 (predicted)","termid":"PBO:0002118"}


id: MONDO:0023660
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary angioedema","termid":"MONDO:0019623"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"angioedema, hereditary, 6","secondary_identifiers":["OMIM:619363","UMLS:C5543516","MEDGEN:1785484"],"synonyms":[{"name":"HAE6","type":"exact"}],"termid":"MONDO:0023660","xrefs":{"Monarch":{"xref_id":"0023660"}}}


id: MONDO:0013851
data:
  {"annotated_genes":["SJAG_01840"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85836],"is_not":false,"summary":null,"term":"MONDO:0013851"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"bone marrow failure syndrome","termid":"MONDO:0000159"},{"relation_name":"is_a","term_name":"inherited aplastic anemia","termid":"MONDO:0001713"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01840":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0002280","MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"autosomal dominant aplasia and myelodysplasia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:814883","OMIM:614675","GARD:17420","NANDO:1200301","Orphanet:314399","UMLS:C3808553"],"synonyms":[{"name":"BMFS1","type":"related"},{"name":"autosomal dominant aplastic anaemia and myelodysplasia","type":"exact"},{"name":"autosomal dominant aplastic anemia and myelodysplasia","type":"exact"},{"name":"bone marrow failure syndrome 1","type":"related"},{"name":"bone marrow failure syndrome type 1","type":"exact"}],"termid":"MONDO:0013851","terms_by_termid":{"MONDO:0013851":null},"xrefs":{"Monarch":{"xref_id":"0013851"}}}


id: MONDO:0100530
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any myopathy in which the cause of the disease is a variation in the CRPPA gene.","direct_ancestors":[{"relation_name":"is_a","term_name":"myopathy","termid":"MONDO:0005336"},{"relation_name":"is_a","term_name":"qualitative or quantitative defects of protein involved in O-glycosylation of alpha-dystroglycan","termid":"MONDO:0016155"},{"relation_name":"is_a","term_name":"hereditary skeletal muscle disorder","termid":"MONDO:0700223"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0024322","MONDO:0005066","MONDO:0005336","MONDO:0002320"],"is_obsolete":false,"name":"myopathy caused by variation in CRPPA","termid":"MONDO:0100530","xrefs":{"Monarch":{"xref_id":"0100530"}}}


id: GO:0090689
data:
  {"annotated_genes":["SJAG_02572","SJAG_03915"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[87504,90788],"is_not":false,"summary":null,"term":"GO:0090689"}]},"cv_name":"cellular_component","definition":"The 'trough' of the cleavage furrow. This is the part of the cleavage furrow closest to the contractile ring.","definition_xrefs":["GOC:vw","PMID:27082518"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"cleavage furrow","termid":"GO:0032154"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02572":null,"SJAG_03915":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005886","GO:0005575"],"is_obsolete":false,"name":"cleavage furrow leading edge","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0090689","terms_by_termid":{"GO:0090689":null}}


id: GO:0043427
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An autotrophic carbon dioxide fixation pathway by which two molecules of carbon dioxide are fixed to form glyoxylate. Acetyl coenzyme A (acetyl-CoA) is assumed to be converted to malate, and two CO2 molecules are thereby fixed. Malyl-CoA is thought to be cleaved to acetyl-CoA, the starting molecule, and glyoxylate, the carbon fixation product.","definition_xrefs":["PMID:11418572","GOC:jl","PMID:15838028"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon fixation","termid":"GO:0015977"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"carbon fixation by 3-hydroxypropionate cycle","synonyms":[{"name":"3-hydroxypropionate cycle","type":"exact"},{"name":"3-hydroxypropionate pathway","type":"exact"},{"name":"hydroxypropionate cycle","type":"exact"},{"name":"hydroxypropionate pathway","type":"exact"}],"termid":"GO:0043427"}


id: GO:0055014
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of an atrial cardiac muscle cell over time, from its formation to the mature state. Cardiac muscle cells are striated muscle cells that are responsible for heart contraction. The atrium is the part of the heart that receives blood into the organ.","definition_xrefs":["GOC:devbiol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiac muscle cell development","termid":"GO:0055013"},{"relation_name":"part_of","term_name":"atrial cardiac muscle cell differentiation","termid":"GO:0055011"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"atrial cardiac muscle cell development","synonyms":[{"name":"atrial cardiomyocyte development","type":"exact"},{"name":"atrial heart muscle development","type":"exact"}],"termid":"GO:0055014"}


id: PBO:0083786
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential protein involved in ribosome biogenesis; putative ATP-dependent RNA helicase of the DEAD-box protein family; human homolog DDX51 complements yeast dbp6 mutant","termid":"PBO:0083786"}


id: PBO:0052847
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin associated protein 4-3","termid":"PBO:0052847"}


id: PBO:0055769
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lncRNA PDCD5 and p53 scaffold","termid":"PBO:0055769"}


id: PBO:0061111
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NLR family pyrin domain containing 3","termid":"PBO:0061111"}


id: MONDO:0023230
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ghose-Sachdev-Kumar syndrome","secondary_identifiers":["MEDGEN:425476","MESH:C537803","UMLS:C2974016"],"synonyms":[{"name":"bilateral nanophthalmos, pigmentary retinal dystrophy, and angle closure glaucoma","type":"related"}],"termid":"MONDO:0023230","xrefs":{"Monarch":{"xref_id":"0023230"}}}


id: GO:0043121
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a neurotrophin, any of a family of growth factors that prevent apoptosis in neurons and promote nerve growth.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"growth factor binding","termid":"GO:0019838"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"neurotrophin binding","secondary_identifiers":["GO:0048405","GO:0048404"],"synonyms":[{"name":"NT 4/5 binding","type":"narrow"},{"name":"NT-3 binding","type":"narrow"},{"name":"NT-4 binding","type":"narrow"},{"name":"NT-4/5 binding","type":"narrow"},{"name":"NT-5 binding","type":"narrow"},{"name":"NT3 binding","type":"narrow"},{"name":"NT4 binding","type":"narrow"},{"name":"NT5 binding","type":"narrow"},{"name":"neurotrophic factor binding","type":"exact"},{"name":"neurotrophin 3 binding","type":"narrow"},{"name":"neurotrophin 4/5 binding","type":"narrow"},{"name":"neurotrophin TRK receptor activity","type":"related"},{"name":"neurotrophin TRKA receptor activity","type":"related"},{"name":"neurotrophin TRKB receptor activity","type":"related"},{"name":"neurotrophin TRKC receptor activity","type":"related"},{"name":"neurotrophin-3 binding","type":"narrow"},{"name":"neurotrophin-4/5 binding","type":"narrow"}],"termid":"GO:0043121"}


id: MONDO:0000011
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete chondrodysplasia (obsolete MONDO:0000011)","termid":"MONDO:0000011","xrefs":{"Monarch":{"xref_id":"0000011"}}}


id: MONDO:0012554
data:
  {"annotated_genes":["SJAG_02828"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85214],"is_not":false,"summary":null,"term":"MONDO:0012554"}]},"cv_name":"mondo","definition":"Any COFS syndrome in which the cause of the disease is a mutation in the ERCC1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"COFS syndrome","termid":"MONDO:0008926"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02828":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0021190"}],"interesting_parent_ids":["MONDO:0021190","MONDO:0005328","MONDO:0005066","MONDO:0006025"],"is_obsolete":false,"name":"cerebrooculofacioskeletal syndrome 4","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0080914","MESH:C565184","GARD:15498","MEDGEN:342798","OMIM:610758","UMLS:C1853100","NCIT:C173104"],"synonyms":[{"name":"COFS syndrome caused by mutation in ERCC1","type":"exact"},{"name":"COFS4","type":"exact"},{"name":"ERCC1 COFS syndrome","type":"exact"},{"name":"cerebrooculofacioskeletal syndrome 4","type":"exact"},{"name":"cerebrooculofacioskeletal syndrome type 4","type":"exact"}],"termid":"MONDO:0012554","terms_by_termid":{"MONDO:0012554":null},"xrefs":{"Monarch":{"xref_id":"0012554"}}}


id: MONDO:0021680
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any of the several infectious disorders caused by members of streptococcus, a genus of gram positive bacteria belonging to the family Streptococcaceae. Streptococcal infections are classified into Groups A, B, C, D and G.","definition_xrefs":["NCIT:C87062"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gram-positive bacterial infections","termid":"MONDO:0021679"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"streptococcal infection","secondary_identifiers":["MESH:D013290","ICD9:041.09","MEDGEN:20963","SCTID:85769006","EFO:1001476","UMLS:C0038395","ICD9:041.00"],"synonyms":[{"name":"Streptococcus caused disease or disorder","type":"exact"},{"name":"Streptococcus disease or disorder","type":"exact"},{"name":"Streptococcus infectious disease","type":"exact"},{"name":"infection, streptococcal","type":"related"},{"name":"infections, streptococcal","type":"related"},{"name":"streptococcal infection","type":"exact"}],"termid":"MONDO:0021680","xrefs":{"Monarch":{"xref_id":"0021680"}}}


id: GO:0110102
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a ribulose bisphosphate carboxylase complex.","definition_xrefs":["PMID:29396988","GOC:tb","PMID:29589905","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex assembly","termid":"GO:0065003"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0065003","GO:0008150","GO:0044085"],"is_obsolete":false,"name":"ribulose bisphosphate carboxylase complex assembly","synonyms":[{"name":"RuBisCO assembly","type":"exact"}],"termid":"GO:0110102"}


id: GO:1990413
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A small pigmented organelle used in single-celled organisms to detect light.","definition_xrefs":["Wikipedia:Eyespot_apparatus"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular membrane-bounded organelle","termid":"GO:0043231"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"eyespot apparatus","synonyms":[{"name":"eyespot","type":"related"},{"name":"stigma","type":"related"}],"termid":"GO:1990413"}


id: MONDO:1012694
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any dwarfism that occurs in dogs due to a mutation in the PRKG2 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"dwarfism, non-human animal","termid":"MONDO:1012971"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dwarfism, PRKG2-related, dog","secondary_identifiers":["OMIA:001485-9615"],"termid":"MONDO:1012694","xrefs":{"Monarch":{"xref_id":"1012694"}}}


id: PBO:0006213
data:
  {"annotation_feature_type":"gene","cv_name":"feature_cvtermprop_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"allele","termid":"PBO:0006213"}


id: PBO:0038419
data:
  {"annotation_feature_type":"gene","cv_name":"feature_cvtermprop_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_throughput_type","termid":"PBO:0038419"}


id: GO:0030825
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of the chemical reactions and pathways involving cGMP.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of cGMP metabolic process (obsolete GO:0030825)","synonyms":[{"name":"activation of cGMP metabolic process","type":"narrow"},{"name":"positive regulation of cGMP metabolism","type":"exact"},{"name":"stimulation of cGMP metabolic process","type":"narrow"},{"name":"up regulation of cGMP metabolic process","type":"exact"},{"name":"up-regulation of cGMP metabolic process","type":"exact"},{"name":"upregulation of cGMP metabolic process","type":"exact"}],"termid":"GO:0030825"}


id: MONDO:0000901
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A diffuse large B-cell lymphoma characterized by less than 50 percent decrease in lesion size with induction therapy or the appearance of new lesions or the appearance of new lesions after attainment of complete remission.","definition_xrefs":["DOID:0080192","PMID:22160081"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diffuse large B-cell lymphoma","termid":"MONDO:0018905"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"relapsed/refractory diffuse large B-cell lymphoma","secondary_identifiers":["MEDGEN:208957","UMLS:C0855112"],"termid":"MONDO:0000901","xrefs":{"Monarch":{"xref_id":"0000901"}}}


id: GO:0044072
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A process in which a symbiont interferes with, inhibits or stops progression through the host cell cycle.","definition_xrefs":["PMID:10946289","PMID:19308257"],"gene_count":0,"genotype_count":0,"name":"obsolete symbiont-mediated suppression of host cell cycle progression (obsolete GO:0044072)","synonyms":[{"name":"cell cycle arrest in host","type":"related"},{"name":"negative regulation by symbiont of host cell cycle","type":"related"},{"name":"suppression of host cell cycle progression","type":"exact"}],"termid":"GO:0044072"}


id: PBO:0030046
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_ferrous_iron_import","termid":"PBO:0030046"}


id: GO:0070777
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which D-aspartate, the D-enantiomer of the anion of (2R)-2-aminobutanedioic acid  is transported across a lipid bilayer, from one side of a membrane to the other, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:rph","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aspartate transmembrane transport","termid":"GO:0015810"},{"relation_name":"is_a","term_name":"D-amino acid transport","termid":"GO:0042940"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0055085","GO:0008150","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"D-aspartate transmembrane transport","termid":"GO:0070777"}


id: PBO:0075294
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sorting nexin 33","termid":"PBO:0075294"}


id: MONDO:0019904
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ring chromosome 3 syndrome is a rare chromosomal anomaly syndrome with a highly variable phenotype principally characterized by pre- and postnatal growth retardation, short stature, developmental delay, mild to severe intellectual disability, microcephaly and mild dysmorphic features (incl. triangular face, dysplastic ears, upslanting palpebral fissures, epicanthic folds, broad nasal bridge, full nasal tip, long philtrum, downturned corners of the mouth, and micro/retrognathia). Additional manifestations reported include hypotonia, mild articular limitation, hearing loss, digital anomalies (i.e. clinodacytyly, brachydactyly), café-au-lait patches and hypospadias.","definition_xrefs":["Orphanet:96172"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome 3 disorder","termid":"MONDO:0700010"},{"relation_name":"is_a","term_name":"ring chromosome disorder","termid":"MONDO:0700091"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring chromosome 3","secondary_identifiers":["GARD:10839","MEDGEN:1643677","NCIT:C121982","SCTID:765486004","UMLS:C4707449"],"synonyms":[{"name":"R3","type":"related"},{"name":"Ring 3","type":"related"},{"name":"Ring chromosome 3 syndrome","type":"related"},{"name":"Ring chromosome type 3","type":"exact"},{"name":"chromosome 3 ring","type":"related"},{"name":"rose cluster 3","type":"exact"}],"termid":"MONDO:0019904","xrefs":{"Monarch":{"xref_id":"0019904"}}}


id: PBO:0048665
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G kinase anchoring protein 1","termid":"PBO:0048665"}


id: MONDO:0009376
data:
  {"annotated_genes":["SJAG_00412","SJAG_00392"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84586,84587],"is_not":false,"summary":null,"term":"MONDO:0009376"}]},"cv_name":"mondo","definition":"Carbamoyl-phosphate synthetase 1 deficiency (CPS1D) is a rare and severe disorder of urea cycle metabolism most commonly characterized by either a neonatal-onset of severe hyperammonemia that occurs few days after birth and manifests with lethargy, vomiting, hypothermia, seizures, coma and death or a presentation outside the newborn period at any age with (sometimes) milder symptoms of hyperammonemia.","definition_xrefs":["Orphanet:147"],"direct_ancestors":[{"relation_name":"is_a","term_name":"urea cycle disorder or inherited hyperammonemia","termid":"MONDO:0800153"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00392":null,"SJAG_00412":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0005066"],"is_obsolete":false,"name":"carbamoyl phosphate synthetase I deficiency disease","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["icd11.foundation:327894003","OMIM:237300","NANDO:2200478","DOID:9280","MESH:D020165","SCTID:62522004","MedDRA:10058297","UMLS:C4082171","NCIT:C84612","EFO:0007193","MEDGEN:907954","GARD:7269","NANDO:1200803"],"synonyms":[{"name":"CPS 1 deficiency","type":"related"},{"name":"CPS I deficiency","type":"exact"},{"name":"CPS1 deficiency","type":"exact"},{"name":"CPS1D","type":"exact"},{"name":"carbamoyl phosphate synthetase 1 deficiency","type":"related"},{"name":"carbamoyl phosphate synthetase 1 deficiency, hyperammonemia due to","type":"related"},{"name":"carbamoyl phosphate synthetase I deficiency disease","type":"exact"},{"name":"carbamoyl phosphate synthetase I deficiency, hyperammonemia due to","type":"related"},{"name":"carbamoyl phosphate synthetase deficiency","type":"exact"},{"name":"carbamoyl-phosphate synthase deficiency disease","type":"exact"},{"name":"carbamoyl-phosphate synthetase 1 deficiency","type":"related"},{"name":"carbamoyl-phosphate synthetase I deficiency","type":"exact"},{"name":"carbamoyl-phosphate synthetase deficiency","type":"exact"},{"name":"carbamoylphosphate synthetase I deficiency","type":"exact"},{"name":"carbamyl phosphate synthetase (CPS) deficiency","type":"related"},{"name":"hyperammonemia due to carbamoyl phosphate synthetase 1 deficiency","type":"related"}],"termid":"MONDO:0009376","terms_by_termid":{"MONDO:0009376":null},"xrefs":{"Monarch":{"xref_id":"0009376"}}}


id: PR:Q9USP8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An isocitrate dehydrogenase [NAD] subunit alpha, mitochondrial that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02477","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"isocitrate dehydrogenase [NAD] subunit 2, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC902.05c","secondary_identifiers":["UniProtKB:Q9USP8"],"synonyms":[{"name":"NAD(+)-specific ICDH (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-IDH3A","type":"exact"},{"name":"isocitric dehydrogenase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9USP8"}


id: MOD:00841
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification produced by formation of an adduct with an isothiocyanate compound.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reagent derivatized residue","termid":"MOD:00848"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"isothiocyanate reagent derivatized residue","termid":"MOD:00841"}


id: MONDO:0800453
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A genetic epilepsy with onset occurring around puberty. Juvenile absence epilepsy is characterized by sporadic occurrence of absence seizures, frequently associated with a long-life prevalence of generalized tonic-clonic seizures (GTCS) and sporadic myoclonic jerks.","definition_xrefs":["Orphanet:1941"],"direct_ancestors":[{"relation_name":"is_a","term_name":"idiopathic generalized epilepsy","termid":"MONDO:0005579"},{"relation_name":"is_a","term_name":"adolescent/adult-onset epilepsy syndrome","termid":"MONDO:0100030"},{"relation_name":"is_a","term_name":"absence epilepsy","termid":"MONDO:0850093"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"juvenile absence epilepsy","secondary_identifiers":["GARD:2162","icd11.foundation:519416529","SCTID:230413002","DOID:0060172","NCIT:C129868","UMLS:C4317339","MEDGEN:1388059"],"synonyms":[{"name":"JAE","type":"exact"},{"name":"epilepsy juvenile absence","type":"related"}],"termid":"MONDO:0800453","xrefs":{"Monarch":{"xref_id":"0800453"}}}


id: PBO:0091380
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial CHCH domain protein Mix17","termid":"PBO:0091380"}


id: FYPO:0000946
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype observed in the vegetative growth phase of the life cycle in which a cell is shaped in the form of a spheroid, and has a normal volume.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"spheroid vegetative cell","termid":"FYPO:0000021"},{"relation_name":"has_part","term_name":"normal volume vegetative cell","termid":"FYPO:0000926"},{"relation_name":"is_a","term_name":"spheroid vegetative cell","termid":"FYPO:0000021"},{"relation_name":"is_a","term_name":"normal volume vegetative cell","termid":"FYPO:0000926"},{"relation_name":"is_a","term_name":"vegetative cell, abnormal cell shape, normal cell size","termid":"FYPO:0001121"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000005"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000257","FYPO:0000005","FYPO:0000002","FYPO:0001312","FYPO:0001985"],"is_obsolete":false,"name":"normal volume spheroid vegetative cell","synonyms":[{"name":"normal volume rounded vegetative cell","type":"exact"},{"name":"normal volume spheroid cell during vegetative growth","type":"exact"},{"name":"normal volume spheroid vegetative cell during mitotic cell cycle","type":"related"}],"termid":"FYPO:0000946"}


id: MONDO:0971036
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A thyroid gland carcinoma that is characterized by the presence of clusters of malignant epithelial cells associated with abundant extracellular mucin deposition.","definition_xrefs":["DOID:0081460"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thyroid gland carcinoma","termid":"MONDO:0015075"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"thyroid gland mucinous carcinoma","termid":"MONDO:0971036","xrefs":{"Monarch":{"xref_id":"0971036"}}}


id: FYPO:0007086
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype in which a vegetative cell is elongated when the cell is subject to sulfur starvation.","definition_xrefs":["PomBase:mah","PMID:28388826"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viable elongated vegetative cell","termid":"FYPO:0001492"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000005","FYPO:0001320","FYPO:0000002","FYPO:0000004","FYPO:0001985"],"is_obsolete":false,"name":"elongated vegetative cell during sulfur starvation","synonyms":[{"name":"elongated cell during sulfur starvation during vegetative growth","type":"exact"},{"name":"elongated vegetative cell during cellular response to sulfur starvation","type":"exact"},{"name":"elongated vegetative cell during sulfur starvation during mitotic cell cycle","type":"related"},{"name":"elongated vegetative cell during sulphur starvation","type":"exact"}],"termid":"FYPO:0007086"}


id: GO:0009819
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of prolonged deprivation of water that restores that organism to a normal (non-stressed) condition.","definition_xrefs":["GOC:lr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to water deprivation","termid":"GO:0009414"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"drought recovery","synonyms":[{"name":"drought tolerance","type":"related"}],"termid":"GO:0009819"}


id: FYPO:0007697
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the activity of a DNA strand exchange inhibitor is decreased.","definition_xrefs":["PMID:33493431","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catalytic activity regulator phenotype","termid":"FYPO:0007690"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000652"],"is_obsolete":false,"name":"decreased DNA strand exchange inhibitor activity","synonyms":[{"name":"decreased RecA-family recombinase inhibitor activity","type":"exact"},{"name":"decreased negative regulation of RecA-family recombinase activity","type":"related"},{"name":"reduced DNA strand exchange inhibitor activity","type":"exact"}],"termid":"FYPO:0007697"}


id: GO:0009433
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Cytoplasmic ring located at the base of the bacterial-type flagellar basal body; acts as a rotor; includes three switch proteins, which generate torque and can change their conformational state in a bimodal fashion, so that the motor direction can switch between clockwise and counterclockwise.","definition_xrefs":["GOC:mtg_sensu","PMID:10572114","GOC:cilia","PMID:12624192"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"bacterial-type flagellum basal body","termid":"GO:0009425"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"bacterial-type flagellum basal body, C ring","synonyms":[{"name":"flagellar basal body, C ring","type":"exact"},{"name":"flagellin-based flagellum basal body, C ring","type":"exact"}],"termid":"GO:0009433"}


id: MONDO:0859367
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"retinitis pigmentosa","termid":"MONDO:0019200"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004736"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0005066","MONDO:0004736"],"is_obsolete":false,"name":"retinitis pigmentosa 96","secondary_identifiers":["UMLS:C5774303","MEDGEN:1824076","OMIM:620228"],"termid":"MONDO:0859367","xrefs":{"Monarch":{"xref_id":"0859367"}}}


id: MONDO:0008049
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"distal myopathy","termid":"MONDO:0018949"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"myopathy, distal, infantile-onset","secondary_identifiers":["DOID:0070196","OMIM:160300","UMLS:C4011725","MEDGEN:860162"],"synonyms":[{"name":"myopathy, distal, infantile-onset","type":"exact"}],"termid":"MONDO:0008049","xrefs":{"Monarch":{"xref_id":"0008049"}}}


id: MONDO:0008347
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Idiopathic and/or familial pulmonary arterial hypertension (IFPAH) is a form or pulmonary arterial hypertension (PAH, see his term) characterized by elevated pulmonary arterial resistance leading to right heart failure; it is progressive and potentially fatal. About 75% of heritable pulmonary arterial hypertension (HPAH) have an identified mutation. HPAH has been linked to mutations in BMPR2 in 75% of cases; other genes implicated in HPAH include ACVR1, BMPR1, CAV1, ENG and SMAD9 and CBLN2. (However, the majority of patients carrying an HPAH mutation do not develop PAH). Idiopathic pulmonary arterial hypertension (IFPAH) refers to those cases of pulmonary arterial hypertension in which etiology remains unknown.","definition_xrefs":["Orphanet:422"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete rare genetic respiratory disease (obsolete MONDO:0015510)","termid":"MONDO:0015510"}],"gene_count":0,"genotype_count":0,"name":"obsolete idiopathic and/or familial pulmonary arterial hypertension (obsolete MONDO:0008347)","synonyms":[{"name":"IFPAH","type":"exact"},{"name":"PPH1","type":"related"},{"name":"idiopathic and/or familial pulmonary arterial hypertension","type":"exact"},{"name":"pulmonary hypertension, primary, 1","type":"related"},{"name":"pulmonary hypertension, primary, type 1","type":"exact"}],"termid":"MONDO:0008347","xrefs":{"Monarch":{"xref_id":"0008347"}}}


id: GO:0006012
data:
  {"annotated_genes":["SJAG_01784","SJAG_03818","SJAG_01209","SJAG_02954","SJAG_02951","SJAG_02950"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[109052,113152,113158,113159,113170],"is_not":false,"summary":null,"term":"GO:0006012"},{"annotations":[108356],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019388"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving galactose, the aldohexose galacto-hexose. D-galactose is widely distributed in combined form in plants, animals and microorganisms as a constituent of oligo- and polysaccharides; it also occurs in galactolipids and as its glucoside in lactose and melibiose.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hexose metabolic process","termid":"GO:0019318"}],"gene_count":6,"genes_by_uniquename":{"SJAG_01209":null,"SJAG_01784":null,"SJAG_02950":null,"SJAG_02951":null,"SJAG_02954":null,"SJAG_03818":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0005975","GO:0044281"],"is_obsolete":false,"name":"galactose metabolic process","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Wikipedia:Galactose"],"synonyms":[{"name":"galactose metabolism","type":"exact"}],"termid":"GO:0006012","terms_by_termid":{"GO:0006012":null,"GO:0019388":null}}


id: PBO:0085315
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Phosphatidylglycerol phospholipase C; regulates phosphatidylglycerol (PG) accumulation via a phospholipase C-type degradation mechanism; PG levels affect mitochondrial function; contains glycerophosphodiester phosphodiesterase motifs","termid":"PBO:0085315"}


id: MONDO:0042487
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Stage 0 includes: (Tis, N0, M0). Tis: Carcinoma in situ. N0: No regional lymph node metastasis. M0: No distant metastasis. (AJCC 6th ed.) - 2003","definition_xrefs":["NCIT:C4000"],"direct_ancestors":[{"relation_name":"is_a","term_name":"uterus carcinoma in situ","termid":"MONDO:0004710"},{"relation_name":"is_a","term_name":"cervical carcinoma","termid":"MONDO:0005131"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"uterine cervix carcinoma in situ","secondary_identifiers":["SCTID:254889004","MEDGEN:163094","UMLS:C0851140","MESH:D018290","ICD9:233.1","DOID:8991"],"synonyms":[{"name":"CIN 3 aJCC v6","type":"exact"},{"name":"CIN III","type":"exact"},{"name":"CIN III - carcinoma in situ of cervix","type":"exact"},{"name":"CIN III - severe dyskaryosis","type":"exact"},{"name":"CIN grade 3 aJCC v6","type":"exact"},{"name":"FIGO stage 0 carcinoma of cervix","type":"exact"},{"name":"FIGO stage 0 carcinoma of cervix uteri","type":"exact"},{"name":"FIGO stage 0 carcinoma of the cervix","type":"exact"},{"name":"FIGO stage 0 carcinoma of the cervix uteri","type":"exact"},{"name":"FIGO stage 0 carcinoma of the uterine cervix","type":"exact"},{"name":"FIGO stage 0 carcinoma of uterine cervix","type":"exact"},{"name":"FIGO stage 0 cervical carcinoma","type":"exact"},{"name":"FIGO stage 0 cervix carcinoma","type":"exact"},{"name":"FIGO stage 0 cervix uteri carcinoma","type":"exact"},{"name":"FIGO stage 0 uterine cervix carcinoma","type":"exact"},{"name":"carcinoma in situ of cervix","type":"exact"},{"name":"carcinoma in situ of cervix aJCC v6","type":"exact"},{"name":"carcinoma in situ of cervix uteri aJCC v6","type":"exact"},{"name":"carcinoma in situ of the cervix aJCC v6","type":"exact"},{"name":"carcinoma in situ of the cervix uteri aJCC v6","type":"exact"},{"name":"carcinoma in situ of the uterine cervix aJCC v6","type":"exact"},{"name":"carcinoma in situ of uterine cervix","type":"exact"},{"name":"carcinoma in situ of uterine cervix aJCC v6","type":"exact"},{"name":"carcinoma of cervix stage 0","type":"exact"},{"name":"cervical Severe dysplasia aJCC v6","type":"exact"},{"name":"cervical cancer stage 0 aJCC v6","type":"exact"},{"name":"cervical carcinoma in situ aJCC v6","type":"exact"},{"name":"cervical intraepithelial neoplasia grade 3 aJCC v6","type":"exact"},{"name":"cervical intraepithelial neoplasia grade III with severe dysplasia","type":"exact"},{"name":"cervix Ca in situ","type":"exact"},{"name":"cervix Severe dysplasia aJCC v6","type":"exact"},{"name":"cervix carcinoma in situ aJCC v6","type":"exact"},{"name":"cervix intraepithelial neoplasia grade 3 aJCC v6","type":"exact"},{"name":"cervix uteri Severe dysplasia aJCC v6","type":"exact"},{"name":"cervix uteri carcinoma in situ","type":"related"},{"name":"cervix uteri carcinoma in situ aJCC v6","type":"exact"},{"name":"cervix uteri intraepithelial neoplasia grade 3 aJCC v6","type":"exact"},{"name":"grade 3 cervical intraepithelial neoplasia aJCC v6","type":"exact"},{"name":"intraepithelial neoplasia of cervix grade 3 aJCC v6","type":"exact"},{"name":"intraepithelial neoplasia of cervix uteri grade 3 aJCC v6","type":"exact"},{"name":"intraepithelial neoplasia of the cervix grade 3 aJCC v6","type":"exact"},{"name":"intraepithelial neoplasia of the cervix uteri grade 3 aJCC v6","type":"exact"},{"name":"intraepithelial neoplasia of the uterine cervix grade 3 aJCC v6","type":"exact"},{"name":"intraepithelial neoplasia of uterine cervix grade 3 aJCC v6","type":"exact"},{"name":"severe cervical dysplasia aJCC v6","type":"exact"},{"name":"severe dysplasia of cervix","type":"exact"},{"name":"severe dysplasia of cervix aJCC v6","type":"exact"},{"name":"severe dysplasia of cervix uteri aJCC v6","type":"exact"},{"name":"severe dysplasia of the cervix aJCC v6","type":"exact"},{"name":"severe dysplasia of the cervix uteri aJCC v6","type":"exact"},{"name":"severe dysplasia of the uterine cervix aJCC v6","type":"exact"},{"name":"severe dysplasia of uterine cervix aJCC v6","type":"exact"},{"name":"squamous intraepithelial neoplasia, grade III","type":"exact"},{"name":"stage 0 cervical cancer","type":"exact"},{"name":"stage 0 cervical cancer aJCC v6","type":"exact"},{"name":"stage 0 uterine cervix carcinoma","type":"exact"},{"name":"uterine cervix Severe dysplasia aJCC v6","type":"exact"},{"name":"uterine cervix carcinoma in situ aJCC v6","type":"exact"},{"name":"uterine cervix intraepithelial neoplasia grade 3 aJCC v6","type":"exact"}],"termid":"MONDO:0042487","xrefs":{"Monarch":{"xref_id":"0042487"}}}


id: GO:0015468
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Plasmid-encoded bacteriocins which are produced by enteric bacteria. Exert a lethal effect on other bacteria including E. coli strains that lack the Col plasmid. Bind to a cell surface receptor and are transported into the periplasm via an energy-dependent process involving a TonB- or TolA-dependent hetero-oligomeric protein complex. Some colicins kill their target cell by inserting into the cytoplasmic membrane where they form voltage-sensitive (trans-negative) channels that depolarize and deenergize the cell, and thereby kill it.","definition_xrefs":["TC:1.C.1.-.-"],"gene_count":0,"genotype_count":0,"name":"obsolete colicin (obsolete GO:0015468)","synonyms":[{"name":"colicin","type":"exact"}],"termid":"GO:0015468"}


id: PBO:0113400
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative SPOUT methyltransferase; may interact with ribosomes, based on co-purification experiments; predicted to be involved in ribosome biogenesis; contributes to the methylation of Cse4-R37 in G2/M phase; overexpression leads to chromosomal instability; null mutant is resistant to fluconazole; GFP-fusion protein localizes to the nucleolus; YGR283C has a paralog, YMR310C, that arose from the whole genome duplication","termid":"PBO:0113400"}


id: PBO:0005026
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA-binding protein involved in ribosome biogenesis (predicted)","termid":"PBO:0005026"}


id: PBO:0039090
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alanine--glyoxylate aminotransferase","termid":"PBO:0039090"}


id: GO:0103054
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: gibberellin A12 + O2 + 2-oxoglutarate = gibberellin A15 + carbon dioxide + succinate.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete gibberellin A12, 2-oxoglutarate:oxygen oxidoreductase activity (gibberellin A15-forming) (obsolete GO:0103054)","termid":"GO:0103054"}


id: PBO:0057063
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 146b","termid":"PBO:0057063"}


id: GO:0098866
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The fusion of the membrane of a multivesicular body with the apical plasma membrane, resulting in release of exosomes from the cell.","definition_xrefs":["PMID:26459596"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle fusion to plasma membrane","termid":"GO:0099500"},{"relation_name":"part_of","term_name":"exosomal secretion","termid":"GO:1990182"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0061024"}],"interesting_parent_ids":["GO:0006810","GO:0016192","GO:0061024","GO:0008150","GO:0044085"],"is_obsolete":false,"name":"multivesicular body fusion to apical plasma membrane","termid":"GO:0098866"}


id: MONDO:0015691
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypereosinophilic syndrome (HES) constitutes a rare and heterogeneous group of disorders, defined as persistent and marked blood eosinophilia and/or tissue eosinophilia associated with a wide range of clinical manifestations reflecting eosinophil-induced tissue/organ damage.","definition_xrefs":["Orphanet:168956"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"non-familial restrictive cardiomyopathy","termid":"MONDO:0016345"},{"relation_name":"is_a","term_name":"eosinophil disorder","termid":"MONDO:0044972"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267","MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"hypereosinophilic syndrome","secondary_identifiers":["ICD9:288.3","NANDO:2200805","EFO:1001467","MedDRA:10048643","GARD:2804","DOID:999","MEDGEN:280990","NCIT:C27038","SCTID:419455006","icd11.foundation:110429919","MESH:D017681","ICDO:9964/3","NANDO:2200806","UMLS:C1540912"],"synonyms":[{"name":"HES","type":"exact"},{"name":"eosinophilia","type":"related"},{"name":"eosinophilic leukocytosis","type":"exact"},{"name":"hypereosinophilic disease","type":"exact"},{"name":"hypereosinophilic disorder","type":"exact"},{"name":"hypereosinophilic syndrome","type":"exact"}],"termid":"MONDO:0015691","xrefs":{"Monarch":{"xref_id":"0015691"}}}


id: MONDO:0018230
data:
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id: MONDO:0004285
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant glandular neoplasm arising from the exocrine pancreas. Microscopically it is characterized by the presence of mucoid stroma formation, papillary patterns, and cystic changes. It has been associated with KRAS and Tp53 gene mutations.","definition_xrefs":["NCIT:C5725"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"pancreatic adenocarcinoma","termid":"MONDO:0006047"},{"relation_name":"is_a","term_name":"exocrine pancreatic carcinoma","termid":"MONDO:0005192"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"pancreatic intraductal papillary-mucinous carcinoma","secondary_identifiers":["MEDGEN:235451","UMLS:C1335304","DOID:7574","Orphanet:424058","GARD:21779"],"synonyms":[{"name":"intraductal papillary mucinous carcinoma of pancreas","type":"exact"},{"name":"intraductal papillary-colloid carcinoma of pancreas","type":"related"},{"name":"intraductal papillary-colloid carcinoma of the pancreas","type":"related"},{"name":"intraductal papillary-colloidal carcinoma of pancreas","type":"related"},{"name":"intraductal papillary-colloidal carcinoma of the pancreas","type":"related"},{"name":"intraductal papillary-mucinous carcinoma of pancreas","type":"exact"},{"name":"intraductal papillary-mucinous carcinoma of the pancreas","type":"related"},{"name":"pancreatic intraductal papillary mucinous carcinoma","type":"exact"},{"name":"pancreatic intraductal papillary-colloid carcinoma","type":"related"},{"name":"pancreatic intraductal papillary-colloidal carcinoma","type":"related"},{"name":"pancreatic intraductal papillary-mucinous carcinoma","type":"exact"}],"termid":"MONDO:0004285","xrefs":{"Monarch":{"xref_id":"0004285"}}}


id: FYPO:0001421
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which protein processing is abnormal. Protein processing is the cleavage of one or more bonds within a protein that leads to the formation of mature, fully functional protein.","definition_xrefs":["GO:0030163","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein metabolic process during vegetative growth","termid":"FYPO:0000328"},{"relation_name":"is_a","term_name":"abnormal protein processing","termid":"FYPO:0006374"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0006551"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0006551","FYPO:0002274","FYPO:0005447","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"abnormal protein processing during vegetative growth","synonyms":[{"name":"abnormal protein cleavage during vegetative growth","type":"related"},{"name":"abnormal protein maturation by peptide bond cleavage during vegetative growth","type":"exact"},{"name":"abnormal protein maturation by peptide bond hydrolysis during vegetative growth","type":"exact"},{"name":"abnormal protein processing during mitotic cell cycle","type":"related"}],"termid":"FYPO:0001421"}


id: GO:0031484
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A myosin complex containing a class XIV myosin heavy chain and associated light chains; myosin XIV heavy chains are the simplest known, containing a motor domain, no classic IQ motif and variable length tails.","definition_xrefs":["PMID:10722873"],"direct_ancestors":[{"relation_name":"is_a","term_name":"unconventional myosin complex","termid":"GO:0016461"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0015629"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0015629"],"is_obsolete":false,"name":"myosin XIV complex","termid":"GO:0031484"}


id: GO:0006469
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of protein kinase activity.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein phosphorylation","termid":"GO:0001933"},{"relation_name":"is_a","term_name":"negative regulation of kinase activity","termid":"GO:0033673"},{"relation_name":"is_a","term_name":"regulation of protein kinase activity","termid":"GO:0045859"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of protein kinase activity","synonyms":[{"name":"down regulation of protein kinase activity","type":"exact"},{"name":"down-regulation of protein kinase activity","type":"exact"},{"name":"downregulation of protein kinase activity","type":"exact"},{"name":"inhibition of protein kinase activity","type":"narrow"}],"termid":"GO:0006469"}


id: MONDO:0000056
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete mandibuloacral dysplasia with lipodystrophy (obsolete MONDO:0000056)","termid":"MONDO:0000056","xrefs":{"Monarch":{"xref_id":"0000056"}}}


id: PBO:0088785
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acetyl-CoA biosynthesis protein","termid":"PBO:0088785"}


id: PBO:0017764
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zf-CCHC type zinc finger protein (predicted)","termid":"PBO:0017764"}


id: MONDO:0000307
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease caused by infection with Ichthyosporea.","definition_xrefs":["MONDO:patterns/infectious_disease_by_agent"],"direct_ancestors":[{"relation_name":"is_a","term_name":"parasitic infectious disease","termid":"MONDO:0005135"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"parasitic Ichthyosporea infectious disease","secondary_identifiers":["DOID:0050291"],"synonyms":[{"name":"Ichthyosporea caused disease or disorder","type":"exact"},{"name":"Ichthyosporea disease or disorder","type":"exact"},{"name":"Ichthyosporea infectious disease","type":"exact"}],"termid":"MONDO:0000307","xrefs":{"Monarch":{"xref_id":"0000307"}}}


id: PBO:0001449
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Aicardi-Goutieres syndrome","termid":"PBO:0001449"}


id: MONDO:0850150
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A kidney disease that is located in the kidney cortex.","definition_xrefs":["DOID:0080616"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kidney disorder","termid":"MONDO:0005240"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"kidney cortex disease","termid":"MONDO:0850150","xrefs":{"Monarch":{"xref_id":"0850150"}}}


id: PBO:0075880
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ST3GAL5 pseudogene 1","termid":"PBO:0075880"}


id: PBO:0059132
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"M-phase phosphoprotein 9","termid":"PBO:0059132"}


id: PBO:0016044
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Suppressor of STe12","termid":"PBO:0016044"}


id: PBO:0041033
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"basic charge Y-linked 2C","termid":"PBO:0041033"}


id: PBO:0083906
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Flavin-linked sulfhydryl oxidase localized to the ER lumen; involved in disulfide bond formation within the endoplasmic reticulum (ER)","termid":"PBO:0083906"}


id: GO:0031917
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that decreases synaptic metaplasticity. Metaplasticity is a higher-order form of plasticity and is manifest as a change in the ability to induce subsequent synaptic plasticity that is the ability of synapses to change as circumstances require.","definition_xrefs":["GOC:mah","PMID:8658594"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of synaptic plasticity","termid":"GO:0031914"},{"relation_name":"is_a","term_name":"regulation of synaptic metaplasticity","termid":"GO:0031916"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"negative regulation of synaptic metaplasticity","synonyms":[{"name":"down regulation of synaptic metaplasticity","type":"exact"},{"name":"down-regulation of synaptic metaplasticity","type":"exact"},{"name":"downregulation of synaptic metaplasticity","type":"exact"},{"name":"inhibition of synaptic metaplasticity","type":"narrow"}],"termid":"GO:0031917"}


id: GO:0071587
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The covalent alteration of one or more amino acid residues within the CAAX box region of CAAX box proteins.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete CAAX-box protein modification (obsolete GO:0071587)","termid":"GO:0071587"}


id: GO:0070921
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of siRNA processing.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of regulatory ncRNA processing","termid":"GO:0070920"},{"relation_name":"regulates","term_name":"siRNA processing","termid":"GO:0030422"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"regulation of siRNA processing","secondary_identifiers":["GO:0090065"],"synonyms":[{"name":"regulation of RNA interference, production of siRNA","type":"exact"},{"name":"regulation of chromatin silencing by small RNA, production of siRNA","type":"exact"},{"name":"regulation of production of siRNA involved in PTGS","type":"related"},{"name":"regulation of production of siRNA involved in RNA interference","type":"exact"},{"name":"regulation of production of siRNA involved in chromatin silencing by small RNA","type":"exact"},{"name":"regulation of production of siRNA involved in gene silencing by small RNA","type":"related"},{"name":"regulation of production of siRNA involved in post-transcriptional gene silencing by RNA","type":"related"},{"name":"regulation of siRNA production","type":"related"}],"termid":"GO:0070921"}


id: PBO:0075782
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SRSF6 pseudogene 2","termid":"PBO:0075782"}


id: GO:0047511
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (S)-methylmalonyl-CoA + H2O = CoA + H+ + methylmalonate.","definition_xrefs":["EC:3.1.2.17","RHEA:17345"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyl-CoA hydrolase activity","termid":"GO:0016289"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016787","GO:0003824","GO:0003674","GO:0016788"],"is_obsolete":false,"name":"(S)-methylmalonyl-CoA hydrolase activity","secondary_identifiers":["MetaCyc:S-METHYLMALONYL-COA-HYDROLASE-RXN","KEGG_REACTION:R02764"],"synonyms":[{"name":"D-methylmalonyl-coenzyme A hydrolase activity","type":"related"}],"termid":"GO:0047511"}


id: PBO:0061706
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear transport factor 2","termid":"PBO:0061706"}


id: FYPO:0000417
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which mitotic cytokinesis does not occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cytokinesis","termid":"FYPO:0000032"},{"relation_name":"is_a","term_name":"abolished cellular process","termid":"FYPO:0005449"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000032"}],"interesting_parent_ids":["FYPO:0000032","FYPO:0000002","FYPO:0001985","FYPO:0001320","FYPO:0005447","FYPO:0000631"],"is_obsolete":false,"name":"abolished cytokinesis","synonyms":[{"name":"abolished cytokinesis during mitotic cell cycle","type":"related"},{"name":"absent cytokinesis","type":"exact"},{"name":"cytokinesis abolished","type":"exact"},{"name":"cytokinesis abolished during vegetative growth","type":"exact"},{"name":"cytokinesis: absent","type":"related"},{"name":"mitotic cytokinesis abolished","type":"exact"}],"termid":"FYPO:0000417"}


id: PATO:0001934
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A shape quality inhering in a bearer by virtue of the bearer's being perfectly circular.","definition_xrefs":["ISBN:0881923214"],"direct_ancestors":[{"relation_name":"is_a","term_name":"circular","termid":"PATO:0000411"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"orbicular","termid":"PATO:0001934"}


id: GO:1903603
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of thermospermine.","definition_xrefs":["PMID:24906355","GOC:TermGenie","GO_REF:0000068"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyamine biosynthetic process","termid":"GO:0006596"},{"relation_name":"is_a","term_name":"thermospermine metabolic process","termid":"GO:1903601"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"thermospermine biosynthetic process","synonyms":[{"name":"thermospermine anabolism","type":"exact"},{"name":"thermospermine biosynthesis","type":"exact"},{"name":"thermospermine formation","type":"exact"},{"name":"thermospermine synthesis","type":"exact"}],"termid":"GO:1903603"}


id: GO:0002131
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the ribose of cytidine at position 34 in the anticodon of a tRNA is post-transcriptionally methylated at the 2'-O position.","definition_xrefs":["ISBN:155581073X","GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"wobble position ribose methylation","termid":"GO:0002130"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006399"}],"interesting_parent_ids":["GO:0006399","GO:0010467","GO:0008150"],"is_obsolete":false,"name":"wobble position cytosine ribose methylation","termid":"GO:0002131"}


id: GO:0043286
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of poly(3-hydroxyalkanoates), polyesters of 3-hydroxyacids produced as intracellular granules by a large variety of bacteria.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of biosynthetic process","termid":"GO:0009889"},{"relation_name":"regulates","term_name":"poly(3-hydroxyalkanoate) biosynthetic process","termid":"GO:0042621"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of poly(3-hydroxyalkanoate) biosynthetic process","synonyms":[{"name":"regulation of PHA","type":"exact"},{"name":"regulation of poly(3-hydroxyalkanoate) anabolism","type":"exact"},{"name":"regulation of poly(3-hydroxyalkanoate) biosynthesis","type":"exact"},{"name":"regulation of poly(3-hydroxyalkanoate) formation","type":"exact"},{"name":"regulation of poly(3-hydroxyalkanoate) synthesis","type":"exact"}],"termid":"GO:0043286"}


id: GO:0098530
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency or extent of strand invasion. Strand invasion is the process in which the nucleoprotein complex (composed of the broken single-strand DNA and the recombinase) searches and identifies a region of homology in intact duplex DNA. The broken single-strand DNA displaces the like strand and forms Watson-Crick base pairs with its complement, forming a duplex in which each strand is from one of the two recombining DNA molecules.","definition_xrefs":["GOC:dos","GOC:tb","GOC:elh","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of DNA metabolic process","termid":"GO:0051054"},{"relation_name":"is_a","term_name":"regulation of strand invasion","termid":"GO:0060542"},{"relation_name":"positively_regulates","term_name":"DNA strand invasion","termid":"GO:0042148"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006259","GO:0008150"],"is_obsolete":false,"name":"positive regulation of strand invasion","synonyms":[{"name":"positive regulation of D-loop biosynthesis","type":"related"},{"name":"positive regulation of D-loop formation","type":"related"},{"name":"positive regulation of Rad51-mediated strand invasion","type":"exact"}],"termid":"GO:0098530"}


id: MONDO:0035738
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"factor VII deficiency","termid":"MONDO:0002244"},{"relation_name":"is_a","term_name":"acquired coagulation factor deficiency","termid":"MONDO:0020599"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"acquired factor VII deficiency","secondary_identifiers":["MEDGEN:1388639","Orphanet:599495","GARD:22409","NCIT:C131625","UMLS:C4331989"],"termid":"MONDO:0035738","xrefs":{"Monarch":{"xref_id":"0035738"}}}


id: _global:during
data:
  {"annotation_feature_type":"gene","cv_name":"go/extensions/gorel","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"during","secondary_identifiers":["GOREL:0000002"],"termid":"_global:during"}


id: MONDO:0035862
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare syndromic intellectual disability without multiple congenital anomalies/dysmorphic syndrome (obsolete MONDO:0035862)","secondary_identifiers":["Orphanet:611314"],"termid":"MONDO:0035862","xrefs":{"Monarch":{"xref_id":"0035862"}}}


id: PBO:0005001
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquinol-cytochrome-c reductase complex core protein Qcr2 (predicted)","termid":"PBO:0005001"}


id: PBO:0080941
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zeta chain of T cell receptor associated protein kinase 70","termid":"PBO:0080941"}


id: MONDO:0006973
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma arising from the sebaceous glands, sweat glands, or the hair follicles. Representative examples include sebaceous carcinoma, apocrine carcinoma, eccrine carcinoma, and pilomatrical carcinoma.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epidermal appendage tumor","termid":"MONDO:0002297"},{"relation_name":"is_a","term_name":"skin carcinoma","termid":"MONDO:0002656"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005093"],"is_obsolete":false,"name":"skin appendage carcinoma","secondary_identifiers":["NCIT:C3775","EFO:1001183","MESH:D018280","UMLS:C0206697","MEDGEN:60209","ONCOTREE:SKAC","ICDO:8390/3","MedDRA:10040798"],"synonyms":[{"name":"adnexal carcinoma","type":"exact"},{"name":"carcinoma of adnexa","type":"exact"},{"name":"carcinoma of cutaneous appendage","type":"exact"},{"name":"carcinoma of skin appendage","type":"exact"},{"name":"carcinoma, adnexal, malignant","type":"exact"},{"name":"cutaneous appendage carcinoma","type":"exact"},{"name":"skin adnexal carcinoma","type":"related"},{"name":"skin appendage carcinoma","type":"exact"}],"termid":"MONDO:0006973","xrefs":{"Monarch":{"xref_id":"0006973"}}}


id: PBO:0047029
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 91 member A4, pseudogene","termid":"PBO:0047029"}


id: PBO:0057512
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 630","termid":"PBO:0057512"}


id: GO:0060198
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A clathrin-sculpted lipid bilayer membrane-enclosed vesicle after clathrin release.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"clathrin-coated vesicle","termid":"GO:0030136"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0031410"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0031410","GO:0005737"],"is_obsolete":false,"name":"clathrin-sculpted vesicle","synonyms":[{"name":"clathrin sculpted vesicle","type":"exact"}],"termid":"GO:0060198"}


id: PATO:0002005
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"Surface shape that refers to the inward or outward curvature of the surface.","definition_xrefs":["PATOC:MAH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"shape","termid":"PATO:0000052"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"concavity","termid":"PATO:0002005"}


id: GO:0030886
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of myeloid dendritic cell activation.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of leukocyte activation","termid":"GO:0002695"},{"relation_name":"is_a","term_name":"regulation of myeloid dendritic cell activation","termid":"GO:0030885"},{"relation_name":"negatively_regulates","term_name":"myeloid dendritic cell activation","termid":"GO:0001773"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of myeloid dendritic cell activation","synonyms":[{"name":"down regulation of myeloid dendritic cell activation","type":"exact"},{"name":"down-regulation of myeloid dendritic cell activation","type":"exact"},{"name":"downregulation of myeloid dendritic cell activation","type":"exact"},{"name":"inhibition of myeloid dendritic cell activation","type":"narrow"}],"termid":"GO:0030886"}


id: PR:000044697
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A histone H3.1, initiator methionine removed K9-methylated form (Schizosaccharomyces pombe) whose methylation type is monomethylation. Example: UniProtKB:P09988-1, 2-136, Lys-10, MOD:00085.","definition_xrefs":["PMID:23849629","PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hht1/Me(K9)","termid":"PR:000027578"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone H3.1, initiator methionine removed K9-monomethylated form (Schizosaccharomyces pombe)","pombase_gene_id":"SPAC1834.04","synonyms":[{"name":"Spom-hht1/InitMet-/K9me1","type":"exact"}],"termid":"PR:000044697"}


id: PBO:0067563
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 716, pseudogene","termid":"PBO:0067563"}


id: GO:0045823
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of heart contraction.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of heart contraction","termid":"GO:0008016"},{"relation_name":"is_a","term_name":"positive regulation of blood circulation","termid":"GO:1903524"},{"relation_name":"positively_regulates","term_name":"heart contraction","termid":"GO:0060047"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of heart contraction","synonyms":[{"name":"activation of heart contraction","type":"narrow"},{"name":"positive regulation of cardiac contraction","type":"exact"},{"name":"stimulation of heart contraction","type":"narrow"},{"name":"up regulation of heart contraction","type":"exact"},{"name":"up-regulation of heart contraction","type":"exact"},{"name":"upregulation of heart contraction","type":"exact"}],"termid":"GO:0045823"}


id: MONDO:0021076
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign or malignant neoplasm that arises from the epithelial cells of the exocrine pancreatic tissue.","definition_xrefs":["NCIT:C4445"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pancreatic neoplasm","termid":"MONDO:0021040"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"pancreatic exocrine neoplasm","secondary_identifiers":["MEDGEN:138030","UMLS:C0345920","SCTID:254604005","ICD9:235.5"],"synonyms":[{"name":"exocrine pancreas neoplasm","type":"exact"},{"name":"exocrine pancreas neoplasm (disease)","type":"exact"},{"name":"exocrine pancreas tumor","type":"exact"},{"name":"exocrine pancreas tumour","type":"exact"},{"name":"neoplasm of exocrine pancreas","type":"exact"},{"name":"neoplasm of the exocrine pancreas","type":"exact"},{"name":"pancreatic exocrine neoplasm","type":"exact"},{"name":"pancreatic exocrine tumor","type":"exact"},{"name":"pancreatic exocrine tumour","type":"exact"},{"name":"tumor of exocrine pancreas","type":"exact"},{"name":"tumor of the exocrine pancreas","type":"exact"},{"name":"tumour of exocrine pancreas","type":"exact"},{"name":"tumour of the exocrine pancreas","type":"exact"}],"termid":"MONDO:0021076","xrefs":{"Monarch":{"xref_id":"0021076"}}}


id: GO:0070961
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the frequency, rate or extent of the directed killing of a symbiont target cell by a neutrophil.","definition_xrefs":["GOC:mah","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of response to biotic stimulus","termid":"GO:0002833"},{"relation_name":"is_a","term_name":"positive regulation of defense response","termid":"GO:0031349"},{"relation_name":"is_a","term_name":"positive regulation of response to external stimulus","termid":"GO:0032103"},{"relation_name":"is_a","term_name":"positive regulation of killing of cells of another organism","termid":"GO:0051712"},{"relation_name":"is_a","term_name":"regulation of neutrophil mediated killing of symbiont cell","termid":"GO:0070949"},{"relation_name":"is_a","term_name":"positive regulation of neutrophil mediated cytotoxicity","termid":"GO:0070960"},{"relation_name":"positively_regulates","term_name":"neutrophil-mediated killing of symbiont cell","termid":"GO:0070943"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of neutrophil mediated killing of symbiont cell","synonyms":[{"name":"activation of neutrophil mediated killing of symbiont cell","type":"narrow"},{"name":"stimulation of neutrophil mediated killing of symbiont cell","type":"narrow"},{"name":"up regulation of neutrophil mediated killing of symbiont cell","type":"exact"},{"name":"up-regulation of neutrophil mediated killing of symbiont cell","type":"exact"},{"name":"upregulation of neutrophil mediated killing of symbiont cell","type":"exact"}],"termid":"GO:0070961"}


id: MONDO:0001287
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"endometriosis","termid":"MONDO:0005133"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endometriosis in cutaneous scar","secondary_identifiers":["ICD9:617.6","ICD10CM:N80.6","icd11.foundation:1586348950","MEDGEN:510252","UMLS:C0156348","SCTID:53913001","DOID:11430"],"synonyms":[{"name":"endometriosis in scar of skin","type":"exact"},{"name":"scar endometriosis","type":"related"}],"termid":"MONDO:0001287","xrefs":{"Monarch":{"xref_id":"0001287"}}}


id: PBO:0038844
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADAM metallopeptidase with thrombospondin type 1 motif 13","termid":"PBO:0038844"}


id: MONDO:0958202
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Moyamoya disease","termid":"MONDO:0016820"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"moyamoya disease 7","secondary_identifiers":["MEDGEN:1851566","OMIM:620687","UMLS:C5882748"],"termid":"MONDO:0958202","xrefs":{"Monarch":{"xref_id":"0958202"}}}


id: GO:0097132
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex consisting of cyclin D2 and cyclin-dependent kinase 6 (CDK6). Cyclins are characterized by periodicity in protein abundance throughout the cell cycle. Cyclin-dependent kinases represent a family of serine/threonine protein kinases that become active upon binding to a cyclin regulatory partner.","definition_xrefs":["GOC:so","PMID:15935619"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cyclin-dependent protein kinase holoenzyme complex","termid":"GO:0000307"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"cyclin D2-CDK6 complex","termid":"GO:0097132"}


id: RO:0002261
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"c has-application-role r iff c has-role r and r is an application role (CHEBI:33232)","direct_ancestors":[{"relation_name":"is_a","term_name":"has_role","termid":"RO:0000087"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_application_role","termid":"RO:0002261"}


id: PBO:0050327
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 29","termid":"PBO:0050327"}


id: MONDO:0800287
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autism, susceptiblity to","termid":"MONDO:0020836"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autism, susceptibility to, 14b","secondary_identifiers":["MEDGEN:766322","UMLS:C3553408"],"synonyms":[{"name":"AUTS14B","type":"exact"}],"termid":"MONDO:0800287","xrefs":{"Monarch":{"xref_id":"0800287"}}}


id: PR:O74388
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- far10 gene.","definition_xrefs":["UniProtKB:O74388","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C3H7.13 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC3H7.13","synonyms":[{"name":"Spom972h-far10","type":"exact"}],"termid":"PR:O74388"}


id: FYECO:0000416
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"Experiments were performed in medium containing glucose (typically <2% w/v), salts, water and with L-glutamatic acid as the nitrogen source.","definition_xrefs":["PomBase:mlr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping defined medium","termid":"FYECO:0000013"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glucose MM, cysteine nitrogen source","synonyms":[{"name":"glucose minimal medium, cysteine nitrogen source","type":"exact"},{"name":"standard glucose minimal medium, cysteine nitrogen source","type":"related"}],"termid":"FYECO:0000416"}


id: GO:1990197
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An ATP-binding cassette (ABC) transporter complex that is capable of methionine-importing activity. An example is the bacterial MetNIQ methionine transporter, that consists of the dimeric ATPase subunit MetN located at the cytoplasmic side of the plasma membrane and the dimeric transmembrane subunit MetI. MetQ is regarded as the periplasmic methionine-binding chaperon subunit, and is capable of transporting methionine from the periplasm into the cytoplasm in an ATP-dependent manner.","definition_xrefs":["GOC:bhm","PMID:22095702"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ATP-binding cassette (ABC) transporter complex","termid":"GO:0043190"},{"relation_name":"is_a","term_name":"methionine-importing complex","termid":"GO:1902509"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005886","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"methionine-importing ABC transporter complex","synonyms":[{"name":"ATP-binding cassette (ABC) methionine importer complex","type":"exact"},{"name":"ATP-dependent methionine importer complex","type":"exact"},{"name":"ATP-dependent methionine importing complex","type":"exact"},{"name":"ATP-dependent methionine-importing complex","type":"exact"},{"name":"MetNI complex","type":"narrow"},{"name":"MetNI transport complex","type":"narrow"},{"name":"MetNI transporter","type":"related"},{"name":"MetNI transporter complex","type":"narrow"},{"name":"MetNIQ complex","type":"narrow"},{"name":"MetNIQ transport complex","type":"narrow"},{"name":"MetNIQ transporter","type":"related"},{"name":"MetNIQ transporter complex","type":"related"},{"name":"methionine transport complex","type":"broad"},{"name":"methionine transporter","type":"related"},{"name":"methionine transporter complex","type":"broad"},{"name":"methionine transporter complex, ATP-dependent","type":"broad"}],"termid":"GO:1990197"}


id: MONDO:0007453
data:
  {"annotated_genes":["SJAG_04334","SJAG_04495"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84670,84671],"is_not":false,"summary":null,"term":"MONDO:0007453"}]},"cv_name":"mondo","definition":"Monogenic diabetes caused by inactivating mutation(s) in the GCK gene, encoding glucokinase. Heterozygous GCK mutations may manifest as mild hyperglycemia, which is not progressive, and usually requires no treatment. Homozygous GCK mutations result in permanent neonatal diabetes.","definition_xrefs":["NCIT:C129741"],"direct_ancestors":[{"relation_name":"is_a","term_name":"maturity-onset diabetes of the young","termid":"MONDO:0018911"}],"gene_count":2,"genes_by_uniquename":{"SJAG_04334":null,"SJAG_04495":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0019254"},{"rel_name":"is_a","termid":"MONDO:0005015"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004335","MONDO:0037792","MONDO:0019254","MONDO:0005015"],"is_obsolete":false,"name":"maturity-onset diabetes of the young type 2","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:237604008","UMLS:C0342277","DOID:0111100","NANDO:2201070","GARD:10657","MEDGEN:87434","OMIM:125851"],"synonyms":[{"name":"GCK maturity-onset diabetes of the young (disease)","type":"exact"},{"name":"GCK-associated diabetes mellitus","type":"exact"},{"name":"MODY 2 monogenic diabetes type 2","type":"exact"},{"name":"MODY glucokinase-related","type":"exact"},{"name":"MODY type 2","type":"exact"},{"name":"MODY, glucokinase-related","type":"related"},{"name":"MODY, type 2","type":"related"},{"name":"MODY, type II","type":"exact"},{"name":"MODY2","type":"exact"},{"name":"diabetes mellitus MODY type 2","type":"related"},{"name":"glucokinase-associated diabetes mellitus","type":"exact"},{"name":"maturity onset diabetes of the Young, type 2","type":"exact"},{"name":"maturity-onset diabetes of the young (disease) caused by mutation in GCK","type":"exact"},{"name":"maturity-onset diabetes of the young, type 2","type":"related"},{"name":"type 2 maturity-onset diabetes of the young","type":"related"}],"termid":"MONDO:0007453","terms_by_termid":{"MONDO:0007453":null},"xrefs":{"Monarch":{"xref_id":"0007453"}}}


id: PBO:0114291
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methyltransferase, sterol related","termid":"PBO:0114291"}


id: GO:0061658
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Isoenergetic transfer of URM1 from one protein to another via the reaction X-URM1 + Y = Y-URM1 + X, where both the X-URM1 and Y-URM1 linkages are thioester bonds between the C-terminal amino acid of URM1 and a sulfhydryl side group of a cysteine residue.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"URM1 transferase activity","termid":"GO:0042294"},{"relation_name":"is_a","term_name":"ubiquitin-like protein conjugating enzyme activity","termid":"GO:0061650"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0019787"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016746","GO:0019787","GO:0003674","GO:0140096","GO:0016740"],"is_obsolete":false,"name":"URM1 conjugating enzyme activity","synonyms":[{"name":"E2","type":"broad"}],"termid":"GO:0061658"}


id: GO:0090441
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of trehalose that occur as a result of a heat stimulus, a temperature stimulus above the optimal temperature for that organism.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"trehalose biosynthetic process","termid":"GO:0005992"},{"relation_name":"is_a","term_name":"trehalose metabolism in response to heat stress","termid":"GO:0070414"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0008150","GO:0005975"],"is_obsolete":false,"name":"trehalose biosynthesis in response to heat stress","synonyms":[{"name":"trehalose biosynthetic process in response to heat stress","type":"exact"}],"termid":"GO:0090441"}


id: MONDO:0014671
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hereditary motor and sensory neuropathy type 6 in which the cause of the disease is a mutation in the SLC25A46 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"motor peripheral neuropathy","termid":"MONDO:0002316"},{"relation_name":"is_a","term_name":"hereditary motor and sensory neuropathy type 6","termid":"MONDO:0019551"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"neuropathy, hereditary motor and sensory, type 6B","secondary_identifiers":["GARD:18092","OMIM:616505","MEDGEN:895482","UMLS:C4225302"],"synonyms":[{"name":"CMT6B","type":"exact"},{"name":"Charcot-Marie-Tooth disease, type 6B","type":"exact"},{"name":"HMSN 6B","type":"exact"},{"name":"HMSN6B","type":"exact"},{"name":"SLC25A46 hereditary motor and sensory neuropathy type 6","type":"exact"},{"name":"hereditary motor and sensory neuropathy type 6 caused by mutation in SLC25A46","type":"exact"},{"name":"neuropathy, hereditary motor and sensory, type 6B","type":"exact"},{"name":"neuropathy, hereditary motor and sensory, type VIB","type":"exact"}],"termid":"MONDO:0014671","xrefs":{"Monarch":{"xref_id":"0014671"}}}


id: PBO:0045049
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dihydrolipoamide dehydrogenase","termid":"PBO:0045049"}


id: GO:0003158
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of an endothelium over time, from its formation to the mature structure. Endothelium refers to the layer of cells lining blood vessels, lymphatics, the heart, and serous cavities, and is derived from bone marrow or mesoderm. Corneal endothelium is a special case, derived from neural crest cells.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelium development","termid":"GO:0060429"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"endothelium development","termid":"GO:0003158"}


id: PR:O14097
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- saf2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14097"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WW domain-containing protein C2F3.14c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC2F3.14c","synonyms":[{"name":"Spom972h-saf2","type":"exact"}],"termid":"PR:O14097"}


id: SO:0001291
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"N4,2'-O-dimethylcytidine is a modified cytidine.","direct_ancestors":[{"relation_name":"is_a","term_name":"modified_cytidine","termid":"SO:0001275"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N4_2_prime_O_dimethylcytidine","secondary_identifiers":["RNAMOD:083"],"synonyms":[{"name":"N4 2 prime O dimethylcytidine","type":"exact"},{"name":"N4,2'-O-dimethylcytidine","type":"exact"},{"name":"m4Cm","type":"exact"}],"termid":"SO:0001291"}


id: PBO:0089885
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NatA N-acetyltransferase complex regulatory subunit Naa15","termid":"PBO:0089885"}


id: PBO:0074853
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 42A","termid":"PBO:0074853"}


id: SO:0001366
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"5_methylaminomethyl_2_selenouridine is a modified uridine base feature.","direct_ancestors":[{"relation_name":"is_a","term_name":"modified_uridine","termid":"SO:0001277"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"five_methylaminomethyl_two_selenouridine","secondary_identifiers":["RNAMOD:074"],"synonyms":[{"name":"5-methylaminomethyl-2-selenouridine","type":"exact"},{"name":"five methylaminomethyl two selenouridine","type":"exact"},{"name":"mnm5se2U","type":"exact"}],"termid":"SO:0001366"}


id: FYPO:0004286
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the occurrence of double-strand break repair via nonhomologous end joining (NHEJ) is normal (i.e. indistinguishable from wild type). NHEJ is the repair of double-strand breaks in DNA in which the two broken ends are rejoined with little or no sequence complementarity.","definition_xrefs":["GO:0006303","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal double-strand break repair","termid":"FYPO:0001033"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000298"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000257","FYPO:0001312","FYPO:0000002","FYPO:0000298"],"is_obsolete":false,"name":"normal double-strand break repair via nonhomologous end joining","synonyms":[{"name":"normal NHEJ","type":"exact"},{"name":"normal double-strand break repair via nonhomologous end joining during mitotic cell cycle","type":"related"},{"name":"normal double-strand break repair via nonhomologous end joining during vegetative growth","type":"exact"},{"name":"normal nonhomologous end joining","type":"exact"}],"termid":"FYPO:0004286"}


id: PBO:0041337
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 3 open reading frame 20","termid":"PBO:0041337"}


id: MONDO:0007534
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Beckwith-Wiedemann syndrome (BWS) is a genetic disorder characterized by overgrowth, tumor predisposition and congenital malformations.","definition_xrefs":["Orphanet:116"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"macroglossia","termid":"MONDO:0015496"},{"relation_name":"excluded_subClassOf","term_name":"obsolete syndrome or malformation associated with head and neck malformations (obsolete MONDO:0015501)","termid":"MONDO:0015501"},{"relation_name":"excluded_subClassOf","term_name":"obsolete syndromic renal or urinary tract malformation (obsolete MONDO:0019721)","termid":"MONDO:0019721"},{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"},{"relation_name":"is_a","term_name":"overgrowth syndrome","termid":"MONDO:0019716"},{"relation_name":"is_a","term_name":"familial hypertrophic cardiomyopathy","termid":"MONDO:0024573"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"Beckwith-Wiedemann syndrome","secondary_identifiers":["UMLS:C0004903","ICD9:759.89","MESH:D001506","MEDGEN:2562","NCIT:C34415","NORD:845","icd11.foundation:803086260","DOID:5572","NANDO:2200959","GARD:3343","MedDRA:10050344","OMIM:130650","SCTID:81780002"],"synonyms":[{"name":"BWS","type":"exact"},{"name":"Beckwith-Wiedemann syndrome","type":"exact"},{"name":"Beckwith-Wiedemann syndrome chromosome region","type":"related"},{"name":"EMG syndrome","type":"related"},{"name":"Wiedemann-Beckwith syndrome","type":"exact"},{"name":"Wiedemann-Beckwith syndrome (WBS)","type":"related"},{"name":"exomphalos macroglossia gigantism syndrome","type":"related"},{"name":"exomphalos-macroglossia-gigantism syndrome","type":"exact"}],"termid":"MONDO:0007534","xrefs":{"Monarch":{"xref_id":"0007534"}}}


id: MONDO:0000763
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"corneal dystrophy","termid":"MONDO:0018102"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"epithelial and subepithelial corneal dystrophy","secondary_identifiers":["DOID:0060440"],"synonyms":[{"name":"epithelial and subepithelial dystrophy","type":"related"}],"termid":"MONDO:0000763","xrefs":{"Monarch":{"xref_id":"0000763"}}}


id: MONDO:0054559
data:
  {"annotated_genes":["SJAG_00578"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86414],"is_not":false,"summary":null,"term":"MONDO:0054559"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital disorder of glycosylation type II","termid":"MONDO:0005501"},{"relation_name":"is_a","term_name":"defect in conserved oligomeric Golgi complex","termid":"MONDO:0017750"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00578":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0024322"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0024322"],"is_obsolete":false,"name":"congenital disorder of glycosylation, type IIq","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:435934","OMIM:617395","DOID:0070269","UMLS:C4479353","MEDGEN:1390458","GARD:17720"],"synonyms":[{"name":"CDG Iiq","type":"related"},{"name":"CDG2Q","type":"related"},{"name":"COG2-CDG","type":"exact"},{"name":"COG2-related congenital disorder of glycosylation","type":"exact"}],"termid":"MONDO:0054559","terms_by_termid":{"MONDO:0054559":null},"xrefs":{"Monarch":{"xref_id":"0054559"}}}


id: PBO:0057810
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3131","termid":"PBO:0057810"}


id: PBO:0077437
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 170B","termid":"PBO:0077437"}


id: PBO:0036475
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exocyst complex ChAPs family (Chs5p-Arf1p-binding) protein Bch1","termid":"PBO:0036475"}


id: MONDO:0017253
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete anterior uveitis (obsolete MONDO:0017253)","termid":"MONDO:0017253","xrefs":{"Monarch":{"xref_id":"0017253"}}}


id: PR:Q9UU89
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An inosine triphosphate pyrophosphatase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR11067:SF7","PRO:DNx","OMA:SCHPO04982"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inosine triphosphate pyrophosphatase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC830.10","secondary_identifiers":["UniProtKB:Q9UU89"],"synonyms":[{"name":"ITPase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"NTPase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-ITPA","type":"exact"},{"name":"inosine triphosphatase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"non-canonical purine NTP pyrophosphatase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"non-standard purine NTP pyrophosphatase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"nucleoside-triphosphate diphosphatase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"nucleoside-triphosphate pyrophosphatase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9UU89"}


id: GO:0106405
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the dephosphorylation of isoprenoid diphosphates.","definition_xrefs":["PMID:33246356"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrophosphatase activity","termid":"GO:0016462"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0003824"],"is_obsolete":false,"name":"isoprenoid diphosphate phosphatase activity","termid":"GO:0106405"}


id: GO:0072470
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that occurs in response to signals generated as a result of cell size control checkpoint signaling.","definition_xrefs":["GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to mitotic cell cycle checkpoint signaling","termid":"GO:0072414"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to cell size control checkpoint signaling","synonyms":[{"name":"cell size control checkpoint effector process","type":"exact"},{"name":"response to mitotic cell cycle cell size control checkpoint signaling","type":"exact"},{"name":"response to signal involved in cell size control checkpoint","type":"exact"}],"termid":"GO:0072470"}


id: GO:2001242
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of intrinsic apoptotic signaling pathway.","definition_xrefs":["GOC:mtg_apoptosis"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of intracellular signal transduction","termid":"GO:1902531"},{"relation_name":"is_a","term_name":"regulation of apoptotic signaling pathway","termid":"GO:2001233"},{"relation_name":"regulates","term_name":"intrinsic apoptotic signaling pathway","termid":"GO:0097193"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"regulation of intrinsic apoptotic signaling pathway","synonyms":[{"name":"regulation of intrinsic apoptosis","type":"narrow"},{"name":"regulation of intrinsic apoptotic pathway","type":"exact"},{"name":"regulation of intrinsic apoptotic signalling pathway","type":"exact"},{"name":"regulation of mitochondrial-mediated apoptotic pathway","type":"exact"}],"termid":"GO:2001242"}


id: GO:0018226
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of peptidyl-cysteine to form peptidyl-S-farnesyl-L-cysteine; formation of S-farnesycysteine may be coupled with subsequent cleavage of a carboxy-terminal tripeptide for the CXXX motif and methyl esterification of the farnesylated cysteine; the residue may be found at the first position in the sequence motif C-X-X-(SAQCMT)* where the second and third positions are usually aliphatic.","definition_xrefs":["RESID:AA0102"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-S-farnesyl-L-cysteine biosynthetic process from peptidyl-cysteine (obsolete GO:0018226)","synonyms":[{"name":"peptidyl-S-farnesyl-L-cysteine anabolism from peptidyl-cysteine","type":"exact"},{"name":"peptidyl-S-farnesyl-L-cysteine formation from peptidyl-cysteine","type":"exact"},{"name":"peptidyl-S-farnesyl-L-cysteine synthesis from peptidyl-cysteine","type":"exact"}],"termid":"GO:0018226"}


id: MONDO:0045011
data:
  {"annotated_genes":["SJAG_01474","SJAG_03349","SJAG_03158","SJAG_02698","SJAG_02488","SJAG_00104","SJAG_04865","SJAG_03352","SJAG_01878","SJAG_00580","SJAG_04167","SJAG_01938","SJAG_04565","SJAG_05011"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84734],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007048"},{"annotations":[85055],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033014"},{"annotations":[85547],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014131"},{"annotations":[85261,85260],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009440"},{"annotations":[84559],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007858"},{"annotations":[86262,86261,86260],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008416"},{"annotations":[86627,86628],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008293"},{"annotations":[85676],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013868"},{"annotations":[85538,85539],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014713"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"integumentary system disorder","termid":"MONDO:0002051"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":14,"genes_by_uniquename":{"SJAG_00104":null,"SJAG_00580":null,"SJAG_01474":null,"SJAG_01878":null,"SJAG_01938":null,"SJAG_02488":null,"SJAG_02698":null,"SJAG_03158":null,"SJAG_03349":null,"SJAG_03352":null,"SJAG_04167":null,"SJAG_04565":null,"SJAG_04865":null,"SJAG_05011":null},"genotype_count":0,"is_obsolete":false,"name":"keratinization disease","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0475811","MEDGEN:635020","SCTID:277905003"],"synonyms":[{"name":"disorder of keratinization","type":"exact"},{"name":"keratinization disease","type":"exact"}],"termid":"MONDO:0045011","terms_by_termid":{"MONDO:0007048":null,"MONDO:0007858":null,"MONDO:0008293":null,"MONDO:0008416":null,"MONDO:0009440":null,"MONDO:0013868":null,"MONDO:0014131":null,"MONDO:0014713":null,"MONDO:0033014":null},"xrefs":{"Monarch":{"xref_id":"0045011"}}}


id: GO:0033233
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the addition of SUMO groups to a protein.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein modification by small protein conjugation or removal","termid":"GO:1903320"},{"relation_name":"regulates","term_name":"protein sumoylation","termid":"GO:0016925"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0070647"}],"interesting_parent_ids":["GO:0008150","GO:0070647"],"is_obsolete":false,"name":"regulation of protein sumoylation","synonyms":[{"name":"regulation of sumoylation","type":"exact"}],"termid":"GO:0033233"}


id: MONDO:0019882
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Distal trisomy 8q is a rare chromosomal anomaly syndrome resulting from the partial duplication of the long arm of chromosome 8, with a highly variable phenotype, typically characterized by growth and developmental delay, intellectual disability, short stature, craniofacial dysmorphism (microcephaly, prominent forehead, hypertelorism, abnormal palpebral fissures, low-set, large ears, anteverted tip of nose, micro/retrognathia), congenital heart defects and skeletal and limb anomalies. Other reported features include ophthalmologic abnormalities (e.g. megalocornea), cryptorchidism, hypertrichosis, and neurologic manifestations (e.g. hypotonia, hearing loss, and seizures).","definition_xrefs":["Orphanet:96100"],"direct_ancestors":[{"relation_name":"is_a","term_name":"partial duplication of the long arm of chromosome 8","termid":"MONDO:0016959"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"distal trisomy 8q","secondary_identifiers":["MEDGEN:1637956","UMLS:C4706365","GARD:19315","SCTID:763277009"],"synonyms":[{"name":"distal duplication 8q","type":"exact"},{"name":"distal trisomy type 8q","type":"exact"},{"name":"telomeric duplication 8q","type":"exact"},{"name":"trisomy 8qter","type":"exact"}],"termid":"MONDO:0019882","xrefs":{"Monarch":{"xref_id":"0019882"}}}


id: PBO:0063220
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protocadherin 9","termid":"PBO:0063220"}


id: GO:0007463
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the R2/R5 photoreceptors commit to their cell fate. R2 and R5 are paired photoreceptors which contribute the outer rhabdomeres.","definition_xrefs":["PMID:3937883","PMID:3076112"],"direct_ancestors":[{"relation_name":"is_a","term_name":"compound eye photoreceptor fate commitment","termid":"GO:0001752"},{"relation_name":"part_of","term_name":"R2/R5 cell differentiation","termid":"GO:0048054"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"R2/R5 cell fate commitment","termid":"GO:0007463"}


id: PBO:0034421
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-regulates_morphogenesis_of","termid":"PBO:0034421"}


id: FYPO:0004114
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a spore germinates to produce an inviable cell that does not divide, and that has a septum with abnormal size, shape, or structure.","definition_xrefs":["PMID:15116432","PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"abnormal septum morphology during vegetative growth","termid":"FYPO:0002023"},{"relation_name":"is_a","term_name":"inviable after spore germination, without cell division","termid":"FYPO:0001991"},{"relation_name":"is_a","term_name":"abnormal septum morphology during vegetative growth","termid":"FYPO:0002023"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"has_part","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000032","FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0000004","FYPO:0000631","FYPO:0001320"],"is_obsolete":false,"name":"inviable after spore germination, without cell division, abnormal septum morphology","synonyms":[{"name":"inviable after spore germination, undivided cell, abnormal septum morphology","type":"exact"},{"name":"inviable after spore germination, without cell division, abnormal septum formation","type":"exact"},{"name":"inviable following spore germination, without cell division, abnormal septum morphology","type":"exact"},{"name":"inviable germinated spore, without cell division, abnormal septum morphology","type":"exact"},{"name":"lethal after spore germination, without cell division, abnormal septum morphology","type":"exact"}],"termid":"FYPO:0004114"}


id: GO:0000812
data:
  {"annotated_genes":["SJAG_03694","SJAG_02466","SJAG_02500","SJAG_02385","SJAG_05192","SJAG_02571","SJAG_03145","SJAG_01465","SJAG_02798","SJAG_04355","SJAG_03036","SJAG_05282","SJAG_04596","SJAG_04097","SJAG_03579","SJAG_02990"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[87496,90207,91881,96150,97740,98464,100466,101178,107344,108523,111685,112590,112759,114159,116709,116893],"is_not":false,"summary":null,"term":"GO:0000812"}]},"cv_name":"cellular_component","definition":"A multisubunit protein complex that is involved in chromatin remodeling. It is required for the incorporation of the histone variant H2AZ into chromatin. In S. cerevisiae, the complex contains Swr1p, a Swi2/Snf2-related ATPase, and 12 additional subunits.","definition_xrefs":["PMID:19355820","GOC:rb","PMID:14645854","PMID:14690608"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone deacetylase complex","termid":"GO:0000118"},{"relation_name":"is_a","term_name":"INO80-type complex","termid":"GO:0097346"},{"relation_name":"part_of","term_name":"nuclear chromosome","termid":"GO:0000228"}],"gene_count":16,"genes_by_uniquename":{"SJAG_01465":null,"SJAG_02385":null,"SJAG_02466":null,"SJAG_02500":null,"SJAG_02571":null,"SJAG_02798":null,"SJAG_02990":null,"SJAG_03036":null,"SJAG_03145":null,"SJAG_03579":null,"SJAG_03694":null,"SJAG_04097":null,"SJAG_04355":null,"SJAG_04596":null,"SJAG_05192":null,"SJAG_05282":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005654"},{"rel_name":"part_of","termid":"GO:0005694"}],"interesting_parent_ids":["GO:0032991","GO:0005634","GO:0005575","GO:0005654","GO:0005694"],"is_obsolete":false,"name":"Swr1 complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"SWR-C","type":"exact"}],"termid":"GO:0000812","terms_by_termid":{"GO:0000812":null}}


id: PBO:0074520
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small NF90 (ILF3) associated RNA A12","termid":"PBO:0074520"}


id: PBO:0001141
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"traub family protein involved in ribosome biogenesis (predicted)","termid":"PBO:0001141"}


id: GO:0019357
data:
  {"annotated_genes":["SJAG_03298","SJAG_00957","SJAG_04467"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90166,88534,109078],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019358"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of nicotinamide nucleotides, any nucleotide that contains combined nicotinate (pyridine 3-carboxylic acid).","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyridine nucleotide biosynthetic process","termid":"GO:0019363"},{"relation_name":"is_a","term_name":"nicotinate nucleotide metabolic process","termid":"GO:0046497"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00957":null,"SJAG_03298":null,"SJAG_04467":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"nicotinate nucleotide biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"nicotinate nucleotide anabolism","type":"exact"},{"name":"nicotinate nucleotide biosynthesis","type":"exact"},{"name":"nicotinate nucleotide formation","type":"exact"},{"name":"nicotinate nucleotide synthesis","type":"exact"}],"termid":"GO:0019357","terms_by_termid":{"GO:0019358":null}}


id: PBO:0061032
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NINJ2 antisense RNA 1","termid":"PBO:0061032"}


id: PBO:0038797
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADAM metallopeptidase domain 3A (pseudogene)","termid":"PBO:0038797"}


id: GO:0042162
data:
  {"annotated_genes":["SJAG_01677","SJAG_01378","SJAG_04863","SJAG_03855","SJAG_05214","SJAG_01698","SJAG_00939","SJAG_04245","SJAG_01777","SJAG_00112","SJAG_05372","SJAG_02194","SJAG_03092","SJAG_05979","SJAG_02212","SJAG_04372","SJAG_02362"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[89283,97067,99225,104579,107405,110403,111011,113733,114972],"is_not":false,"summary":null,"term":"GO:0042162"},{"annotations":[88691,105612,89281],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003691"},{"annotations":[94594],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098505"},{"annotations":[95570,94595,88693,109827,111009,107585,114055,110984],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043047"}]},"cv_name":"molecular_function","definition":"Binding to a telomere, a specific structure at the end of a linear chromosome required for the integrity and maintenance of the end.","definition_xrefs":["GOC:jl","SO:0000624"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sequence-specific DNA binding","termid":"GO:0043565"}],"gene_count":17,"genes_by_uniquename":{"SJAG_00112":null,"SJAG_00939":null,"SJAG_01378":null,"SJAG_01677":null,"SJAG_01698":null,"SJAG_01777":null,"SJAG_02194":null,"SJAG_02212":null,"SJAG_02362":null,"SJAG_03092":null,"SJAG_03855":null,"SJAG_04245":null,"SJAG_04372":null,"SJAG_04863":null,"SJAG_05214":null,"SJAG_05372":null,"SJAG_05979":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003677"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0003677"],"is_obsolete":false,"name":"telomeric DNA binding","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"telomere binding","type":"exact"},{"name":"telomeric repeat binding","type":"exact"}],"termid":"GO:0042162","terms_by_termid":{"GO:0003691":null,"GO:0042162":null,"GO:0043047":null,"GO:0098505":null}}


id: SO:0000771
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A quantitative trait locus (QTL) is a polymorphic locus which contains alleles that differentially affect the expression of a continuously distributed phenotypic trait. Usually it is a marker described by statistical association to quantitative variation in the particular phenotypic trait that is thought to be controlled by the cumulative action of alleles at multiple loci.","direct_ancestors":[{"relation_name":"is_a","term_name":"biological_region","termid":"SO:0001411"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"QTL","synonyms":[{"name":"quantitative trait locus","type":"exact"}],"termid":"SO:0000771"}


id: PBO:0075452
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spermatogenesis associated 4","termid":"PBO:0075452"}


id: MONDO:1030015
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A porphyria disorder that is acquired during the lifetime of the individual.","definition_xrefs":["MONDO:patterns/acquired"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acquired metabolic disease","termid":"MONDO:0006504"},{"relation_name":"is_a","term_name":"porphyria","termid":"MONDO:0037939"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"acquired porphyria","secondary_identifiers":["MESH:D011164","NCIT:C97096"],"termid":"MONDO:1030015","xrefs":{"Monarch":{"xref_id":"1030015"}}}


id: GO:0102171
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (3S,6E)-nerolidol + O2 + reduced [NADPH--hemoprotein reductase] = (3E)-4,8-dimethylnona-1,3,7-triene + but-3-en-2-one + H+ + 2 H2O + oxidized [NADPH--hemoprotein reductase].","definition_xrefs":["RHEA:55424"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen","termid":"GO:0016712"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"DMNT synthase activity","secondary_identifiers":["EC:1.14.14.59","MetaCyc:RXN-11911"],"termid":"GO:0102171"}


id: MONDO:0054763
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"neurodegeneration with brain iron accumulation","termid":"MONDO:0018307"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0002039","MONDO:0005559"],"is_obsolete":false,"name":"neurodegeneration with brain iron accumulation 7","secondary_identifiers":["MEDGEN:1647672","OMIM:617916","UMLS:C4693583"],"synonyms":[{"name":"NBIA7","type":"related"},{"name":"neurodegeneration with brain iron accumulation 7","type":"exact"}],"termid":"MONDO:0054763","xrefs":{"Monarch":{"xref_id":"0054763"}}}


id: MONDO:1011348
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Post-Infectious disorder that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-human animal disease","termid":"MONDO:0005583"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"post-infectious disorder, non-human animal","termid":"MONDO:1011348","xrefs":{"Monarch":{"xref_id":"1011348"}}}


id: PBO:0017727
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP-dependent DNA helicase/ ubiquitin-protein ligase E3 (predicted)","termid":"PBO:0017727"}


id: GO:0033303
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways leading to the formation of O-glucosylated derivatives of quercetin.","definition_xrefs":["MetaCyc:PWY-5321","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycoside biosynthetic process","termid":"GO:0016138"},{"relation_name":"is_a","term_name":"quercetin O-glucoside metabolic process","termid":"GO:0033302"},{"relation_name":"is_a","term_name":"flavone biosynthetic process","termid":"GO:0051553"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"quercetin O-glucoside biosynthetic process","synonyms":[{"name":"quercetin O-glucoside anabolism","type":"exact"},{"name":"quercetin O-glucoside biosynthesis","type":"exact"},{"name":"quercetin O-glucoside formation","type":"exact"},{"name":"quercetin O-glucoside synthesit","type":"exact"}],"termid":"GO:0033303"}


id: GO:0075065
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The increase in size or mass of symbiont, or the progression of the symbiont from an initial condition to a later condition, occurring in its host's cell. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete growth or development of symbiont in host cell (obsolete GO:0075065)","synonyms":[{"name":"growth or development of symbiont in host cell","type":"exact"}],"termid":"GO:0075065"}


id: PBO:0050063
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HLF transcription factor, PAR bZIP family member","termid":"PBO:0050063"}


id: GO:0045311
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The growth of colonies in filamentous chains of cells as a result of a pheromone stimulus.","definition_xrefs":["GOC:dph","GOC:mcc","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"invasive filamentous growth","termid":"GO:0036267"},{"relation_name":"part_of","term_name":"response to pheromone","termid":"GO:0019236"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"invasive growth in response to pheromone","termid":"GO:0045311"}


id: PBO:0076749
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thymine DNA glycosylase","termid":"PBO:0076749"}


id: PBO:0085499
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein anchored to mitochondrial inner membrane; may have a redundant function with Sco1p in delivery of copper to cytochrome c oxidase; interacts with Cox2p; SCO2 has a paralog, SCO1, that arose from the whole genome duplication","termid":"PBO:0085499"}


id: PBO:0028496
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_protein_degradation_via_N-end_rule_pathway_during_vegetative_growth","termid":"PBO:0028496"}


id: PBO:0089257
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein phosphatase PP2A catalytic subunit Ppa3","termid":"PBO:0089257"}


id: MONDO:0000228
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Astrakhan spotted fever (obsolete MONDO:0000228)","termid":"MONDO:0000228","xrefs":{"Monarch":{"xref_id":"0000228"}}}


id: PR:O13872
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A vacuolar protein sorting-associated protein 28 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02052","PANTHER:PTHR12937:SF0","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar protein sorting-associated protein 28 homolog (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1B3.07c","secondary_identifiers":["UniProtKB:O13872"],"synonyms":[{"name":"ESCRT-I complex subunit vps28 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-VPS28","type":"exact"}],"termid":"PR:O13872"}


id: FYPO:0000148
data:
  {"alleles_by_uniquename":{"SJAG_01330:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01330","name":"mad2delta","uniquename":"SJAG_01330:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[118702,118742],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0004318"}]},"cv_name":"fission_yeast_phenotype","definition":"A regulation phenotype in which regulation of the mitotic cell cycle is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic cell cycle","termid":"FYPO:0000059"},{"relation_name":"is_a","term_name":"regulation phenotype during vegetative growth","termid":"FYPO:0001334"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01330":null},"genotype_count":1,"genotypes_by_uniquename":{"mad2delta":{"display_name":"mad2delta","display_uniquename":"mad2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01330:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000631","FYPO:0005447","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"abnormal regulation of mitotic cell cycle","references_by_uniquename":{"PMID:21802294":null,"PMID:32109380":null},"single_locus_annotated_genes":["SJAG_01330"],"single_locus_genotype_uniquenames":["mad2delta"],"termid":"FYPO:0000148","terms_by_termid":{"FYECO:0000162":null,"FYPO:0004318":null}}


id: SO:0001211
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The region of mRNA 1 base long that is skipped during the process of translational frameshifting (GO:0006452), causing the reading frame to be different.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"translational_frameshift","termid":"SO:0001210"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plus_1_translational_frameshift","synonyms":[{"name":"plus 1 ribosomal frameshift","type":"exact"},{"name":"plus 1 translational frameshift","type":"exact"}],"termid":"SO:0001211"}


id: PBO:0038544
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"abhydrolase domain containing 16A, phospholipase","termid":"PBO:0038544"}


id: GO:1905621
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of alpha-(1->3)-fucosyltransferase activity.","definition_xrefs":["PMID:15364955","GOC:TermGenie","GO_REF:0000059"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of alpha-(1->3)-fucosyltransferase activity (obsolete GO:1905621)","synonyms":[{"name":"activation of alpha(1,3)-fucosyltransferase activity","type":"narrow"},{"name":"activation of alpha-(1,3)-fucosyltransferase activity","type":"narrow"},{"name":"activation of alpha-(1->3)-fucosyltransferase activity","type":"narrow"},{"name":"activation of alpha-1,3-fucosyltransferase activity","type":"narrow"},{"name":"positive regulation of alpha(1,3)-fucosyltransferase activity","type":"exact"},{"name":"positive regulation of alpha-(1,3)-fucosyltransferase activity","type":"exact"},{"name":"positive regulation of alpha-1,3-fucosyltransferase activity","type":"exact"},{"name":"up regulation of alpha(1,3)-fucosyltransferase activity","type":"exact"},{"name":"up regulation of alpha-(1,3)-fucosyltransferase activity","type":"exact"},{"name":"up regulation of alpha-(1->3)-fucosyltransferase activity","type":"exact"},{"name":"up regulation of alpha-1,3-fucosyltransferase activity","type":"exact"},{"name":"up-regulation of alpha(1,3)-fucosyltransferase activity","type":"exact"},{"name":"up-regulation of alpha-(1,3)-fucosyltransferase activity","type":"exact"},{"name":"up-regulation of alpha-(1->3)-fucosyltransferase activity","type":"exact"},{"name":"up-regulation of alpha-1,3-fucosyltransferase activity","type":"exact"},{"name":"upregulation of alpha(1,3)-fucosyltransferase activity","type":"exact"},{"name":"upregulation of alpha-(1,3)-fucosyltransferase activity","type":"exact"},{"name":"upregulation of alpha-(1->3)-fucosyltransferase activity","type":"exact"},{"name":"upregulation of alpha-1,3-fucosyltransferase activity","type":"exact"}],"termid":"GO:1905621"}


id: PBO:0091372
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER zinc importer, CDF family, Zhf1","termid":"PBO:0091372"}


id: GO:0045705
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of salivary gland determination.","definition_xrefs":["GOC:tb","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of salivary gland boundary specification","termid":"GO:0045704"},{"relation_name":"is_a","term_name":"negative regulation of developmental process","termid":"GO:0051093"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"negatively_regulates","term_name":"salivary gland boundary specification","termid":"GO:0007432"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of salivary gland boundary specification","synonyms":[{"name":"down regulation of salivary gland determination","type":"exact"},{"name":"down-regulation of salivary gland determination","type":"exact"},{"name":"downregulation of salivary gland determination","type":"exact"},{"name":"inhibition of salivary gland determination","type":"narrow"},{"name":"negative regulation of salivary gland determination","type":"exact"}],"termid":"GO:0045705"}


id: PBO:0073146
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SEC23 interacting protein","termid":"PBO:0073146"}


id: GO:0008017
data:
  {"annotated_genes":["SJAG_03073","SJAG_02045","SJAG_02795","SJAG_00773","SJAG_04841","SJAG_00930","SJAG_02609","SJAG_00851","SJAG_00723","SJAG_01546","SJAG_02814","SJAG_01613","SJAG_01297","SJAG_00042","SJAG_02336","SJAG_03835","SJAG_02040","SJAG_04745","SJAG_02624","SJAG_01760","SJAG_00332","SJAG_03540"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[58659,59294,61105,62006,63422,63632,65996,67890,68556,73288,73564,75469,75846,76588,76681,78273],"is_not":false,"summary":null,"term":"GO:0008017"},{"annotations":[71177,70669],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051011"},{"annotations":[68198,79428,70133,64931],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051010"}]},"cv_name":"molecular_function","definition":"Binding to a microtubule, a filament composed of tubulin monomers.","definition_xrefs":["GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tubulin binding","termid":"GO:0015631"}],"gene_count":22,"genes_by_uniquename":{"SJAG_00042":null,"SJAG_00332":null,"SJAG_00723":null,"SJAG_00773":null,"SJAG_00851":null,"SJAG_00930":null,"SJAG_01297":null,"SJAG_01546":null,"SJAG_01613":null,"SJAG_01760":null,"SJAG_02040":null,"SJAG_02045":null,"SJAG_02336":null,"SJAG_02609":null,"SJAG_02624":null,"SJAG_02795":null,"SJAG_02814":null,"SJAG_03073":null,"SJAG_03540":null,"SJAG_03835":null,"SJAG_04745":null,"SJAG_04841":null},"genotype_count":0,"in_subsets":["mf_goslim_japonicus"],"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0008092"}],"interesting_parent_ids":["GO:0005515","GO:0005488","GO:0003674","GO:0008092"],"is_obsolete":false,"name":"microtubule binding","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-9614343"],"synonyms":[{"name":"microtubule severing activity","type":"related"},{"name":"microtubule/chromatin interaction","type":"related"}],"termid":"GO:0008017","terms_by_termid":{"GO:0008017":null,"GO:0051010":null,"GO:0051011":null}}


id: GO:0046547
data:
  {"annotated_genes":["SJAG_02973"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[94185,94189],"is_not":false,"summary":null,"term":"GO:0046547"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine(1+) + trans-aconitate = (E)-2-(methoxycarbonylmethyl)but-2-enedioate + S-adenosyl-L-homocysteine.","definition_xrefs":["EC:2.1.1.145","RHEA:22200"],"direct_ancestors":[{"relation_name":"is_a","term_name":"S-adenosylmethionine-dependent methyltransferase activity","termid":"GO:0008757"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02973":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016740","GO:0016741"],"is_obsolete":false,"name":"trans-aconitate 3-methyltransferase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["KEGG_REACTION:R05764","MetaCyc:2.1.1.145-RXN"],"synonyms":[{"name":"S-adenosyl-L-methionine:(E)-prop-1-ene-1,2,3-tricarboxylate 3'-O-methyltransferase activity","type":"related"}],"termid":"GO:0046547","terms_by_termid":{"GO:0046547":null}}


id: GO:0051592
data:
  {"annotated_genes":["SJAG_01233","SJAG_03631","SJAG_03799","SJAG_02858","SJAG_04454","SJAG_03879"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[115572,100485,114122,97610,112799,109619],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071277"}]},"cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a calcium ion stimulus.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to metal ion","termid":"GO:0010038"}],"gene_count":6,"genes_by_uniquename":{"SJAG_01233":null,"SJAG_02858":null,"SJAG_03631":null,"SJAG_03799":null,"SJAG_03879":null,"SJAG_04454":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to calcium ion","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"response to Ca2+ ion","type":"exact"}],"termid":"GO:0051592","terms_by_termid":{"GO:0071277":null}}


id: MONDO:0024430
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neurological disorder in which a sensory stimulus, usually tactile but more rarely other sensory modalities, is misperceived in a location distant from the original stimulus.","definition_xrefs":["MESH:D066190"],"direct_ancestors":[{"relation_name":"is_a","term_name":"perceptual disorders","termid":"MONDO:0024417"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"allesthesia","secondary_identifiers":["MEDGEN:827104","UMLS:C3850010"],"synonyms":[{"name":"Allachesthesia","type":"related"},{"name":"Allachesthesias","type":"related"},{"name":"Allesthesias","type":"related"},{"name":"Alloesthesia","type":"related"},{"name":"Alloesthesias","type":"related"},{"name":"Dyschirias","type":"related"},{"name":"allochiria","type":"related"},{"name":"dyschiria","type":"related"},{"name":"false allochiria","type":"related"}],"termid":"MONDO:0024430","xrefs":{"Monarch":{"xref_id":"0024430"}}}


id: MONDO:0008966
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cholestasis-lymphedema syndrome is a rare genetic disorder characterized by neonatal intrahepatic cholestasis, often lessening and becoming intermittent with age, and severe chronic lymphedema which mainly affects the lower limbs. Patients often present with fat malabsorption leading to failure to thrive, fat soluble vitamin deficiency with bleeding, rickets, and neuropathy. In 25% of cases, cirrhosis occurs during childhood or later in life.","definition_xrefs":["Orphanet:1414"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"liver disorder","termid":"MONDO:0005154"},{"relation_name":"is_a","term_name":"primary lymphedema","termid":"MONDO:0019175"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0002515","MONDO:0004335"],"is_obsolete":false,"name":"Aagenaes syndrome","secondary_identifiers":["NCIT:C35709","DOID:6691","ICD10CM:Q82.0","MESH:C535330","GARD:370","ICD9:576.8","MEDGEN:78658","SCTID:28724005","UMLS:C0268314","OMIM:214900"],"synonyms":[{"name":"Aagenaes syndrome","type":"exact"},{"name":"Chls","type":"related"},{"name":"LCS","type":"related"},{"name":"LCS1","type":"related"},{"name":"cholestasis lymphedema syndrome","type":"related"},{"name":"cholestasis-edema syndrome, Norwegian type","type":"exact"},{"name":"cholestasis-lymphedema syndrome","type":"related"},{"name":"lymphedema cholestasis syndrome","type":"related"},{"name":"lymphedema-cholestasis syndrome","type":"related"}],"termid":"MONDO:0008966","xrefs":{"Monarch":{"xref_id":"0008966"}}}


id: MONDO:0012462
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"brain disorder","termid":"MONDO:0005560"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autosomal recessive frontotemporal pachygyria","secondary_identifiers":["OMIM:610279","MESH:C538092","Orphanet:329329","MEDGEN:343995","GARD:21489","UMLS:C1853215"],"synonyms":[{"name":"pachygyria, frontotemporal","type":"related"}],"termid":"MONDO:0012462","xrefs":{"Monarch":{"xref_id":"0012462"}}}


id: GO:0008143
data:
  {"annotated_genes":["SJAG_03747","SJAG_03214","SJAG_03448","SJAG_01650","SJAG_01910","SJAG_04427","SJAG_04601","SJAG_02808","SJAG_04271","SJAG_03283","SJAG_01222","SJAG_00425"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[72514,74188,88597,88961,89000,91442,96616,97045,98019,103786,107189,108665],"is_not":false,"summary":null,"term":"GO:0008143"}]},"cv_name":"molecular_function","definition":"Binding to a sequence of adenylyl residues in an RNA molecule, such as the poly(A) tail, a sequence of adenylyl residues at the 3' end of eukaryotic mRNA.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"poly-purine tract binding","termid":"GO:0070717"}],"gene_count":12,"genes_by_uniquename":{"SJAG_00425":null,"SJAG_01222":null,"SJAG_01650":null,"SJAG_01910":null,"SJAG_02808":null,"SJAG_03214":null,"SJAG_03283":null,"SJAG_03448":null,"SJAG_03747":null,"SJAG_04271":null,"SJAG_04427":null,"SJAG_04601":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003723"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0003723"],"is_obsolete":false,"name":"poly(A) binding","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"poly(A) binding, within an RNA molecule","type":"exact"},{"name":"poly(rA) binding","type":"exact"},{"name":"poly-A binding","type":"exact"},{"name":"polyadenylate binding","type":"exact"}],"termid":"GO:0008143","terms_by_termid":{"GO:0008143":null}}


id: PBO:0038976
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADPGK antisense RNA 1","termid":"PBO:0038976"}


id: GO:1903938
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an acrylamide stimulus.","definition_xrefs":["GOC:TermGenie","PMID:16292499","GO_REF:0000071"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to nitrogen compound","termid":"GO:1901699"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"},{"relation_name":"is_a","term_name":"response to acrylamide","termid":"GO:1903937"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to acrylamide","termid":"GO:1903938"}


id: MONDO:0004442
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare malignant germ cell tumor that arises from the testis and is characterized by the presence of embryoid bodies.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malignant testicular germ cell tumor","termid":"MONDO:0003510"},{"relation_name":"is_a","term_name":"polyembryoma","termid":"MONDO:0015863"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"testis polyembryoma","secondary_identifiers":["MEDGEN:271324","DOID:8042","UMLS:C1514200","NCIT:C40962"],"synonyms":[{"name":"polyembryoma of testis","type":"exact"},{"name":"polyembryoma of the testis","type":"exact"},{"name":"testicular polyembryoma","type":"exact"}],"termid":"MONDO:0004442","xrefs":{"Monarch":{"xref_id":"0004442"}}}


id: PBO:0079622
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin conjugating enzyme E2 M","termid":"PBO:0079622"}


id: GO:0019836
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cytolytic destruction of red blood cells, with the release of intracellular hemoglobin, in the host organism by a symbiont. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:add","UniProtKB-KW:KW-0354"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated cytolysis of host cell","termid":"GO:0001897"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"hemolysis by symbiont of host erythrocytes","synonyms":[{"name":"haemolysis in host","type":"exact"},{"name":"hemolysin activity","type":"related"},{"name":"hemolysis by symbiont of host RBCs","type":"exact"},{"name":"hemolysis by symbiont of host red blood cells","type":"exact"},{"name":"pathogenesis","type":"related"},{"name":"regulation of cytolysis of host cells by symbiont","type":"exact"}],"termid":"GO:0019836"}


id: GO:0075733
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a virus, or part of a virus, within the host cell.","definition_xrefs":["GOC:bf","GOC:jl","PMID:11733033","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biological process involved in symbiotic interaction","termid":"GO:0044403"},{"relation_name":"is_a","term_name":"transport of virus","termid":"GO:0046794"},{"relation_name":"part_of","term_name":"viral life cycle","termid":"GO:0019058"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"intracellular transport of virus","secondary_identifiers":["GO:0046788","GO:0046795","Reactome:R-HSA-168271","Reactome:R-HSA-168274","Reactome:R-HSA-174490","GO:0046796"],"synonyms":[{"name":"egress of virus within host cell","type":"exact"},{"name":"intracellular transport of viral material","type":"exact"},{"name":"intracellular virion transport","type":"related"},{"name":"movement of virus within host cell","type":"exact"},{"name":"viral egress","type":"related"},{"name":"viral genome transport in host cell","type":"exact"}],"termid":"GO:0075733"}


id: MONDO:0004553
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete extrinsic allergic alveolitis (obsolete MONDO:0004553)","termid":"MONDO:0004553","xrefs":{"Monarch":{"xref_id":"0004553"}}}


id: GO:1902508
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex which is capable of 2-iminoacetate synthase activity.","definition_xrefs":["GOC:bhm","PMID:12650933","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catalytic complex","termid":"GO:1902494"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"2-iminoacetate synthase complex","synonyms":[{"name":"ThiH-ThiG complex","type":"narrow"}],"termid":"GO:1902508"}


id: PBO:0055224
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long intergenic non-protein coding RNA 2650","termid":"PBO:0055224"}


id: PBO:0051946
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ITPK1 pseudogene 1","termid":"PBO:0051946"}


id: PBO:0068050
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 355","termid":"PBO:0068050"}


id: PBO:0066977
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 280","termid":"PBO:0066977"}


id: GO:0042429
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of serotonin (5-hydroxytryptamine), a monoamine neurotransmitter occurring in the peripheral and central nervous systems, also having hormonal properties.","definition_xrefs":["ISBN:0198506732","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenol-containing compound catabolic process","termid":"GO:0019336"},{"relation_name":"is_a","term_name":"serotonin metabolic process","termid":"GO:0042428"},{"relation_name":"is_a","term_name":"indole-containing compound catabolic process","termid":"GO:0042436"},{"relation_name":"is_a","term_name":"primary amino compound catabolic process","termid":"GO:1901161"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"serotonin catabolic process","secondary_identifiers":["Reactome:R-HSA-380612"],"synonyms":[{"name":"serotonin breakdown","type":"exact"},{"name":"serotonin catabolism","type":"exact"},{"name":"serotonin degradation","type":"exact"}],"termid":"GO:0042429"}


id: PBO:0031533
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_peptide-N4-(N-acetyl-beta-glucosaminyl)asparagine_amidase_activity","termid":"PBO:0031533"}


id: GO:0106004
data:
  {"annotated_genes":["SJAG_04680","SJAG_04848"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[115157,118422],"is_not":false,"summary":null,"term":"GO:0106004"}]},"cv_name":"biological_process","definition":"The process whereby a guanine in a tRNA is methylated at the N7 position of guanine.","definition_xrefs":["GOC:hjd","PMID:17382321"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA methylation","termid":"GO:0030488"},{"relation_name":"is_a","term_name":"RNA (guanine-N7)-methylation","termid":"GO:0036265"}],"gene_count":2,"genes_by_uniquename":{"SJAG_04680":null,"SJAG_04848":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0006399"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0006399"],"is_obsolete":false,"name":"tRNA (guanine-N7)-methylation","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0106004","terms_by_termid":{"GO:0106004":null}}


id: PBO:0070779
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L12 pseudogene 9","termid":"PBO:0070779"}


id: PBO:0002429
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hydantoin racemase family (predicted)","termid":"PBO:0002429"}


id: PBO:0111792
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AAA family ATPase","termid":"PBO:0111792"}


id: PBO:0012233
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pombe AP-1-like gene","termid":"PBO:0012233"}


id: GO:0018465
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: O2 + vanillyl alcohol = H2O2 + vanillin.","definition_xrefs":["RHEA:10036","EC:1.1.3.38"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, oxygen as acceptor","termid":"GO:0016899"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"vanillyl-alcohol oxidase activity","secondary_identifiers":["KEGG_REACTION:R02877","MetaCyc:1.1.3.38-RXN","UM-BBD_reactionID:r0651"],"synonyms":[{"name":"4-hydroxy-2-methoxybenzyl alcohol oxidase activity","type":"related"},{"name":"vanillyl alcohol:oxygen oxidoreductase activity","type":"related"}],"termid":"GO:0018465"}


id: PBO:0083045
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Deoxyhypusine hydroxylase; HEAT-repeat containing metalloenzyme that catalyzes hypusine formation; binds to and is required for the modification of Hyp2p (eIF5A); complements S. pombe mmd1 mutants defective in mitochondrial positioning; protein abundance increases in response to DNA replication stress","termid":"PBO:0083045"}


id: GO:0102449
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: kaempferol + S-adenosyl-L-methionine = 3-O-methylkaempferol + H+ + S-adenosyl-L-homocysteine.","definition_xrefs":["RHEA:74743"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methyltransferase activity","termid":"GO:0008168"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016741"}],"interesting_parent_ids":["GO:0016741","GO:0003824","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"kaempferol 3-O-methyltransferase activity","secondary_identifiers":["MetaCyc:RXN-13935"],"termid":"GO:0102449"}


id: GO:0062059
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a FACT complex.","definition_xrefs":["PMID:10682845"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex binding","termid":"GO:0044877"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"FACT complex binding","termid":"GO:0062059"}


id: FYPO:0007579
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A localization phenotype observed in the vegetative growth phase of the life cycle in which the distribution of sterols in the medial membrane band is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah","PMID:15517003","GO:0032178"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal plasma membrane sterol distribution","termid":"FYPO:0004963"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257","FYPO:0001312","FYPO:0001320","FYPO:0000138"],"is_obsolete":false,"name":"normal medial membrane band sterol distribution","synonyms":[{"name":"normal medial membrane band sterol distribution during mitotic cell cycle","type":"related"},{"name":"normal medial membrane band sterol distribution during vegetative growth","type":"exact"},{"name":"normal medial membrane domain sterol distribution","type":"exact"}],"termid":"FYPO:0007579"}


id: MOD:00160
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-asparagine residue to an N4-glycosyl-L-asparagine.","definition_xrefs":["PubMed:1694179","PubMed:5490222","PubMed:111247","RESID:AA0151#var"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-glycosylated residue","termid":"MOD:00006"},{"relation_name":"is_a","term_name":"modified L-asparagine residue","termid":"MOD:00903"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00764"}],"interesting_parent_ids":["MOD:00764"],"is_obsolete":false,"name":"N4-glycosyl-L-asparagine","synonyms":[{"name":"N4GlycoAsn","type":"exact"}],"termid":"MOD:00160"}


id: PR:O60087
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- meu17 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O60087"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glucoamylase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC14C8.05c","synonyms":[{"name":"1,4-alpha-D-glucan glucohydrolase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-meu17","type":"exact"},{"name":"glucan 1,4-alpha-glucosidase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"meiotic expression up-regulated protein 17 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O60087"}


id: PBO:0077289
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 30C, pseudogene","termid":"PBO:0077289"}


id: GO:0006807
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways involving organic or inorganic compounds that contain nitrogen.","definition_xrefs":["ISBN:0198506732","GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete nitrogen compound metabolic process (obsolete GO:0006807)","termid":"GO:0006807"}


id: GO:0032194
data:
  {"annotated_genes":["SJAG_00933"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[107630],"is_not":false,"summary":null,"term":"GO:0032194"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of ubiquinone, via the intermediates 3,4-dihydroxy-5-polyprenylbenzoate and 3-methoxy-4-hydroxy-5-polyprenylbenzoate.","definition_xrefs":["GOC:mah","PMID:11583838"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ubiquinone biosynthetic process","termid":"GO:0006744"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00933":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006744"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006744","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"ubiquinone biosynthetic process via 3,4-dihydroxy-5-polyprenylbenzoate","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0032194","terms_by_termid":{"GO:0032194":null}}


id: PBO:0003018
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"membrane transporter, pseudogene","termid":"PBO:0003018"}


id: PBO:0048445
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gastrulation brain homeobox 1","termid":"PBO:0048445"}


id: PBO:0069893
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1183, pseudogene","termid":"PBO:0069893"}


id: PBO:0065090
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRKACB divergent transcript","termid":"PBO:0065090"}


id: PBO:0110064
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RQT complex subunit Rqt4","termid":"PBO:0110064"}


id: MONDO:0971056
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"squamous cell neoplasm","termid":"MONDO:0002532"},{"relation_name":"is_a","term_name":"eye neoplasm","termid":"MONDO:0021220"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"ocular surface squamous neoplasia","secondary_identifiers":["Orphanet:659744"],"termid":"MONDO:0971056","xrefs":{"Monarch":{"xref_id":"0971056"}}}


id: PBO:0049150
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutathione peroxidase 7","termid":"PBO:0049150"}


id: PBO:0084761
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial methionyl-tRNA synthetase (MetRS); functions as a monomer in mitochondrial protein synthesis; functions similarly to cytoplasmic MetRS although the cytoplasmic form contains a zinc-binding domain not found in Msm1p","termid":"PBO:0084761"}


id: FYPO:0005528
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the formation of chromatin knobs in subtelomeric regions is decreased. Chromatin knobs are highly condensed chromatin bodies formed from subtelomeric heterochromatin (observed on chromosomes 1 and 2).","definition_xrefs":["PMID:26205977","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal heterochromatin organization during vegetative growth","termid":"FYPO:0004543"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320","FYPO:0005447","FYPO:0000641"],"is_obsolete":false,"name":"decreased subtelomeric chromatin knob formation","synonyms":[{"name":"decreased frequency of knob-containing nuclei","type":"related"},{"name":"decreased subtelomeric chromatin condensation","type":"broad"},{"name":"decreased subtelomeric chromatin knob assembly","type":"exact"},{"name":"reduced subtelomeric chromatin knob formation","type":"exact"}],"termid":"FYPO:0005528"}


id: GO:0039017
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any developmental process that results in the creation of defined areas or spaces within the pronephros to which cells respond and eventually are instructed to differentiate.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pattern specification involved in kidney development","termid":"GO:0061004"},{"relation_name":"part_of","term_name":"pronephros development","termid":"GO:0048793"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"pattern specification involved in pronephros development","synonyms":[{"name":"pattern specification involved in pronephric kidney development","type":"exact"}],"termid":"GO:0039017"}


id: MONDO:0014552
data:
  {"annotated_genes":["SJAG_00773"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84954],"is_not":false,"summary":null,"term":"MONDO:0014552"}]},"cv_name":"mondo","definition":"Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome is a rare, genetic developmental defect during embryogenesis malformation syndrome characterized by intrauterine growth restriction, flexion arthrogryposis of all joints, severe microcephaly, renal cystic dysplasia/agenesis/hypoplasia and complex malformations of the brain (cerebral and cerebellar hypoplasia, vermis, corpus callosum and/or occipital lobe agenesis, with or without arhinencephaly), as well as of the genitourinary tract (ureteral agenesis/hypoplasia, uterine hypoplasia and/or vaginal atresia), leading to fetal demise.","definition_xrefs":["Orphanet:439897"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"arthrogryposis multiplex congenita","termid":"MONDO:0015168"},{"relation_name":"is_a","term_name":"Meckel syndrome","termid":"MONDO:0018921"},{"relation_name":"is_a","term_name":"central nervous system malformation","termid":"MONDO:0020022"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00773":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0020022"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0020022","MONDO:0002320"],"is_obsolete":false,"name":"lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:17743","UMLS:C4015701","MEDGEN:864138","OMIM:616258"],"synonyms":[{"name":"MKS12","type":"related"},{"name":"Meckel syndrome 12","type":"related"},{"name":"Meckel syndrome type 12","type":"exact"}],"termid":"MONDO:0014552","terms_by_termid":{"MONDO:0014552":null},"xrefs":{"Monarch":{"xref_id":"0014552"}}}


id: GO:0103001
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reactions: dimethyl sulfoxide + H+ + NADH + O2 = dimethyl sulfone + H2O + NAD+ and dimethyl sulfide + H+ + NADH + O2 = dimethyl sulfoxide + H2O + NAD+.","definition_xrefs":["EC:1.14.13.245","PMID:9345770"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen","termid":"GO:0016709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"dimethylsulfoxide oxygenase activity","synonyms":[{"name":"assimilatory dimethylsulfide S-monooxygenase activity","type":"exact"}],"termid":"GO:0103001"}


id: MONDO:0008035
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"muscular hypoplasia, congenital universal, of Krabbe","secondary_identifiers":["OMIM:159100","UMLS:C1834651","MEDGEN:320398","MESH:C563553"],"synonyms":[{"name":"muscular hypoplasia, congenital universal, of Krabbe","type":"exact"}],"termid":"MONDO:0008035","xrefs":{"Monarch":{"xref_id":"0008035"}}}


id: GO:0120211
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Fusion of the membrane of proacrosomal vesicle with the membrane of another proacrosomal vesicle to form the acrosome.","definition_xrefs":["GOC:krc","PMID:29991750"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle fusion","termid":"GO:0006906"},{"relation_name":"part_of","term_name":"acrosome assembly","termid":"GO:0001675"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044085","GO:0006810","GO:0016192","GO:0061024","GO:0008150"],"is_obsolete":false,"name":"proacrosomal vesicle fusion","termid":"GO:0120211"}


id: PBO:0075196
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nuclear ribonucleoprotein polypeptide G pseudogene 8","termid":"PBO:0075196"}


id: FYPO:0002469
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cell population phenotype in which a cell undergoes one or a few rounds of cell division before cells die, resulting in the formation a colony that contains only a few inviable cells that are longer than normal and taper at one end to a diameter smaller than the other. Up to 6 rounds of cell division (generating 64 cells) may be observed, but 3 divisions or fewer is more typical.","definition_xrefs":["PomBase:mah","PomBase:vw"],"gene_count":0,"genotype_count":0,"name":"obsolete inviable microcolony, elongated tapered cells (obsolete FYPO:0002469)","synonyms":[{"name":"inviable microcolony, elongated bottle/skittle cells","type":"exact"},{"name":"inviable microcolony, elongated skittle-shaped cells","type":"exact"},{"name":"inviable microcolony, elongated tapered vegetative cells","type":"exact"}],"termid":"FYPO:0002469"}


id: MONDO:0008621
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Uncombable hair syndrome (UHS), or pili trianguli et canaliculi, is a rare scalp hair shaft dysplasia.","definition_xrefs":["Orphanet:1410"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hair anomaly","termid":"MONDO:0019278"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncombable hair syndrome","secondary_identifiers":["MESH:C536939","UMLS:C0432347","SCTID:254230001","MEDGEN:96596","icd11.foundation:244892708","GARD:5404"],"synonyms":[{"name":"cheveux incoiffables","type":"related"},{"name":"pili trianguli et canaliculi","type":"exact"},{"name":"spun glass hair","type":"related"},{"name":"uncombable hair syndrome","type":"exact"},{"name":"unmanageable hair syndrome","type":"related"}],"termid":"MONDO:0008621","xrefs":{"Monarch":{"xref_id":"0008621"}}}


id: PBO:0042111
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CCDC183 antisense RNA 1","termid":"PBO:0042111"}


id: MONDO:0021578
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign or malignant neoplasm that affects the sternum.","definition_xrefs":["NCIT:C6730"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skeletal system disorder","termid":"MONDO:0005172"},{"relation_name":"is_a","term_name":"neoplasm of thorax","termid":"MONDO:0021350"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sternal neoplasm","secondary_identifiers":["UMLS:C1290244","ICD9:239.2","MEDGEN:226935","SCTID:126559003"],"synonyms":[{"name":"neoplasm of sternum","type":"exact"},{"name":"neoplasm of sternum (disease)","type":"exact"},{"name":"neoplasm of sternum (disorder)","type":"exact"},{"name":"neoplasm of the sternum","type":"exact"},{"name":"sternal neoplasm","type":"exact"},{"name":"sternal tumor","type":"exact"},{"name":"sternal tumour","type":"exact"},{"name":"sternum neoplasm","type":"exact"},{"name":"sternum neoplasm (disease)","type":"exact"},{"name":"sternum tumor","type":"exact"},{"name":"sternum tumour","type":"exact"},{"name":"tumor of sternum","type":"exact"},{"name":"tumor of the sternum","type":"exact"},{"name":"tumour of sternum","type":"exact"},{"name":"tumour of the sternum","type":"exact"}],"termid":"MONDO:0021578","xrefs":{"Monarch":{"xref_id":"0021578"}}}


id: MONDO:0006003
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm involving the body of uterus.","direct_ancestors":[{"relation_name":"is_a","term_name":"uterine cancer","termid":"MONDO:0002715"},{"relation_name":"is_a","term_name":"corpus uteri neoplasm","termid":"MONDO:0021254"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"uterine corpus cancer","secondary_identifiers":["ICD9:182","DOID:9460","SCTID:371972005","NCIT:C61574","UMLS:C1883486","MEDGEN:364875","EFO:0007532"],"synonyms":[{"name":"body of uterus cancer","type":"exact"},{"name":"cancer of body of uterus","type":"exact"},{"name":"cancer of the corpus uteri","type":"exact"},{"name":"corpus uteri cancer","type":"exact"},{"name":"endometrial cancer","type":"related"},{"name":"malignant body of uterus neoplasm","type":"exact"},{"name":"malignant neoplasm of body of uterus","type":"exact"},{"name":"uterine (including endometrial) cancer","type":"exact"},{"name":"uterine corpus cancer","type":"exact"}],"termid":"MONDO:0006003","xrefs":{"Monarch":{"xref_id":"0006003"}}}


id: PBO:0089234
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ENTH/VHS domain protein","termid":"PBO:0089234"}


id: GO:0061384
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of shaping a trabecula in the heart. A trabecula is a small, often microscopic, tissue element in the form of a small beam, strut or rod, which generally has a mechanical function. Trabecula are usually but not necessarily, composed of dense collagenous tissue.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"trabecula morphogenesis","termid":"GO:0061383"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"heart trabecula morphogenesis","termid":"GO:0061384"}


id: PBO:0061951
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 2 subfamily A member 3 pseudogene","termid":"PBO:0061951"}


id: PBO:0053380
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long intergenic non-protein coding RNA 307","termid":"PBO:0053380"}


id: PR:Q9P6I8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An uncharacterized zinc-type alcohol dehydrogenase-like protein YbdR that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02347","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc-type alcohol dehydrogenase-like protein C1198.01 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1198.01","secondary_identifiers":["UniProtKB:Q9P6I8"],"synonyms":[{"name":"Spom972h-ybdR","type":"exact"}],"termid":"PR:Q9P6I8"}


id: GO:0001882
data:
  {"annotated_genes":["SJAG_03578","SJAG_04030","SJAG_04410","SJAG_00637"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[115133],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905108"},{"annotations":[97654,112584,93604],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032549"}]},"cv_name":"molecular_function","definition":"Binding to a nucleoside, a compound consisting of a purine or pyrimidine nitrogenous base linked either to ribose or deoxyribose.","definition_xrefs":["GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic cyclic compound binding","termid":"GO:0097159"},{"relation_name":"is_a","term_name":"carbohydrate derivative binding","termid":"GO:0097367"},{"relation_name":"is_a","term_name":"heterocyclic compound binding","termid":"GO:1901363"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00637":null,"SJAG_03578":null,"SJAG_04030":null,"SJAG_04410":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"nucleoside binding","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0001882","terms_by_termid":{"GO:0032549":null,"GO:1905108":null}}


id: MONDO:0040500
data:
  {"annotated_genes":["SJAG_04119"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84613],"is_not":false,"summary":null,"term":"MONDO:0040500"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"inherited lipid metabolism disorder","termid":"MONDO:0002525"},{"relation_name":"is_a","term_name":"congenital disorder of glycosylation","termid":"MONDO:0015286"},{"relation_name":"is_a","term_name":"autosomal recessive non-syndromic intellectual disability","termid":"MONDO:0019502"},{"relation_name":"is_a","term_name":"disorder of GPI anchor biosynthesis","termid":"MONDO:0024321"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04119":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0002525"}],"interesting_parent_ids":["MONDO:0024322","MONDO:0005066","MONDO:0006025","MONDO:0002525","MONDO:0002320","MONDO:0037792"],"is_obsolete":false,"name":"glycosylphosphatidylinositol biosynthesis defect 16","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1628197","UMLS:C4540521","OMIM:617816","DOID:0081223","GARD:22577"],"synonyms":[{"name":"GPIBD16","type":"related"},{"name":"glycosylphosphatidylinositol biosynthesis defect 16","type":"exact"},{"name":"intellectual disability, autosomal recessive 62","type":"related"},{"name":"mental retardation, autosomal recessive 62","type":"related"}],"termid":"MONDO:0040500","terms_by_termid":{"MONDO:0040500":null},"xrefs":{"Monarch":{"xref_id":"0040500"}}}


id: PBO:0028269
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_cellular_nitric_oxide_level_during_cellular_response_to_cadmium_ion","termid":"PBO:0028269"}


id: FYPO:0004761
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which histone exchange occurs to a greater extent than normal in regions of pericentric heterochromatin. Histone exchange is replacement, within chromatin, of resident histones or histone subunits with alternative, sometimes variant, histones or subunits.","definition_xrefs":["GO:0005721","PMID:24095277","GO:0043486","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal chromatin remodeling","termid":"FYPO:0006356"},{"relation_name":"is_a","term_name":"increased protein exchange at pericentric heterochromatin","termid":"FYPO:0006360"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000138","FYPO:0000002","FYPO:0001985","FYPO:0000641","FYPO:0001320"],"is_obsolete":false,"name":"increased histone exchange at pericentric heterochromatin","synonyms":[{"name":"increased histone exchange at dh repeat","type":"narrow"},{"name":"increased histone exchange at pericentric heterochromatin during mitotic cell cycle","type":"related"},{"name":"increased histone exchange at pericentric heterochromatin during vegetative growth","type":"exact"}],"termid":"FYPO:0004761"}


id: MONDO:0012162
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any patterned macular dystrophy in which the cause of the disease is a mutation in the CTNNA1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"patterned macular dystrophy","termid":"MONDO:0020381"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"patterned macular dystrophy 2","secondary_identifiers":["MEDGEN:332348","GARD:18238","DOID:0060864","OMIM:608970","UMLS:C1837029"],"synonyms":[{"name":"CTNNA1 patterned macular dystrophy","type":"exact"},{"name":"MDPT2","type":"exact"},{"name":"butterfly-shaped pigmentary maculary dystrophy 2","type":"exact"},{"name":"macular dystrophy, butterfly-Shaped pigmentary, 2","type":"related"},{"name":"macular dystrophy, patterned, 2","type":"related"},{"name":"macular dystrophy, patterned, type 2","type":"exact"},{"name":"patterned macular dystrophy caused by mutation in CTNNA1","type":"exact"},{"name":"patterned macular dystrophy type 2","type":"exact"}],"termid":"MONDO:0012162","xrefs":{"Monarch":{"xref_id":"0012162"}}}


id: PBO:0002338
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA-binding protein Rsd1 (predicted)","termid":"PBO:0002338"}


id: PBO:0043454
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calponin 3 pseudogene 1","termid":"PBO:0043454"}


id: MONDO:0010958
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial long QT syndrome","termid":"MONDO:0019171"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"cardiac arrhythmia, ankyrin-B-related","secondary_identifiers":["DOID:0111701","OMIM:600919","UMLS:C1970119","GARD:10432","SCTID:764457005","MEDGEN:370181","DOID:0111700"],"synonyms":[{"name":"LQT4","type":"related"},{"name":"ankyrin-B syndrome","type":"exact"},{"name":"cardiac arrhythmia, ankyrin-b-related","type":"exact"}],"termid":"MONDO:0010958","xrefs":{"Monarch":{"xref_id":"0010958"}}}


id: PBO:0089524
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5'-methylthioribulose-1-phosphate dehydratase, adducin Mta3","termid":"PBO:0089524"}


id: MONDO:0030822
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"renal agenesis","termid":"MONDO:0018470"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"renal hypodysplasia/aplasia 4","secondary_identifiers":["MEDGEN:1808595","UMLS:C5676993","OMIM:619887"],"synonyms":[{"name":"RHDA4","type":"exact"},{"name":"renal hypodysplasia/aplasia 4","type":"exact"}],"termid":"MONDO:0030822","xrefs":{"Monarch":{"xref_id":"0030822"}}}


id: FYPO:0006631
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to chromatin is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to chromatin","termid":"FYPO:0001679"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0001985","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"decreased protein localization to chromatin","synonyms":[{"name":"decreased protein localisation to chromatin","type":"exact"},{"name":"reduced protein localization to chromatin","type":"exact"}],"termid":"FYPO:0006631"}


id: PBO:0074943
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 108","termid":"PBO:0074943"}


id: GO:0160148
data:
  {"annotated_genes":["SJAG_04065"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[101985],"is_not":false,"summary":null,"term":"GO:0160148"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: uridine(55) in tRNA = pseudouridine(55) in tRNA.","definition_xrefs":["EC:5.4.99.25"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA pseudouridine synthase activity","termid":"GO:0106029"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04065":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140101"},{"rel_name":"is_a","termid":"GO:0140098"}],"interesting_parent_ids":["GO:0003824","GO:0016853","GO:0140101","GO:0140098","GO:0003674"],"is_obsolete":false,"name":"tRNA pseudouridine(55) synthase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["RHEA:42532"],"termid":"GO:0160148","terms_by_termid":{"GO:0160148":null}}


id: MONDO:0004473
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm that affects the epiglottis. The vast majority of cases are squamous cell carcinomas.","definition_xrefs":["NCIT:C4836"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epiglottis neoplasm","termid":"MONDO:0004109"},{"relation_name":"is_a","term_name":"carcinoma of supraglottis","termid":"MONDO:0004357"},{"relation_name":"is_a","term_name":"hypopharyngeal carcinoma","termid":"MONDO:0005216"},{"relation_name":"is_a","term_name":"oropharyngeal carcinoma","termid":"MONDO:0044926"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"epiglottis cancer","secondary_identifiers":["ICD9:146.4","ICD10CM:C10.1","UMLS:C1112382","MEDGEN:249035","DOID:8133","NCIT:C35697","SCTID:187681002"],"synonyms":[{"name":"cancer of epiglottis","type":"exact"},{"name":"epiglottic cancer","type":"exact"},{"name":"epiglottic carcinoma","type":"narrow"},{"name":"epiglottic throat cancer","type":"exact"},{"name":"epiglottis cancer","type":"exact"},{"name":"malignant Epiglottis neoplasm","type":"exact"},{"name":"malignant Epiglottis tumor","type":"exact"},{"name":"malignant Epiglottis tumour","type":"exact"},{"name":"malignant epiglottic neoplasm","type":"exact"},{"name":"malignant epiglottic tumor","type":"exact"},{"name":"malignant epiglottic tumour","type":"exact"},{"name":"malignant epiglottis neoplasm","type":"exact"},{"name":"malignant neoplasm of Epiglottis","type":"exact"},{"name":"malignant neoplasm of anterior aspect of epiglottis","type":"narrow"},{"name":"malignant neoplasm of anterior epiglottis","type":"exact"},{"name":"malignant neoplasm of anterior surface of epiglottis","type":"narrow"},{"name":"malignant neoplasm of epiglottis","type":"exact"},{"name":"malignant neoplasm of the Epiglottis","type":"exact"},{"name":"malignant tumor of Epiglottis","type":"exact"},{"name":"malignant tumor of the Epiglottis","type":"exact"},{"name":"malignant tumour of Epiglottis","type":"exact"},{"name":"malignant tumour of the Epiglottis","type":"exact"}],"termid":"MONDO:0004473","xrefs":{"Monarch":{"xref_id":"0004473"}}}


id: PBO:0052371
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kinesin family member 18B","termid":"PBO:0052371"}


id: MONDO:0035133
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome","secondary_identifiers":["GARD:22367","MEDGEN:1641154","Orphanet:589905","OMIM:617991","UMLS:C4693860"],"synonyms":[{"name":"Chung-Jansen syndrome","type":"exact"},{"name":"DIDOD","type":"related"},{"name":"developmental delay, intellectual disability, obesity, and dysmorphic features","type":"exact"}],"termid":"MONDO:0035133","xrefs":{"Monarch":{"xref_id":"0035133"}}}


id: PBO:0049709
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hyaluronan synthase 3","termid":"PBO:0049709"}


id: MONDO:0035684
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete epidermolysis bullosa simplex without extracutaneous involvement (obsolete MONDO:0035684)","secondary_identifiers":["Orphanet:595346"],"synonyms":[{"name":"EBS without extracutaneous involvement","type":"exact"}],"termid":"MONDO:0035684","xrefs":{"Monarch":{"xref_id":"0035684"}}}


id: PBO:0077748
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"toll interacting protein","termid":"PBO:0077748"}


id: MONDO:0012562
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any holoprosencephaly in which the cause of the disease is a mutation in the PTCH1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"holoprosencephaly","termid":"MONDO:0016296"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"holoprosencephaly 7","secondary_identifiers":["MESH:C563660","MEDGEN:372134","UMLS:C1835820","DOID:0110876","OMIM:610828"],"synonyms":[{"name":"HPE7","type":"exact"},{"name":"PTCH1 holoprosencephaly","type":"exact"},{"name":"holoprosencephaly 7","type":"exact"},{"name":"holoprosencephaly caused by mutation in PTCH1","type":"exact"},{"name":"holoprosencephaly type 7","type":"exact"}],"termid":"MONDO:0012562","xrefs":{"Monarch":{"xref_id":"0012562"}}}


id: PBO:0041139
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"basic transcription factor 3","termid":"PBO:0041139"}


id: MONDO:0005983
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A severe, chronic fungal skin infection, usually of the scalp, characterized by the development of thick, yellow cup-shaped crusts and scarring over hair follicles.","definition_xrefs":["NCIT:C35072"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tinea infection","termid":"MONDO:0005982"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"tinea favosa","secondary_identifiers":["MESH:D014007","UMLS:C0040254","MEDGEN:52758","SCTID:85375000","ICD10CM:B35","DOID:4336"],"synonyms":[{"name":"favus","type":"exact"}],"termid":"MONDO:0005983","xrefs":{"Monarch":{"xref_id":"0005983"}}}


id: GO:0042983
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of amyloid precursor protein (APP), the precursor of amyloid-beta, a glycoprotein associated with Alzheimer's disease.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"macromolecule biosynthetic process","termid":"GO:0009059"},{"relation_name":"is_a","term_name":"amyloid precursor protein metabolic process","termid":"GO:0042982"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"amyloid precursor protein biosynthetic process","synonyms":[{"name":"APP biosynthesis","type":"exact"},{"name":"APP biosynthetic process","type":"exact"},{"name":"amyloid precursor protein anabolism","type":"exact"},{"name":"amyloid precursor protein biosynthesis","type":"exact"},{"name":"amyloid precursor protein formation","type":"exact"},{"name":"amyloid precursor protein synthesis","type":"exact"}],"termid":"GO:0042983"}


id: GO:1990500
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that causes translational repression in Drosophila. Prevents assembly of ribosomes at the mRNA by interfacing with a sequence-specific RNA-binding protein leading to recruitment of the CCR4 complex and consequently, reduction of the mRNA's poly(A) tail length. The complex is also required for dorso-ventral pattern formation in the embryo.","definition_xrefs":["GOC:bhm","PMID:14723848"],"direct_ancestors":[{"relation_name":"is_a","term_name":"translation repressor complex","termid":"GO:1903502"},{"relation_name":"part_of","term_name":"P-body","termid":"GO:0000932"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0000932"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0000932","GO:0032991","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"eif4e-cup complex","synonyms":[{"name":"eukaryotic translation initiation factor 4E-cup complex","type":"exact"}],"termid":"GO:1990500"}


id: GO:0016993
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: precorrin-8X = hydrogenobyrinate.","definition_xrefs":["EC:5.4.99.61"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular acyltransferase activity","termid":"GO:0016867"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016853"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016853"],"is_obsolete":false,"name":"precorrin-8X methylmutase activity","secondary_identifiers":["RHEA:22512","MetaCyc:5.4.1.2-RXN"],"synonyms":[{"name":"HBA synthase activity","type":"related"},{"name":"hydrogenobyrinic acid-binding protein activity","type":"narrow"},{"name":"precorrin isomerase activity","type":"related"},{"name":"precorrin-8X 11,12-methylmutase activity","type":"exact"}],"termid":"GO:0016993"}


id: PR:O74418
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC162.01c gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74418"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U4/U6.U5 tri-snRNP-associated protein 3-like protein C162.01c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC162.01c","synonyms":[{"name":"Spom972h-SPCC162.01c","type":"exact"}],"termid":"PR:O74418"}


id: GO:0102856
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 1-18:2-2-18:2-sn-glycerol-3-phosphocholine + O2 + a reduced electron acceptor = 1-18:3-2-18:2-phosphatidylcholine + 2 H2O + an oxidized electron acceptor.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 1-18:2-2-18:2-sn-glycerol-3-phosphocholine desaturase activity (obsolete GO:0102856)","termid":"GO:0102856"}


id: GO:0072155
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The orderly movement of epithelial cells within a renal tubule that contributes to nephron tubule morphogenesis.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial cell migration","termid":"GO:0010631"},{"relation_name":"is_a","term_name":"cell migration involved in kidney development","termid":"GO:0035787"},{"relation_name":"part_of","term_name":"nephron tubule morphogenesis","termid":"GO:0072078"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"epithelial cell migration involved in nephron tubule morphogenesis","termid":"GO:0072155"}


id: PBO:0045044
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dickkopf WNT signaling pathway inhibitor 4","termid":"PBO:0045044"}


id: MOD:00199
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-isoleucine residue to a D-allo-isoleucine.","definition_xrefs":["PubMed:8223491","RESID:AA0192","ChEBI:30007"],"direct_ancestors":[{"relation_name":"is_a","term_name":"residues isobaric at 113.084064 Da","termid":"MOD:00306"},{"relation_name":"is_a","term_name":"stereoisomerized residue","termid":"MOD:00664"},{"relation_name":"is_a","term_name":"modified L-isoleucine residue","termid":"MOD:00910"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"D-allo-isoleucine","synonyms":[{"name":"(2R,3S)-2-amino-3-methylpentanoic acid","type":"exact"},{"name":"2-azanyl-3-methylpentanoic acid","type":"exact"},{"name":"3-methyl-norvaline","type":"exact"},{"name":"D-Ile","type":"exact"},{"name":"D-allo-isoleucine","type":"exact"},{"name":"D-threo-isoleucine","type":"exact"},{"name":"MOD_RES D-allo-isoleucine","type":"exact"},{"name":"allo-D-isoleucine","type":"exact"},{"name":"alpha-amino-beta-methylvaleric acid","type":"exact"}],"termid":"MOD:00199"}


id: PBO:0028336
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_histone_H4-K5,_H4-K8,_H4-K12_and_H4-K16_acetylation_at_centromere_central_core","termid":"PBO:0028336"}


id: RO:0002518
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"x has end sequence y if the end of x is identical to the end of y, and x has y as a subsequence","direct_ancestors":[{"relation_name":"is_a","term_name":"has_subsequence","termid":"RO:0002524"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_end_sequence","termid":"RO:0002518"}


id: PBO:0028909
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_heterochromatin_organization_during_vegetative_growth","termid":"PBO:0028909"}


id: PBO:0086372
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative aryl-alcohol dehydrogenase; involved in oxidative stress response; similar to P. chrysosporium aryl-alcohol dehydrogenase; expression induced in cells treated with the mycotoxin patulin; members of the AAD gene family comprise three pairs (AAD3 + AAD15, AAD6/AAD16 + AAD4, AAD10 + AAD14) whose two genes are more related to one another than to other members of the family","termid":"PBO:0086372"}


id: GO:0043769
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A complex composed of four polypeptides, a telomere-protecting terminal protein (Tpg), a telomere-associated protein (Tap), DNA polymerase (PolA) and topoisomerase I (TopA), that functions in the replication of the telomeric regions of linear chromosomes, plasmids and circular replicons of some bacterial species.","definition_xrefs":["PMID:15353591"],"direct_ancestors":[{"relation_name":"is_a","term_name":"telomere cap complex","termid":"GO:0000782"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005694"}],"interesting_parent_ids":["GO:0005575","GO:0005694","GO:0032991"],"is_obsolete":false,"name":"Tpg-containing telomere binding complex","synonyms":[{"name":"telomere complex","type":"broad"}],"termid":"GO:0043769"}


id: GO:0072552
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: monoferuloyl di-(hydroxyferuloyl) spermidine + NADPH + O2 = tri-(hydroxyferuloyl) spermidine + NADP+ + H2O.","definition_xrefs":["PMID:19779199","GOC:kad"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tri-(feruloyl or hydroxyferuloyl) spermidine meta-hydroxylase activity","termid":"GO:0072532"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"monoferuloyl di-(hydroxyferuloyl) spermidine meta-hydroxylase activity","termid":"GO:0072552"}


id: MOD:01317
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Chemical derivative -","definition_xrefs":["Unimod:178#T","PubMed:12216740"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphorylation to amine thiol","termid":"MOD:00535"},{"relation_name":"is_a","term_name":"modified L-threonine residue","termid":"MOD:00917"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphorylation to amine thiol - site T","synonyms":[{"name":"DAET","type":"related"},{"name":"phosphorylation to amine thiol","type":"related"}],"termid":"MOD:01317"}


id: MOD:01589
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-serine residue to O-(2,4-diacetamido-2,4-dideoxyglucosyl)-L-serine.","definition_xrefs":["PubMed:16949362","RESID:AA0499","PubMed:15249686"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-glycosyl-L-serine","termid":"MOD:00002"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00764"}],"interesting_parent_ids":["MOD:00764"],"is_obsolete":false,"name":"O-(2,4-diacetamido-2,4-dideoxyglucosyl)-L-serine","synonyms":[{"name":"(2S)-2-amino-3-[(2,4-diacetamido-2,4-dideoxy-beta-D-glucopyranosyl)oxy]propanoic acid","type":"exact"},{"name":"CARBOHYD O-linked (DADDGlc) serine","type":"exact"},{"name":"DADDGlc","type":"exact"},{"name":"O-(2,4-diacetamido-2,4-dideoxy-D-glucosyl)-L-serine","type":"exact"},{"name":"O-(2,4-diacetamido-2,4-dideoxy-beta-D-glucopyranosyl)-L-serine","type":"exact"},{"name":"O-[2,4-bis(acetylamino)]glucosyl-L-serine","type":"exact"},{"name":"O-seryl-beta-2,4-bis(acetylamino)glucoside","type":"exact"},{"name":"O3-(2,4-diacetamido-2,4-dideoxy-beta-D-glucopyranosyl)-L-serine","type":"exact"}],"termid":"MOD:01589"}


id: PBO:0089830
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat/BOP1NT protein Erb1","termid":"PBO:0089830"}


id: MONDO:0018573
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"diabetes mellitus","termid":"MONDO:0005015"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intrauterine growth restriction-short stature-early adult-onset diabetes syndrome","secondary_identifiers":["GARD:21818","UMLS:C5681180","Orphanet:436144","MEDGEN:1801791"],"termid":"MONDO:0018573","xrefs":{"Monarch":{"xref_id":"0018573"}}}


id: MONDO:0007026
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete non-alcoholic fatty liver (obsolete MONDO:0007026)","termid":"MONDO:0007026","xrefs":{"Monarch":{"xref_id":"0007026"}}}


id: GO:0050288
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-sorbose + A = 5-dehydro-D-fructose + AH(2).","definition_xrefs":["EC:1.1.99.12","RHEA:14713"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on CH-OH group of donors","termid":"GO:0016614"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"sorbose dehydrogenase activity","secondary_identifiers":["MetaCyc:SORBOSE-DEHYDROGENASE-RXN","KEGG_REACTION:R01696"],"synonyms":[{"name":"L-sorbose:(acceptor) 5-oxidoreductase activity","type":"related"},{"name":"L-sorbose:acceptor 5-oxidoreductase activity","type":"related"}],"termid":"GO:0050288"}


id: PBO:0050246
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group nucleosomal binding domain 2 pseudogene 24","termid":"PBO:0050246"}


id: GO:0017182
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways involving peptidyl-diphthamide, a modified histidine residue.","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-diphthamide metabolic process (obsolete GO:0017182)","synonyms":[{"name":"peptidyl-diphthamide metabolism","type":"exact"}],"termid":"GO:0017182"}


id: PBO:0003381
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cortical anchoring factor for dynein Mcp5/Num1","termid":"PBO:0003381"}


id: GO:0051435
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a BH4 protein domain, present in Bcl-2 family members. All anti-apoptotic proteins contain BH1 and BH2 domains; some also contain an additional N-terminal BH4 domain, which is almost never seen in pro-apoptotic proteins. Loss of the BH4 domain can diminish or abrogate anti-apoptotic function or even impart outright death-promoting properties to the protein.","definition_xrefs":["InterPro:IPR003093","PMID:11048732","PMID:9704409","PMID:9020082","Prosite:PS01260","Prosite:PS50063","PMID:12133724"],"direct_ancestors":[{"relation_name":"is_a","term_name":"BH domain binding","termid":"GO:0051400"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005515","GO:0005488"],"is_obsolete":false,"name":"BH4 domain binding","termid":"GO:0051435"}


id: GO:0016087
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"The action characteristic of ecdysiostatic hormone, a peptide hormone that inhibits ecdysone secretion.","definition_xrefs":["GOC:mah","DOI:10.1002/(SICI)1520-6327(1997)35:1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuropeptide hormone activity","termid":"GO:0005184"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0140677"}],"interesting_parent_ids":["GO:0098772","GO:0005515","GO:0003674","GO:0140677","GO:0005488"],"is_obsolete":false,"name":"ecdysiostatic hormone activity","termid":"GO:0016087"}


id: PBO:0049991
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histidine triad nucleotide binding protein 3","termid":"PBO:0049991"}


id: PBO:0058226
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4516","termid":"PBO:0058226"}


id: GO:1901325
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an antimycin A stimulus.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to organic cyclic compound","termid":"GO:0014070"},{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"},{"relation_name":"is_a","term_name":"response to oxygen-containing compound","termid":"GO:1901700"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to antimycin A","termid":"GO:1901325"}


id: GO:0032327
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of the W-molybdopterin cofactor, essential for the catalytic activity of some enzymes. The cofactor consists of a mononuclear tungsten ion (W) coordinated by one or two molybdopterin ligands.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"molybdopterin cofactor catabolic process","termid":"GO:0032325"},{"relation_name":"is_a","term_name":"W-molybdopterin cofactor metabolic process","termid":"GO:0042046"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"W-molybdopterin cofactor catabolic process","synonyms":[{"name":"Moco catabolic process","type":"broad"},{"name":"Moco catabolism","type":"broad"},{"name":"W-molybdopterin cofactor breakdown","type":"exact"},{"name":"W-molybdopterin cofactor catabolism","type":"exact"},{"name":"W-molybdopterin cofactor degradation","type":"exact"}],"termid":"GO:0032327"}


id: PBO:0083419
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the uncharacterized gene YFR055W","termid":"PBO:0083419"}


id: PR:O74764
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An ATP-dependent RNA helicase DDX55 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03226","PANTHER:PTHR24031:SF26","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP-dependent rRNA helicase spb4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC24C6.02","secondary_identifiers":["UniProtKB:O74764"],"synonyms":[{"name":"Spom972h-DDX55","type":"exact"}],"termid":"PR:O74764"}


id: MONDO:0012168
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"excluded_subClassOf","term_name":"dyslexia","termid":"MONDO:0005489"},{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dyslexia, susceptibility to, 8","secondary_identifiers":["OMIM:608995","MEDGEN:332344","UMLS:C1837009"],"synonyms":[{"name":"DYX8","type":"exact"},{"name":"dyslexia, susceptibility to, 8","type":"exact"},{"name":"dyslexia, susceptibility to, 8, multifactorial","type":"exact"}],"termid":"MONDO:0012168","xrefs":{"Monarch":{"xref_id":"0012168"}}}


id: PBO:0091547
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae SPT15","termid":"PBO:0091547"}


id: GO:0044679
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex which catalyzes the conversion of methanophenazine and hydrogen to form dihydromethanophenazine. This typically consists of three polypeptides.","definition_xrefs":["PMID:9555882","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase complex","termid":"GO:1990204"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"methanophenazine reducing hydrogenase complex","termid":"GO:0044679"}


id: PBO:0050706
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HSPB2-C11orf52 readthrough (NMD candidate)","termid":"PBO:0050706"}


id: GO:0060697
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency, or extent of phospholipid catabolism, the chemical reactions and pathways resulting in the breakdown of phospholipids, any lipid containing phosphoric acid as a mono- or diester.","definition_xrefs":["GOC:tb","GOC:BHF","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of lipid catabolic process","termid":"GO:0050996"},{"relation_name":"is_a","term_name":"regulation of phospholipid catabolic process","termid":"GO:0060696"},{"relation_name":"is_a","term_name":"positive regulation of phospholipid metabolic process","termid":"GO:1903727"},{"relation_name":"positively_regulates","term_name":"phospholipid catabolic process","termid":"GO:0009395"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"positive regulation of phospholipid catabolic process","termid":"GO:0060697"}


id: MONDO:0017601
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Diffuse large B-cell lymphoma with chronic inflammation is an Epstein-Barr virus-associated malignant lymphoproliferative disorder, developing in a context of long-standing or slow-growing, chronically inflamed lesions, such as chronic pyothorax, metallic implants in bones and joints, chronic osteomyelitis, chronic venous ulcer, or, rarely granulomatous inflammation. The tumor is usually primarily localized, with no involvement of other organs.","definition_xrefs":["Orphanet:300888"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Epstein-Barr virus-associated malignant lymphoproliferative disorder","termid":"MONDO:0017343"},{"relation_name":"is_a","term_name":"diffuse large B-cell lymphoma","termid":"MONDO:0018905"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"diffuse large B-cell lymphoma with chronic inflammation","secondary_identifiers":["GARD:21250","MEDGEN:1374328","UMLS:C4511460"],"synonyms":[{"name":"DLBCL with chronic inflammation","type":"exact"}],"termid":"MONDO:0017601","xrefs":{"Monarch":{"xref_id":"0017601"}}}


id: FYPO:0000814
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which nucleolus organization is abnormal. Nucleolus organization results in the assembly, arrangement of constituent parts, or disassembly of the nucleolus.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal nucleus organization","termid":"FYPO:0000810"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"abnormal nucleolus organization","synonyms":[{"name":"abnormal nucleolus organisation","type":"exact"},{"name":"abnormal nucleolus organization during mitotic cell cycle","type":"related"},{"name":"abnormal nucleolus organization during vegetative growth","type":"exact"}],"termid":"FYPO:0000814"}


id: PBO:0113208
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial HMG-box protein; limits the copy number of mitochondrial DNA (mtDNA), antagonizing HMG-box containing protein Abf2p, a mtDNA packaging factor; localizes to the mitochondrial matrix; contains two HMG-boxes similar to Abf2p; null mutant is viable","termid":"PBO:0113208"}


id: GO:2000431
data:
  {"annotated_genes":["SJAG_02795","SJAG_02592","SJAG_04597","SJAG_01805","SJAG_03048","SJAG_00082"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[97783],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000432"},{"annotations":[101856],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903500"},{"annotations":[93917,89508],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903501"},{"annotations":[118919,93883,93311],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903499"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cytokinesis, actomyosin contractile ring assembly.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytokinetic process","termid":"GO:0032954"},{"relation_name":"is_a","term_name":"regulation of cellular component biogenesis","termid":"GO:0044087"},{"relation_name":"is_a","term_name":"regulation of actomyosin structure organization","termid":"GO:0110020"},{"relation_name":"regulates","term_name":"actomyosin contractile ring assembly","termid":"GO:0000915"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00082":null,"SJAG_01805":null,"SJAG_02592":null,"SJAG_02795":null,"SJAG_03048":null,"SJAG_04597":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0030036"},{"rel_name":"regulates","termid":"GO:0007010"},{"rel_name":"regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0044085","GO:0007010","GO:0030036","GO:0007049","GO:0008150"],"is_obsolete":false,"name":"regulation of cytokinesis, actomyosin contractile ring assembly","references_by_uniquename":{"GO_REF:0000107":null,"PMID:32915139":null},"synonyms":[{"name":"regulation of contractile ring assembly","type":"exact"}],"termid":"GO:2000431","terms_by_termid":{"GO:0120306":null,"GO:1903499":null,"GO:1903500":null,"GO:1903501":null,"GO:2000432":null}}


id: PBO:0040385
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPase H+ transporting V1 subunit A","termid":"PBO:0040385"}


id: PBO:0108763
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"4-phosphoerythronate phosphatase/2-phosphoglycolate phophatase, involved in detoxification of glycolytic by-products","termid":"PBO:0108763"}


id: GO:0052154
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont alters or subverts the B-cell mediated immune response of the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host immune response","termid":"GO:0052553"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated perturbation of host B-cell mediated immune response","secondary_identifiers":["GO:0052293"],"synonyms":[{"name":"modulation by organism of B-cell mediated immune response of other organism involved in symbiotic interaction","type":"broad"},{"name":"modulation by symbiont of host B-cell mediated immune response","type":"exact"},{"name":"perturbation of host B-cell mediated immune response","type":"exact"},{"name":"regulation by organism of host B-cell mediated immune response","type":"exact"},{"name":"symbiont-mediated perturbation of host humoral immune response","type":"exact"}],"termid":"GO:0052154"}


id: GO:0016457
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The aggregation, arrangement and bonding together of proteins on DNA to form the complex that mediates dosage compensation on the X chromosome of the heterogametic sex, ultimately resulting in a two-fold increase in transcription from this chromosome. An example of this is found in Drosophila melanogaster.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete dosage compensation complex assembly involved in dosage compensation by hyperactivation of X chromosome (obsolete GO:0016457)","synonyms":[{"name":"dosage compensation complex assembly during dosage compensation by hyperactivation of X chromosome","type":"related"}],"termid":"GO:0016457"}


id: PBO:0074358
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"structural maintenance of chromosomes 4 pseudogene 1","termid":"PBO:0074358"}


id: GO:0097512
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A cardiac myofibril is a myofibril specific to cardiac muscle cells.","definition_xrefs":["GOC:cjm","GOC:devbiol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myofibril","termid":"GO:0030016"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005737"],"is_obsolete":false,"name":"cardiac myofibril","termid":"GO:0097512"}


id: MONDO:0012181
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hereditary spastic paraplegia that has material basis in variation in the chromosome region 10q22.1-q24.1.","definition_xrefs":["DOID:0110778","PMID:15455396"],"direct_ancestors":[{"relation_name":"is_a","term_name":"complex hereditary spastic paraplegia","termid":"MONDO:0015150"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"hereditary spastic paraplegia 27","secondary_identifiers":["Orphanet:101007","GARD:16940","MESH:C563807","UMLS:C1836899","MEDGEN:373203","OMIM:609041"],"synonyms":[{"name":"SPG27","type":"exact"},{"name":"autosomal recessive spastic paraplegia 27","type":"exact"},{"name":"autosomal recessive spastic paraplegia type 27","type":"exact"},{"name":"hereditary spastic paraplegia type 27","type":"exact"},{"name":"spastic paraplegia 27, autosomal recessive","type":"related"}],"termid":"MONDO:0012181","xrefs":{"Monarch":{"xref_id":"0012181"}}}


id: PBO:0017729
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SNARE Use1 (predicted)","termid":"PBO:0017729"}


id: PBO:0050576
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heparan sulfate-glucosamine 3-sulfotransferase 1","termid":"PBO:0050576"}


id: PBO:0041466
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 10 open reading frame 126","termid":"PBO:0041466"}


id: MONDO:0060556
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with multiple joint dislocations (obsolete MONDO:0019700)","termid":"MONDO:0019700"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"developmental defect during embryogenesis","termid":"MONDO:0019755"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"joint laxity, short stature, and myopia","secondary_identifiers":["Orphanet:527450","UMLS:C4540020","OMIM:617662","GARD:17963","MEDGEN:1621331"],"synonyms":[{"name":"JLSM","type":"related"},{"name":"joint laxity, short stature, and myopia","type":"exact"}],"termid":"MONDO:0060556","xrefs":{"Monarch":{"xref_id":"0060556"}}}


id: MOD:00966
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an N-terminal L-tryptophan residue by a formadehyde adduct to 1,2,3,4-tetrahydro-beta-carboline-3-carboxylic acid.","definition_xrefs":["DeltaMass:339"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-tryptophan residue","termid":"MOD:00918"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1,2,3,4-tetrahydro-beta-carboline-3-carboxylic acid","termid":"MOD:00966"}


id: PBO:0082944
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cytoplasmic heavy chain dynein; microtubule motor protein; member of the AAA+ protein family, required for anaphase spindle elongation; involved in spindle assembly, chromosome movement, and spindle orientation during cell division, targeted to microtubule tips by Pac1p; motility along microtubules inhibited by She1p","termid":"PBO:0082944"}


id: FYPO:0000950
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which a cell does not contain a septum and is elongated.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"aseptate","termid":"FYPO:0000949"},{"relation_name":"has_part","term_name":"elongated vegetative cell","termid":"FYPO:0001122"},{"relation_name":"is_a","term_name":"aseptate","termid":"FYPO:0000949"},{"relation_name":"is_a","term_name":"elongated vegetative cell","termid":"FYPO:0001122"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000005","FYPO:0000002","FYPO:0001320","FYPO:0001985","FYPO:0000032","FYPO:0000631"],"is_obsolete":false,"name":"elongated aseptate vegetative cell","synonyms":[{"name":"elongated aseptate cell during mitotic cell cycle","type":"related"},{"name":"elongated aseptate cell during vegetative growth","type":"exact"}],"termid":"FYPO:0000950"}


id: GO:0046169
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of methanol, CH3-OH, a colorless, flammable, mobile, poisonous liquid, widely used as a solvent.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methanol metabolic process","termid":"GO:0015945"},{"relation_name":"is_a","term_name":"primary alcohol biosynthetic process","termid":"GO:0034309"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"methanol biosynthetic process","synonyms":[{"name":"methanol anabolism","type":"exact"},{"name":"methanol biosynthesis","type":"exact"},{"name":"methanol formation","type":"exact"},{"name":"methanol synthesis","type":"exact"}],"termid":"GO:0046169"}


id: PBO:0091940
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small non-coding RNA, expressed in stationary phase and quiescence","termid":"PBO:0091940"}


id: MONDO:0020508
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete malformation of the neurenteric canal, spinal cord and column (obsolete MONDO:0017085)","termid":"MONDO:0017085"},{"relation_name":"is_a","term_name":"syringomyelia","termid":"MONDO:0017987"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primary syringomyelia","secondary_identifiers":["icd11.foundation:257905685","Orphanet:99856","GARD:19691","SCTID:371076006","UMLS:C1299627","MEDGEN:721465"],"synonyms":[{"name":"congenital syringomyelia","type":"exact"}],"termid":"MONDO:0020508","xrefs":{"Monarch":{"xref_id":"0020508"}}}


id: RO:0002100
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Relation between a neuron and an anatomical structure that its soma is part of.","direct_ancestors":[{"relation_name":"is_a","term_name":"overlaps","termid":"RO:0002131"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_soma_location","termid":"RO:0002100"}


id: GO:0032369
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the directed movement of lipids into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of lipid transport","termid":"GO:0032368"},{"relation_name":"is_a","term_name":"negative regulation of transport","termid":"GO:0051051"},{"relation_name":"is_a","term_name":"negative regulation of lipid localization","termid":"GO:1905953"},{"relation_name":"negatively_regulates","term_name":"lipid transport","termid":"GO:0006869"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"negative regulation of lipid transport","synonyms":[{"name":"down regulation of lipid transport","type":"exact"},{"name":"down-regulation of lipid transport","type":"exact"},{"name":"downregulation of lipid transport","type":"exact"},{"name":"inhibition of lipid transport","type":"narrow"}],"termid":"GO:0032369"}


id: GO:0072003
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The developmental process pertaining to the initial formation of a kidney rudiment from unspecified parts. A kidney is an organ that filters the blood and excretes the end products of body metabolism in the form of urine.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure formation involved in morphogenesis","termid":"GO:0048646"},{"relation_name":"part_of","term_name":"kidney morphogenesis","termid":"GO:0060993"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"kidney rudiment formation","synonyms":[{"name":"kidney anlage formation","type":"related"}],"termid":"GO:0072003"}


id: MONDO:0850123
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"benign neoplasm of peripheral nervous system","termid":"MONDO:0056804"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autonomic nervous system benign neoplasm","secondary_identifiers":["DOID:0080321"],"termid":"MONDO:0850123","xrefs":{"Monarch":{"xref_id":"0850123"}}}


id: PBO:0062284
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 5 subfamily K member 1","termid":"PBO:0062284"}


id: PBO:0046057
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation initiation factor 3 subunit H","termid":"PBO:0046057"}


id: PBO:0048345
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 56","termid":"PBO:0048345"}


id: PBO:0054641
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long intergenic non-protein coding RNA 2046","termid":"PBO:0054641"}


id: PR:Q9Y7Y5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rtt109 gene.","definition_xrefs":["UniProtKB:Q9Y7Y5","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone acetyltransferase rtt109 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC342.06c","synonyms":[{"name":"Spom972h-rtt109","type":"exact"}],"termid":"PR:Q9Y7Y5"}


id: MONDO:0011797
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infantile-onset ascending hereditary spastic paralysis (IAHSP) is a very rare motor neuron disease characterized by severe spasticity of the lower limbs in early life, progression of spasticity to the upper limbs in late childhood, and dysarthria.","definition_xrefs":["Orphanet:293168"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ALS2-related motor neuron disease","termid":"MONDO:0100227"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"infantile-onset ascending hereditary spastic paralysis","secondary_identifiers":["MEDGEN:419413","ICD9:343.8","MESH:C537217","OMIM:607225","SCTID:703543005","UMLS:C2931441","GARD:4914"],"synonyms":[{"name":"IAHSP","type":"exact"},{"name":"spastic paralysis, infantile onset ascending","type":"related"},{"name":"spastic paralysis, infantile-onset ascending","type":"related"}],"termid":"MONDO:0011797","xrefs":{"Monarch":{"xref_id":"0011797"}}}


id: PBO:0059952
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND2 pseudogene 38","termid":"PBO:0059952"}


id: PBO:0067460
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 585, pseudogene","termid":"PBO:0067460"}


id: MOD:00872
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"OBSOLETE because redundant and identical to MOD:01970. Remap to MOD:01970.","definition_xrefs":["PubMed:15525938","PubMed:10747868","Unimod:450","RESID:AA0202#var","PubMed:1680872"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE MOD:00872 L-isoglutamyl monoglutamic acid (obsolete MOD:00872)","synonyms":[{"name":"Glu","type":"related"},{"name":"N alpha -(gamma-Glutamyl)-Glu","type":"exact"},{"name":"monoglutamyl","type":"related"}],"termid":"MOD:00872"}


id: PBO:0043821
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coproporphyrinogen oxidase","termid":"PBO:0043821"}


id: FYPO:0005259
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell population phenotype in which a population reaches stationary phase at, and maintains, a higher cell density than wild type.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell population phenotype","termid":"FYPO:0000003"},{"relation_name":"is_a","term_name":"abnormal phenotype","termid":"FYPO:0001985"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0001985"],"is_obsolete":false,"name":"increased cell density in stationary phase","termid":"FYPO:0005259"}


id: GO:0000819
data:
  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id: GO:0030495
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of bacteriochlorophyll, any of the chlorophylls of photosynthetic bacteria. They differ structurally from the chlorophylls of higher plants.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chlorophyll catabolic process","termid":"GO:0015996"},{"relation_name":"is_a","term_name":"bacteriochlorophyll metabolic process","termid":"GO:0030493"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0033013"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0033013","GO:0008150"],"is_obsolete":false,"name":"bacteriochlorophyll catabolic process","synonyms":[{"name":"bacteriochlorophyll breakdown","type":"exact"},{"name":"bacteriochlorophyll catabolism","type":"exact"},{"name":"bacteriochlorophyll degradation","type":"exact"}],"termid":"GO:0030495"}


id: FYECO:0000251
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  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which amitrole (3-amino-1,2,4-triazole) was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ amitrole","synonyms":[{"name":"+ 3-AT","type":"exact"},{"name":"+ 3-amino-1,2,4-triazole","type":"exact"},{"name":"+ 3AT","type":"exact"}],"termid":"FYECO:0000251"}


id: GO:0106184
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  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the translocation of other compounds not included in EC:7.1 through EC:7.5 .","definition_xrefs":["GOC:hjd"],"gene_count":0,"genotype_count":0,"name":"obsolete translocation activity acting on other compounds (obsolete GO:0106184)","termid":"GO:0106184"}


id: PBO:0085960
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; overexpression causes cell cycle delay or arrest; green fluorescent protein (GFP)-fusion protein localizes to vacuole; null mutant displays elevated frequency of mitochondrial genome loss; relocalizes from nucleus to cytoplasm upon DNA replication stress; AIM20 has a paralog, SKG1, that arose from the whole genome duplication","termid":"PBO:0085960"}


id: PBO:0069529
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 798, pseudogene","termid":"PBO:0069529"}


id: MONDO:0013912
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the TAC3 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypogonadotropic hypogonadism","termid":"MONDO:0018555"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypogonadotropic hypogonadism 10 with or without anosmia","secondary_identifiers":["GARD:18600","ICD10CM:E23.0","OMIM:614839","UMLS:C3553843","MEDGEN:766757","DOID:0090089"],"synonyms":[{"name":"HH10","type":"related"},{"name":"TAC3 hypogonadotropic hypogonadism","type":"exact"},{"name":"hypogonadotropic hypogonadism 10 with or without anosmia","type":"exact"},{"name":"hypogonadotropic hypogonadism caused by mutation in TAC3","type":"exact"}],"termid":"MONDO:0013912","xrefs":{"Monarch":{"xref_id":"0013912"}}}


id: PBO:0042845
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cilia and flagella associated protein 53","termid":"PBO:0042845"}


id: GO:0008510
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: Na+(out) + HCO3-(out) = Na+(in) + HCO3-(in).","definition_xrefs":["TC:2.A.31.2.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"solute:sodium symporter activity","termid":"GO:0015370"},{"relation_name":"is_a","term_name":"monoatomic cation:bicarbonate symporter activity","termid":"GO:0140410"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"sodium:bicarbonate symporter activity","secondary_identifiers":["Reactome:R-HSA-425483","Reactome:R-HSA-5656219","Reactome:R-HSA-8878664","RHEA:70267"],"synonyms":[{"name":"sodium/bicarbonate cotransporter activity","type":"broad"},{"name":"sodium:bicarbonate cotransporter activity","type":"broad"},{"name":"sodium:hydrogencarbonate symporter activity","type":"exact"}],"termid":"GO:0008510"}


id: GO:0002721
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of B cell cytokine production.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of B cell mediated immunity","termid":"GO:0002712"},{"relation_name":"is_a","term_name":"regulation of cytokine production involved in immune response","termid":"GO:0002718"},{"relation_name":"regulates","term_name":"B cell cytokine production","termid":"GO:0002368"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"regulation of B cell cytokine production","synonyms":[{"name":"regulation of B lymphocyte cytokine production","type":"exact"},{"name":"regulation of B-cell cytokine production","type":"exact"},{"name":"regulation of B-lymphocyte cytokine production","type":"exact"}],"termid":"GO:0002721"}


id: PBO:0048259
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"galactokinase 1","termid":"PBO:0048259"}


id: PBO:0056575
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAPK regulated corepressor interacting protein 2 pseudogene 2","termid":"PBO:0056575"}


id: GO:0061347
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of molecular signals initiated by binding of a Wnt protein to a receptor on the surface of the target cell where activated receptors signal via downstream effectors including C-Jun N-terminal kinase (JNK) to modulate cytoskeletal elements and control cell polarity that contributes to the shaping of the outflow tract.","definition_xrefs":["GOC:dph","GOC:mtg_heart","PMID:19056682"],"gene_count":0,"genotype_count":0,"name":"obsolete planar cell polarity pathway involved in outflow tract morphogenesis (obsolete GO:0061347)","termid":"GO:0061347"}


id: PBO:0060600
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-SMC condensin II complex subunit G2","termid":"PBO:0060600"}


id: GO:0022410
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A behavioral process involved in the cycle from wakefulness through an orderly succession of sleep states and stages that occurs on an approximately 24 hour rhythm.","definition_xrefs":["GOC:isa_complete"],"direct_ancestors":[{"relation_name":"is_a","term_name":"circadian behavior","termid":"GO:0048512"},{"relation_name":"part_of","term_name":"circadian sleep/wake cycle","termid":"GO:0042745"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"circadian sleep/wake cycle process","termid":"GO:0022410"}


id: MONDO:0011956
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  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autism, susceptiblity to","termid":"MONDO:0020836"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autism, susceptibility to, 3","secondary_identifiers":["OMIM:608049","MEDGEN:334211","UMLS:C1842632"],"synonyms":[{"name":"AUTS3","type":"exact"},{"name":"autism susceptibility 3, isolated cases","type":"exact"},{"name":"autism, susceptibility to, 3","type":"exact"}],"termid":"MONDO:0011956","xrefs":{"Monarch":{"xref_id":"0011956"}}}


id: FYPO:0005145
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  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which proteasome regulatory particle binding by a gene product (usually a protein) in a mutant does not occur. The affected gene product may be encoded by the mutated gene, or by a different gene.","definition_xrefs":["PMID:16096059","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein-protein interaction","termid":"FYPO:0000705"},{"relation_name":"is_a","term_name":"abnormal protein complex binding","termid":"FYPO:0003591"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000702"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000702","FYPO:0001985","FYPO:0000707","FYPO:0000652"],"is_obsolete":false,"name":"abolished proteasome regulatory particle binding","synonyms":[{"name":"proteasome regulatory particle binding abolished","type":"exact"}],"termid":"FYPO:0005145"}


id: GO:1903877
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  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to 21-deoxycortisol.","definition_xrefs":["GOC:TermGenie","PMID:10802282","GOC:mr","GO_REF:0000067"],"direct_ancestors":[{"relation_name":"is_a","term_name":"steroid binding","termid":"GO:0005496"},{"relation_name":"is_a","term_name":"alcohol binding","termid":"GO:0043178"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008289"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0008289"],"is_obsolete":false,"name":"21-deoxycortisol binding","termid":"GO:1903877"}


id: GO:1990467
data:
  {"annotated_genes":["SJAG_02165"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[90266],"is_not":false,"summary":null,"term":"GO:1990467"}]},"cv_name":"cellular_component","definition":"A NuA3 complex that catalyzes the acetylation of Histone H3. In S. cerevisiae, this complex consists of Eaf6p, Nto1p, Sas3p, Taf14p, Yng1p and associates with H3K4me3 using Yng1p.","definition_xrefs":["PMID:25104842","GOC:rb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"NuA3 histone acetyltransferase complex","termid":"GO:0033100"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02165":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005694","GO:0032991"],"is_obsolete":false,"name":"NuA3a histone acetyltransferase complex","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1990467","terms_by_termid":{"GO:1990467":null}}


id: PBO:0067971
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 273","termid":"PBO:0067971"}


id: PBO:0039678
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adaptor related protein complex 5 subunit zeta 1","termid":"PBO:0039678"}


id: GO:0002279
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The change in morphology and behavior of a mast cell resulting from exposure to a cytokine, chemokine, soluble factor, or to (at least in mammals) an antigen which the mast cell has specifically bound via IgE bound to Fc-epsilonRI receptors, leading to the initiation or perpetuation of an immune response.","definition_xrefs":["ISBN:0781735149","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myeloid cell activation involved in immune response","termid":"GO:0002275"},{"relation_name":"is_a","term_name":"mast cell activation","termid":"GO:0045576"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"mast cell activation involved in immune response","synonyms":[{"name":"mast cell activation during immune response","type":"related"}],"termid":"GO:0002279"}


id: PBO:0039148
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AK3 pseudogene 3","termid":"PBO:0039148"}


id: PBO:0051011
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"insulin like growth factor 1 receptor","termid":"PBO:0051011"}


id: GO:1900114
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of histone H3-K9 trimethylation.","definition_xrefs":["GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of histone H3-K9 trimethylation (obsolete GO:1900114)","synonyms":[{"name":"activation of histone H3-K9 trimethylation","type":"narrow"},{"name":"up regulation of histone H3-K9 trimethylation","type":"exact"},{"name":"up-regulation of histone H3-K9 trimethylation","type":"exact"},{"name":"upregulation of histone H3-K9 trimethylation","type":"exact"}],"termid":"GO:1900114"}


id: MONDO:0043069
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"excluded_subClassOf","term_name":"intellectual disability","termid":"MONDO:0001071"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary endocrine growth disease","termid":"MONDO:0015514"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Zerres Rietschel Majewski syndrome","secondary_identifiers":["GARD:338","MESH:C536724","UMLS:C2931301","MEDGEN:419769"],"synonyms":[{"name":"postnatal short stature, microcephaly, severe syndactyly of hands and feet, dysmorphic face, and intellectual disability","type":"related"},{"name":"postnatal short stature, microcephaly, severe syndactyly of hands and feet, dysmorphic face, and mental retardation","type":"related"}],"termid":"MONDO:0043069","xrefs":{"Monarch":{"xref_id":"0043069"}}}


id: PBO:0074077
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLC25A51 pseudogene 1","termid":"PBO:0074077"}


id: PBO:0109128
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cripto, EGF-CFC family member 3","termid":"PBO:0109128"}


id: PBO:0026874
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_meiotic_DNA_double-strand_break_resectioning","termid":"PBO:0026874"}


id: GO:0033812
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: succinyl-CoA + acetyl-CoA = CoA + 3-oxoadipyl-CoA.","definition_xrefs":["RHEA:19481"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acetyl-CoA C-acyltransferase activity","termid":"GO:0003988"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016746","GO:0003674","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"3-oxoadipyl-CoA thiolase activity","secondary_identifiers":["MetaCyc:RXN-3641","EC:2.3.1.174"],"synonyms":[{"name":"succinyl-CoA:acetyl-CoA C-succinyltransferase activity","type":"related"}],"termid":"GO:0033812"}


id: PBO:0036372
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uridine ribohydrolase Urh1 (predicted)","termid":"PBO:0036372"}


id: PBO:0086509
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function","termid":"PBO:0086509"}


id: FYECO:0000149
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which 1-deoxynojirimycin (1-DNJ) was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ 1-DNJ","synonyms":[{"name":"1-deoxynojirimycin added","type":"exact"},{"name":"DNJ added","type":"exact"},{"name":"deoxynojirimycin added","type":"exact"}],"termid":"FYECO:0000149"}


id: PBO:0029592
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_protein_phosphorylation_during_cellular_response_to_heat","termid":"PBO:0029592"}


id: MONDO:0021068
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign, borderline, or malignant neoplasm involving the ovary.","definition_xrefs":["NCIT:C4984"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ovarian disorder","termid":"MONDO:0005558"},{"relation_name":"is_a","term_name":"female reproductive system neoplasm","termid":"MONDO:0021148"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ovarian neoplasm","secondary_identifiers":["EFO:0003893","SCTID:123843001","MEDGEN:181539","UMLS:C0919267","ICD9:239.5"],"synonyms":[{"name":"neoplasm of ovary","type":"exact"},{"name":"neoplasm of the ovary","type":"exact"},{"name":"ovarian neoplasm","type":"exact"},{"name":"ovarian tumor","type":"exact"},{"name":"ovarian tumors","type":"exact"},{"name":"ovarian tumour","type":"exact"},{"name":"ovarian tumours","type":"exact"},{"name":"ovary neoplasm","type":"exact"},{"name":"ovary neoplasm (disease)","type":"exact"},{"name":"ovary tumor","type":"exact"},{"name":"ovary tumour","type":"exact"},{"name":"tumor of ovary","type":"exact"},{"name":"tumor of the ovary","type":"exact"},{"name":"tumour of ovary","type":"exact"},{"name":"tumour of the ovary","type":"exact"}],"termid":"MONDO:0021068","xrefs":{"Monarch":{"xref_id":"0021068"}}}


id: GO:0047286
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: peptide diphthamide + NAD+ = peptide N-(ADP-D-ribosyl)diphthamide + niacinamide.","definition_xrefs":["EC:2.4.2.36"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pentosyltransferase activity","termid":"GO:0016763"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016757","GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"NAD+-diphthamide ADP-ribosyltransferase activity","secondary_identifiers":["RHEA:11820","Reactome:R-HSA-5336421","MetaCyc:RXN-11372"],"synonyms":[{"name":"ADP-ribosyltransferase activity","type":"broad"},{"name":"NAD+:peptide-diphthamide N-(ADP-D-ribosyl)transferase activity","type":"related"},{"name":"NAD-diphthamide ADP-ribosyltransferase activity","type":"exact"},{"name":"mono(ADP-ribosyl)transferase activity","type":"broad"}],"termid":"GO:0047286"}


id: FYPO:0003110
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to a combination of caffeine and rapamycin. Cells stop growing (and may die) at concentrations of caffeine and rapamycin that allow wild type cells to grow.","definition_xrefs":["PomBase:mah","PMID:23551936"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0002683","FYPO:0005447","FYPO:0000139","FYPO:0000003"],"is_obsolete":false,"name":"sensitive to caffeine and rapamycin","synonyms":[{"name":"hypersensitive to caffeine and rapamycin","type":"exact"},{"name":"sensitive to caffeine and rapamycin during mitotic cell cycle","type":"related"},{"name":"sensitive to caffeine and rapamycin during vegetative growth","type":"exact"},{"name":"sensitive to caffeine and rapamycin in combination","type":"exact"}],"termid":"FYPO:0003110"}


id: PBO:0052205
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"potassium voltage-gated channel subfamily Q member 2","termid":"PBO:0052205"}


id: MONDO:0004688
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete sideroblastic anemia (obsolete MONDO:0004688)","termid":"MONDO:0004688","xrefs":{"Monarch":{"xref_id":"0004688"}}}


id: MONDO:0100134
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial complex I deficiency","termid":"MONDO:0100133"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005066"],"is_obsolete":false,"name":"mitochondrial complex I deficiency, mitochondrial type","termid":"MONDO:0100134","xrefs":{"Monarch":{"xref_id":"0100134"}}}


