# terms

id: GO:0004743
data:
  {"annotated_genes":["SJAG_02796"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[79788],"is_not":false,"summary":null,"term":"GO:0004743"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: = ADP + H+ + phosphoenolpyruvate => ATP + pyruvate.","definition_xrefs":["EC:2.7.1.40","RHEA:18159"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02796":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"pyruvate kinase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["MetaCyc:PEPDEPHOS-RXN","Reactome:R-HSA-71670"],"synonyms":[{"name":"ATP:pyruvate 2-O-phosphotransferase activity","type":"related"},{"name":"phosphoenol transphosphorylase activity","type":"related"},{"name":"phosphoenolpyruvate kinase activity","type":"related"}],"termid":"GO:0004743","terms_by_termid":{"GO:0004743":null}}


id: PBO:0045907
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EF-hand calcium binding domain 5","termid":"PBO:0045907"}


id: PBO:0039715
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"apolipoprotein B mRNA editing enzyme catalytic subunit 1","termid":"PBO:0039715"}


id: MONDO:0010719
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":"radiation sensitivity of natural killer activity","secondary_identifiers":["UMLS:C1839408","OMIM:312210","MEDGEN:333311","MESH:C564066"],"synonyms":[{"name":"X-Ray Nk sensitivity","type":"related"},{"name":"radiation sensitivity of natural killer activity","type":"exact"}],"termid":"MONDO:0010719","xrefs":{"Monarch":{"xref_id":"0010719"}}}


id: PBO:0070075
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6atac small nuclear 32, pseudogene","termid":"PBO:0070075"}


id: MONDO:0008826
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Arthrogryposis-hyperkeratosis syndrome, lethal form is an arthrogryposis syndrome, described in two siblings to date, characterized by the association of multiple congenital joint contractures (of the large joints, fingers and toes) and hyperkeratosis (i.e. thick, scaling and fissured skin), with death occurring in early infancy. There have been no further reports in the literature since 1993.","definition_xrefs":["Orphanet:1485"],"direct_ancestors":[{"relation_name":"is_a","term_name":"arthrogryposis multiplex congenita","termid":"MONDO:0015168"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arthrogryposis-hyperkeratosis syndrome, lethal form","secondary_identifiers":["MESH:C535883","GARD:3053","MEDGEN:349230","SCTID:726620005","OMIM:208158","UMLS:C1859710"],"synonyms":[{"name":"Johnston Aarons Schelley syndrome","type":"related"},{"name":"Johnston-Aarons-Schelley syndrome","type":"exact"},{"name":"Joint contractures, hyperkeratosis, and severe hypoplasia of the posterior columns","type":"related"},{"name":"arthrogryposis with hyperkeratosis","type":"related"}],"termid":"MONDO:0008826","xrefs":{"Monarch":{"xref_id":"0008826"}}}


id: PBO:0052074
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"katanin regulatory subunit B1","termid":"PBO:0052074"}


id: FYECO:0000451
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"Experiments were performed in minimal medium containing a high concentration of lactate (>2%) as carbon source, salts and water.","definition_xrefs":["PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping defined medium","termid":"FYECO:0000013"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ lactate","termid":"FYECO:0000451"}


id: PBO:0086764
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; separated from neighboring gene, YAP7, by frame shift and corresponds to C-terminal part of YAP7 orthologs in other species; identified as interacting with Hsc82p and Hsp82p in high-throughput two-hybrid screens","termid":"PBO:0086764"}


id: MONDO:0054561
data:
  {"annotated_genes":["SJAG_04582"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87236],"is_not":false,"summary":null,"term":"MONDO:0054561"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"anauxetic dysplasia","termid":"MONDO:0011773"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04582":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"anauxetic dysplasia 2","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:617396","DOID:0080962","MEDGEN:1384439","UMLS:C4479357"],"synonyms":[{"name":"ANXD2","type":"related"},{"name":"anauxetic dysplasia 2","type":"exact"}],"termid":"MONDO:0054561","terms_by_termid":{"MONDO:0054561":null},"xrefs":{"Monarch":{"xref_id":"0054561"}}}


id: PR:Q9Y7K2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A serine/threonine-protein kinase mTOR that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR11139:SF9","PRO:DNx","OMA:SCHPO02637"],"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":"phosphatidylinositol 3-kinase tor2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC216.07c","secondary_identifiers":["UniProtKB:Q9Y7K2"],"synonyms":[{"name":"PI3-kinase tor2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"PI3K tor2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"PtdIns-3-kinase tor2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-MTOR","type":"exact"}],"termid":"PR:Q9Y7K2"}


id: PBO:0110463
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ACO2 pseudogene 2","termid":"PBO:0110463"}


id: PBO:0043600
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"colorectal cancer associated 1","termid":"PBO:0043600"}


id: PBO:0061853
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactomedin 3","termid":"PBO:0061853"}


id: GO:1902448
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of shade avoidance.","definition_xrefs":["PMID:23763263","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of response to stimulus","termid":"GO:0048584"},{"relation_name":"is_a","term_name":"regulation of shade avoidance","termid":"GO:1902446"},{"relation_name":"positively_regulates","term_name":"shade avoidance","termid":"GO:0009641"}],"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 shade avoidance","synonyms":[{"name":"activation of shade avoidance","type":"narrow"},{"name":"up regulation of shade avoidance","type":"exact"},{"name":"up-regulation of shade avoidance","type":"exact"},{"name":"upregulation of shade avoidance","type":"exact"}],"termid":"GO:1902448"}


id: PBO:0087319
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sm-like protein involved in docking and fusion of exocytic vesicles; binds to assembled SNARE complexes at the membrane and stimulates membrane fusion; localization to sites of secretion (bud neck and bud tip) is dependent on SNARE function; interacts directly with essential exocyst subunit Sec6p","termid":"PBO:0087319"}


id: PBO:0116778
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UBE2I antisense RNA 1","termid":"PBO:0116778"}


id: PBO:0088970
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rhomboid family protease, unknown biological role, associated with COP1 coated vesicle","termid":"PBO:0088970"}


id: FYPO:0004075
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which cell growth is decreased. Cell growth is the irreversible increase in size over time by accretion and biosynthetic production of matter similar to that already present.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell growth","termid":"FYPO:0002862"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"decreased cell growth","synonyms":[{"name":"reduced cell growth","type":"exact"}],"termid":"FYPO:0004075"}


id: MONDO:0016113
data:
  {"annotated_genes":["SJAG_04321","SJAG_01260","SJAG_04084","SJAG_04907","SJAG_03328","SJAG_00754"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86662],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013853"},{"annotations":[86956],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010190"},{"annotations":[87423],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012890"},{"annotations":[87427],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012891"},{"annotations":[87252],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014485"},{"annotations":[86444],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014874"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spinal muscular atrophy","termid":"MONDO:0001516"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00754":null,"SJAG_01260":null,"SJAG_03328":null,"SJAG_04084":null,"SJAG_04321":null,"SJAG_04907":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"bulbospinal muscular atrophy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0393547","SCTID:230253001","Orphanet:206701","NANDO:1200001","GARD:20365","icd11.foundation:1604214898","MEDGEN:95977"],"synonyms":[{"name":"SBMA","type":"exact"},{"name":"bulbospinal muscular atrophy","type":"exact"},{"name":"spinal and bulbal muscular atrophy","type":"exact"},{"name":"spinal-bulbar muscular atrophy","type":"exact"}],"termid":"MONDO:0016113","terms_by_termid":{"MONDO:0010190":null,"MONDO:0012890":null,"MONDO:0012891":null,"MONDO:0013853":null,"MONDO:0014485":null,"MONDO:0014874":null},"xrefs":{"Monarch":{"xref_id":"0016113"}}}


id: MONDO:0013960
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Sinoatrial node dysfunction and deafness is a rare genetic disease characterized by congenital severe to profound deafness with no evidence of vestibular dysfunction, associated with sinoatrial node dysfunction with pronounced bradycardia and increased variability of heart rate at rest and episodic syncopes that may be triggered by enhanced physical activity and stress.","definition_xrefs":["Orphanet:324321"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiac rhythm disease","termid":"MONDO:0007263"},{"relation_name":"is_a","term_name":"cardiogenetic disease","termid":"MONDO:0100547"}],"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":"sinoatrial node dysfunction and deafness","secondary_identifiers":["UMLS:C3554018","OMIM:614896","GARD:17484","MEDGEN:766932"],"synonyms":[{"name":"SANDD","type":"related"},{"name":"sinoatrial node dysfunction and deafness","type":"exact"}],"termid":"MONDO:0013960","xrefs":{"Monarch":{"xref_id":"0013960"}}}


id: GO:1903651
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of cytoplasmic transport.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:25049409"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of cytoplasmic transport (obsolete GO:1903651)","synonyms":[{"name":"activation of cytoplasmic streaming","type":"narrow"},{"name":"activation of cytoplasmic transport","type":"narrow"},{"name":"positive regulation of cytoplasmic streaming","type":"narrow"},{"name":"up regulation of cytoplasmic streaming","type":"narrow"},{"name":"up regulation of cytoplasmic transport","type":"exact"},{"name":"up-regulation of cytoplasmic streaming","type":"narrow"},{"name":"up-regulation of cytoplasmic transport","type":"exact"},{"name":"upregulation of cytoplasmic streaming","type":"narrow"},{"name":"upregulation of cytoplasmic transport","type":"exact"}],"termid":"GO:1903651"}


id: MONDO:1010897
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any lysosomal disease characterized by the accumulation of sphingomyelin and cholesterol in lysosomes that occurs in cats due to a mutation in the SMPD1 gene.","definition_xrefs":["PMID:32347185"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lysosomal storage disease, domestic cat","termid":"MONDO:1010861"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Niemann-Pick disease, SMPD1-related, domestic cat","secondary_identifiers":["OMIA:001795-9685"],"synonyms":[{"name":"Niemann-Pick disease, type A, domestic cat","type":"related"}],"termid":"MONDO:1010897","xrefs":{"Monarch":{"xref_id":"1010897"}}}


id: MONDO:0002049
data:
  {"annotated_genes":["SJAG_02431","SJAG_02509","SJAG_04003","SJAG_01784","SJAG_02951","SJAG_01852","SJAG_02744","SJAG_03818","SJAG_03703","SJAG_04387","SJAG_04509","SJAG_04621","SJAG_01732"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86708,86709],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0015912"},{"annotations":[86988],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0800047"},{"annotations":[87306,87307],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030827"},{"annotations":[86256],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014757"},{"annotations":[85508],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014078"},{"annotations":[87540],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010743"},{"annotations":[87502,87503,87501],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0958333"},{"annotations":[86657],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012775"},{"annotations":[87436],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010121"}]},"cv_name":"mondo","definition":"A laboratory test result indicating that there is an abnormally small number of platelets in the circulating blood.","definition_xrefs":["NCIT:C3408"],"direct_ancestors":[{"relation_name":"is_a","term_name":"blood platelet disease","termid":"MONDO:0002245"}],"gene_count":13,"genes_by_uniquename":{"SJAG_01732":null,"SJAG_01784":null,"SJAG_01852":null,"SJAG_02431":null,"SJAG_02509":null,"SJAG_02744":null,"SJAG_02951":null,"SJAG_03703":null,"SJAG_03818":null,"SJAG_04003":null,"SJAG_04387":null,"SJAG_04509":null,"SJAG_04621":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"thrombocytopenia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:52737","ICD9:287.5","MESH:D013921","SCTID:302215000","UMLS:C0040034","icd11.foundation:683583694","DOID:1588"],"synonyms":[{"name":"platelet count decreased","type":"exact"},{"name":"thrombocytopenic disorder","type":"exact"}],"termid":"MONDO:0002049","terms_by_termid":{"MONDO:0010121":null,"MONDO:0010743":null,"MONDO:0012775":null,"MONDO:0014078":null,"MONDO:0014757":null,"MONDO:0015912":null,"MONDO:0030827":null,"MONDO:0800047":null,"MONDO:0958333":null},"xrefs":{"Monarch":{"xref_id":"0002049"}}}


id: PBO:0044829
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"defensin beta 116","termid":"PBO:0044829"}


id: MONDO:0009688
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Myasthenia gravis (MG) is a rare, clinically heterogeneous, autoimmune disorder of the neuromuscular junction characterized by fatigable weakness of voluntary muscles.","definition_xrefs":["Orphanet:589"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune disorder of peripheral nervous system","termid":"MONDO:0000590"}],"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":"myasthenia gravis","secondary_identifiers":["ICD10CM:G70.0","NCIT:C60989","ICD9:358.00","MEDGEN:7764","SCTID:91637004","EFO:0004991","ICD9:358.0","OMIM:254200","UMLS:C0026896","DOID:437","MESH:D009157","NORD:1478","MedDRA:10028417","GARD:7122","NANDO:2200906","NANDO:2100252","icd11.foundation:1270100227","NANDO:1200020"],"synonyms":[{"name":"MG","type":"related"},{"name":"acquired myasthenia","type":"exact"},{"name":"autoimmune myasthenia gravis","type":"exact"},{"name":"myasthenia gravis","type":"exact"}],"termid":"MONDO:0009688","xrefs":{"Monarch":{"xref_id":"0009688"}}}


id: PBO:0028762
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_cytoplasmic_translational_initiation","termid":"PBO:0028762"}


id: PBO:0089976
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"snoRNP assembly factor Naf1","termid":"PBO:0089976"}


id: PBO:0075026
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 115-37","termid":"PBO:0075026"}


id: GO:0080189
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Growth of a plant structure from the time of its initiation by an apical meristem until its expansion is completed.","definition_xrefs":["ISBN:0471245208"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multicellular organismal process","termid":"GO:0032501"},{"relation_name":"is_a","term_name":"growth","termid":"GO:0040007"}],"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":"primary growth","termid":"GO:0080189"}


id: FYPO:0001297
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of palmitoyl-CoA ligase activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal long-chain fatty acid-CoA ligase activity","termid":"FYPO:0001305"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0001985","FYPO:0000707","FYPO:0000654","FYPO:0005447","FYPO:0000002","FYPO:0000652"],"is_obsolete":false,"name":"abnormal palmitoyl-CoA ligase activity","synonyms":[{"name":"abnormal palmitoyl-CoA synthetase activity","type":"exact"}],"termid":"FYPO:0001297"}


id: MONDO:1012338
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"reduced glutathione deficiency, non-human animal","termid":"MONDO:1011699"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"reduced glutathione deficiency, goat","secondary_identifiers":["OMIA:001235-9925"],"termid":"MONDO:1012338","xrefs":{"Monarch":{"xref_id":"1012338"}}}


id: PBO:0062138
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 F member 5","termid":"PBO:0062138"}


id: PBO:0044453
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome P450 family 4 subfamily F member 32, pseudogene","termid":"PBO:0044453"}


id: PBO:0073148
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SEC24 homolog A pseudogene 1","termid":"PBO:0073148"}


id: PBO:0001511
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"human TMEM165 homolog","termid":"PBO:0001511"}


id: GO:1904415
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of xenophagy.","definition_xrefs":["GOC:PARL","GOC:TermGenie","PMID:21617041","GOC:pad","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of response to biotic stimulus","termid":"GO:0002831"},{"relation_name":"is_a","term_name":"regulation of macroautophagy","termid":"GO:0016241"},{"relation_name":"is_a","term_name":"regulation of response to external stimulus","termid":"GO:0032101"},{"relation_name":"regulates","term_name":"xenophagy","termid":"GO:0098792"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006914"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006914","GO:0008150"],"is_obsolete":false,"name":"regulation of xenophagy","termid":"GO:1904415"}


id: PBO:0070149
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 63 pseudogene","termid":"PBO:0070149"}


id: FYPO:0001683
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which mitotic spindle assembly does not occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_output","term_name":"mitotic spindle absent from cell","termid":"FYPO:0002018"},{"relation_name":"is_a","term_name":"abnormal mitotic spindle assembly","termid":"FYPO:0000177"},{"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":"part_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000054"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000641","FYPO:0005447","FYPO:0000631","FYPO:0000337","FYPO:0000002","FYPO:0000054","FYPO:0001320"],"is_obsolete":false,"name":"abolished mitotic spindle assembly","synonyms":[{"name":"abolished mitotic spindle assembly during vegetative growth","type":"exact"},{"name":"abolished spindle assembly during mitotic cell cycle","type":"related"},{"name":"spindle assembly involved in mitosis abolished","type":"exact"}],"termid":"FYPO:0001683"}


id: PBO:0052577
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lysine methyltransferase 5C","termid":"PBO:0052577"}


id: GO:0098917
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Cell-cell signaling from post to pre-synapse, across the synaptic cleft.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"trans-synaptic signaling","termid":"GO:0099537"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"retrograde trans-synaptic signaling","termid":"GO:0098917"}


id: GO:0090309
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that increases the rate, frequency, or extent of DNA methylation-dependent heterochromatin formation.","definition_xrefs":["GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of DNA methylation-dependent heterochromatin formation (obsolete GO:0090309)","synonyms":[{"name":"positive regulation of DNA methylation-dependent heterochromatin assembly","type":"exact"},{"name":"positive regulation of methylation-dependent chromatin silencing","type":"broad"}],"termid":"GO:0090309"}


id: FYPO:0001453
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An increased chemical resistance phenotype observed in the vegetative growth phase of the life cycle in which cells grow in the presence of a higher concentration of ethanol than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002682"}],"interesting_parent_ids":["FYPO:0002682","FYPO:0000003","FYPO:0005447","FYPO:0001985","FYPO:0000139"],"is_obsolete":false,"name":"resistance to ethanol","synonyms":[{"name":"resistance to ethanol during mitotic cell cycle","type":"related"},{"name":"resistance to ethanol during vegetative growth","type":"exact"},{"name":"resistance to ethyl alcohol","type":"exact"},{"name":"resistant to ethanol","type":"exact"}],"termid":"FYPO:0001453"}


id: GO:0021894
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a cerebral cortex GABAergic interneuron over time, from initial commitment to its fate, to the fully functional differentiated cell.","definition_xrefs":["GOC:jid","PMID:12626695","GOC:dph","GO_REF:0000021","GOC:cls","GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"forebrain neuron development","termid":"GO:0021884"},{"relation_name":"part_of","term_name":"cerebral cortex GABAergic interneuron differentiation","termid":"GO:0021892"}],"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":"cerebral cortex GABAergic interneuron development","termid":"GO:0021894"}


id: MONDO:0018444
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete female infertility due to fertilization defect (obsolete MONDO:0018444)","secondary_identifiers":["Orphanet:404469"],"synonyms":[{"name":"female infertility due to fecundation defect","type":"exact"},{"name":"rare female infertility due to oocyte maturation","type":"related"},{"name":"rare female infertility due to oocyte maturation defect","type":"related"}],"termid":"MONDO:0018444","xrefs":{"Monarch":{"xref_id":"0018444"}}}


id: PBO:0066367
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RDH10 antisense RNA 1","termid":"PBO:0066367"}


id: GO:0005205
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete chondroitin sulfate/dermatan sulfate proteoglycan (obsolete GO:0005205)","synonyms":[{"name":"chondroitin sulfate/dermatan sulfate proteoglycan","type":"exact"},{"name":"chondroitin sulphate/dermatan sulphate proteoglycan","type":"exact"}],"termid":"GO:0005205"}


id: GO:0031928
data:
  {"annotated_genes":["SJAG_03652","SJAG_02962","SJAG_03808","SJAG_02152"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[90490,90491,117774,119053],"is_not":false,"summary":null,"term":"GO:0031928"}]},"cv_name":"molecular_function","definition":"Enables the transfer of pyridoxine from one side of a membrane to the other. Pyridoxine, 2-methyl-3-hydroxy-4,5-bis(hydroxymethyl)pyridine, is one of the vitamin B6 compounds. Pyridoxal, pyridoxamine and pyridoxine are collectively known as vitamin B6, and are efficiently converted to the biologically active form of vitamin B6, pyridoxal phosphate.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane transporter activity","termid":"GO:0022857"}],"gene_count":4,"genes_by_uniquename":{"SJAG_02152":null,"SJAG_02962":null,"SJAG_03652":null,"SJAG_03808":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0022857","GO:0005215"],"is_obsolete":false,"name":"pyridoxine transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"pyridoxine transporter activity","type":"broad"}],"termid":"GO:0031928","terms_by_termid":{"GO:0031928":null}}


id: GO:0047689
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-aspartate = D-aspartate.","definition_xrefs":["RHEA:14973","EC:5.1.1.13"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino-acid racemase activity","termid":"GO:0047661"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016853"],"is_obsolete":false,"name":"aspartate racemase activity","secondary_identifiers":["KEGG_REACTION:R00491","MetaCyc:ASPARTATE-RACEMASE-RXN"],"synonyms":[{"name":"D-aspartate racemase activity","type":"related"}],"termid":"GO:0047689"}


id: PBO:0062346
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 6 subfamily K member 5 pseudogene","termid":"PBO:0062346"}


id: GO:0007300
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Transfer of constituents synthesized in the ovarian nurse cells to the oocyte, through the ring canals, as the egg chamber is growing. An example of this is found in Drosophila melanogaster.","definition_xrefs":["GOC:mtg_sensu","ISBN:0879694238"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transport","termid":"GO:0006810"},{"relation_name":"part_of","term_name":"oogenesis","termid":"GO:0048477"}],"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"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"ovarian nurse cell to oocyte transport","synonyms":[{"name":"nurse cell to oocyte transport","type":"broad"}],"termid":"GO:0007300"}


id: MOD:01150
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively crosslinks the N6-amino of a peptidyl lysine with the carboxyl-terminal glycine of a nedd8 protein.","definition_xrefs":["PubMed:12612601","PubMed:11125103","PubMed:18688235"],"direct_ancestors":[{"relation_name":"contains","term_name":"N6-glycyl-L-lysine","termid":"MOD:00134"},{"relation_name":"is_a","term_name":"N6-acylated L-lysine","termid":"MOD:01875"},{"relation_name":"is_a","term_name":"crosslinked glycine residue","termid":"MOD:02047"},{"relation_name":"is_a","term_name":"crosslinked L-lysine residue","termid":"MOD:02051"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01875"}],"interesting_parent_ids":["MOD:01875"],"is_obsolete":false,"name":"neddylated lysine","termid":"MOD:01150"}


id: PBO:0044489
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome P450 family 46 subfamily A member 1","termid":"PBO:0044489"}


id: PBO:0076862
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis expressed 12","termid":"PBO:0076862"}


id: GO:0010156
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Formation and development of sporocyte, the haploid spores of angiosperms which are initiated by the differentiation of a subset of floral cells into sporocytes, which then undergo meiotic divisions to form microspores and megaspores.","definition_xrefs":["PMID:10465788"],"gene_count":0,"genotype_count":0,"name":"obsolete sporocyte morphogenesis (obsolete GO:0010156)","synonyms":[{"name":"sporocyte morphogenesis","type":"exact"}],"termid":"GO:0010156"}


id: GO:0106071
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of an adenylate cyclase-activating G protein-coupled receptor signaling pathway.","definition_xrefs":["GOC:hjd","PMID:19246489"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of G protein-coupled receptor signaling pathway","termid":"GO:0045745"},{"relation_name":"is_a","term_name":"regulation of adenylate cyclase-activating G protein-coupled receptor signaling pathway","termid":"GO:0106070"},{"relation_name":"positively_regulates","term_name":"adenylate cyclase-activating G protein-coupled receptor signaling pathway","termid":"GO:0007189"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"positive regulation of adenylate cyclase-activating G protein-coupled receptor signaling pathway","synonyms":[{"name":"positive regulation of adenylate cyclase-activating G-protein coupled receptor signaling pathway","type":"exact"}],"termid":"GO:0106071"}


id: PR:G2TRM1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC977.18 gene.","definition_xrefs":["PRO:DNx","UniProtKB:G2TRM1"],"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":"UPF0768 protein C977.18 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC977.18","synonyms":[{"name":"Spom972h-SPAC977.18","type":"exact"}],"termid":"PR:G2TRM1"}


id: PBO:0027638
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_spindle_during_meiosis_I","termid":"PBO:0027638"}


id: PBO:0045702
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dual specificity tyrosine phosphorylation regulated kinase 1B","termid":"PBO:0045702"}


id: PBO:0071461
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L32 pseudogene 2","termid":"PBO:0071461"}


id: GO:1990188
data:
  {"annotated_genes":["SJAG_03689","SJAG_00471"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[105709,116294],"is_not":false,"summary":null,"term":"GO:1990188"}]},"cv_name":"molecular_function","definition":"Binding to euchromatin, a dispersed and relatively uncompacted form of chromatin.","definition_xrefs":["GOC:vw","PMID:22431512"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromatin binding","termid":"GO:0003682"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00471":null,"SJAG_03689":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":"euchromatin binding","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1990188","terms_by_termid":{"GO:1990188":null}}


id: FYPO:0007403
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 anaphase-promoting complex (APC) is present for longer than normal. The APC normally forms in prometaphase and disassembles before anaphase; in mutants it may remain present during anaphase.","definition_xrefs":["PMID:24583014","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein complex organization during vegetative growth","termid":"FYPO:0007402"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"increased duration of anaphase-promoting complex presence","synonyms":[{"name":"APC present during mitotic anaphase","type":"narrow"},{"name":"increased duration of APC presence","type":"exact"},{"name":"increased duration of anaphase-promoting complex presence during mitotic cell cycle","type":"related"},{"name":"increased duration of anaphase-promoting complex presence during vegetative growth","type":"exact"},{"name":"increased persistence of anaphase-promoting complex","type":"related"}],"termid":"FYPO:0007403"}


id: PBO:0041552
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 19 open reading frame 18","termid":"PBO:0041552"}


id: MONDO:0022673
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant cataract","termid":"MONDO:0022672"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0000426"],"is_obsolete":false,"name":"autosomal dominant non-nuclear cataract","secondary_identifiers":["MEDGEN:318648","OMIM:601286","UMLS:C1832526","MESH:C538284"],"synonyms":[{"name":"CCP","type":"related"},{"name":"PCC","type":"related"},{"name":"autosomal dominant nonnuclear polymorphic congenital cataract","type":"related"},{"name":"cataract congenital dominant non nuclear","type":"related"},{"name":"cataract, Nonnuclear polymorphic congenital, autosomal dominant","type":"related"},{"name":"cataract, polymorphic congenital","type":"related"}],"termid":"MONDO:0022673","xrefs":{"Monarch":{"xref_id":"0022673"}}}


id: PBO:0027138
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_DNA/DNA_annealing_activity","termid":"PBO:0027138"}


id: GO:0052672
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (2E,6E,10E)-geranylgeraniol + CTP = (2E,6E,10E)-geranylgeranyl phosphate + CDP + H+.","definition_xrefs":["RHEA:63456"],"direct_ancestors":[{"relation_name":"is_a","term_name":"geranylgeraniol kinase activity","termid":"GO:0052671"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"CTP:geranylgeraniol kinase activity","secondary_identifiers":["MetaCyc:RXN-11629"],"synonyms":[{"name":"CTP:geranylgeraniol phosphotransferase activity","type":"exact"}],"termid":"GO:0052672"}


id: MONDO:0002988
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An aggressive malignant tumor of melanocytic origin that arises from the cervix.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mucosal melanoma","termid":"MONDO:0000544"},{"relation_name":"is_a","term_name":"cervical cancer","termid":"MONDO:0002974"}],"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":"cervix melanoma","secondary_identifiers":["DOID:4413","MEDGEN:163764","UMLS:C0877611","NCIT:C40239"],"synonyms":[{"name":"cervical melanoma","type":"exact"},{"name":"melanoma of the cervix","type":"exact"},{"name":"primary malignant melanoma of the cervix uteri","type":"related"},{"name":"primary malignant melanoma of the uterine cervix","type":"related"}],"termid":"MONDO:0002988","xrefs":{"Monarch":{"xref_id":"0002988"}}}


id: GO:0015736
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which hexuronate is transported across a lipid bilayer, from one side of a membrane to the other. A hexuronate is any monocarboxylic acid derived from a hexose by oxidation of C-6.","definition_xrefs":["GOC:ai","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"uronic acid transmembrane transport","termid":"GO:0015735"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0055085","GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"hexuronate transmembrane transport","synonyms":[{"name":"hexuronate transport","type":"related"}],"termid":"GO:0015736"}


id: PR:Q9HGM2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- get1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9HGM2"],"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":"protein get1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC543.10","synonyms":[{"name":"Spom972h-get1","type":"exact"},{"name":"guided entry of tail-anchored proteins 1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9HGM2"}


id: GO:0006363
data:
  {"annotated_genes":["SJAG_04855","SJAG_03689","SJAG_02922","SJAG_04106"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[96717,102597,114518,116288],"is_not":false,"summary":null,"term":"GO:0006363"}]},"cv_name":"biological_process","definition":"A transcription termination process that completes the production of a ribosomal RNA transcript. RNAP I termination requires binding of a terminator protein to specific sequences downstream of the transcription unit.","definition_xrefs":["PMID:27371117","GOC:txnOH","GOC:mah","PMID:10684922"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA-templated transcription termination","termid":"GO:0006353"},{"relation_name":"part_of","term_name":"transcription by RNA polymerase I","termid":"GO:0006360"}],"gene_count":4,"genes_by_uniquename":{"SJAG_02922":null,"SJAG_03689":null,"SJAG_04106":null,"SJAG_04855":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006351"}],"interesting_parent_ids":["GO:0006351","GO:0008150","GO:0010467"],"is_obsolete":false,"name":"termination of RNA polymerase I transcription","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0019223","Reactome:R-HSA-73863","GO:0001185"],"synonyms":[{"name":"RNA polymerase I transcription termination","type":"exact"},{"name":"RNA polymerase I transcription termination factor activity","type":"related"},{"name":"termination of RNA polymerase I transcription from promoter for nuclear large rRNA transcript","type":"narrow"},{"name":"transcription termination from Pol I promoter","type":"exact"},{"name":"transcription termination from RNA polymerase I promoter","type":"exact"}],"termid":"GO:0006363","terms_by_termid":{"GO:0006363":null}}


id: PBO:0116772
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TGF-beta induced TARBP2 interacting lncRNA","termid":"PBO:0116772"}


id: PATO:0001753
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A peramorphic growth quality which is due to an increased rate.","definition_xrefs":["PATOC:mh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peramorphic growth","termid":"PATO:0001752"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"accelerated growth","termid":"PATO:0001753"}


id: MONDO:0003097
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mediastinal neural neoplasm","termid":"MONDO:0003098"},{"relation_name":"is_a","term_name":"childhood neoplasm","termid":"MONDO:0021079"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"childhood mediastinal neurogenic neoplasm","secondary_identifiers":["DOID:4690","UMLS:C1332981","NCIT:C5429","MEDGEN:234134"],"synonyms":[{"name":"childhood mediastinal neurogenic neoplasm","type":"exact"},{"name":"childhood mediastinal neurogenic tumor","type":"exact"},{"name":"childhood mediastinal neurogenic tumour","type":"exact"},{"name":"childhood neurogenic neoplasm of mediastinum","type":"exact"},{"name":"childhood neurogenic neoplasm of the mediastinum","type":"exact"},{"name":"childhood neurogenic tumor of mediastinum","type":"exact"},{"name":"childhood neurogenic tumor of the mediastinum","type":"exact"},{"name":"childhood neurogenic tumour of mediastinum","type":"exact"},{"name":"childhood neurogenic tumour of the mediastinum","type":"exact"},{"name":"paediatric mediastinal neurogenic neoplasm","type":"exact"},{"name":"paediatric mediastinal neurogenic tumour","type":"exact"},{"name":"paediatric neurogenic neoplasm of mediastinum","type":"exact"},{"name":"paediatric neurogenic neoplasm of the mediastinum","type":"exact"},{"name":"paediatric neurogenic tumour of mediastinum","type":"exact"},{"name":"paediatric neurogenic tumour of the mediastinum","type":"exact"},{"name":"pediatric mediastinal neurogenic neoplasm","type":"exact"},{"name":"pediatric mediastinal neurogenic tumor","type":"exact"},{"name":"pediatric neurogenic neoplasm of mediastinum","type":"exact"},{"name":"pediatric neurogenic neoplasm of the mediastinum","type":"exact"},{"name":"pediatric neurogenic tumor of mediastinum","type":"exact"},{"name":"pediatric neurogenic tumor of the mediastinum","type":"exact"}],"termid":"MONDO:0003097","xrefs":{"Monarch":{"xref_id":"0003097"}}}


id: PBO:0085266
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Peroxin required for peroxisomal matrix protein targeting; acts on proteins containing the PTS2 targeting sequence; interacts with Pex7p; constitutively expressed; partially redundant with Pex18p; required for import of the Gpd1p-Pnc1p heterodimer in which only Gpd1p has a peroxisomal targeting signal; relative distribution to cytoplasmic foci increases upon DNA replication stress","termid":"PBO:0085266"}


id: PBO:0029054
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_degradation","termid":"PBO:0029054"}


id: PBO:0064808
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase 1 regulatory inhibitor subunit 2","termid":"PBO:0064808"}


id: GO:0031906
data:
  {"annotated_genes":["SJAG_02432"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[97961],"is_not":false,"summary":null,"term":"GO:0031906"}]},"cv_name":"cellular_component","definition":"The volume enclosed by the membrane of a late endosome.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endosome lumen","termid":"GO:0031904"},{"relation_name":"part_of","term_name":"late endosome","termid":"GO:0005770"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02432":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0031410"},{"rel_name":"part_of","termid":"GO:0005768"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005768","GO:0031410","GO:0005737"],"is_obsolete":false,"name":"late endosome lumen","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0031906","terms_by_termid":{"GO:0031906":null}}


id: PBO:0038343
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_eggs_laid_on_by","termid":"PBO:0038343"}


id: PBO:0090856
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleobase transmembrane transporter","termid":"PBO:0090856"}


id: MONDO:0005586
data:
  {"annotated_genes":["SJAG_03429","SJAG_03677","SJAG_03453"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87520],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014937"},{"annotations":[87082],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009050"},{"annotations":[86236],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008097"}]},"cv_name":"mondo","definition":"A benign or malignant neoplasm that affects the anatomic structures of the head and neck region. Representative examples of benign neoplasms include salivary gland pleomorphic adenoma and nasal cavity papilloma. Representative examples of malignant neoplasms include oral cavity squamous cell carcinoma, laryngeal squamous cell carcinoma, and salivary gland carcinoma.","definition_xrefs":["NCIT:C3077"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neoplasm","termid":"MONDO:0005070"}],"gene_count":3,"genes_by_uniquename":{"SJAG_03429":null,"SJAG_03453":null,"SJAG_03677":null},"genotype_count":0,"is_obsolete":false,"name":"head and neck neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0018671","ONCOTREE:HEADNECK","SCTID:255055008","EFO:0005950","ICD9:239.89","MEDGEN:6728"],"synonyms":[{"name":"craniocervical region neoplasm","type":"exact"},{"name":"craniocervical region neoplasm (disease)","type":"exact"},{"name":"craniocervical region tumor","type":"exact"},{"name":"craniocervical region tumour","type":"exact"},{"name":"head and neck neoplasm","type":"exact"},{"name":"head and neck neoplasm (excluding central nervous system)","type":"exact"},{"name":"head and neck tumor","type":"exact"},{"name":"head and neck tumour","type":"exact"},{"name":"neoplasm of craniocervical region","type":"exact"},{"name":"neoplasm of head and neck","type":"exact"},{"name":"neoplasm of the head and neck","type":"exact"},{"name":"tumor of craniocervical region","type":"exact"},{"name":"tumor of head and neck","type":"exact"},{"name":"tumor of the head and neck","type":"exact"},{"name":"tumour of craniocervical region","type":"exact"},{"name":"tumour of head and neck","type":"exact"},{"name":"tumour of the head and neck","type":"exact"}],"termid":"MONDO:0005586","terms_by_termid":{"MONDO:0008097":null,"MONDO:0009050":null,"MONDO:0014937":null},"xrefs":{"Monarch":{"xref_id":"0005586"}}}


id: PBO:0038485
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP binding cassette subfamily B member 10","termid":"PBO:0038485"}


id: MONDO:0958204
data:
  {"annotated_genes":["SJAG_00898"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87441],"is_not":false,"summary":null,"term":"MONDO:0958204"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive non-syndromic intellectual disability","termid":"MONDO:0019502"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00898":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0037792","MONDO:0005066","MONDO:0006025"],"is_obsolete":false,"name":"intellectual developmental disorder, autosomal recessive 81","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1844192","OMIM:620700","UMLS:C5882758"],"termid":"MONDO:0958204","terms_by_termid":{"MONDO:0958204":null},"xrefs":{"Monarch":{"xref_id":"0958204"}}}


id: CHEBI:192760
data:
  {"annotation_feature_type":"gene","cv_name":"chebi_ontology","definition":"A benzoate ester resulting from the formal condensation of the carboxy group of vanillic acid with the hydroxy group of cyclohexanol.","direct_ancestors":[{"relation_name":"is_a","term_name":"chemical entity","termid":"CHEBI:24431"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mochimganine","termid":"CHEBI:192760"}


id: PBO:0080184
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VDAC2 pseudogene 5","termid":"PBO:0080184"}


id: PBO:0087757
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the tRNA splicing endonuclease; tRNA splicing endonuclease (Sen complex) is composed of Sen2p, Sen15p, Sen34p, and Sen54p; Sen complex also cleaves the CBP1 mRNA at the mitochondrial surface; Sen2p contains the active site for tRNA 5' splice site cleavage and has similarity to Sen34p and to Archaeal tRNA splicing endonuclease;","termid":"PBO:0087757"}


id: PBO:0068134
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 441","termid":"PBO:0068134"}


id: PBO:0087582
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the Anaphase-Promoting Complex/Cyclosome (APC/C); APC/C is a ubiquitin-protein ligase required for degradation of anaphase inhibitors, including mitotic cyclins, during the metaphase/anaphase transition; component of the platform domain of the APC/C, based on structural analysis; relative distribution to nuclear foci decreases upon DNA replication stress","termid":"PBO:0087582"}


id: MONDO:0014942
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the GABRB1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"undetermined early-onset epileptic encephalopathy","termid":"MONDO:0018614"},{"relation_name":"is_a","term_name":"neonatal-onset developmental and epileptic encephalopathy","termid":"MONDO:0100455"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0700092"},{"rel_name":"is_a","termid":"MONDO:0005027"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004736","MONDO:0700092","MONDO:0005027"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy, 45","secondary_identifiers":["OMIM:617153","MEDGEN:934658","DOID:0080428","UMLS:C4310691","GARD:16203"],"synonyms":[{"name":"DEE45","type":"exact"},{"name":"EIEE45","type":"exact"},{"name":"GABRB1 early infantile epileptic encephalopathy","type":"exact"},{"name":"developmental and epileptic encephalopathy 45","type":"exact"},{"name":"early infantile epileptic encephalopathy caused by mutation in GABRB1","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 45","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 45; EIEE45","type":"exact"},{"name":"epileptic encephalopathy, early infantile, type 45","type":"exact"}],"termid":"MONDO:0014942","xrefs":{"Monarch":{"xref_id":"0014942"}}}


id: PBO:0085586
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in assembly and export of the large ribosomal subunit; nucleolar protein; constituent of 66S pre-ribosomal particles; contains a sigma(70)-like motif, which is thought to bind RNA","termid":"PBO:0085586"}


id: FYPO:0002863
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which cells elongate more slowly than normal when the cells are returned to nitrogen-rich medium following nitrogen starvation.","definition_xrefs":["PomBase:al","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell growth rate","termid":"FYPO:0006820"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"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:0005447","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"slow cell growth during recovery from nitrogen starvation","synonyms":[{"name":"slow cell growth during recovery from nitrogen depletion","type":"exact"},{"name":"slow cell growth during recovery from nitrogen deprivation","type":"exact"}],"termid":"FYPO:0002863"}


id: PBO:0039549
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ANKRD44 divergent transcript","termid":"PBO:0039549"}


id: MONDO:0002879
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A primary malignant neoplasm of the uterine corpus characterized by the presence of an epithelial and a mesenchymal component. This category includes carcinosarcoma, carcinofibroma, and adenosarcoma.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malignant mixed neoplasm","termid":"MONDO:0005853"},{"relation_name":"is_a","term_name":"uterine corpus cancer","termid":"MONDO:0006003"},{"relation_name":"is_a","term_name":"uterine corpus mixed epithelial and mesenchymal neoplasm","termid":"MONDO:0016255"}],"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 body mixed cancer","secondary_identifiers":["NCIT:C6311","UMLS:C1334628","MEDGEN:233163","DOID:4114"],"synonyms":[{"name":"malignant body of uterus mixed neoplasm","type":"exact"},{"name":"malignant body of uterus mixed tumor","type":"exact"},{"name":"malignant body of uterus mixed tumour","type":"exact"},{"name":"malignant corpus uteri mixed neoplasm","type":"exact"},{"name":"malignant corpus uteri mixed tumor","type":"exact"},{"name":"malignant corpus uteri mixed tumour","type":"exact"},{"name":"malignant mixed neoplasm of body of uterus","type":"exact"},{"name":"malignant mixed neoplasm of corpus uteri","type":"exact"},{"name":"malignant mixed neoplasm of the body of uterus","type":"exact"},{"name":"malignant mixed neoplasm of the corpus uteri","type":"exact"},{"name":"malignant mixed neoplasm of the uterine body","type":"exact"},{"name":"malignant mixed neoplasm of the uterine corpus","type":"exact"},{"name":"malignant mixed neoplasm of uterine body","type":"exact"},{"name":"malignant mixed neoplasm of uterine corpus","type":"exact"},{"name":"malignant mixed tumor of body of uterus","type":"exact"},{"name":"malignant mixed tumor of corpus uteri","type":"exact"},{"name":"malignant mixed tumor of the body of uterus","type":"exact"},{"name":"malignant mixed tumor of the corpus uteri","type":"exact"},{"name":"malignant mixed tumor of the uterine body","type":"exact"},{"name":"malignant mixed tumor of the uterine corpus","type":"exact"},{"name":"malignant mixed tumor of uterine body","type":"exact"},{"name":"malignant mixed tumor of uterine corpus","type":"exact"},{"name":"malignant mixed tumour of body of uterus","type":"exact"},{"name":"malignant mixed tumour of corpus uteri","type":"exact"},{"name":"malignant mixed tumour of the body of uterus","type":"exact"},{"name":"malignant mixed tumour of the corpus uteri","type":"exact"},{"name":"malignant mixed tumour of the uterine body","type":"exact"},{"name":"malignant mixed tumour of the uterine corpus","type":"exact"},{"name":"malignant mixed tumour of uterine body","type":"exact"},{"name":"malignant mixed tumour of uterine corpus","type":"exact"},{"name":"malignant uterine body mixed neoplasm","type":"exact"},{"name":"malignant uterine body mixed tumor","type":"exact"},{"name":"malignant uterine body mixed tumour","type":"exact"},{"name":"malignant uterine corpus mixed epithelial and mesenchymal neoplasm","type":"exact"},{"name":"malignant uterine corpus mixed tumor","type":"exact"},{"name":"malignant uterine corpus mixed tumour","type":"exact"}],"termid":"MONDO:0002879","xrefs":{"Monarch":{"xref_id":"0002879"}}}


id: MONDO:0100153
data:
  {"annotated_genes":["SJAG_04003"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87117],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010912"}]},"cv_name":"mondo","definition":"A nervous system disorder characterized by complex cortical malformations including in most cases dysmorphic basal ganglia and/or corpus callosum in which the cause of the disease is a variation in a tubulin gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene","DOID:0112227"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder","termid":"MONDO:0005071"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04003":null},"genotype_count":0,"is_obsolete":false,"name":"tubulinopathy","references_by_uniquename":{"PB_REF:0000006":null},"termid":"MONDO:0100153","terms_by_termid":{"MONDO:0010912":null},"xrefs":{"Monarch":{"xref_id":"0100153"}}}


id: PBO:0078272
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Cys (anticodon GCA) 8-1","termid":"PBO:0078272"}


id: PBO:0038997
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"apoptosis enhancing nuclease","termid":"PBO:0038997"}


id: GO:1990094
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The positive regulation of the receptor clustering process in which N-methyl-D-aspartate (NMDA) receptors are localized to distinct domains in the cell membrane.","definition_xrefs":["PMID:18442977"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of N-methyl-D-aspartate receptor clustering (obsolete GO:1990094)","synonyms":[{"name":"positive regulation of N-methyl-D-aspartate receptor clustering","type":"exact"},{"name":"positive regulation of NMDA receptor clustering","type":"exact"}],"termid":"GO:1990094"}


id: PBO:0065734
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PX domain containing 1","termid":"PBO:0065734"}


id: MONDO:0006875
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Abnormally high intraocular pressure.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypertensive disorder","termid":"MONDO:0005044"},{"relation_name":"is_a","term_name":"eye disorder","termid":"MONDO:0005328"}],"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 hypertension","secondary_identifiers":["icd11.foundation:535283437","UMLS:C0028840","MedDRA:10030043","DOID:9282","MEDGEN:10423","ICD9:365.04","MESH:D009798","SCTID:4210003","EFO:1001069"],"termid":"MONDO:0006875","xrefs":{"Monarch":{"xref_id":"0006875"}}}


id: PBO:0066254
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RBMX2 pseudogene 2","termid":"PBO:0066254"}


id: PBO:0058676
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6804","termid":"PBO:0058676"}


id: MONDO:0011996
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A chronic myeloproliferative neoplasm characterized by the expression of the BCR-ABL1 fusion gene. It presents with neutrophilic leukocytosis. It can appear at any age, but it mostly affects middle aged and older individuals. Patients usually present with fatigue, weight loss, anemia, night sweats, and splenomegaly. If untreated, it follows a biphasic or triphasic natural course; an initial indolent chronic phase which is followed by an accelerated phase, a blast phase, or both. Allogeneic stem cell transplantation and tyrosine kinase inhibitors delay disease progression and prolong overall survival.","definition_xrefs":["NCIT:C3174"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myeloid leukemia","termid":"MONDO:0004643"},{"relation_name":"is_a","term_name":"hereditary disorder of connective tissue","termid":"MONDO:0023603"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046","MONDO:0004992"],"is_obsolete":false,"name":"chronic myelogenous leukemia, BCR-ABL1 positive","secondary_identifiers":["ICD9:205.1","DOID:0081088","MedDRA:10009013","DOID:8552","MEDGEN:75993","UMLS:C0279543","NANDO:2200013","OMIM:608232","NCIT:C3177","ONCOTREE:CML","Orphanet:521","ICDO:9863/3","EFO:0000339","ICDO:9875/3","GARD:6105"],"synonyms":[{"name":"BCR-ABL Positive chronic myelogenous leukaemia","type":"exact"},{"name":"BCR-ABL Positive chronic myelogenous leukemia","type":"exact"},{"name":"CML","type":"exact"},{"name":"CML - chronic myelogenous leukaemia","type":"exact"},{"name":"CML - chronic myelogenous leukemia","type":"exact"},{"name":"chronic granulocytic leukaemia","type":"exact"},{"name":"chronic granulocytic leukemia","type":"exact"},{"name":"chronic myelocytic leukaemia","type":"exact"},{"name":"chronic myelocytic leukemia","type":"exact"},{"name":"chronic myelogenous leukaemia","type":"exact"},{"name":"chronic myelogenous leukaemia (CML)","type":"exact"},{"name":"chronic myelogenous leukemia","type":"exact"},{"name":"chronic myelogenous leukemia (CML)","type":"exact"},{"name":"chronic myelogenous leukemia, BCR-ABL1 Positive","type":"exact"},{"name":"chronic myelogenous leukemias","type":"exact"},{"name":"chronic myeloid leukaemia","type":"exact"},{"name":"chronic myeloid leukemia","type":"exact"},{"name":"hematopoeitic - chronic myelocytic leukaemia (CML)","type":"exact"},{"name":"hematopoeitic - chronic myelocytic leukemia (CML)","type":"exact"},{"name":"leukemia, Philadelphia chromosome-positive, resistant to imatinib, Somatic mutation","type":"exact"},{"name":"leukemia, chronic myelogenous","type":"related"},{"name":"leukemia, chronic myeloid","type":"related"},{"name":"leukemia, chronic myeloid, Philadelphia chromosome positive, somatic","type":"exact"},{"name":"leukemia, chronic myeloid, atypical","type":"related"},{"name":"myeloid leukemia, chronic","type":"exact"}],"termid":"MONDO:0011996","xrefs":{"Monarch":{"xref_id":"0011996"}}}


id: PBO:0068069
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 374","termid":"PBO:0068069"}


id: PBO:0049617
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H3 histone pseudogene 20","termid":"PBO:0049617"}


id: PBO:0061840
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"8-oxoguanine DNA glycosylase","termid":"PBO:0061840"}


id: MONDO:0005219
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Fibrosis associated with cyst formation in the breast parenchyma.","definition_xrefs":["NCIT:C3039"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"breast benign neoplasm","termid":"MONDO:0000620"},{"relation_name":"is_a","term_name":"breast disorder","termid":"MONDO:0002657"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"breast fibrocystic disease","secondary_identifiers":["UMLS:C0016034","EFO:0003014","ICD9:610.1","MEDGEN:42015","MESH:D005348","DOID:10354"],"synonyms":[{"name":"benign breast disease","type":"exact"},{"name":"breast fibrocystic change","type":"exact"},{"name":"cystic disease of breast","type":"exact"},{"name":"cystic disease of the breast","type":"exact"},{"name":"diffuse cystic mastopathy","type":"exact"},{"name":"fibrocystic breast","type":"exact"},{"name":"fibrocystic breast changes","type":"exact"},{"name":"fibrocystic breast disease","type":"exact"},{"name":"fibrocystic change of breast","type":"exact"},{"name":"fibrocystic change of the breast","type":"exact"},{"name":"fibrocystic disease","type":"exact"},{"name":"fibrocystic disease of breast","type":"exact"},{"name":"fibrocystic disease of the breast","type":"exact"},{"name":"fibrocystic mastopathy","type":"exact"},{"name":"mammary dysplasia","type":"exact"}],"termid":"MONDO:0005219","xrefs":{"Monarch":{"xref_id":"0005219"}}}


id: GO:0019743
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of hopanoids, pentacyclic sterol-like compounds based on the hopane nucleus.","definition_xrefs":["ISBN:0198547684"],"direct_ancestors":[{"relation_name":"is_a","term_name":"triterpenoid catabolic process","termid":"GO:0016105"},{"relation_name":"is_a","term_name":"hopanoid metabolic process","termid":"GO:0019744"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"hopanoid catabolic process","synonyms":[{"name":"hopanoid breakdown","type":"exact"},{"name":"hopanoid catabolism","type":"exact"},{"name":"hopanoid degradation","type":"exact"}],"termid":"GO:0019743"}


id: PBO:0078900
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Gln (anticodon CTG) 9-1","termid":"PBO:0078900"}


id: PBO:0044935
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"D-glutamate cyclase","termid":"PBO:0044935"}


id: MONDO:0011269
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any psoriasis in which the cause of the disease is a mutation in the CARD14 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"psoriasis","termid":"MONDO:0005083"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005046"],"is_obsolete":false,"name":"psoriasis 2","secondary_identifiers":["MEDGEN:351141","DOID:0080475","OMIM:602723","NANDO:2200443","UMLS:C1864497"],"synonyms":[{"name":"CARD14 psoriasis","type":"exact"},{"name":"PSORS2","type":"related"},{"name":"psoriasis 2","type":"exact"},{"name":"psoriasis caused by mutation in CARD14","type":"exact"},{"name":"psoriasis type 2","type":"exact"}],"termid":"MONDO:0011269","xrefs":{"Monarch":{"xref_id":"0011269"}}}


id: PBO:0081039
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger CCCH-type containing 15","termid":"PBO:0081039"}


id: MONDO:0030748
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"junctional epidermolysis bullosa","termid":"MONDO:0017612"}],"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":"epidermolysis bullosa, junctional 3A, intermediate","secondary_identifiers":["UMLS:C5676938","OMIM:619785","MEDGEN:1812940"],"synonyms":[{"name":"JEB3A","type":"exact"},{"name":"epidermolysis bullosa, junctional 3A, generalised intermediate","type":"exact"},{"name":"epidermolysis bullosa, junctional 3A, generalized intermediate","type":"exact"},{"name":"epidermolysis bullosa, junctional 3A, intermediate","type":"exact"},{"name":"epidermolysis bullosa, junctional 3A, non-herlitz IIA","type":"exact"}],"termid":"MONDO:0030748","xrefs":{"Monarch":{"xref_id":"0030748"}}}


id: GO:1903061
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of protein lipidation.","definition_xrefs":["GOC:rph","GO_REF:0000058","GOC:TermGenie","PMID:21909394"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein modification process","termid":"GO:0031401"},{"relation_name":"is_a","term_name":"positive regulation of lipoprotein metabolic process","termid":"GO:0050747"},{"relation_name":"is_a","term_name":"regulation of protein lipidation","termid":"GO:1903059"},{"relation_name":"positively_regulates","term_name":"protein lipidation","termid":"GO:0006497"}],"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 protein lipidation","synonyms":[{"name":"activation of lipid:protein modification","type":"narrow"},{"name":"activation of protein amino acid lipidation","type":"narrow"},{"name":"activation of protein lipidation","type":"narrow"},{"name":"positive regulation of lipid:protein modification","type":"exact"},{"name":"positive regulation of protein amino acid lipidation","type":"exact"},{"name":"up regulation of lipid:protein modification","type":"exact"},{"name":"up regulation of protein amino acid lipidation","type":"exact"},{"name":"up regulation of protein lipidation","type":"exact"},{"name":"up-regulation of lipid:protein modification","type":"exact"},{"name":"up-regulation of protein amino acid lipidation","type":"exact"},{"name":"up-regulation of protein lipidation","type":"exact"},{"name":"upregulation of lipid:protein modification","type":"exact"},{"name":"upregulation of protein amino acid lipidation","type":"exact"},{"name":"upregulation of protein lipidation","type":"exact"}],"termid":"GO:1903061"}


id: PBO:0003869
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"copper transporting ATPase Ccc2 (predicted)","termid":"PBO:0003869"}


id: PBO:0060393
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitotic spindle organizing protein 2A","termid":"PBO:0060393"}


id: PBO:0042922
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclic GMP-AMP synthase","termid":"PBO:0042922"}


id: PBO:0072509
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein SA pseudogene 38","termid":"PBO:0072509"}


id: MONDO:0000714
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete crest syndrome (obsolete MONDO:0000714)","termid":"MONDO:0000714","xrefs":{"Monarch":{"xref_id":"0000714"}}}


id: PBO:0000457
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tryptophan-tRNA ligase Wrs1 (predicted)","termid":"PBO:0000457"}


id: PBO:0109952
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 51 member A","termid":"PBO:0109952"}


id: PBO:0079415
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tubulin beta 8 class VIII pseudogene 9","termid":"PBO:0079415"}


id: PBO:0085272
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Peroxisomal importomer complex component; integral peroxisomal membrane protein required for docking and translocation of peroxisomal matrix proteins; interacts with the PTS1 signal recognition factor Pex5p and the PTS2 signal recognition factor Pex7p; forms a complex with Pex14p and Pex17p; human homolog PEX13 complements yeast null mutant","termid":"PBO:0085272"}


id: PBO:0109965
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SNX7 divergent transcript","termid":"PBO:0109965"}


id: PR:Q10326
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mug8 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q10326"],"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":"meiotically up-regulated gene 8 protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC32A11.01","synonyms":[{"name":"Spom972h-mug8","type":"exact"}],"termid":"PR:Q10326"}


id: MONDO:0008449
data:
  {"annotated_genes":["SJAG_04156","SJAG_03712","SJAG_04042","SJAG_00106","SJAG_01466","SJAG_04425","SJAG_04459"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87702,87704,87707,87703,87701,87705,87706],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011120"}]},"cv_name":"mondo","definition":"A congenital neural tube defect in which vertebrae are not fully formed. It results in the protrusion of the spinal cord through the opening of the vertebrae.","definition_xrefs":["NCIT:C101214"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"spinal cord disorder","termid":"MONDO:0002545"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00106":null,"SJAG_01466":null,"SJAG_03712":null,"SJAG_04042":null,"SJAG_04156":null,"SJAG_04425":null,"SJAG_04459":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"spina bifida","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD9:741","MESH:D016135","EFO:0003105","HP:0002414","icd11.foundation:2036217905","DOID:0080016","UMLS:C0080178","MEDGEN:38283","SCTID:67531005"],"synonyms":[{"name":"NTD","type":"related"},{"name":"neural tube defects, susceptibility to","type":"related"},{"name":"rachischisis","type":"exact"},{"name":"spina bifida","type":"exact"},{"name":"spina bifida (disease)","type":"exact"},{"name":"spinal meningocele","type":"exact"},{"name":"spinal myelocele","type":"exact"},{"name":"spinal myelomeningocele","type":"exact"}],"termid":"MONDO:0008449","terms_by_termid":{"MONDO:0011120":null},"xrefs":{"Monarch":{"xref_id":"0008449"}}}


id: GO:0034174
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by a ligand binding to the endolysosomal toll-like receptor 12.","definition_xrefs":["GOC:add","PMID:17328678","PMID:16551253"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endolysosomal toll-like receptor signaling pathway","termid":"GO:0140894"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"toll-like receptor 12 signaling pathway","synonyms":[{"name":"TLR12 signaling pathway","type":"exact"},{"name":"toll-like receptor 12 signalling pathway","type":"exact"}],"termid":"GO:0034174"}


id: GO:0047401
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + trithionate = H+ + sulfate + thiosulfate.","definition_xrefs":["RHEA:21884"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on acid sulfur-sulfur bonds","termid":"GO:0016828"}],"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:0003674","GO:0016787","GO:0003824"],"is_obsolete":false,"name":"trithionate hydrolase activity","secondary_identifiers":["EC:3.12.1.1","MetaCyc:3.12.1.1-RXN","KEGG_REACTION:R01930"],"synonyms":[{"name":"trithionate thiosulfohydrolase activity","type":"related"}],"termid":"GO:0047401"}


id: GO:0140631
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binds to and stops, prevents or reduces the activity of aldehyde dehydrogenase (NAD+).","definition_xrefs":["PMID:33495566"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme inhibitor activity","termid":"GO:0004857"},{"relation_name":"negatively_regulates","term_name":"aldehyde dehydrogenase (NAD+) activity","termid":"GO:0004029"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0004857"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"negatively_regulates","termid":"GO:0016491"},{"rel_name":"negatively_regulates","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140678"},{"rel_name":"regulates","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0004857","GO:0140678","GO:0030234","GO:0016491","GO:0098772","GO:0003674"],"is_obsolete":false,"name":"aldehyde dehydrogenase (NAD+) inhibitor activity","termid":"GO:0140631"}


id: PBO:0063886
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PIGO antisense RNA 1","termid":"PBO:0063886"}


id: GO:0061011
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the hepatic duct over time, from its formation to the mature structure. The hepatic duct is the duct that leads from the liver to the common bile duct.","definition_xrefs":["PMID:20614624","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"common bile duct development","termid":"GO:0061009"}],"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":"hepatic duct development","termid":"GO:0061011"}


id: MONDO:0009554
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any 3MC syndrome in which the cause of the disease is a mutation in the COLEC10 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"3MC syndrome","termid":"MONDO:0017398"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3MC syndrome 3","secondary_identifiers":["Orphanet:2453","DOID:0060577","UMLS:C0796032","MEDGEN:208657","GARD:8531","MESH:C535704","OMIM:248340"],"synonyms":[{"name":"3MC syndrome 3","type":"exact"},{"name":"3MC syndrome caused by mutation in COLEC10","type":"exact"},{"name":"3MC syndrome type 3","type":"exact"},{"name":"3MC3","type":"related"},{"name":"3Mc syndrome type 3","type":"exact"},{"name":"COLEC10 3MC syndrome","type":"exact"},{"name":"Malpuech Facial clefting syndrome","type":"related"},{"name":"Malpuech Facial clefting syndrome, formerly","type":"related"},{"name":"facial clefting syndrome, Gypsy type","type":"related"}],"termid":"MONDO:0009554","xrefs":{"Monarch":{"xref_id":"0009554"}}}


id: GO:0048106
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Orientation along the body surface of bristles, sensory organs originating from a sensory organ precursor cell, such that they all point in a uniform direction.","definition_xrefs":["GOC:tb","GOC:jid","GOC:ascb_2009","FBbt:00004298","FBbt:00004408","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment of body hair or bristle planar orientation","termid":"GO:0048104"},{"relation_name":"part_of","term_name":"chaeta morphogenesis","termid":"GO:0008407"}],"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":"establishment of thoracic bristle planar orientation","synonyms":[{"name":"establishment of body bristle planar orientation","type":"exact"}],"termid":"GO:0048106"}


id: MONDO:0000152
data:
  {"annotated_genes":["SJAG_00835","SJAG_03362"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85927],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011790"},{"annotations":[86995],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013761"},{"annotations":[87374],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013382"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of thiamine metabolism and transport","termid":"MONDO:0017578"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00835":null,"SJAG_03362":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"thiamine-responsive dysfunction syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIMPS:249270"],"synonyms":[{"name":"thiamine-responsive dysfunction syndrome","type":"exact"}],"termid":"MONDO:0000152","terms_by_termid":{"MONDO:0011790":null,"MONDO:0013382":null,"MONDO:0013761":null},"xrefs":{"Monarch":{"xref_id":"0000152"}}}


id: PBO:0046507
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ERICH2 divergent transcript","termid":"PBO:0046507"}


id: PR:O74413
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A chorismate synthase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO04860"],"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":"chorismate synthase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1223.14","secondary_identifiers":["UniProtKB:O74413"],"synonyms":[{"name":"5-enolpyruvylshikimate-3-phosphate phospholyase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-aroC","type":"exact"}],"termid":"PR:O74413"}


id: GO:0032935
data:
  {"annotated_genes":["SJAG_03715"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[115208],"is_not":false,"summary":null,"term":"GO:0032935"}]},"cv_name":"molecular_function","definition":"Binding to and responding, e.g. by conformational change, to changes in the cellular level of a sterol.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipid sensor activity","termid":"GO:0106254"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03715":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0140299"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0098772","GO:0140299","GO:0003674"],"is_obsolete":false,"name":"sterol sensor activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"sterol sensing activity","type":"exact"},{"name":"sterol-sensing domain","type":"narrow"}],"termid":"GO:0032935","terms_by_termid":{"GO:0032935":null}}


id: PBO:0045968
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"early growth response 1","termid":"PBO:0045968"}


id: PBO:0045915
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EFCAB10 antisense RNA 1","termid":"PBO:0045915"}


id: PBO:0001620
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribose-phosphate pyrophosphokinase (predicted)","termid":"PBO:0001620"}


id: GO:0046993
data:
  {"annotated_genes":["SJAG_00832"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[103944],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061686"}]},"cv_name":"molecular_function","definition":"Catalysis of an oxidation-reduction (redox) reaction in which X-H and Y-H form X-Y and the acceptor is oxygen.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on X-H and Y-H to form an X-Y bond","termid":"GO:0046992"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00832":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"oxidoreductase activity, acting on X-H and Y-H to form an X-Y bond, with oxygen as acceptor","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["EC:1.21.3.-"],"termid":"GO:0046993","terms_by_termid":{"GO:0061686":null}}


id: FYPO:0005094
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell cycle checkpoint phenotype in which the duration of cell cycle arrest or delay due to regulation by the S-phase DNA damage checkpoint is lower than in wild type during a cellular response to hydroxyurea.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic cell cycle regulation during cellular response to hydroxyurea","termid":"FYPO:0001933"},{"relation_name":"is_a","term_name":"decreased duration of S-phase DNA damage checkpoint","termid":"FYPO:0004371"}],"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:0000298"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000298","FYPO:0005447","FYPO:0001985","FYPO:0001320","FYPO:0000631"],"is_obsolete":false,"name":"decreased duration of S-phase DNA damage checkpoint during cellular response to hydroxyurea","synonyms":[{"name":"decreased duration of S-phase DNA damage checkpoint activation during cellular response to hydroxyurea","type":"exact"},{"name":"decreased duration of S-phase DNA damage checkpoint during cellular response to HU","type":"exact"},{"name":"decreased duration of S-phase DNA damage checkpoint during cellular response to hydroxyurea during mitotic cell cycle","type":"exact"},{"name":"decreased duration of S-phase DNA damage checkpoint during cellular response to hydroxyurea during vegetative growth","type":"exact"},{"name":"decreased duration of intra-S DNA damage checkpoint during cellular response to hydroxyurea","type":"exact"},{"name":"decreased duration of mitotic S-phase DNA damage checkpoint during cellular response to hydroxyurea","type":"exact"},{"name":"premature S-phase DNA damage checkpoint deactivation during cellular response to hydroxyurea","type":"related"},{"name":"reduced duration of S-phase DNA damage checkpoint during cellular response to hydroxyurea","type":"exact"}],"termid":"FYPO:0005094"}


id: PBO:0081199
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger with KRAB and SCAN domains 1","termid":"PBO:0081199"}


id: GO:0051231
data:
  {"annotated_genes":["SJAG_00794","SJAG_02624","SJAG_01297","SJAG_04003","SJAG_00930","SJAG_03073","SJAG_01215","SJAG_02336","SJAG_04841","SJAG_02761","SJAG_01224","SJAG_03048","SJAG_04597","SJAG_00082","SJAG_04745","SJAG_01613","SJAG_02246","SJAG_00773","SJAG_03540","SJAG_04464","SJAG_00244"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[95644,76116,78190],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000073"},{"annotations":[101754],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051232"},{"annotations":[118963,118450,107740],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000022"},{"annotations":[100707,103862,95109],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061805"},{"annotations":[100181,101760,97614,98951,100708,104217,108576],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061804"},{"annotations":[97615,77543,109170,99557,95111],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051256"},{"annotations":[102686],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1902845"},{"annotations":[90342,94750],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1902846"},{"annotations":[111327],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0032888"},{"annotations":[115352],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0110162"}]},"cv_name":"biological_process","definition":"The cell cycle process in which the distance is lengthened between poles of the spindle.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microtubule-based process","termid":"GO:0007017"},{"relation_name":"is_a","term_name":"cell cycle process","termid":"GO:0022402"},{"relation_name":"part_of","term_name":"spindle organization","termid":"GO:0007051"},{"relation_name":"part_of","term_name":"nuclear chromosome segregation","termid":"GO:0098813"}],"gene_count":21,"genes_by_uniquename":{"SJAG_00082":null,"SJAG_00244":null,"SJAG_00773":null,"SJAG_00794":null,"SJAG_00930":null,"SJAG_01215":null,"SJAG_01224":null,"SJAG_01297":null,"SJAG_01613":null,"SJAG_02246":null,"SJAG_02336":null,"SJAG_02624":null,"SJAG_02761":null,"SJAG_03048":null,"SJAG_03073":null,"SJAG_03540":null,"SJAG_04003":null,"SJAG_04464":null,"SJAG_04597":null,"SJAG_04745":null,"SJAG_04841":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007010"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0000226"}],"interesting_parent_ids":["GO:0008150","GO:0007010","GO:0007049","GO:0000226"],"is_obsolete":false,"name":"spindle elongation","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0051231","terms_by_termid":{"GO:0000022":null,"GO:0000073":null,"GO:0032888":null,"GO:0051232":null,"GO:0051256":null,"GO:0061804":null,"GO:0061805":null,"GO:0110162":null,"GO:1902845":null,"GO:1902846":null}}


id: PR:P87154
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A DNA polymerase epsilon catalytic subunit A that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03630","PRO:DNx","PANTHER:PTHR10670:SF0"],"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":"DNA polymerase epsilon catalytic subunit A (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC25H2.13c","secondary_identifiers":["UniProtKB:P87154"],"synonyms":[{"name":"DNA polymerase II subunit A (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-POLE","type":"exact"}],"termid":"PR:P87154"}


id: GO:0006837
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of serotonin into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. Serotonin (5-hydroxytryptamine) is a monoamine neurotransmitter occurring in the peripheral and central nervous systems.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monoamine transport","termid":"GO:0015844"},{"relation_name":"is_a","term_name":"organic hydroxy compound transport","termid":"GO:0015850"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"serotonin transport","termid":"GO:0006837"}


id: PBO:0066684
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring finger protein, LIM domain interacting pseudogene 2","termid":"PBO:0066684"}


id: GO:0003309
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which relatively unspecialized cells acquire specialized structural and/or functional features of a type B pancreatic cell. A type B pancreatic cell is a cell located towards center of the islets of Langerhans that secretes insulin.","definition_xrefs":["GOC:dph","CL:0000169","PMID:11076772"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enteroendocrine cell differentiation","termid":"GO:0035883"},{"relation_name":"part_of","term_name":"endocrine pancreas development","termid":"GO:0031018"}],"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":"type B pancreatic cell differentiation","synonyms":[{"name":"pancreatic B cell differentiation","type":"exact"},{"name":"pancreatic beta cell differentiation","type":"exact"}],"termid":"GO:0003309"}


id: FYPO:0008302
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed during prophase of the first division of the meiotic cell cycle in which the localization of a protein to discrete regions in the nucleus, visible as foci or dots by microscopy, is abolished.","definition_xrefs":["PomBase:pc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal punctate nuclear protein localization during meiotic prophase I","termid":"FYPO:0008300"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"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:0001985","FYPO:0000138","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"abolished punctate nuclear protein localization during meiotic prophase I","termid":"FYPO:0008302"}


id: PBO:0083728
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential 3-hydroxyacyl-CoA dehydratase of the ER membrane; involved in elongation of very long-chain fatty acids; evolutionarily conserved, similar to mammalian PTPLA and PTPLB; involved in sphingolipid biosynthesis and protein trafficking","termid":"PBO:0083728"}


id: MONDO:0021851
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A syndrome characterized by total alopecia (hair loss), total vitíligo, and nail changes. The nail changes consist of fine pitting, associated with softness, and friability and may include horizontal splitting. The vitiligo is characterized by complete, rapid uniform loss of pigment which occurs without going through a patchy state. The entire cutaneous surface is light and translucent-appearing and is prone to burning on exposure to the sun.","definition_xrefs":["PMID:14043609"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alopecia","termid":"MONDO:0004907"},{"relation_name":"is_a","term_name":"vitiligo","termid":"MONDO:0008661"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005093"],"is_obsolete":false,"name":"alopecia universalis onychodystrophy vitiligo","secondary_identifiers":["MESH:C537056","UMLS:C2931408","GARD:615","MEDGEN:444049"],"synonyms":[{"name":"alopecia universalis, onychodystrophy, and total vitiligo","type":"related"}],"termid":"MONDO:0021851","xrefs":{"Monarch":{"xref_id":"0021851"}}}


id: PBO:0083020
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Deleted ORF; does not encode a protein; included in the original annotation of Chromosome I but later withdrawn","termid":"PBO:0083020"}


id: PBO:0030814
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_isocitrate_dehydrogenase_(NAD+)_activity","termid":"PBO:0030814"}


id: PBO:0047899
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fragile site, aphidicolin type, common, fra(7)(q22)","termid":"PBO:0047899"}


id: FYPO:0006022
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which the size, shape, or structure of the spindle pole body is abnormal during the first meiotic nuclear division.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal spindle pole body morphology during meiotic cell cycle","termid":"FYPO:0006406"},{"relation_name":"output_of","term_name":"abnormal prospore-specific spindle pole body remodeling","termid":"FYPO:0003561"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0000054"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"output_of","termid":"FYPO:0000121"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000631","FYPO:0000054","FYPO:0000121","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"abnormal spindle pole body morphology during meiosis I","synonyms":[{"name":"abnormal SPB morphology during meiosis I","type":"exact"},{"name":"abnormal spindle pole body morphology during first meiotic nuclear division","type":"exact"},{"name":"abnormal spindle pole body structure during meiosis I","type":"narrow"}],"termid":"FYPO:0006022"}


id: PBO:0001383
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Polo kinase Plo1","termid":"PBO:0001383"}


id: PBO:0087217
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S-AdoMet-dependent methyltransferase involved in lipid homeostasis; mediates resistance to a drug cantharidin","termid":"PBO:0087217"}


id: PBO:0058469
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5571","termid":"PBO:0058469"}


id: GO:0008526
data:
  {"annotated_genes":["SJAG_03721","SJAG_03741","SJAG_03746","SJAG_01225","SJAG_03172"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[70407,73604,74886,76657,76940],"is_not":false,"summary":null,"term":"GO:0008526"}]},"cv_name":"molecular_function","definition":"Removes phosphatidylinositol from a membrane or a monolayer lipid particle, transports it through the aqueous phase while protected in a hydrophobic pocket, and brings it to an acceptor membrane or lipid particle.","definition_xrefs":["PMID:25797198","PMID:20823909","GOC:krc","PMID:24220498"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phospholipid transfer activity","termid":"GO:0120014"}],"gene_count":5,"genes_by_uniquename":{"SJAG_01225":null,"SJAG_03172":null,"SJAG_03721":null,"SJAG_03741":null,"SJAG_03746":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0120013"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0120013"],"is_obsolete":false,"name":"phosphatidylinositol transfer activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-8874470","Reactome:R-HSA-1483229","Reactome:R-HSA-8869241","GO:0120018"],"synonyms":[{"name":"intermembrane phosphatidylinositol transfer activity","type":"narrow"},{"name":"intermembrane phosphotidylinositol transfer activity","type":"narrow"},{"name":"phosphatidylinositol carrier activity","type":"exact"},{"name":"phosphatidylinositol transporter activity","type":"broad"}],"termid":"GO:0008526","terms_by_termid":{"GO:0008526":null}}


id: PBO:0088572
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial carrier, ATP:ADP antiporter","termid":"PBO:0088572"}


id: PBO:0072897
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SR-related CTD associated factor 1","termid":"PBO:0072897"}


id: SO:0000609
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The string of non-encoded U's at the 3' end of a guide RNA (SO:0000602).","direct_ancestors":[{"relation_name":"adjacent_to","term_name":"guide_RNA","termid":"SO:0000602"},{"relation_name":"is_a","term_name":"biological_region","termid":"SO:0001411"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oligo_U_tail","synonyms":[{"name":"oligo U tail","type":"exact"}],"termid":"SO:0000609"}


id: GO:0005308
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of creatine from one side of a membrane to the other. Creatine is a compound synthesized from the amino acids arginine, glycine, and methionine that occurs in muscle.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxylic acid transmembrane transporter activity","termid":"GO:0046943"},{"relation_name":"is_a","term_name":"modified amino acid transmembrane transporter activity","termid":"GO:0072349"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"creatine transmembrane transporter activity","termid":"GO:0005308"}


id: PBO:0050862
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inhibitor of DNA binding 1","termid":"PBO:0050862"}


id: PBO:0047424
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Fc alpha and mu receptor","termid":"PBO:0047424"}


id: PBO:0113172
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Invertase; sucrose hydrolyzing enzyme; seven closely related but non-identical invertase genes have been described in yeast (SUC1-5, 7, 8) but only SUC2 is in the reference strain (S288C); mapped to 146.0 cM on chrII","termid":"PBO:0113172"}


id: PBO:0069142
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 393, pseudogene","termid":"PBO:0069142"}


id: GO:0023062
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which a signal is conveyed via transcytosis. Transcytosis is the directed movement of endocytosed material through the cell and its exocytosis from the plasma membrane at the opposite side.","definition_xrefs":["ISBN:0716731363","GOC:mtg_signal"],"gene_count":0,"genotype_count":0,"name":"obsolete signal transmission via transcytosis (obsolete GO:0023062)","synonyms":[{"name":"signal transmission via transcytosis","type":"exact"}],"termid":"GO:0023062"}


id: PBO:0058775
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 7109","termid":"PBO:0058775"}


id: PBO:0056995
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 34b","termid":"PBO:0056995"}


id: CHEBI:17345
data:
  {"annotation_feature_type":"gene","cv_name":"chebi_ontology","direct_ancestors":[{"relation_name":"is_a","term_name":"chemical entity","termid":"CHEBI:24431"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GMP","termid":"CHEBI:17345"}


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","MEDGEN:895482","UMLS:C4225302","OMIM:616505"],"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: GO:0098781
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The transcription of non (protein) coding RNA from a DNA template.","definition_xrefs":["GOC:dos"],"gene_count":0,"genotype_count":0,"name":"obsolete ncRNA transcription (obsolete GO:0098781)","termid":"GO:0098781"}


id: PR:P41888
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- tnr3 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P41888"],"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":"thiamine pyrophosphokinase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC6F12.05c","synonyms":[{"name":"Spom972h-tnr3","type":"exact"},{"name":"TPK (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"thiamine kinase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P41888"}


id: PBO:0036093
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_histone_H4-K12_acetylation_during_vegetative_growth","termid":"PBO:0036093"}


id: PBO:0089822
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ndc80 complex subunit Spc24","termid":"PBO:0089822"}


id: GO:0044672
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A multifunctional enzyme complex composed of five different polypeptides that catalyzes the decarbonylation of acetyl-CoA, cleaves the C-C and C-S bonds in the acetyl moiety of acetyl-CoA, oxidizes the carbonyl group to CO2 and transfers the methyl group to tetrahydrosarcinapterin. These reactions are important for methanogenesis.","definition_xrefs":["GOC:mengo_curators","PMID:8955306","PMID:7693685","PMID:11607176"],"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":"acetyl-CoA decarbonylase/synthase-carbon monoxide dehydrogenase complex","synonyms":[{"name":"CO dehydrogenase complex","type":"broad"},{"name":"CO dehydrogenase/acetyl-CoA synthase complex","type":"exact"},{"name":"CODH","type":"broad"},{"name":"CODH/ACS complex","type":"exact"},{"name":"carbon monoxide dehydrogenase","type":"broad"},{"name":"carbon-monoxide:(acceptor) oxidoreductase complex","type":"broad"}],"termid":"GO:0044672"}


id: MONDO:0018259
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"melanocytic nevus","termid":"MONDO:0005073"}],"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":"didymosis aplasticosebacea","secondary_identifiers":["Orphanet:370046","UMLS:C4751600","GARD:21591","MEDGEN:1650408"],"synonyms":[{"name":"aplasia cutis congenita-nevus sebaceus syndrome","type":"exact"}],"termid":"MONDO:0018259","xrefs":{"Monarch":{"xref_id":"0018259"}}}


id: PBO:0089564
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit S17","termid":"PBO:0089564"}


id: GO:1905445
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of clathrin coat assembly.","definition_xrefs":["PMID:15533940","GO_REF:0000058","GOC:PARL","GOC:TermGenie","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein-containing complex assembly","termid":"GO:0031334"},{"relation_name":"is_a","term_name":"regulation of clathrin coat assembly","termid":"GO:1905443"},{"relation_name":"positively_regulates","term_name":"clathrin coat assembly","termid":"GO:0048268"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0065003"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"positively_regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0065003"}],"interesting_parent_ids":["GO:0044085","GO:0065003","GO:0008150"],"is_obsolete":false,"name":"positive regulation of clathrin coat assembly","synonyms":[{"name":"activation of clathrin cage assembly","type":"narrow"},{"name":"activation of clathrin coat assembly","type":"narrow"},{"name":"positive regulation of clathrin cage assembly","type":"exact"},{"name":"up regulation of clathrin cage assembly","type":"exact"},{"name":"up regulation of clathrin coat assembly","type":"exact"},{"name":"up-regulation of clathrin cage assembly","type":"exact"},{"name":"up-regulation of clathrin coat assembly","type":"exact"},{"name":"upregulation of clathrin cage assembly","type":"exact"},{"name":"upregulation of clathrin coat assembly","type":"exact"}],"termid":"GO:1905445"}


id: PBO:0088467
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dolichyl pyrophosphate Man7GlcNAc2 alpha-1,6-mannosyltransferase Alg12","termid":"PBO:0088467"}


id: MONDO:0010445
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete McLeod syndrome (obsolete MONDO:0010445)","termid":"MONDO:0010445","xrefs":{"Monarch":{"xref_id":"0010445"}}}


id: PBO:0054821
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 2234","termid":"PBO:0054821"}


id: PBO:0074400
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small integral membrane protein 9","termid":"PBO:0074400"}


id: GO:0102934
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: germacra-1(10),4,11(13)-trien-12-oate + O2 + NADPH + 2 H+ = costunolide + 2 H2O + NADP.","definition_xrefs":["RHEA:28230","GOC:pz"],"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:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"costunolide synthase activity","secondary_identifiers":["EC:1.14.14.150","MetaCyc:RXN-8971"],"termid":"GO:0102934"}


id: PBO:0027988
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_after_spore_germination,_without_cell_division,_abnormal_septum_morphology,_enlarged_nucleus","termid":"PBO:0027988"}


id: GO:0075217
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of spore encystment on host. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell development","termid":"GO:0010721"},{"relation_name":"is_a","term_name":"modulation of spore encystment on host","termid":"GO:0075215"},{"relation_name":"negatively_regulates","term_name":"spore encystment","termid":"GO:0075214"}],"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 spore encystment on host","termid":"GO:0075217"}


id: PBO:0090143
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translation initiation factor","termid":"PBO:0090143"}


id: PBO:0000473
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SAGA complex ubiquitin C-terminal hydrolase Ubp8","termid":"PBO:0000473"}


id: GO:1905207
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cardiocyte differentiation.","definition_xrefs":["GO_REF:0000058","GOC:BHF_miRNA","PMID:23069713","GOC:bc","GOC:BHF","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell differentiation","termid":"GO:0045595"},{"relation_name":"regulates","term_name":"cardiocyte differentiation","termid":"GO:0035051"}],"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 cardiocyte differentiation","synonyms":[{"name":"regulation of cardiac cell differentiation","type":"exact"},{"name":"regulation of heart cell differentiation","type":"exact"}],"termid":"GO:1905207"}


id: PR:000045537
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A GTP-binding nuclear protein spi1 that is encoded in the genome of Schizosaccharomyces pombe.","definition_xrefs":["PRO:CNA"],"direct_ancestors":[{"relation_name":"is_a","term_name":"GTP-binding nuclear protein spi1","termid":"PR:000027715"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTP-binding nuclear protein spi1 (Schizosaccharomyces pombe)","pombase_gene_id":"SPBC1289.03c","synonyms":[{"name":"Spom-spi1","type":"exact"}],"termid":"PR:000045537"}


id: PBO:0046636
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endogenous retrovirus group W member 17","termid":"PBO:0046636"}


id: MONDO:0017106
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cystic malformation of the posterior fossa","termid":"MONDO:0020134"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0020022"}],"interesting_parent_ids":["MONDO:0020022"],"is_obsolete":false,"name":"retrocerebellar cyst","secondary_identifiers":["HP:0006951","UMLS:C1845370","MEDGEN:335172","Orphanet:269200"],"synonyms":[{"name":"Retrocerebellar arachnoid cyst","type":"exact"},{"name":"Retrocerebellar cyst","type":"exact"},{"name":"retrocerebellar cyst (disease)","type":"exact"}],"termid":"MONDO:0017106","xrefs":{"Monarch":{"xref_id":"0017106"}}}


id: MONDO:0011164
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"malignant hyperthermia, susceptibility to","termid":"MONDO:0800188"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"malignant hyperthermia, susceptibility to, 6","secondary_identifiers":["MEDGEN:356150","OMIM:601888","MESH:C535699","UMLS:C1866076"],"synonyms":[{"name":"MHS6","type":"related"},{"name":"Mhs6","type":"related"},{"name":"malignant hyperpyrexia susceptibility type 6","type":"related"},{"name":"malignant hyperthermia susceptibility 6","type":"exact"},{"name":"malignant hyperthermia susceptibility type 6","type":"related"},{"name":"malignant hyperthermia, susceptibility to, 6","type":"exact"},{"name":"malignant hyperthermia, susceptibility to, type 6","type":"exact"}],"termid":"MONDO:0011164","xrefs":{"Monarch":{"xref_id":"0011164"}}}


id: PBO:0089967
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial Mam33 family protein","termid":"PBO:0089967"}


id: GO:0015834
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of peptidoglycan peptides into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. Peptidoglycan peptides are the oligopeptides found in peptidoglycan networks which cross-link the polysaccharide chains.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptide transport","termid":"GO:0015833"}],"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":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"peptidoglycan-associated peptide transport","synonyms":[{"name":"murein peptide transport","type":"exact"},{"name":"muropeptide transport","type":"exact"},{"name":"peptidoglycan peptide transport","type":"exact"}],"termid":"GO:0015834"}


id: GO:0001787
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The expansion of a natural killer cell population by cell division.","definition_xrefs":["ISBN:0781735149","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"natural killer cell activation","termid":"GO:0030101"},{"relation_name":"is_a","term_name":"lymphocyte proliferation","termid":"GO:0046651"}],"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":"natural killer cell proliferation","synonyms":[{"name":"NK cell proliferation","type":"exact"}],"termid":"GO:0001787"}


id: PBO:0041642
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcium voltage-gated channel subunit alpha1 H","termid":"PBO:0041642"}


id: PBO:0043129
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CIBAR1 pseudogene 1","termid":"PBO:0043129"}


id: PBO:0114080
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schizosaccharomyces specific methyltransferase","termid":"PBO:0114080"}


id: GO:0047842
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 3-dehydro-L-gulonate + H+ = L-xylulose + CO2.","definition_xrefs":["RHEA:11084","EC:4.1.1.34"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxy-lyase activity","termid":"GO:0016831"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016829"],"is_obsolete":false,"name":"dehydro-L-gulonate decarboxylase activity","secondary_identifiers":["KEGG_REACTION:R01905","MetaCyc:DEHYDRO-L-GULONATE-DECARBOXYLASE-RXN","Reactome:R-HSA-5662473"],"synonyms":[{"name":"3-dehydro-L-gulonate carboxy-lyase (L-xylulose-forming)","type":"related"},{"name":"3-dehydro-L-gulonate carboxy-lyase activity","type":"related"},{"name":"3-keto-L-gulonate decarboxylase activity","type":"related"},{"name":"keto-L-gulonate decarboxylase activity","type":"related"}],"termid":"GO:0047842"}


id: FYPO:0001368
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 contractile ring assembly is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal actin cytoskeleton organization","termid":"FYPO:0001366"},{"relation_name":"is_a","term_name":"normal cytokinesis","termid":"FYPO:0001367"},{"relation_name":"is_a","term_name":"normal actomyosin contractile ring organization","termid":"FYPO:0007827"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002","FYPO:0001312","FYPO:0001320"],"is_obsolete":false,"name":"normal actomyosin contractile ring assembly","synonyms":[{"name":"normal actomyosin contractile ring assembly during mitotic cell cycle","type":"related"},{"name":"normal actomyosin contractile ring assembly during vegetative growth","type":"exact"},{"name":"normal actomyosin contractile ring formation","type":"related"},{"name":"normal contractile ring assembly","type":"exact"},{"name":"normal cytokinesis, actomyosin contractile ring assembly","type":"exact"},{"name":"normal cytokinetic contractile ring assembly","type":"exact"},{"name":"normal cytokinetic ring assembly","type":"related"},{"name":"normal cytokinetic ring formation","type":"related"},{"name":"normal mitotic contractile ring assembly","type":"exact"}],"termid":"FYPO:0001368"}


id: MONDO:1011607
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Vestibular disease that occurs in Sumatran tiger.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vestibular disease, non-human animal","termid":"MONDO:1011414"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vestibular disease, Sumatran tiger","secondary_identifiers":["OMIA:002263-9695"],"termid":"MONDO:1011607","xrefs":{"Monarch":{"xref_id":"1011607"}}}


id: PBO:0078966
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Ser (AGA) 5-1","termid":"PBO:0078966"}


id: PBO:0040235
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATF6 divergent transcript","termid":"PBO:0040235"}


id: MONDO:0004750
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A category of disorders characterized by an impairment in the development of an individual's language capabilities, which is in contrast to his/her non-verbal intellect.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"communication disorder","termid":"MONDO:0002182"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"language disorder","secondary_identifiers":["NCIT:C97155","DOID:93","MEDGEN:44069","MESH:D007806","HP:0002463","UMLS:C0023015"],"termid":"MONDO:0004750","xrefs":{"Monarch":{"xref_id":"0004750"}}}


id: PBO:0116221
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5-oxoprolinase (ATP-hydrolyzing), Oxp1","termid":"PBO:0116221"}


id: GO:0002018
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which an increase in active angiotensin stimulates the adrenal cortices to secrete aldosterone.","definition_xrefs":["ISBN:0721643949"],"direct_ancestors":[{"relation_name":"is_a","term_name":"renal system process involved in regulation of systemic arterial blood pressure","termid":"GO:0003071"},{"relation_name":"is_a","term_name":"regulation of aldosterone secretion","termid":"GO:2000858"},{"relation_name":"part_of","term_name":"regulation of blood volume by renin-angiotensin","termid":"GO:0002016"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052","GO:0006810"],"is_obsolete":false,"name":"renin-angiotensin regulation of aldosterone production","synonyms":[{"name":"renin-angiotensin control of aldosterone production","type":"related"}],"termid":"GO:0002018"}


id: PBO:0109348
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"9 [SWVTETVTSGSVGFTTTIATPIGTTAGTVLVDIPTP-consensus] repeats reported (5 copies in reference)","termid":"PBO:0109348"}


id: PBO:0061302
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aminopeptidase like 1","termid":"PBO:0061302"}


id: GO:0071223
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 a lipoteichoic acid stimulus; lipoteichoic acid is a major component of the cell wall of gram-positive bacteria and typically consists of a chain of glycerol-phosphate repeating units linked to a glycolipid anchor.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to lipoteichoic acid","termid":"GO:0070391"},{"relation_name":"is_a","term_name":"cellular response to molecule of bacterial origin","termid":"GO:0071219"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"}],"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 lipoteichoic acid","synonyms":[{"name":"cellular response to LTA","type":"exact"}],"termid":"GO:0071223"}


id: GO:0050313
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-sulfanylglutathione + O2 + H2O = sulfite + glutathione + 2 H+.","definition_xrefs":["EC:1.13.11.18"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen","termid":"GO:0016702"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"sulfur dioxygenase activity","secondary_identifiers":["RHEA:12981","MetaCyc:RXN-13161","Reactome:R-HSA-1614605"],"synonyms":[{"name":"S-sulfanylglutathione:oxygen oxidoreductase activity","type":"related"},{"name":"sulfur oxygenase activity","type":"related"},{"name":"sulfur:oxygen oxidoreductase activity","type":"related"},{"name":"sulphur dioxygenase activity","type":"exact"}],"termid":"GO:0050313"}


id: PBO:0035703
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-K16_acetylation_at_telomere_during_vegetative_growth","termid":"PBO:0035703"}


id: MONDO:0001247
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An anxiety disorder characterized by an intense, irrational fear of one or more social or performance situations in which the individual believes that he or she will be scrutinized by others. Exposure to social situations immediately provokes an anxiety response. In adults, the social phobia is recognized as excessive or unreasonable.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phobic disorder","termid":"MONDO:0003699"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"social phobia","secondary_identifiers":["MEDGEN:19254","DOID:11257","EFO:1001917","MESH:D000072861","ICD9:300.23","NCIT:C34927","SCTID:25501002","UMLS:C0031572"],"synonyms":[{"name":"social anxiety disorder","type":"exact"}],"termid":"MONDO:0001247","xrefs":{"Monarch":{"xref_id":"0001247"}}}


id: PBO:0057098
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 193b","termid":"PBO:0057098"}


id: MONDO:0009518
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any leprosy in which the cause of the disease is a mutation in the TLR2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leprosy, susceptibility to, 3","secondary_identifiers":["UMLS:C1968668","MEDGEN:368500","OMIM:246300"],"synonyms":[{"name":"LPRS3","type":"related"},{"name":"TLR2 leprosy","type":"exact"},{"name":"leprosy caused by mutation in TLR2","type":"exact"},{"name":"leprosy, susceptibility to","type":"exact"},{"name":"leprosy, susceptibility to, 3","type":"exact"},{"name":"leprosy, susceptibility to, type 3","type":"exact"},{"name":"susceptibility to leprosy 3","type":"related"}],"termid":"MONDO:0009518","xrefs":{"Monarch":{"xref_id":"0009518"}}}


id: MONDO:0009956
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":"red skin pigment anomaly of new guinea","secondary_identifiers":["UMLS:C1849451","OMIM:266350","MESH:C535515","MEDGEN:341457"],"synonyms":[{"name":"Red skin pigment, New Guinea type","type":"related"},{"name":"red skin pigment anomaly of new guinea","type":"exact"}],"termid":"MONDO:0009956","xrefs":{"Monarch":{"xref_id":"0009956"}}}


id: PBO:0035940
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_methyltransferase_activity","termid":"PBO:0035940"}


id: GO:0010345
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of suberin monomers and suberin polyesters. Suberin monomers are derived from fatty acids and trans-cinnamic acids. The monomers are then cross-linked with glycerols.","definition_xrefs":["PMID:17259262"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenylpropanoid biosynthetic process","termid":"GO:0009699"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0019748","GO:0008150"],"is_obsolete":false,"name":"suberin biosynthetic process","secondary_identifiers":["MetaCyc:PWY-1121"],"termid":"GO:0010345"}


id: MONDO:0013323
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any cranioectodermal dysplasia in which the cause of the disease is a mutation in the WDR35 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cranioectodermal dysplasia","termid":"MONDO:0009032"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"},{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005497"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005497","MONDO:0006025","MONDO:0005240"],"is_obsolete":false,"name":"cranioectodermal dysplasia 2","secondary_identifiers":["MEDGEN:462224","DOID:0080804","OMIM:613610","UMLS:C3150874","GARD:15680"],"synonyms":[{"name":"CED2","type":"related"},{"name":"CRANIOECTODERMAL dysplasia 2","type":"related"},{"name":"Cranioectodermal dysplasia type 2","type":"exact"},{"name":"WDR35 cranioectodermal dysplasia","type":"exact"},{"name":"WDR35-related cranioectodermal dysplasia","type":"exact"},{"name":"cranioectodermal dysplasia 2","type":"exact"},{"name":"cranioectodermal dysplasia caused by mutation in WDR35","type":"exact"}],"termid":"MONDO:0013323","xrefs":{"Monarch":{"xref_id":"0013323"}}}


id: MONDO:0000466
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder characterized by an electrocardiographic finding of prolonged PR interval for a specific population. For adults one common threshold is a PR interval greater than 0.20 seconds.","definition_xrefs":["NCIT:C62015"],"direct_ancestors":[{"relation_name":"is_a","term_name":"atrioventricular block","termid":"MONDO:0000465"},{"relation_name":"is_a","term_name":"cardiac rhythm disease","termid":"MONDO:0007263"}],"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":"first-degree atrioventricular block","secondary_identifiers":["SCTID:270492004","UMLS:C0085614","DOID:0050821","MEDGEN:43215","ICD9:426.11"],"synonyms":[{"name":"AV block first degree","type":"exact"},{"name":"atrioventricular block first degree","type":"exact"},{"name":"atrioventricular block, first degree","type":"exact"},{"name":"first degree AV block","type":"exact"},{"name":"first degree atrioventricular block","type":"exact"}],"termid":"MONDO:0000466","xrefs":{"Monarch":{"xref_id":"0000466"}}}


id: PBO:0057677
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1268a","termid":"PBO:0057677"}


id: PBO:0063204
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PCBP2 overlapping transcript 1","termid":"PBO:0063204"}


id: PBO:0078349
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Glu (CTC) 15-1","termid":"PBO:0078349"}


id: RO:0002246
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"g is under-expressed in t iff g is expressed in t, and the expression level of g is decreased relative to some background.","direct_ancestors":[{"relation_name":"is_a","term_name":"expressed_in","termid":"RO:0002206"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"under-expressed_in","termid":"RO:0002246"}


id: PBO:0056156
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mono-ADP ribosylhydrolase 1","termid":"PBO:0056156"}


id: GO:0000127
data:
  {"annotated_genes":["SJAG_05339","SJAG_00585","SJAG_03546","SJAG_03354","SJAG_01827","SJAG_02815"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[70167,71466,72444,74128,76831,88527],"is_not":false,"summary":null,"term":"GO:0000127"}]},"cv_name":"cellular_component","definition":"A heterotrimeric transcription factor complex that is involved in regulating transcription from RNA polymerase III (Pol III) promoters. TFIIIC contains three conserved subunits that associate with the proximal Pol III promoter element, and additional subunits that associate with sequence elements downstream of the promoter and are more diverged among species. It also functions as a boundary element to partition genome content into distinct domains outside Pol III promoter regions.","definition_xrefs":["GOC:vw","PMID:16751097","PMID:11433012","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA polymerase III transcription regulator complex","termid":"GO:0090576"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00585":null,"SJAG_01827":null,"SJAG_02815":null,"SJAG_03354":null,"SJAG_03546":null,"SJAG_05339":null},"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":"transcription factor TFIIIC complex","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0000127","terms_by_termid":{"GO:0000127":null}}


id: GO:0072645
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The appearance of interferon-delta due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["GOC:mah","PMID:15546383","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"type I interferon production","termid":"GO:0032606"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"interferon-delta production","secondary_identifiers":["GO:0072646"],"synonyms":[{"name":"IFN-delta production","type":"exact"},{"name":"IFND production","type":"exact"},{"name":"interferon-delta secretion","type":"narrow"}],"termid":"GO:0072645"}


id: PBO:0049348
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"general transcription factor IIi pseudogene 6","termid":"PBO:0049348"}


id: GO:0019711
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of peptidyl-beta-carboxyaspartic acid from other compounds, including peptidyl-aspartic acid.","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-beta-carboxyaspartic acid biosynthetic process from peptidyl-aspartic acid (obsolete GO:0019711)","synonyms":[{"name":"peptidyl-beta-carboxyaspartic acid anabolism from peptidyl-aspartic acid","type":"exact"},{"name":"peptidyl-beta-carboxyaspartic acid formation from peptidyl-aspartic acid","type":"exact"},{"name":"peptidyl-beta-carboxyaspartic acid synthesis from peptidyl-aspartic acid","type":"exact"}],"termid":"GO:0019711"}


id: PBO:0071014
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 16","termid":"PBO:0071014"}


id: PBO:0047180
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 200 member A","termid":"PBO:0047180"}


id: PBO:0039005
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AFF1 antisense RNA 1","termid":"PBO:0039005"}


id: MONDO:0008272
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Polysyndactyly or PPD4 is a form of preaxial polydactyly of fingers, a limb malformation syndrome, characterized by the presence of a thumb showing the mildest degree of duplication, being broad, bifid or with radially deviated distal phalanx. Syndactyly of various degrees of third-and-fourth fingers is occasionally present.","definition_xrefs":["Orphanet:93338"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"metabolic disease","termid":"MONDO:0005066"},{"relation_name":"is_a","term_name":"non-syndromic synpolydactyly","termid":"MONDO:0000722"},{"relation_name":"is_a","term_name":"preaxial polydactyly of fingers","termid":"MONDO:0017425"},{"relation_name":"is_a","term_name":"inborn errors of metabolism","termid":"MONDO:0019052"},{"relation_name":"is_a","term_name":"polydactyly-syndactyly-triphalangism","termid":"MONDO:0800066"}],"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":"polysyndactyly 4","secondary_identifiers":["GARD:9903","ICD9:755.10","UMLS:C1868111","icd11.foundation:973656080","MEDGEN:357420","MedDRA:10063143","OMIM:174700"],"synonyms":[{"name":"PPD4","type":"exact"},{"name":"crossed polydactyly type 1","type":"related"},{"name":"crossed polydactyly, type 1","type":"related"},{"name":"polydactyly preaxial 4","type":"related"},{"name":"polydactyly, preaxial 4","type":"related"},{"name":"polydactyly, preaxial IV","type":"related"},{"name":"polydactyly, preaxial type 4","type":"exact"},{"name":"polydactyly, preaxial, type IV","type":"exact"},{"name":"polysyndactyly uncomplicated","type":"related"},{"name":"polysyndactyly, uncomplicated","type":"related"},{"name":"preaxial polydactyly 4","type":"related"},{"name":"preaxial polydactyly type 4","type":"exact"}],"termid":"MONDO:0008272","xrefs":{"Monarch":{"xref_id":"0008272"}}}


id: MONDO:0010424
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary pulmonary alveolar proteinosis","termid":"MONDO:0012580"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"surfactant metabolism dysfunction, pulmonary, 4","secondary_identifiers":["UMLS:C2677877","GARD:15263","MESH:C567461","OMIM:300770","MEDGEN:393858"],"synonyms":[{"name":"Csf2Ra deficiency","type":"related"},{"name":"Pap due to Csf2Ra deficiency","type":"related"},{"name":"SMDP4","type":"related"},{"name":"pulmonary alveolar proteinosis, congenital, 4","type":"related"},{"name":"surfactant metabolism dysfunction, pulmonary, 4","type":"exact"},{"name":"surfactant metabolism dysfunction, pulmonary, type 4","type":"exact"}],"termid":"MONDO:0010424","xrefs":{"Monarch":{"xref_id":"0010424"}}}


id: GO:0043912
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: D-lysine + H2O + O2 = 6-amino-2-oxohexanoate + H2O2 + NH4+.","definition_xrefs":["PMID:17259313"],"gene_count":0,"genotype_count":0,"name":"obsolete D-lysine oxidase activity (obsolete GO:0043912)","termid":"GO:0043912"}


id: PBO:0089509
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial inheritance GTPase, tubulin-like","termid":"PBO:0089509"}


id: PBO:0065436
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome 26S subunit, ATPase 1 pseudogene 9","termid":"PBO:0065436"}


id: GO:0021769
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the orbitofrontal cortex over time from its initial formation until its mature state. The orbitofrontal cortex is a cerebral cortex region located in the frontal lobe.","definition_xrefs":["GOC:dph","ISBN:0878937420","GOC:dgh","GOC:jid","GOC:cls","GO_REF:0000021"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"limbic system development","termid":"GO:0021761"}],"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":"orbitofrontal cortex development","termid":"GO:0021769"}


id: GO:0030374
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. A transcription coactivator activity that activates or increases the transcription of specific gene sets via binding to a DNA-bound nuclear receptor, either on its own or as part of a complex. Coactivators often act by altering chromatin structure and modifications. For example, one class of transcription coregulators modifies chromatin structure through covalent modification of histones. A second class remodels the conformation of chromatin in an ATP-dependent fashion. A third class modulates interactions of DNA-bound DNA-binding transcription factors with other transcription coregulators. A fourth class of coactivator activity is the bridging of a DNA-binding transcription factor to the general (basal) transcription machinery. The Mediator complex, which bridges sequence-specific DNA binding transcription factors and RNA polymerase, is also a transcription coactivator.","definition_xrefs":["GOC:dph","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete nuclear receptor coactivator activity (obsolete GO:0030374)","synonyms":[{"name":"ligand-activated RNA polymerase II transcription factor binding transcription factor activity","type":"exact"},{"name":"ligand-dependent nuclear receptor transcription co-activator activity","type":"exact"},{"name":"ligand-dependent nuclear receptor transcription coactivator activity","type":"exact"},{"name":"nuclear receptor transcription coactivator activity","type":"exact"},{"name":"transcription factor activity, ligand-activated RNA polymerase II transcription factor binding","type":"exact"}],"termid":"GO:0030374"}


id: PBO:0042520
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclin dependent kinase 2 associated protein 1","termid":"PBO:0042520"}


id: PBO:0057484
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 602","termid":"PBO:0057484"}


id: PBO:0036369
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"helper of TIM Hot13 (predicted)","termid":"PBO:0036369"}


id: GO:0098673
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process by which a virus inhibits DNA replication in its host cell. Some bacteriophages are known to do this, possibly as a way of increasing the pool of nucleotides available for virus replication.","definition_xrefs":["PMID:21205014","PMID:17010157"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host cellular process","termid":"GO:0044068"}],"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 suppression of host DNA replication","secondary_identifiers":["VZ:3948"],"synonyms":[{"name":"inhibition of host DNA replication by virus","type":"narrow"}],"termid":"GO:0098673"}


id: PBO:0040224
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"activating transcription factor 1","termid":"PBO:0040224"}


id: PBO:0062026
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 N member 1 pseudogene","termid":"PBO:0062026"}


id: PBO:0044871
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DENN domain containing 3","termid":"PBO:0044871"}


id: GO:0052719
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of ester linkages immediately 5' to an apurinic/apyrimidinic (AP; also called abasic) site within a ribonucleic acid molecule by creating internal breaks, generating a single-strand break with 5'-ribose phosphate and 3'-hydroxyl ends.","definition_xrefs":["PMID:19401441"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA endonuclease activity, producing 5'-phosphomonoesters","termid":"GO:0016891"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0003824","GO:0140098","GO:0016788"],"is_obsolete":false,"name":"RNA-(apurinic or apyrimidinic site) endonuclease activity","synonyms":[{"name":"AP endoribonuclease activity","type":"exact"},{"name":"abasic endoribonuclease activity","type":"exact"},{"name":"apurinic endoribonuclease activity","type":"narrow"},{"name":"apyrimidinic endoribonuclease activity","type":"narrow"}],"termid":"GO:0052719"}


id: MONDO:0000889
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infections of the nervous system caused by bacteria of the genus haemophilus, and marked by prominent inflammation of the meninges. haemophilus influenzae type B is the most common causative organism. The condition primarily affects children under 6 years of age but may occur in adults.","definition_xrefs":["MESH:D008583"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bacterial meningitis","termid":"MONDO:0006670"},{"relation_name":"is_a","term_name":"haemophilus infectious disease","termid":"MONDO:0006926"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"haemophilus meningitis","secondary_identifiers":["SCTID:5900006","SCTID:192643004","EFO:1000955","UMLS:C0025292","DOID:0080179","ICD9:320.0","MedDRA:10018953","MEDGEN:7535"],"synonyms":[{"name":"Haemophilus influenzae bacterial meningitis","type":"exact"},{"name":"Haemophilus influenzae caused bacterial meningitis","type":"exact"}],"termid":"MONDO:0000889","xrefs":{"Monarch":{"xref_id":"0000889"}}}


id: GO:0160036
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of postsynaptic density assembly.","definition_xrefs":["PMID:17626212"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of postsynaptic density assembly","termid":"GO:0099151"},{"relation_name":"is_a","term_name":"positive regulation of organelle assembly","termid":"GO:1902117"},{"relation_name":"is_a","term_name":"positive regulation of postsynaptic density organization","termid":"GO:1905876"},{"relation_name":"positively_regulates","term_name":"postsynaptic density assembly","termid":"GO:0097107"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"positive regulation of postsynaptic density assembly","termid":"GO:0160036"}


id: PBO:0029693
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_cellular_iron_level","termid":"PBO:0029693"}


id: GO:0035995
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events by which a muscle stretch stimulus is received by a cell and converted into a molecular signal.","definition_xrefs":["PMID:14583192"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to muscle stretch","termid":"GO:0035994"},{"relation_name":"is_a","term_name":"detection of mechanical stimulus","termid":"GO:0050982"}],"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":"detection of muscle stretch","termid":"GO:0035995"}


id: MONDO:1011996
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"vision disorder, non-human animal","termid":"MONDO:1011367"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ocular melanosis, non-human animal","secondary_identifiers":["OMIA:001804"],"termid":"MONDO:1011996","xrefs":{"Monarch":{"xref_id":"1011996"}}}


id: PATO:0000153
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000153 absolute threshold (obsolete PATO:0000153)","termid":"PATO:0000153"}


id: PBO:0006183
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_regulation_target","termid":"PBO:0006183"}


id: FYPO:0008312
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which mitotic sister chromatid cohesion is increased at the centromeres in early mitosis. Contromeric cohesion is usually protected until  the metaphase anaphase transition.","definition_xrefs":["PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic sister chromatid cohesion","termid":"FYPO:0006521"}],"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:0001320"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000641","FYPO:0001985","FYPO:0000631","FYPO:0005447","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"increased split sister centromeres in early mitosis","synonyms":[{"name":"increased sister kinetochore dissociation at centromeres","type":"exact"},{"name":"increased split sister centromeres in mitosis","type":"broad"}],"termid":"FYPO:0008312"}


id: PBO:0080547
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WBP1L pseudogene 6","termid":"PBO:0080547"}


id: PBO:0081302
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 84","termid":"PBO:0081302"}


id: MONDO:0006640
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Excess production of adrenal cortex hormones.","definition_xrefs":["MESH:D000308"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adrenal cortex disorder","termid":"MONDO:0002816"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adrenal gland hyperfunction","secondary_identifiers":["UMLS:C0001622","DOID:3947","HP:0003118","EFO:1000797","MEDGEN:7899","ICD9:255.3","SCTID:275437005"],"synonyms":[{"name":"adrenal gland hyperfunction","type":"exact"},{"name":"adrenocortical hyperfunction","type":"exact"},{"name":"disorder of corticoadrenal overactivity","type":"related"},{"name":"hyperadrenalism","type":"exact"},{"name":"hyperadrenocorticism","type":"related"},{"name":"hypercorticism","type":"related"},{"name":"hypercortisolemia","type":"exact"},{"name":"hypercortisolism","type":"exact"},{"name":"hyperfunction, adrenal gland","type":"related"},{"name":"hyperfunction, adrenocortical","type":"related"}],"termid":"MONDO:0006640","xrefs":{"Monarch":{"xref_id":"0006640"}}}


id: GO:0052738
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of an oxidation-reduction (redox) reaction in which an aldehyde or ketone (oxo) group acts as a hydrogen or electron donor and reduces a quinone or similar compound.","definition_xrefs":["EC:1.2.5.-"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the aldehyde or oxo group of donors","termid":"GO:0016903"}],"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:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"oxidoreductase activity, acting on the aldehyde or oxo group of donors, with a quinone or similar compound as acceptor","termid":"GO:0052738"}


id: FYPO:0002314
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 all-trans-geranylgeranyl diphosphate (GGPP) measured in a cell is too low to detect.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"substance absent from cell during vegetative growth","termid":"FYPO:0001208"},{"relation_name":"is_a","term_name":"decreased cellular GGPP level","termid":"FYPO:0002323"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"GGPP absent from cell","synonyms":[{"name":"2-trans,6-trans,10-trans-geranylgeranyl diphosphate absent from cell","type":"exact"},{"name":"GGPP absent from cell during mitotic cell cycle","type":"related"},{"name":"GGPP absent from cell during vegetative growth","type":"exact"},{"name":"all-trans-geranylgeranyl diphosphate absent from cell","type":"exact"},{"name":"all-trans-geranylgeranyl pyrophosphate absent from cell","type":"exact"}],"termid":"FYPO:0002314"}


id: PBO:0084841
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial ribosomal protein of the large subunit; appears as two protein spots (YmL34 and YmL38) on two-dimensional SDS gels; protein abundance increases in response to DNA replication stress","termid":"PBO:0084841"}


id: PBO:0090381
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exocyst complex subunit Sec15","termid":"PBO:0090381"}


id: PBO:0083163
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; almost completely overlaps the verified gene SSB1","termid":"PBO:0083163"}


id: GO:0071247
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 a chromate stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to chromate","termid":"GO:0046687"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"}],"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 chromate","termid":"GO:0071247"}


id: GO:0036485
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The movement of trunk neural crest cells from the neural tube, travelling dorso-laterally into the ectoderm and continuing toward the ventral midline of the belly. These migrating trunk neural crest cells become melanocytes, the melanin-forming pigment cells.","definition_xrefs":["GOC:PARL","PMID:2387238","GOC:bf","GOC:mat"],"direct_ancestors":[{"relation_name":"is_a","term_name":"trunk neural crest cell migration","termid":"GO:0036484"}],"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":"dorsolateral trunk neural crest cell migration","synonyms":[{"name":"dorsolateral trunk NCC migration","type":"exact"}],"termid":"GO:0036485"}


id: PBO:0049129
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor class C group 6 member A","termid":"PBO:0049129"}


id: PBO:0086556
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; conserved among S. cerevisiae strains; YHL005C is not an essential gene","termid":"PBO:0086556"}


id: PBO:0088252
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial mRNA processing protein Cox24/Pet20","termid":"PBO:0088252"}


id: GO:0008904
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + hygromycin B = 7''-O-phosphohygromycin B + ADP + 2 H+.","definition_xrefs":["RHEA:23388","EC:2.7.1.119"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aminoglycoside phosphotransferase activity","termid":"GO:0034071"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0016301","GO:0003824"],"is_obsolete":false,"name":"hygromycin-B 7''-O-phosphotransferase activity","secondary_identifiers":["MetaCyc:HYGROMYCIN-B-KINASE-RXN","KEGG_REACTION:R03770"],"synonyms":[{"name":"APH(7'') activity","type":"related"},{"name":"ATP:hygromycin-B 7''-O-phosphotransferase activity","type":"related"},{"name":"destomic acid ring 7''-O-phosphotransferase activity","type":"exact"},{"name":"hygromycin B kinase activity","type":"broad"},{"name":"hygromycin B phosphotransferase activity","type":"broad"},{"name":"hygromycin-B kinase activity","type":"broad"}],"termid":"GO:0008904"}


id: MONDO:0015493
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary lipodystrophy","termid":"MONDO:0020087"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005066"],"is_obsolete":false,"name":"lipoatrophy with diabetes, leukomelanodermic papules, liver steatosis, and hypertrophic cardiomyopathy","secondary_identifiers":["Orphanet:156156"],"termid":"MONDO:0015493","xrefs":{"Monarch":{"xref_id":"0015493"}}}


id: GO:0047098
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 O2 + donor-H2 + Latia luciferin = light + H2O + acceptor + formate + CO2 + oxidized Latia luciferin.","definition_xrefs":["EC:1.14.99.21"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen","termid":"GO:0016705"},{"relation_name":"is_a","term_name":"luciferin monooxygenase activity","termid":"GO:0045289"}],"gene_count":0,"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:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"Latia-luciferin monooxygenase (demethylating) activity","secondary_identifiers":["RHEA:12677","MetaCyc:1.14.99.21-RXN"],"synonyms":[{"name":"Latia luciferin monooxygenase (demethylating)","type":"related"},{"name":"Latia-luciferin,hydrogen-donor:oxygen oxidoreductase (demethylating)","type":"related"},{"name":"luciferase (Latia luciferin)","type":"related"}],"termid":"GO:0047098"}


id: MONDO:0017879
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An infection caused by Hantaviruses. It manifests with flu-like symptoms but it rapidly progresses to life-threatening respiratory problems.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"lung disorder","termid":"MONDO:0005275"},{"relation_name":"is_a","term_name":"hantavirus infectious disease","termid":"MONDO:0005780"},{"relation_name":"is_a","term_name":"viral hemorrhagic fever","termid":"MONDO:0018087"},{"relation_name":"is_a","term_name":"viral respiratory tract infection","termid":"MONDO:0024352"},{"relation_name":"is_a","term_name":"vector-borne disease","termid":"MONDO:0100120"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hantavirus pulmonary syndrome","secondary_identifiers":["Orphanet:319247","MEDGEN:66205","EFO:0007296","GARD:69","NCIT:C84747","ICD10EXP:J17.1*","SCTID:120639003","ICD9:480.8","DOID:14472","icd11.foundation:582624609","NORD:1216","UMLS:C0243025","MedDRA:10019143","ICD10EXP:B33.4+","MESH:D018804"],"synonyms":[{"name":"HARDS","type":"related"},{"name":"Hantavirus","type":"related"},{"name":"Hantavirus-associated respiratory distress syndrome","type":"related"},{"name":"four corners hantavirus","type":"related"}],"termid":"MONDO:0017879","xrefs":{"Monarch":{"xref_id":"0017879"}}}


id: GO:0070763
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of homodimer of the Notch ligand Delta1.","definition_xrefs":["PMID:12794186"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005886","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"Delta1 complex","synonyms":[{"name":"Delta1 homodimer complex","type":"exact"}],"termid":"GO:0070763"}


id: PBO:0078917
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Gln (anticodon TTG) 6-1","termid":"PBO:0078917"}


id: FYPO:0007010
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 secondary siRNA measured in a cell is too low to detect. Secondary siRNAs are sequences homologous to regions 5' and 3' to the initial siRNA, and their production amplifies the primary siRNA signal.","definition_xrefs":["PMID:20062003","PomBase:mah","PomBase:al","PMID:22542102"],"direct_ancestors":[{"relation_name":"is_a","term_name":"siRNA absent from cell","termid":"FYPO:0006076"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0006551","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"secondary siRNA absent from cell","synonyms":[{"name":"secondary siRNA absent from cell during mitotic cell cycle","type":"related"},{"name":"secondary siRNA absent from cell during vegetative growth","type":"exact"},{"name":"secondary small interfering RNA absent from cell","type":"exact"}],"termid":"FYPO:0007010"}


id: PR:P23566
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A ubiquitin-conjugating enzyme E2 B that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["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":"ubiquitin-conjugating enzyme E2 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC18B11.07c","secondary_identifiers":["UniProtKB:P23566"],"synonyms":[{"name":"RAD6 homolog (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"SPAC18B11.07c","type":"related"},{"name":"Spom972h-UBE2B","type":"exact"},{"name":"ubc2","type":"related"},{"name":"ubiquitin carrier protein 2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"ubiquitin-protein ligase 2 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P23566"}


id: PBO:0091554
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"4-alpha-hydroxytetrahydrobiopterin dehydratase","termid":"PBO:0091554"}


id: GO:0009243
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of the O side chain of a lipopolysaccharide, which determines the antigenic specificity of the organism. It is made up of about 50 repeating units of a branched tetrasaccharide.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polysaccharide biosynthetic process","termid":"GO:0000271"},{"relation_name":"is_a","term_name":"O antigen metabolic process","termid":"GO:0046402"},{"relation_name":"part_of","term_name":"lipopolysaccharide biosynthetic process","termid":"GO:0009103"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0008150","GO:0005975","GO:0006629"],"is_obsolete":false,"name":"O antigen biosynthetic process","synonyms":[{"name":"O antigen anabolism","type":"exact"},{"name":"O antigen biosynthesis","type":"exact"},{"name":"O antigen formation","type":"exact"},{"name":"O antigen synthesis","type":"exact"}],"termid":"GO:0009243"}


id: PBO:0026771
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_uracil_import","termid":"PBO:0026771"}


id: MONDO:0022790
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":"cleft tongue","secondary_identifiers":["UMLS:C0266111","MEDGEN:82731"],"synonyms":[{"name":"bifid tongue","type":"related"},{"name":"cleft tongue syndrome","type":"related"}],"termid":"MONDO:0022790","xrefs":{"Monarch":{"xref_id":"0022790"}}}


id: GO:0034193
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving L-galactonate, the anion of L-galactonic acid.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"galactonate metabolic process","termid":"GO:0019583"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0005975"],"is_obsolete":false,"name":"L-galactonate metabolic process","synonyms":[{"name":"L-galactonate metabolism","type":"exact"}],"termid":"GO:0034193"}


id: PBO:0064821
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase 1 regulatory subunit 3C","termid":"PBO:0064821"}


id: PBO:0000053
data:
  {"annotation_feature_type":"gene","cv_name":"genome_org","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"present at telomere ends","termid":"PBO:0000053"}


id: GO:0007569
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. An aging process that has as participant a cell after a cell has stopped dividing. Cell aging may occur when a cell has temporarily stopped dividing through cell cycle arrest (GO:0007050) or when a cell has permanently stopped dividing, in which case it is undergoing cellular senescence (GO:0090398). May precede cell death (GO:0008219) and succeed cell maturation (GO:0048469).","definition_xrefs":["GOC:PO_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete cell aging (obsolete GO:0007569)","synonyms":[{"name":"cell ageing","type":"exact"}],"termid":"GO:0007569"}


id: PBO:0076852
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thymocyte expressed, positive selection associated 1","termid":"PBO:0076852"}


id: GO:0003984
data:
  {"annotated_genes":["SJAG_03985","SJAG_06635"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[76452],"is_not":false,"summary":null,"term":"GO:0003984"},{"annotations":[64044],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1990610"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: H+ + 2 pyruvate = (2S)-2-acetolactate + CO2. Can also convert 2-oxobutanoate and pyruvate to (S)-2-ethyl-2-hydroxy-3-oxobutanoate.","definition_xrefs":["EC:2.2.1.6"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transketolase or transaldolase activity","termid":"GO:0016744"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03985":null,"SJAG_06635":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016744"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0016744","GO:0003824"],"is_obsolete":false,"name":"acetolactate synthase activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null},"secondary_identifiers":["MetaCyc:ACETOLACTSYN-RXN"],"synonyms":[{"name":"acetohydroxy acid synthetase activity","type":"related"},{"name":"acetohydroxyacid synthase activity","type":"related"},{"name":"acetolactate pyruvate-lyase (carboxylating) activity","type":"related"},{"name":"acetolactic synthetase activity","type":"related"},{"name":"alpha-acetohydroxy acid synthetase activity","type":"related"},{"name":"alpha-acetohydroxyacid synthase activity","type":"related"},{"name":"alpha-acetolactate synthase activity","type":"related"},{"name":"alpha-acetolactate synthetase activity","type":"related"},{"name":"pyruvate:pyruvate acetaldehydetransferase (decarboxylating)","type":"related"}],"termid":"GO:0003984","terms_by_termid":{"GO:0003984":null,"GO:1990610":null}}


id: PBO:0056600
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mdm1 nuclear protein","termid":"PBO:0056600"}


id: PBO:0033818
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TRAPP complex subunit 2-like Tca17 (predicted)","termid":"PBO:0033818"}


id: FYPO:0006490
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell cycle phenotype in which the duration of M phase of the mitotic cell cycle is shorter than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic M phase progression","termid":"FYPO:0000607"},{"relation_name":"is_a","term_name":"decreased duration of mitotic cell cycle phase","termid":"FYPO:0001070"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0000631","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"decreased duration of mitotic M phase","synonyms":[{"name":"decreased duration of M phase during mitotic cell cycle","type":"exact"},{"name":"decreased duration of mitosis","type":"related"},{"name":"decreased duration of mitosis during mitotic cell cycle","type":"related"},{"name":"decreased duration of mitosis during vegetative growth","type":"related"},{"name":"decreased duration of mitotic nuclear division","type":"related"},{"name":"decreased mitotic M phase duration","type":"exact"},{"name":"decreased mitotic M phase duration during vegetative growth","type":"exact"},{"name":"reduced duration of mitotic M phase","type":"exact"}],"termid":"FYPO:0006490"}


id: GO:0050433
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the regulated release of catecholamines.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of amine transport","termid":"GO:0051952"},{"relation_name":"is_a","term_name":"regulation of secretion by cell","termid":"GO:1903530"},{"relation_name":"regulates","term_name":"catecholamine secretion","termid":"GO:0050432"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"regulation of catecholamine secretion","termid":"GO:0050433"}


id: PBO:0076689
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription elongation factor A like 6","termid":"PBO:0076689"}


id: PBO:0029397
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-delayed_onset_of_protein_localization_to_nucleoplasm","termid":"PBO:0029397"}


id: PBO:0080832
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"YAP1 pseudogene 3","termid":"PBO:0080832"}


id: GO:0006163
data:
  {"annotated_genes":["SJAG_02009","SJAG_02105","SJAG_07003","SJAG_00461","SJAG_03091","SJAG_MIT37","SJAG_00522","SJAG_01500","SJAG_04849","SJAG_04681","SJAG_01814","SJAG_02850","SJAG_04495","SJAG_02038","SJAG_04192","SJAG_01471","SJAG_05314","SJAG_04122","SJAG_00438","SJAG_02297","SJAG_02618","SJAG_04882","SJAG_02135","SJAG_03373","SJAG_00070","SJAG_04870","SJAG_03174","SJAG_01070","SJAG_02154","SJAG_03946","SJAG_02148","SJAG_00964","SJAG_00915","SJAG_00839","SJAG_03934","SJAG_03811","SJAG_00044","SJAG_03355","SJAG_06621","SJAG_00685","SJAG_MIT15","SJAG_03903","SJAG_02481","SJAG_04362","SJAG_04693","SJAG_04334","SJAG_02598","SJAG_04487","SJAG_02369","SJAG_01081","SJAG_01661","SJAG_02107","SJAG_05204","SJAG_02785","SJAG_02364","SJAG_02191","SJAG_06622","SJAG_04123","SJAG_00027","SJAG_01582","SJAG_00836","SJAG_01310","SJAG_00605","SJAG_03925","SJAG_02889","SJAG_00542","SJAG_00985","SJAG_04634","SJAG_03298","SJAG_00501","SJAG_01824","SJAG_02887","SJAG_04970","SJAG_03852","SJAG_01298","SJAG_02564","SJAG_00133","SJAG_MIT09","SJAG_02945","SJAG_02696","SJAG_03114","SJAG_02796","SJAG_00136","SJAG_01566","SJAG_01859","SJAG_03140","SJAG_06634","SJAG_04422","SJAG_00633","SJAG_04048","SJAG_03660","SJAG_03828","SJAG_04263"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[77151,79181],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044208"},{"annotations":[77123,65565,57099,72092,64558,58002,60147,70286],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006189"},{"annotations":[79556],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901911"},{"annotations":[72269],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006172"},{"annotations":[76776,59482],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046033"},{"annotations":[57088,74295],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044209"},{"annotations":[59483,67803,67722],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046034"},{"annotations":[116678],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006198"},{"annotations":[109702,109701,103700,105778,109703,95350,78210,98321,109704,106148,94861,103956,109707,116650,105780,98592,109706,106149,105779,109705],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061621"},{"annotations":[99314],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035863"},{"annotations":[64496],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046710"},{"annotations":[88947],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061613"},{"annotations":[63136,59501,75080],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006177"},{"annotations":[64495],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046037"},{"annotations":[75995],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032263"},{"annotations":[64615,75212,102556],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006183"},{"annotations":[79182],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046040"},{"annotations":[65070,75996],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032264"},{"annotations":[96891],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043490"},{"annotations":[113392,75100,77806],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009435"},{"annotations":[99668,80285],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034355"},{"annotations":[72570],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019677"},{"annotations":[67010,58520,69422],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019674"},{"annotations":[72572],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006734"},{"annotations":[95445,95444],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006735"},{"annotations":[78296,80207,71445],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006741"},{"annotations":[72573],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006742"},{"annotations":[74217],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006739"},{"annotations":[76377,73408],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0045820"},{"annotations":[118303],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1905707"},{"annotations":[68385],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006098"},{"annotations":[74087,108743,73453,74878,104671],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0009052"},{"annotations":[98511,97313,73419,80742,97224],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0009051"},{"annotations":[90032],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1905857"},{"annotations":[94209,89470,109103,116145,102136,108122,93195,103351,103968,95179,108214,119358,119370,93626,119364,103997,105332],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042776"},{"annotations":[98040,72764,74224],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006164"},{"annotations":[70420],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0006110"},{"annotations":[76376],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0043456"},{"annotations":[75997],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032265"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving a purine nucleotide, a compound consisting of nucleoside (a purine base linked to a deoxyribose or ribose sugar) esterified with a phosphate group at either the 3' or 5'-hydroxyl group of the sugar.","definition_xrefs":["ISBN:0198506732","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide metabolic process","termid":"GO:0009117"},{"relation_name":"is_a","term_name":"purine-containing compound metabolic 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nucleotide metabolic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000108":null},"synonyms":[{"name":"purine metabolic process","type":"narrow"},{"name":"purine metabolism","type":"narrow"},{"name":"purine nucleotide metabolism","type":"exact"}],"termid":"GO:0006163","terms_by_termid":{"GO:0006098":null,"GO:0006110":null,"GO:0006164":null,"GO:0006172":null,"GO:0006177":null,"GO:0006183":null,"GO:0006189":null,"GO:0006198":null,"GO:0006734":null,"GO:0006735":null,"GO:0006739":null,"GO:0006741":null,"GO:0006742":null,"GO:0009051":null,"GO:0009052":null,"GO:0009435":null,"GO:0019674":null,"GO:0019677":null,"GO:0032263":null,"GO:0032264":null,"GO:0032265":null,"GO:0034355":null,"GO:0035863":null,"GO:0042776":null,"GO:0043456":null,"GO:0043490":null,"GO:0044208":null,"GO:0044209":null,"GO:0045820":null,"GO:0046033":null,"GO:0046034":null,"GO:0046037":null,"GO:0046040":null,"GO:0046710":null,"GO:0061613":null,"GO:0061621":null,"GO:1901911":null,"GO:1905707":null,"GO:1905857":null}}


id: GO:0018038
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The formation of a C-terminal peptidyl-cysteine amide by hydrolysis and oxidation of an interior Cys-Gly peptide in a secreted protein.","definition_xrefs":["RESID:AA0085"],"gene_count":0,"genotype_count":0,"name":"obsolete C-terminal peptidyl-cysteine amidation (obsolete GO:0018038)","termid":"GO:0018038"}


id: PBO:0041770
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calpain 10","termid":"PBO:0041770"}


id: MONDO:0020784
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete short sleep, familial natural, 1 (obsolete MONDO:0020784)","secondary_identifiers":["OMIM:612975"],"synonyms":[{"name":"FNSS1","type":"related"},{"name":"SHORT SLEEP, FAMILIAL NATURAL, 1","type":"related"},{"name":"Short Sleep Phenotype","type":"related"},{"name":"short sleep, familial natural, 1","type":"exact"}],"termid":"MONDO:0020784","xrefs":{"Monarch":{"xref_id":"0020784"}}}


id: PR:O14161
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- cwf21 gene.","definition_xrefs":["UniProtKB:O14161","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":"pre-mRNA-splicing factor cwf21 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4A8.09c","synonyms":[{"name":"Spom972h-cwf21","type":"exact"},{"name":"complexed with cdc5 protein 21 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14161"}


id: PBO:0028664
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-loss_of_gross_chromosomal_rearrangement_during_replication_fork_processing","termid":"PBO:0028664"}


id: GO:0090443
data:
  {"annotated_genes":["SJAG_04455","SJAG_01790","SJAG_03508","SJAG_06270","SJAG_02514","SJAG_00229"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[70889,74990,95967,101587,107848,110476],"is_not":false,"summary":null,"term":"GO:0090443"}]},"cv_name":"cellular_component","definition":"A conserved protein phosphatase type 2A complex which contains a protein phosphatase type 2A, a protein phosphatase regulatory subunit, a striatin, an FHA domain protein and other subunits (at least six proteins). In fission yeast this complex negatively regulate the septation initiation network at the spindle pole body.","definition_xrefs":["PMID:21561862","PMID:22119525","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00229":null,"SJAG_01790":null,"SJAG_02514":null,"SJAG_03508":null,"SJAG_04455":null,"SJAG_06270":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"FAR/SIN/STRIPAK complex","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"FAR complex","type":"related"},{"name":"SIN inhibitory phosphatase (SIP) complex","type":"exact"},{"name":"SIN inhibitory phosphatase complex","type":"exact"},{"name":"SIP complex","type":"exact"},{"name":"STRIPAK signalling complex","type":"related"},{"name":"striatin interacting phosphatase and kinase complex","type":"exact"}],"termid":"GO:0090443","terms_by_termid":{"GO:0090443":null}}


id: MONDO:0015817
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete aggressive primary cutaneous T-cell lymphoma (obsolete MONDO:0015817)","secondary_identifiers":["Orphanet:178551"],"termid":"MONDO:0015817","xrefs":{"Monarch":{"xref_id":"0015817"}}}


id: FYPO:0003834
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell cycle phenotype in the duration of meiotic interphase, which begins after cytokinesis and ends when meiotic prophase begins, is normal (i.e. indistinguishable from wild type).","definition_xrefs":["GO:0051328","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cell cycle phase","termid":"FYPO:0003833"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal duration of meiotic interphase","termid":"FYPO:0003834"}


id: PBO:0090412
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L15","termid":"PBO:0090412"}


id: PBO:0044059
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cystatin D","termid":"PBO:0044059"}


id: PATO:0000391
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000391 intense (obsolete PATO:0000391)","termid":"PATO:0000391"}


id: MONDO:0001917
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chronic form of perichondritis of auricle.","definition_xrefs":["MONDO:patterns/chronic"],"direct_ancestors":[{"relation_name":"is_a","term_name":"perichondritis of auricle","termid":"MONDO:0002246"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chronic perichondritis of pinna","secondary_identifiers":["UMLS:C0155391","ICD9:380.02","MEDGEN:509947","DOID:14243","SCTID:45431004"],"synonyms":[{"name":"chronic perichondritis of auricle","type":"exact"},{"name":"chronic pinna perichondritis","type":"exact"},{"name":"perichondritis of auricle, chronic","type":"exact"}],"termid":"MONDO:0001917","xrefs":{"Monarch":{"xref_id":"0001917"}}}


id: PBO:0040198
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"argininosuccinate synthetase 1 pseudogene 11","termid":"PBO:0040198"}


id: GO:0008556
data:
  {"annotated_genes":["SJAG_04167"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[112657],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008900"}]},"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: ATP + H2O + K+(out) = ADP + phosphate + K+(in).","definition_xrefs":["RHEA:16777"],"direct_ancestors":[{"relation_name":"is_a","term_name":"potassium ion transmembrane transporter activity","termid":"GO:0015079"},{"relation_name":"is_a","term_name":"P-type ion transporter activity","termid":"GO:0015662"},{"relation_name":"is_a","term_name":"ATPase-coupled monoatomic cation transmembrane transporter activity","termid":"GO:0019829"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04167":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"P-type potassium transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:TRANS-RXN-2","EC:7.2.2.6","GO:0015618"],"synonyms":[{"name":"ATP phosphohydrolase (K+-importing)","type":"related"},{"name":"ATP-dependent potassium transmembrane transporter activity","type":"exact"},{"name":"ATPase-coupled potassium transmembrane transporter activity","type":"related"},{"name":"K(+)-importing ATPase activity","type":"narrow"},{"name":"K(+)-transporting ATPase activity","type":"related"},{"name":"K+-importing ATPase activity","type":"related"},{"name":"K+-transporting ATPase activity","type":"exact"},{"name":"potassium ABC transporter","type":"narrow"},{"name":"potassium transmembrane transporter activity, phosphorylative mechanism","type":"exact"},{"name":"potassium transporting ATPase activity","type":"exact"},{"name":"potassium-importing ATPase activity","type":"narrow"},{"name":"potassium-transporting ATPase activity","type":"exact"},{"name":"potassium-uptake-ATPase activity","type":"exact"}],"termid":"GO:0008556","terms_by_termid":{"GO:0008900":null}}


id: GO:0062029
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that starts or increases the rate, frequency or extent of stress-granule assembly, the aggregation, arrangement and bonding together of proteins and RNA molecules to form a stress granule.","definition_xrefs":["PMID:20180778"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of stress granule assembly","termid":"GO:0062028"},{"relation_name":"is_a","term_name":"positive regulation of organelle assembly","termid":"GO:1902117"},{"relation_name":"positively_regulates","term_name":"stress granule assembly","termid":"GO:0034063"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"positively_regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"positive regulation of stress granule assembly","termid":"GO:0062029"}


id: PBO:0090626
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homoserine O-acetyltransferase","termid":"PBO:0090626"}


id: RO:HOM0000001
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Similarity that results from common evolutionary origin.","direct_ancestors":[{"relation_name":"is_a","term_name":"shares_ancestor_with","termid":"RO:0002158"},{"relation_name":"is_a","term_name":"in_similarity_relationship_with","termid":"RO:HOM0000000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"in_homology_relationship_with","synonyms":[{"name":"homologous to","type":"exact"}],"termid":"RO:HOM0000001"}


id: PBO:0038309
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein_degradation","termid":"PBO:0038309"}


id: MONDO:0009299
data:
  {"annotated_genes":["SJAG_04148","SJAG_04950","SJAG_03051"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87304],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030736"},{"annotations":[85991],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013689"},{"annotations":[86749],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054850"}]},"cv_name":"mondo","definition":"46,XX gonadal dysgenesis (46,XX GD) is a primary ovarian defect leading to premature ovarian failure (POF) in otherwise normal 46,XX females as a result of failure of the gonads to develop or due to resistance to gonadotrophin stimulation.","definition_xrefs":["Orphanet:243"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gonadal dysgenesis","termid":"MONDO:0001967"},{"relation_name":"is_a","term_name":"inherited primary ovarian failure","termid":"MONDO:0019852"}],"gene_count":3,"genes_by_uniquename":{"SJAG_03051":null,"SJAG_04148":null,"SJAG_04950":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"46 XX gonadal dysgenesis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0685837","MEDGEN:146899","GARD:5671","icd11.foundation:1742528605","OMIMPS:233300","SCTID:95198001","MESH:D023961","NANDO:2200384","NCIT:C120197","DOID:14450"],"synonyms":[{"name":"46,XX complete gonadal dysgenesis","type":"exact"},{"name":"46,XX gonadal dysgenesis","type":"exact"},{"name":"46,XX ovarian dysgenesis","type":"exact"},{"name":"46,XX pure gonadal dysgenesis","type":"exact"},{"name":"FSH-RO","type":"exact"},{"name":"XX female gonadal dysgenesis","type":"exact"},{"name":"XX gonadal dysgenesis","type":"related"},{"name":"XX-GD","type":"exact"},{"name":"follicular stimulating hormone-resistant ovaries","type":"exact"},{"name":"hypergonadotropic ovarian dysgenesis","type":"exact"},{"name":"ovarian dysgenesis","type":"related"}],"termid":"MONDO:0009299","terms_by_termid":{"MONDO:0013689":null,"MONDO:0030736":null,"MONDO:0054850":null},"xrefs":{"Monarch":{"xref_id":"0009299"}}}


id: GO:0030316
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized monocyte acquires the specialized features of an osteoclast. An osteoclast is a specialized phagocytic cell associated with the absorption and removal of the mineralized matrix of bone tissue.","definition_xrefs":["GOC:add","PMID:12161749","CL:0000092","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myeloid leukocyte differentiation","termid":"GO:0002573"}],"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":"osteoclast differentiation","synonyms":[{"name":"osteoclast cell differentiation","type":"exact"}],"termid":"GO:0030316"}


id: MONDO:0013165
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal recessive spastic paraplegia type 45 is a rare, pure or complex form of hereditary spastic paraplegia characterized by onset in infancy of progressive lower limb spasticity, abnormal gait, increased deep tendon reflexes and extensor plantar responses, that may be associated with intellectual disability. Additional signs, such as contractures in the lower limbs, amyotrophy, clubfoot and optic atrophy, have also been reported.","definition_xrefs":["Orphanet:320396"],"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 45","secondary_identifiers":["UMLS:C3888209","GARD:17477","OMIM:613162","SCTID:765753004","DOID:0110797","MEDGEN:854816"],"synonyms":[{"name":"NT5C2 autosomal recessive complex spastic paraplegia","type":"exact"},{"name":"SPG45","type":"exact"},{"name":"SPG65","type":"exact"},{"name":"autosomal recessive complex spastic paraplegia caused by mutation in NT5C2","type":"exact"},{"name":"autosomal recessive spastic paraplegia 45","type":"exact"},{"name":"autosomal recessive spastic paraplegia type 45","type":"exact"},{"name":"autosomal recessive spastic paraplegia type 65","type":"exact"},{"name":"hereditary spastic paraplegia type 45","type":"exact"},{"name":"spastic paraplegia 45, autosomal recessive","type":"related"}],"termid":"MONDO:0013165","xrefs":{"Monarch":{"xref_id":"0013165"}}}


id: GO:1904088
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of epiboly involved in gastrulation with mouth forming second.","definition_xrefs":["PMID:24892953","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of epiboly involved in gastrulation with mouth forming second","termid":"GO:1904086"},{"relation_name":"is_a","term_name":"positive regulation of morphogenesis of an epithelium","termid":"GO:1905332"},{"relation_name":"positively_regulates","term_name":"epiboly involved in gastrulation with mouth forming second","termid":"GO:0055113"}],"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 epiboly involved in gastrulation with mouth forming second","synonyms":[{"name":"activation of epiboly involved in gastrulation with mouth forming second","type":"narrow"},{"name":"up regulation of epiboly involved in gastrulation with mouth forming second","type":"exact"},{"name":"up-regulation of epiboly involved in gastrulation with mouth forming second","type":"exact"},{"name":"upregulation of epiboly involved in gastrulation with mouth forming second","type":"exact"}],"termid":"GO:1904088"}


id: GO:0015385
data:
  {"annotated_genes":["SJAG_04616","SJAG_01541"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[78462,80410],"is_not":false,"summary":null,"term":"GO:0015385"}]},"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) + H+(in) = Na+(in) + H+(out).","definition_xrefs":["TC:2.A.36.-.-","TC:2.A.35.1.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sodium ion transmembrane transporter activity","termid":"GO:0015081"},{"relation_name":"is_a","term_name":"metal cation:proton antiporter activity","termid":"GO:0051139"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01541":null,"SJAG_04616":null},"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:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"sodium:proton antiporter activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-425983","Reactome:R-HSA-2872463","Reactome:R-HSA-425994","Reactome:R-HSA-5661039","Reactome:R-HSA-426015","Reactome:R-HSA-5661086","RHEA:29251","GO:0015502","Reactome:R-HSA-2872444","Reactome:R-HSA-425965","MetaCyc:TRANS-RXN-129","Reactome:R-HSA-2889070"],"synonyms":[{"name":"pH-dependent sodium:hydrogen antiporter activity","type":"narrow"},{"name":"pH-dependent sodium:proton antiporter activity","type":"narrow"},{"name":"sodium/hydrogen antiporter activity","type":"exact"},{"name":"sodium:hydrogen antiporter activity","type":"exact"},{"name":"sodium:hydrogen exchange activity","type":"exact"},{"name":"sodium:hydrogen exchanger","type":"exact"}],"termid":"GO:0015385","terms_by_termid":{"GO:0015385":null}}


id: FYPO:0007363
data:
  {"alleles_by_uniquename":{"SJAG_02796:allele-1":{"allele_type":"amino_acid_mutation","description":"A343T","gene_uniquename":"SJAG_02796","name":"pyk1-A343T","uniquename":"SJAG_02796:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[119710],"is_not":false,"summary":null,"term":"FYPO:0007363"}]},"cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of pyruvate kinase activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal catalytic activity","termid":"FYPO:0000661"},{"relation_name":"is_a","term_name":"abnormal metabolic process","termid":"FYPO:0000860"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02796":null},"genotype_count":1,"genotypes_by_uniquename":{"pyk1-A343T-A343T-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"pyk1-A343T(aa)","display_uniquename":"pyk1-A343T-A343T-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02796:allele-1","expression":"Not assayed or wild type"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000707","FYPO:0000654","FYPO:0000652","FYPO:0000002","FYPO:0005447","FYPO:0000661"],"is_obsolete":false,"name":"abnormal pyruvate kinase activity","references_by_uniquename":{"PMID:37164017":null},"single_locus_annotated_genes":["SJAG_02796"],"single_locus_genotype_uniquenames":["pyk1-A343T-A343T-amino_acid_mutation-expression-not_assayed_or_wild_type"],"termid":"FYPO:0007363","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000126":null,"FYPO:0007363":null,"FYPO_EXT:0000002":null}}


id: GO:0005213
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"The action of a molecule that contributes to the structural integrity of an egg chorion. An example of this is found in Drosophila melanogaster.","definition_xrefs":["GOC:mah","GOC:sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"structural molecule activity","termid":"GO:0005198"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005198"}],"interesting_parent_ids":["GO:0003674","GO:0005198"],"is_obsolete":false,"name":"structural constituent of egg chorion","synonyms":[{"name":"structural constituent of chorion","type":"broad"},{"name":"structural protein of chorion","type":"narrow"}],"termid":"GO:0005213"}


id: GO:0071129
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of an alphaV-beta3 integrin complex bound to lipid phosphate phosphohydrolase-3.","definition_xrefs":["PMID:16099422"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"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:0005886"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005886"],"is_obsolete":false,"name":"alphaV-beta3 integrin-LPP3 complex","synonyms":[{"name":"ITGAV-ITGB3-PPAP2B complex","type":"narrow"}],"termid":"GO:0071129"}


id: MONDO:0000391
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Bethlem myopathy (obsolete MONDO:0000391)","termid":"MONDO:0000391","xrefs":{"Monarch":{"xref_id":"0000391"}}}


id: MONDO:1011678
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"endocrine system disorder, non-human animal","termid":"MONDO:1011317"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primary hypothyroidism, non-human animal","secondary_identifiers":["OMIA:000538"],"termid":"MONDO:1011678","xrefs":{"Monarch":{"xref_id":"1011678"}}}


id: GO:0045208
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of a MAPK phosphatase from the nucleus to the cytoplasm.","definition_xrefs":["GOC:ebc"],"gene_count":0,"genotype_count":0,"name":"obsolete MAPK phosphatase export from nucleus (obsolete GO:0045208)","synonyms":[{"name":"MAPK phosphatase export from cell nucleus","type":"exact"},{"name":"MAPK phosphatase export out of nucleus","type":"exact"},{"name":"MAPK phosphatase transport from nucleus to cytoplasm","type":"exact"},{"name":"MAPK phosphatase-nucleus export","type":"exact"}],"termid":"GO:0045208"}


id: PR:Q76PC7
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mti3 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q76PC7"],"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":"translation initiation factor, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC18E5.13","synonyms":[{"name":"Spom972h-mti3","type":"exact"}],"termid":"PR:Q76PC7"}


id: PBO:0073251
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"septin 4","termid":"PBO:0073251"}


id: GO:0009467
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete monoheme class I cytochrome c (obsolete GO:0009467)","synonyms":[{"name":"monoheme class I cytochrome c","type":"exact"}],"termid":"GO:0009467"}


id: PBO:0069304
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 560, pseudogene","termid":"PBO:0069304"}


id: GO:0005537
data:
  {"annotated_genes":["SJAG_02839","SJAG_04571","SJAG_01991","SJAG_03535"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[79600,111059,114070,118816],"is_not":false,"summary":null,"term":"GO:0005537"}]},"cv_name":"molecular_function","definition":"Binding to mannose, a monosaccharide hexose, stereoisomeric with glucose, that occurs naturally only in polymerized forms called mannans.","definition_xrefs":["ISBN:0192800981","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monosaccharide binding","termid":"GO:0048029"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01991":null,"SJAG_02839":null,"SJAG_03535":null,"SJAG_04571":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:0003674","GO:0005488"],"is_obsolete":false,"name":"D-mannose binding","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-947991"],"synonyms":[{"name":"mannose binding","type":"broad"},{"name":"mannose binding lectin","type":"related"}],"termid":"GO:0005537","terms_by_termid":{"GO:0005537":null}}


id: MONDO:0100431
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A migraine disorder characterized by episodes that occur in the absence of preceding focal neurological symptoms.","definition_xrefs":["NCIT:C117004"],"direct_ancestors":[{"relation_name":"is_a","term_name":"migraine disorder","termid":"MONDO:0005277"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"migraine without aura","secondary_identifiers":["MEDGEN:137899","MESH:D020326","SCTID:56097005","UMLS:C0338480","DOID:12783","icd11.foundation:2048783472"],"synonyms":[{"name":"common migraine","type":"exact"}],"termid":"MONDO:0100431","xrefs":{"Monarch":{"xref_id":"0100431"}}}


id: PBO:0074449
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"survival of motor neuron 1, telomeric","termid":"PBO:0074449"}


id: MONDO:0044228
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Since the initial discovery of the human electroencephalogram (EEG) by {1:Berger (1929)}, it has been speculated that neural oscillations play a broad role in nervous systems and form the basis for higher cognitive functions and consciousness. The presence of a beta/gamma oscillation (18 to 50 Hz) is thought to represent an activated state of the underlying neuronal network. These beta (12-29 Hz) and gamma (30-50 Hz) brain rhythms involve gamma-aminobutyric acid type A (GABA-A) receptor action ({2:Haenschel et al., 2000}; summary by {3:Porjesz et al., 2002}).","definition_xrefs":["OMIM:130190"],"gene_count":0,"genotype_count":0,"name":"obsolete eegbqtl (obsolete MONDO:0044228)","synonyms":[{"name":"EEGBQTL","type":"related"},{"name":"ELECTROENCEPHALOGRAPHIC pattern, BETA frequency, quantitative trait locus","type":"related"}],"termid":"MONDO:0044228","xrefs":{"Monarch":{"xref_id":"0044228"}}}


id: GO:0033488
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of cholesterol, cholest-5-en-3 beta-ol, via the intermediate 24,25-dihydrolanosterol.","definition_xrefs":["MetaCyc:PWY66-3","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cholesterol biosynthetic process","termid":"GO:0006695"}],"gene_count":0,"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:0006629"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0006629"],"is_obsolete":false,"name":"cholesterol biosynthetic process via 24,25-dihydrolanosterol","synonyms":[{"name":"cholesterol anabolism via 24,25-dihydrolanosterol","type":"exact"},{"name":"cholesterol biosynthesis via 24,25-dihydrolanosterol","type":"exact"},{"name":"cholesterol formation via 24,25-dihydrolanosterol","type":"exact"},{"name":"cholesterol synthesis via 24,25-dihydrolanosterol","type":"exact"}],"termid":"GO:0033488"}


id: PBO:0031750
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_histone_methylation","termid":"PBO:0031750"}


id: PBO:0031613
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_vacuolar_transport","termid":"PBO:0031613"}


id: PBO:0009122
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gamma-tubulin Gtb1","termid":"PBO:0009122"}


id: PBO:0109310
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ligand of numb-protein X 2B, pseudogene","termid":"PBO:0109310"}


id: MONDO:0035466
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete nephrotic syndrome without extrarenal manifestations (obsolete MONDO:0035466)","secondary_identifiers":["Orphanet:567564"],"termid":"MONDO:0035466","xrefs":{"Monarch":{"xref_id":"0035466"}}}


id: PBO:0086430
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative integral membrane protein; member of DUP240 gene family","termid":"PBO:0086430"}


id: PR:O13874
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC1B3.09c gene.","definition_xrefs":["PRO:DNx","UniProtKB:O13874"],"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 NOC2 family protein C1B3.09c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1B3.09c","synonyms":[{"name":"Spom972h-SPAC1B3.09c","type":"exact"}],"termid":"PR:O13874"}


id: PBO:0047390
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box protein 30","termid":"PBO:0047390"}


id: MONDO:0015206
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome","termid":"MONDO:0015160"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"short stature-heart defect-craniofacial anomalies syndrome","secondary_identifiers":["Orphanet:1088","MEDGEN:419321","MESH:C535871","UMLS:C2931050"],"synonyms":[{"name":"Rommen Mueller Sybert syndrome","type":"related"},{"name":"Rommen-Mueller-Sybert syndrome","type":"exact"},{"name":"short stature heart defect and craniofacial anomalies","type":"related"}],"termid":"MONDO:0015206","xrefs":{"Monarch":{"xref_id":"0015206"}}}


id: PBO:0082128
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Actin; structural protein involved in cell polarization, endocytosis, and other cytoskeletal functions; monomeric actin in the nucleus plays a role in INO80 chromatin remodeling","termid":"PBO:0082128"}


id: GO:0061100
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a neuroendocrine cell of the lung epithelium.","definition_xrefs":["GOC:dph","PMID:9126746"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuroendocrine cell differentiation","termid":"GO:0061101"},{"relation_name":"is_a","term_name":"lung secretory cell differentiation","termid":"GO:0061140"}],"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":"lung neuroendocrine cell differentiation","termid":"GO:0061100"}


id: GO:0045892
data:
  {"annotated_genes":["SJAG_01804","SJAG_01799","SJAG_02846","SJAG_01157","SJAG_03845","SJAG_04312","SJAG_04539","SJAG_01254","SJAG_00142","SJAG_04921","SJAG_00926","SJAG_00969","SJAG_03067","SJAG_00861","SJAG_00441","SJAG_03319","SJAG_02981","SJAG_00124","SJAG_02255","SJAG_01680","SJAG_04039","SJAG_00266","SJAG_02858","SJAG_00802","SJAG_04249","SJAG_04268","SJAG_00792","SJAG_03473","SJAG_00290","SJAG_04584","SJAG_02444","SJAG_02752","SJAG_02104","SJAG_00163","SJAG_02730","SJAG_02385","SJAG_04613","SJAG_00996","SJAG_03081","SJAG_01199","SJAG_00987","SJAG_01000","SJAG_01311","SJAG_04026","SJAG_01230","SJAG_04381","SJAG_02898","SJAG_01707","SJAG_00410","SJAG_03143","SJAG_04512","SJAG_01728","SJAG_04607"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[101392],"is_not":false,"summary":null,"term":"GO:0045892"},{"annotations":[108283],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0060195"},{"annotations":[77376,108546,109327,111456,74661,107046,112399,113279,107066,93738,108285,72552,94978,99212,73597,92476,96617,70477,87933,101317,94081,102168,104273,103871,106231,108888,106573,114566,114133,117668,91523,94567,94223,74435,80791,111033,95061,74010,72256,79855,93640,74205,77114,75710,70920,91595,92500,104574,106137,106815],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000122"},{"annotations":[74062],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016480"},{"annotations":[101318],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010621"},{"annotations":[118234],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034244"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of cellular DNA-templated transcription.","definition_xrefs":["GOC:go_curators","GOC:txnOH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of DNA-templated transcription","termid":"GO:0006355"},{"relation_name":"is_a","term_name":"negative regulation of RNA biosynthetic process","termid":"GO:1902679"},{"relation_name":"negatively_regulates","term_name":"DNA-templated transcription","termid":"GO:0006351"}],"gene_count":53,"genes_by_uniquename":{"SJAG_00124":null,"SJAG_00142":null,"SJAG_00163":null,"SJAG_00266":null,"SJAG_00290":null,"SJAG_00410":null,"SJAG_00441":null,"SJAG_00792":null,"SJAG_00802":null,"SJAG_00861":null,"SJAG_00926":null,"SJAG_00969":null,"SJAG_00987":null,"SJAG_00996":null,"SJAG_01000":null,"SJAG_01157":null,"SJAG_01199":null,"SJAG_01230":null,"SJAG_01254":null,"SJAG_01311":null,"SJAG_01680":null,"SJAG_01707":null,"SJAG_01728":null,"SJAG_01799":null,"SJAG_01804":null,"SJAG_02104":null,"SJAG_02255":null,"SJAG_02385":null,"SJAG_02444":null,"SJAG_02730":null,"SJAG_02752":null,"SJAG_02846":null,"SJAG_02858":null,"SJAG_02898":null,"SJAG_02981":null,"SJAG_03067":null,"SJAG_03081":null,"SJAG_03143":null,"SJAG_03319":null,"SJAG_03473":null,"SJAG_03845":null,"SJAG_04026":null,"SJAG_04039":null,"SJAG_04249":null,"SJAG_04268":null,"SJAG_04312":null,"SJAG_04381":null,"SJAG_04512":null,"SJAG_04539":null,"SJAG_04584":null,"SJAG_04607":null,"SJAG_04613":null,"SJAG_04921":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006355"},{"rel_name":"regulates","termid":"GO:0006351"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006351"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0006351","GO:0008150","GO:0006355"],"is_obsolete":false,"name":"negative regulation of DNA-templated transcription","references_by_uniquename":{"GO_REF:0000024":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0032582","GO:0061021","GO:0016481"],"synonyms":[{"name":"down regulation of gene-specific transcription","type":"related"},{"name":"down regulation of transcription, DNA-dependent","type":"exact"},{"name":"down-regulation of gene-specific transcription","type":"related"},{"name":"down-regulation of transcription, DNA-dependent","type":"exact"},{"name":"downregulation of gene-specific transcription","type":"related"},{"name":"downregulation of transcription, DNA-dependent","type":"exact"},{"name":"inhibition of gene-specific transcription","type":"related"},{"name":"inhibition of transcription, DNA-dependent","type":"narrow"},{"name":"negative regulation of cellular transcription, DNA-dependent","type":"exact"},{"name":"negative regulation of gene-specific transcription","type":"related"},{"name":"negative regulation of transcription, DNA-dependent","type":"exact"},{"name":"negative regulation of transcription, DNA-templated","type":"exact"},{"name":"transcription repressor activity","type":"related"}],"termid":"GO:0045892","terms_by_termid":{"GO:0000122":null,"GO:0010621":null,"GO:0016480":null,"GO:0034244":null,"GO:0045892":null,"GO:0060195":null}}


id: GO:0141113
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the Wnt signaling pathway, planar cell polarity pathway.","definition_xrefs":["PMID:19056682"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of non-canonical Wnt signaling pathway","termid":"GO:2000051"},{"relation_name":"is_a","term_name":"regulation of Wnt signaling pathway, planar cell polarity pathway","termid":"GO:2000095"},{"relation_name":"negatively_regulates","term_name":"Wnt signaling pathway, planar cell polarity pathway","termid":"GO:0060071"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of Wnt signaling pathway, planar cell polarity pathway","termid":"GO:0141113"}


id: GO:0002786
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of antibacterial peptide production.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of antimicrobial peptide production","termid":"GO:0002784"},{"relation_name":"regulates","term_name":"antibacterial peptide production","termid":"GO:0002778"}],"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:0008150","GO:0010467"],"is_obsolete":false,"name":"regulation of antibacterial peptide production","termid":"GO:0002786"}


id: MONDO:1012361
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"bird disease","termid":"MONDO:0024905"},{"relation_name":"is_a","term_name":"yellow-semen syndrome, non-human animal","termid":"MONDO:1011920"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"yellow-semen syndrome, turkey","secondary_identifiers":["OMIA:001304-9103"],"termid":"MONDO:1012361","xrefs":{"Monarch":{"xref_id":"1012361"}}}


id: PATO:0001617
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A morphological quality inhering in a bearer by virtue of the bearer's being distorted in form.","definition_xrefs":["thefreedictionary.com:thefreedictionary.com"],"direct_ancestors":[{"relation_name":"is_a","term_name":"morphology","termid":"PATO:0000051"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deformed","synonyms":[{"name":"disfigured","type":"related"},{"name":"distorted","type":"related"}],"termid":"PATO:0001617"}


id: PBO:0059791
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CYB pseudogene 17","termid":"PBO:0059791"}


id: PBO:0080687
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WIZ pseudogene 1","termid":"PBO:0080687"}


id: GO:1904711
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of Wnt-Frizzled-LRP5/6 complex assembly.","definition_xrefs":["GOC:bf","GOC:TermGenie","GO_REF:0000058","GOC:PARL"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein-containing complex assembly","termid":"GO:0043254"},{"relation_name":"regulates","term_name":"Wnt-Frizzled-LRP5/6 complex assembly","termid":"GO:1904701"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0065003"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044085","GO:0065003","GO:0008150"],"is_obsolete":false,"name":"regulation of Wnt-Frizzled-LRP5/6 complex assembly","synonyms":[{"name":"regulation of Frizzled-LRP5/6 complex assembly","type":"related"},{"name":"regulation of Frizzled-LRP5/6 complex formation","type":"related"},{"name":"regulation of WNT-FZD-LRP5 complex assembly","type":"narrow"},{"name":"regulation of WNT-FZD-LRP5 complex formation","type":"narrow"},{"name":"regulation of WNT-FZD-LRP6 complex assembly","type":"narrow"},{"name":"regulation of WNT-FZD-LRP6 complex formation","type":"narrow"},{"name":"regulation of Wnt receptor complex assembly","type":"broad"},{"name":"regulation of Wnt-FZD-LRP5/6 trimeric complex assembly","type":"exact"},{"name":"regulation of Wnt-FZD-LRP5/6 trimeric complex formation","type":"exact"},{"name":"regulation of Wnt-induced Frizzled-LRP5/6 complex assembly","type":"related"},{"name":"regulation of Wnt-induced Frizzled-LRP5/6 complex formation","type":"related"}],"termid":"GO:1904711"}


id: MONDO:0023303
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Hamanishi-Ueba-Tsuji syndrome (obsolete MONDO:0023303)","termid":"MONDO:0023303","xrefs":{"Monarch":{"xref_id":"0023303"}}}


id: GO:0044735
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which an organism inhibits or disrupts the activity of a pH-gated (also known as acid-sensing ion channel (ASIC)) in another organism via the action of a venom.","definition_xrefs":["GOC:fj","GOC:jl","PMID:23034652"],"direct_ancestors":[{"relation_name":"is_a","term_name":"venom-mediated perturbation of pH-gated ion channel activity","termid":"GO:0044733"}],"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":"venom-mediated inhibition of pH-gated ion channel activity","synonyms":[{"name":"envenomation resulting in negative regulation of ASIC channel activity in other organism","type":"exact"},{"name":"envenomation resulting in negative regulation of acid-sensing ion channel activity in another organism","type":"exact"},{"name":"envenomation resulting in negative regulation of acid-sensing ion channel activity in other organism","type":"exact"},{"name":"venom-mediated inhibition of acid-sensing ion channel activity","type":"related"}],"termid":"GO:0044735"}


id: MONDO:0006436
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An aggressive carcinoma that arises from the submandibular gland. It is characterized by the presence of malignant epithelial and myoepithelial cells forming cribriform, tubular, and solid patterns. It usually presents as a slow growing mass. Patients develop pain because of the tendency of these carcinomas to invade perineural tissues.","definition_xrefs":["NCIT:C5935"],"direct_ancestors":[{"relation_name":"is_a","term_name":"submandibular gland cancer","termid":"MONDO:0004724"},{"relation_name":"is_a","term_name":"major salivary gland adenoid cystic carcinoma","termid":"MONDO:0045063"}],"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:0004335","MONDO:0004992"],"is_obsolete":false,"name":"submandibular gland adenoid cystic carcinoma","secondary_identifiers":["MEDGEN:277773","EFO:1000555","SCTID:423189008","UMLS:C1336522"],"synonyms":[{"name":"adenoid cystic carcinoma of submandibular gland","type":"exact"},{"name":"adenoid cystic carcinoma of the submandibular gland","type":"exact"},{"name":"submandibular gland adenoid cystic carcinoma","type":"exact"}],"termid":"MONDO:0006436","xrefs":{"Monarch":{"xref_id":"0006436"}}}


id: PBO:0045201
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DnaJ heat shock protein family (Hsp40) member B12","termid":"PBO:0045201"}


id: PBO:0051444
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin lambda variable 3-30 (pseudogene)","termid":"PBO:0051444"}


id: MONDO:0005722
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute upper respiratory airways infection that results in the swelling of the larynx. It is usually caused by parainfluenza viruses. Signs include a characteristic barking cough and stridor.","definition_xrefs":["NCIT:C26735"],"direct_ancestors":[{"relation_name":"is_a","term_name":"laryngotracheitis","termid":"MONDO:0000263"},{"relation_name":"is_a","term_name":"bronchitis","termid":"MONDO:0003781"},{"relation_name":"is_a","term_name":"acute laryngitis","termid":"MONDO:0004777"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"croup","secondary_identifiers":["SCTID:71186008","UMLS:C0010380","DOID:9395","MEDGEN:3668","ICD9:464.4","MESH:D003440","EFO:0007227"],"synonyms":[{"name":"acute laryngotracheitis","type":"related"},{"name":"acute laryngotracheobronchitis","type":"exact"},{"name":"acute obstructive laryngitis","type":"exact"},{"name":"croup syndrome","type":"exact"}],"termid":"MONDO:0005722","xrefs":{"Monarch":{"xref_id":"0005722"}}}


id: GO:2001295
data:
  {"annotated_genes":["SJAG_03313"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[66262],"is_not":false,"summary":null,"term":"GO:2001295"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of malonyl-CoA, the S-malonyl derivative of coenzyme A.","definition_xrefs":["UniPathway:UPA00655","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyl-CoA biosynthetic process","termid":"GO:0071616"},{"relation_name":"is_a","term_name":"malonyl-CoA metabolic process","termid":"GO:2001293"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03313":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:0006790"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0055086","GO:0006790","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"malonyl-CoA biosynthetic process","references_by_uniquename":{"GO_REF:0000041":null},"synonyms":[{"name":"malonyl-CoA anabolism","type":"exact"},{"name":"malonyl-CoA biosynthesis","type":"exact"},{"name":"malonyl-CoA formation","type":"exact"},{"name":"malonyl-CoA synthesis","type":"exact"}],"termid":"GO:2001295","terms_by_termid":{"GO:2001295":null}}


id: GO:0005689
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Any spliceosomal complex that forms during the splicing of a messenger RNA primary transcript to excise an intron; the series of U12-type spliceosomal complexes is involved in the splicing of the majority of introns that contain atypical AT-AC terminal dinucleotides, as well as other non-canonical introns. The entire splice site signal, not just the terminal dinucleotides, is involved in determining which spliceosome utilizes the site.","definition_xrefs":["PMID:11971955","GOC:mah","PMID:11574683","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spliceosomal complex","termid":"GO:0005681"}],"gene_count":0,"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"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005634"],"is_obsolete":false,"name":"U12-type spliceosomal complex","secondary_identifiers":["Wikipedia:Minor_spliceosome"],"synonyms":[{"name":"AT-AC spliceosomal complex","type":"narrow"},{"name":"minor (U12-type) spliceosomal complex","type":"exact"},{"name":"minor spliceosomal complex","type":"exact"}],"termid":"GO:0005689"}


id: FYPO:0002693
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An increased chemical resistance phenotype observed in the vegetative growth phase of the life cycle in which cells grow in the presence of a higher concentration of diamide (N,N,N',N'-tetramethyldiazene-1,2-dicarboxamide) than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002682"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000139","FYPO:0001985","FYPO:0002682","FYPO:0000003"],"is_obsolete":false,"name":"resistance to diamide","synonyms":[{"name":"resistance to N,N,N',N'-tetramethyldiazene-1,2-dicarboxamide","type":"exact"},{"name":"resistance to diamide during mitotic cell cycle","type":"related"},{"name":"resistance to diamide during vegetative growth","type":"exact"},{"name":"resistant to diamide","type":"exact"}],"termid":"FYPO:0002693"}


id: MONDO:0005987
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infections with nematodes of the genus toxascaris.","definition_xrefs":["MESH:D017227"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Ascaridida infectious disease","termid":"MONDO:0005656"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"toxascariasis","secondary_identifiers":["UMLS:C0040522","MEDGEN:21221","DOID:3107"],"synonyms":[{"name":"Toxascaris caused disease or disorder","type":"exact"},{"name":"Toxascaris disease or disorder","type":"exact"},{"name":"Toxascaris infectious disease","type":"exact"}],"termid":"MONDO:0005987","xrefs":{"Monarch":{"xref_id":"0005987"}}}


id: MONDO:0021486
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that involves the ciliary body.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ciliary body neoplasm","termid":"MONDO:0021229"},{"relation_name":"is_a","term_name":"benign neoplasm of iris","termid":"MONDO:0021485"}],"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":"benign neoplasm of ciliary body","secondary_identifiers":["NCIT:C4779","SCTID:92060009","MEDGEN:96927","UMLS:C0496894","ICD9:224.0","icd11.foundation:1138156221"],"synonyms":[{"name":"benign ciliary body neoplasm","type":"exact"},{"name":"benign ciliary body tumor","type":"exact"},{"name":"benign ciliary body tumour","type":"exact"},{"name":"benign neoplasm of the ciliary body","type":"exact"},{"name":"benign tumor of ciliary body","type":"exact"},{"name":"benign tumor of the ciliary body","type":"exact"},{"name":"benign tumour of ciliary body","type":"exact"},{"name":"benign tumour of the ciliary body","type":"exact"},{"name":"ciliary body benign neoplasm","type":"exact"}],"termid":"MONDO:0021486","xrefs":{"Monarch":{"xref_id":"0021486"}}}


id: PBO:0028930
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_localization_to_growing_cell_tip","termid":"PBO:0028930"}


id: PBO:0038322
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"malacards_disease_name","termid":"PBO:0038322"}


id: PBO:0110382
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KLHL5 pseudogene 1","termid":"PBO:0110382"}


id: SO:0002118
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A polymorphic pseudogene transcript that contains a CDS but has one or more splice junctions >50bp downstream of stop codon. Premature stop codon is not introduced, directly or indirectly, as a result of the variation i.e. must be present in both protein_coding and pseudogenic alleles.","definition_xrefs":["GENCODE:http://www.gencodegenes.org/gencode_biotypes.html"],"direct_ancestors":[{"relation_name":"is_a","term_name":"NMD_transcript","termid":"SO:0002114"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NMD_polymorphic_pseudogene_transcript","synonyms":[{"name":"NMD polymorphic pseudogene transcript","type":"exact"},{"name":"nonsense_mediated_decay_polymorphic_pseudogene","type":"exact"}],"termid":"SO:0002118"}


id: PBO:0002235
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.6.1.52","termid":"PBO:0002235"}


id: MONDO:0014355
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete syndrome associated with dilated cardiomyopathy (obsolete MONDO:0016337)","termid":"MONDO:0016337"},{"relation_name":"excluded_subClassOf","term_name":"obsolete inherited odontologic disease (obsolete MONDO:0019183)","termid":"MONDO:0019183"},{"relation_name":"is_a","term_name":"arrhythmogenic cardiomyopathy with wooly hair and keratoderma","termid":"MONDO:0011581"},{"relation_name":"is_a","term_name":"erythrokeratoderma","termid":"MONDO:0019270"}],"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":"cardiomyopathy, dilated, with wooly hair, keratoderma, and tooth agenesis","secondary_identifiers":["GARD:16014","OMIM:615821","Orphanet:476096","UMLS:C4014393","MEDGEN:862830"],"synonyms":[{"name":"DCWHKTA","type":"related"},{"name":"EKC syndrome","type":"exact"},{"name":"cardiomyopathy, dilated, with wooly hair, keratoderma, and tooth agenesis","type":"exact"},{"name":"dilated cardiomyopathy with woolly hair, keratoderma, and tooth agenesis","type":"exact"},{"name":"dilated cardiomyopathy with wooly hair, keratoderma, and tooth agenesis","type":"exact"},{"name":"erythrokeratodermia-cardiomyopathy syndrome","type":"exact"}],"termid":"MONDO:0014355","xrefs":{"Monarch":{"xref_id":"0014355"}}}


id: PBO:0087832
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Thiamine pyrophosphokinase; phosphorylates thiamine to produce the coenzyme thiamine pyrophosphate (thiamine diphosphate)","termid":"PBO:0087832"}


id: GO:0060515
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that results in the delineation of a specific region of the urogenital sinus epithelium into the area in which the prostate gland will develop.","definition_xrefs":["PMID:18977204","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"is_a","term_name":"specification of animal organ identity","termid":"GO:0010092"},{"relation_name":"part_of","term_name":"prostatic bud formation","termid":"GO:0060513"}],"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":"prostate field specification","termid":"GO:0060515"}


id: MONDO:0007576
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A primary or metastatic malignant neoplasm involving the esophagus.","definition_xrefs":["NCIT:C7478"],"direct_ancestors":[{"relation_name":"is_a","term_name":"digestive system cancer","termid":"MONDO:0002516"},{"relation_name":"is_a","term_name":"thoracic cancer","termid":"MONDO:0003274"},{"relation_name":"is_a","term_name":"neoplasm of esophagus","termid":"MONDO:0021355"}],"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":"esophageal cancer","secondary_identifiers":["UMLS:C0546837","OMIM:133239","ICD9:150.8","MEDGEN:107792","DOID:5041","NCIT:C4764","ICD9:150.9","ICD9:150.3","ICD9:150.5","ICD9:150.2","ICD9:150.4","SCTID:187724003","SCTID:363402007"],"synonyms":[{"name":"Aerodigestive tract cancer, susceptibility to","type":"related"},{"name":"Ca lower third esophagus","type":"narrow"},{"name":"Ca lower third oesophagus","type":"narrow"},{"name":"Ca middle third esophagus","type":"narrow"},{"name":"Ca middle third oesophagus","type":"narrow"},{"name":"Escc, susceptibility to","type":"related"},{"name":"cancer of esophagus","type":"exact"},{"name":"cancer of oesophagus","type":"exact"},{"name":"esophageal cancer","type":"exact"},{"name":"esophageal cancer, somatic","type":"exact"},{"name":"esophageal carcinoma, somatic","type":"exact"},{"name":"esophageal squamous cell carcinoma, somatic","type":"exact"},{"name":"esophageal squamous cell carcinoma, susceptibility to","type":"related"},{"name":"esophagus cancer","type":"exact"},{"name":"gastric cardia adenocarcinoma, susceptibility to","type":"related"},{"name":"malignant esophageal neoplasm","type":"exact"},{"name":"malignant esophageal tumor","type":"exact"},{"name":"malignant esophageal tumour","type":"exact"},{"name":"malignant esophagus neoplasm","type":"exact"},{"name":"malignant esophagus tumor","type":"exact"},{"name":"malignant neoplasm of distal third of esophagus","type":"narrow"},{"name":"malignant neoplasm of distal third of oesophagus","type":"narrow"},{"name":"malignant neoplasm of esophagus","type":"exact"},{"name":"malignant neoplasm of lower third of esophagus","type":"narrow"},{"name":"malignant neoplasm of lower third of oesophagus","type":"narrow"},{"name":"malignant neoplasm of middle third of esophagus","type":"narrow"},{"name":"malignant neoplasm of middle third of oesophagus","type":"narrow"},{"name":"malignant neoplasm of oesophagus","type":"exact"},{"name":"malignant neoplasm of proximal third of esophagus","type":"narrow"},{"name":"malignant neoplasm of proximal third of oesophagus","type":"narrow"},{"name":"malignant neoplasm of the esophagus","type":"exact"},{"name":"malignant neoplasm of the oesophagus","type":"exact"},{"name":"malignant neoplasm of upper third esophagus","type":"narrow"},{"name":"malignant neoplasm of upper third oesophagus","type":"narrow"},{"name":"malignant oesophagus neoplasm","type":"exact"},{"name":"malignant oesophagus tumour","type":"exact"},{"name":"malignant tumor of abdominal esophagus","type":"narrow"},{"name":"malignant tumor of distal third of esophagus","type":"narrow"},{"name":"malignant tumor of esophagus","type":"exact"},{"name":"malignant tumor of proximal third of esophagus","type":"narrow"},{"name":"malignant tumor of the esophagus","type":"exact"},{"name":"malignant tumor of the middle third of the esophagus","type":"narrow"},{"name":"malignant tumour of abdominal oesophagus","type":"narrow"},{"name":"malignant tumour of distal third of oesophagus","type":"narrow"},{"name":"malignant tumour of oesophagus","type":"exact"},{"name":"malignant tumour of proximal third of oesophagus","type":"narrow"},{"name":"malignant tumour of the middle third of the oesophagus","type":"narrow"},{"name":"malignant tumour of the oesophagus","type":"exact"},{"name":"oesophagus cancer","type":"exact"}],"termid":"MONDO:0007576","xrefs":{"Monarch":{"xref_id":"0007576"}}}


id: GO:1900691
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of gliotoxin biosynthetic process.","definition_xrefs":["GOC:di","GOC:TermGenie"],"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 sulfur metabolic process","termid":"GO:0051176"},{"relation_name":"is_a","term_name":"positive regulation of secondary metabolite biosynthetic process","termid":"GO:1900378"},{"relation_name":"is_a","term_name":"regulation of gliotoxin biosynthetic process","termid":"GO:1900689"},{"relation_name":"positively_regulates","term_name":"gliotoxin biosynthetic process","termid":"GO:2001310"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0019748"},{"rel_name":"regulates","termid":"GO:0006790"},{"rel_name":"positively_regulates","termid":"GO:0006790"},{"rel_name":"regulates","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0008150","GO:0019748","GO:0006790"],"is_obsolete":false,"name":"positive regulation of gliotoxin biosynthetic process","synonyms":[{"name":"activation of gliotoxin anabolism","type":"exact"},{"name":"activation of gliotoxin biosynthesis","type":"exact"},{"name":"activation of gliotoxin biosynthetic process","type":"narrow"},{"name":"activation of gliotoxin formation","type":"exact"},{"name":"activation of gliotoxin synthesis","type":"exact"},{"name":"positive regulation of gliotoxin anabolism","type":"exact"},{"name":"positive regulation of gliotoxin biosynthesis","type":"exact"},{"name":"positive regulation of gliotoxin formation","type":"exact"},{"name":"positive regulation of gliotoxin synthesis","type":"exact"},{"name":"up regulation of gliotoxin anabolism","type":"exact"},{"name":"up regulation of gliotoxin biosynthesis","type":"exact"},{"name":"up regulation of gliotoxin biosynthetic process","type":"exact"},{"name":"up regulation of gliotoxin formation","type":"exact"},{"name":"up regulation of gliotoxin synthesis","type":"exact"},{"name":"up-regulation of gliotoxin anabolism","type":"exact"},{"name":"up-regulation of gliotoxin biosynthesis","type":"exact"},{"name":"up-regulation of gliotoxin biosynthetic process","type":"exact"},{"name":"up-regulation of gliotoxin formation","type":"exact"},{"name":"up-regulation of gliotoxin synthesis","type":"exact"},{"name":"upregulation of gliotoxin anabolism","type":"exact"},{"name":"upregulation of gliotoxin biosynthesis","type":"exact"},{"name":"upregulation of gliotoxin biosynthetic process","type":"exact"},{"name":"upregulation of gliotoxin formation","type":"exact"},{"name":"upregulation of gliotoxin synthesis","type":"exact"}],"termid":"GO:1900691"}


id: GO:1990218
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which an organism activates, maintains or increases the frequency, rate or extent of the abscisic acid levels in the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:17304219"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation by symbiont of abscisic acid levels in host (obsolete GO:1990218)","termid":"GO:1990218"}


id: MONDO:0043723
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Fracture in the proximal half of the shaft of the ulna, with dislocation of the head of the radius.","definition_xrefs":["MESH:D009011"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ulna fracture","termid":"MONDO:0005322"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Monteggia's fracture","secondary_identifiers":["SCTID:123973009"],"synonyms":[{"name":"Monteggia fracture","type":"related"},{"name":"Monteggias fracture","type":"related"},{"name":"fracture, Monteggia's","type":"related"},{"name":"monteggia fracture","type":"related"},{"name":"monteggia fracture dislocation","type":"related"},{"name":"monteggia's dislocation","type":"related"},{"name":"monteggia's fracture","type":"exact"}],"termid":"MONDO:0043723","xrefs":{"Monarch":{"xref_id":"0043723"}}}


id: GO:0048103
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The self-renewing division of a somatic stem cell, a stem cell that can give rise to cell types of the body other than those of the germ-line.","definition_xrefs":["GOC:jid","ISBN:0582227089"],"direct_ancestors":[{"relation_name":"is_a","term_name":"stem cell division","termid":"GO:0017145"}],"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":"somatic stem cell division","synonyms":[{"name":"somatic stem cell renewal","type":"exact"}],"termid":"GO:0048103"}


id: PBO:0000251
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pleckstrin homology domain","termid":"PBO:0000251"}


id: SO:0000230
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A primary transcript encoding valyl tRNA (SO:000273).","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA_primary_transcript","termid":"SO:0000210"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"valine_tRNA_primary_transcript","synonyms":[{"name":"valine tRNA primary transcript","type":"exact"}],"termid":"SO:0000230"}


id: SO:0000456
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene that is recombinationally rearranged.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"recombinationally_rearranged","termid":"SO:0000940"},{"relation_name":"is_a","term_name":"gene","termid":"SO:0000704"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"recombinationally_rearranged_gene","synonyms":[{"name":"recombinationally rearranged gene","type":"exact"}],"termid":"SO:0000456"}


id: PBO:0068031
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 336","termid":"PBO:0068031"}


id: MONDO:0012649
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete FTSD (obsolete MONDO:0012649)","termid":"MONDO:0012649","xrefs":{"Monarch":{"xref_id":"0012649"}}}


id: MONDO:0019586
data:
  {"annotated_genes":["SJAG_04882","SJAG_03811","SJAG_02016"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85738,85737],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010577"},{"annotations":[87527],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010378"}]},"cv_name":"mondo","definition":"X-linked form of nonsyndromic deafness.","definition_xrefs":["MONDO:patterns/x_linked"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"prelingual non-syndromic genetic hearing loss","termid":"MONDO:0016297"},{"relation_name":"excluded_subClassOf","term_name":"postlingual non-syndromic genetic hearing loss","termid":"MONDO:0016298"},{"relation_name":"is_a","term_name":"nonsyndromic genetic hearing loss","termid":"MONDO:0019497"},{"relation_name":"is_a","term_name":"X-linked deafness","termid":"MONDO:0020768"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02016":null,"SJAG_03811":null,"SJAG_04882":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"}],"interesting_parent_ids":["MONDO:0019497"],"is_obsolete":false,"name":"X-linked nonsyndromic hearing loss","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:90625","GARD:16790","MEDGEN:1825990","DOID:0050566","UMLS:C5680192"],"synonyms":[{"name":"X-linked deafness","type":"narrow"},{"name":"X-linked isolated neurosensory deafness type DFN","type":"narrow"},{"name":"X-linked isolated neurosensory hearing loss type DFN","type":"exact"},{"name":"X-linked isolated sensorineural deafness type DFN","type":"narrow"},{"name":"X-linked isolated sensorineural hearing loss type DFN","type":"exact"},{"name":"X-linked non-syndromic neurosensory deafness type DFN","type":"narrow"},{"name":"X-linked non-syndromic neurosensory hearing loss type DFN","type":"exact"},{"name":"X-linked non-syndromic sensorineural deafness type DFN","type":"narrow"},{"name":"X-linked non-syndromic sensorineural hearing loss type DFN","type":"exact"},{"name":"X-linked nonsyndromic deafness","type":"narrow"},{"name":"X-linked nonsyndromic genetic deafness","type":"narrow"},{"name":"nonsyndromic deafness, X-linked","type":"narrow"},{"name":"nonsyndromic genetic deafness, X-linked","type":"narrow"}],"termid":"MONDO:0019586","terms_by_termid":{"MONDO:0010378":null,"MONDO:0010577":null},"xrefs":{"Monarch":{"xref_id":"0019586"}}}


id: PBO:0031582
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_cell_population_growth_rate","termid":"PBO:0031582"}


id: PBO:0053475
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 445","termid":"PBO:0053475"}


id: PBO:0065226
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proline rich 7, synaptic","termid":"PBO:0065226"}


id: GO:1902447
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of shade avoidance.","definition_xrefs":["GOC:TermGenie","PMID:23763263"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of response to stimulus","termid":"GO:0048585"},{"relation_name":"is_a","term_name":"regulation of shade avoidance","termid":"GO:1902446"},{"relation_name":"negatively_regulates","term_name":"shade avoidance","termid":"GO:0009641"}],"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 shade avoidance","synonyms":[{"name":"down regulation of shade avoidance","type":"exact"},{"name":"down-regulation of shade avoidance","type":"exact"},{"name":"downregulation of shade avoidance","type":"exact"},{"name":"inhibition of shade avoidance","type":"narrow"}],"termid":"GO:1902447"}


id: MONDO:0019724
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Secondary glomerular diseases are conditions with glomerular pathology in which an underlying cause can be established.","gene_count":0,"genotype_count":0,"name":"obsolete secondary glomerular disease (obsolete MONDO:0019724)","secondary_identifiers":["Orphanet:93551"],"termid":"MONDO:0019724","xrefs":{"Monarch":{"xref_id":"0019724"}}}


id: MONDO:0001865
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete autoimmune polyendocrinopathy syndrome (obsolete MONDO:0001865)","termid":"MONDO:0001865","xrefs":{"Monarch":{"xref_id":"0001865"}}}


id: MONDO:0032906
data:
  {"annotated_genes":["SJAG_04628"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87050],"is_not":false,"summary":null,"term":"MONDO:0032906"}]},"cv_name":"mondo","definition":"Any hereditary spastic paraplegia in which the cause of the disease is an autosomal recessive mutation in the PCYT2 gene.","definition_xrefs":["PMID:31637422","MONDO:patterns/hereditary"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary spastic paraplegia","termid":"MONDO:0019064"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04628":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"spastic paraplegia 82, autosomal recessive","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0112343","OMIM:618770","Orphanet:631073","MEDGEN:1710411","UMLS:C5394037"],"synonyms":[{"name":"SPG82","type":"exact"},{"name":"autosomal recessive spastic paraplegia type 82","type":"exact"},{"name":"spastic paraplegia 82, autosomal recessive","type":"exact"}],"termid":"MONDO:0032906","terms_by_termid":{"MONDO:0032906":null},"xrefs":{"Monarch":{"xref_id":"0032906"}}}


id: PBO:0030278
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_vegetative_cell_population_growth_rate","termid":"PBO:0030278"}


id: PBO:0004721
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F0-ATPase subunit (predicted)","termid":"PBO:0004721"}


id: PBO:0069037
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 282, pseudogene","termid":"PBO:0069037"}


id: FYPO:0005733
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of glutamate-ammonia ligase activity is increased during a cellular response to iron ion starvation.","definition_xrefs":["PMID:20435771","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased glutamate-ammonia ligase activity","termid":"FYPO:0002270"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000654","FYPO:0001985","FYPO:0000652","FYPO:0000707","FYPO:0000661"],"is_obsolete":false,"name":"increased glutamate-ammonia ligase activity during cellular response to iron ion starvation","synonyms":[{"name":"increased GS activity during cellular response to iron ion starvation","type":"exact"},{"name":"increased glutamate-ammonia ligase activity during iron ion starvation","type":"exact"},{"name":"increased glutamine synthetase activity during cellular response to iron ion starvation","type":"exact"},{"name":"increased glutamylhydroxamic synthetase activity during cellular response to iron ion starvation","type":"exact"}],"termid":"FYPO:0005733"}


id: PBO:0049322
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"general transcription factor IIA subunit 1","termid":"PBO:0049322"}


id: PBO:0043105
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chondroitin sulfate synthase 3","termid":"PBO:0043105"}


id: GO:0031932
data:
  {"annotated_genes":["SJAG_01320","SJAG_04460","SJAG_03067","SJAG_00117","SJAG_04987","SJAG_01020"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[72959,77445,77912,79284,99704,108886],"is_not":false,"summary":null,"term":"GO:0031932"}]},"cv_name":"cellular_component","definition":"A protein complex that contains at least TOR (target of rapamycin) and Rictor (rapamycin-insensitive companion of TOR), or orthologs of, in complex with other signaling components. Mediates the phosphorylation and activation of PKB (also called AKT). In Saccharomyces, the complex contains Avo1p, Avo2p, Tsc11p, Lst8p, Bit61p, Slm1p, Slm2p, and Tor2p.","definition_xrefs":["PMID:21548787","GOC:bf","PMID:15780592","GOC:jh","PMID:14736892","PMID:16469695"],"direct_ancestors":[{"relation_name":"is_a","term_name":"TOR complex","termid":"GO:0038201"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00117":null,"SJAG_01020":null,"SJAG_01320":null,"SJAG_03067":null,"SJAG_04460":null,"SJAG_04987":null},"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":"TORC2 complex","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Wikipedia:MTORC1"],"synonyms":[{"name":"TOR complex 2","type":"exact"},{"name":"TORC 2 complex","type":"exact"},{"name":"TORC2","type":"exact"},{"name":"mTORC2","type":"narrow"},{"name":"rapamycin and nutrient-insensitive TOR complex","type":"exact"}],"termid":"GO:0031932","terms_by_termid":{"GO:0031932":null}}


id: CHEBI:16907
data:
  {"annotation_feature_type":"gene","cv_name":"chebi_ontology","direct_ancestors":[{"relation_name":"is_a","term_name":"chemical entity","termid":"CHEBI:24431"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"4-nitroquinoline N-oxide","termid":"CHEBI:16907"}


id: FYECO:0000270
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which TEV protease was added to the medium or assay buffer. TEV protease cleaves a highly specific protein sequence and thus allows for artificial proteolytic regulation of genes engineered to contain the cleavage site.","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":"+ TEV protease","termid":"FYECO:0000270"}


id: MONDO:0009186
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":"epilepsy, photogenic, with spastic diplegia and intellectual disability","secondary_identifiers":["OMIM:226800","MESH:C565587","UMLS:C1856931","MEDGEN:347333"],"synonyms":[{"name":"epilepsy, photogenic, with spastic diplegia and intellectual disability","type":"exact"},{"name":"epilepsy, photogenic, with spastic diplegia and mental retardation","type":"exact"}],"termid":"MONDO:0009186","xrefs":{"Monarch":{"xref_id":"0009186"}}}


id: FYPO:0002093
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which cohesion between sister chromatids is decreased during meiosis.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal meiotic sister chromatid cohesion","termid":"FYPO:0002092"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0000641","FYPO:0005447","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"decreased meiotic sister chromatid cohesion","synonyms":[{"name":"decreased sister chromatid cohesion during meiosis","type":"exact"},{"name":"reduced meiotic sister chromatid cohesion","type":"exact"}],"termid":"FYPO:0002093"}


id: PBO:0075394
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sp7 transcription factor","termid":"PBO:0075394"}


id: PBO:0111903
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"wtf element","termid":"PBO:0111903"}


id: PBO:0080292
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vomeronasal 1 receptor 56 pseudogene","termid":"PBO:0080292"}


id: PBO:0058229
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4519","termid":"PBO:0058229"}


id: PR:P48011
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A DNA-directed RNA polymerases I, II, and III subunit RPABC4 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR12056:SF0","OMA:SCHPO02953","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":"DNA-directed RNA polymerases I, II, and III subunit RPABC4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC19C2.03","secondary_identifiers":["UniProtKB:P48011"],"synonyms":[{"name":"ABC10-alpha (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"RNA polymerases I, II, and III subunit ABC4 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-POLR2K","type":"exact"}],"termid":"PR:P48011"}


id: GO:0052048
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. An interaction with the host organism mediated by a substance secreted by the other (symbiont) organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete interaction with host via secreted substance (obsolete GO:0052048)","synonyms":[{"name":"interaction with host via secreted substance during symbiotic interaction","type":"related"},{"name":"interaction with host via secreted substance involved in symbiotic interaction","type":"related"}],"termid":"GO:0052048"}


id: GO:1900936
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of nonadec-1-ene biosynthetic process.","definition_xrefs":["GOC:TermGenie","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of olefin biosynthetic process","termid":"GO:1900912"},{"relation_name":"is_a","term_name":"negative regulation of nonadec-1-ene metabolic process","termid":"GO:1900933"},{"relation_name":"is_a","term_name":"regulation of nonadec-1-ene biosynthetic process","termid":"GO:1900935"},{"relation_name":"negatively_regulates","term_name":"nonadec-1-ene biosynthetic process","termid":"GO:1900877"}],"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 nonadec-1-ene biosynthetic process","synonyms":[{"name":"down regulation of nonadec-1-ene anabolism","type":"exact"},{"name":"down regulation of nonadec-1-ene biosynthesis","type":"exact"},{"name":"down regulation of nonadec-1-ene biosynthetic process","type":"exact"},{"name":"down regulation of nonadec-1-ene formation","type":"exact"},{"name":"down regulation of nonadec-1-ene synthesis","type":"exact"},{"name":"down-regulation of nonadec-1-ene anabolism","type":"exact"},{"name":"down-regulation of nonadec-1-ene biosynthesis","type":"exact"},{"name":"down-regulation of nonadec-1-ene biosynthetic process","type":"exact"},{"name":"down-regulation of nonadec-1-ene formation","type":"exact"},{"name":"down-regulation of nonadec-1-ene synthesis","type":"exact"},{"name":"downregulation of nonadec-1-ene anabolism","type":"exact"},{"name":"downregulation of nonadec-1-ene biosynthesis","type":"exact"},{"name":"downregulation of nonadec-1-ene biosynthetic process","type":"exact"},{"name":"downregulation of nonadec-1-ene formation","type":"exact"},{"name":"downregulation of nonadec-1-ene synthesis","type":"exact"},{"name":"inhibition of nonadec-1-ene anabolism","type":"exact"},{"name":"inhibition of nonadec-1-ene biosynthesis","type":"exact"},{"name":"inhibition of nonadec-1-ene biosynthetic process","type":"narrow"},{"name":"inhibition of nonadec-1-ene formation","type":"exact"},{"name":"inhibition of nonadec-1-ene synthesis","type":"exact"},{"name":"negative regulation of nonadec-1-ene anabolism","type":"exact"},{"name":"negative regulation of nonadec-1-ene biosynthesis","type":"exact"},{"name":"negative regulation of nonadec-1-ene formation","type":"exact"},{"name":"negative regulation of nonadec-1-ene synthesis","type":"exact"}],"termid":"GO:1900936"}


id: MONDO:0032658
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":"macrocephaly, acquired, with impaired intellectual development","secondary_identifiers":["UMLS:C4748993","MEDGEN:1648471","OMIM:618286"],"synonyms":[{"name":"MACID","type":"related"},{"name":"MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT","type":"related"},{"name":"Macrocephaly, Acquired, With Mental Retardation","type":"related"}],"termid":"MONDO:0032658","xrefs":{"Monarch":{"xref_id":"0032658"}}}


id: GO:2001116
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of a methanopterin.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pteridine-containing compound biosynthetic process","termid":"GO:0042559"},{"relation_name":"is_a","term_name":"organophosphate biosynthetic process","termid":"GO:0090407"},{"relation_name":"is_a","term_name":"methanopterin-containing compound metabolic process","termid":"GO:2001115"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0042559"}],"interesting_parent_ids":["GO:0008150","GO:0042559"],"is_obsolete":false,"name":"methanopterin-containing compound biosynthetic process","synonyms":[{"name":"methanopterin biosynthesis","type":"exact"}],"termid":"GO:2001116"}


id: PBO:0072166
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S15 pseudogene 3","termid":"PBO:0072166"}


id: GO:0035027
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The commitment of cells to leading edge cell fate and their capacity to differentiate into leading edge cells. Leading edge cells are found at the front of a migrating epithelial sheet.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial cell fate commitment","termid":"GO:0072148"},{"relation_name":"part_of","term_name":"leading edge cell differentiation","termid":"GO:0035026"}],"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":"leading edge cell fate commitment","termid":"GO:0035027"}


id: GO:0014704
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A complex cell-cell junction at which myofibrils terminate in cardiomyocytes; mediates mechanical and electrochemical integration between individual cardiomyocytes. The intercalated disc contains regions of tight mechanical attachment (fasciae adherentes and desmosomes) and electrical coupling (gap junctions) between adjacent cells.","definition_xrefs":["GOC:mtg_muscle","PMID:11732910"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-cell contact zone","termid":"GO:0044291"}],"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":"intercalated disc","secondary_identifiers":["Wikipedia:Intercalated_disc"],"synonyms":[{"name":"intercalated disk","type":"exact"}],"termid":"GO:0014704"}


id: MONDO:0016565
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete syndromic genetic obesity (obsolete MONDO:0016565)","secondary_identifiers":["Orphanet:240371"],"synonyms":[{"name":"syndrome associated with obesity (disease)","type":"exact"},{"name":"syndromic obesity (disease)","type":"exact"}],"termid":"MONDO:0016565","xrefs":{"Monarch":{"xref_id":"0016565"}}}


id: GO:0030833
data:
  {"annotated_genes":["SJAG_01894","SJAG_02566","SJAG_00521","SJAG_04479","SJAG_03086","SJAG_00279","SJAG_04100","SJAG_01993","SJAG_02700"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[67297,68426,76970,77641,79783],"is_not":false,"summary":null,"term":"GO:0030833"},{"annotations":[92665,76057,79524,80555],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051016"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the assembly of actin filaments by the addition of actin monomers to a filament.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of actin polymerization or depolymerization","termid":"GO:0008064"},{"relation_name":"is_a","term_name":"regulation of protein polymerization","termid":"GO:0032271"},{"relation_name":"regulates","term_name":"actin filament polymerization","termid":"GO:0030041"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00279":null,"SJAG_00521":null,"SJAG_01894":null,"SJAG_01993":null,"SJAG_02566":null,"SJAG_02700":null,"SJAG_03086":null,"SJAG_04100":null,"SJAG_04479":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0007010"},{"rel_name":"regulates","termid":"GO:0065003"},{"rel_name":"regulates","termid":"GO:0030036"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0030036","GO:0008150","GO:0007010","GO:0065003","GO:0044085"],"is_obsolete":false,"name":"regulation of actin filament polymerization","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"regulation of actin polymerization","type":"exact"}],"termid":"GO:0030833","terms_by_termid":{"GO:0030833":null,"GO:0051016":null}}


id: PBO:0065952
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAD18 E3 ubiquitin protein ligase","termid":"PBO:0065952"}


id: PBO:0077332
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 69","termid":"PBO:0077332"}


id: MONDO:0004022
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A meningioma that affects the superior sagittal sinus and invades the parasagittal angle.","definition_xrefs":["NCIT:C4960"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"cerebral convexity meningioma","termid":"MONDO:0003774"},{"relation_name":"is_a","term_name":"cerebral meningioma","termid":"MONDO:0003772"}],"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":"parasagittal meningioma","secondary_identifiers":["UMLS:C0751304","DOID:6869","MEDGEN:155845"],"termid":"MONDO:0004022","xrefs":{"Monarch":{"xref_id":"0004022"}}}


id: MONDO:1010701
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pyruvate kinase deficiency of erythrocyte that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyruvate kinase deficiency of erythrocyte, non-human animal","termid":"MONDO:1010099"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyruvate kinase deficiency of erythrocyte, dog","secondary_identifiers":["OMIA:000844-9615"],"termid":"MONDO:1010701","xrefs":{"Monarch":{"xref_id":"1010701"}}}


id: SO:0000479
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A transcript that is trans-spliced.","definition_xrefs":["SO:xp"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"trans_spliced","termid":"SO:0000870"},{"relation_name":"is_a","term_name":"transcript","termid":"SO:0000673"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trans_spliced_transcript","synonyms":[{"name":"INSDC_feature:tRNA","type":"broad"},{"name":"INSDC_qualifier:trans_splicing","type":"exact"},{"name":"trans spliced transcript","type":"exact"},{"name":"trans-spliced transcript","type":"exact"}],"termid":"SO:0000479"}


id: GO:0001114
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A macromolecular complex containing protein, DNA, and RNA molecules.","definition_xrefs":["GOC:txnOH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"}],"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:0032991","GO:0005575"],"is_obsolete":false,"name":"protein-DNA-RNA complex","termid":"GO:0001114"}


id: GO:0046483
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways involving heterocyclic compounds, those with a cyclic molecular structure and at least two different atoms in the ring (or rings).","definition_xrefs":["ISBN:0198506732"],"gene_count":0,"genotype_count":0,"name":"obsolete heterocycle metabolic process (obsolete GO:0046483)","termid":"GO:0046483"}


id: PBO:0075827
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"signal sequence receptor subunit 2","termid":"PBO:0075827"}


id: GO:0097029
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which antigen-activated dendritic cells acquire the specialized features of a mature conventional dendritic cell. Mature conventional dendritic cells upregulate the surface expression of MHC molecules, chemokine receptors and adhesion molecules, and increase the number of dendrites (cytoplasmic protrusions) in preparation for migration to lymphoid organs where they present antigen to T cells.","definition_xrefs":["PMID:15845453","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myeloid leukocyte differentiation","termid":"GO:0002573"},{"relation_name":"is_a","term_name":"dendritic cell differentiation","termid":"GO:0097028"}],"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":"mature conventional dendritic cell differentiation","termid":"GO:0097029"}


id: PBO:0063287
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protocadherin gamma subfamily B, 1","termid":"PBO:0063287"}


id: GO:0019914
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Modulation of the activity of the enzyme cyclin-dependent protein kinase activating kinase.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein kinase regulator activity","termid":"GO:0019887"},{"relation_name":"regulates","term_name":"cyclin-dependent protein kinase activating kinase activity","termid":"GO:0019912"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"regulates","termid":"GO:0016301"},{"rel_name":"regulates","termid":"GO:0004672"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"regulates","termid":"GO:0098772"},{"rel_name":"regulates","termid":"GO:0140096"},{"rel_name":"regulates","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"regulates","termid":"GO:0003824"},{"rel_name":"regulates","termid":"GO:0030234"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016740","GO:0016301","GO:0140096","GO:0098772","GO:0004672","GO:0030234"],"is_obsolete":false,"name":"cyclin-dependent protein kinase activating kinase regulator activity","synonyms":[{"name":"cyclin-dependent protein kinase activating kinase, intrinsic regulator activity","type":"narrow"}],"termid":"GO:0019914"}


id: GO:0005532
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete mannose binding lectin (obsolete GO:0005532)","synonyms":[{"name":"mannose binding lectin","type":"exact"},{"name":"mannose receptor","type":"related"}],"termid":"GO:0005532"}


id: MONDO:0022874
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"brain disorder","termid":"MONDO:0005560"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"corpus callosum dysgenesis hypopituitarism","termid":"MONDO:0022874","xrefs":{"Monarch":{"xref_id":"0022874"}}}


id: PBO:0060048
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND4 pseudogene 36","termid":"PBO:0060048"}


id: PBO:0040965
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BCL2 interacting protein 3 pseudogene 36","termid":"PBO:0040965"}


id: MONDO:0012142
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any orofacial cleft in which the cause of the disease is a mutation in the MSX1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cleft lip and alveolus","termid":"MONDO:0015420"},{"relation_name":"is_a","term_name":"isolated cleft lip","termid":"MONDO:0016043"},{"relation_name":"is_a","term_name":"cleft lip/palate","termid":"MONDO:0016044"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"orofacial cleft 5","secondary_identifiers":["MESH:C563843","MEDGEN:373280","GARD:18305","OMIM:608874","DOID:0080399","UMLS:C1837210"],"synonyms":[{"name":"MSX1 orofacial cleft","type":"exact"},{"name":"OFC5","type":"related"},{"name":"cleft lip with or without cleft palate, nonsyndromic, 5","type":"related"},{"name":"orofacial cleft 5","type":"exact"},{"name":"orofacial cleft caused by mutation in MSX1","type":"exact"},{"name":"orofacial cleft type 5","type":"exact"}],"termid":"MONDO:0012142","xrefs":{"Monarch":{"xref_id":"0012142"}}}


id: GO:0021790
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a branchiomotor neuron growth cone in the branchial arch mesenchyme is directed to a specific target site in the branchial arch mesenchyme in response to a repulsive chemical cue. Branchiomotor neurons are located in the hindbrain and innervate branchial arch-derived muscles that control jaw movements, facial expression, the larynx, and the pharynx.","definition_xrefs":["GOC:jid","GOC:dph","PMID:14699587","GOC:cls","GO_REF:0000021","GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"branchiomotor neuron axon guidance in branchial arch mesenchyme","termid":"GO:0021789"},{"relation_name":"is_a","term_name":"chemorepulsion of branchiomotor axon","termid":"GO:0021793"}],"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":"chemorepulsion of branchiomotor neuron axon in branchial arch mesenchyme","synonyms":[{"name":"negative chemotaxis of branchiomotor neuron axon in branchial arch mesenchyme","type":"exact"}],"termid":"GO:0021790"}


id: GO:0047620
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + acylglycerol = ADP + acyl-sn-glycerol 3-phosphate.","definition_xrefs":["MetaCyc:ACYLGLYCEROL-KINASE-RXN","EC:2.7.1.94"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinase activity","termid":"GO:0016301"},{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016301","GO:0016740","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"acylglycerol kinase activity","secondary_identifiers":["RHEA:19293","Reactome:R-HSA-5696074"],"synonyms":[{"name":"ATP:acylglycerol 3-phosphotransferase activity","type":"related"},{"name":"MGK","type":"related"},{"name":"monoacylglycerol kinase (phosphorylating)","type":"related"},{"name":"monoacylglycerol kinase activity","type":"related"},{"name":"monoglyceride kinase activity","type":"related"},{"name":"monoglyceride phosphokinase activity","type":"related"},{"name":"sn-2-monoacylglycerol kinase activity","type":"related"}],"termid":"GO:0047620"}


id: PBO:0057223
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 379","termid":"PBO:0057223"}


id: PBO:0082933
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cytoplasmic assembly chaperone for ribosomal protein Rps2p; co-translationally associates with the N-terminal extension of Rps2p to facilitate expression, solubility and ribosome assembly; released prior to the nuclear import of Rps2p; required for correct processing of 20S pre-rRNA at site D to generate mature 18S rRNA; essential gene in the S288C background but not in CEN.PK2; homologous to human PDCD2L and PDCD2","termid":"PBO:0082933"}


id: MONDO:0024358
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A distinct form of sleep-disordered breathing characterized as central sleep apnea (CSA), and presents in obstructive sleep apnea (OSA) patients during initial treatment with a continuous positive airway pressure (CPAP) device.","definition_xrefs":["PMID:23861580"],"direct_ancestors":[{"relation_name":"is_a","term_name":"central sleep apnea syndrome","termid":"MONDO:0004731"},{"relation_name":"is_a","term_name":"obstructive sleep apnea syndrome","termid":"MONDO:0007147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"complex sleep apnea","secondary_identifiers":["DOID:0080302","MEDGEN:83271","SCTID:230493001","UMLS:C0338495"],"synonyms":[{"name":"CompSAS","type":"exact"},{"name":"complex sleep apnea","type":"exact"},{"name":"mixed sleep apnea","type":"exact"}],"termid":"MONDO:0024358","xrefs":{"Monarch":{"xref_id":"0024358"}}}


id: PBO:0073423
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"splicing factor 1","termid":"PBO:0073423"}


id: MOD:01219
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Chemical derivative -","definition_xrefs":["Unimod:286#D","PubMed:9254591","PubMed:9750125"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Sulfanilic Acid (SA), heavy C13","termid":"MOD:00606"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sulfanilic Acid (SA), heavy C13 - site D","synonyms":[{"name":"Heavy Sulfanilic Acid (SA) C13","type":"related"},{"name":"SulfanilicAcid:13C(6)","type":"related"}],"termid":"MOD:01219"}


id: GO:1904026
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of collagen fibril organization.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:25451920"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of supramolecular fiber organization","termid":"GO:1902903"},{"relation_name":"is_a","term_name":"regulation of extracellular matrix organization","termid":"GO:1903053"},{"relation_name":"regulates","term_name":"collagen fibril organization","termid":"GO:0030199"}],"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 collagen fibril organization","synonyms":[{"name":"regulation of collagen fibril organisation","type":"exact"},{"name":"regulation of collagen fibrillogenesis","type":"related"},{"name":"regulation of fibrillar collagen organization","type":"exact"}],"termid":"GO:1904026"}


id: MONDO:0006744
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An accumulation of endolymph in the inner ear (labyrinth) leading to buildup of pressure and distortion of intralabyrinthine structures, such as cochlea and semicircular canals. It is characterized by sensorineural hearing loss; tinnitus; and sometimes vertigo.","definition_xrefs":["MESH:D018159"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peripheral vertigo","termid":"MONDO:0004900"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endolymphatic hydrops","secondary_identifiers":["DOID:9848","MedDRA:10049934","UMLS:C0206586","ICD9:386.8","MEDGEN:60183","SCTID:27621000119100","EFO:1000918"],"synonyms":[{"name":"labyrinthine hydrops","type":"exact"}],"termid":"MONDO:0006744","xrefs":{"Monarch":{"xref_id":"0006744"}}}


id: PBO:0000125
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sim Four and mal Two Associated protein","termid":"PBO:0000125"}


id: PBO:0068181
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 488","termid":"PBO:0068181"}


id: MOD:01192
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Isotopic label -","definition_xrefs":["PubMed:11760118","Unimod:211#Y","PubMed:12766232"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-ethyl iodoacetamide-d0","termid":"MOD:00561"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-ethyl iodoacetamide-d0 - site Y","synonyms":[{"name":"N-ethyl iodoacetamide-d0","type":"related"},{"name":"NEIAA","type":"related"}],"termid":"MOD:01192"}


id: GO:0050597
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H+ + NADPH + O2 + taxa-4(20),11-dien-5alpha-yl acetate = 10beta-hydroxytaxa-4(20),11-dien-5alpha-yl acetate + H2O + NADP+.","definition_xrefs":["EC:1.14.14.105","RHEA:15241"],"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:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"taxane 10-beta-hydroxylase activity","secondary_identifiers":["KEGG_REACTION:R06309","MetaCyc:1.14.13.76-RXN"],"synonyms":[{"name":"5-alpha-taxadienol-10-beta-hydroxylase activity","type":"related"},{"name":"taxa-4(20),11-dien-5alpha-yl acetate,NADPH:oxygen oxidoreductase (10beta-hydroxylating)","type":"related"},{"name":"taxane 10b-hydroxylase activity","type":"exact"},{"name":"taxane 10beta-hydroxylase activity","type":"related"}],"termid":"GO:0050597"}


id: PBO:0001597
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F0-ATPase subunit K (predicted)","termid":"PBO:0001597"}


id: MOD:00961
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively reduces the disulfide bond of cystine to form two cysteine residues.","definition_xrefs":["DeltaMass:333"],"direct_ancestors":[{"relation_name":"derives_from","term_name":"L-cystine (cross-link)","termid":"MOD:00034"},{"relation_name":"is_a","term_name":"modified L-cysteine residue","termid":"MOD:00905"},{"relation_name":"is_a","term_name":"hydrogenated residue","termid":"MOD:01473"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"reduction of disulfide crosslink in cystine to two cysteines","termid":"MOD:00961"}


id: GO:1902696
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of glycine to isobutanol.","definition_xrefs":["GOC:mengo_curators","GO_REF:0000093","PMID:23642236","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycine catabolic process","termid":"GO:0006546"},{"relation_name":"is_a","term_name":"isobutanol metabolic process","termid":"GO:1901960"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006520","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"glycine catabolic process to isobutanol","secondary_identifiers":["GO:1990293"],"synonyms":[{"name":"glycine breakdown to isobutanol","type":"exact"},{"name":"glycine catabolism to isobutanol","type":"exact"},{"name":"glycine degradation to isobutanol","type":"exact"}],"termid":"GO:1902696"}


id: PBO:0079363
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tubulin alpha 4b","termid":"PBO:0079363"}


id: MONDO:0003196
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma that arises from epithelial cells of the vermiform appendix","direct_ancestors":[{"relation_name":"is_a","term_name":"appendix cancer","termid":"MONDO:0001235"},{"relation_name":"is_a","term_name":"cecum carcinoma","termid":"MONDO:0006029"},{"relation_name":"is_a","term_name":"epithelial tumor of the appendix","termid":"MONDO:0018511"}],"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":"appendix carcinoma","secondary_identifiers":["NCIT:C9330","SCTID:448992002","DOID:4902","MEDGEN:196398","UMLS:C0728951"],"synonyms":[{"name":"Ca appendix","type":"exact"},{"name":"appendix cancer","type":"broad"},{"name":"appendix carcinoma","type":"exact"},{"name":"carcinoma of appendix","type":"exact"},{"name":"carcinoma of the appendix","type":"exact"},{"name":"carcinoma of vermiform appendix","type":"exact"},{"name":"vermiform appendix carcinoma","type":"exact"}],"termid":"MONDO:0003196","xrefs":{"Monarch":{"xref_id":"0003196"}}}


id: FYPO:0005311
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 methylation of lysine at position 4 of histone H3 is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal histone methylation during vegetative growth","termid":"FYPO:0000861"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0000002","FYPO:0001320","FYPO:0000257"],"is_obsolete":false,"name":"normal histone H3-K4 methylation during vegetative growth","synonyms":[{"name":"normal histone H3 K4 methylation during vegetative growth","type":"exact"},{"name":"normal histone H3-K4 methylation during mitotic cell cycle","type":"related"},{"name":"normal histone H3K4me during vegetative growth","type":"exact"},{"name":"normal histone lysine H3 K4 methylation during vegetative growth","type":"exact"}],"termid":"FYPO:0005311"}


id: FYPO:0004450
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 phosphorylation of one or more specific proteins is normal (i.e. indistinguishable from wild type) during a cellular response to calcium ions.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein phosphorylation during vegetative growth","termid":"FYPO:0000776"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0000257","FYPO:0001312"],"is_obsolete":false,"name":"normal protein phosphorylation during cellular response to calcium ion","synonyms":[{"name":"normal protein phosphorylation during cellular response to calcium","type":"exact"},{"name":"normal protein phosphorylation during cellular response to calcium ion during mitotic cell cycle","type":"related"},{"name":"normal protein phosphorylation during cellular response to calcium ion during vegetative growth","type":"exact"}],"termid":"FYPO:0004450"}


id: SO:0001922
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A scaffold composed of mitochondrial contigs.","definition_xrefs":["GMOD:ea"],"direct_ancestors":[{"relation_name":"is_a","term_name":"supercontig","termid":"SO:0000148"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial_supercontig","synonyms":[{"name":"mitochondrial scaffold","type":"exact"},{"name":"mitochondrial supercontig","type":"exact"},{"name":"mitochondrial_scaffold","type":"exact"}],"termid":"SO:0001922"}


id: PBO:0029339
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_level_of_mitochondrial_tRNA_processing_intermediates_with_3'_extensions","termid":"PBO:0029339"}


id: PBO:0063004
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"platelet activating factor acetylhydrolase 1b regulatory subunit 1 pseudogene 1","termid":"PBO:0063004"}


id: PBO:0028732
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_cellular_hercynylcysteine_sulfoxide_level_during_vegetative_growth","termid":"PBO:0028732"}


id: PBO:0083165
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; almost completely overlaps uncharacterized ORF YER085C","termid":"PBO:0083165"}


id: GO:0032465
data:
  {"annotated_genes":["SJAG_01790","SJAG_03309","SJAG_01386","SJAG_03681","SJAG_04455","SJAG_04597","SJAG_02838","SJAG_00514","SJAG_03342","SJAG_02807","SJAG_00082","SJAG_00845","SJAG_00229","SJAG_01114","SJAG_02232","SJAG_01188","SJAG_02392","SJAG_01805","SJAG_03048","SJAG_03887","SJAG_03631","SJAG_01837","SJAG_03508","SJAG_03704","SJAG_01863","SJAG_04412","SJAG_01456","SJAG_00883","SJAG_03353","SJAG_01787","SJAG_03592","SJAG_00256","SJAG_00526","SJAG_03581","SJAG_06270","SJAG_04943","SJAG_02169","SJAG_04468","SJAG_02380","SJAG_02514","SJAG_02795","SJAG_03936","SJAG_04776","SJAG_04551","SJAG_05290","SJAG_04666","SJAG_02592","SJAG_01464","SJAG_03376","SJAG_03692"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[98602],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000432"},{"annotations":[102683],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903500"},{"annotations":[104014],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903472"},{"annotations":[93184,107412,102462,99993],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902413"},{"annotations":[102688],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905757"},{"annotations":[93185,95972,105363,107854,73126,99916,93269,116203,91066,110479,101595,92071,107548,107413,93803],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031030"},{"annotations":[94748,90339],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903501"},{"annotations":[113669,94749,87876,94917,110834],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903473"},{"annotations":[119587,91108,104019,111076],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903617"},{"annotations":[113670,105503,115772,107364,94144,118190,106703,90209,78274,92759],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140281"},{"annotations":[92760,87877,94752],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905758"},{"annotations":[119900,94150],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903499"},{"annotations":[92184,109526,118991,90155,101263,117818,107457,77401,103808],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902412"},{"annotations":[88193,101709,111684],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902472"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the division of the cytoplasm of a cell and its separation into two daughter cells.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell cycle process","termid":"GO:0010564"},{"relation_name":"is_a","term_name":"regulation of cell division","termid":"GO:0051302"},{"relation_name":"regulates","term_name":"cytokinesis","termid":"GO:0000910"}],"gene_count":50,"genes_by_uniquename":{"SJAG_00082":null,"SJAG_00229":null,"SJAG_00256":null,"SJAG_00514":null,"SJAG_00526":null,"SJAG_00845":null,"SJAG_00883":null,"SJAG_01114":null,"SJAG_01188":null,"SJAG_01386":null,"SJAG_01456":null,"SJAG_01464":null,"SJAG_01787":null,"SJAG_01790":null,"SJAG_01805":null,"SJAG_01837":null,"SJAG_01863":null,"SJAG_02169":null,"SJAG_02232":null,"SJAG_02380":null,"SJAG_02392":null,"SJAG_02514":null,"SJAG_02592":null,"SJAG_02795":null,"SJAG_02807":null,"SJAG_02838":null,"SJAG_03048":null,"SJAG_03309":null,"SJAG_03342":null,"SJAG_03353":null,"SJAG_03376":null,"SJAG_03508":null,"SJAG_03581":null,"SJAG_03592":null,"SJAG_03631":null,"SJAG_03681":null,"SJAG_03692":null,"SJAG_03704":null,"SJAG_03887":null,"SJAG_03936":null,"SJAG_04412":null,"SJAG_04455":null,"SJAG_04468":null,"SJAG_04551":null,"SJAG_04597":null,"SJAG_04666":null,"SJAG_04776":null,"SJAG_04943":null,"SJAG_05290":null,"SJAG_06270":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"regulation of cytokinesis","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"PMID:25866389":null,"PMID:32915139":null},"secondary_identifiers":["GO:0071775"],"synonyms":[{"name":"regulation of cell cycle cytokinesis","type":"exact"}],"termid":"GO:0032465","terms_by_termid":{"GO:0031030":null,"GO:0120306":null,"GO:0140281":null,"GO:1902412":null,"GO:1902413":null,"GO:1902472":null,"GO:1903472":null,"GO:1903473":null,"GO:1903499":null,"GO:1903500":null,"GO:1903501":null,"GO:1903617":null,"GO:1905757":null,"GO:1905758":null,"GO:2000432":null}}


id: PBO:0084823
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial protein, regulator of COB mRNA stability and translation; interacts with the 5'-untranslated region of the COB mRNA; found in a complex at the inner membrane along with Pet309p; localizes to mitochondrial foci upon DNA replication stress","termid":"PBO:0084823"}


id: GO:0033890
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the exonucleolytic cleavage that removes extra residues from the 3'-terminus of tRNA to produce 5'-mononucleotides.","definition_xrefs":["EC:3.1.13.5"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA exonuclease activity, producing 5'-phosphomonoesters","termid":"GO:0016896"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0004527"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0140098"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016788","GO:0140098","GO:0004527","GO:0016787"],"is_obsolete":false,"name":"ribonuclease D activity","secondary_identifiers":["MetaCyc:3.1.13.5-RXN"],"synonyms":[{"name":"RNase D activity","type":"related"}],"termid":"GO:0033890"}


id: GO:0080192
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Lateral growth of a plant axis (shoot axis or root) that is an increase in thickness resulting from the activity of a primary thickening meristem.","definition_xrefs":["PO:0005039","PO:0025004","ISBN:0471245208","JSTOR:4354165"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lateral growth","termid":"GO:0080190"}],"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":"primary thickening","termid":"GO:0080192"}


id: MONDO:0001110
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Persistent pyelonephritis.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chronic kidney disease","termid":"MONDO:0005300"},{"relation_name":"is_a","term_name":"pyelonephritis","termid":"MONDO:0006939"}],"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":"chronic pyelonephritis","secondary_identifiers":["NCIT:C123216","icd11.foundation:1346439976","MEDGEN:39090","NANDO:2200137","ICD9:590.0","SCTID:63302006","NANDO:2100012","DOID:1076","UMLS:C0085697"],"synonyms":[{"name":"pyelonephritis, chronic","type":"exact"}],"termid":"MONDO:0001110","xrefs":{"Monarch":{"xref_id":"0001110"}}}


id: GO:1902126
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of (+)-pinoresinol.","definition_xrefs":["PMID:9872995","GOC:TermGenie","PMID:8910615"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lignan biosynthetic process","termid":"GO:0009807"},{"relation_name":"is_a","term_name":"phenol-containing compound biosynthetic process","termid":"GO:0046189"},{"relation_name":"is_a","term_name":"ether biosynthetic process","termid":"GO:1901503"},{"relation_name":"is_a","term_name":"(+)-pinoresinol metabolic process","termid":"GO:1902124"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0019748","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"(+)-pinoresinol biosynthetic process","synonyms":[{"name":"(+)-pinoresinol anabolism","type":"exact"},{"name":"(+)-pinoresinol biosynthesis","type":"exact"},{"name":"(+)-pinoresinol formation","type":"exact"},{"name":"(+)-pinoresinol synthesis","type":"exact"}],"termid":"GO:1902126"}


id: PBO:0055971
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LRRFIP2 pseudogene 1","termid":"PBO:0055971"}


id: PBO:0065502
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paraspeckle component 1","termid":"PBO:0065502"}


id: PBO:0050326
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 28","termid":"PBO:0050326"}


id: PBO:0041525
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 16 open reading frame 86","termid":"PBO:0041525"}


id: MONDO:0000330
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A bacterial infection caused by Rickettsia typhi.","definition_xrefs":["Wikipedia:Murine_typhus"],"direct_ancestors":[{"relation_name":"is_a","term_name":"typhus","termid":"MONDO:0001246"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endemic typhus","secondary_identifiers":["MEDGEN:11977","UMLS:C0041472","icd11.foundation:4659958","MedDRA:10028282","DOID:0050481","MESH:D014437","NCIT:C84688","GARD:19033","Orphanet:83315"],"synonyms":[{"name":"Rickettsia felis spotted fever","type":"exact"},{"name":"cat flea rickettsiosis","type":"exact"},{"name":"endemic flea-borne typhus","type":"exact"},{"name":"endemic typhus fever","type":"exact"},{"name":"fleaborne typhus","type":"exact"},{"name":"murine typhus","type":"exact"},{"name":"rat-flea typhus","type":"exact"},{"name":"shop typhus","type":"related"},{"name":"toulon typhus","type":"exact"},{"name":"urban typhus","type":"exact"},{"name":"urban typhus of Malaya","type":"exact"}],"termid":"MONDO:0000330","xrefs":{"Monarch":{"xref_id":"0000330"}}}


id: MONDO:0012300
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"prostate cancer, hereditary","termid":"MONDO:0700275"}],"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":"prostate cancer, hereditary, 6","secondary_identifiers":["GARD:15462","MEDGEN:322797","MESH:C563699","OMIM:609558","UMLS:C1836005"],"synonyms":[{"name":"HPC6","type":"related"},{"name":"prostate cancer, hereditary, 6","type":"exact"},{"name":"prostate cancer, hereditary, type 6","type":"exact"},{"name":"prostate cancer, susceptibility to","type":"related"}],"termid":"MONDO:0012300","xrefs":{"Monarch":{"xref_id":"0012300"}}}


id: GO:0070093
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the regulated release of glucagon.","definition_xrefs":["GOC:mah","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of glucagon secretion","termid":"GO:0070092"},{"relation_name":"is_a","term_name":"negative regulation of peptide hormone secretion","termid":"GO:0090278"},{"relation_name":"negatively_regulates","term_name":"glucagon secretion","termid":"GO:0070091"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"negative regulation of glucagon secretion","synonyms":[{"name":"down regulation of glucagon secretion","type":"exact"},{"name":"down-regulation of glucagon secretion","type":"exact"},{"name":"downregulation of glucagon secretion","type":"exact"},{"name":"inhibition of glucagon secretion","type":"narrow"}],"termid":"GO:0070093"}


id: MONDO:0005256
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Heart failure characterized by marked limitation in activity due to symptoms, even during less-than-ordinary activity, e.g. walking short distances (20b100 m). Patients with moderate heart failure are comfortable only at rest.","definition_xrefs":["EFO:0003148"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symptomatic heart failure","termid":"MONDO:0005254"}],"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":"moderate heart failure","secondary_identifiers":["Wikipedia:New_York_Heart_Association_Functional_Classification"],"termid":"MONDO:0005256","xrefs":{"Monarch":{"xref_id":"0005256"}}}


id: PBO:0000617
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RecQ type DNA helicase Rqh1","termid":"PBO:0000617"}


id: PBO:0040754
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"brain derived neurotrophic factor","termid":"PBO:0040754"}


id: SO:0000108
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An mRNA with a frameshift.","definition_xrefs":["SO:xp"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"frameshift","termid":"SO:0000865"},{"relation_name":"is_a","term_name":"mRNA","termid":"SO:0000234"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mRNA_with_frameshift","synonyms":[{"name":"frameshifted mRNA","type":"exact"},{"name":"mRNA with frameshift","type":"exact"}],"termid":"SO:0000108"}


id: GO:2001103
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a maltohexaoseacetate into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hexasaccharide transport","termid":"GO:2001102"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"maltohexaose transport","termid":"GO:2001103"}


id: PBO:0074298
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"secreted LY6/PLAUR domain containing 1","termid":"PBO:0074298"}


id: PBO:0067221
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 290, pseudogene","termid":"PBO:0067221"}


id: PBO:0047363
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box and leucine rich repeat protein 17","termid":"PBO:0047363"}


id: PBO:0045538
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dual oxidase 2","termid":"PBO:0045538"}


id: MONDO:0022575
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A syndromic disease characterized by a small ductal system and reduction in the number of interlobular bile ducts.","definition_xrefs":["PMID:12664410"],"gene_count":0,"genotype_count":0,"name":"obsolete biliary hypoplasia (obsolete MONDO:0022575)","termid":"MONDO:0022575","xrefs":{"Monarch":{"xref_id":"0022575"}}}


id: PBO:0041315
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 2 open reading frame 69 pseudogene 1","termid":"PBO:0041315"}


id: PBO:0042329
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CD52 molecule","termid":"PBO:0042329"}


id: PBO:0046155
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ELAV like RNA binding protein 3","termid":"PBO:0046155"}


id: PBO:0082393
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Beta subunit of C-terminal domain kinase I (CTDK-I); which phosphorylates both RNA pol II subunit Rpo21p to affect transcription and pre-mRNA 3' end processing, and ribosomal protein Rps2p to increase translational fidelity; relocalizes to the cytosol in response to hypoxia","termid":"PBO:0082393"}


id: GO:2000343
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of chemokine (C-X-C motif) ligand 2 production.","definition_xrefs":["GOC:mah","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of chemokine production","termid":"GO:0032722"},{"relation_name":"is_a","term_name":"regulation of chemokine (C-X-C motif) ligand 2 production","termid":"GO:2000341"},{"relation_name":"positively_regulates","term_name":"chemokine (C-X-C motif) ligand 2 production","termid":"GO:0072567"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"positively_regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"positive regulation of chemokine (C-X-C motif) ligand 2 production","secondary_identifiers":["GO:1904209"],"synonyms":[{"name":"positive regulation of CCL2 secretion","type":"exact"},{"name":"positive regulation of CXCL2 production","type":"exact"},{"name":"positive regulation of MIP-2 production","type":"exact"},{"name":"positive regulation of MIP2 production","type":"exact"},{"name":"positive regulation of SCYB2 production","type":"exact"},{"name":"positive regulation of chemokine (C-C motif) ligand 2 secretion","type":"narrow"}],"termid":"GO:2000343"}


id: PBO:0030566
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_cellular_methionine_level","termid":"PBO:0030566"}


id: GO:0051144
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of propanediol, a sweet, colorless, viscous, hygroscopic liquid with the formula CH3-CHOH-CH2OH.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycol catabolic process","termid":"GO:0042846"},{"relation_name":"is_a","term_name":"propanediol metabolic process","termid":"GO:0051143"}],"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:0044281","GO:0008150"],"is_obsolete":false,"name":"propanediol catabolic process","synonyms":[{"name":"1,2-dihydroxypropane catabolic process","type":"exact"},{"name":"1,2-dihydroxypropane catabolism","type":"exact"},{"name":"propanediol breakdown","type":"exact"},{"name":"propanediol catabolism","type":"exact"},{"name":"propanediol degradation","type":"exact"},{"name":"propylene glycol catabolic process","type":"exact"},{"name":"propylene glycol catabolism","type":"exact"}],"termid":"GO:0051144"}


id: GO:0090380
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A developmental process, independent of morphogenetic (shape) change, that is required for a seed trichome to attain its fully functional state.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"is_a","term_name":"cellular process involved in reproduction in multicellular organism","termid":"GO:0022412"},{"relation_name":"is_a","term_name":"cell maturation","termid":"GO:0048469"},{"relation_name":"part_of","term_name":"seed trichome differentiation","termid":"GO:0090376"}],"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":"seed trichome maturation","termid":"GO:0090380"}


id: GO:0000232
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A chromosome found in the nucleus during interphase.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete nuclear interphase chromosome (obsolete GO:0000232)","synonyms":[{"name":"nuclear interphase chromosome","type":"exact"}],"termid":"GO:0000232"}


id: FYPO:0002568
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 the nuclear periphery is abolished.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to nucleus during vegetative growth","termid":"FYPO:0001424"},{"relation_name":"is_a","term_name":"abnormal protein localization to nuclear periphery","termid":"FYPO:0002338"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320","FYPO:0000138","FYPO:0005447"],"is_obsolete":false,"name":"abolished protein localization to nuclear periphery","synonyms":[{"name":"abolished protein localisation to nuclear periphery","type":"exact"},{"name":"abolished protein localization to nuclear periphery during mitotic cell cycle","type":"related"},{"name":"abolished protein localization to nuclear periphery during vegetative growth","type":"exact"},{"name":"protein localization to nuclear periphery abolished","type":"exact"}],"termid":"FYPO:0002568"}


id: PBO:0060359
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myogenic differentiation 1","termid":"PBO:0060359"}


id: GO:0071902
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency, or extent of protein serine/threonine kinase activity.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein kinase activity","termid":"GO:0045860"},{"relation_name":"is_a","term_name":"regulation of protein serine/threonine kinase activity","termid":"GO:0071900"}],"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 protein serine/threonine kinase activity","termid":"GO:0071902"}


id: MONDO:0032570
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Joubert syndrome","termid":"MONDO:0018772"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Joubert syndrome 35","secondary_identifiers":["OMIM:618161","MEDGEN:1648453","GARD:16297","UMLS:C4748442"],"synonyms":[{"name":"JBTS35","type":"related"},{"name":"JOUBERT SYNDROME 35","type":"related"}],"termid":"MONDO:0032570","xrefs":{"Monarch":{"xref_id":"0032570"}}}


id: PBO:0060187
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MUC5B antisense RNA 1","termid":"PBO:0060187"}


id: MONDO:0002119
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A well circumscribed lesion of the bone, most frequently arising from the posterior mandible. It is characterized by the presence of fibrous tissue and a mineralized component which may be woven bone, lamellar bone, or cementum-like material. Complete removal is recommended, since it continues to enlarge if left untreated.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bone benign neoplasm","termid":"MONDO:0000631"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ossifying fibroma","secondary_identifiers":["NORD:111729","ICDO:9262/0","MEDGEN:104906","DOID:180","UMLS:C0206640","NCIT:C173820","ICDO:9274/0","MESH:D018214","HP:0030426","NCIT:C8422"],"synonyms":[{"name":"Cementifying fibroma","type":"exact"},{"name":"Juvenile Ossifying Fibroma","type":"narrow"},{"name":"cemento-ossifying fibroma","type":"exact"},{"name":"fibro-osteoma","type":"exact"},{"name":"fibroma, ossifying, benign","type":"exact"},{"name":"juvenile ossifying fibroma","type":"narrow"},{"name":"ossifying fibroma","type":"exact"},{"name":"ossifying fibroma (disease)","type":"exact"},{"name":"peripheral ossifying fibroma","type":"related"}],"termid":"MONDO:0002119","xrefs":{"Monarch":{"xref_id":"0002119"}}}


id: PBO:0002544
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3.1.30.-","termid":"PBO:0002544"}


id: PBO:0044188
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chymotrypsinogen B1","termid":"PBO:0044188"}


id: PBO:0051594
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 21 receptor","termid":"PBO:0051594"}


id: FYPO:0004832
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 the mitotic spindle midzone during anaphase A does not occur. The mitotic spindle midzone is the area in the center of the mitotic spindle where the spindle microtubules from opposite poles overlap. Anaphase A is the stage of mitosis in which the kinetochore microtubules shorten as chromosomes move toward the spindle poles.","definition_xrefs":["GO:1990023","PMID:16824200","PomBase:mah","GO:1902967","GO:0000091"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to mitotic spindle midzone during anaphase","termid":"FYPO:0004412"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0000138","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"abolished protein localization to mitotic spindle midzone during anaphase A","synonyms":[{"name":"abolished protein localization to spindle midzone during mitotic anaphase A","type":"exact"},{"name":"protein absent from mitotic spindle midzone during anaphase A","type":"related"},{"name":"protein localisation to mitotic spindle midzone abolished during anaphase A","type":"exact"},{"name":"protein localization to mitotic spindle midzone abolished during anaphase A","type":"exact"},{"name":"protein localization to spindle midzone abolished during anaphase A during vegetative growth","type":"exact"}],"termid":"FYPO:0004832"}


id: PBO:0086269
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein translocase and chaperone required for Complex III assembly; member of the AAA ATPase family; forms a homo-oligomeric complex in the mitochondrial inner membrane that translocates the C-terminal domain of Rip1p from the matrix across the inner membrane and delivers it to an assembly intermediate of respiratory Complex III; also required for assembly of the Qcr10p subunit; mutation is functionally complemented by human homolog BCS1L, linked to neonatal diseases","termid":"PBO:0086269"}


id: PBO:0109607
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 90 member A15","termid":"PBO:0109607"}


id: SO:0001447
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A polar amino acid encoded by the codons TGT and TGC.","direct_ancestors":[{"relation_name":"is_a","term_name":"amino_acid","termid":"SO:0001237"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cysteine","synonyms":[{"name":"C","type":"exact"},{"name":"Cys","type":"exact"}],"termid":"SO:0001447"}


id: PBO:0074260
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLCO4A1 antisense RNA 1","termid":"PBO:0074260"}


id: PBO:0075102
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 151","termid":"PBO:0075102"}


id: MONDO:1011154
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Osteoporosis that occurs in horse.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"osteoporosis, non-human animal","termid":"MONDO:1010295"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"osteoporosis, horse","secondary_identifiers":["OMIA:000105-9796"],"termid":"MONDO:1011154","xrefs":{"Monarch":{"xref_id":"1011154"}}}


id: PBO:0083516
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 verified ORF MES1/YGR264C, which encodes methionyl-tRNA synthetase","termid":"PBO:0083516"}


id: SO:0000191
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An intron that is not the most 3-prime or the most 5-prime in a given transcript.","direct_ancestors":[{"relation_name":"is_a","term_name":"intron","termid":"SO:0000188"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interior_intron","synonyms":[{"name":"interior intron","type":"exact"}],"termid":"SO:0000191"}


id: PBO:0047614
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibrinogen C domain containing 1","termid":"PBO:0047614"}


id: GO:0085041
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Highly branched symbiont haustoria within host root cortex cells, responsible for nutrient exchange.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"haustorium","termid":"GO:0085035"}],"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":"arbuscule","termid":"GO:0085041"}


id: MONDO:0030043
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital disorder of glycosylation type II","termid":"MONDO:0005501"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0024322","MONDO:0005066"],"is_obsolete":false,"name":"congenital disorder of glycosylation, type iit","secondary_identifiers":["UMLS:C5394387","MEDGEN:1709627","OMIM:618885"],"synonyms":[{"name":"CDG2T","type":"exact"},{"name":"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIt","type":"exact"},{"name":"Cdg Iit","type":"exact"}],"termid":"MONDO:0030043","xrefs":{"Monarch":{"xref_id":"0030043"}}}


id: GO:0043158
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cellular developmental process by which a cell becomes a heterocyst, a cell that carries out nitrogen fixation. This process involves changes to the cell wall, expression of nitrogenase and other proteins involved in nitrogen fixation, and degradation of photosystem II, which produces oxygen. This process is known to occur in some cyanobacteria.","definition_xrefs":["PMID:35744626","PMID:11121783"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular developmental process","termid":"GO:0048869"}],"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":"heterocyst development","synonyms":[{"name":"heterocyst cell differentiation","type":"related"},{"name":"heterocyst differentiation","type":"related"},{"name":"heterocyst formation","type":"exact"}],"termid":"GO:0043158"}


id: PATO:0001196
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A spatial quality inhering in a bearer by virtue of the bearer's being located toward the abdomen of an organism relative to another entity.","definition_xrefs":["PATOC:nw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"position","termid":"PATO:0000140"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ventral to","synonyms":[{"name":"anterior_ to","type":"exact"}],"termid":"PATO:0001196"}


id: GO:0071001
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A ribonucleoprotein complex that contains the extensively base paired small nuclear RNAs U4 and U6, a heptameric ring of Sm proteins associated with U4, the Lsm2-8 heptameric ring complex associated with U6, as well as several proteins that are unique to the U4 snRNP or U6 snRNPs, some of which remain associated with the U4/U6 snRNA both while the U4 snRNP is free or assembled into a series of spliceosomal complexes.","definition_xrefs":["ISBN:0879695897","GOC:krc","PMID:14685174","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spliceosomal snRNP complex","termid":"GO:0097525"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005634"],"is_obsolete":false,"name":"U4/U6 snRNP","termid":"GO:0071001"}


id: PBO:0076608
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TBC1D26 antisense RNA 1","termid":"PBO:0076608"}


id: FYPO:0004774
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 L-proline measured in the vacuole is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased level of substance in vacuole","termid":"FYPO:0001730"},{"relation_name":"is_a","term_name":"increased cellular proline level","termid":"FYPO:0005237"}],"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:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"increased vacuolar proline level","synonyms":[{"name":"increased level of proline in vacuole","type":"exact"},{"name":"increased vacuolar L-proline level","type":"exact"},{"name":"increased vacuolar proline level during mitotic cell cycle","type":"related"},{"name":"increased vacuolar proline level during vegetative growth","type":"exact"}],"termid":"FYPO:0004774"}


id: PR:O94243
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mug9 gene.","definition_xrefs":["UniProtKB:O94243","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":"meiotically up-regulated gene 9 protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC70.09c","synonyms":[{"name":"Spom972h-mug9","type":"exact"}],"termid":"PR:O94243"}


id: GO:1900312
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of maltohexaose transport.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of hexasaccharide transport","termid":"GO:1900297"},{"relation_name":"regulates","term_name":"maltohexaose transport","termid":"GO:2001103"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"regulation of maltohexaose transport","termid":"GO:1900312"}


id: GO:0090676
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a calcium ion is transported from one side of a membrane to the other by means of a low voltage-gated calcium channel.","definition_xrefs":["GOC:PARL","PMID:20371816","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"calcium ion transmembrane transport","termid":"GO:0070588"}],"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":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0055085","GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"calcium ion transmembrane transport via low voltage-gated calcium channel","synonyms":[{"name":"generation of T-type calcium current","type":"related"}],"termid":"GO:0090676"}


id: MONDO:1010049
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acromegaly that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endocrine system disorder, non-human animal","termid":"MONDO:1011317"},{"relation_name":"is_a","term_name":"nervous system disorder, non-human animal","termid":"MONDO:1011336"},{"relation_name":"is_a","term_name":"reproductive system disorder, non-human animal","termid":"MONDO:1011354"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acromegaly, non-human animal","secondary_identifiers":["OMIA:000008"],"termid":"MONDO:1010049","xrefs":{"Monarch":{"xref_id":"1010049"}}}


id: GO:0031424
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the cytoplasm of the outermost cells of the vertebrate epidermis is replaced by keratin. Keratinization occurs in the stratum corneum, feathers, hair, claws, nails, hooves, and horns.","definition_xrefs":["GOC:dph","GOC:sdb_2009","GOC:tb","GOC:ebc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multicellular organismal process","termid":"GO:0032501"},{"relation_name":"part_of","term_name":"keratinocyte differentiation","termid":"GO:0030216"}],"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":"keratinization","secondary_identifiers":["Reactome:R-HSA-6805567"],"termid":"GO:0031424"}


id: PATO:0001429
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An medium acidity quality inhering in a solution by virtue of the bearer's a high concentration of H+ ions.","definition_xrefs":["chemicool:chemicool"],"direct_ancestors":[{"relation_name":"is_a","term_name":"medium acidity","termid":"PATO:0001428"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acidic","termid":"PATO:0001429"}


id: PBO:0018106
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"does not functionally complement S. cerevisiae RAD7","termid":"PBO:0018106"}


id: GO:0180051
data:
  {"annotated_genes":["SJAG_02180","SJAG_04635","SJAG_03472","SJAG_01659","SJAG_01576","SJAG_03433","SJAG_02856","SJAG_02704","SJAG_04891","SJAG_02601","SJAG_05221","SJAG_04900","SJAG_03629","SJAG_00786","SJAG_03678","SJAG_03788","SJAG_04772","SJAG_03147","SJAG_01117","SJAG_00308","SJAG_02628","SJAG_02471","SJAG_01487","SJAG_00466","SJAG_00338","SJAG_03461","SJAG_02189","SJAG_01643","SJAG_02307","SJAG_02390","SJAG_04351","SJAG_05271","SJAG_00662","SJAG_03996","SJAG_02812","SJAG_02376","SJAG_01954","SJAG_05003","SJAG_01518","SJAG_01696","SJAG_03223","SJAG_05332","SJAG_04744","SJAG_02017","SJAG_01851","SJAG_01438","SJAG_02493","SJAG_03732","SJAG_02353","SJAG_04283","SJAG_00507","SJAG_04981","SJAG_02164","SJAG_03232","SJAG_02995","SJAG_02738","SJAG_04157"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[80137,80332,118783,77705,73894,57237,119257,69107,77988,77260,79724,92330,80503,73216],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003746"},{"annotations":[62188],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008135"},{"annotations":[72605,68772,75451,78306,93116,72280,62063,74706,105937,74462,60536,77815,75176,71978,71769,78001,78861,80472,115920,72754,76915,76017,105912,59610,58156,61423,72259,72767,63943,74855,79360,74276,77811,87868],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003743"},{"annotations":[107494,116336,69215,66496,72816],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003747"},{"annotations":[98979],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016150"},{"annotations":[74167],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016149"},{"annotations":[109487,105027,109486],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008079"}]},"cv_name":"molecular_function","definition":"A molecular function required for translation of a mRNA into a protein functioning as part of initiation, elongation or termination of translation.","definition_xrefs":["GOC:pg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"molecular_function","termid":"GO:0003674"}],"gene_count":57,"genes_by_uniquename":{"SJAG_00308":null,"SJAG_00338":null,"SJAG_00466":null,"SJAG_00507":null,"SJAG_00662":null,"SJAG_00786":null,"SJAG_01117":null,"SJAG_01438":null,"SJAG_01487":null,"SJAG_01518":null,"SJAG_01576":null,"SJAG_01643":null,"SJAG_01659":null,"SJAG_01696":null,"SJAG_01851":null,"SJAG_01954":null,"SJAG_02017":null,"SJAG_02164":null,"SJAG_02180":null,"SJAG_02189":null,"SJAG_02307":null,"SJAG_02353":null,"SJAG_02376":null,"SJAG_02390":null,"SJAG_02471":null,"SJAG_02493":null,"SJAG_02601":null,"SJAG_02628":null,"SJAG_02704":null,"SJAG_02738":null,"SJAG_02812":null,"SJAG_02856":null,"SJAG_02995":null,"SJAG_03147":null,"SJAG_03223":null,"SJAG_03232":null,"SJAG_03433":null,"SJAG_03461":null,"SJAG_03472":null,"SJAG_03629":null,"SJAG_03678":null,"SJAG_03732":null,"SJAG_03788":null,"SJAG_03996":null,"SJAG_04157":null,"SJAG_04283":null,"SJAG_04351":null,"SJAG_04635":null,"SJAG_04744":null,"SJAG_04772":null,"SJAG_04891":null,"SJAG_04900":null,"SJAG_04981":null,"SJAG_05003":null,"SJAG_05221":null,"SJAG_05271":null,"SJAG_05332":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674"],"is_obsolete":false,"name":"translation factor activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"termid":"GO:0180051","terms_by_termid":{"GO:0003743":null,"GO:0003746":null,"GO:0003747":null,"GO:0008079":null,"GO:0008135":null,"GO:0016149":null,"GO:0016150":null}}


id: PBO:0036064
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_rate_of_protein_exchange_in_actomyosin_contractile_ring","termid":"PBO:0036064"}


id: PBO:0060338
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myosin VB pseudogene 3","termid":"PBO:0060338"}


id: GO:0141081
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont interferes with, inhibits or stops an inflammasome-mediated signal transduction pathway in the host organism by interfering with its normal execution. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:27214553","PMID:34324582","PMID:36227980","PMID:29061850","PMID:26687278"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated suppression of cytoplasmic pattern recognition receptor signaling pathway","termid":"GO:0039537"}],"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 suppression of host inflammasome-mediated signal transduction","synonyms":[{"name":"perturbation of host inflammasome-mediated signal transduction","type":"broad"}],"termid":"GO:0141081"}


id: PBO:0034027
data:
  {"annotation_feature_type":"gene","cv_name":"pubprop_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"canto_curator_email","termid":"PBO:0034027"}


id: GO:0035035
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to an histone acetyltransferase.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme binding","termid":"GO:0019899"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"histone acetyltransferase binding","synonyms":[{"name":"histone acetylase binding","type":"exact"}],"termid":"GO:0035035"}


id: PR:O60166
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- nud3 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O60166"],"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":"nuclear movement protein nudc (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC19F8.02","synonyms":[{"name":"Spom972h-nud3","type":"exact"},{"name":"nuclear distribution protein C homolog (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O60166"}


id: PBO:0074309
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SMAD1 antisense RNA 2","termid":"PBO:0074309"}


id: MONDO:0003241
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hemangioma arising from the brain and spinal cord.","definition_xrefs":["NCIT:C7004"],"direct_ancestors":[{"relation_name":"is_a","term_name":"central nervous system organ benign neoplasm","termid":"MONDO:0000628"},{"relation_name":"is_a","term_name":"hemangioma","termid":"MONDO:0006500"},{"relation_name":"is_a","term_name":"neurovascular disorder","termid":"MONDO:0043218"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"central nervous system hemangioma","secondary_identifiers":["MEDGEN:272703","DOID:501","UMLS:C1333957"],"synonyms":[{"name":"central nervous system hemangioma","type":"exact"},{"name":"hemangioma of CNS","type":"exact"},{"name":"hemangioma of central nervous system","type":"exact"},{"name":"hemangioma of the CNS","type":"exact"},{"name":"hemangioma of the central nervous system","type":"exact"}],"termid":"MONDO:0003241","xrefs":{"Monarch":{"xref_id":"0003241"}}}


id: PBO:0066249
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RBMS3 antisense RNA 2","termid":"PBO:0066249"}


id: GO:0030289
data:
  {"annotated_genes":["SJAG_00369","SJAG_00823"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[73025,107716],"is_not":false,"summary":null,"term":"GO:0030289"}]},"cv_name":"cellular_component","definition":"A protein serine/threonine phosphatase complex formed by the catalytic subunit of protein phosphatase 4 plus one or more regulatory subunits.","definition_xrefs":["PMID:10026142","GOC:bhm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein serine/threonine phosphatase complex","termid":"GO:0008287"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00369":null,"SJAG_00823":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"protein phosphatase 4 complex","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0030289","terms_by_termid":{"GO:0030289":null}}


id: PBO:0036176
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-delayed_onset_of_protein_phosphorylation_during_mitosis","termid":"PBO:0036176"}


id: GO:0043971
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of histone H3 by the addition of an acetyl group to a lysine residue at position 18 of the histone.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete histone H3-K18 acetylation (obsolete GO:0043971)","synonyms":[{"name":"histone H3 acetylation at K18","type":"exact"},{"name":"histone H3K18 acetylation","type":"exact"}],"termid":"GO:0043971"}


id: MONDO:0026181
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete genetic renal or urinary tract malformation (obsolete MONDO:0026181)","secondary_identifiers":["Orphanet:183539"],"termid":"MONDO:0026181","xrefs":{"Monarch":{"xref_id":"0026181"}}}


id: PR:O59799
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- coa4 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O59799"],"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":"coiled-coil-helix-coiled-coil-helix domain-containing protein C550.01c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC550.01c","synonyms":[{"name":"Spom972h-coa4","type":"exact"}],"termid":"PR:O59799"}


id: FYPO:0006188
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 rate, or speed, of protein exchange in the actomyosin contractile ring is decreased. Normally, proteins including actin and myosin are turned over between the contractile ring and elsewhere in the cytoplasm; exchange is faster during than before ring constriction.","definition_xrefs":["PMID:19570908","PMID:20110347","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization during vegetative growth","termid":"FYPO:0000443"},{"relation_name":"is_a","term_name":"abnormal actomyosin contractile ring organization","termid":"FYPO:0004738"},{"relation_name":"is_a","term_name":"abnormal dynamic protein localization pattern","termid":"FYPO:0006606"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0004803"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000138","FYPO:0005447","FYPO:0000631","FYPO:0001985","FYPO:0004803","FYPO:0000002"],"is_obsolete":false,"name":"decreased rate of protein exchange in actomyosin contractile ring","synonyms":[{"name":"decreased rate of protein exchange in actomyosin contractile ring during mitotic cell cycle","type":"related"},{"name":"decreased rate of protein exchange in actomyosin contractile ring during vegetative growth","type":"exact"},{"name":"reduced rate of protein exchange in actomyosin contractile ring","type":"exact"}],"termid":"FYPO:0006188"}


id: MONDO:0029140
data:
  {"annotated_genes":["SJAG_05278"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86719],"is_not":false,"summary":null,"term":"MONDO:0029140"}]},"cv_name":"mondo","direct_ancestors":[{"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":"disorder of GPI anchor biosynthesis","termid":"MONDO:0024321"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05278":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0024322"}],"interesting_parent_ids":["MONDO:0002525","MONDO:0024322","MONDO:0005066"],"is_obsolete":false,"name":"glycosylphosphatidylinositol biosynthesis defect 18","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0070382","MEDGEN:1648478","UMLS:C4748357","OMIM:618143"],"synonyms":[{"name":"GPIBD18","type":"related"},{"name":"developmental and epileptic encephalopathy 95","type":"exact"},{"name":"glycosylphosphatidylinositol biosynthesis defect 18","type":"exact"}],"termid":"MONDO:0029140","terms_by_termid":{"MONDO:0029140":null},"xrefs":{"Monarch":{"xref_id":"0029140"}}}


id: PBO:0066402
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"regenerating family member 4","termid":"PBO:0066402"}


id: PBO:0113504
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA methyltransferase; methylates the N-1 of guanine at position 9 in tRNAs; involved in the methylation of guanosine and uridine ribonucleosides in mRNA; member of the SPOUT (SpoU-TrmD) methyltransferase family; human ortholog TRMT10A plays a role in the pathogenesis of microcephaly and early onset diabetes; an 18-mer ncRNA originates from the TRM10 locus; genetic analysis shows the 18-mer ncRNA is a translational regulator; protein abundance increases in response to DNA replication stress","termid":"PBO:0113504"}


id: GO:1903389
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of synaptic vesicle uncoating.","definition_xrefs":["GO_REF:0000058","GOC:PARL","GOC:TermGenie","GOC:pad","PMID:21563316"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of synaptic vesicle endocytosis","termid":"GO:1900243"},{"relation_name":"is_a","term_name":"negative regulation of protein depolymerization","termid":"GO:1901880"},{"relation_name":"is_a","term_name":"regulation of synaptic vesicle uncoating","termid":"GO:1903388"},{"relation_name":"negatively_regulates","term_name":"synaptic vesicle uncoating","termid":"GO:0016191"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0016192"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0016192"],"is_obsolete":false,"name":"negative regulation of synaptic vesicle uncoating","synonyms":[{"name":"down regulation of synaptic vesicle coat depolymerization","type":"exact"},{"name":"down regulation of synaptic vesicle coat protein depolymerization","type":"exact"},{"name":"down regulation of synaptic vesicle uncoating","type":"exact"},{"name":"down-regulation of synaptic vesicle coat depolymerization","type":"exact"},{"name":"down-regulation of synaptic vesicle coat protein depolymerization","type":"exact"},{"name":"down-regulation of synaptic vesicle uncoating","type":"exact"},{"name":"downregulation of synaptic vesicle coat depolymerization","type":"exact"},{"name":"downregulation of synaptic vesicle coat protein depolymerization","type":"exact"},{"name":"downregulation of synaptic vesicle uncoating","type":"exact"},{"name":"inhibition of synaptic vesicle coat depolymerization","type":"narrow"},{"name":"inhibition of synaptic vesicle coat protein depolymerization","type":"narrow"},{"name":"inhibition of synaptic vesicle uncoating","type":"narrow"},{"name":"negative regulation of synaptic vesicle coat depolymerization","type":"exact"},{"name":"negative regulation of synaptic vesicle coat protein depolymerization","type":"exact"}],"termid":"GO:1903389"}


id: PBO:0073977
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 23 member 2","termid":"PBO:0073977"}


id: MONDO:0012969
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any microvascular complications of diabetes, susceptibility in which the cause of the disease is a mutation in the PON1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microvascular complications of diabetes, susceptibility","termid":"MONDO:0000065"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microvascular complications of diabetes, susceptibility to, 5","secondary_identifiers":["OMIM:612633","MEDGEN:436225","UMLS:C2674665"],"synonyms":[{"name":"MVCD5","type":"related"},{"name":"PON1 microvascular complications of diabetes, susceptibility","type":"exact"},{"name":"microvascular complications of diabetes 5","type":"exact"},{"name":"microvascular complications of diabetes, susceptibility caused by mutation in PON1","type":"exact"},{"name":"microvascular complications of diabetes, susceptibility to, 5","type":"exact"},{"name":"microvascular complications of diabetes, susceptibility to, type 5","type":"exact"},{"name":"retinopathy, diabetic, susceptibility to","type":"related"}],"termid":"MONDO:0012969","xrefs":{"Monarch":{"xref_id":"0012969"}}}


id: GO:0052872
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: tocotrienol + O2 + NADPH + H+ = 13'-hydroxy-tocotrienol + NADP+ + H2O .","definition_xrefs":["MetaCyc:RXN-11003"],"gene_count":0,"genotype_count":0,"name":"obsolete tocotrienol omega-hydroxylase activity (obsolete GO:0052872)","synonyms":[{"name":"tocotrienol 13-hydroxylase activity","type":"exact"}],"termid":"GO:0052872"}


id: GO:0075205
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which the host organism modulates the frequency, rate or extent of cAMP-mediated signal transduction in the symbiont. The cAMP-mediated signal transduction is defined as a series of molecular signals in which a cell uses cyclic AMP to convert an extracellular signal into a response. 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 modulation by host of symbiont cAMP-mediated signal transduction (obsolete GO:0075205)","synonyms":[{"name":"modulation by host of symbiont cAMP-mediated signaling","type":"related"},{"name":"modulation by host of symbiont cAMP-mediated signalling","type":"exact"},{"name":"regulation by host of symbiont cAMP-mediated signaling","type":"exact"}],"termid":"GO:0075205"}


id: RO:0002264
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"c acts upstream of or within p if c is enables 'p' and p' causally upstream of or within p","direct_ancestors":[{"relation_name":"is_a","term_name":"causal_agent_in","termid":"RO:0002500"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acts_upstream_of_or_within","synonyms":[{"name":"affects","type":"related"}],"termid":"RO:0002264"}


id: MONDO:0016152
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete qualitative or quantitative defects of calpain (obsolete MONDO:0016152)","secondary_identifiers":["Orphanet:207104"],"termid":"MONDO:0016152","xrefs":{"Monarch":{"xref_id":"0016152"}}}


id: MONDO:0019786
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Severe intellectual disability-epilepsy-anal anomalies-distal phalangeal hypoplasia is characterized by severe intellectual deficit, epilepsy, hypoplasia of the terminal phalanges, and an anteriorly displaced anus. It has been described in two sisters born to consanguineous parents. The syndrome is transmitted as an autosomal recessive trait and appears to be caused by anomalies in to chromosome regions, one localized to chromosome 1 and the other to chromosome 14.","definition_xrefs":["Orphanet:94066"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"severe intellectual disability-epilepsy-anal anomalies-distal phalangeal hypoplasia","secondary_identifiers":["UMLS:C4510007","GARD:19247","MEDGEN:1372948"],"termid":"MONDO:0019786","xrefs":{"Monarch":{"xref_id":"0019786"}}}


id: GO:0120063
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which force is generated within gastric smooth muscle tissue, resulting in a change in muscle geometry. This process occurs throughout the length of the stomach.","definition_xrefs":["GOC:sl","PMID:15890336"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gastro-intestinal system smooth muscle contraction","termid":"GO:0014831"}],"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":"stomach smooth muscle contraction","termid":"GO:0120063"}


id: PBO:0081844
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 778","termid":"PBO:0081844"}


id: GO:0060155
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of a platelet dense granule. A platelet dense granule is an electron-dense granule occurring in blood platelets that stores and secretes adenosine nucleotides and serotonin. They contain a highly condensed core consisting of serotonin, histamine, calcium, magnesium, ATP, ADP, pyrophosphate and membrane lysosomal proteins.","definition_xrefs":["GOC:dph","PMID:11487378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secretory granule organization","termid":"GO:0033363"}],"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":"platelet dense granule organization","synonyms":[{"name":"bull's eye body organization and biogenesis","type":"related"},{"name":"platelet dense body organization and biogenesis","type":"related"},{"name":"platelet dense granule organisation","type":"exact"},{"name":"platelet dense granule organization and biogenesis","type":"related"}],"termid":"GO:0060155"}


id: PBO:0080979
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger and BTB domain containing 12B, pseudogene","termid":"PBO:0080979"}


id: FYPO:0005325
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 error-free translesion synthesis is normal (i.e. indistinguishable from wild type). Error-free translesion synthesis a DNA repair process that results in the conversion of DNA-damage induced single-stranded gaps into large molecular weight DNA after replication by using a specialized DNA polymerase or replication complex to insert a defined nucleotide across from the lesion.","definition_xrefs":["GO:0070987","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal DNA repair","termid":"FYPO:0006569"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000298","FYPO:0000002","FYPO:0001312","FYPO:0001320","FYPO:0000257"],"is_obsolete":false,"name":"normal error-free translesion synthesis","synonyms":[{"name":"normal error-free translesion synthesis during mitotic cell cycle","type":"related"},{"name":"normal error-free translesion synthesis during vegetative growth","type":"exact"}],"termid":"FYPO:0005325"}


id: PBO:0081882
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 830","termid":"PBO:0081882"}


id: PBO:0078405
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Gly (anticodon CCC) 1-1","termid":"PBO:0078405"}


id: GO:0010625
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the frequency or rate of the multiplication or reproduction of Schwann cells, resulting in the expansion of their population. Schwann cells are a type of glial cell in the peripheral nervous system.","definition_xrefs":["GOC:tb","GOC:dph","GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of Schwann cell proliferation","termid":"GO:0010624"},{"relation_name":"is_a","term_name":"positive regulation of glial cell proliferation","termid":"GO:0060252"},{"relation_name":"positively_regulates","term_name":"Schwann cell proliferation","termid":"GO:0014010"}],"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 Schwann cell proliferation","termid":"GO:0010625"}


id: GO:0046134
data:
  {"annotated_genes":["SJAG_04264","SJAG_05029","SJAG_00694"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[98065,114118],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043097"},{"annotations":[73715],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046132"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of one of a family of organic molecules consisting of a pyrimidine base covalently bonded to a sugar ribose (a ribonucleoside) or deoxyribose (a deoxyribonucleoside).","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine nucleoside metabolic process","termid":"GO:0006213"},{"relation_name":"is_a","term_name":"nucleoside biosynthetic process","termid":"GO:0009163"},{"relation_name":"is_a","term_name":"pyrimidine-containing compound biosynthetic process","termid":"GO:0072528"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00694":null,"SJAG_04264":null,"SJAG_05029":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:0044281","GO:0008150","GO:0055086"],"is_obsolete":false,"name":"pyrimidine nucleoside biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-500753"],"synonyms":[{"name":"pyrimidine nucleoside anabolism","type":"exact"},{"name":"pyrimidine nucleoside biosynthesis","type":"exact"},{"name":"pyrimidine nucleoside formation","type":"exact"},{"name":"pyrimidine nucleoside synthesis","type":"exact"}],"termid":"GO:0046134","terms_by_termid":{"GO:0043097":null,"GO:0046132":null}}


id: PBO:0090563
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-binding transcription factor, MADS-box Pvg4","termid":"PBO:0090563"}


id: PBO:0050831
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypoxia up-regulated 1","termid":"PBO:0050831"}


id: GO:0032204
data:
  {"annotated_genes":["SJAG_03624","SJAG_02194"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[97515],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032215"},{"annotations":[77245],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032210"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of a process that affects and monitors the activity of telomeric proteins and the length of telomeric DNA.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of chromosome organization","termid":"GO:0033044"},{"relation_name":"is_a","term_name":"regulation of DNA metabolic process","termid":"GO:0051052"},{"relation_name":"regulates","term_name":"telomere maintenance","termid":"GO:0000723"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02194":null,"SJAG_03624":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0032200"}],"interesting_parent_ids":["GO:0006259","GO:0008150","GO:0032200"],"is_obsolete":false,"name":"regulation of telomere maintenance","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0032204","terms_by_termid":{"GO:0032210":null,"GO:0032215":null}}


id: MONDO:0100383
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any acute myeloid leukemia that has the chromosomal anomaly t(11;19)(q23;p13). (A cytogenetic abnormality that refers to the translocation of the long arm (q23) of chromosome 11 and the short arm (p13) of chromosome 19. It is associated with KMT2A (MLL) fusions, including those with MLLT1 (ENL) and ELL, and acute myeloid leukemia.)","definition_xrefs":["NCIT:C168764"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute myeloid leukemia","termid":"MONDO:0018874"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0004992","MONDO:0005046"],"is_obsolete":false,"name":"acute myeloid leukemia, t(11;19)(q23;p13)","synonyms":[{"name":"AML, t(11;19)(q23;p13)","type":"exact"}],"termid":"MONDO:0100383","xrefs":{"Monarch":{"xref_id":"0100383"}}}


id: PBO:0069513
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 782, pseudogene","termid":"PBO:0069513"}


id: SO:0001158
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence element characteristic of some RNA polymerase II promoters, usually located between -60 and +1 relative to the TSS. Consensus sequence is AWCAGCTGWT. Tends to co-occur with DMv2 (SO:0001161). Tends to not occur with DPE motif (SO:0000015).","definition_xrefs":["PMID:12537576:16827941"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA_motif","termid":"SO:0000713"},{"relation_name":"part_of","term_name":"RNApol_II_promoter","termid":"SO:0000170"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"E_box_motif","synonyms":[{"name":"AWCAGCTGWT","type":"narrow"},{"name":"E box motif","type":"exact"},{"name":"NDM5","type":"related"},{"name":"generic E box motif","type":"exact"}],"termid":"SO:0001158"}


id: PBO:0081267
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 33B","termid":"PBO:0081267"}


id: MONDO:0002608
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete gangliosidosis GM2 (obsolete MONDO:0002608)","termid":"MONDO:0002608","xrefs":{"Monarch":{"xref_id":"0002608"}}}


id: PBO:0062039
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 T member 8","termid":"PBO:0062039"}


id: PBO:0046372
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ectonucleoside triphosphate diphosphohydrolase 7","termid":"PBO:0046372"}


id: PATO:0000807
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000807 proprioreception value (obsolete PATO:0000807)","termid":"PATO:0000807"}


id: MONDO:0700116
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A brain disorder caused by biallelic variants in NDE1 that is characterized by extreme microcephaly (typically head circumference of more than 10 standard deviations (SD) below the mean), profound motor and intellectual disability, spasticity, and incomplete cerebral formation. Radiologic studies demonstrate overt microcephaly with cortical dysgenesis ranging from simplification to pachygyria/lissencephaly to hydranencephaly. Agenesis of the corpus callosum as well as hypoplasia of the brainstem and cerebellum are typically present.","definition_xrefs":["PMID:22526350","PMID:21529751"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microcephaly","termid":"MONDO:0001149"},{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"microcephaly with lissencephaly and/or hydranencephaly","termid":"MONDO:0700116","xrefs":{"Monarch":{"xref_id":"0700116"}}}


id: GO:0061597
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction GTP = cyclic pyranopterin phosphate + diphosphate.","definition_xrefs":["GOC:dph","EC:4.1.99.18","PMID:18154309"],"gene_count":0,"genotype_count":0,"name":"obsolete cyclic pyranopterin monophosphate synthase activity (obsolete GO:0061597)","termid":"GO:0061597"}


id: PBO:0049473
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"granzyme H","termid":"PBO:0049473"}


id: PBO:0005189
data:
  {"annotation_feature_type":"gene","cv_name":"DNA_binding_specificity","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"binds 5'-TA[AG]GCAGNTN[CT]AACG[AC]G-3'","termid":"PBO:0005189"}


id: FYPO:0007174
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 the kinetochore of a chromosome is abnormal during interphase of the mitotic cell cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to kinetochore during vegetative growth","termid":"FYPO:0001268"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"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:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000138","FYPO:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"abnormal protein localization to kinetochore during mitotic interphase","synonyms":[{"name":"abnormal protein localisation to kinetochore during interphase during vegetative growth","type":"exact"},{"name":"abnormal protein localization to kinetochore during interphase of mitotic cell cycle","type":"related"}],"termid":"FYPO:0007174"}


id: GO:0010744
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency or extent of macrophage derived foam cell differentiation. Macrophage derived foam cell differentiation is the process in which a macrophage acquires the specialized features of a foam cell. A foam cell is a type of cell containing lipids in small vacuoles and typically seen in atherosclerotic lesions, as well as other conditions.","definition_xrefs":["GOC:add","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of macrophage derived foam cell differentiation","termid":"GO:0010743"},{"relation_name":"is_a","term_name":"positive regulation of cell differentiation","termid":"GO:0045597"},{"relation_name":"positively_regulates","term_name":"macrophage derived foam cell differentiation","termid":"GO:0010742"}],"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 macrophage derived foam cell differentiation","termid":"GO:0010744"}


