# terms

id: GO:0047173
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a 1,2-diacyl-sn-glycero-3-phosphocholine + all-trans-retinol--[retinol-binding protein] = a 2-acyl-sn-glycero-3-phosphocholine + an all-trans-retinyl ester + apo--[retinol-binding protein]. Recognizes the substrate both in free form and when bound to cellular-retinol-binding-protein, but has higher affinity for the bound form.","definition_xrefs":["RHEA:17469"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-acyltransferase activity","termid":"GO:0008374"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016746","GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"phosphatidylcholine-retinol O-acyltransferase activity","secondary_identifiers":["MetaCyc:2.3.1.135-RXN","Reactome:R-HSA-975608","EC:2.3.1.135"],"synonyms":[{"name":"lecithin--retinol acyltransferase activity","type":"related"},{"name":"phosphatidylcholine:retinol-(cellular-retinol-binding-protein) O-acyltransferase activity","type":"related"},{"name":"phosphatidylcholine:retinol-[cellular-retinol-binding-protein] O-acyltransferase activity","type":"related"}],"termid":"GO:0047173"}


id: PBO:0077429
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 167A","termid":"PBO:0077429"}


id: PBO:0113483
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Telomere-linked gene, silencing of which is strictly Sir2-dependent","termid":"PBO:0113483"}


id: GO:0044017
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: acetyl-CoA + histone H3 L-lysine (position 27) = CoA + histone H3 N6-acetyl-L-lysine (position 27).","definition_xrefs":["PMID:18552846"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H3 acetyltransferase activity","termid":"GO:0010484"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0034212"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016746"}],"interesting_parent_ids":["GO:0003674","GO:0034212","GO:0140096","GO:0016746","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"histone H3K27 acetyltransferase activity","synonyms":[{"name":"histone H3-K27 acetyltransferase activity","type":"exact"},{"name":"histone acetylase activity (H3-K27 specific)","type":"exact"},{"name":"histone acetyltransferase activity (H3-K27 specific)","type":"exact"},{"name":"histone lysine N-acetyltransferase activity (H3-K27 specific)","type":"exact"}],"termid":"GO:0044017"}


id: GO:1904451
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of hydrogen:potassium-exchanging ATPase activity.","definition_xrefs":["GOC:TermGenie","PMID:11897793","GO_REF:0000059"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of proton transport","termid":"GO:0010155"},{"relation_name":"is_a","term_name":"regulation of ATP-dependent activity","termid":"GO:0043462"},{"relation_name":"is_a","term_name":"regulation of potassium ion transmembrane transporter activity","termid":"GO:1901016"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0055085","GO:0006810"],"is_obsolete":false,"name":"regulation of potassium:proton exchanging ATPase activity","synonyms":[{"name":"regulation of (K+ + H+)-ATPase activity","type":"exact"},{"name":"regulation of ATP phosphohydrolase (H+/K+-exchanging)","type":"exact"},{"name":"regulation of H+-K+-ATPase activity","type":"exact"},{"name":"regulation of H+/K(+)-ATPase activity","type":"exact"},{"name":"regulation of H+/K(+)-exchanging ATPase activity","type":"exact"},{"name":"regulation of H+/K+-ATPase activity","type":"exact"},{"name":"regulation of H+/K+-exchanging ATPase activity","type":"exact"},{"name":"regulation of H,K-ATPase activity","type":"exact"},{"name":"regulation of gastric H+/K(+) ATPase activity","type":"narrow"},{"name":"regulation of gastric H+/K+ ATPase","type":"narrow"},{"name":"regulation of hydrogen/potassium-exchanging ATPase activity","type":"exact"},{"name":"regulation of hydrogen:potassium exchanging ATPase activity","type":"exact"},{"name":"regulation of hydrogen:potassium-exchanging ATPase activity","type":"exact"},{"name":"regulation of proton pump activity","type":"broad"}],"termid":"GO:1904451"}


id: GO:0045741
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of EGF-activated receptor activity.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of epidermal growth factor-activated receptor activity","termid":"GO:0007176"},{"relation_name":"is_a","term_name":"positive regulation of protein tyrosine kinase activity","termid":"GO:0061098"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of epidermal growth factor-activated receptor activity","synonyms":[{"name":"activation of epidermal growth factor receptor activity","type":"narrow"},{"name":"positive regulation of EGF receptor activity","type":"exact"},{"name":"positive regulation of EGFR activity","type":"exact"},{"name":"positive regulation of epidermal growth factor receptor activity","type":"exact"},{"name":"stimulation of epidermal growth factor receptor activity","type":"narrow"},{"name":"up regulation of epidermal growth factor receptor activity","type":"exact"},{"name":"up-regulation of epidermal growth factor receptor activity","type":"exact"},{"name":"upregulation of epidermal growth factor receptor activity","type":"exact"}],"termid":"GO:0045741"}


id: MONDO:0010562
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Colonic atresia is a congenital intestinal malformation resulting in a non-latent segment of the colon and characterized by lower intestinal obstruction manifesting with abdominal distention and failure to pass meconium in newborns.","definition_xrefs":["Orphanet:1198"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"colonic atresia","secondary_identifiers":["MEDGEN:75605","NCIT:C101024","GARD:1446","OMIM:303650","MESH:C562562","UMLS:C0266190","SCTID:37054000","HP:0010448"],"synonyms":[{"name":"atresia of colon","type":"exact"},{"name":"colon atresia","type":"exact"},{"name":"colonic atresia","type":"exact"},{"name":"colonic atresia (disease)","type":"exact"},{"name":"congenital atresia of colon","type":"exact"}],"termid":"MONDO:0010562","xrefs":{"Monarch":{"xref_id":"0010562"}}}


id: GO:0030100
data:
  {"annotated_genes":["SJAG_04343","SJAG_00514","SJAG_03631","SJAG_00649","SJAG_04465","SJAG_02684","SJAG_03268","SJAG_03987","SJAG_04052","SJAG_01373","SJAG_04666","SJAG_03581","SJAG_00402","SJAG_00845"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[79277,80192,89336,90430,91899,92185,102462,112825,112955],"is_not":false,"summary":null,"term":"GO:0030100"},{"annotations":[94068],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045806"},{"annotations":[103226],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045807"},{"annotations":[110603,111250,118487],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000369"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of endocytosis.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cellular component organization","termid":"GO:0051128"},{"relation_name":"is_a","term_name":"regulation of vesicle-mediated transport","termid":"GO:0060627"},{"relation_name":"regulates","term_name":"endocytosis","termid":"GO:0006897"}],"gene_count":14,"genes_by_uniquename":{"SJAG_00402":null,"SJAG_00514":null,"SJAG_00649":null,"SJAG_00845":null,"SJAG_01373":null,"SJAG_02684":null,"SJAG_03268":null,"SJAG_03581":null,"SJAG_03631":null,"SJAG_03987":null,"SJAG_04052":null,"SJAG_04343":null,"SJAG_04465":null,"SJAG_04666":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0016192"],"is_obsolete":false,"name":"regulation of endocytosis","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0030100","terms_by_termid":{"GO:0030100":null,"GO:0045806":null,"GO:0045807":null,"GO:2000369":null}}


id: PBO:0055523
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 2957","termid":"PBO:0055523"}


id: PBO:0088905
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER membrane CoA pyrophosphatase (FIT) family lipid storage protein Fit1","termid":"PBO:0088905"}


id: PBO:0108965
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ciliary microtubule associated protein 1B","termid":"PBO:0108965"}


id: GO:0042727
data:
  {"annotated_genes":["SJAG_02360","SJAG_00376","SJAG_01054","SJAG_01937","SJAG_04711","SJAG_00480","SJAG_02491","SJAG_00491","SJAG_04845"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[80369],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006747"},{"annotations":[74604],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009398"},{"annotations":[67159,80489,60599,79735,116782,73004,78201],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009231"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of a flavin, any derivative of the dimethylisoalloxazine (7,8-dimethylbenzo[g]pteridine-2,4(3H,10H)-dione) skeleton, with a substituent on the 10 position.","definition_xrefs":["GOC:jl","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biosynthetic process","termid":"GO:0009058"},{"relation_name":"is_a","term_name":"flavin-containing compound metabolic process","termid":"GO:0042726"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00376":null,"SJAG_00480":null,"SJAG_00491":null,"SJAG_01054":null,"SJAG_01937":null,"SJAG_02360":null,"SJAG_02491":null,"SJAG_04711":null,"SJAG_04845":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"flavin-containing compound biosynthetic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"flavin-containing compound anabolism","type":"exact"},{"name":"flavin-containing compound biosynthesis","type":"exact"},{"name":"flavin-containing compound formation","type":"exact"},{"name":"flavin-containing compound synthesis","type":"exact"},{"name":"riboflavin and derivative biosynthesis","type":"related"},{"name":"riboflavin and derivative biosynthetic process","type":"related"},{"name":"vitamin B2 and derivative biosynthesis","type":"related"},{"name":"vitamin B2 and derivative biosynthetic process","type":"related"}],"termid":"GO:0042727","terms_by_termid":{"GO:0006747":null,"GO:0009231":null,"GO:0009398":null}}


id: FYPO:0003289
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 medial cortical nodes is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to medial cortex during vegetative growth","termid":"FYPO:0000731"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000138","FYPO:0005447","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"abnormal protein localization to medial cortical node","synonyms":[{"name":"abnormal protein localisation to medial cortical node","type":"exact"},{"name":"abnormal protein localization to cortical medial dot","type":"exact"},{"name":"abnormal protein localization to cytokinetic nodes","type":"related"},{"name":"abnormal protein localization to medial cortical node during mitotic cell cycle","type":"related"},{"name":"abnormal protein localization to medial cortical node during vegetative growth","type":"exact"},{"name":"abnormal protein localization to medial cortical nodes","type":"exact"},{"name":"abnormal protein recruitment to medial cortical node","type":"related"}],"termid":"FYPO:0003289"}


id: GO:0050192
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-phospho-D-glycerate + H2O = D-glycerate + phosphate.","definition_xrefs":["RHEA:21156","EC:3.1.3.20"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatase activity","termid":"GO:0016791"}],"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"},{"rel_name":"is_a","termid":"GO:0016788"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016788","GO:0016787"],"is_obsolete":false,"name":"phosphoglycerate phosphatase activity","secondary_identifiers":["MetaCyc:PHOSPHOGLYCERATE-PHOSPHATASE-RXN","KEGG_REACTION:R01748"],"synonyms":[{"name":"D-2-phosphoglycerate phosphatase activity","type":"related"},{"name":"D-glycerate-2-phosphate phosphohydrolase activity","type":"related"},{"name":"glycerophosphate phosphatase activity","type":"related"}],"termid":"GO:0050192"}


id: PBO:0002492
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.4.1.183","termid":"PBO:0002492"}


id: PR:O14011
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A pre-mRNA-processing factor 19 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO02137"],"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-processing factor 19 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC29A4.08c","secondary_identifiers":["UniProtKB:O14011"],"synonyms":[{"name":"Spom972h-PRPF19","type":"exact"},{"name":"complexed with cdc5 protein 8 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14011"}


id: MONDO:0020259
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete myopathy with eye involvement (obsolete MONDO:0020259)","secondary_identifiers":["Orphanet:98689"],"termid":"MONDO:0020259","xrefs":{"Monarch":{"xref_id":"0020259"}}}


id: SO:0002128
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Mitochondrial rRNA is an RNA component of the small or large subunits of mitochondrial ribosomes.","definition_xrefs":["GENCODE:http://www.gencodegenes.org/gencode_biotypes.html"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rRNA","termid":"SO:0000252"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mt_rRNA","synonyms":[{"name":"Mt rRNA","type":"exact"},{"name":"Mt_rRNA","type":"exact"},{"name":"mitochondrial rRNA","type":"exact"},{"name":"mitochondrial_rRNA","type":"exact"}],"termid":"SO:0002128"}


id: PBO:0039604
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acidic nuclear phosphoprotein 32 family member D","termid":"PBO:0039604"}


id: PBO:0039961
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADP ribosylation factor like GTPase 2 binding protein pseudogene 4","termid":"PBO:0039961"}


id: GO:1990588
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex required for prokaryotic cell division (FtsZ-dependent cytokinesis). Part of the divisome. Assembled independently of the other divisome components in the cytoplasm prior to transport to the cell septum. In E. coli consists of FtsB and FtsL.","definition_xrefs":["PMID:15165235","PMID:21784946","GOC:bhm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"divisome complex","termid":"GO:1990586"},{"relation_name":"part_of","term_name":"cytosol","termid":"GO:0005829"},{"relation_name":"part_of","term_name":"FtsQBL complex","termid":"GO:1990587"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005829"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0005829","GO:0032991"],"is_obsolete":false,"name":"FtsBL complex","synonyms":[{"name":"FtsB-FtsL complex","type":"exact"}],"termid":"GO:1990588"}


id: GO:0090017
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation of anterior end of the flat, thickened layer of ectodermal cells known as the neural plate.","definition_xrefs":["GOC:tb","GOC:dph","GOC:sdb_2009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure formation involved in morphogenesis","termid":"GO:0048646"},{"relation_name":"part_of","term_name":"neural plate formation","termid":"GO:0021990"}],"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":"anterior neural plate formation","secondary_identifiers":["Reactome:R-HSA-9823739"],"termid":"GO:0090017"}


id: PBO:0086072
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function that may interact with ribosomes; green fluorescent protein (GFP)-fusion protein localizes to the nucleolus; predicted to be involved in ribosome biogenesis","termid":"PBO:0086072"}


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:0005198"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005198","GO:0003674"],"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: PBO:0074858
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 45B","termid":"PBO:0074858"}


id: GO:0046379
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways involving polysaccharides used in extracellular structures.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete extracellular polysaccharide metabolic process (obsolete GO:0046379)","synonyms":[{"name":"extracellular polysaccharide metabolism","type":"exact"}],"termid":"GO:0046379"}


id: PBO:0064375
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidase, mitochondrial processing subunit beta","termid":"PBO:0064375"}


id: PATO:0001646
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering into a bearer by virtue of the bearer's extending out above or beyond its surface or boundary and outwards in relation to the physical space occupied by another entity.","definition_xrefs":["PATOC:nc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protruding","termid":"PATO:0001598"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protruding out of","synonyms":[{"name":"exits through","type":"related"},{"name":"exposed","type":"related"},{"name":"extruding from","type":"exact"}],"termid":"PATO:0001646"}


id: PBO:0054617
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 2022","termid":"PBO:0054617"}


id: PBO:0003921
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptionally regulates mfm1","termid":"PBO:0003921"}


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":["GARD:17484","UMLS:C3554018","MEDGEN:766932","OMIM:614896"],"synonyms":[{"name":"SANDD","type":"related"},{"name":"sinoatrial node dysfunction and deafness","type":"exact"}],"termid":"MONDO:0013960","xrefs":{"Monarch":{"xref_id":"0013960"}}}


id: PBO:0046493
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ergosterol biosynthesis 28 homolog","termid":"PBO:0046493"}


id: GO:0042195
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of gallate, the anion of gallic acid, in the presence of oxygen.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gallate catabolic process","termid":"GO:0019396"}],"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":"aerobic gallate catabolic process","synonyms":[{"name":"aerobic gallate breakdown","type":"exact"},{"name":"aerobic gallate catabolism","type":"exact"},{"name":"aerobic gallate degradation","type":"exact"},{"name":"aerobic gallic acid catabolic process","type":"exact"},{"name":"aerobic gallic acid catabolism","type":"exact"}],"termid":"GO:0042195"}


id: PBO:0000255
data:
  {"annotation_feature_type":"gene","cv_name":"m_f_g","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chaperone","termid":"PBO:0000255"}


id: MONDO:0032594
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"intellectual disability","termid":"MONDO:0001071"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intellectual developmental disorder and retinitis pigmentosa; IDDRP","secondary_identifiers":["GARD:16306","UMLS:C4748658","MEDGEN:1648358","OMIM:618195"],"synonyms":[{"name":"IDDRP","type":"related"},{"name":"INTELLECTUAL DEVELOPMENTAL DISORDER AND RETINITIS PIGMENTOSA","type":"related"}],"termid":"MONDO:0032594","xrefs":{"Monarch":{"xref_id":"0032594"}}}


id: FYPO:0007920
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 alternative polyadenylation of ncRNA is decreased. ncRNA alternative polyadenylation generates RNA molecules with variable 3'-end lengths from a given RNA by differential use of cleavage and polyadenylation signals. Includes differences in the relative usage levels of alternative polyadenylation sites.","direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal RNA alternative polyadenylation","termid":"FYPO:0007919"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000294","FYPO:0006551","FYPO:0001320","FYPO:0005447","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"decreased ncRNA alternative polyadenylation","termid":"FYPO:0007920"}


id: GO:1902729
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of proteoglycans, any glycoprotein in which the carbohydrate units are glycosaminoglycans.","definition_xrefs":["PMID:23212449","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of glycoprotein biosynthetic process","termid":"GO:0010561"},{"relation_name":"negatively_regulates","term_name":"proteoglycan biosynthetic process","termid":"GO:0030166"}],"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 proteoglycan biosynthetic process","synonyms":[{"name":"down regulation of proteoglycan anabolism","type":"exact"},{"name":"down regulation of proteoglycan biosynthesis","type":"exact"},{"name":"down regulation of proteoglycan biosynthetic process","type":"exact"},{"name":"down regulation of proteoglycan formation","type":"exact"},{"name":"down regulation of proteoglycan synthesis","type":"exact"},{"name":"down-regulation of proteoglycan anabolism","type":"exact"},{"name":"down-regulation of proteoglycan biosynthesis","type":"exact"},{"name":"down-regulation of proteoglycan biosynthetic process","type":"exact"},{"name":"down-regulation of proteoglycan formation","type":"exact"},{"name":"down-regulation of proteoglycan synthesis","type":"exact"},{"name":"downregulation of proteoglycan anabolism","type":"exact"},{"name":"downregulation of proteoglycan biosynthesis","type":"exact"},{"name":"downregulation of proteoglycan biosynthetic process","type":"exact"},{"name":"downregulation of proteoglycan formation","type":"exact"},{"name":"downregulation of proteoglycan synthesis","type":"exact"},{"name":"inhibition of proteoglycan anabolism","type":"narrow"},{"name":"inhibition of proteoglycan biosynthesis","type":"narrow"},{"name":"inhibition of proteoglycan biosynthetic process","type":"narrow"},{"name":"inhibition of proteoglycan formation","type":"narrow"},{"name":"inhibition of proteoglycan synthesis","type":"narrow"},{"name":"negative regulation of proteoglycan anabolism","type":"exact"},{"name":"negative regulation of proteoglycan biosynthesis","type":"exact"},{"name":"negative regulation of proteoglycan formation","type":"exact"},{"name":"negative regulation of proteoglycan synthesis","type":"exact"}],"termid":"GO:1902729"}


id: PBO:0044567
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deleted in azoospermia like","termid":"PBO:0044567"}


id: PBO:0050976
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interferon related developmental regulator 2","termid":"PBO:0050976"}


id: GO:1900953
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of 18-methylnonadec-1-ene metabolic process.","definition_xrefs":["GOC:TermGenie","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of olefin metabolic process","termid":"GO:1900908"},{"relation_name":"regulates","term_name":"18-methylnonadec-1-ene metabolic process","termid":"GO:1900880"}],"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 18-methylnonadec-1-ene metabolic process","synonyms":[{"name":"regulation of 18-methylnonadec-1-ene metabolism","type":"exact"}],"termid":"GO:1900953"}


id: PBO:0086997
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Reverse transcriptase required for splicing of the COX1 pre-mRNA; encoded by a mobile group II intron within the mitochondrial COX1 gene","termid":"PBO:0086997"}


id: GO:0071622
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency or extent of granulocyte chemotaxis. Granulocyte chemotaxis is the movement of a granulocyte in response to an external stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of leukocyte chemotaxis","termid":"GO:0002688"},{"relation_name":"regulates","term_name":"granulocyte chemotaxis","termid":"GO:0071621"}],"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 granulocyte chemotaxis","termid":"GO:0071622"}


id: GO:0031887
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a lipid droplet along a microtubule, mediated by motor proteins.","definition_xrefs":["PMID:9491895"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organelle transport along microtubule","termid":"GO:0072384"}],"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:0006810","GO:0051179"],"is_obsolete":false,"name":"lipid droplet transport along microtubule","synonyms":[{"name":"adiposome transport along microtubule","type":"exact"},{"name":"lipid body transport along microtubule","type":"exact"},{"name":"lipid particle transport along microtubule","type":"exact"}],"termid":"GO:0031887"}


id: PBO:0004782
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterotrimeric G protein gamma subunit Git11","termid":"PBO:0004782"}


id: GO:0009861
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The jasmonic acid and ethylene (ethene) dependent process that confers broad spectrum systemic resistance to disease in response to wounding or a pathogen.","definition_xrefs":["GOC:jy","PMID:10234273"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to wounding","termid":"GO:0009611"},{"relation_name":"is_a","term_name":"defense response to symbiont","termid":"GO:0140546"}],"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":"jasmonic acid and ethylene-dependent systemic resistance","synonyms":[{"name":"jasmonic acid and ethene-dependent systemic resistance","type":"exact"},{"name":"jasmonic acid/ethylene-dependent systemic resistance","type":"exact"}],"termid":"GO:0009861"}


id: MONDO:0012515
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"juvenile open angle glaucoma","termid":"MONDO:0020367"}],"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":"glaucoma 1, open angle, M","secondary_identifiers":["OMIM:610535","MEDGEN:400584","GARD:18230","UMLS:C1864653","MESH:C566436"],"synonyms":[{"name":"GLC1M","type":"exact"},{"name":"JOAG1M","type":"exact"},{"name":"glaucoma 1, open angle, M","type":"exact"}],"termid":"MONDO:0012515","xrefs":{"Monarch":{"xref_id":"0012515"}}}


id: PBO:0028893
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_transcription_at_telomere","termid":"PBO:0028893"}


id: GO:0047442
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 17alpha-hydroxyprogesterone + O2 + reduced NADPH--hemoprotein reductase = acetate + androst-4-ene-3,17-dione + 2 H+ + H2O + oxidized NADPH--hemoprotein reductase.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete 17-alpha-hydroxyprogesterone aldolase activity (obsolete GO:0047442)","termid":"GO:0047442"}


id: MONDO:0002549
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A schwannoma that involves the hypoglossal nerve.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"schwannoma","termid":"MONDO:0002546"},{"relation_name":"is_a","term_name":"hypoglossal nerve neoplasm","termid":"MONDO:0002550"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"schwannoma of twelfth cranial nerve","secondary_identifiers":["MEDGEN:235581","DOID:3197","UMLS:C1335928","NCIT:C5434"],"synonyms":[{"name":"hypoglossal nerve neurilemmoma","type":"exact"},{"name":"hypoglossal nerve schwannoma","type":"exact"},{"name":"hypoglossal neurilemmoma","type":"exact"},{"name":"hypoglossal schwannoma","type":"exact"},{"name":"neurilemmoma of hypoglossal nerve","type":"exact"},{"name":"neurilemmoma of the hypoglossal nerve","type":"exact"},{"name":"neurilemmoma of the twelfth cranial nerve","type":"exact"},{"name":"neurilemmoma of twelfth cranial nerve","type":"exact"},{"name":"schwannoma of hypoglossal nerve","type":"exact"},{"name":"schwannoma of the hypoglossal nerve","type":"exact"},{"name":"schwannoma of the twelfth cranial nerve","type":"exact"},{"name":"schwannoma of twelfth cranial nerve","type":"exact"},{"name":"twelfth cranial nerve neurilemmoma","type":"exact"},{"name":"twelfth cranial nerve schwannoma","type":"exact"}],"termid":"MONDO:0002549","xrefs":{"Monarch":{"xref_id":"0002549"}}}


id: PBO:0027861
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_kinase_activity_during_mitotic_S_phase","termid":"PBO:0027861"}


id: GO:0001742
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires the specialized features of an oenocyte. Oenocytes are large secretory cells found in clusters underlying the epidermis of larval abdominal segments.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"}],"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":"oenocyte differentiation","synonyms":[{"name":"oenocyte cell differentiation","type":"exact"}],"termid":"GO:0001742"}


id: GO:0034881
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: citrazinate + H2O = cis-aconitamide.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete citrazinate hydrolase activity (obsolete GO:0034881)","termid":"GO:0034881"}


id: PATO:0001282
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A color consisting of purple color and low saturation.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purple","termid":"PATO:0000951"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"desaturated purple","synonyms":[{"name":"pale purple","type":"exact"}],"termid":"PATO:0001282"}


id: PBO:0091297
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dolichyl-phosphate-glucose-glycolipid alpha-glucosyltransferase Alg10","termid":"PBO:0091297"}


id: FYPO:0008387
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to autophagic structure is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PMID:37939137"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization","termid":"FYPO:0003627"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal protein localization to autophagic structure","termid":"FYPO:0008387"}


id: PBO:0082614
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Coiled-coil 12S polarisome subunit; required for polarity establishment, apical bud growth, shmoo formation, filamentous differentiation; involved in Bni1p localization at sites of polarized growth, controlling polarized assembly of actin cables; role in apical growth affects diploid-specific bipolar bud site selection; retains Slt2p at bud tip to regulate ER inheritance; role in Ca2+ influx, cell fusion; S288C allele encoding Leu409 rather than Met linked with non-invasion","termid":"PBO:0082614"}


id: FYPO:0002179
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A mixed population phenotype in which a microcolony forms, all cells in the population are inviable and have abnormal morphology (i.e. size, shape, or structure), some cells may divide, and some cells are longer than normal.","definition_xrefs":["PomBase:jh","PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete inviable mixed population, vegetative cells with abnormal morphology, including long cells (obsolete FYPO:0002179)","synonyms":[{"name":"inviable microcolony of vegetative cells with abnormal morphology, including long cells","type":"exact"}],"termid":"FYPO:0002179"}


id: GO:0034074
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: oxidosqualene = marneral.","definition_xrefs":["PMID:16425307","GOC:cb","PMID:18033581"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidosqualene cyclase activity","termid":"GO:0031559"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016853","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"marneral synthase activity","secondary_identifiers":["RHEA:31875","MetaCyc:RXN-9664"],"termid":"GO:0034074"}


id: PBO:0061761
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2'-5'-oligoadenylate synthetase like","termid":"PBO:0061761"}


id: PBO:0082264
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Aminopeptidase yscII; may have a role in obtaining leucine from dipeptide substrates; APE2 has a paralog, AAP1, that arose from the whole genome duplication","termid":"PBO:0082264"}


id: PBO:0090394
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosome biogenesis protein Urb2","termid":"PBO:0090394"}


id: FYPO:0003830
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell cycle checkpoint phenotype in which the cytokinesis checkpoint of a mitotic cell cycle is abnormal. The cytokinesis checkpoint normally delays the G2/M transition of a mitotic cell cycle if cytokinesis was not completed correctly in the previous cell cycle. In a mutant, the checkpoint may fail to arrest or delay cell cycle progression under appropriate conditions, or the incidence or duration of arrest or delay may differ from wild type under any specified set of conditions.","definition_xrefs":["GO:0044878","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal regulation of G2/M transition of mitotic cell cycle","termid":"FYPO:0000166"},{"relation_name":"is_a","term_name":"abnormal mitotic cell cycle checkpoint","termid":"FYPO:0001704"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"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"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000298"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0000002","FYPO:0000298","FYPO:0001985","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"abnormal cytokinesis checkpoint","synonyms":[{"name":"abnormal cytokinesis after mitosis checkpoint","type":"exact"},{"name":"abnormal cytokinesis checkpoint activation","type":"related"},{"name":"abnormal mitotic cell cycle cytokinesis checkpoint","type":"exact"}],"termid":"FYPO:0003830"}


id: MONDO:0010971
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infundibulopelvic stenosis-multicystic kidney syndrome is a rare, genetic renal malformation syndrome characterized by variable degrees of malformation in the pelvicalyceal system (including unilateral or bilateral calyceal dilatation, infundibular stenosis, hypoplasia or stenosis of the renal pelvis) which lead to multicystic kidney. Clinically it exhibits abdominal, lumbar or flank pain, recurrent urinary tract infections, hypertension, proteinuria and often progresses to renal insufficiency. Calyceal dilatation and hydronephrosis are frequently seen on imaging.","definition_xrefs":["Orphanet:1849"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"infundibulopelvic stenosis-multicystic kidney syndrome","secondary_identifiers":["OMIM:600989","SCTID:725905005","MEDGEN:318751","MESH:C535528","UMLS:C1832949"],"synonyms":[{"name":"infundibulopelvic dysgenesis","type":"related"}],"termid":"MONDO:0010971","xrefs":{"Monarch":{"xref_id":"0010971"}}}


id: MONDO:1011962
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"musculoskeletal system disorder, non-human animal","termid":"MONDO:1011335"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vitamin D-deficiency rickets, non-type I, non-type II, non-human animal","secondary_identifiers":["OMIA:001614"],"termid":"MONDO:1011962","xrefs":{"Monarch":{"xref_id":"1011962"}}}


id: GO:0070958
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the frequency, rate or extent of the directed killing of a gram-positive bacterium by a neutrophil.","definition_xrefs":["GOC:add","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of neutrophil mediated killing of gram-positive bacterium","termid":"GO:0070952"},{"relation_name":"is_a","term_name":"negative regulation of neutrophil mediated killing of bacterium","termid":"GO:0070956"},{"relation_name":"negatively_regulates","term_name":"neutrophil-mediated killing of gram-positive bacterium","termid":"GO:0070946"}],"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 neutrophil mediated killing of gram-positive bacterium","synonyms":[{"name":"down regulation of neutrophil mediated killing of gram-positive bacterium","type":"exact"},{"name":"down-regulation of neutrophil mediated killing of gram-positive bacterium","type":"exact"},{"name":"downregulation of neutrophil mediated killing of gram-positive bacterium","type":"exact"},{"name":"inhibition of neutrophil mediated killing of gram-positive bacterium","type":"narrow"}],"termid":"GO:0070958"}


id: GO:0106164
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of exonucleolytic nuclear-transcribed mRNA catabolic process involved in deadenylation-dependent decay.","definition_xrefs":["PMID:30601114","GOC:vw"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of exonucleolytic catabolism of deadenylated mRNA (obsolete GO:0106164)","termid":"GO:0106164"}


id: PATO:0000066
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A texture quality inhering in a bearer by virtue of the bearer's having hair or bristles.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"texture","termid":"PATO:0000150"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pilosity","termid":"PATO:0000066"}


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


id: PR:O74957
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ago1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74957"],"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 argonaute (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC736.11","synonyms":[{"name":"PAZ Piwi domain protein ago1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"RNA interference pathway protein ago1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-ago1","type":"exact"},{"name":"cell cycle control protein ago1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"eukaryotic translation initiation factor 2C 2-like protein ago1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"protein slicer (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74957"}


id: GO:0070645
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A small, granular structure that is found in the extracellular matrix of cell of the secretory tapetal layer that surrounds developing pollen grains. Ubisch bodies have a sporopollenin coat, are attached to the peritapetal wall, and may play a role in pollen development.","definition_xrefs":["GOC:ecd","PMID:14612572","PMID:16524248","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"specialized extracellular matrix","termid":"GO:0140047"}],"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":"Ubisch body","synonyms":[{"name":"orbicule","type":"exact"}],"termid":"GO:0070645"}


id: PBO:0039803
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADP ribosylation factor 1 pseudogene 1","termid":"PBO:0039803"}


id: PBO:0066260
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RBMX like 3","termid":"PBO:0066260"}


id: PBO:0077891
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TP53RK binding protein","termid":"PBO:0077891"}


id: PR:Q10182
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- erf4 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q10182"],"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":"ras modification protein erf4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC3F10.07c","synonyms":[{"name":"Spom972h-erf4","type":"exact"},{"name":"meiotically up-regulated gene 91 protein (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q10182"}


id: PBO:0077134
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TIPIN pseudogene 1","termid":"PBO:0077134"}


id: PBO:0003942
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RRM-containing cyclophilin regulating transcription Rct1","termid":"PBO:0003942"}


id: PR:O13882
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mrps18 gene.","definition_xrefs":["UniProtKB:O13882","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":"37S ribosomal protein S18, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1B3.18c","synonyms":[{"name":"Spom972h-mrps18","type":"exact"}],"termid":"PR:O13882"}


id: PBO:0065947
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAD9 checkpoint clamp component A","termid":"PBO:0065947"}


id: GO:1905322
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of mesenchymal stem cell migration.","definition_xrefs":["PMID:26846297","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell migration","termid":"GO:0030335"},{"relation_name":"is_a","term_name":"regulation of mesenchymal stem cell migration","termid":"GO:1905320"},{"relation_name":"positively_regulates","term_name":"mesenchymal stem cell migration","termid":"GO:1905319"}],"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 mesenchymal stem cell migration","synonyms":[{"name":"activation of mesenchymal stem cell migration","type":"narrow"},{"name":"up regulation of mesenchymal stem cell migration","type":"exact"},{"name":"up-regulation of mesenchymal stem cell migration","type":"exact"},{"name":"upregulation of mesenchymal stem cell migration","type":"exact"}],"termid":"GO:1905322"}


id: PBO:0005455
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear export mediator factor NEMF","termid":"PBO:0005455"}


id: PBO:0053407
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 342","termid":"PBO:0053407"}


id: FYECO:0000297
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which sodium arsenite (NaAsO2) was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ NaAsO2","synonyms":[{"name":"sodium arsenite added","type":"exact"}],"termid":"FYECO:0000297"}


id: PBO:0001467
data:
  {"annotation_feature_type":"gene","cv_name":"subunit_composition","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"monomeric","termid":"PBO:0001467"}


id: FYPO:0001465
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 intracellular calcium ion (Ca2+) concentration briefly increases to a lesser extent than normal immediately following an extracellular Ca2+ stimulus. Normally, the intracellular Ca2+ concentration increases to a peak in a \\\"burst\\\" within one minute, and then decreases to a new steady-state concentration.","definition_xrefs":["PMID:21811607","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal immediate intracellular calcium spike following extracellular calcium stimulus","termid":"FYPO:0001463"}],"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:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"decreased immediate intracellular calcium spike following extracellular calcium stimulus","synonyms":[{"name":"decreased immediate intracellular calcium spike following extracellular calcium stimulus during mitotic cell cycle","type":"related"},{"name":"decreased immediate intracellular calcium spike following extracellular calcium stimulus during vegetative growth","type":"exact"},{"name":"reduced immediate intracellular calcium spike following extracellular calcium stimulus","type":"exact"}],"termid":"FYPO:0001465"}


id: PBO:0077253
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane p24 trafficking protein 4","termid":"PBO:0077253"}


id: MONDO:0012447
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"non-syndromic synpolydactyly","termid":"MONDO:0000722"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"synpolydactyly type 3","secondary_identifiers":["MESH:C565216","OMIM:610234","UMLS:C1853255","icd11.foundation:1671501762","Orphanet:295199","MEDGEN:344005","GARD:17360"],"synonyms":[{"name":"SD2, Malik type","type":"exact"},{"name":"SD2c","type":"exact"},{"name":"SPD, Malik type","type":"exact"},{"name":"SPD3","type":"exact"},{"name":"synpolydactyly 3","type":"related"},{"name":"synpolydactyly, Malik type","type":"exact"}],"termid":"MONDO:0012447","xrefs":{"Monarch":{"xref_id":"0012447"}}}


id: MONDO:0004701
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign protruding lesion arising either from the endometrial cavity (endometrial polyp) or the endocervix (endocervical polyp). It may occasionally recur following complete resection.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"uterine disorder","termid":"MONDO:0002654"},{"relation_name":"is_a","term_name":"polyp","termid":"MONDO:0005079"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uterine polyp","secondary_identifiers":["SCTID:11314008","NCIT:C3662","EFO:0009484","DOID:9042","ICD10CM:N84.0","MEDGEN:57628","ICD9:621.0","UMLS:C0156369"],"synonyms":[{"name":"endometrial/uterine polyp","type":"exact"},{"name":"polyp of corpus uteri","type":"exact"},{"name":"polyp of endometrium","type":"narrow"},{"name":"polyp of the uterus","type":"exact"},{"name":"polyp of uterus","type":"exact"},{"name":"polyp, uterus","type":"exact"},{"name":"uterine polyp","type":"exact"},{"name":"uterus polyp","type":"exact"}],"termid":"MONDO:0004701","xrefs":{"Monarch":{"xref_id":"0004701"}}}


id: PBO:0005892
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F0-ATPase subunit 6 (predicted)","termid":"PBO:0005892"}


id: PR:Q9P7V8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A phosphate carrier protein, mitochondrial that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO03484","PANTHER:PTHR24089:SF22"],"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":"mitochondrial phosphate carrier protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1703.13c","secondary_identifiers":["UniProtKB:Q9P7V8"],"synonyms":[{"name":"Spom972h-SLC25A3","type":"exact"}],"termid":"PR:Q9P7V8"}


id: GO:0004189
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the cleavage of the Glu-Tyr bond to release the C-terminal tyrosine residue from the native tyrosinated tubulin. Inactive on Z-Glu-Tyr.","definition_xrefs":["EC:3.4.17.17"],"gene_count":0,"genotype_count":0,"name":"obsolete tubulinyl-Tyr carboxypeptidase activity (obsolete GO:0004189)","synonyms":[{"name":"TTCPase activity","type":"related"},{"name":"brain I carboxypeptidase activity","type":"related"},{"name":"carboxypeptidase-tubulin activity","type":"related"},{"name":"soluble carboxypeptidase activity","type":"related"},{"name":"tubulin carboxypeptidase activity","type":"related"},{"name":"tubulin-tyrosine carboxypeptidase activity","type":"related"},{"name":"tubulinyl-Tyr carboxypeptidase activity","type":"exact"},{"name":"tubulinyl-tyrosine carboxypeptidase activity","type":"exact"},{"name":"tubulinyltyrosine carboxypeptidase activity","type":"related"},{"name":"tyrosinotubulin carboxypeptidase activity","type":"related"},{"name":"tyrosyltubulin carboxypeptidase activity","type":"related"}],"termid":"GO:0004189"}


id: PATO:0001858
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A functionality quality inhering in a bearer by virtue of being not completely paralysed.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"movement behavioral quality","termid":"PATO:0002076"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partially paralysed","termid":"PATO:0001858"}


id: PATO:0001798
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A shape quality inhering in a bearer by virtue of the bearer's having multiple angles in its length.","definition_xrefs":["thefreedictionary.com:thefreedictionary.com"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bent","termid":"PATO:0000617"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kinked","synonyms":[{"name":"tightly curled","type":"related"},{"name":"twisted","type":"related"}],"termid":"PATO:0001798"}


id: FYPO:0006283
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 dihydroxylation of one or more proline residues in specific proteins, or at specific protein sites, does not occur.","definition_xrefs":["PomBase:mah","PMID:29083304"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein modification during vegetative growth","termid":"FYPO:0000544"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0001320","FYPO:0002494","FYPO:0002274","FYPO:0001985"],"is_obsolete":false,"name":"abolished protein-proline dihydroxylation during vegetative growth","synonyms":[{"name":"abolished protein-proline dihydroxylation during mitotic cell cycle","type":"related"},{"name":"abolished protein-proline dioxygenation during vegetative growth","type":"exact"},{"name":"protein-proline dihydroxylation abolished during vegetative growth","type":"exact"}],"termid":"FYPO:0006283"}


id: MONDO:0004541
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A morphologic variant of testicular seminoma characterized by the presence of seminoma cells arranged in pseudoglandular patterns and few lymphocytes.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"testicular seminoma","termid":"MONDO:0003669"}],"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":"pseudoglandular variant testicular seminoma","secondary_identifiers":["MEDGEN:273633","DOID:8358","NCIT:C40958","UMLS:C1515293"],"synonyms":[{"name":"testicular seminoma, pseudoglandular variant","type":"exact"}],"termid":"MONDO:0004541","xrefs":{"Monarch":{"xref_id":"0004541"}}}


id: PBO:0117186
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DPP6 antisense RNA 1","termid":"PBO:0117186"}


id: GO:0030700
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Complex that possesses glycine reductase activity; usually comprises three subunits, of which two are selenoproteins; the subunits are typically designated selenoprotein A, selenoprotein B and protein C.","definition_xrefs":["GOC:mah","PMID:2018775"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase complex","termid":"GO:1990204"},{"relation_name":"part_of","term_name":"cytoplasm","termid":"GO:0005737"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005737"],"is_obsolete":false,"name":"glycine reductase complex","termid":"GO:0030700"}


id: PBO:0076707
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor 7 like 1","termid":"PBO:0076707"}


id: MONDO:0001797
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chancroid is a bacterial infection that is spread through sexual contact. It is caused by a type of bacteria called Haemophilus ducreyi. Chancroid is characterized by a small bump on the genital which becomes a painful ulcer. Men may have just one ulcer, but women often develop four or more.About half of the people who are infected with a chancroid will develop enlarged inguinal lymph nodes, the nodes located in the fold between the leg and the lower abdomen. In some cases, the nodes will break through the skin and cause draining abscesses. The swollen lymph nodes and abscesses are often called buboes. Chancroid infections can be treated with antibiotics, including azithromycin, ceftriaxone, ciprofloxacin, and erythromycin. Large lymph node swellings need to be drained, either with a needle or local surgery.","direct_ancestors":[{"relation_name":"is_a","term_name":"primary bacterial infectious disease","termid":"MONDO:0000314"},{"relation_name":"is_a","term_name":"bacterial sexually transmitted disease","termid":"MONDO:0005323"},{"relation_name":"is_a","term_name":"haemophilus infectious disease","termid":"MONDO:0006926"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chancroid","secondary_identifiers":["UMLS:C0007947","ICD9:099.0","DOID:13778","MEDGEN:872","GARD:9522","ICD10CM:A57","icd11.foundation:1357024926","MESH:D002602","SCTID:266143009"],"synonyms":[{"name":"Chancroids","type":"related"},{"name":"Ulcus molle, skin","type":"exact"}],"termid":"MONDO:0001797","xrefs":{"Monarch":{"xref_id":"0001797"}}}


id: PBO:0041763
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calpain 2","termid":"PBO:0041763"}


id: MONDO:1010985
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hydrocephalus that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrocephalus, non-human animal","termid":"MONDO:1010233"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hydrocephalus, domestic cat","secondary_identifiers":["OMIA:000487-9685"],"termid":"MONDO:1010985","xrefs":{"Monarch":{"xref_id":"1010985"}}}


id: PR:Q10369
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- snt1 gene.","definition_xrefs":["UniProtKB:Q10369","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C22E12.19 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC22E12.19","synonyms":[{"name":"Spom972h-snt1","type":"exact"}],"termid":"PR:Q10369"}


id: GO:1902787
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 dodecane stimulus.","definition_xrefs":["GO_REF:0000071","GOC:TermGenie","GOC:mengo_curators","PMID:23826995"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to alkane","termid":"GO:1902779"},{"relation_name":"is_a","term_name":"response to dodecane","termid":"GO:1902786"}],"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 dodecane","termid":"GO:1902787"}


id: GO:0043861
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: agmatine(out) + putrescine(in) = agmatine(in) + putrescine(out).","definition_xrefs":["GOC:jl","PMID:17028272"],"direct_ancestors":[{"relation_name":"is_a","term_name":"antiporter activity","termid":"GO:0015297"},{"relation_name":"is_a","term_name":"putrescine transmembrane transporter activity","termid":"GO:0015489"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"agmatine:putrescine antiporter activity","synonyms":[{"name":"agmatine-putrescine antiporter activity","type":"exact"},{"name":"agmatine/putrescine antiporter activity","type":"exact"}],"termid":"GO:0043861"}


id: PBO:0048189
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gamma-aminobutyric acid type B receptor subunit 1","termid":"PBO:0048189"}


id: MONDO:0021225
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplasm (disease) that involves the uvea.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"uveal disorder","termid":"MONDO:0002661"},{"relation_name":"is_a","term_name":"eye neoplasm","termid":"MONDO:0021220"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"uvea neoplasm","secondary_identifiers":["NCIT:C3436","UMLS:C0042162","MEDGEN:52960"],"synonyms":[{"name":"neoplasm of the uvea","type":"exact"},{"name":"neoplasm of uvea","type":"exact"},{"name":"tumor of the uvea","type":"exact"},{"name":"tumor of uvea","type":"exact"},{"name":"tumour of the uvea","type":"exact"},{"name":"tumour of uvea","type":"exact"},{"name":"uvea neoplasm (disease)","type":"exact"},{"name":"uvea tumor","type":"exact"},{"name":"uvea tumour","type":"exact"},{"name":"uveal neoplasm","type":"exact"},{"name":"uveal tumor","type":"exact"},{"name":"uveal tumour","type":"exact"}],"termid":"MONDO:0021225","xrefs":{"Monarch":{"xref_id":"0021225"}}}


id: MONDO:0002438
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An instance of polycythemia that is acquired during the lifetime of the individual.","definition_xrefs":["MONDO:patterns/acquired"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polycythemia","termid":"MONDO:0005571"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"acquired polycythemia","secondary_identifiers":["ICD9:289.0","DOID:2834","NCIT:C27178"],"synonyms":[{"name":"acquired polycythemia","type":"exact"},{"name":"acquired polycythemia (disease)","type":"exact"}],"termid":"MONDO:0002438","xrefs":{"Monarch":{"xref_id":"0002438"}}}


id: MONDO:0005074
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant cystic serous or mucinous epithelial neoplasm characterized by the presence of malignant glandular epithelial cells forming papillary structures. Stromal invasion is present.","definition_xrefs":["NCIT:C3777"],"direct_ancestors":[{"relation_name":"is_a","term_name":"papillary adenocarcinoma","termid":"MONDO:0002512"},{"relation_name":"is_a","term_name":"cystadenocarcinoma","termid":"MONDO:0005596"},{"relation_name":"is_a","term_name":"papillary cystic neoplasm","termid":"MONDO:0006349"}],"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":"papillary cystadenocarcinoma","secondary_identifiers":["MEDGEN:64635","EFO:0000639","ICDO:8450/3","MESH:D018283","UMLS:C0206700","DOID:3110"],"synonyms":[{"name":"cystadenocarcinoma, papillary, malignant","type":"exact"},{"name":"papillary cystadenocarcinoma","type":"exact"},{"name":"papillary cystadenocarcinoma (morphologic abnormality)","type":"exact"},{"name":"papillary cystadenocarcinoma, NOS (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0005074","xrefs":{"Monarch":{"xref_id":"0005074"}}}


id: SO:0001605
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant within a CDS resulting in the gain of an amino acid to the resulting polypeptide.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polypeptide_sequence_variant","termid":"SO:0001603"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amino_acid_insertion","synonyms":[{"name":"amino acid insertion","type":"exact"}],"termid":"SO:0001605"}


id: PBO:0002711
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aspartyl aminopeptidase Aap1","termid":"PBO:0002711"}


id: MONDO:0012387
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"This syndrome is characterized by sclerosing bone dysplasia, ichthyosis vulgaris and premature ovarian failure. The bone disorder affects all metaphyseal-diaphyseal regions of the long bones, the skull, and the metacarpals.","definition_xrefs":["Orphanet:75325"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with increased bone density (obsolete MONDO:0019703)","termid":"MONDO:0019703"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"inherited primary ovarian failure","termid":"MONDO:0019852"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"osteosclerosis-ichthyosis-premature ovarian failure syndrome","secondary_identifiers":["GARD:9904","OMIM:609993","MESH:C536064","UMLS:C1864942","SCTID:722114007","MEDGEN:355875"],"synonyms":[{"name":"osteosclerosis with ichthyosis and POF","type":"related"},{"name":"osteosclerosis with ichthyosis and premature ovarian failure","type":"related"},{"name":"sclerosing dysplasia of bone with ichthyosis and premature ovarian failure","type":"related"},{"name":"sclerosing dysplasia of bone-ichthyosis-premature ovarian failure syndrome","type":"exact"}],"termid":"MONDO:0012387","xrefs":{"Monarch":{"xref_id":"0012387"}}}


id: PBO:0082096
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"6-phosphogluconolactonase; protein abundance increases in response to DNA replication stress; SOL4 has a paralog, SOL3, that arose from the whole genome duplication","termid":"PBO:0082096"}


id: PATO:0001540
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An amylose composition quality inhering in an bearer by virtue of the bearer's having negligible or no amylose content.","definition_xrefs":["TO:TO"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amylose composition","termid":"PATO:0001539"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutinous","termid":"PATO:0001540"}


id: PBO:0061544
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NOP2/Sun RNA methyltransferase family member 7","termid":"PBO:0061544"}


id: MONDO:0024291
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-neoplastic disorder that is the result of defects of vascular morphogenesis.","direct_ancestors":[{"relation_name":"is_a","term_name":"vascular disorder","termid":"MONDO:0005385"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vascular malformation","secondary_identifiers":["EFO:0006888","MEDGEN:56387","UMLS:C0158570","NANDO:2100295","MESH:D054079"],"synonyms":[{"name":"malformation, vascular","type":"related"},{"name":"malformations, vascular","type":"related"},{"name":"vascular malformation","type":"exact"}],"termid":"MONDO:0024291","xrefs":{"Monarch":{"xref_id":"0024291"}}}


id: PBO:0053356
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 260","termid":"PBO:0053356"}


id: SO:0002065
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An insertion of sequence from the SVA family of mobile elements.","definition_xrefs":["NCBI:th"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mobile_element_insertion","termid":"SO:0001837"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SVA_insertion","termid":"SO:0002065"}


id: PBO:0051725
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"INSYN1 antisense RNA 1","termid":"PBO:0051725"}


id: MONDO:0005430
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A form of hypertension with early onset relative to normal range for a given population.","definition_xrefs":["EFO:0004772"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypertensive disorder","termid":"MONDO:0005044"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"early onset hypertension","termid":"MONDO:0005430","xrefs":{"Monarch":{"xref_id":"0005430"}}}


id: GO:1903328
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of tRNA metabolic process.","definition_xrefs":["GO_REF:0000058","GOC:vw","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of RNA metabolic process","termid":"GO:0051254"},{"relation_name":"is_a","term_name":"regulation of tRNA metabolic process","termid":"GO:1903326"},{"relation_name":"positively_regulates","term_name":"tRNA metabolic process","termid":"GO:0006399"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006399"},{"rel_name":"regulates","termid":"GO:0006399"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006399","GO:0008150"],"is_obsolete":false,"name":"positive regulation of tRNA metabolic process","synonyms":[{"name":"activation of tRNA metabolic process","type":"narrow"},{"name":"activation of tRNA metabolism","type":"narrow"},{"name":"positive regulation of tRNA metabolism","type":"exact"},{"name":"up regulation of tRNA metabolic process","type":"exact"},{"name":"up regulation of tRNA metabolism","type":"exact"},{"name":"up-regulation of tRNA metabolic process","type":"exact"},{"name":"up-regulation of tRNA metabolism","type":"exact"},{"name":"upregulation of tRNA metabolic process","type":"exact"},{"name":"upregulation of tRNA metabolism","type":"exact"}],"termid":"GO:1903328"}


id: SO:0002205
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A regulatory element that acts in response to a stimulus, usually via transcription factor binding.","direct_ancestors":[{"relation_name":"is_a","term_name":"transcriptional_cis_regulatory_region","termid":"SO:0001055"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"response_element","synonyms":[{"name":"INSDC_feature:regulatory","type":"broad"},{"name":"INSDC_qualifier:response_element","type":"exact"},{"name":"response element","type":"exact"}],"termid":"SO:0002205"}


id: GO:0070670
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an interleukin-4 stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to cytokine","termid":"GO:0034097"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to interleukin-4","synonyms":[{"name":"response to IL-4","type":"exact"}],"termid":"GO:0070670"}


id: MONDO:0014050
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any isolated microphthalmia in which the cause of the disease is a mutation in the ALDH1A3 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isolated microphthalmia","termid":"MONDO:0000062"},{"relation_name":"is_a","term_name":"isolated anophthalmia-microphthalmia syndrome","termid":"MONDO:0016764"}],"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":"isolated microphthalmia 8","secondary_identifiers":["MEDGEN:767438","UMLS:C3554524","DOID:0060841","OMIM:615113"],"synonyms":[{"name":"ALDH1A3 isolated microphthalmia","type":"exact"},{"name":"MCOP8","type":"exact"},{"name":"isolated microphthalmia 8","type":"exact"},{"name":"isolated microphthalmia caused by mutation in ALDH1A3","type":"exact"},{"name":"isolated microphthalmia type 8","type":"exact"},{"name":"microphthalmia, isolated 8","type":"related"},{"name":"microphthalmia, isolated type 8","type":"exact"}],"termid":"MONDO:0014050","xrefs":{"Monarch":{"xref_id":"0014050"}}}


id: PBO:0027210
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-large_vacuoles_present_in_decreased_numbers_during_salt_stress","termid":"PBO:0027210"}


id: PBO:0044279
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-X-C motif chemokine receptor 2 pseudogene 1","termid":"PBO:0044279"}


id: PBO:0066003
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ral GTPase activating protein catalytic subunit alpha 2","termid":"PBO:0066003"}


id: GO:0009791
data:
  {"annotated_genes":["SJAG_00845"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[59452],"is_not":false,"summary":null,"term":"GO:0009791"}]},"cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the organism over time, from the completion of embryonic development to the mature structure. See embryonic development.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multicellular organismal process","termid":"GO:0032501"},{"relation_name":"part_of","term_name":"multicellular organism development","termid":"GO:0007275"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00845":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"post-embryonic development","references_by_uniquename":{"GO_REF:0000117":null},"termid":"GO:0009791","terms_by_termid":{"GO:0009791":null}}


id: GO:0033425
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A triplet codon-amino acid adaptor activity that recognizes a CAU codon.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"triplet codon-amino acid adaptor activity","termid":"GO:0030533"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0060090"},{"rel_name":"is_a","termid":"GO:0003723"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0060090","GO:0003723","GO:0003674"],"is_obsolete":false,"name":"CAU codon-amino acid adaptor activity","synonyms":[{"name":"CAT codon-amino acid adaptor activity","type":"exact"},{"name":"histidine tRNA","type":"related"}],"termid":"GO:0033425"}


id: GO:0016821
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete hydrolase activity, acting on acid anhydrides, involved in cellular and subcellular movement (obsolete GO:0016821)","synonyms":[{"name":"hydrolase activity, acting on acid anhydrides, involved in cellular and subcellular movement","type":"exact"}],"termid":"GO:0016821"}


id: GO:0047469
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 4-carboxymethyl-4-methylbut-2-en-1,4-olide = 4-carboxymethyl-3-methylbut-2-en-1,4-olide.","definition_xrefs":["RHEA:19237","EC:5.4.99.14"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular transferase activity","termid":"GO:0016866"}],"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:0016853","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"4-carboxymethyl-4-methylbutenolide mutase activity","secondary_identifiers":["KEGG_REACTION:R04510","MetaCyc:5.4.99.14-RXN"],"synonyms":[{"name":"4-carboxymethyl-4-methylbut-2-en-1,4-olide methylmutase activity","type":"related"},{"name":"4-methyl-2-enelactone isomerase activity","type":"related"},{"name":"4-methyl-2-enelactone methyl-isomerase activity","type":"related"},{"name":"4-methyl-3-enelactone methyl isomerase activity","type":"related"},{"name":"4-methylmuconolactone methylisomerase activity","type":"related"}],"termid":"GO:0047469"}


id: MONDO:0019532
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Warm autoimmune hemolytic anemia is the most common form of autoimmune hemolytic anemia defined by the presence of warm autoantibodies against red blood cells (autoantibodies that are active at temperatures between 37-40B0C).","definition_xrefs":["Orphanet:90033"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune hemolytic anemia","termid":"MONDO:0020108"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0002280","MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"autoimmune hemolytic anemia, warm type","secondary_identifiers":["NANDO:1200306","GARD:7876","NORD:1837","icd11.foundation:880772122","UMLS:C0272118","NCIT:C162611","SCTID:3978000","MedDRA:10047822","MEDGEN:450541"],"synonyms":[{"name":"Warm Autoimmune Hemolytic Anemia","type":"exact"},{"name":"wAHA","type":"exact"},{"name":"wAIHA","type":"exact"},{"name":"warm AIHA","type":"exact"},{"name":"warm antibody AIHA","type":"related"},{"name":"warm antibody autoimmune hemolytic anaemia","type":"related"},{"name":"warm antibody autoimmune hemolytic anemia","type":"related"},{"name":"warm antibody hemolytic anaemia","type":"related"},{"name":"warm antibody hemolytic anemia","type":"related"},{"name":"warm-reacting-antibody hemolytic anaemia","type":"related"},{"name":"warm-reacting-antibody hemolytic anemia","type":"related"}],"termid":"MONDO:0019532","xrefs":{"Monarch":{"xref_id":"0019532"}}}


id: FYPO:0006179
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the lateral attachment of sister chromatids to mitotic spindle microtubules is abnormal. Normally, sister chromatids become laterally attached to spindle microtubules as part of mitotic metaphase plate congression. Attachment precedes migration along microtubules towards the spindle equator (metaphase plate).","definition_xrefs":["GO:0099607","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal attachment of mitotic spindle microtubules to kinetochore","termid":"FYPO:0004213"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0000641"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0000337","FYPO:0000631","FYPO:0005447","FYPO:0001985","FYPO:0000641","FYPO:0000138"],"is_obsolete":false,"name":"abnormal lateral attachment of mitotic spindle microtubules to kinetochore","synonyms":[{"name":"abnormal lateral attachment of mitotic spindle microtubules to kinetochore during vegetative growth","type":"exact"},{"name":"abnormal lateral attachment of spindle microtubules to kinetochore during mitosis","type":"exact"},{"name":"abnormal lateral attachment of spindle microtubules to kinetochore during mitotic cell cycle","type":"related"}],"termid":"FYPO:0006179"}


id: GO:0180050
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"The binding activity of a molecule that brings together a protein or protein complex and a mitochondrial outer membrane lipid or membrane-associated protein, in order to maintain the localization of the protein, or protein complex at a specific mitochondrial outer membrane location.","definition_xrefs":["GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane-membrane adaptor activity","termid":"GO:0043495"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0030674"},{"rel_name":"is_a","termid":"GO:0060090"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0060090","GO:0003674","GO:0030674"],"is_obsolete":false,"name":"protein-mitochondrial outer membrane tethering activity","termid":"GO:0180050"}


id: PR:P08091
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pho1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P08091"],"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":"acid phosphatase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBP4G3.02","synonyms":[{"name":"Spom972h-pho1","type":"exact"}],"termid":"PR:P08091"}


id: GO:0004158
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: (S)-dihydroorotate + O2 = H2O2 + orotate.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete dihydroorotate oxidase activity (obsolete GO:0004158)","synonyms":[{"name":"(S)-dihydroorotate:oxygen oxidoreductase activity","type":"related"},{"name":"4,5-L-dihydroorotate:oxygen oxidoreductase activity","type":"related"}],"termid":"GO:0004158"}


id: PBO:0029410
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_response_to_mitotic_G2/M_transition_checkpoint_signaling","termid":"PBO:0029410"}


id: GO:0140816
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of ADP-ribose groups to the serine-6 or an equivalent residue of the N-terminal tail of histone H2B.","definition_xrefs":["PMID:34874266"],"direct_ancestors":[{"relation_name":"is_a","term_name":"NAD+-protein-serine ADP-ribosyltransferase activity","termid":"GO:0140805"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0140096","GO:0003674","GO:0003824","GO:0016757","GO:0016740"],"is_obsolete":false,"name":"NAD+-histone H2BS6 serine ADP-ribosyltransferase activity","synonyms":[{"name":"NAD+-histone H2B-S6 serine ADP-ribosyltransferase activity","type":"exact"},{"name":"NAD+-histone-serine ADP-ribosyltransferase activity (H2B-S6 specific)","type":"exact"}],"termid":"GO:0140816"}


id: PBO:0050697
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock protein family A (Hsp70) member 12A","termid":"PBO:0050697"}


id: PBO:0088133
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Vacuolar membrane protein of unknown function; member of the multidrug resistance family; YCR023C is not an essential gene","termid":"PBO:0088133"}


id: PBO:0073465
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sideroflexin 1","termid":"PBO:0073465"}


id: MOD:00090
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-alanine residue to L-alanine amide.","definition_xrefs":["RESID:AA0081","PubMed:2069951","PubMed:1377792","PubMed:8472537","PubMed:952951"],"direct_ancestors":[{"relation_name":"is_a","term_name":"C1-amidated residue","termid":"MOD:00883"},{"relation_name":"is_a","term_name":"modified L-alanine residue","termid":"MOD:00901"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-alanine amide","synonyms":[{"name":"(2S)-2-aminopropanamide","type":"exact"},{"name":"AlaN","type":"exact"},{"name":"L-alanine amide","type":"exact"},{"name":"MOD_RES Alanine amide","type":"exact"},{"name":"alaninamide","type":"exact"},{"name":"amidated L-alanine","type":"exact"}],"termid":"MOD:00090"}


id: PBO:0077957
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Ala (anticodon AGC) 13-1","termid":"PBO:0077957"}


id: GO:0070305
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a cGMP (cyclic GMP, guanosine 3',5'-cyclophosphate) stimulus.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to purine-containing compound","termid":"GO:0014074"},{"relation_name":"is_a","term_name":"response to organophosphorus","termid":"GO:0046683"},{"relation_name":"is_a","term_name":"response to oxygen-containing compound","termid":"GO:1901700"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to cGMP","synonyms":[{"name":"response to 3',5' cGMP","type":"exact"},{"name":"response to 3',5'-cGMP","type":"exact"},{"name":"response to cyclic GMP","type":"exact"},{"name":"response to guanosine 3',5'-cyclophosphate","type":"exact"}],"termid":"GO:0070305"}


id: PBO:0075335
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sorbin and SH3 domain containing 3","termid":"PBO:0075335"}


id: MONDO:0005498
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A serious bacterial infection caused by botulinum toxin which is produced by Clostridium botulinum. Patients are infected usually by ingestion of contaminated food or wound contamination. It leads to muscle paralysis which may result in respiratory failure.","definition_xrefs":["NCIT:C84599"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary bacterial infectious disease","termid":"MONDO:0000314"},{"relation_name":"is_a","term_name":"Clostridium infectious disease","termid":"MONDO:0024388"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"botulism","secondary_identifiers":["Orphanet:1267","SCTID:398565003","DOID:11976","icd11.foundation:78422942","MEDGEN:14204","UMLS:C0006057","CSP:5000-0060","GARD:943","MedDRA:10006041","MESH:D001906","EFO:0005542","NORD:867"],"synonyms":[{"name":"botulism","type":"exact"},{"name":"botulism poisoning","type":"exact"},{"name":"food poisoning due to Clostridium botulinum","type":"narrow"},{"name":"foodborne botulism","type":"narrow"},{"name":"foodborne botulism (subtype)","type":"related"},{"name":"infant botulism (subtype)","type":"related"},{"name":"infection due to Clostridium botulinum","type":"exact"},{"name":"intoxication with Clostridium botulinum toxin","type":"narrow"},{"name":"wound botulism (subtype)","type":"narrow"}],"termid":"MONDO:0005498","xrefs":{"Monarch":{"xref_id":"0005498"}}}


id: PBO:0076254
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"synaptic vesicle glycoprotein 2C","termid":"PBO:0076254"}


id: PBO:0048482
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glucosaminyl (N-acetyl) transferase 4","termid":"PBO:0048482"}


id: GO:0019382
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of carbon tetrachloride, a toxic, carcinogenic compound which is used as a general solvent in industrial degreasing operations. It is also used as grain fumigant and a chemical intermediate in the production of refrigerants.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon tetrachloride metabolic process","termid":"GO:0018885"},{"relation_name":"is_a","term_name":"halogenated hydrocarbon catabolic process","termid":"GO:0042206"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"carbon tetrachloride catabolic process","synonyms":[{"name":"carbon tetrachloride breakdown","type":"exact"},{"name":"carbon tetrachloride catabolism","type":"exact"},{"name":"carbon tetrachloride degradation","type":"exact"}],"termid":"GO:0019382"}


id: MONDO:0014446
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Bardet-Biedl syndrome in which the cause of the disease is a mutation in the BBIP1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Bardet-Biedl syndrome","termid":"MONDO:0015229"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"Bardet-Biedl syndrome 18","secondary_identifiers":["MEDGEN:812504","OMIM:615995","GARD:16042","DOID:0110140","UMLS:C3806174"],"synonyms":[{"name":"BBIP1 Bardet-Biedl syndrome","type":"exact"},{"name":"BBS18","type":"exact"},{"name":"Bardet-Biedl syndrome 18","type":"exact"},{"name":"Bardet-Biedl syndrome caused by mutation in BBIP1","type":"exact"},{"name":"Bardet-Biedl syndrome type 18","type":"exact"}],"termid":"MONDO:0014446","xrefs":{"Monarch":{"xref_id":"0014446"}}}


id: PBO:0061356
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleophosmin 1 pseudogene 14","termid":"PBO:0061356"}


id: PBO:0040806
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"betaine--homocysteine S-methyltransferase 2","termid":"PBO:0040806"}


id: PBO:0072219
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S19 pseudogene 2","termid":"PBO:0072219"}


id: MOD:00482
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-methionine residue to N-formyl-L-methionine (not known as a natural, post-translational modification process).","definition_xrefs":["PubMed:11152118","PubMed:3042771","PubMed:2165784","RESID:AA0021#MET"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-formyl-L-methionine residue","termid":"MOD:00030"},{"relation_name":"is_a","term_name":"modified L-methionine residue","termid":"MOD:00913"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-formyl-L-methionine (Met)","synonyms":[{"name":"(2S)-2-formylamino-4-(methylsulfanyl)butanoic acid","type":"exact"},{"name":"2-formamido-4-(methylsulfanyl)butanoic acid","type":"exact"},{"name":"2-formylamino-4-(methylthio)butanoic acid","type":"exact"},{"name":"2-formylazanyl-4-(methylsulfanyl)butanoic acid","type":"exact"},{"name":"MOD_RES N-formylmethionine","type":"exact"},{"name":"N-formyl-L-methionine","type":"exact"},{"name":"N-formylated L-methionine","type":"exact"},{"name":"NFoMet","type":"exact"}],"termid":"MOD:00482"}


id: GO:0018333
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The transient phosphorylation of peptidyl-threonine to form O-phospho-L-threonine.","definition_xrefs":["RESID:AA0038"],"gene_count":0,"genotype_count":0,"name":"obsolete enzyme active site formation via O-phospho-L-threonine (obsolete GO:0018333)","termid":"GO:0018333"}


id: MONDO:0003612
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A primary or metastatic malignant neoplasm that affects the uterine ligament.","definition_xrefs":["NCIT:C126498"],"direct_ancestors":[{"relation_name":"is_a","term_name":"musculoskeletal system cancer","termid":"MONDO:0000637"},{"relation_name":"is_a","term_name":"cervical cancer","termid":"MONDO:0002974"},{"relation_name":"is_a","term_name":"uterine ligament neoplasm","termid":"MONDO:0021629"}],"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 ligament cancer","secondary_identifiers":["UMLS:C0864950","DOID:5727","MEDGEN:923070"],"synonyms":[{"name":"cancer of uterine ligament","type":"exact"},{"name":"malignant neoplasm of uterine ligament","type":"exact"},{"name":"malignant uterine ligament neoplasm","type":"exact"},{"name":"tumour of the uterine ligament","type":"related"},{"name":"uterine ligament cancer","type":"exact"}],"termid":"MONDO:0003612","xrefs":{"Monarch":{"xref_id":"0003612"}}}


id: GO:0017163
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Any transcription regulator activity that prevents or downregulates basal transcription. Basal transcription results from transcription that is controlled by the minimal complement of proteins necessary to reconstitute transcription from a minimal promoter.","definition_xrefs":["GOC:dph","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete basal transcription repressor activity (obsolete GO:0017163)","synonyms":[{"name":"basal transcription repressor activity","type":"exact"}],"termid":"GO:0017163"}


id: PBO:0062286
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 5 subfamily K member 3","termid":"PBO:0062286"}


id: PBO:0051656
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inosine monophosphate dehydrogenase 1 pseudogene 11","termid":"PBO:0051656"}


id: GO:0046149
data:
  {"annotated_genes":["SJAG_00366"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[106153],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042167"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of a pigment, any general or particular coloring matter in living organisms, e.g. melanin.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pigment metabolic process","termid":"GO:0042440"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00366":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"pigment catabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"pigment breakdown","type":"exact"},{"name":"pigment catabolism","type":"exact"},{"name":"pigment degradation","type":"exact"}],"termid":"GO:0046149","terms_by_termid":{"GO:0042167":null}}


id: PBO:0080976
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 11","termid":"PBO:0080976"}


id: PBO:0071994
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S6 pseudogene 23","termid":"PBO:0071994"}


id: PBO:0079857
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"unc-93 homolog B6 (pseudogene)","termid":"PBO:0079857"}


id: PR:O42826
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pdh1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O42826"],"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 pdh1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1235.08c","synonyms":[{"name":"Spom972h-pdh1","type":"exact"}],"termid":"PR:O42826"}


id: PBO:0041192
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BUB1B-PAK6 readthrough","termid":"PBO:0041192"}


id: PR:P0CH06
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ubi1 gene.","definition_xrefs":["UniProtKB:P0CH06","PRO:DAN"],"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-60S ribosomal protein L40-1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC11G7.04","synonyms":[{"name":"SPAC11G7.04","type":"related"},{"name":"Spom972h-ubi1","type":"exact"}],"termid":"PR:P0CH06"}


id: PBO:0065776
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyroglutamylated RFamide peptide","termid":"PBO:0065776"}


id: PBO:0048329
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 40","termid":"PBO:0048329"}


id: GO:0004097
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 catechol + O2 = 2 1,2-benzoquinone + 2 H2O. This reaction catalyzes exclusively the oxidation of catechols (i.e., o-diphenols) to the corresponding o-quinones.","definition_xrefs":["PMID:22120533","EC:1.10.3.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monooxygenase activity","termid":"GO:0004497"},{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on diphenols and related substances as donors, oxygen as acceptor","termid":"GO:0016682"}],"gene_count":0,"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:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"catechol oxidase activity","secondary_identifiers":["GO:0036263","GO:0036264","RHEA:21632","GO:0102316","MetaCyc:CATECHOL-OXIDASE-RXN"],"synonyms":[{"name":"L-DOPA monooxygenase activity","type":"narrow"},{"name":"L-dopa oxidase activity","type":"narrow"},{"name":"catecholase","type":"exact"},{"name":"diphenol oxidase activity","type":"exact"},{"name":"dopamine monooxygenase activity","type":"narrow"},{"name":"o-diphenol oxidoreductase","type":"exact"},{"name":"o-diphenolase activity","type":"exact"},{"name":"phenolase activity","type":"broad"},{"name":"polyphenol oxidase activity","type":"related"},{"name":"pyrocatechol oxidase","type":"broad"},{"name":"tyrosinase activity","type":"broad"}],"termid":"GO:0004097"}


id: SO:0001881
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant, caused by an alteration of the genomic sequence, where the structural change, a translocation, is greater than the extent of the underlying genomic features.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"structural_variant","termid":"SO:0001537"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"feature_translocation","synonyms":[{"name":"feature translocation","type":"exact"}],"termid":"SO:0001881"}


id: GO:0106228
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: glutaryl-CoA + L-lysyl-[protein] = CoA + H+ + N6-glutaryl-L-lysyl-[protein].","definition_xrefs":["GOC:sp","PMID:31542297"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-acyltransferase activity","termid":"GO:0016410"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016746","GO:0016740","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"peptide glutaryltransferase activity","secondary_identifiers":["RHEA:18009"],"termid":"GO:0106228"}


id: MONDO:0009927
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any 3MC syndrome in which the cause of the disease is a mutation in the COLEC11 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 2","secondary_identifiers":["MEDGEN:167115","OMIM:265050","DOID:0060576","EFO:1001977","Orphanet:2998","GARD:18428","UMLS:C0796279","MESH:C535586"],"synonyms":[{"name":"3MC syndrome 2","type":"exact"},{"name":"3MC syndrome caused by mutation in COLEC11","type":"exact"},{"name":"3MC syndrome type 2","type":"exact"},{"name":"3MC2","type":"related"},{"name":"3Mc syndrome type 2","type":"exact"},{"name":"COLEC11 3MC syndrome","type":"exact"},{"name":"Carnevale syndrome","type":"related"},{"name":"Carnevale syndrome, formerly","type":"related"},{"name":"Osa syndrome","type":"related"},{"name":"oculo-skeletal-abdominal syndrome","type":"related"},{"name":"ptosis of eyelids with diastasis recti and hip dysplasia","type":"related"}],"termid":"MONDO:0009927","xrefs":{"Monarch":{"xref_id":"0009927"}}}


id: MONDO:0012453
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare type of hereditary spastic paraplegia usually characterized by a pure phenotype of proximal weakness of the lower extremities with spastic gait and brisk reflexes, with a bimodal age of onset of either childhood or adulthood (>30 years). In some cases, it can present as a complex phenotype with additional associated manifestations including peripheral neuropathy, bulbar palsy (with dysarthria and dysphagia), distal amyotrophy, and impaired distal vibration sense.","definition_xrefs":["Orphanet:101011"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary spastic paraplegia","termid":"MONDO:0019064"}],"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 31","secondary_identifiers":["UMLS:C1853247","MEDGEN:377858","MESH:C565210","DOID:0110782","GARD:10817","OMIM:610250","SCTID:763068005"],"synonyms":[{"name":"REEP1 hereditary spastic paraplegia","type":"exact"},{"name":"SPG31","type":"exact"},{"name":"autosomal dominant spastic paraplegia 31","type":"exact"},{"name":"autosomal dominant spastic paraplegia type 31","type":"exact"},{"name":"hereditary spastic paraplegia caused by mutation in REEP1","type":"exact"},{"name":"hereditary spastic paraplegia type 31","type":"exact"},{"name":"spastic paraplegia 31","type":"related"},{"name":"spastic paraplegia 31, autosomal dominant","type":"related"}],"termid":"MONDO:0012453","xrefs":{"Monarch":{"xref_id":"0012453"}}}


id: GO:0044596
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: S-adenosyl-L-methionine + 3-demethylubiquinol-10 = S-adenosyl-L-homocysteine + ubiquinol-10.","definition_xrefs":["PMID:10777520"],"gene_count":0,"genotype_count":0,"name":"obsolete 3-demethylubiquinol-10 3-O-methyltransferase activity (obsolete GO:0044596)","termid":"GO:0044596"}


id: PBO:0059688
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO1 pseudogene 54","termid":"PBO:0059688"}


id: PBO:0011099
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"copper membrane transporter, meiotic Mfc1","termid":"PBO:0011099"}


id: PBO:0067190
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 252, pseudogene","termid":"PBO:0067190"}


id: MONDO:0011284
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Unequal curvature of the refractive surfaces of the eye. Thus a point source of light cannot be brought to a point focus on the retina but is spread over a more or less diffuse area. This results from the radius of curvature in one plane being longer or shorter than the radius at right angles to it. (Dorland, 27th ed)","definition_xrefs":["MESH:D001251"],"direct_ancestors":[{"relation_name":"is_a","term_name":"refractive error","termid":"MONDO:0004892"}],"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":"astigmatism","secondary_identifiers":["ICD9:367.2","OMIM:603047","HP:0000483","ICD9:367.20","DOID:11782","SCTID:82649003","MEDGEN:2473","UMLS:C0004106","icd11.foundation:402558626","CSP:1116-1831"],"synonyms":[{"name":"astigmatism","type":"exact"},{"name":"astigmatism (disease)","type":"exact"}],"termid":"MONDO:0011284","xrefs":{"Monarch":{"xref_id":"0011284"}}}


id: PBO:0060238
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myosin binding protein C1","termid":"PBO:0060238"}


id: GO:1903018
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of glycoprotein metabolic process.","definition_xrefs":["PMID:23544079","GO_REF:0000058","GOC:BHF","GOC:rl","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein metabolic process","termid":"GO:0051246"},{"relation_name":"regulates","term_name":"glycoprotein metabolic process","termid":"GO:0009100"}],"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 glycoprotein metabolic process","synonyms":[{"name":"regulation of glycoprotein metabolism","type":"exact"}],"termid":"GO:1903018"}


id: MONDO:0019957
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"PPoma is a type of pancreatic endocrine tumor that hypersecretes pancreatic polypeptide (PP) but that does not cause a hypersecretion syndrome (is non-functioning) and instead presents with only non-specific symptoms such as weight loss, abdominal pain, jaundice, diarrhea and/or an abdominal mass, hence leading to a late diagnosis. PPoma can be associated with multiple endocrine neoplasia 1 (MEN-1).","definition_xrefs":["Orphanet:97278"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pancreatic neuroendocrine tumor","termid":"MONDO:0019954"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"PPoma","secondary_identifiers":["icd11.foundation:1180851464","GARD:19358","ICD9:239.89","MEDGEN:577392","NCIT:C67453","UMLS:C0346407","ICDO:8152/1","SCTID:255039001"],"synonyms":[{"name":"pancreatic polypeptide neoplasm","type":"exact"},{"name":"pancreatic polypeptide tumor","type":"exact"},{"name":"pancreatic polypeptide tumour","type":"exact"},{"name":"pancreatic polypeptidoma","type":"exact"}],"termid":"MONDO:0019957","xrefs":{"Monarch":{"xref_id":"0019957"}}}


id: SO:0000652
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Cytosolic 5S rRNA is an RNA component of the large subunit of cytosolic ribosomes in both prokaryotes and eukaryotes.","direct_ancestors":[{"relation_name":"derives_from","term_name":"cytosolic_rRNA_5S_gene","termid":"SO:0002238"},{"relation_name":"is_a","term_name":"cytosolic_LSU_rRNA","termid":"SO:0000651"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytosolic_5S_rRNA","secondary_identifiers":["http://en.wikipedia.org/wiki/5S_ribosomal_RNA"],"synonyms":[{"name":"cytosolic 5S LSU rRNA","type":"exact"},{"name":"cytosolic 5S rRNA","type":"exact"},{"name":"cytosolic 5S ribosomal RNA","type":"exact"},{"name":"cytosolic rRNA 5S","type":"exact"}],"termid":"SO:0000652"}


id: GO:0052460
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in which an organism modulates the frequency, rate or extent of the release of nutrients from a symbiont organism. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host-mediated perturbation of symbiont process","termid":"GO:0051851"},{"relation_name":"part_of","term_name":"acquisition of nutrients from symbiont","termid":"GO:0051850"}],"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":"modulation of nutrient release by symbiont","synonyms":[{"name":"modulation by host of nutrient release from symbiont","type":"exact"}],"termid":"GO:0052460"}


id: GO:0061798
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: GTP=(8S)-3',8-cyclo-7,8-dihydroguanosine 5'-triphosphate.","definition_xrefs":["GOC:dph","GOC:ik","PMID:25896388"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-carbon lyase activity","termid":"GO:0016830"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016829","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"GTP 3',8'-cyclase activity","secondary_identifiers":["MetaCyc:RXN-8340","RHEA:49576","EC:4.1.99.22"],"termid":"GO:0061798"}


id: FYPO:0002261
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 N-glycan processing is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular process","termid":"FYPO:0000628"},{"relation_name":"is_a","term_name":"cellular metabolism phenotype during vegetative growth","termid":"FYPO:0001348"}],"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:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"abnormal N-glycan processing","synonyms":[{"name":"abnormal N-glycan catabolism","type":"related"},{"name":"abnormal N-glycan degradation","type":"related"},{"name":"abnormal N-glycan processing during mitotic cell cycle","type":"related"},{"name":"abnormal N-glycan processing during vegetative growth","type":"exact"},{"name":"abnormal N-linked glycoprotein maturation","type":"exact"}],"termid":"FYPO:0002261"}


id: PR:Q9UTQ4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC1071.11 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9UTQ4"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C1071.11 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1071.11","synonyms":[{"name":"Spom972h-SPAC1071.11","type":"exact"}],"termid":"PR:Q9UTQ4"}


id: GO:0098678
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process by which the range of hosts which a virus can bind and infect is changed. Examples include phages that switch between types of fibers via the action of a virally encoded invertase.","definition_xrefs":["PMID:6232613","VZ:4498"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral process","termid":"GO:0016032"}],"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":"viral tropism switching","termid":"GO:0098678"}


id: MONDO:0010145
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":"tibia, absence of, with congenital deafness","secondary_identifiers":["UMLS:C1848758","MESH:C564764","MEDGEN:336413","OMIM:275230"],"synonyms":[{"name":"tibia, absence of, with congenital deafness","type":"exact"}],"termid":"MONDO:0010145","xrefs":{"Monarch":{"xref_id":"0010145"}}}


id: GO:0004179
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the release of an N-terminal amino acid, Xaa-Xbb- from a peptide, amide or arylamide. Xaa is preferably Ala, but may be most amino acids including Pro (slow action). When a terminal hydrophobic residue is followed by a prolyl residue, the two may be released as an intact Xaa-Pro dipeptide.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete membrane alanyl aminopeptidase activity (obsolete GO:0004179)","synonyms":[{"name":"membrane alanyl aminopeptidase activity","type":"exact"}],"termid":"GO:0004179"}


id: MONDO:0007051
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acromegaloid facial appearance (AFA) syndrome is a multiple congenital anomalies/dysmorphic syndrome with a probable autosomal dominant inheritance, characterized by a progressively coarse acromegaloid-like facial appearance with thickening of the lips and intraoral mucosa, large and doughy hands and, in some cases, developmental delay. AFA syndrome appears to be part of a phenotypic spectrum that includes hypertrichotic osteochondrodysplasia, Cantu type and hypertrichosis-acromegaloid facial appearance syndrome.","definition_xrefs":["Orphanet:965"],"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":"acromegaloid facial appearance syndrome","secondary_identifiers":["OMIM:102150","GARD:501","MESH:C535655","MEDGEN:167116","SCTID:720456009","UMLS:C0796280"],"synonyms":[{"name":"AFA syndrome","type":"related"},{"name":"acromegaloid facial appearance syndrome","type":"exact"},{"name":"thick lips and oral mucosa","type":"related"}],"termid":"MONDO:0007051","xrefs":{"Monarch":{"xref_id":"0007051"}}}


id: GO:0102802
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: thebaine + 2-oxoglutarate + O2 = neopinone + formaldehyde + succinate + carbon dioxide.","definition_xrefs":["GOC:pz","EC:1.14.11.31"],"direct_ancestors":[{"relation_name":"is_a","term_name":"2-oxoglutarate-dependent dioxygenase activity","termid":"GO:0016706"}],"gene_count":0,"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:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"thebaine 6-O-demethylase activity","secondary_identifiers":["MetaCyc:RXN-8147","RHEA:27477"],"termid":"GO:0102802"}


id: MONDO:0002040
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Superficial infections of the skin or its appendages by any of various fungi.","definition_xrefs":["MESH:D003881"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cutaneous mycosis","termid":"MONDO:0000254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dermatomycosis","secondary_identifiers":["SCTID:47382004","ICD9:111","MEDGEN:8330","DOID:1563","ICD9:111.9","UMLS:C0011630"],"termid":"MONDO:0002040","xrefs":{"Monarch":{"xref_id":"0002040"}}}


id: GO:0042190
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of vanillin, an aromatic hydrocarbon which occurs naturally in black vanilla bean pods.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vanillin metabolic process","termid":"GO:0018982"},{"relation_name":"is_a","term_name":"phenol-containing compound catabolic process","termid":"GO:0019336"},{"relation_name":"is_a","term_name":"aldehyde catabolic process","termid":"GO:0046185"},{"relation_name":"is_a","term_name":"ether catabolic process","termid":"GO:1901502"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"vanillin catabolic process","synonyms":[{"name":"vanillic aldehyde catabolic process","type":"exact"},{"name":"vanillic aldehyde catabolism","type":"exact"},{"name":"vanillin breakdown","type":"exact"},{"name":"vanillin catabolism","type":"exact"},{"name":"vanillin degradation","type":"exact"}],"termid":"GO:0042190"}


id: PBO:0048731
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamate dehydrogenase 1 pseudogene 2","termid":"PBO:0048731"}


id: MONDO:0975755
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"benign vascular tumor","termid":"MONDO:0971115"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eccrine angiomatous hamartoma","secondary_identifiers":["Orphanet:673568","UMLS:C0406801","MEDGEN:98361"],"termid":"MONDO:0975755","xrefs":{"Monarch":{"xref_id":"0975755"}}}


id: PBO:0066988
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 291","termid":"PBO:0066988"}


id: GO:1902601
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of silver (Ag+) ions across a membrane.","definition_xrefs":["GOC:TermGenie","GO_REF:0000069","GOC:pr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"silver ion transport","termid":"GO:0015673"},{"relation_name":"is_a","term_name":"monoatomic cation transmembrane transport","termid":"GO:0098655"},{"relation_name":"is_a","term_name":"inorganic cation transmembrane transport","termid":"GO:0098662"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055085"},{"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:0055085","GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"silver ion transmembrane transport","synonyms":[{"name":"silver transmembrane transport","type":"broad"}],"termid":"GO:1902601"}


id: PBO:0035923
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_number_of_Rad52_foci_during_mitotic_S_phase","termid":"PBO:0035923"}


id: MONDO:0000618
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"breast carcinoma by gene expression profile","termid":"MONDO:0006116"}],"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":"Her2-receptor negative breast cancer","secondary_identifiers":["NCIT:C168519","UMLS:C4733095","MEDGEN:1684659","EFO:0009780","SCTID:431396003","DOID:0060080"],"termid":"MONDO:0000618","xrefs":{"Monarch":{"xref_id":"0000618"}}}


id: PBO:0071281
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L26 pseudogene 4","termid":"PBO:0071281"}


id: PBO:0059206
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAS related GPR family member X13, pseudogene","termid":"PBO:0059206"}


id: PBO:0017998
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat/BOP1NT protein Erb1 (predicted)","termid":"PBO:0017998"}


id: MONDO:0030522
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spermatogenic failure","termid":"MONDO:0004983"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"spermatogenic failure 64","secondary_identifiers":["DOID:0112353","UMLS:C5562062","OMIM:619696","MEDGEN:1794272"],"synonyms":[{"name":"SPGF64","type":"exact"}],"termid":"MONDO:0030522","xrefs":{"Monarch":{"xref_id":"0030522"}}}


id: MONDO:0030895
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial nephrotic syndrome","termid":"MONDO:0002350"}],"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":"nephrotic syndrome, type 22","secondary_identifiers":["MEDGEN:1745920","DOID:0112268","OMIM:619155","GARD:16428","UMLS:C5436909"],"synonyms":[{"name":"NPHS22","type":"exact"},{"name":"nephrotic syndrome, type 22","type":"exact"}],"termid":"MONDO:0030895","xrefs":{"Monarch":{"xref_id":"0030895"}}}


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


id: MONDO:0023554
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Testicular failure, the cause of which is not present at birth.","definition_xrefs":["NCIT:C131091"],"direct_ancestors":[{"relation_name":"is_a","term_name":"testicular disorder","termid":"MONDO:0002329"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acquired testicular failure","secondary_identifiers":["SCTID:236811002","MEDGEN:588672","UMLS:C0403818"],"synonyms":[{"name":"acquired testicular failure","type":"exact"}],"termid":"MONDO:0023554","xrefs":{"Monarch":{"xref_id":"0023554"}}}


id: PBO:0047359
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 13","termid":"PBO:0047359"}


id: GO:0006884
data:
  {"annotated_genes":["SJAG_03401","SJAG_04668","SJAG_02532","SJAG_02019"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[75175,95174,113518],"is_not":false,"summary":null,"term":"GO:0006884"},{"annotations":[91878],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009992"}]},"cv_name":"biological_process","definition":"Any process involved in maintaining the steady state of a cell's volume. The cell's volume refers to the three-dimensional space occupied by a cell.","definition_xrefs":["GOC:dph","GOC:go_curators","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell size","termid":"GO:0008361"},{"relation_name":"is_a","term_name":"cellular homeostasis","termid":"GO:0019725"}],"gene_count":4,"genes_by_uniquename":{"SJAG_02019":null,"SJAG_02532":null,"SJAG_03401":null,"SJAG_04668":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cell volume homeostasis","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"regulation of cell volume","type":"exact"}],"termid":"GO:0006884","terms_by_termid":{"GO:0006884":null,"GO:0009992":null}}


id: MONDO:0015670
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete cardiomyopathy (obsolete MONDO:0015670)","termid":"MONDO:0015670","xrefs":{"Monarch":{"xref_id":"0015670"}}}


id: PBO:0051329
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin kappa variable 2-23 (pseudogene)","termid":"PBO:0051329"}


id: PBO:0026969
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-actin_cortical_patches_present_in_decreased_numbers","termid":"PBO:0026969"}


id: FYPO:0000115
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to valproic acid. Cells stop growing (and may die) at a concentration of valproic acid that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0002683","FYPO:0001985","FYPO:0000003","FYPO:0000139","FYPO:0005447"],"is_obsolete":false,"name":"sensitive to valproic acid","synonyms":[{"name":"hypersensitive to valproic acid","type":"exact"},{"name":"sensitive to valproic acid during mitotic cell cycle","type":"related"},{"name":"sensitive to valproic acid during vegetative growth","type":"exact"}],"termid":"FYPO:0000115"}


id: GO:0090019
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of transcription from an RNA polymerase II promoter contributing to the formation of the anterior neural plate.","definition_xrefs":["GOC:sdb_2009","GOC:dph","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of transcription involved in anterior neural plate formation (obsolete GO:0090019)","termid":"GO:0090019"}


id: MONDO:0036595
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign or malignant sex cord-stromal tumor arising from the ovary. It is characterized by the presence of neoplastic Leydig cells. Signs and symptoms include hirsutism, menorrhagia and metrorrhagia. It may be associated with trisomy 8.","definition_xrefs":["NCIT:C2880"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ovarian sertoli-stromal cell tumor","termid":"MONDO:0020807"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ovarian Sertoli-Leydig cell tumor","secondary_identifiers":["MEDGEN:2038","SCTID:254866007","UMLS:C0003810"],"synonyms":[{"name":"Sertoli-Leydig cell tumor of ovary","type":"exact"},{"name":"Sertoli-Leydig cell tumor of the ovary","type":"exact"},{"name":"Sertoli-Leydig cell tumour of ovary","type":"exact"},{"name":"Sertoli-Leydig cell tumour of the ovary","type":"exact"},{"name":"Sertoli-Leydig neoplasm of ovary","type":"exact"},{"name":"Sertoli-Leydig neoplasm of the ovary","type":"exact"},{"name":"androblastoma","type":"exact"},{"name":"arrhenoblastoma","type":"exact"},{"name":"ovarian Sertoli-Leydig cell neoplasm","type":"exact"},{"name":"ovarian Sertoli-Leydig cell tumor","type":"exact"}],"termid":"MONDO:0036595","xrefs":{"Monarch":{"xref_id":"0036595"}}}


id: PBO:0015220
data:
  {"annotation_feature_type":"gene","cv_name":"subunit_composition","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homooligomeric","termid":"PBO:0015220"}


id: PBO:0054504
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 1904","termid":"PBO:0054504"}


id: PBO:0089687
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"20S proteasome complex subunit alpha 1","termid":"PBO:0089687"}


id: GO:0031037
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The disassembly of a bipolar filament composed of myosin II molecules.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myosin filament disassembly","termid":"GO:0031035"},{"relation_name":"is_a","term_name":"myosin II filament organization","termid":"GO:0031038"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0007010"},{"rel_name":"is_a","termid":"GO:0030036"}],"interesting_parent_ids":["GO:0007010","GO:0030036","GO:0008150"],"is_obsolete":false,"name":"myosin II filament disassembly","synonyms":[{"name":"myosin II depolymerization","type":"related"}],"termid":"GO:0031037"}


id: PBO:0062941
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prolyl 4-hydroxylase, transmembrane","termid":"PBO:0062941"}


id: PBO:0086921
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative Zn(II)2Cys6 motif containing transcription factor; non-essential gene identified in a screen for mutants with increased levels of rDNA transcription; similar to S. kluyveri Urc2p involved in uracil catabolism","termid":"PBO:0086921"}


id: MONDO:0009358
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":"Hutterite cerebroosteonephrodysplasia syndrome","secondary_identifiers":["MESH:C536074","OMIM:236450","UMLS:C1856054","MEDGEN:343466"],"synonyms":[{"name":"Hutterite cerebroosteonephrodysplasia syndrome","type":"exact"},{"name":"cerebroosteonephosis syndrome","type":"related"},{"name":"cond","type":"related"}],"termid":"MONDO:0009358","xrefs":{"Monarch":{"xref_id":"0009358"}}}


id: PBO:0080646
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat domain 95, pseudogene","termid":"PBO:0080646"}


id: GO:1900629
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving methanophenazine.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metabolic process","termid":"GO:0008152"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"methanophenazine metabolic process","synonyms":[{"name":"methanophenazine metabolism","type":"exact"}],"termid":"GO:1900629"}


id: GO:0007473
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The establishment, maintenance and elaboration of the proximal/distal axis of the wing disc, a precursor to the adult wing.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proximal/distal pattern formation, imaginal disc","termid":"GO:0007449"},{"relation_name":"is_a","term_name":"wing disc pattern formation","termid":"GO:0035222"}],"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":"wing disc proximal/distal pattern formation","termid":"GO:0007473"}


id: PBO:0088622
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acid phosphatase","termid":"PBO:0088622"}


id: MONDO:0000578
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete CD3gamma deficiency (obsolete MONDO:0000578)","termid":"MONDO:0000578","xrefs":{"Monarch":{"xref_id":"0000578"}}}


id: PBO:0045866
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EEF1AKMT4-ECE2 readthrough","termid":"PBO:0045866"}


id: GO:0039677
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of the viral genome or a viral particle out of the host cell nucleus that involves disruption of the nuclear membrane envelope by the virus.","definition_xrefs":["VZ:2176"],"direct_ancestors":[{"relation_name":"is_a","term_name":"exit of virus from host cell nucleus","termid":"GO:0039674"}],"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":"exit of virus from host cell nucleus via nuclear envelope disassembly","synonyms":[{"name":"exit of virus from host cell nucleus via nuclear envelope breakdown","type":"exact"}],"termid":"GO:0039677"}


id: GO:0086045
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which AV node cardiac muscle cell membrane potential changes in the depolarizing direction from the negative resting potential towards the positive membrane potential that will be the peak of the action potential.","definition_xrefs":["GOC:mtg_cardiac_conduct_nov11","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane depolarization during cardiac muscle cell action potential","termid":"GO:0086012"},{"relation_name":"part_of","term_name":"AV node cell action potential","termid":"GO:0086016"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"membrane depolarization during AV node cell action potential","synonyms":[{"name":"membrane depolarization during AV node cardiac muscle cell action potential","type":"exact"},{"name":"membrane depolarization during atrioventricular node cardiac muscle cell action potential","type":"exact"}],"termid":"GO:0086045"}


id: GO:0033685
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 luteinizing hormone.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of gonadotropin secretion","termid":"GO:0032277"},{"relation_name":"is_a","term_name":"regulation of luteinizing hormone secretion","termid":"GO:0033684"},{"relation_name":"negatively_regulates","term_name":"luteinizing hormone secretion","termid":"GO:0032275"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"negative regulation of luteinizing hormone secretion","synonyms":[{"name":"down regulation of luteinizing hormone secretion","type":"exact"},{"name":"down-regulation of luteinizing hormone secretion","type":"exact"},{"name":"downregulation of luteinizing hormone secretion","type":"exact"},{"name":"inhibition of luteinizing hormone secretion","type":"narrow"}],"termid":"GO:0033685"}


id: PBO:0069736
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1017, pseudogene","termid":"PBO:0069736"}


id: PBO:0012007
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rRNA processing protein Rrp12 (predicted)","termid":"PBO:0012007"}


id: FYPO:0005419
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which the size, shape, or structure of the mitochondrial cristae is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitochondrial morphology","termid":"FYPO:0000359"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"abnormal mitochondrial crista morphology","synonyms":[{"name":"abnormal mitochondrial crista morphology during mitotic cell cycle","type":"related"},{"name":"abnormal mitochondrial crista morphology during vegetative growth","type":"exact"},{"name":"abnormal mitochondrial cristae morphology","type":"exact"}],"termid":"FYPO:0005419"}


id: PR:Q9UR27
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mrpl31 gene.","definition_xrefs":["UniProtKB:Q9UR27","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":"54S ribosomal protein L31, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC16A11.11","synonyms":[{"name":"Spom972h-mrpl31","type":"exact"},{"name":"negative regulator of cdc42 protein nrf20 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9UR27"}


id: PBO:0029800
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-thick_actin_cables","termid":"PBO:0029800"}


id: GO:0035362
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of proteins and DNA molecules to form a protein-DNA complex, in which the complex is formed through interaction of the protein(s) with a interferon-stimulated response element (ISRE) in the DNA.","definition_xrefs":["GOC:amm","PMID:11747630"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-DNA complex assembly","termid":"GO:0065004"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0065003"}],"interesting_parent_ids":["GO:0044085","GO:0008150","GO:0065003"],"is_obsolete":false,"name":"protein-DNA ISRE complex assembly","synonyms":[{"name":"protein-DNA interferon-stimulated response element complex assembly","type":"exact"}],"termid":"GO:0035362"}


id: GO:0106161
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of small RNA loading onto RISC.","definition_xrefs":["GOC:ha","PMID:29775584"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of small RNA loading onto RISC (obsolete GO:0106161)","termid":"GO:0106161"}


id: GO:1900324
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of maltotriulose transport.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transport","termid":"GO:0051049"},{"relation_name":"regulates","term_name":"maltotriulose transport","termid":"GO:2001090"}],"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:0006810","GO:0008150"],"is_obsolete":false,"name":"regulation of maltotriulose transport","termid":"GO:1900324"}


id: MONDO:0021061
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hereditary neoplastic syndrome in which tumors grow in the nervous system. There are typically 3 main types recognized, but other forms with uncertain etiology exist.","definition_xrefs":["NCIT:C6727","Wikipedia:Neurofibromatosis"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"},{"relation_name":"is_a","term_name":"neurocutaneous syndrome","termid":"MONDO:0042983"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"neurofibromatosis","secondary_identifiers":["MEDGEN:58149","EFO:0008514","NANDO:2201003","ICD9:237.7","MESH:D017253","NANDO:1200227","UMLS:C0162678","NANDO:1200226","SCTID:19133005","ICD9:237.71","DOID:8712","ICD9:237.70","ICD9:237.72","ICDO:9540/1","GARD:10420","NANDO:1200225"],"synonyms":[{"name":"Recklinghausen's neurofibromatosis","type":"exact"},{"name":"acoustic neurofibromatosis","type":"exact"},{"name":"central Neurofibromatosis","type":"exact"},{"name":"neurofibromatosis","type":"exact"},{"name":"neurofibromatosis syndrome","type":"exact"},{"name":"neurofibromatosis type 2","type":"narrow"},{"name":"neurofibromatosis type 4","type":"narrow"},{"name":"neurofibromatosis type IV","type":"narrow"},{"name":"peripheral Neurofibromatosis","type":"exact"},{"name":"type IV neurofibromatosis of riccardi","type":"exact"},{"name":"von Reklinghausen disease","type":"exact"}],"termid":"MONDO:0021061","xrefs":{"Monarch":{"xref_id":"0021061"}}}


id: PBO:0083221
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; completely overlaps verified gene RPB3/YIL021W; identified by gene-trapping, expression analysis, and genome-wide homology searching","termid":"PBO:0083221"}


id: MONDO:0600018
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any acinar dysplasia in which the cause of the disease is a mutation in the FGFR2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"acinar dysplasia","termid":"MONDO:0600016"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acinar dysplasia caused by mutation in FGFR2","synonyms":[{"name":"FGFR2 acinar dysplasia","type":"exact"},{"name":"FGFR2 related acinar dysplasia","type":"exact"}],"termid":"MONDO:0600018","xrefs":{"Monarch":{"xref_id":"0600018"}}}


id: PBO:0046146
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EARP complex and GARP complex interacting protein 1","termid":"PBO:0046146"}


id: PBO:0000375
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone demethylase SWIRM2 (predicted)","termid":"PBO:0000375"}


id: PBO:0083495
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 gene YJL168C/SET2","termid":"PBO:0083495"}


id: PBO:0032726
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_stress_response_gene_antisense_RNA_level","termid":"PBO:0032726"}


id: PBO:0062374
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 7 subfamily A member 17","termid":"PBO:0062374"}


id: PR:Q9US59
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- skb5 gene.","definition_xrefs":["UniProtKB:Q9US59","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":"shk1 kinase-binding protein 5 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC24B10.13","synonyms":[{"name":"Spom972h-skb5","type":"exact"}],"termid":"PR:Q9US59"}


id: MONDO:0024597
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete CD3epsilon deficiency (obsolete MONDO:0024597)","termid":"MONDO:0024597","xrefs":{"Monarch":{"xref_id":"0024597"}}}


id: PBO:0047099
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FAM151A pseudogene 1","termid":"PBO:0047099"}


id: PBO:0056159
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MACROD2 intronic transcript 1","termid":"PBO:0056159"}


id: GO:0140220
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A membrane-bound intracellular compartment that is formed upon internalization of a pathogen into a host cell, and in which the pathogen resides.","definition_xrefs":["PMID:26842840","PMID:10560000"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host cell part","termid":"GO:0033643"}],"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":"pathogen-containing vacuole","synonyms":[{"name":"pathogen inclusion","type":"related"},{"name":"pathogen-containing compartment","type":"related"}],"termid":"GO:0140220"}


id: PBO:0062416
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 7 subfamily E member 47 pseudogene","termid":"PBO:0062416"}


id: PATO:0001550
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A sensitivity toward an external stimulus which is lower than normal/average.","definition_xrefs":["PATO:GVG"],"direct_ancestors":[{"relation_name":"decreased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"sensitive toward","termid":"PATO:0000516"},{"relation_name":"is_a","term_name":"decreased object quality","termid":"PATO:0002303"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"decreased sensitivity toward","synonyms":[{"name":"decreased sensitivity","type":"exact"},{"name":"low sensitivity toward","type":"exact"}],"termid":"PATO:0001550"}


id: MONDO:0013061
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Selcen type muscular dystrophy is characterized by progressive limb and axial muscle weakness associated with cardiomyopathy and severe respiratory insufficiency during adolescence. The disease manifests during childhood and progresses rapidly.","definition_xrefs":["Orphanet:199340"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myofibrillar myopathy","termid":"MONDO:0018943"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"myofibrillar myopathy 6","secondary_identifiers":["GARD:17096","MEDGEN:414119","DOID:0080097","OMIM:612954","UMLS:C2751831","MESH:C567843"],"synonyms":[{"name":"BAG3 myofibrillar myopathy (disease)","type":"exact"},{"name":"BAG3-related myofibrillar myopathy","type":"related"},{"name":"MFM6","type":"related"},{"name":"muscular dystrophy, Selcen type","type":"related"},{"name":"myofibrillar myopathy (disease) caused by mutation in BAG3","type":"exact"},{"name":"myofibrillar myopathy 6","type":"exact"},{"name":"myofibrillar myopathy type 6","type":"exact"},{"name":"myopathy, myofibrillar, 6","type":"related"},{"name":"myopathy, myofibrillar, Bag3-related","type":"related"},{"name":"myopathy, myofibrillar, type 6","type":"exact"}],"termid":"MONDO:0013061","xrefs":{"Monarch":{"xref_id":"0013061"}}}


id: PBO:0078526
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripartite motif containing 16 like","termid":"PBO:0078526"}


id: PBO:0049392
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTP binding protein 6 (putative)","termid":"PBO:0049392"}


id: FYPO:0006014
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which one cell forms multiple mating projections that engage multiple partner cells.","definition_xrefs":["PomBase:mah","PMID:28410370"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mating","termid":"FYPO:0000031"}],"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:0000301"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000301"],"is_obsolete":false,"name":"promiscuous mating","synonyms":[{"name":"conjugation with multiple partner cells","type":"exact"},{"name":"formation of multiple mating projections","type":"related"},{"name":"formation of multiple shmoos","type":"related"},{"name":"mating with multiple partner cells","type":"exact"},{"name":"promiscuous conjugation","type":"exact"}],"termid":"FYPO:0006014"}


id: GO:0030099
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized myeloid precursor cell acquires the specialized features of any cell of the myeloid leukocyte, megakaryocyte, thrombocyte, or erythrocyte lineages.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"},{"relation_name":"part_of","term_name":"hemopoiesis","termid":"GO:0030097"}],"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":"myeloid cell differentiation","termid":"GO:0030099"}


id: GO:0031392
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of prostaglandin.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of unsaturated fatty acid biosynthetic process","termid":"GO:2001279"},{"relation_name":"regulates","term_name":"prostaglandin biosynthetic process","termid":"GO:0001516"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0006629"],"is_obsolete":false,"name":"regulation of prostaglandin biosynthetic process","synonyms":[{"name":"regulation of prostaglandin anabolism","type":"exact"},{"name":"regulation of prostaglandin biosynthesis","type":"exact"},{"name":"regulation of prostaglandin formation","type":"exact"},{"name":"regulation of prostaglandin synthesis","type":"exact"}],"termid":"GO:0031392"}


id: PBO:0043035
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"charged multivesicular body protein 5","termid":"PBO:0043035"}


id: PBO:0052555
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"killer cell lectin like receptor F2","termid":"PBO:0052555"}


id: GO:0047651
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: bromochloromethane + H2O = bromide + chloride + formaldehyde + 2 H+.","definition_xrefs":["RHEA:13765"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on acid halide bonds, in C-halide compounds","termid":"GO:0019120"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"alkylhalidase activity","secondary_identifiers":["KEGG_REACTION:R03523"],"synonyms":[{"name":"alkyl-halide halidohydrolase activity","type":"related"},{"name":"haloalkane halidohydrolase activity","type":"related"},{"name":"halogenase activity","type":"related"}],"termid":"GO:0047651"}


id: MONDO:0007350
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"coloboma","termid":"MONDO:0001476"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"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":"coloboma, ocular, autosomal dominant","secondary_identifiers":["MEDGEN:1859952","OMIM:120200","UMLS:C5886785"],"synonyms":[{"name":"coloboma of iris, choroid, and retina","type":"related"},{"name":"coloboma, Uveoretinal","type":"related"},{"name":"coloboma, ocular","type":"exact"},{"name":"coloboma, ocular, autosomal dominant","type":"exact"}],"termid":"MONDO:0007350","xrefs":{"Monarch":{"xref_id":"0007350"}}}


id: PBO:0047337
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibulin 5","termid":"PBO:0047337"}


id: PR:O60170
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A cationic amino acid transporter 3 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":"amino-acid permease meu22 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC19F8.06c","secondary_identifiers":["UniProtKB:O60170"],"synonyms":[{"name":"SPBC19F8.06c","type":"related"},{"name":"Spom972h-SLC7A3","type":"exact"},{"name":"meiotic expression up-regulated protein 22 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O60170"}


id: SO:0002194
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The pseudogene has arisen from a copy of the parent gene by duplication followed by accumulation of random mutation. The changes, compared to their functional homolog, include insertions, deletions, premature stop codons, frameshifts and a higher proportion of non-synonymous versus synonymous substitutions.","direct_ancestors":[{"relation_name":"is_a","term_name":"pseudogenic_rRNA","termid":"SO:0000777"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"unprocessed_pseudogenic_rRNA","synonyms":[{"name":"INSDC_feature:rRNA","type":"broad"},{"name":"INSDC_qualifier:unprocessed","type":"exact"},{"name":"unprocessed pseudogenic rRNA","type":"exact"}],"termid":"SO:0002194"}


id: FYPO:0004284
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of oxanine DNA N-glycosylase activity is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased catalytic activity","termid":"FYPO:0000663"},{"relation_name":"is_a","term_name":"abnormal oxanine DNA N-glycosylase activity","termid":"FYPO:0004283"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000654","FYPO:0000707","FYPO:0000661","FYPO:0000652"],"is_obsolete":false,"name":"decreased oxanine DNA N-glycosylase activity","synonyms":[{"name":"reduced oxanine DNA N-glycosylase activity","type":"exact"}],"termid":"FYPO:0004284"}


id: PBO:0064328
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PLS1 pseudogene 1","termid":"PBO:0064328"}


id: MONDO:0007753
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autonomic disorder characterized by excessive sweating of the forehead, upper lip, perioral region, or sternum subsequent to gustatory stimuli. The auriculotemporal syndrome features facial flushing or sweating limited to the distribution of the auriculotemporal nerve and may develop after trauma to the parotid gland, in association with parotid neoplasms, or following their surgical removal. (From Ann Neurol 1997 Dec;42(6):973-5)","definition_xrefs":["MESH:D013547"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autonomic nervous system disorder","termid":"MONDO:0001292"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Frey syndrome","secondary_identifiers":["DOID:11599","SCTID:238758008","Orphanet:662240","UMLS:C0038994","EFO:1000940","OMIM:144100","MEDGEN:21041"],"synonyms":[{"name":"Baillarger syndrome","type":"exact"},{"name":"Frey syndrome","type":"exact"},{"name":"Frey's syndrome","type":"related"},{"name":"HYPRG","type":"related"},{"name":"auriculotemporal nerve syndrome","type":"related"},{"name":"gustatory hyperhidrosis","type":"exact"},{"name":"gustatory sweating","type":"exact"},{"name":"hyperhidrosis gustatory","type":"related"},{"name":"hyperhidrosis, gustatory","type":"related"}],"termid":"MONDO:0007753","xrefs":{"Monarch":{"xref_id":"0007753"}}}


id: MONDO:0011961
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hereditary sensory and autonomic neuropathy, type 1B (HSAN1B) is characterized by the association of type 1 HSAN with paroxysmal cough and gastroesophageal reflux (GOR).","definition_xrefs":["Orphanet:139564"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary sensory and autonomic neuropathy type 1","termid":"MONDO:0018213"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244","MONDO:0002525","MONDO:0005066"],"is_obsolete":false,"name":"hereditary sensory and autonomic neuropathy type 1B","secondary_identifiers":["OMIM:608088","SCTID:717825008","PMID:12870133","UMLS:C1842586","MEDGEN:330880","GARD:16958","DOID:0070148","MESH:C564296","PMID:16311270"],"synonyms":[{"name":"HSAN with cough and gastroesophageal reflux","type":"exact"},{"name":"HSAN1B","type":"exact"},{"name":"hereditary sensory and autonomic neuropathy type 1 with cough and gastroesophageal reflux","type":"exact"},{"name":"hereditary sensory and autonomic neuropathy type IB","type":"exact"},{"name":"hereditary sensory neuropathy type 1B","type":"related"},{"name":"hereditary sensory neuropathy type IB","type":"exact"},{"name":"neuropathy, hereditary sensory and autonomic, type 1B","type":"related"},{"name":"neuropathy, hereditary sensory and autonomic, type I, with cough and gastroesophageal reflux","type":"related"},{"name":"neuropathy, hereditary sensory, type 1B","type":"related"},{"name":"neuropathy, hereditary sensory, type IB","type":"exact"}],"termid":"MONDO:0011961","xrefs":{"Monarch":{"xref_id":"0011961"}}}


id: PBO:0048783
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GNA13 pseudogene 1","termid":"PBO:0048783"}


id: PBO:0111842
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rab subfamily","termid":"PBO:0111842"}


id: MONDO:0009267
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Gaucher disease type 3 is the subacute neurological form of Gaucher disease (GD) characterized by progressive encephalopathy and associated with the systemic manifestations (organomegaly, bone involvement, cytopenia) of GD type 1.","definition_xrefs":["Orphanet:77261"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"lysosomal storage disease","termid":"MONDO:0002561"},{"relation_name":"excluded_subClassOf","term_name":"familial restrictive cardiomyopathy","termid":"MONDO:0016340"},{"relation_name":"excluded_subClassOf","term_name":"interstitial lung disease specific to childhood","termid":"MONDO:0017014"},{"relation_name":"excluded_subClassOf","term_name":"secondary avascular necrosis","termid":"MONDO:0018374"},{"relation_name":"excluded_subClassOf","term_name":"obsolete avascular necrosis of genetic origin (obsolete MONDO:0018384)","termid":"MONDO:0018384"},{"relation_name":"excluded_subClassOf","term_name":"sphingolipidosis","termid":"MONDO:0019255"},{"relation_name":"excluded_subClassOf","term_name":"cerebral lipidosis with dementia","termid":"MONDO:0020143"},{"relation_name":"is_a","term_name":"Gaucher disease","termid":"MONDO:0018150"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002561"},{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0002525","MONDO:0005066","MONDO:0005328","MONDO:0002561"],"is_obsolete":false,"name":"Gaucher disease type III","secondary_identifiers":["OMIM:231000","DOID:0110959","GARD:2443","MEDGEN:78653","NANDO:1200059","SCTID:5963005","NANDO:2201212","UMLS:C0268251"],"synonyms":[{"name":"GD III","type":"exact"},{"name":"Gaucher disease type 3","type":"related"},{"name":"Gaucher disease type III","type":"exact"},{"name":"Gaucher disease, Norrbottnian type","type":"related"},{"name":"Gaucher disease, Subacute neuronopathic type","type":"exact"},{"name":"Gaucher disease, chronic neuronopathic type","type":"exact"},{"name":"Gaucher disease, juvenile and adult, cerebral","type":"exact"},{"name":"Gaucher disease, subacute neuronopathic type","type":"exact"},{"name":"Gaucher disease, type 3","type":"related"},{"name":"Gaucher disease, type 3A","type":"related"},{"name":"Gaucher disease, type 3B","type":"related"},{"name":"Gaucher disease, type III","type":"related"},{"name":"Gaucher's disease type III","type":"exact"},{"name":"Gd 3","type":"related"},{"name":"cerebral juvenile and adult form of Gaucher disease","type":"exact"},{"name":"chronic neuronopathic Gaucher disease","type":"exact"}],"termid":"MONDO:0009267","xrefs":{"Monarch":{"xref_id":"0009267"}}}


id: PBO:0030175
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-slow_cell_population_growth_during_recovery_from_stationary_phase","termid":"PBO:0030175"}


id: RO:0002262
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"c has-chemical-role r iff c has-role r and r is a chemical role (CHEBI:51086)","direct_ancestors":[{"relation_name":"is_a","term_name":"has_role","termid":"RO:0000087"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_chemical_role","termid":"RO:0002262"}


id: MONDO:1010225
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cystic hygroma that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neoplasm, non-human animal","termid":"MONDO:0700098"},{"relation_name":"is_a","term_name":"cardiovascular disorder, non-human animal","termid":"MONDO:1011306"},{"relation_name":"is_a","term_name":"lymphoid system disorder, non-human animal","termid":"MONDO:1011330"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cystic hygroma, non-human animal","secondary_identifiers":["OMIA:002369"],"termid":"MONDO:1010225","xrefs":{"Monarch":{"xref_id":"1010225"}}}


id: PBO:0030971
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_H3-K9_dimethylation_at_centromere","termid":"PBO:0030971"}


id: PBO:0042513
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cadherin related family member 18, pseudogene","termid":"PBO:0042513"}


id: PBO:0028350
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_mitotic_anaphase_B","termid":"PBO:0028350"}


id: PR:G2TRN0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC4H3.16 gene.","definition_xrefs":["PRO:DNx","UniProtKB:G2TRN0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C4H3.16 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4H3.16","synonyms":[{"name":"Spom972h-SPAC4H3.16","type":"exact"}],"termid":"PR:G2TRN0"}


id: PBO:0075816
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"scavenger receptor cysteine rich family member with 5 domains","termid":"PBO:0075816"}


id: PBO:0069311
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 567, pseudogene","termid":"PBO:0069311"}


id: GO:0097377
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the migration of an axon growth cone of a spinal cord interneuron is directed to a specific target site in response to a combination of attractive and repulsive cues. A spinal cord interneuron is a CNS interneuron located in the spinal cord.","definition_xrefs":["GOC:pr","CL:0005000"],"direct_ancestors":[{"relation_name":"is_a","term_name":"interneuron axon guidance","termid":"GO:0097376"}],"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":"spinal cord interneuron axon guidance","termid":"GO:0097377"}


id: GO:0045992
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of embryonic development.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of embryonic development","termid":"GO:0045995"},{"relation_name":"is_a","term_name":"negative regulation of developmental process","termid":"GO:0051093"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"negatively_regulates","term_name":"embryo development","termid":"GO:0009790"}],"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 embryonic development","synonyms":[{"name":"down regulation of embryonic development","type":"exact"},{"name":"down-regulation of embryonic development","type":"exact"},{"name":"downregulation of embryonic development","type":"exact"},{"name":"inhibition of embryonic development","type":"narrow"}],"termid":"GO:0045992"}


id: PBO:0028294
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_dioxygenase_activity","termid":"PBO:0028294"}


id: GO:0038085
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a vascular endothelial growth factor.","definition_xrefs":["PMID:17470632"],"direct_ancestors":[{"relation_name":"is_a","term_name":"growth factor binding","termid":"GO:0019838"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0003674","GO:0005515","GO:0005488"],"is_obsolete":false,"name":"vascular endothelial growth factor binding","synonyms":[{"name":"VEGF binding","type":"exact"}],"termid":"GO:0038085"}


id: PBO:0080321
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vomeronasal 1 receptor 85 pseudogene","termid":"PBO:0080321"}


id: PBO:0069449
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 714, pseudogene","termid":"PBO:0069449"}


id: PBO:0030450
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-growth_auxotrophic_for_lysine_and_cysteine","termid":"PBO:0030450"}


id: MONDO:0014248
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"SLC35A3-CDG is a form of congenital disorders of N-linked glycosylation characterized by distal arthrogryposis (mild flexion contractures of the fingers, deviation of the distal phalanges, swan-neck deformity), retromicrognathia, general muscle hypotonia, delayed psychomotor development, autism spectrum disorder (speech delay, abnormal use of speech, difficulties in initiating, understanding and maintaining social interaction, limited non-verbal communication and repetitive behavior), seizures, microcephaly and mild to moderate intellectual disability that becomes apparent with age. The disease is caused by mutations in the gene SLC35A3 (1p21).","definition_xrefs":["Orphanet:370943"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental anomaly of metabolic origin","termid":"MONDO:0015327"},{"relation_name":"is_a","term_name":"disorder of protein N-glycosylation","termid":"MONDO:0017740"},{"relation_name":"is_a","term_name":"distal arthrogryposis","termid":"MONDO:0019942"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0024322"}],"interesting_parent_ids":["MONDO:0024322","MONDO:0005066"],"is_obsolete":false,"name":"autism spectrum disorder - epilepsy - arthrogryposis syndrome","secondary_identifiers":["MEDGEN:816240","OMIM:615553","UMLS:C3809910","GARD:17604"],"synonyms":[{"name":"AMRS","type":"related"},{"name":"SLC35A3-CDG","type":"exact"},{"name":"arthrogryposis, impaired intellectual development, and seizures","type":"exact"},{"name":"arthrogryposis, intellectual disability, and seizures","type":"related"},{"name":"arthrogryposis, mental retardation, and seizures","type":"related"}],"termid":"MONDO:0014248","xrefs":{"Monarch":{"xref_id":"0014248"}}}


id: PBO:0067926
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 228","termid":"PBO:0067926"}


id: PBO:0048275
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polypeptide N-acetylgalactosaminyltransferase 11","termid":"PBO:0048275"}


id: GO:0047357
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-N-acetyl-alpha-D-glucosamine + UDP-D-galactose = H+ + UDP-N-acetyl-6-(D-galactose-1-phospho)-D-glucosamine + UMP.","definition_xrefs":["RHEA:22440","EC:2.7.8.18"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphotransferase activity, for other substituted phosphate groups","termid":"GO:0016780"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016780"},{"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:0016780","GO:0003674","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"UDP-galactose-UDP-N-acetylglucosamine galactose phosphotransferase activity","secondary_identifiers":["MetaCyc:2.7.8.18-RXN","KEGG_REACTION:R00504"],"synonyms":[{"name":"UDP-galactose:UDP-N-acetyl-D-glucosamine galactose phosphotransferase activity","type":"related"},{"name":"UDPgalactose-UDP-N-acetylglucosamine galactose phosphotransferase activity","type":"related"},{"name":"UDPgalactose:UDP-N-acetyl-D-glucosamine galactose phosphotransferase activity","type":"related"},{"name":"galactose-1-phosphotransferase activity","type":"related"},{"name":"galactosyl phosphotransferase activity","type":"related"},{"name":"uridine diphosphogalactose-uridine diphosphoacetylglucosamine galactose-1-phosphotransferase activity","type":"related"}],"termid":"GO:0047357"}


id: PBO:0036057
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-C-shaped_cytoplasmic_microtubules","termid":"PBO:0036057"}


id: FYPO:0001645
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the binding of one protein to another occurs to a lower extent than normal. The relevant proteins may include the one encoded by the mutated gene, or may both be encoded by different genes.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein-protein interaction","termid":"FYPO:0000704"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000702"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000702","FYPO:0000707","FYPO:0001985"],"is_obsolete":false,"name":"decreased protein-protein interaction","secondary_identifiers":["FYPO:0004636"],"synonyms":[{"name":"decreased protein binding","type":"exact"},{"name":"reduced protein-protein interaction","type":"exact"}],"termid":"FYPO:0001645"}


id: GO:0034919
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2-methyl-3-oxohexanoyl-CoA + CoA = propanoyl-CoA + butyryl-CoA.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete butyryl-CoA 2-C-propionyltransferase activity (obsolete GO:0034919)","termid":"GO:0034919"}


id: PBO:0045264
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynein heavy chain domain 1","termid":"PBO:0045264"}


id: PBO:0068101
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 408","termid":"PBO:0068101"}


id: MONDO:0043137
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"microcephaly","termid":"MONDO:0001149"}],"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":"isolated microcephaly","secondary_identifiers":["MEDGEN:419828","MESH:C537542","UMLS:C2931527"],"synonyms":[{"name":"Nonsyndromal microcephaly","type":"related"},{"name":"microcephaly, non-syndromic","type":"related"},{"name":"nonsyndromic microcephaly","type":"related"}],"termid":"MONDO:0043137","xrefs":{"Monarch":{"xref_id":"0043137"}}}


id: GO:0031410
data:
  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id: GO:0075274
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of zygosporangium development, a process in which a fruiting body called zygosporangium is formed.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of spore-bearing organ development","termid":"GO:0075262"},{"relation_name":"is_a","term_name":"regulation of zygosporangium development","termid":"GO:0075272"},{"relation_name":"negatively_regulates","term_name":"zygosporangium development","termid":"GO:0075271"}],"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 zygosporangium development","termid":"GO:0075274"}


id: GO:0006061
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of sorbitol (D-glucitol), one of the ten stereoisomeric hexitols. It can be derived from glucose by reduction of the aldehyde group.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sorbitol metabolic process","termid":"GO:0006060"},{"relation_name":"is_a","term_name":"hexitol biosynthetic process","termid":"GO:0019406"}],"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:0005975"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0005975"],"is_obsolete":false,"name":"sorbitol biosynthetic process","synonyms":[{"name":"sorbitol anabolism","type":"exact"},{"name":"sorbitol biosynthesis","type":"exact"},{"name":"sorbitol formation","type":"exact"},{"name":"sorbitol synthesis","type":"exact"}],"termid":"GO:0006061"}


id: GO:1903668
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of chemorepellent activity.","definition_xrefs":["PMID:22711818","PMID:24390142","GOC:TermGenie","GO_REF:0000059"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of chemorepellent activity (obsolete GO:1903668)","synonyms":[{"name":"down regulation of chemorepellant activity","type":"exact"},{"name":"down regulation of chemorepellent activity","type":"exact"},{"name":"down-regulation of chemorepellant activity","type":"exact"},{"name":"down-regulation of chemorepellent activity","type":"exact"},{"name":"downregulation of chemorepellant activity","type":"exact"},{"name":"downregulation of chemorepellent activity","type":"exact"},{"name":"inhibition of chemorepellant activity","type":"narrow"},{"name":"inhibition of chemorepellent activity","type":"narrow"},{"name":"negative regulation of chemorepellant activity","type":"exact"}],"termid":"GO:1903668"}


id: GO:0007227
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of molecular signals that are initiated by the transmembrane protein Smoothened. In the presence of a Hedgehog signaling molecule, the Patched protein no longer inhibits the activity of Smoothened, and Smoothened signals via the Hedgehog signaling complex to activate downstream components of the Hedgehog signaling pathway.","definition_xrefs":["PMID:15057936"],"gene_count":0,"genotype_count":0,"name":"obsolete signal transduction downstream of smoothened (obsolete GO:0007227)","termid":"GO:0007227"}


id: PBO:0044373
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CYLD lysine 63 deubiquitinase","termid":"PBO:0044373"}


id: PBO:0049516
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H2AC histone family pseudogene 1","termid":"PBO:0049516"}


id: GO:0036008
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of sucrose, which proceeds by phosphorylation of sucrose to form sucrose-6-phosphate. The subsequent actions of a hydrolase and a fructokinase generate fructose-6-phosphate and glucose-6-phosphate.","definition_xrefs":["GOC:bf","MetaCyc:SUCUTIL-PWY","GOC:dgf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sucrose catabolic process","termid":"GO:0005987"},{"relation_name":"is_a","term_name":"fructose 6-phosphate metabolic process","termid":"GO:0006002"},{"relation_name":"is_a","term_name":"glucose 6-phosphate metabolic process","termid":"GO:0051156"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0005975"],"is_obsolete":false,"name":"sucrose catabolic process to fructose-6-phosphate and glucose-6-phosphate","termid":"GO:0036008"}


id: PBO:0000436
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"expression cell cycle regulated","termid":"PBO:0000436"}


id: GO:0061561
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that gives rise to the trigeminal ganglion. This process pertains to the initial formation of a structure from unspecified parts.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cranial ganglion formation","termid":"GO:0061560"},{"relation_name":"part_of","term_name":"trigeminal ganglion morphogenesis","termid":"GO:0061556"}],"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":"trigeminal ganglion formation","synonyms":[{"name":"trigeminal ganglia formation","type":"related"}],"termid":"GO:0061561"}


id: MONDO:0020205
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete bulbar conjunctival dermoid or conjunctival dermolipoma (obsolete MONDO:0020205)","secondary_identifiers":["Orphanet:98617"],"termid":"MONDO:0020205","xrefs":{"Monarch":{"xref_id":"0020205"}}}


id: MONDO:0010793
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":"nephropathy, chronic tubulointerstitial","secondary_identifiers":["MEDGEN:333200","MESH:C564016","OMIM:551200","UMLS:C1838875"],"synonyms":[{"name":"nephropathy, chronic tubulointerstitial","type":"exact"}],"termid":"MONDO:0010793","xrefs":{"Monarch":{"xref_id":"0010793"}}}


id: FYPO:0000844
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to mercaptoethanol. Cells stop growing (and may die) at a concentration of mercaptoethanol that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0002683","FYPO:0001985","FYPO:0005447","FYPO:0000139"],"is_obsolete":false,"name":"sensitive to mercaptoethanol","synonyms":[{"name":"hypersensitive to mercaptoethanol","type":"exact"},{"name":"sensitive to 2-sulfanylethanol","type":"exact"},{"name":"sensitive to mercaptoethanol during mitotic cell cycle","type":"related"},{"name":"sensitive to mercaptoethanol during vegetative growth","type":"exact"}],"termid":"FYPO:0000844"}


id: FYPO:0006202
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of RNA measured in a cell during a cellular response to hydroxyurea is normal (i.e. indistinguishable from wild type). Total RNA or a specific RNA may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal RNA level during vegetative growth","termid":"FYPO:0001317"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO: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:0001312","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"normal RNA level during cellular response to hydroxyurea","synonyms":[{"name":"normal RNA accumulation during cellular response to hydroxyurea","type":"related"},{"name":"normal RNA level during cellular response to HU","type":"exact"},{"name":"normal RNA level during cellular response to hydroxyurea during mitotic cell cycle","type":"related"},{"name":"normal RNA level during cellular response to hydroxyurea during vegetative growth","type":"exact"},{"name":"normal mRNA level during cellular response to hydroxyurea","type":"narrow"},{"name":"normal transcript level during cellular response to hydroxyurea","type":"exact"}],"termid":"FYPO:0006202"}


id: GO:0000208
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of a MAP kinase to the nucleus during osmolarity sensing.","definition_xrefs":["PMID:9561267"],"gene_count":0,"genotype_count":0,"name":"obsolete MAPK import into nucleus involved in osmosensory signaling pathway (obsolete GO:0000208)","synonyms":[{"name":"MAPK import into nucleus during osmolarity sensing","type":"exact"},{"name":"MAPK import into nucleus involved in osmosensory signalling pathway","type":"exact"},{"name":"nuclear translocation of MAPK during osmolarity sensing","type":"exact"},{"name":"nuclear translocation of MAPK involved in osmosensory signaling pathway","type":"narrow"},{"name":"nuclear translocation of MAPK involved in osmosensory signalling pathway","type":"narrow"},{"name":"osmolarity sensing, MAPK import into nucleus","type":"exact"},{"name":"osmolarity sensing, nuclear translocation of MAPK","type":"narrow"}],"termid":"GO:0000208"}


id: GO:0005597
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A collagen trimer containing alpha(XVI) chains; type XVI trimers can associate with microfibrils.","definition_xrefs":["GOC:mah","PMID:12782140"],"direct_ancestors":[{"relation_name":"is_a","term_name":"FACIT collagen trimer","termid":"GO:0005593"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"collagen type XVI trimer","termid":"GO:0005597"}


id: PBO:0068992
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 236, pseudogene","termid":"PBO:0068992"}


id: MONDO:0008041
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"early myoclonic encephalopathy","termid":"MONDO:0016022"},{"relation_name":"is_a","term_name":"myoclonic epilepsy","termid":"MONDO:0100577"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"myoclonic epilepsy, Hartung type","secondary_identifiers":["MEDGEN:371857","OMIM:159600","UMLS:C1834581","MESH:C563550"],"synonyms":[{"name":"myoclonic epilepsy, Hartung type","type":"exact"}],"termid":"MONDO:0008041","xrefs":{"Monarch":{"xref_id":"0008041"}}}


id: SO:0001122
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A motif of two consecutive residues with dihedral angles: Residue(i): -140 degrees < phi < -20 degrees, -90 degrees < psi < +40 degrees. Residue(i+1): +20 degrees < phi < +140 degrees, -40 degrees < psi < +90 degrees.","definition_xrefs":["EBIBS:GAR"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polypeptide_nest_motif","termid":"SO:0001120"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"SO:0000839"}],"interesting_parent_ids":["SO:0000839"],"is_obsolete":false,"name":"polypeptide_nest_right_left_motif","secondary_identifiers":["BS:00225"],"synonyms":[{"name":"nest_right_left","type":"exact"},{"name":"nest_rl","type":"exact"},{"name":"polypeptide nest right left motif","type":"exact"}],"termid":"SO:0001122"}


id: PBO:0048271
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polypeptide N-acetylgalactosaminyltransferase 8","termid":"PBO:0048271"}


id: MONDO:0032565
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":"ophthalmoplegia, external, with rib and vertebral anomalies","secondary_identifiers":["OMIM:618155","MEDGEN:1648445","UMLS:C4748418"],"synonyms":[{"name":"EORVA","type":"related"},{"name":"OPHTHALMOPLEGIA, EXTERNAL, WITH RIB AND VERTEBRAL ANOMALIES","type":"related"}],"termid":"MONDO:0032565","xrefs":{"Monarch":{"xref_id":"0032565"}}}


id: PBO:0081725
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 653","termid":"PBO:0081725"}


id: MONDO:0009810
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal recessive distal osteolysis syndrome is an early-onset distal osteolysis characterized by severe resorption of the hands and feet and absence of the distal and middle phalanges. It has been described in a son and daughter born to consanguineous parents. Other manifestations include distal muscular hypertrophy, flexion contractures, short stature, mild intellectual deficit and characteristic facies (maxillary hypoplasia, exophthalmos, and a broad nasal tip). It is transmitted as an autosomal recessive trait.","definition_xrefs":["Orphanet:2776"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary osteolysis","termid":"MONDO:0019707"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autosomal recessive distal osteolysis syndrome","secondary_identifiers":["icd11.foundation:1878981266","MEDGEN:376714","MESH:C536052","OMIM:259610","SCTID:715487005","UMLS:C1850143","GARD:4299"],"synonyms":[{"name":"Petit-Fryns syndrome","type":"exact"},{"name":"distal osteolysis-short stature-intellectual disability syndrome","type":"exact"},{"name":"osteolysis syndrome recessive","type":"related"},{"name":"osteolysis syndrome, recessive","type":"related"},{"name":"osteolysis, distal, with short stature, intellectual disability, and characteristic Facial appearance","type":"related"},{"name":"osteolysis, distal, with short stature, intellectual disability, and characteristic facial appearance","type":"related"},{"name":"osteolysis, distal, with short stature, mental retardation, and characteristic Facial appearance","type":"related"},{"name":"osteolysis, distal, with short stature, mental retardation, and characteristic facial appearance","type":"related"}],"termid":"MONDO:0009810","xrefs":{"Monarch":{"xref_id":"0009810"}}}


id: PBO:0059267
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MRPL32 pseudogene 1","termid":"PBO:0059267"}


id: GO:0016872
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"The catalysis of certain rearrangements of a molecule to break or form a ring.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isomerase activity","termid":"GO:0016853"}],"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:0016853"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016853"],"is_obsolete":false,"name":"intramolecular lyase activity","secondary_identifiers":["EC:5.5.1.-"],"termid":"GO:0016872"}


id: PBO:0081293
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 75B, pseudogene","termid":"PBO:0081293"}


id: PBO:0048662
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycerol kinase 4 pseudogene","termid":"PBO:0048662"}


id: PBO:0029604
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_transporter_activity","termid":"PBO:0029604"}


id: PBO:0048971
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycerol-3-phosphate acyltransferase 2, mitochondrial","termid":"PBO:0048971"}


id: GO:0061812
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: cyclic ADP-ribose + H20 = ADP-ribose (ADPR).","definition_xrefs":["PMID:11866528","GOC:pad","GOC:PARL","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete cyclic ADP-ribose hydrolase (obsolete GO:0061812)","termid":"GO:0061812"}


id: PBO:0056279
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mannosidase alpha class 2B member 1","termid":"PBO:0056279"}


id: GO:0021676
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that contributes to creating the structural organization of rhombomere 8. This process pertains to the physical shaping of a rudimentary structure. Rhombomeres are transverse segments of the developing rhombencephalon. Rhombomeres are lineage restricted, express different genes from one another, and adopt different developmental fates. Rhombomeres are numbered in an anterior to posterior order.","definition_xrefs":["GOC:dgh","GOC:jid","GOC:cls","GO_REF:0000021","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rhombomere structural organization","termid":"GO:0021595"},{"relation_name":"part_of","term_name":"rhombomere 8 morphogenesis","termid":"GO:0021674"}],"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":"rhombomere 8 structural organization","synonyms":[{"name":"rhombomere 8 structural organisation","type":"exact"}],"termid":"GO:0021676"}


id: PBO:0026653
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_plasma_membrane_at_cell_division_site_during_vegetative_growth","termid":"PBO:0026653"}


id: MONDO:0013787
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":"psychomotor retardation, epilepsy, and craniofacial dysmorphism","secondary_identifiers":["MEDGEN:482685","OMIM:614501","UMLS:C3281055"],"synonyms":[{"name":"PMRED","type":"related"},{"name":"neurodevelopmental disorder with hypotonia, craniofacial abnormalities, and seizures","type":"exact"},{"name":"psychomotor retardation, epilepsy, and craniofacial dysmorphism","type":"exact"}],"termid":"MONDO:0013787","xrefs":{"Monarch":{"xref_id":"0013787"}}}


id: PBO:0086702
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; may be involved in the uptake of chloride ions; does not appear to be involved in monocarboxylic acid transport; green fluorescent protein (GFP)-fusion protein localizes to the vacuole","termid":"PBO:0086702"}


id: PBO:0000917
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae ERG20","termid":"PBO:0000917"}


id: PBO:0087810
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Telomere end-binding and capping protein; plays a key role with Pol12p in linking telomerase action with completion of lagging strand synthesis, and in a regulatory step required for telomere capping; similar to human Stn1","termid":"PBO:0087810"}


id: GO:0001995
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of norepinephrine or epinephrine in the bloodstream.","definition_xrefs":["GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epinephrine catabolic process","termid":"GO:0042419"},{"relation_name":"part_of","term_name":"regulation of systemic arterial blood pressure by norepinephrine-epinephrine","termid":"GO:0001993"}],"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":"norepinephrine-epinephrine catabolic process in blood stream","synonyms":[{"name":"noradrenaline-adrenalin catabolic process in blood stream","type":"exact"}],"termid":"GO:0001995"}


id: GO:0001906
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in an organism that results in the killing of its own cells or those of another organism, including in some cases the death of the other organism. Killing here refers to the induction of death in one cell by another cell, not cell-autonomous death due to internal or other environmental conditions.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular process","termid":"GO:0009987"}],"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":"cell killing","synonyms":[{"name":"necrosis","type":"related"}],"termid":"GO:0001906"}


id: MONDO:0001300
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited or acquired peripheral neuropathy affecting the autonomic nervous system. It results in disruption of the involuntary body functions. Inherited causes include Fabry disease and porphyrias. Acquired causes include diabetes, uremia, hepatic disorders, vitamin deficiencies, toxins, and drug toxicities.","definition_xrefs":["NCIT:C27033"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autonomic nervous system disorder","termid":"MONDO:0001292"},{"relation_name":"is_a","term_name":"peripheral neuropathy","termid":"MONDO:0005244"}],"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":"autonomic neuropathy","secondary_identifiers":["UMLS:C0259749","DOID:11504","CSP:2049-9000","DOID:0060054","CSP:2042-2001","MEDGEN:82621","SCTID:277879009"],"synonyms":[{"name":"autonomic nervous system peripheral neuropathy","type":"exact"},{"name":"autonomic peripheral neuropathy","type":"exact"},{"name":"peripheral neuropathy of autonomic nervous system","type":"exact"}],"termid":"MONDO:0001300","xrefs":{"Monarch":{"xref_id":"0001300"}}}


id: MONDO:0956986
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A connective tissue cancer that is characterized as the combination of solitary fibrous tumors and hemangiopericytomas.","definition_xrefs":["DOID:0080897"],"direct_ancestors":[{"relation_name":"is_a","term_name":"connective tissue neoplasm","termid":"MONDO:0021581"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solitary fibrous tumor/hemangiopericytoma","termid":"MONDO:0956986","xrefs":{"Monarch":{"xref_id":"0956986"}}}


id: MONDO:0002019
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hypohidrotic ectodermal dysplasia (obsolete MONDO:0002019)","termid":"MONDO:0002019","xrefs":{"Monarch":{"xref_id":"0002019"}}}


id: GO:0046070
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving dGTP, guanosine triphosphate.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine deoxyribonucleotide metabolic process","termid":"GO:0009151"},{"relation_name":"is_a","term_name":"purine deoxyribonucleoside triphosphate metabolic process","termid":"GO:0009215"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0055086","GO:0008150"],"is_obsolete":false,"name":"dGTP metabolic process","synonyms":[{"name":"dGTP metabolism","type":"exact"}],"termid":"GO:0046070"}


id: GO:1903295
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of glutamate secretion, neurotransmission.","definition_xrefs":["PMID:16782817","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of glutamate secretion","termid":"GO:0014050"},{"relation_name":"is_a","term_name":"negative regulation of neurotransmitter secretion","termid":"GO:0046929"},{"relation_name":"is_a","term_name":"negative regulation of synaptic transmission, glutamatergic","termid":"GO:0051967"},{"relation_name":"is_a","term_name":"regulation of glutamate secretion, neurotransmission","termid":"GO:1903294"},{"relation_name":"negatively_regulates","term_name":"glutamate secretion, neurotransmission","termid":"GO:0061535"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of glutamate secretion, neurotransmission","synonyms":[{"name":"down regulation of glutamate secretion, neurotransmission","type":"exact"},{"name":"down-regulation of glutamate secretion, neurotransmission","type":"exact"},{"name":"downregulation of glutamate secretion, neurotransmission","type":"exact"},{"name":"inhibition of glutamate secretion, neurotransmission","type":"narrow"}],"termid":"GO:1903295"}


id: PBO:0001792
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"P-type ATPase, calcium transporting Cta4","termid":"PBO:0001792"}


id: PBO:0038426
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"A2ML1 antisense RNA 2","termid":"PBO:0038426"}


id: MONDO:0019883
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Distal trisomy 9q is a rare chromosomal anomaly, resulting from the partial trisomy of the long arm of chromosome 9, with a variable phenotype mostly characterized by psychomotor and speech delay, intellectual disability, hypotonia, long narrow habitus, craniofacial dysmorphism (incl. micro/dolichocephaly, facial asymmetry, narrow palpebral fissures, deep-set eyes, strabismus, microphthalmia, abnormally shaped ears, microstomia, micro/retrognathia) and hand and feet anomalies (incl. arachnodactyly, camptodactyly, abnormal implantation of digits). Congenital flexion contractures and limited joint movements have also been observed.","definition_xrefs":["Orphanet:96101"],"direct_ancestors":[{"relation_name":"is_a","term_name":"partial trisomy of the long arm of chromosome 9","termid":"MONDO:0016960"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"distal trisomy 9q","secondary_identifiers":["MEDGEN:1645202","SCTID:764520001","UMLS:C4706939","GARD:19316"],"synonyms":[{"name":"distal duplication 9q","type":"exact"},{"name":"distal trisomy type 9q","type":"exact"},{"name":"telomeric duplication 9q","type":"exact"},{"name":"trisomy 9qter","type":"exact"}],"termid":"MONDO:0019883","xrefs":{"Monarch":{"xref_id":"0019883"}}}


id: PATO:0000562
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000562 mass value (obsolete PATO:0000562)","termid":"PATO:0000562"}


id: SO:0001743
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence alteration whereby the copy number of a given region is less than the reference sequence.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"copy_number_variation","termid":"SO:0001019"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"copy_number_loss","synonyms":[{"name":"copy number loss","type":"exact"},{"name":"loss","type":"related"}],"termid":"SO:0001743"}


id: GO:0036291
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The phosphorylation by a protein of one or more of its own amino acid residues.","definition_xrefs":["GOC:jsg","PMID:9201908"],"gene_count":0,"genotype_count":0,"name":"obsolete protein cis-autophosphorylation (obsolete GO:0036291)","synonyms":[{"name":"cis-autophosphorylation","type":"exact"}],"termid":"GO:0036291"}


id: FYPO:0007992
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 pole body is decreased during metaphase.","definition_xrefs":["PomBase:mlr","PMID:35286199"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein localization to mitotic spindle pole body during mitosis","termid":"FYPO:0002822"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0000138","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"decreased protein localization to mitotic spindle pole body during metaphase","synonyms":[{"name":"decreased protein localisation to mitotic spindle pole body during metaphase","type":"exact"},{"name":"decreased protein localization to mitotic SPB during metaphase","type":"exact"}],"termid":"FYPO:0007992"}


id: FYPO:0004927
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which prospore formation assembly is normal (i.e. indistinguishable from wild type). In prospore formation, the nascent membrane forms at the meiotic outer plaque and grows until closure occurs and forespores, or prospores, are formed.","definition_xrefs":["GO:0032120","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular component organization","termid":"FYPO:0006003"},{"relation_name":"is_a","term_name":"normal meiotic cell cycle process","termid":"FYPO:0007078"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal prospore membrane formation","synonyms":[{"name":"normal ascospore-type prospore membrane assembly","type":"exact"},{"name":"normal forespore membrane formation","type":"exact"}],"termid":"FYPO:0004927"}


id: FYPO:0006767
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of a cyclin-dependent protein kinase activity is increased during the meiotic cell cycle, in cells that have not arrested the meiotic cell cycle under conditions that normally trigger meiotic DNA replication checkpoint signaling and response.","definition_xrefs":["PomBase:mah","PMID:10521402"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased cyclin-dependent protein kinase activity","termid":"FYPO:0004319"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000661"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0001985","FYPO:0000654","FYPO:0000707","FYPO:0000652"],"is_obsolete":false,"name":"increased cyclin-dependent protein kinase activity in absence of meiotic DNA replication checkpoint arrest","synonyms":[{"name":"increased cyclin-dependent protein kinase activity with abolished meiotic DNA replication checkpoint arrest","type":"exact"}],"termid":"FYPO:0006767"}


id: PBO:0058170
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4465","termid":"PBO:0058170"}


id: PBO:0044182
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"catenin delta 2","termid":"PBO:0044182"}


id: MONDO:0014586
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A congenital myasthenic syndrome characterized by autosomal recessive inheritance of postsynaptic neuromuscular junction defects, early-onset progressive muscle weakness, and kinetic abnormalities of the AChR channel that has material basis in homozygous or compound heterozygous mutation in the CHRNE gene on chromosome 17p13.","definition_xrefs":["PMID:25792100","PMID:8755487","DOID:0110677"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital myasthenic syndrome 4","termid":"MONDO:1040021"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"congenital myasthenic syndrome 4B","secondary_identifiers":["GARD:16087","MEDGEN:904424","UMLS:C4225369","OMIM:616324"],"synonyms":[{"name":"CMS4B","type":"exact"},{"name":"congenital myasthenic syndrome 4B fast-channel","type":"exact"},{"name":"congenital myasthenic syndrome type 4B","type":"exact"},{"name":"myasthenic syndrome, congenital, 4B, FAST-channel","type":"related"}],"termid":"MONDO:0014586","xrefs":{"Monarch":{"xref_id":"0014586"}}}


id: GO:0043076
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The nucleus of a megasporocyte, a diploid cell that undergoes meiosis to produce four megaspores, and its descendents.","definition_xrefs":["GOC:jl","ISBN:0618254153"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleus","termid":"GO:0005634"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005634"],"is_obsolete":false,"name":"megasporocyte nucleus","synonyms":[{"name":"megaspore mother cell nucleus","type":"exact"}],"termid":"GO:0043076"}


id: PBO:0067807
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 109","termid":"PBO:0067807"}


id: GO:0102400
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2 S-adenosyl-L-methionine + dTDP-3-amino-4-dehydro-2,3,6-trideoxy-alpha-D-glucose = 2 S-adenosyl-L-homocysteine + dTDP-3-N,N-dimethylamino-4-oxo-2,3,6-trideoxy-alpha-D-glucose + 2 H+.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete dTDP-3-amino-4-oxo-2,3,6-trideoxy-alpha-D-glucose N,N-dimethyltransferase activity (obsolete GO:0102400)","termid":"GO:0102400"}


id: PBO:0060927
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NFAT activating protein with ITAM motif 1","termid":"PBO:0060927"}


id: GO:1903092
data:
  {"annotated_genes":["SJAG_03652","SJAG_02152","SJAG_02962","SJAG_03808"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89606,89607,117079,118381],"is_not":false,"summary":null,"term":"GO:1903092"}]},"cv_name":"biological_process","definition":"The process in which pyridoxine is transported across a membrane.","definition_xrefs":["GOC:TermGenie","PMID:15701794","GO_REF:0000069"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyridoxine transport","termid":"GO:0031923"},{"relation_name":"is_a","term_name":"vitamin transmembrane transport","termid":"GO:0035461"}],"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:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0055085","GO:0006810"],"is_obsolete":false,"name":"pyridoxine transmembrane transport","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1903092","terms_by_termid":{"GO:1903092":null}}


id: MONDO:0021168
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare benign slow growing adipose tissue tumor, characterized by the presence of polygonal brown fat cells with multivacuolated and/or granular cytoplasm. The tumor is usually painless and is most often seen in young adults.","definition_xrefs":["NCIT:C3702"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipoma","termid":"MONDO:0005106"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hibernoma","secondary_identifiers":["UMLS:C0205822","MEDGEN:61456","SCTID:404064001","ICDO:8880/0"],"synonyms":[{"name":"Brown fat neoplasm","type":"exact"},{"name":"Brown fat tumor","type":"exact"},{"name":"Brown fat tumour","type":"exact"},{"name":"fetal fat cell lipoma","type":"exact"},{"name":"foetal fat cell lipoma","type":"exact"},{"name":"hibernoma","type":"exact"},{"name":"hibernoma, benign","type":"exact"}],"termid":"MONDO:0021168","xrefs":{"Monarch":{"xref_id":"0021168"}}}


id: MONDO:0002683
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A choroid plexus neoplasm that occurs in an adult.","definition_xrefs":["MONDO:design_pattern"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"choroid plexus cancer","termid":"MONDO:0002681"},{"relation_name":"is_a","term_name":"choroid plexus neoplasm","termid":"MONDO:0016717"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adult choroid plexus neoplasm","secondary_identifiers":["DOID:3542","NCIT:C8568","UMLS:C0796430","MEDGEN:163268"],"synonyms":[{"name":"adult choroid plexus cancer","type":"related"},{"name":"adult choroid plexus neoplasm","type":"exact"},{"name":"adult choroid plexus tumor","type":"exact"},{"name":"adult choroid plexus tumour","type":"exact"},{"name":"choroid plexus neoplasm","type":"broad"},{"name":"choroid plexus neoplasm of adults","type":"exact"},{"name":"neoplasm of adult choroid plexus","type":"exact"},{"name":"neoplasm of the adult choroid plexus","type":"exact"},{"name":"tumor of adult choroid plexus","type":"exact"},{"name":"tumor of the adult choroid plexus","type":"exact"},{"name":"tumour of adult choroid plexus","type":"exact"},{"name":"tumour of the adult choroid plexus","type":"exact"}],"termid":"MONDO:0002683","xrefs":{"Monarch":{"xref_id":"0002683"}}}


id: MONDO:0001600
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign cyst located in the salivary gland that is lined by epithelium and filled with mucoid fluid, tissue, or other material; it is usually caused by duct obstruction.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"salivary gland disorder","termid":"MONDO:0001142"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mucocele of salivary gland","secondary_identifiers":["MESH:D011900","ICD10CM:K11.6","DOID:12904","icd11.foundation:48444833","ICD9:527.6","UMLS:C0026686","MEDGEN:10117","SCTID:69825009"],"synonyms":[{"name":"mucous retention cyst of salivary gland","type":"exact"},{"name":"ranula","type":"exact"},{"name":"salivary cyst","type":"exact"},{"name":"salivary gland mucocele","type":"exact"}],"termid":"MONDO:0001600","xrefs":{"Monarch":{"xref_id":"0001600"}}}


id: MONDO:0011972
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A complication of ovulation induction in infertility treatment. It is graded by the severity of symptoms which include ovary enlargement, multiple ovarian follicles; ovarian cysts; ascites; and generalized edema. The full-blown syndrome may lead to renal failure, respiratory distress, and even death. Increased capillary permeability is caused by the vasoactive substances, such as vascular endothelial growth factors, secreted by the overly-stimulated ovaries.","definition_xrefs":["MESH:D016471"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"ovarian disorder","termid":"MONDO:0005558"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ovarian hyperstimulation syndrome","secondary_identifiers":["ICD9:256.1","UMLS:C0085083","MEDGEN:38966","MedDRA:10033266","Orphanet:64739","GARD:16668","DOID:5425","OMIM:608115","SCTID:129635004","icd11.foundation:1216664013"],"synonyms":[{"name":"OHSS","type":"exact"},{"name":"ovarian hyperstimulation syndrome","type":"exact"},{"name":"ovarian hyperstimulation syndrome, familial gestational spontaneous","type":"related"},{"name":"secondary Meig's syndrome","type":"exact"}],"termid":"MONDO:0011972","xrefs":{"Monarch":{"xref_id":"0011972"}}}


id: PBO:0043049
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cysteine and histidine rich domain containing 2, pseudogene","termid":"PBO:0043049"}


id: SO:0000754
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The lambda bacteriophage is the vector for the linear lambda clone. The genes involved in the lysogenic pathway are removed from the from the viral DNA. Up to 25 kb of foreign DNA can then be inserted into the lambda genome.","definition_xrefs":["ISBN:0-1767-2380-8"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vector_replicon","termid":"SO:0000440"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lambda_vector","synonyms":[{"name":"lambda vector","type":"exact"}],"termid":"SO:0000754"}


id: PBO:0083416
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 ORF PTC2/YER089C; identified by gene-trapping, expression analysis, and homology searching","termid":"PBO:0083416"}


id: GO:0030351
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: inositol-1,3,4,5,6-pentakisphosphate + H2O = inositol-1,4,5,6-tetrakisphosphate + phosphate.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inositol pentakisphosphate phosphatase activity","termid":"GO:0052827"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016788"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016787","GO:0016788"],"is_obsolete":false,"name":"inositol-1,3,4,5,6-pentakisphosphate 3-phosphatase activity","secondary_identifiers":["Reactome:R-HSA-1855163"],"termid":"GO:0030351"}


id: PBO:0029676
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_septum_morphology_during_vegetative_growth","termid":"PBO:0029676"}


id: PBO:0046401
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"erythrocyte membrane protein band 4.1 like 4B","termid":"PBO:0046401"}


id: PBO:0055250
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 2677","termid":"PBO:0055250"}


id: MOD:00418
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a hydrogen atom with an (pyridin-3-yl)acetyl group.","definition_xrefs":["PubMed:9276974","Unimod:25"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acylated residue","termid":"MOD:00649"},{"relation_name":"is_a","term_name":"reagent derivatized residue","termid":"MOD:00848"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyridylacetylated residue","synonyms":[{"name":"Pyridylacetyl","type":"related"},{"name":"pyridylacetyl","type":"related"}],"termid":"MOD:00418"}


id: PBO:0056538
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methylmalonyl-CoA epimerase","termid":"PBO:0056538"}


id: GO:1903795
data:
  {"annotated_genes":["SJAG_04990"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[98903],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000185"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of inorganic anion transmembrane transport.","definition_xrefs":["GO_REF:0000058","PMID:11336802","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transmembrane transport","termid":"GO:0034762"},{"relation_name":"regulates","term_name":"inorganic anion transmembrane transport","termid":"GO:0098661"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04990":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0055085"],"is_obsolete":false,"name":"regulation of inorganic anion transmembrane transport","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"regulation of inorganic anion membrane transport","type":"exact"},{"name":"regulation of transmembrane inorganic anion transport","type":"exact"}],"termid":"GO:1903795","terms_by_termid":{"GO:2000185":null}}


id: PBO:0017532
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial Release Factor","termid":"PBO:0017532"}


id: GO:0140935
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A histone deubiquitinase that cleaves ubiquitin from the conserved C-terminal lysine residue of a histone H2B protein to which it is conjugated. The conserved lysine residue is K119 in fission yeast, K123 in budding yeast, and K120 in mammals.","definition_xrefs":["PMID:15657442"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H2B deubiquitinase activity","termid":"GO:0140936"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0008233"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0008233","GO:0016787","GO:0140096"],"is_obsolete":false,"name":"histone H2B conserved C-terminal lysine deubiquitinase activity","synonyms":[{"name":"histone conserved C-terminal lysine deubiquitination","type":"related"}],"termid":"GO:0140935"}


id: PBO:0056344
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitogen-activated protein kinase kinase kinase kinase 3","termid":"PBO:0056344"}


id: MONDO:0024340
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neuroblastoma arising from the retina.","definition_xrefs":["NCIT:C6956"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuroblastoma","termid":"MONDO:0005072"},{"relation_name":"is_a","term_name":"retina neoplasm","termid":"MONDO:0021231"}],"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":"retinal neuroblastoma","secondary_identifiers":["UMLS:C5779888","MEDGEN:1830429"],"synonyms":[{"name":"neuroblastoma of retina","type":"exact"},{"name":"neuroblastoma of the retina","type":"exact"},{"name":"retina neuroblastoma","type":"exact"},{"name":"retinal neuroblastoma","type":"exact"}],"termid":"MONDO:0024340","xrefs":{"Monarch":{"xref_id":"0024340"}}}


id: PBO:0091746
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome b translation regulator Cbp7","termid":"PBO:0091746"}


id: MONDO:0019604
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare monoclonalgammopathy characterized by renal proximal tubule dysfunction secondary to monoclonal kappa light chain deposits in proximal tubular cells. Clinical presentation is with variable chronic kidney disease, low molecular weight proteinuria, aminoaciduria, hyperphosphaturia, uricosuria, bicarbonaturia, and non-diabetic glycosuria. Renal phosphate and urate wasting may cause hypophosphatemia and hypouricaemia.","definition_xrefs":["Orphanet:91136"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monoclonal gammopathy","termid":"MONDO:0004960"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"acquired monoclonal Ig light chain-associated Fanconi syndrome","secondary_identifiers":["GARD:19154","MEDGEN:1375627","UMLS:C4510369","SCTID:724099000"],"synonyms":[{"name":"acquired Fanconi syndrome secondary to monoclonal gammopathy","type":"exact"},{"name":"acquired monoclonal immunoglobulin light chain-associated Fanconi syndrome","type":"exact"}],"termid":"MONDO:0019604","xrefs":{"Monarch":{"xref_id":"0019604"}}}


id: PR:O59814
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC794.04c gene.","definition_xrefs":["PRO:DNx","UniProtKB:O59814"],"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 transporter C794.04c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC794.04c","synonyms":[{"name":"Spom972h-SPCC794.04c","type":"exact"}],"termid":"PR:O59814"}


id: MONDO:0850101
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cutaneous melanoma","termid":"MONDO:0005012"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005093"],"is_obsolete":false,"name":"spitzoid melanoma","secondary_identifiers":["DOID:0070326","MEDGEN:1713307","NCIT:C165497","UMLS:C3495721"],"termid":"MONDO:0850101","xrefs":{"Monarch":{"xref_id":"0850101"}}}


id: GO:0007338
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The union of male and female gametes to form a zygote.","definition_xrefs":["GOC:ems","GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fertilization","termid":"GO:0009566"}],"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":"single fertilization","secondary_identifiers":["Reactome:R-HSA-1187000"],"synonyms":[{"name":"zygote biosynthesis","type":"related"},{"name":"zygote formation","type":"related"}],"termid":"GO:0007338"}


id: MONDO:0013172
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare genetic syndrome with central nervous system malformations characterized by severe developmental delay, neonatal hypotonia, seizures, optic nerve hypoplasia and distinct central nervous system malformations including extensive bilateral polymicrogyria, dysplastic or absent corpus callosum and malformed brainstem with loss of demarcation of the pontomedullary junction.","definition_xrefs":["Orphanet:250972"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"excluded_subClassOf","term_name":"obsolete syndrome with a central nervous system malformation as major feature (obsolete MONDO:0015220)","termid":"MONDO:0015220"},{"relation_name":"excluded_subClassOf","term_name":"obsolete syndromic optic nerve hypoplasia (obsolete MONDO:0015310)","termid":"MONDO:0015310"},{"relation_name":"excluded_subClassOf","term_name":"obsolete cerebral malformation with epilepsy (obsolete MONDO:0015655)","termid":"MONDO:0015655"},{"relation_name":"is_a","term_name":"complex cortical dysplasia with other brain malformations","termid":"MONDO:0000904"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polymicrogyria with optic nerve hypoplasia","secondary_identifiers":["GARD:20687","MEDGEN:442565","MESH:C567715","OMIM:613180","UMLS:C2750798"],"synonyms":[{"name":"CDCBM8","type":"related"},{"name":"cortical dysplasia, Complex, with Other brain malformations 8","type":"related"},{"name":"cortical dysplasia, complex, with other brain malformations 8","type":"related"},{"name":"polymicrogyria with optic nerve hypoplasia","type":"exact"}],"termid":"MONDO:0013172","xrefs":{"Monarch":{"xref_id":"0013172"}}}


id: GO:0045647
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of erythrocyte differentiation.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of myeloid cell differentiation","termid":"GO:0045638"},{"relation_name":"is_a","term_name":"regulation of erythrocyte differentiation","termid":"GO:0045646"},{"relation_name":"negatively_regulates","term_name":"erythrocyte differentiation","termid":"GO:0030218"}],"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 erythrocyte differentiation","synonyms":[{"name":"down regulation of erythrocyte differentiation","type":"exact"},{"name":"down-regulation of erythrocyte differentiation","type":"exact"},{"name":"downregulation of erythrocyte differentiation","type":"exact"},{"name":"inhibition of erythrocyte differentiation","type":"narrow"},{"name":"negative regulation of RBC differentiation","type":"exact"},{"name":"negative regulation of red blood cell differentiation","type":"exact"}],"termid":"GO:0045647"}


id: GO:0018959
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving a phenol, any compound containing one or more hydroxyl groups directly attached to an aromatic carbon ring, in the presence of oxygen.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenol-containing compound metabolic process","termid":"GO:0018958"}],"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":"aerobic phenol-containing compound metabolic process","secondary_identifiers":["UM-BBD_pathwayID:pba"],"synonyms":[{"name":"aerobic phenol-containing compound metabolism","type":"exact"}],"termid":"GO:0018959"}


id: MONDO:0044345
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An infection that is caused by Schistosoma mansoni.","definition_xrefs":["NCIT:C35002"],"direct_ancestors":[{"relation_name":"is_a","term_name":"schistosomiasis","termid":"MONDO:0015254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schistosoma mansoni infectious disease","secondary_identifiers":["MESH:D012555","SCTID:750009"],"synonyms":[{"name":"Schistosoma mansoni caused disease or disorder","type":"exact"},{"name":"Schistosoma mansoni disease or disorder","type":"exact"},{"name":"Schistosoma mansoni infection","type":"exact"}],"termid":"MONDO:0044345","xrefs":{"Monarch":{"xref_id":"0044345"}}}


id: PBO:0058428
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4798","termid":"PBO:0058428"}


id: MONDO:0008671
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Waardenburg syndrome Type 2 caused by mutations in the MITF gene.","definition_xrefs":["NCIT:C75011"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Waardenburg syndrome type 2","termid":"MONDO:0019517"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"Waardenburg syndrome type 2A","secondary_identifiers":["DOID:0110950","MESH:C536464","OMIM:193510","GARD:5521","MEDGEN:349786","UMLS:C1860339"],"synonyms":[{"name":"MITF Waardenburg syndrome type 2","type":"exact"},{"name":"WS2A","type":"exact"},{"name":"Waardenburg syndrome type 2 caused by mutation in MITF","type":"exact"},{"name":"Waardenburg syndrome type 2A","type":"exact"},{"name":"Waardenburg syndrome type IIA","type":"exact"},{"name":"Waardenburg syndrome without dystopia canthorum","type":"related"},{"name":"Waardenburg syndrome, type 2A","type":"related"},{"name":"Ws2","type":"related"}],"termid":"MONDO:0008671","xrefs":{"Monarch":{"xref_id":"0008671"}}}


id: PBO:0054162
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 1531","termid":"PBO:0054162"}


id: PBO:0036293
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Defective in Mitotic Arrest","termid":"PBO:0036293"}


id: PBO:0077637
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TMX2-CTNND1 readthrough (NMD candidate)","termid":"PBO:0077637"}


id: PBO:0061010
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"niban apoptosis regulator 3","termid":"PBO:0061010"}


id: PBO:0031141
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-septation_following_abnormal_mitotic_chromosome_segregation","termid":"PBO:0031141"}


id: PBO:0005710
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"human aprataxin homolog, involved in DNA repair (predicted)","termid":"PBO:0005710"}


id: PR:O42852
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sec20 gene.","definition_xrefs":["UniProtKB:O42852","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":"protein transport protein sec20 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC23A1.15c","synonyms":[{"name":"Spom972h-sec20","type":"exact"}],"termid":"PR:O42852"}


id: PBO:0083007
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Daughter cell-specific secreted protein with similarity to glucanases; degrades cell wall from the daughter side causing daughter to separate from mother","termid":"PBO:0083007"}


id: PBO:0117241
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial peptidyl-tRNA hydrolase Pth2","termid":"PBO:0117241"}


id: GO:0061552
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of ganglion are generated and organized.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tissue morphogenesis","termid":"GO:0048729"},{"relation_name":"part_of","term_name":"ganglion development","termid":"GO:0061548"}],"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":"ganglion morphogenesis","synonyms":[{"name":"ganglia morphogenesis","type":"related"}],"termid":"GO:0061552"}


id: MONDO:0015038
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lissencephaly with cerebellar hypoplasia type E (LCHe) is a form of lissencephaly with cerebellar hypoplasia, characterized by an abrupt transition from agyria to gyral simplification, near the boundary between frontal and parietal cortex, microcephaly (B1 3 SD) and brainstem hypoplasia.","definition_xrefs":["Orphanet:100015"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lissencephaly with cerebellar hypoplasia","termid":"MONDO:0019450"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"lissencephaly with cerebellar hypoplasia type E","secondary_identifiers":["UMLS:C5191422","MEDGEN:1676990","GARD:19735","icd11.foundation:252327835"],"termid":"MONDO:0015038","xrefs":{"Monarch":{"xref_id":"0015038"}}}


id: GO:1903703
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires the specialized features of an enterocyte.","definition_xrefs":["GO_REF:0000086","PMID:16782882","GOC:TermGenie","Wikipedia:List_of_intestinal_epithelial_differentiation_genes"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intestinal epithelial cell differentiation","termid":"GO:0060575"}],"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":"enterocyte differentiation","termid":"GO:1903703"}


id: PBO:0066739
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 36","termid":"PBO:0066739"}


id: GO:1990456
data:
  {"annotated_genes":["SJAG_03416","SJAG_04370","SJAG_01305","SJAG_03710","SJAG_01929"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[71696,71740,76533,81856,116219],"is_not":false,"summary":null,"term":"GO:1990456"}]},"cv_name":"biological_process","definition":"The attachment of a mitochondrion and an endoplasmic reticulum via molecular tethers that physically bridge their respective membranes and attach them to each other. The tethering may facilitate exchange of metabolites between the organelles.","definition_xrefs":["PMID:27875684","PMID:19556461"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular component organization","termid":"GO:0016043"},{"relation_name":"is_a","term_name":"organelle localization by membrane tethering","termid":"GO:0140056"}],"gene_count":5,"genes_by_uniquename":{"SJAG_01305":null,"SJAG_01929":null,"SJAG_03416":null,"SJAG_03710":null,"SJAG_04370":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140056"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0140056","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"mitochondrion-endoplasmic reticulum membrane tethering","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"mitochondrion-ER attachment","type":"exact"},{"name":"mitochondrion-ER membrane tethering","type":"exact"},{"name":"mitochondrion-ER tethering","type":"exact"},{"name":"mitochondrion-endoplasmic reticulum attachment","type":"exact"},{"name":"mitochondrion-endoplasmic reticulum tethering","type":"exact"}],"termid":"GO:1990456","terms_by_termid":{"GO:1990456":null}}


id: MONDO:0010679
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Duchenne muscular dystrophy (DMD) is a neuromuscular disease characterized by rapidly progressive muscle weakness and wasting due to degeneration of skeletal, smooth and cardiac muscle.","definition_xrefs":["Orphanet:98896"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete neuro-ophthalmological disease (obsolete MONDO:0015368)","termid":"MONDO:0015368"},{"relation_name":"is_a","term_name":"DMD-related muscular dystrophy","termid":"MONDO:0700285"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"Duchenne muscular dystrophy","secondary_identifiers":["MedDRA:10013801","MEDGEN:3925","OMIM:310200","GARD:6291","NANDO:2200856","NCIT:C75482","NANDO:1200488","DOID:11723","MESH:D020388","NORD:1065","SCTID:76670001","icd11.foundation:1479561744","UMLS:C0013264"],"synonyms":[{"name":"DMD","type":"exact"},{"name":"Duchenne muscular dystrophy","type":"exact"},{"name":"Duchenne muscular dystrophy, X-linked recessive","type":"exact"},{"name":"muscular dystrophy, Duchenne","type":"exact"},{"name":"muscular dystrophy, Duchenne type","type":"related"},{"name":"muscular dystrophy, pseudohypertrophic progressive, Duchenne type","type":"related"},{"name":"severe dystrophinopathy, Duchenne type","type":"exact"}],"termid":"MONDO:0010679","xrefs":{"Monarch":{"xref_id":"0010679"}}}


id: PBO:0090682
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Thioredoxin reductase superfamily protein","termid":"PBO:0090682"}


id: PBO:0001090
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA Glycine","termid":"PBO:0001090"}


id: GO:1990370
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A response that results in a state of tolerance to aldehyde.","definition_xrefs":["PMID:23356676","GOC:mengo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete process resulting in tolerance to aldehyde (obsolete GO:1990370)","termid":"GO:1990370"}


id: PBO:0053535
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 537","termid":"PBO:0053535"}


id: PBO:0043509
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CNTNAP3 pseudogene 4","termid":"PBO:0043509"}


id: PBO:0002635
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Golgi GDP-mannose transporter Vrg4 (predicted)","termid":"PBO:0002635"}


id: GO:0060437
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The increase in size or mass of a lung. In all air-breathing vertebrates the lungs are developed from the ventral wall of the oesophagus as a pouch which divides into two sacs. In amphibians and many reptiles the lungs retain very nearly this primitive sac-like character, but in the higher forms the connection with the esophagus becomes elongated into the windpipe and the inner walls of the sacs become more and more divided, until, in the mammals, the air spaces become minutely divided into tubes ending in small air cells, in the walls of which the blood circulates in a fine network of capillaries. In mammals the lungs are more or less divided into lobes, and each lung occupies a separate cavity in the thorax.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organ growth","termid":"GO:0035265"},{"relation_name":"part_of","term_name":"lung development","termid":"GO:0030324"}],"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 growth","termid":"GO:0060437"}


id: PBO:0111301
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U1 snRNP-associated protein Prp39","termid":"PBO:0111301"}


id: MONDO:0011371
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An instance of hydroa vacciniforme that is caused by an inherited modification of the individual's genome.","definition_xrefs":["MONDO:patterns/hereditary"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydroa vacciniforme","termid":"MONDO:0018024"},{"relation_name":"is_a","term_name":"hereditary skin disorder","termid":"MONDO:0100118"}],"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":"hydroa vacciniforme, familial","secondary_identifiers":["GARD:10079","MEDGEN:355003","MESH:C536077","OMIM:603794","UMLS:C1863533"],"synonyms":[{"name":"familial hydroa vacciniforme","type":"related"},{"name":"hereditary hydroa vacciniforme","type":"exact"},{"name":"hydroa vacciniforme, familial","type":"exact"}],"termid":"MONDO:0011371","xrefs":{"Monarch":{"xref_id":"0011371"}}}


id: GO:0015344
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: siderophore-iron(ferrioxamine)(out) + H+(out) = siderophore-iron(ferrioxamine)(in) + H+(in).","definition_xrefs":["TC:2.A.1.16.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"siderophore-iron transmembrane transporter activity","termid":"GO:0015343"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"siderophore uptake transmembrane transporter activity","synonyms":[{"name":"ferrioxamine uptake transmembrane transporter activity","type":"related"},{"name":"siderochrome-iron (ferrioxamine) uptake transporter","type":"narrow"},{"name":"siderophore-iron uptake transmembrane transporter activity","type":"related"}],"termid":"GO:0015344"}


id: PBO:0080816
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5'-3' exoribonuclease 1","termid":"PBO:0080816"}


id: PBO:0043877
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cAMP responsive element binding protein 5","termid":"PBO:0043877"}


id: GO:0046823
data:
  {"annotated_genes":["SJAG_01311"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[105358],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042308"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the directed movement of substances between the cytoplasm and the nucleus.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of intracellular transport","termid":"GO:0032387"},{"relation_name":"is_a","term_name":"regulation of nucleocytoplasmic transport","termid":"GO:0046822"},{"relation_name":"negatively_regulates","term_name":"nucleocytoplasmic transport","termid":"GO:0006913"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01311":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0006913"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006913"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0006913"],"is_obsolete":false,"name":"negative regulation of nucleocytoplasmic transport","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of nucleocytoplasmic transport","type":"exact"},{"name":"down-regulation of nucleocytoplasmic transport","type":"exact"},{"name":"downregulation of nucleocytoplasmic transport","type":"exact"},{"name":"inhibition of nucleocytoplasmic transport","type":"narrow"}],"termid":"GO:0046823","terms_by_termid":{"GO:0042308":null}}


id: MONDO:0010739
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":"Taqi polymorphism","secondary_identifiers":["MEDGEN:374172","OMIM:313480","UMLS:C1839238"],"synonyms":[{"name":"TAQ1","type":"related"},{"name":"TaqI polymorphism","type":"related"},{"name":"Taqi polymorphism","type":"exact"}],"termid":"MONDO:0010739","xrefs":{"Monarch":{"xref_id":"0010739"}}}


id: FYPO:0003931
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which a cell has no septum and is inviable.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"aseptate","termid":"FYPO:0000949"},{"relation_name":"has_part","term_name":"inviable vegetative cell","termid":"FYPO:0001489"},{"relation_name":"is_a","term_name":"aseptate","termid":"FYPO:0000949"},{"relation_name":"is_a","term_name":"inviable vegetative cell","termid":"FYPO:0001489"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0000004","FYPO:0000002","FYPO:0000631","FYPO:0000032","FYPO:0001985","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"inviable aseptate vegetative cell","synonyms":[{"name":"inviable aseptate cell during mitotic cell cycle","type":"related"},{"name":"inviable aseptate cell during vegetative growth","type":"exact"},{"name":"lethal; aseptate vegetative cell","type":"exact"}],"termid":"FYPO:0003931"}


id: MONDO:0013577
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Disorder of adipose tissue characterized by symmetric and bilateral enlargement of the lower extremities due to abnormal deposition of subcutaneous fat often in obese women. It is associated with hematoma, pain and may progress to secondary lymphedema which is known as lipolymphedema.","definition_xrefs":["MESH:D065134"],"direct_ancestors":[{"relation_name":"is_a","term_name":"subcutaneous tissue disorder","termid":"MONDO:0019296"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Lipedema","secondary_identifiers":["HP:0100695","Orphanet:77243","UMLS:C0398370","SCTID:234102003","MedDRA:10063955","MEDGEN:451048","OMIM:614103"],"synonyms":[{"name":"Lipedema (disease)","type":"exact"},{"name":"lipedema","type":"exact"}],"termid":"MONDO:0013577","xrefs":{"Monarch":{"xref_id":"0013577"}}}


id: PBO:0044976
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DEAH-box helicase 16","termid":"PBO:0044976"}


id: FYPO:0002882
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which transcription occurs to is normal (i.e. indistinguishable from wild type) in extent, timing, start or termination site, etc. All genes, or a specific subset of genes, may be measured.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcription phenotype","termid":"FYPO:0004847"},{"relation_name":"is_a","term_name":"normal RNA metabolic process","termid":"FYPO:0004850"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000294","FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal transcription","synonyms":[{"name":"normal transcription, DNA-dependent","type":"exact"}],"termid":"FYPO:0002882"}


id: PBO:0047507
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FER1L6 antisense RNA 2","termid":"PBO:0047507"}


id: PATO:0001386
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An aneuploidy quality inhering in a bearer by virtue of the bearer's containing only one chromosome from a pair in a cell's nucleus.","definition_xrefs":["Wikipedia:http://en.wikipedia.org/wiki/Monosomy"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aneuploid","termid":"PATO:0001385"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"monosomy","termid":"PATO:0001386"}


id: PBO:0034769
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, calcium binding subfamily (predicted)","termid":"PBO:0034769"}


id: MONDO:0000839
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Any abnormality, anatomical or biochemical, evident at birth or during the neonatal period.","definition_xrefs":["NCIT:C2849"],"gene_count":0,"genotype_count":0,"name":"obsolete congenital abnormality (obsolete MONDO:0000839)","secondary_identifiers":["DOID:0080015","SCTID:276654001","NANDO:1200957","ICD9:759.9","MESH:D000013","ICD9:759.89"],"synonyms":[{"name":"CM - congenital malformation","type":"related"},{"name":"SCONG","type":"exact"},{"name":"birth defect","type":"exact"},{"name":"congenital Abnormality","type":"exact"},{"name":"congenital abnormality","type":"exact"},{"name":"congenital anatomic Abnormality","type":"exact"},{"name":"congenital anatomical Abnormality","type":"exact"},{"name":"congenital anomalies of fetus","type":"exact"},{"name":"congenital anomaly","type":"exact"},{"name":"congenital anomaly or birth defect","type":"exact"},{"name":"congenital defect","type":"exact"},{"name":"congenital defect/deformity","type":"exact"},{"name":"congenital deformity","type":"exact"},{"name":"congenital malformation","type":"exact"},{"name":"defect/deformity, Congenital","type":"exact"},{"name":"defect/deformity, congenital","type":"exact"},{"name":"deformity/defect, Congenital","type":"exact"},{"name":"fetal developmental abnormality","type":"related"},{"name":"fetal malformation","type":"related"},{"name":"physical disorder","type":"exact"}],"termid":"MONDO:0000839","xrefs":{"Monarch":{"xref_id":"0000839"}}}


id: PBO:0045263
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"delta/notch like EGF repeat containing","termid":"PBO:0045263"}


id: MONDO:0017081
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"isolated encephalocele","termid":"MONDO:0016057"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"parietal encephalocele","secondary_identifiers":["GARD:20970","Orphanet:268826","SCTID:253109005","UMLS:C0431294","MEDGEN:488903","icd11.foundation:1122294944"],"termid":"MONDO:0017081","xrefs":{"Monarch":{"xref_id":"0017081"}}}


id: PBO:0049470
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"granzyme A","termid":"PBO:0049470"}


id: FYPO:0008337
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 addition of one or more uridylyl residues to the 3' ends of non-polyadenylated RNA molecules occurs to a lower extent than normal.","definition_xrefs":["PMID:39333464"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased RNA modification","termid":"FYPO:0000372"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"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:0000294"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000294","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"decreased 3' end uridylation of non-polyadenylated RNA","termid":"FYPO:0008337"}


id: SO:0001416
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A flanking region located five prime of a specific region.","definition_xrefs":["SO:chado"],"direct_ancestors":[{"relation_name":"is_a","term_name":"flanking_region","termid":"SO:0000239"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"five_prime_flanking_region","synonyms":[{"name":"5' flanking region","type":"related"},{"name":"five prime flanking region","type":"exact"}],"termid":"SO:0001416"}


id: GO:0007559
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The breakdown of tissues; usually, if not always, accompanied by cell death, followed by the complete dissolution of dead tissue.","definition_xrefs":["GOC:ma","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete histolysis (obsolete GO:0007559)","secondary_identifiers":["Wikipedia:Histolysis"],"termid":"GO:0007559"}


id: PBO:0005606
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DUF1715 family protein","termid":"PBO:0005606"}


id: PBO:0053991
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 1310","termid":"PBO:0053991"}


id: FYPO:0003456
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"Auxotrophy in which a cell is unable to synthesize methionine or purines, and therefore requires methionine and at least one purine in the medium for vegetative cell growth.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"growth auxotrophic for methionine","termid":"FYPO:0000040"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"growth auxotrophic for methionine and purine","synonyms":[{"name":"growth auxotrophic for methionine and purine during mitotic cell cycle","type":"related"},{"name":"growth auxotrophic for methionine and purine during vegetative growth","type":"exact"},{"name":"methionine and purine auxotrophy","type":"exact"}],"termid":"FYPO:0003456"}


id: MONDO:0017093
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Unilateral focal polymicrogyria (BFPP) is the mildest sub-type of polymicrogyria (PMG), a cerebral cortical malformation characterized by excessive cortical folding and abnormal cortical layering, that affects only one small region of the brain and that may show no neurologic involvement.","definition_xrefs":["Orphanet:268947"],"direct_ancestors":[{"relation_name":"is_a","term_name":"unilateral polymicrogyria","termid":"MONDO:0017092"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"unilateral focal polymicrogyria","secondary_identifiers":["DOID:0080919","GARD:20981","MEDGEN:1842371","icd11.foundation:1006662041","UMLS:C5680773"],"termid":"MONDO:0017093","xrefs":{"Monarch":{"xref_id":"0017093"}}}


id: GO:0000350
data:
  {"annotated_genes":["SJAG_01152","SJAG_01200","SJAG_01214","SJAG_02455"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[74898,79116,104395,109119],"is_not":false,"summary":null,"term":"GO:0000350"}]},"cv_name":"biological_process","definition":"Conformational rearrangement of the spliceosomal complex containing the RNA products from the 1st step of splicing to form the catalytic site for the second step of splicing.","definition_xrefs":["ISBN:0879695897","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-RNA complex assembly","termid":"GO:0022618"},{"relation_name":"part_of","term_name":"spliceosomal conformational changes to generate catalytic conformation","termid":"GO:0000393"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01152":null,"SJAG_01200":null,"SJAG_01214":null,"SJAG_02455":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"part_of","termid":"GO:0065003"},{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0016071"}],"interesting_parent_ids":["GO:0016071","GO:0010467","GO:0065003","GO:0008150","GO:0044085"],"is_obsolete":false,"name":"generation of catalytic spliceosome for second transesterification step","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0000359","GO:0000358"],"synonyms":[{"name":"catalytic spliceosome assembly for second transesterification step","type":"related"},{"name":"formation of catalytic U12-type spliceosome for second transesterification step","type":"narrow"},{"name":"formation of catalytic U2-type spliceosome for second transesterification step","type":"narrow"},{"name":"formation of catalytic spliceosome for second transesterification step","type":"exact"},{"name":"formation of spliceosomal A2-2 complex","type":"narrow"},{"name":"formation of spliceosomal C1 complex","type":"narrow"},{"name":"lariat formation, 5'-splice site cleavage","type":"related"},{"name":"spliceosomal A2-3 complex biosynthesis","type":"narrow"},{"name":"spliceosomal A2-3 complex formation","type":"narrow"},{"name":"spliceosomal C2 complex biosynthesis","type":"narrow"},{"name":"spliceosomal C2 complex formation","type":"narrow"}],"termid":"GO:0000350","terms_by_termid":{"GO:0000350":null}}


id: GO:1900294
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of heptasaccharide transport.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transport","termid":"GO:0051049"},{"relation_name":"regulates","term_name":"heptasaccharide transport","termid":"GO:2001104"}],"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 heptasaccharide transport","termid":"GO:1900294"}


id: PBO:0117053
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MYO7B antisense RNA 1","termid":"PBO:0117053"}


id: MONDO:0015085
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Bathing suit ichthyosis (BSI) is a rare variant of autosomal recessive congenital ichthyosis (ARCI) characterized by the presence of large dark scales in specific areas of the body.","definition_xrefs":["Orphanet:100976"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive congenital ichthyosis","termid":"MONDO:0017265"}],"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":"bathing suit ichthyosis","secondary_identifiers":["icd11.foundation:174005370","MEDGEN:1386460","UMLS:C4511230","SCTID:725588002","GARD:16938"],"synonyms":[{"name":"BSI","type":"exact"}],"termid":"MONDO:0015085","xrefs":{"Monarch":{"xref_id":"0015085"}}}


id: GO:0000032
data:
  {"annotated_genes":["SJAG_03082","SJAG_00816","SJAG_04770","SJAG_01276","SJAG_04906","SJAG_01021","SJAG_00598","SJAG_02519","SJAG_01264"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[73768,76449,76578,78748,79300,79791,81121,82219,86947],"is_not":false,"summary":null,"term":"GO:0000032"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of cell wall mannoproteins, any cell wall protein that contains covalently bound mannose residues.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mannoprotein biosynthetic process","termid":"GO:0006057"},{"relation_name":"is_a","term_name":"cell wall glycoprotein biosynthetic process","termid":"GO:0031506"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00598":null,"SJAG_00816":null,"SJAG_01021":null,"SJAG_01264":null,"SJAG_01276":null,"SJAG_02519":null,"SJAG_03082":null,"SJAG_04770":null,"SJAG_04906":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0071554"}],"interesting_parent_ids":["GO:0071554","GO:0008150"],"is_obsolete":false,"name":"cell wall mannoprotein biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"cell wall mannoprotein anabolism","type":"exact"},{"name":"cell wall mannoprotein biosynthesis","type":"exact"},{"name":"cell wall mannoprotein formation","type":"exact"},{"name":"cell wall mannoprotein synthesis","type":"exact"}],"termid":"GO:0000032","terms_by_termid":{"GO:0000032":null}}


id: GO:0007485
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the male genitalia over time, from formation as part of the genital disc to the mature structure. An example of this is found in Drosophila melanogaster.","definition_xrefs":["GOC:ai","GOC:sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"imaginal disc-derived genitalia development","termid":"GO:0007484"}],"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":"imaginal disc-derived male genitalia development","synonyms":[{"name":"male genital development","type":"broad"}],"termid":"GO:0007485"}


id: PR:O59715
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- dsd1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O59715"],"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":"sphingolipid delta(4)-desaturase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC3B8.07c","synonyms":[{"name":"Spom972h-dsd1","type":"exact"},{"name":"delta 4-(E)-sphingolipid desaturase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"dihydroceramide desaturase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O59715"}


id: PBO:0057993
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3917","termid":"PBO:0057993"}


id: PR:O42970
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC1E8.05 gene.","definition_xrefs":["UniProtKB:O42970","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized serine-rich protein C1E8.05 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1E8.05","synonyms":[{"name":"Spom972h-SPBC1E8.05","type":"exact"}],"termid":"PR:O42970"}


id: PBO:0071515
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L34 pseudogene 18","termid":"PBO:0071515"}


id: FYPO:0000339
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which a cell has a septum in an abnormal location. The normal location is at the midpoint of the long axis of the cell. The site of septum assembly is normally determined by the location of the actomyosin contractile ring.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal septum during vegetative growth","termid":"FYPO:0002455"},{"relation_name":"is_a","term_name":"mislocalized septum","termid":"FYPO:0004293"},{"relation_name":"output_of","term_name":"abnormal actomyosin contractile ring localization","termid":"FYPO:0000033"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0000138","FYPO:0001985","FYPO:0001320","FYPO:0000032","FYPO:0000631"],"is_obsolete":false,"name":"mislocalized septum during vegetative growth","secondary_identifiers":["FYPO:0002154"],"synonyms":[{"name":"abnormal contractile ring localization resulting in abnormal septum site selection","type":"related"},{"name":"abnormal contractile ring localization resulting in mislocalized septum","type":"related"},{"name":"abnormal division septum site selection","type":"related"},{"name":"abnormal septum localization during vegetative growth","type":"related"},{"name":"abnormal septum location during vegetative growth","type":"exact"},{"name":"abnormal septum position during vegetative growth","type":"exact"},{"name":"abnormal septum positioning during vegetative growth","type":"related"},{"name":"abnormal septum postitioning","type":"exact"},{"name":"abnormal septum site selection","type":"related"},{"name":"abnormal septum site selection during mitotic cell cycle","type":"related"},{"name":"abnormal septum site selection during vegetative growth","type":"related"},{"name":"asymmetric septum during vegetative growth","type":"exact"},{"name":"asymmetrically located septum during vegetative growth","type":"exact"},{"name":"mislocalised septum during vegetative growth","type":"exact"},{"name":"mislocalized septum during mitotic cell cycle","type":"related"},{"name":"misplaced septum during vegetative growth","type":"exact"},{"name":"septum site selection defects","type":"related"}],"termid":"FYPO:0000339"}


id: PBO:0050847
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"islet cell autoantigen 1 like","termid":"PBO:0050847"}


id: PBO:0059565
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metallothionein 1H like 1","termid":"PBO:0059565"}


id: PBO:0046318
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"enolase 1","termid":"PBO:0046318"}


id: MONDO:0011604
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Spondylo-ocular syndrome is a very rare association of spinal and ocular manifestations that is characterized by dense cataracts, and retinal detachment along with generalized osteoporosis and platyspondyly. Mild craniofacial dysphormism has been reported including short neck, large head and prominent eyebrows.","definition_xrefs":["Orphanet:85194"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with decreased bone density (obsolete MONDO:0019704)","termid":"MONDO:0019704"},{"relation_name":"is_a","term_name":"congenital vitreoretinal dysplasia","termid":"MONDO:0020247"},{"relation_name":"is_a","term_name":"osteogenesis imperfecta and a reduction of bone mineral density.","termid":"MONDO:0800064"},{"relation_name":"is_a","term_name":"linkeropathy","termid":"MONDO:1040022"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0002320","MONDO:0005497"],"is_obsolete":false,"name":"spondylo-ocular syndrome","secondary_identifiers":["UMLS:C4225412","OMIM:605822","GARD:16740","MEDGEN:900371","icd11.foundation:1611450426","SCTID:715653007"],"synonyms":[{"name":"SOS","type":"related"},{"name":"spondyloocular syndrome","type":"related"}],"termid":"MONDO:0011604","xrefs":{"Monarch":{"xref_id":"0011604"}}}


id: PBO:0055580
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 3016","termid":"PBO:0055580"}


id: GO:0051985
data:
  {"annotated_genes":["SJAG_01679","SJAG_01837","SJAG_04884","SJAG_00460","SJAG_03353","SJAG_03048","SJAG_00883","SJAG_03126","SJAG_02169","SJAG_01330","SJAG_03327","SJAG_03681","SJAG_02451","SJAG_01297","SJAG_01082","SJAG_04259","SJAG_04126","SJAG_04999","SJAG_01515","SJAG_02336","SJAG_04699"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[106784,99099,111544,113375,113868,90188,107814,103422,115502],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1902426"},{"annotations":[105867,114095],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905318"},{"annotations":[77147,116273],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033316"},{"annotations":[115159,114098,98941,109478,105869,101323],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007094"},{"annotations":[101889],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902424"},{"annotations":[98199],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902103"},{"annotations":[102807],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000816"},{"annotations":[93677],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0140499"},{"annotations":[113380],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1905326"},{"annotations":[116280],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0090267"},{"annotations":[100863],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1905325"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of chromosome segregation, the process in which genetic material, in the form of chromosomes, is organized and then physically separated and apportioned to two or more sets.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell cycle process","termid":"GO:0010948"},{"relation_name":"is_a","term_name":"regulation of chromosome segregation","termid":"GO:0051983"},{"relation_name":"negatively_regulates","term_name":"chromosome segregation","termid":"GO:0007059"}],"gene_count":21,"genes_by_uniquename":{"SJAG_00460":null,"SJAG_00883":null,"SJAG_01082":null,"SJAG_01297":null,"SJAG_01330":null,"SJAG_01515":null,"SJAG_01679":null,"SJAG_01837":null,"SJAG_02169":null,"SJAG_02336":null,"SJAG_02451":null,"SJAG_03048":null,"SJAG_03126":null,"SJAG_03327":null,"SJAG_03353":null,"SJAG_03681":null,"SJAG_04126":null,"SJAG_04259":null,"SJAG_04699":null,"SJAG_04884":null,"SJAG_04999":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"negative regulation of chromosome segregation","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of chromosome segregation","type":"exact"},{"name":"down-regulation of chromosome segregation","type":"exact"},{"name":"downregulation of chromosome segregation","type":"exact"},{"name":"inhibition of chromosome segregation","type":"narrow"}],"termid":"GO:0051985","terms_by_termid":{"GO:0007094":null,"GO:0033316":null,"GO:0090267":null,"GO:0140499":null,"GO:1902103":null,"GO:1902424":null,"GO:1902426":null,"GO:1905318":null,"GO:1905325":null,"GO:1905326":null,"GO:2000816":null}}


id: MOD:01285
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-leucine residue to 6x(13)C,1x(15)N isotope labeled L-leucine.","definition_xrefs":["Unimod:695#L","PubMed:12175151","PubMed:11857757","PubMed:11999733"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-leucine residue","termid":"MOD:00911"},{"relation_name":"is_a","term_name":"6x(13)C,1x(15)N labeled residue","termid":"MOD:01370"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"6x(13)C,1x(15)N labeled L-leucine","synonyms":[{"name":"13C(6) 15N(1) Silac label","type":"related"},{"name":"Label:13C(6)15N(1)","type":"related"}],"termid":"MOD:01285"}


id: MONDO:0043988
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Herpes zoster but without eruption of vesicles. Patients exhibit the characteristic pain minus the skin rash, sometimes making diagnosis difficult.","definition_xrefs":["MESH:D031368"],"direct_ancestors":[{"relation_name":"is_a","term_name":"herpes zoster","termid":"MONDO:0005609"}],"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":"zoster sine herpete","secondary_identifiers":["SCTID:449783002","MEDGEN:253902","UMLS:C1135841"],"synonyms":[{"name":"Zoster sine Eruptione","type":"related"},{"name":"zoster sine herpete","type":"exact"}],"termid":"MONDO:0043988","xrefs":{"Monarch":{"xref_id":"0043988"}}}


id: MONDO:1011099
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Alkaptonuria that occurs in rabbit.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alkaptonuria, non-human animal","termid":"MONDO:1010270"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alkaptonuria, rabbit","secondary_identifiers":["OMIA:001243-9986"],"termid":"MONDO:1011099","xrefs":{"Monarch":{"xref_id":"1011099"}}}


id: PBO:0047927
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(11)(p13)","termid":"PBO:0047927"}


id: FYPO:0006699
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 hercynylcysteine sulfoxide measured in a cell is lower than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased level of substance in cell during vegetative growth","termid":"FYPO:0001329"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"decreased cellular hercynylcysteine sulfoxide level during vegetative growth","synonyms":[{"name":"decreased cellular hercynylcysteine sulfoxide level during mitotic cell cycle","type":"related"},{"name":"decreased cellular hercynylcysteine sulphoxide level during vegetative growth","type":"exact"},{"name":"decreased hercynylcysteine sulfoxide level during vegetative growth","type":"exact"},{"name":"reduced cellular hercynylcysteine sulfoxide level during vegetative growth","type":"exact"}],"termid":"FYPO:0006699"}


id: PBO:0046353
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 11","termid":"PBO:0046353"}


id: MONDO:0001054
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"pterygium","termid":"MONDO:0005085"}],"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":"double pterygium","secondary_identifiers":["DOID:10525","MEDGEN:509817","SCTID:41564009","ICD9:372.44","UMLS:C0155157"],"termid":"MONDO:0001054","xrefs":{"Monarch":{"xref_id":"0001054"}}}


id: FYPO:0000434
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 fermentation is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular process during vegetative growth","termid":"FYPO:0001319"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001312","FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal fermentation","synonyms":[{"name":"fermentative metabolism: normal","type":"related"},{"name":"normal fermentation during mitotic cell cycle","type":"related"},{"name":"normal fermentation during vegetative growth","type":"exact"},{"name":"normal fermentative metabolism","type":"exact"}],"termid":"FYPO:0000434"}


id: FYPO:0000804
data:
  {"alleles_by_uniquename":{"SJAG_00426:allele-1":{"allele_type":"amino_acid_mutation","description":"P363S","gene_uniquename":"SJAG_00426","name":"bbl1-P363S","uniquename":"SJAG_00426:allele-1"},"SJAG_01242:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01242","name":"vps32delta","uniquename":"SJAG_01242:allele-1"},"SJAG_01745:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01745","name":"lem2delta","uniquename":"SJAG_01745:allele-1"},"SJAG_01906:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01906","name":"nem1delta","uniquename":"SJAG_01906:allele-1"},"SJAG_02763:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02763","name":"ned1delta","uniquename":"SJAG_02763:allele-1"},"SJAG_02763:allele-2":{"allele_type":"amino_acid_mutation","description":"D422E,D424E","gene_uniquename":"SJAG_02763","name":"ned1cat","synonyms":[{"name":"Catalytic mutant","reference":"PMID:26774782","type":"exact"}],"uniquename":"SJAG_02763:allele-2"},"SJAG_02763:allele-4":{"allele_type":"amino_acid_mutation","description":"S235E; S651E","gene_uniquename":"SJAG_02763","name":"ned1S235E/S651E","synonyms":[{"name":"phosphomimetic","reference":"PMID:26774782","type":"exact"}],"uniquename":"SJAG_02763:allele-4"},"SJAG_02763:allele-5":{"allele_type":"amino_acid_mutation","description":"S499E; S538E; T620E; T638E; S651E","gene_uniquename":"SJAG_02763","name":"ned1-5E","uniquename":"SJAG_02763:allele-5"},"SJAG_03449:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03449","name":"man1delta","uniquename":"SJAG_03449:allele-1"},"SJAG_03449:allele-2":{"allele_type":"partial_amino_acid_deletion","description":"man1DHEH","gene_uniquename":"SJAG_03449","name":"Man1DHEH","uniquename":"SJAG_03449:allele-2"},"SJAG_03449:allele-3":{"allele_type":"amino_acid_insertion_and_deletion","description":"man1-1-488","gene_uniquename":"SJAG_03449","name":"man1-1-488","uniquename":"SJAG_03449:allele-3"},"SJAG_03891:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03891","name":"alx1delta","uniquename":"SJAG_03891:allele-1"},"SJAG_03892:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03892","name":"vps4delta","uniquename":"SJAG_03892:allele-1"},"SJAG_03940:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03940","name":"nem2delta","uniquename":"SJAG_03940:allele-1"},"SJAG_04284:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04284","name":"nup61delta","uniquename":"SJAG_04284:allele-1"},"SJAG_04464:allele-1":{"allele_type":"amino_acid_mutation","description":"R152C","gene_uniquename":"SJAG_04464","name":"pim1-R152C","synonyms":[{"name":"Inferred CDK-phospho-mimic mutation","reference":"PMID:28954740","type":"exact"}],"uniquename":"SJAG_04464:allele-1"},"SJAG_05207:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_05207","name":"cmp7delta","uniquename":"SJAG_05207:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[119106,119029,119027,119022],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0003779"},{"annotations":[119156],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000815"},{"annotations":[119238],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0006433"},{"annotations":[118783,119080,118775,119107,118776,118782,119087,119079],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007772"},{"annotations":[119047,119056,119044,119045,119059],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0001784"},{"annotations":[119050,119046,119055,119043,119058,119042],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0001556"},{"annotations":[119150],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0003976"}]},"cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which endomembrane system organization is abnormal. 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S538E; T620E; T638E; S651E aa)","display_uniquename":"ned1-5E-S499E__S538E__T620E__T638E__S651E-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02763:allele-5","expression":"Not assayed or wild type"}]}]},"ned1S235E_S651E-S235E__S651E-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"ned1S235E/S651E(S235E; S651E aa)","display_uniquename":"ned1S235E_S651E-S235E__S651E-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02763:allele-4","expression":"Not assayed or wild type"}]}]},"ned1cat-D422E,D424E-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"ned1cat(D422E,D424E aa)","display_uniquename":"ned1cat-D422E,D424E-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02763:allele-2","expression":"Not assayed or wild type"}]}]},"ned1delta":{"display_name":"ned1delta","display_uniquename":"ned1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02763:allele-1","expression":"Null"}]}]},"nem1delta":{"display_name":"nem1delta","display_uniquename":"nem1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01906:allele-1","expression":"Null"}]}]},"nem2delta":{"display_name":"nem2delta","display_uniquename":"nem2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03940:allele-1","expression":"Null"}]}]},"nup61delta":{"display_name":"nup61delta","display_uniquename":"nup61delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04284:allele-1","expression":"Null"}]}]},"pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"pim1-R152C(aa)","display_uniquename":"pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04464:allele-1","expression":"Not assayed or wild type"}]}]},"vps32delta":{"display_name":"vps32delta","display_uniquename":"vps32delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01242:allele-1","expression":"Null"}]}]},"vps4delta":{"display_name":"vps4delta","display_uniquename":"vps4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03892:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"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:0005447","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"abnormal endomembrane system organization","references_by_uniquename":{"PMID:21802294":null,"PMID:24184107":null,"PMID:25318672":null,"PMID:26774782":null,"PMID:28954740":null,"PMID:32109380":null,"PMID:32243490":null},"single_locus_annotated_genes":["SJAG_05207","SJAG_04284","SJAG_01242","SJAG_00426","SJAG_03940","SJAG_04464","SJAG_02763","SJAG_01745","SJAG_03892","SJAG_03891","SJAG_01906","SJAG_03449"],"single_locus_genotype_uniquenames":["man1delta","vps32delta","ned1cat-D422E,D424E-amino_acid_mutation-expression-not_assayed_or_wild_type","lem2delta","nem2delta","nem1delta","cmp7delta","pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type","Man1DHEH-man1DHEH-partial_amino_acid_deletion-expression-not_assayed_or_wild_type","vps4delta","nup61delta","ned1delta","bbl1-P363S-P363S-amino_acid_mutation-expression-not_assayed_or_wild_type","man1-1-488-man1-1-488-amino_acid_insertion_and_deletion-expression-not_assayed_or_wild_type","alx1delta","ned1S235E_S651E-S235E__S651E-amino_acid_mutation-expression-not_assayed_or_wild_type","ned1-5E-S499E__S538E__T620E__T638E__S651E-amino_acid_mutation-expression-not_assayed_or_wild_type"],"synonyms":[{"name":"abnormal endomembrane system organisation","type":"exact"},{"name":"abnormal endomembrane system organization during mitotic cell cycle","type":"related"},{"name":"abnormal endomembrane system organization during vegetative growth","type":"exact"}],"termid":"FYPO:0000804","terms_by_termid":{"FYECO:0000004":null,"FYECO:0000005":null,"FYECO:0000137":null,"FYECO:0000162":null,"FYPO:0000815":null,"FYPO:0001556":null,"FYPO:0001784":null,"FYPO:0003779":null,"FYPO:0003976":null,"FYPO:0006433":null,"FYPO:0007772":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null,"FYPO_EXT:0000003":null}}


id: GO:0033945
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of cellobiose from the reducing end of xyloglucans consisting of a beta-(1->4) linked glucan carrying alpha-D-xylosyl groups on O-6 of the glucose residues. To be a substrate, the first residue must be unsubstituted, the second residue may bear a xylosyl group, whether further glycosylated or not, and the third residue, which becomes the new terminus by the action of the enzyme, is preferably xylosylated, but this xylose residue must not be further substituted.","definition_xrefs":["EC:3.2.1.150"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, hydrolyzing O-glycosyl compounds","termid":"GO:0004553"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016787","GO:0016798"],"is_obsolete":false,"name":"oligoxyloglucan reducing-end-specific cellobiohydrolase activity","secondary_identifiers":["MetaCyc:3.2.1.150-RXN"],"synonyms":[{"name":"oligoxyloglucan reducing end-specific cellobiohydrolase activity","type":"related"},{"name":"oligoxyloglucan reducing-end cellobiohydrolase activity","type":"related"}],"termid":"GO:0033945"}


id: PBO:0080699
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Wnt family member 5A","termid":"PBO:0080699"}


id: GO:0010743
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates 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:BHF","GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell differentiation","termid":"GO:0045595"},{"relation_name":"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":"regulation of macrophage derived foam cell differentiation","termid":"GO:0010743"}


id: MONDO:1011978
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":"central retinal degeneration, non-human animal","secondary_identifiers":["OMIA:000867"],"termid":"MONDO:1011978","xrefs":{"Monarch":{"xref_id":"1011978"}}}


id: MONDO:0008482
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"thoracic malformation","termid":"MONDO:0015929"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sprengel deformity","secondary_identifiers":["SCTID:79120002","MEDGEN:56291","NORD:1736","UMLS:C0152438","icd11.foundation:2144522441","MedDRA:10010455","OMIM:184400","Orphanet:3181","GARD:7693","MESH:C535802","HP:0000912"],"synonyms":[{"name":"Sprengel deformity","type":"exact"},{"name":"Sprengel deformity (disease)","type":"exact"},{"name":"Sprengel's deformity","type":"related"},{"name":"Sprengel's shoulder","type":"related"},{"name":"congenital elevation of the scapula","type":"related"},{"name":"congenital upward displacement of the scapula","type":"related"},{"name":"high scapula","type":"exact"}],"termid":"MONDO:0008482","xrefs":{"Monarch":{"xref_id":"0008482"}}}


id: PBO:0027111
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-incomplete_cell_wall_disassembly_at_cell_fusion_site","termid":"PBO:0027111"}


id: PBO:0031577
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_chromatin_organization","termid":"PBO:0031577"}


id: PR:P79081
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A diamine acetyltransferase 2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00741","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":"N-acetyltransferase ats1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1002.07c","secondary_identifiers":["UniProtKB:P79081"],"synonyms":[{"name":"Spom972h-SAT2","type":"exact"}],"termid":"PR:P79081"}


id: SO:0001624
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A UTR variant of the 3' UTR.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UTR_variant","termid":"SO:0001622"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3_prime_UTR_variant","secondary_identifiers":["http:www.ensembl.org/info/genome/variation/predicted_data.html#consequences","http://snp.gs.washington.edu/SeattleSeqAnnotation137/HelpHowToUse.jsp","http://snpeff.sourceforge.net/SnpEff_manual.html"],"synonyms":[{"name":"3'UTR variant","type":"exact"},{"name":"3PRIME_UTR","type":"exact"},{"name":"ANNOVAR:UTR3","type":"related"},{"name":"Jannovar:3_prime_utr_variant","type":"exact"},{"name":"Seattleseq:3-prime-UTR","type":"exact"},{"name":"VAAST:3_prime_UTR_variant","type":"exact"},{"name":"VAAST:three_prime_UTR_variant","type":"exact"},{"name":"VEP:3_prime_UTR_variant","type":"exact"},{"name":"snpEff:UTR_3_PRIME","type":"exact"},{"name":"three prime UTR variant","type":"exact"},{"name":"untranslated-3","type":"exact"}],"termid":"SO:0001624"}


id: FYPO:0004375
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to Ku-0063794. Cells stop growing (and may die) at a concentration of Ku-0063794 that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002683"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0001985","FYPO:0002683","FYPO:0000003","FYPO:0005447"],"is_obsolete":false,"name":"sensitive to Ku-0063794","synonyms":[{"name":"hypersensitive to Ku-0063794","type":"exact"},{"name":"sensitive to KU 0063794","type":"exact"},{"name":"sensitive to Ku-0063794 during mitotic cell cycle","type":"related"},{"name":"sensitive to Ku-0063794 during vegetative growth","type":"exact"}],"termid":"FYPO:0004375"}


id: PBO:0000647
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"40S ribosomal protein S3a (predicted)","termid":"PBO:0000647"}


id: GO:0019322
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of a pentose, any monosaccharide with a chain of five carbon atoms in the molecule.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pentose metabolic process","termid":"GO:0019321"},{"relation_name":"is_a","term_name":"monosaccharide biosynthetic process","termid":"GO:0046364"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0005975","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"pentose biosynthetic process","synonyms":[{"name":"pentose anabolism","type":"exact"},{"name":"pentose biosynthesis","type":"exact"},{"name":"pentose formation","type":"exact"},{"name":"pentose synthesis","type":"exact"}],"termid":"GO:0019322"}


id: GO:0036482
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals in which an intracellular signal is conveyed to trigger the apoptotic death of a neuron in response to hydrogen peroxide.","definition_xrefs":["GOC:bf","GOC:PARL"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuron intrinsic apoptotic signaling pathway in response to oxidative stress","termid":"GO:0036480"},{"relation_name":"is_a","term_name":"intrinsic apoptotic signaling pathway in response to hydrogen peroxide","termid":"GO:0036481"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"neuron intrinsic apoptotic signaling pathway in response to hydrogen peroxide","synonyms":[{"name":"H2O2-induced neuron intrinsic apoptotic signaling pathway","type":"exact"},{"name":"hydrogen peroxide-induced neuron apoptosis","type":"broad"},{"name":"hydrogen peroxide-induced neuronal apoptosis","type":"broad"},{"name":"neuron apoptosis in response to hydrogen peroxide","type":"related"},{"name":"neuron intrinsic apoptotic signaling pathway in response to H2O2","type":"exact"}],"termid":"GO:0036482"}


id: PR:O74807
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mhf1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74807"],"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":"MHF histone-fold complex subunit 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC2D10.16","synonyms":[{"name":"Spom972h-mhf1","type":"exact"}],"termid":"PR:O74807"}


id: FYPO:0001419
data:
  {"alleles_by_uniquename":{"SJAG_03360:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03360","name":"shc1delta","uniquename":"SJAG_03360:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[119226],"is_not":false,"summary":null,"term":"FYPO:0001419"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell population phenotype in which a population of cells grows at the same rate as wild type.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viable cell population","termid":"FYPO:0002058"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03360":null},"genotype_count":1,"genotypes_by_uniquename":{"shc1delta":{"display_name":"shc1delta","display_uniquename":"shc1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03360:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002057"}],"interesting_parent_ids":["FYPO:0002058","FYPO:0000003","FYPO:0002057"],"is_obsolete":false,"name":"normal cell population growth rate","references_by_uniquename":{"PMID:40195311":null},"single_locus_annotated_genes":["SJAG_03360"],"single_locus_genotype_uniquenames":["shc1delta"],"synonyms":[{"name":"normal cell population proliferation","type":"related"},{"name":"normal cell proliferation","type":"related"},{"name":"normal growth rate","type":"broad"}],"termid":"FYPO:0001419","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000137":null,"FYPO:0001419":null}}


id: PBO:0088332
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial thioredoxin family protein, implicated in sulfur cluster assembly","termid":"PBO:0088332"}


id: MOD:00631
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Chemical derivative","definition_xrefs":["Unimod:320"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reagent derivatized residue","termid":"MOD:00848"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hydrolyzed N-ethylmaleimide adduct","synonyms":[{"name":"Nethylmaleimide+water","type":"related"},{"name":"Nethylmaleimidehydrolysis","type":"related"}],"termid":"MOD:00631"}


id: PBO:0086571
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; YPR053C is not an essential gene; partially overlaps verified ORF NHP6A/YPR052C","termid":"PBO:0086571"}


id: PBO:0068761
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U5F small nuclear 6, pseudogene","termid":"PBO:0068761"}


id: PBO:0080987
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZBTB20 antisense RNA 3","termid":"PBO:0080987"}


id: PBO:0053898
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 1186","termid":"PBO:0053898"}


id: GO:0039588
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process by which a symbiont inhibits or disrupts the normal processing and presentation of a peptide antigen on its cell surface in association with an MHC protein complex.","definition_xrefs":["VZ:815"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated suppression of host adaptive immune response","termid":"GO:0039504"}],"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 antigen processing and presentation","synonyms":[{"name":"suppression by virus of host antigen processing and presentation","type":"narrow"}],"termid":"GO:0039588"}


id: GO:0016482
data:
  {"annotated_genes":["SJAG_00971","SJAG_04629","SJAG_01488","SJAG_02912","SJAG_04609","SJAG_00380","SJAG_01039","SJAG_02811","SJAG_00287","SJAG_04359","SJAG_03756","SJAG_00143","SJAG_03963","SJAG_00379","SJAG_06588","SJAG_02177","SJAG_01598","SJAG_04112","SJAG_01448","SJAG_04552","SJAG_01809","SJAG_04219","SJAG_02852","SJAG_05030","SJAG_01027","SJAG_02282","SJAG_02750","SJAG_02193","SJAG_03504","SJAG_02823","SJAG_04023","SJAG_04902","SJAG_04338","SJAG_04275","SJAG_04822","SJAG_02240","SJAG_00314","SJAG_00632","SJAG_03005","SJAG_04966","SJAG_04565","SJAG_02277","SJAG_01645"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[73268,114822],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034498"},{"annotations":[62221,75284,88613,79517,79491,99427,81562,99770,99828,100640,112594,116576,78634,118058],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006895"},{"annotations":[82095],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034499"},{"annotations":[79111,72774,100652,102192,98193,118129,72253,71710,81798,73343,77561,96649,63432,79293,91761,77747,112596,81416,73709,73308,79040,101658,112377,105075,65006,77881,94440,118517,97254,80478],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042147"}]},"cv_name":"biological_process","definition":"The directed movement of substances or organelles within the cytosol.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular transport","termid":"GO:0046907"}],"gene_count":43,"genes_by_uniquename":{"SJAG_00143":null,"SJAG_00287":null,"SJAG_00314":null,"SJAG_00379":null,"SJAG_00380":null,"SJAG_00632":null,"SJAG_00971":null,"SJAG_01027":null,"SJAG_01039":null,"SJAG_01448":null,"SJAG_01488":null,"SJAG_01598":null,"SJAG_01645":null,"SJAG_01809":null,"SJAG_02177":null,"SJAG_02193":null,"SJAG_02240":null,"SJAG_02277":null,"SJAG_02282":null,"SJAG_02750":null,"SJAG_02811":null,"SJAG_02823":null,"SJAG_02852":null,"SJAG_02912":null,"SJAG_03005":null,"SJAG_03504":null,"SJAG_03756":null,"SJAG_03963":null,"SJAG_04023":null,"SJAG_04112":null,"SJAG_04219":null,"SJAG_04275":null,"SJAG_04338":null,"SJAG_04359":null,"SJAG_04552":null,"SJAG_04565":null,"SJAG_04609":null,"SJAG_04629":null,"SJAG_04822":null,"SJAG_04902":null,"SJAG_04966":null,"SJAG_05030":null,"SJAG_06588":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"cytosolic transport","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0016482","terms_by_termid":{"GO:0006895":null,"GO:0034498":null,"GO:0034499":null,"GO:0042147":null}}


id: PBO:0091776
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"not functionally complemented by S. japonicus SJAG_02066.2","termid":"PBO:0091776"}


id: SO:0000263
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A tRNA sequence that has an isoleucine anticodon, and a 3' isoleucine binding region.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"derives_from","term_name":"isoleucine_tRNA_primary_transcript","termid":"SO:0000220"},{"relation_name":"is_a","term_name":"tRNA","termid":"SO:0000253"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"isoleucyl_tRNA","synonyms":[{"name":"isoleucyl tRNA","type":"exact"},{"name":"isoleucyl-transfer RNA","type":"exact"},{"name":"isoleucyl-transfer ribonucleic acid","type":"exact"}],"termid":"SO:0000263"}


id: PBO:0027958
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_pyridoxine:NADP_4-dehydrogenase_activity","termid":"PBO:0027958"}


id: PBO:0119992
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PTPRN2 antisense RNA 3","termid":"PBO:0119992"}


id: GO:0034304
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which differentiated, resting cells are formed from a substrate mycelium; characteristic of many members of the order Actinomycetales.","definition_xrefs":["GOC:ds","ISBN:0122268008"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reproductive process in single-celled organism","termid":"GO:0022413"},{"relation_name":"is_a","term_name":"asexual sporulation resulting in formation of a cellular spore","termid":"GO:0043936"}],"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":"actinomycete-type spore formation","termid":"GO:0034304"}


id: PBO:0084356
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Lectin-like protein involved in flocculation; cell wall protein that binds mannose chains on the surface of other cells, confers floc-forming ability that is chymotrypsin sensitive and heat resistant; important for co-flocculation with other yeasts, mediating interaction with specific species; FLO1 has a paralog, FLO5, that arose from a segmental duplication","termid":"PBO:0084356"}


id: GO:0090012
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents, or reduces the frequency, rate or extent of any TGF-beta receptor signaling pathway that contributes to the formation of the primitive streak.","definition_xrefs":["GOC:sdb_2009","GOC:tb","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of transforming growth factor beta receptor signaling pathway involved in primitive streak formation (obsolete GO:0090012)","synonyms":[{"name":"negative regulation of transforming growth factor beta receptor signalling pathway involved in primitive streak formation","type":"exact"}],"termid":"GO:0090012"}


id: MONDO:1012113
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"primary hypoadrenocorticism, non-human animal","termid":"MONDO:1011676"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primary hypoadrenocorticism, dog","secondary_identifiers":["OMIA:000520-9615"],"termid":"MONDO:1012113","xrefs":{"Monarch":{"xref_id":"1012113"}}}


id: GO:1990058
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the fruit replum over time, from its formation to the mature structure. The fruit replum is a portion of fruit placenta tissue that divides a fruit into two or more chambers and develops from a replum.","definition_xrefs":["PO:0025267","PMID:23133401"],"direct_ancestors":[{"relation_name":"is_a","term_name":"post-embryonic development","termid":"GO:0009791"},{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"fruit development","termid":"GO:0010154"}],"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":"fruit replum development","termid":"GO:1990058"}


id: GO:0010480
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process aimed at the progression of a microsporocyte cell over time, from initial commitment of the cell to a specific fate, to the fully functional differentiated cell. A microsporocyte is a diploid (2n) cell that undergoes meiosis and forms four haploid (1n) microspores; also called microspore mother cell and, in seed plants, pollen mother cell.","definition_xrefs":["PMID:16751349","CL:0000248"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"is_a","term_name":"sporocyte differentiation","termid":"GO:0048533"},{"relation_name":"part_of","term_name":"anther development","termid":"GO:0048653"}],"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":"microsporocyte differentiation","synonyms":[{"name":"pollen mother cell differentiation","type":"related"}],"termid":"GO:0010480"}


id: PBO:0057773
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 2276","termid":"PBO:0057773"}


id: PR:O74742
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A folylpolyglutamate synthase, mitochondrial that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","PANTHER:PTHR11136: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":"folylpolyglutamate synthase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1709.17","secondary_identifiers":["UniProtKB:O74742"],"synonyms":[{"name":"FPGS (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"SPBC1709.17","type":"related"},{"name":"Spom972h-FPGS","type":"exact"},{"name":"folylpoly-gamma-glutamate synthetase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"tetrahydrofolate synthase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"tetrahydrofolylpolyglutamate synthase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74742"}


id: GO:0052639
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: salicylic acid + UDP-glucose = salicylic acid glucose ester + UDP.","definition_xrefs":["RHEA:62316","MetaCyc:RXN-11659"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glucosyltransferase activity","termid":"GO:0035251"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016757"}],"interesting_parent_ids":["GO:0003674","GO:0016757","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"salicylic acid glucosyltransferase (ester-forming) activity","synonyms":[{"name":"UDP:glucose:2-hydroxybenzoic acid glucosyltransferase (ester-forming) activity","type":"exact"},{"name":"UDP:glucose:SA glucosyltransferase (ester-forming) activity","type":"exact"},{"name":"UDP:glucose:salicylate glucosyltransferase (ester-forming) activity","type":"exact"},{"name":"UDP:glucose:salicylic acid glucosyltransferase (ester-forming) activity","type":"exact"},{"name":"salicylic acid glucosyltransferase activity","type":"broad"}],"termid":"GO:0052639"}


id: GO:0061215
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a nephron in the mesonephros over time, from its formation to the mature structure. A nephron is the functional unit of the kidney.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nephron development","termid":"GO:0072006"},{"relation_name":"part_of","term_name":"mesonephros development","termid":"GO:0001823"}],"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":"mesonephric nephron development","termid":"GO:0061215"}


id: MONDO:0012838
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inflammatory bowel disease that has material basis in variation in the chromosome region 9q32.","definition_xrefs":["PMID:18587394","DOID:0110896"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inflammatory bowel disease","termid":"MONDO:0005265"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0004335"],"is_obsolete":false,"name":"inflammatory bowel disease 16","secondary_identifiers":["OMIM:612259","UMLS:C2677093","MEDGEN:383024","MESH:C567380"],"synonyms":[{"name":"IBD16","type":"exact"},{"name":"inflammatory bowel disease 16","type":"exact"},{"name":"inflammatory bowel disease type 16","type":"exact"}],"termid":"MONDO:0012838","xrefs":{"Monarch":{"xref_id":"0012838"}}}


id: PBO:0055767
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucyl and cystinyl aminopeptidase","termid":"PBO:0055767"}


id: PBO:0053102
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"late cornified envelope pseudogene 1","termid":"PBO:0053102"}


id: FYPO:0006361
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 dimethylation of lysine at position 9 of histone H3 in heterochromatin at subtelomeric regions occurs to a greater extent than normal.","definition_xrefs":["PomBase:mah","PMID:26438724","PMID:29214404"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased histone H3-K9 dimethylation during vegetative growth","termid":"FYPO:0000873"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0002494","FYPO:0001985","FYPO:0002274","FYPO:0000002"],"is_obsolete":false,"name":"increased histone H3-K9 dimethylation at subtelomeric heterochromatin during vegetative growth","synonyms":[{"name":"increased histone H3 K9 dimethylation at subtelomeric heterochromatin during vegetative growth","type":"exact"},{"name":"increased histone H3-K9 dimethylation at subtelomeres during vegetative growth","type":"exact"},{"name":"increased histone H3-K9 dimethylation at subtelomeric heterochromatin during mitotic cell cycle","type":"related"},{"name":"increased histone H3-K9 dimethylation at telomeric heterochromatin during vegetative growth","type":"related"},{"name":"increased histone H3K9me2 at subtelomeric heterochromatin during vegetative growth","type":"exact"},{"name":"increased histone lysine H3 K9 dimethylation at subtelomeric heterochromatin during vegetative growth","type":"exact"}],"termid":"FYPO:0006361"}


id: GO:1905809
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of synapse organization.","definition_xrefs":["GOC:TermGenie","PMID:27779093","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of synapse organization","termid":"GO:0050807"},{"relation_name":"is_a","term_name":"negative regulation of cellular component organization","termid":"GO:0051129"},{"relation_name":"negatively_regulates","term_name":"synapse organization","termid":"GO:0050808"}],"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 synapse organization","synonyms":[{"name":"down regulation of synapse development","type":"exact"},{"name":"down regulation of synapse morphogenesis","type":"related"},{"name":"down regulation of synapse organisation","type":"exact"},{"name":"down regulation of synapse organization","type":"exact"},{"name":"down regulation of synapse organization and biogenesis","type":"related"},{"name":"down-regulation of synapse development","type":"exact"},{"name":"down-regulation of synapse morphogenesis","type":"related"},{"name":"down-regulation of synapse organisation","type":"exact"},{"name":"down-regulation of synapse organization","type":"exact"},{"name":"down-regulation of synapse organization and biogenesis","type":"related"},{"name":"downregulation of synapse development","type":"exact"},{"name":"downregulation of synapse morphogenesis","type":"related"},{"name":"downregulation of synapse organisation","type":"exact"},{"name":"downregulation of synapse organization","type":"exact"},{"name":"downregulation of synapse organization and biogenesis","type":"related"},{"name":"inhibition of synapse development","type":"narrow"},{"name":"inhibition of synapse morphogenesis","type":"related"},{"name":"inhibition of synapse organisation","type":"narrow"},{"name":"inhibition of synapse organization","type":"narrow"},{"name":"inhibition of synapse organization and biogenesis","type":"related"},{"name":"negative regulation of synapse development","type":"exact"},{"name":"negative regulation of synapse morphogenesis","type":"related"},{"name":"negative regulation of synapse organisation","type":"exact"},{"name":"negative regulation of synapse organization and biogenesis","type":"related"}],"termid":"GO:1905809"}


id: PBO:0049233
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GRM5 antisense RNA 1","termid":"PBO:0049233"}


id: GO:1903843
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an arsenite ion stimulus.","definition_xrefs":["GOC:TermGenie","GOC:mr","PMID:12106899","GO_REF:0000071"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to arsenic-containing substance","termid":"GO:0071243"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"},{"relation_name":"is_a","term_name":"response to arsenite ion","termid":"GO:1903842"}],"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 arsenite ion","termid":"GO:1903843"}


id: MONDO:0100275
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any disorder of plasmalogen biosynthesis in which the cause of the disease is a mutation in the FAR1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of plasmalogens biosynthesis","termid":"MONDO:0017986"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0019053"},{"rel_name":"is_a","termid":"MONDO:0002525"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0019053","MONDO:0002525"],"is_obsolete":false,"name":"fatty acyl-CoA reductase defects","synonyms":[{"name":"FAR1 defect","type":"exact"},{"name":"fatty acyl-CoA reductase defects","type":"exact"}],"termid":"MONDO:0100275","xrefs":{"Monarch":{"xref_id":"0100275"}}}


id: MONDO:0008609
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":"Tristichiasis","secondary_identifiers":["UMLS:C1860785","MEDGEN:349889","OMIM:190800"],"synonyms":[{"name":"Tristichiasis","type":"exact"},{"name":"eyelashes, three rows of","type":"related"}],"termid":"MONDO:0008609","xrefs":{"Monarch":{"xref_id":"0008609"}}}


id: GO:0102687
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: UDP-alpha-D-glucose + dihydrozeatin = H+ + dihydrozeatin-7-N-glucose + UDP.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete UDP-glucose:dihydrozeatin 7-N-glucosyltransferase activity (obsolete GO:0102687)","termid":"GO:0102687"}


id: FYPO:0006737
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell population phenotype in which the proportion of cells in the population remains viable after entering stationary phase does not change in the presence of alpha-hibitakanine. Normally, wild-type cell populations survive longer in the presence of alpha-hibitakanine than in its absence.","definition_xrefs":["PomBase:mah","PMID:29900664"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell population phenotype","termid":"FYPO:0000003"},{"relation_name":"is_a","term_name":"abnormal phenotype","termid":"FYPO:0001985"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000003"],"is_obsolete":false,"name":"stationary phase viability unaffected by alpha-hibitakanine","synonyms":[{"name":"chronological lifespan unaffected by alpha-hibitakanine","type":"related"},{"name":"loss of chronological lifespan extension by alpha-hibitakanine","type":"related"},{"name":"loss of stationary phase viability extension in presence of alpha-hibitakanine","type":"exact"}],"termid":"FYPO:0006737"}


id: MONDO:0036688
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign mesenchymal tumor arising from skeletal or cardiac muscle.","definition_xrefs":["NCIT:C3358"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign muscle neoplasm","termid":"MONDO:0003061"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rhabdomyoma","secondary_identifiers":["MESH:D012207","UMLS:C0035411","icd11.foundation:1253205675","SCTID:402877008","MEDGEN:48445","ICDO:8900/0"],"synonyms":[{"name":"Rhabdomyomatous neoplasm","type":"exact"},{"name":"rhabdomyoma","type":"exact"},{"name":"rhabdomyoma, benign","type":"exact"}],"termid":"MONDO:0036688","xrefs":{"Monarch":{"xref_id":"0036688"}}}


id: PBO:0089033
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial Rieske ISP assembly ATPase Bcs1","termid":"PBO:0089033"}


id: MONDO:0056804
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"central nervous system organ benign neoplasm","termid":"MONDO:0000628"},{"relation_name":"is_a","term_name":"peripheral nervous system neoplasm","termid":"MONDO:0001406"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign neoplasm of peripheral nervous system","secondary_identifiers":["DOID:0080320","MEDGEN:199653","UMLS:C0751427"],"termid":"MONDO:0056804","xrefs":{"Monarch":{"xref_id":"0056804"}}}


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: MONDO:0850096
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spondylometaphyseal dysplasia","termid":"MONDO:0016763"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SBDS-related severe neonatal spondylometaphyseal dysplasia","secondary_identifiers":["UMLS:C5680412","GARD:22491","Orphanet:622934","MEDGEN:1843152"],"termid":"MONDO:0850096","xrefs":{"Monarch":{"xref_id":"0850096"}}}


id: PBO:0034140
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-in_1_to_many_homology_relationship_with","termid":"PBO:0034140"}


id: GO:0010177
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: acetyl-CoA + an omega-(methylsulfanyl)-2-oxoalkanoate + H2O = a 2-(omega-methylsulfanyl)alkylmalate + CoA + H+.","definition_xrefs":["RHEA:50624"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyltransferase activity, acyl groups converted into alkyl on transfer","termid":"GO:0046912"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016746"}],"interesting_parent_ids":["GO:0016746","GO:0003674","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"methylthioalkylmalate synthase activity","secondary_identifiers":["EC:2.3.3.17","MetaCyc:RXN-18197"],"synonyms":[{"name":"2-(2'-methylthio)ethylmalate synthase activity","type":"narrow"}],"termid":"GO:0010177"}


id: PR:O59669
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A zinc finger HIT domain-containing protein 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR13093:SF0","OMA:SCHPO03105","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":"SWR1 complex subunit vps71 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC29A3.05","secondary_identifiers":["UniProtKB:O59669"],"synonyms":[{"name":"Spom972h-ZNHIT1","type":"exact"}],"termid":"PR:O59669"}


id: GO:0042479
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of eye photoreceptor development.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell development","termid":"GO:0010720"},{"relation_name":"is_a","term_name":"regulation of eye photoreceptor cell development","termid":"GO:0042478"},{"relation_name":"is_a","term_name":"positive regulation of photoreceptor cell differentiation","termid":"GO:0046534"},{"relation_name":"positively_regulates","term_name":"eye photoreceptor cell development","termid":"GO:0042462"}],"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 eye photoreceptor cell development","synonyms":[{"name":"activation of eye photoreceptor cell development","type":"narrow"},{"name":"positive regulation of eye photoreceptor development","type":"exact"},{"name":"stimulation of eye photoreceptor cell development","type":"narrow"},{"name":"up regulation of eye photoreceptor cell development","type":"exact"},{"name":"up-regulation of eye photoreceptor cell development","type":"exact"},{"name":"upregulation of eye photoreceptor cell development","type":"exact"}],"termid":"GO:0042479"}


id: MONDO:0016253
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare cancer of corpus uteri (obsolete MONDO:0016253)","secondary_identifiers":["Orphanet:213569"],"synonyms":[{"name":"rare malignant tumor of corpus uteri","type":"exact"}],"termid":"MONDO:0016253","xrefs":{"Monarch":{"xref_id":"0016253"}}}


id: PBO:0057843
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3156-3","termid":"PBO:0057843"}


id: PBO:0052870
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin associated protein 5-14, pseudogene","termid":"PBO:0052870"}


id: GO:0004513
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: CMP-N-acetylneuraminate + beta-D-galactosyl-1,4-N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,4-beta-D-glucosylceramide = CMP + alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,4-N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,4-D-glucosylceramide.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete neolactotetraosylceramide alpha-2,3-sialyltransferase activity (obsolete GO:0004513)","synonyms":[{"name":"N-acetyllactosaminide alpha-2,3-sialyltransferase","type":"broad"},{"name":"alpha2->3 sialyltransferase activity","type":"related"},{"name":"neolactotetraosylceramide alpha-2,3-sialyltransferase","type":"related"}],"termid":"GO:0004513"}


id: GO:0014872
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process resulting in the physical partitioning and separation of a myoblast into daughter cells. A myoblast is a mononucleate cell type that, by fusion with other myoblasts, gives rise to the myotubes that eventually develop into skeletal muscle fibers.","definition_xrefs":["GOC:ef","CL:0000056","GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell division","termid":"GO:0051301"}],"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":"myoblast division","termid":"GO:0014872"}


id: PBO:0045050
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DLEC1 cilia and flagella associated protein","termid":"PBO:0045050"}


id: MONDO:0020434
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"atrial septal defect","termid":"MONDO:0006664"}],"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":"atrial septal defect, ostium secundum type","secondary_identifiers":["MedDRA:10031303","icd11.foundation:1875768490","MEDGEN:91034","UMLS:C0344724","NANDO:2200266","MedDRA:10031302","GARD:5865","Orphanet:99103"],"synonyms":[{"name":"ASD ostium secundum type","type":"related"},{"name":"ASD, ostium secundum type","type":"exact"},{"name":"osASD","type":"related"},{"name":"ostium secundum ASD","type":"related"},{"name":"ostium secundum atrial septal defect","type":"related"}],"termid":"MONDO:0020434","xrefs":{"Monarch":{"xref_id":"0020434"}}}


id: GO:0050169
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: peptide tryptophan + O2 = peptide formylkynurenine.","definition_xrefs":["PMID:4403729"],"gene_count":0,"genotype_count":0,"name":"obsolete peptide-tryptophan 2,3-dioxygenase activity (obsolete GO:0050169)","termid":"GO:0050169"}


id: GO:0046210
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of nitric oxide, nitrogen monoxide (NO), a colorless gas only slightly soluble in water.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catabolic process","termid":"GO:0009056"},{"relation_name":"is_a","term_name":"nitric oxide metabolic process","termid":"GO:0046209"}],"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":"nitric oxide catabolic process","synonyms":[{"name":"nitric oxide breakdown","type":"exact"},{"name":"nitric oxide catabolism","type":"exact"},{"name":"nitric oxide degradation","type":"exact"}],"termid":"GO:0046210"}


id: MONDO:0004704
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete peroxisomal disease (obsolete MONDO:0004704)","termid":"MONDO:0004704","xrefs":{"Monarch":{"xref_id":"0004704"}}}


id: PBO:0085837
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm and nucleus; protein abundance increases in response to DNA replication stress; YKR018C has a paralog, IML2, that arose from the whole genome duplication","termid":"PBO:0085837"}


id: PBO:0067902
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 204","termid":"PBO:0067902"}


id: GO:0004584
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the transfer of an alpha-D-mannosyl residue from dolichyl-phosphate D-mannose into membrane lipid-linked oligosaccharide.","definition_xrefs":["EC:2.4.1.130"],"gene_count":0,"genotype_count":0,"name":"obsolete dolichyl-phosphate-mannose-glycolipid alpha-mannosyltransferase activity (obsolete GO:0004584)","synonyms":[{"name":"dolichol phosphomannose-oligosaccharide-lipid mannosyltransferase activity","type":"related"},{"name":"dolichyl-phosphate-D-mannose:glycolipid alpha-D-mannosyltransferase activity","type":"related"},{"name":"oligomannosylsynthase activity","type":"broad"}],"termid":"GO:0004584"}


id: MONDO:0011839
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any cone-rod dystrophy in which the cause of the disease is a mutation in the RLBP1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cone-rod dystrophy","termid":"MONDO:0015993"},{"relation_name":"is_a","term_name":"RLBP1-related retinopathy","termid":"MONDO:0100444"}],"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":"Newfoundland cone-rod dystrophy","secondary_identifiers":["MEDGEN:334840","MESH:C564391","DOID:0111015","OMIM:607476","UMLS:C1843815"],"synonyms":[{"name":"NFRCD","type":"exact"},{"name":"Newfoundland ROD-cone dystrophy","type":"related"},{"name":"RLBP1 cone-rod dystrophy","type":"exact"},{"name":"cone-rod dystrophy caused by mutation in RLBP1","type":"exact"}],"termid":"MONDO:0011839","xrefs":{"Monarch":{"xref_id":"0011839"}}}


id: PBO:0044473
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome P450 family 11 subfamily B member 2","termid":"PBO:0044473"}


id: GO:0090143
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of the nucleoid. The nucleoid is the region of a bacterial cell, virion, mitochondrion or chloroplast to which the DNA is confined.","definition_xrefs":["GOC:ascb_2009","GOC:dph","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete nucleoid organization (obsolete GO:0090143)","synonyms":[{"name":"nucleoid organisation","type":"exact"}],"termid":"GO:0090143"}


id: GO:0000902
data:
  {"annotated_genes":["SJAG_04724","SJAG_01894","SJAG_00661","SJAG_02536","SJAG_00236","SJAG_04666","SJAG_03581","SJAG_00028","SJAG_00596","SJAG_02864","SJAG_00333","SJAG_02392","SJAG_01943","SJAG_00610","SJAG_03705","SJAG_04509","SJAG_02022","SJAG_01456","SJAG_01799","SJAG_02989","SJAG_02700","SJAG_02222","SJAG_00216","SJAG_00845","SJAG_00514","SJAG_02838","SJAG_01993","SJAG_01017","SJAG_00244","SJAG_03486","SJAG_04461","SJAG_03637","SJAG_04322","SJAG_02169","SJAG_04522"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89328,95341,94066],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0051519"},{"annotations":[93496,87340],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042815"},{"annotations":[117514,106406,116084,87505,99252,103016,110336],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0051523"},{"annotations":[98488,91988,113921,98406,87713,97794],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1904600"},{"annotations":[90191],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0051517"},{"annotations":[107167,116190],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:2000784"},{"annotations":[93218,99694,104901],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:2000247"},{"annotations":[103229],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0061361"},{"annotations":[114649],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0051516"},{"annotations":[119185,119186],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0008360"},{"annotations":[94072,112636,118417,104072,90611,95154],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:2000100"},{"annotations":[105659,102375,87349,91900],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:2000769"}]},"cv_name":"biological_process","definition":"The developmental process in which the size or shape of a cell is generated and organized.","definition_xrefs":["GOC:go_curators","GOC:tb","GOC:dph","GOC:clt"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"}],"gene_count":35,"genes_by_uniquename":{"SJAG_00028":null,"SJAG_00216":null,"SJAG_00236":null,"SJAG_00244":null,"SJAG_00333":null,"SJAG_00514":null,"SJAG_00596":null,"SJAG_00610":null,"SJAG_00661":null,"SJAG_00845":null,"SJAG_01017":null,"SJAG_01456":null,"SJAG_01799":null,"SJAG_01894":null,"SJAG_01943":null,"SJAG_01993":null,"SJAG_02022":null,"SJAG_02169":null,"SJAG_02222":null,"SJAG_02392":null,"SJAG_02536":null,"SJAG_02700":null,"SJAG_02838":null,"SJAG_02864":null,"SJAG_02989":null,"SJAG_03486":null,"SJAG_03581":null,"SJAG_03637":null,"SJAG_03705":null,"SJAG_04322":null,"SJAG_04461":null,"SJAG_04509":null,"SJAG_04522":null,"SJAG_04666":null,"SJAG_04724":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cell morphogenesis","references_by_uniquename":{"GO_REF:0000107":null,"PMID:30664646":null},"secondary_identifiers":["GO:0045790","GO:0045791","GO:0007148"],"synonyms":[{"name":"cellular morphogenesis","type":"exact"}],"termid":"GO:0000902","terms_by_termid":{"GO:0008360":null,"GO:0042815":null,"GO:0051516":null,"GO:0051517":null,"GO:0051519":null,"GO:0051523":null,"GO:0061361":null,"GO:1904600":null,"GO:2000100":null,"GO:2000247":null,"GO:2000769":null,"GO:2000784":null}}


id: GO:0003160
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structure of the endocardium is generated and organized. The endocardium is an anatomical structure comprised of an endothelium and an extracellular matrix that forms the innermost layer of tissue of the heart, and lines the heart chambers.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"},{"relation_name":"part_of","term_name":"endocardium development","termid":"GO:0003157"}],"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":"endocardium morphogenesis","termid":"GO:0003160"}


id: PBO:0066131
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ras association domain family member 9","termid":"PBO:0066131"}


id: MONDO:1010024
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Atrial fibrillation that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heart disorder, non-human animal","termid":"MONDO:1012982"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"atrial fibrillation, non-human animal","secondary_identifiers":["OMIA:001181"],"termid":"MONDO:1010024","xrefs":{"Monarch":{"xref_id":"1010024"}}}


id: SO:0000700
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A comment about the sequence.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"experimental_feature","termid":"SO:0001410"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"remark","termid":"SO:0000700"}


id: PBO:0036164
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-mitotic_spindle_elongation_without_chromosome_separation_with_centromeric_DNA_associated_with_spindle","termid":"PBO:0036164"}


id: GO:1900557
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of emericellamide.","definition_xrefs":["GOC:TermGenie","GOC:di"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipid biosynthetic process","termid":"GO:0008610"},{"relation_name":"is_a","term_name":"secondary metabolite biosynthetic process","termid":"GO:0044550"},{"relation_name":"is_a","term_name":"depsipeptide biosynthetic process","termid":"GO:0050763"},{"relation_name":"is_a","term_name":"lactam biosynthetic process","termid":"GO:0072339"},{"relation_name":"is_a","term_name":"emericellamide metabolic process","termid":"GO:1900555"},{"relation_name":"is_a","term_name":"lactone biosynthetic process","termid":"GO:1901336"}],"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"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0019748","GO:0008150","GO:0006629","GO:0044281"],"is_obsolete":false,"name":"emericellamide biosynthetic process","synonyms":[{"name":"emericellamide anabolism","type":"exact"},{"name":"emericellamide biosynthesis","type":"exact"},{"name":"emericellamide formation","type":"exact"},{"name":"emericellamide synthesis","type":"exact"}],"termid":"GO:1900557"}


id: PBO:0046878
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 8 member A3, pseudogene","termid":"PBO:0046878"}


id: GO:0016888
data:
  {"annotated_genes":["SJAG_01832","SJAG_03994","SJAG_01648","SJAG_04183","SJAG_05237","SJAG_01173"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[73032,76325,77365,80250,67758,74531],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017108"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of ester linkages within deoxyribonucleic acids by creating internal breaks to yield 5'-phosphomonoesters.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA endonuclease activity","termid":"GO:0004520"},{"relation_name":"is_a","term_name":"hydrolase activity, acting on ester bonds","termid":"GO:0016788"}],"gene_count":6,"genes_by_uniquename":{"SJAG_01173":null,"SJAG_01648":null,"SJAG_01832":null,"SJAG_03994":null,"SJAG_04183":null,"SJAG_05237":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140097"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003824","GO:0140097","GO:0016788","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"DNA endonuclease activity, producing 5'-phosphomonoesters","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null},"secondary_identifiers":["EC:3.1.21.-","Reactome:R-HSA-912368"],"synonyms":[{"name":"endodeoxyribonuclease activity, producing 5' phosphomonoesters","type":"exact"},{"name":"endodeoxyribonuclease activity, producing 5'-phosphomonoesters","type":"exact"}],"termid":"GO:0016888","terms_by_termid":{"GO:0017108":null}}


id: PATO:0000487
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A response quality inhering in a bearer by virtue of the bearer's disposition to react to a stimulus or an agent.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to","termid":"PATO:0000077"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"responsive to","synonyms":[{"name":"responsive","type":"exact"}],"termid":"PATO:0000487"}


id: GO:0047422
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: N-acyl-D-aspartate + H2O = D-aspartate + a carboxylate.","definition_xrefs":["RHEA:18285","EC:3.5.1.83"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides","termid":"GO:0016811"}],"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:0016810"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016787","GO:0003674","GO:0003824","GO:0016810"],"is_obsolete":false,"name":"N-acyl-D-aspartate deacylase activity","secondary_identifiers":["KEGG_REACTION:R02182","MetaCyc:3.5.1.83-RXN"],"synonyms":[{"name":"N-acyl-D-aspartate amidohydrolase activity","type":"related"}],"termid":"GO:0047422"}


id: MONDO:0033015
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"erythrokeratodermia variabilis","termid":"MONDO:0017851"}],"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":"erythrokeratodermia variabilis et progressiva 5","secondary_identifiers":["UMLS:C4540331","OMIM:617756","DOID:0080251","MEDGEN:1626376","GARD:18669"],"synonyms":[{"name":"EKVP5","type":"related"},{"name":"erythrokeratodermia variabilis ET progressiva 5","type":"related"}],"termid":"MONDO:0033015","xrefs":{"Monarch":{"xref_id":"0033015"}}}


id: PBO:0001104
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptionally regulated by ammonia","termid":"PBO:0001104"}


id: PBO:0092039
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sulfonate/alpha-ketoglutarate dioxygenase","termid":"PBO:0092039"}


id: GO:0008519
data:
  {"annotated_genes":["SJAG_04136","SJAG_04731"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[71583,77129],"is_not":false,"summary":null,"term":"GO:0008519"}]},"cv_name":"molecular_function","definition":"Enables the energy-independent facilitated diffusion of ammonium through a transmembrane aqueous pore or channel.","definition_xrefs":["PMID:17710640"],"direct_ancestors":[{"relation_name":"is_a","term_name":"channel activity","termid":"GO:0015267"},{"relation_name":"is_a","term_name":"inorganic cation transmembrane transporter activity","termid":"GO:0022890"}],"gene_count":2,"genes_by_uniquename":{"SJAG_04136":null,"SJAG_04731":null},"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":"ammonium channel activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["GO:0051739","Reactome:R-HSA-446277","Reactome:R-HSA-446278","Reactome:R-HSA-5623051","Reactome:R-HSA-444419","Reactome:R-HSA-444416","TC:1.A.11","GO:0015251","MetaCyc:RXN-9615","Reactome:R-HSA-444393"],"synonyms":[{"name":"ammonia transmembrane transporter activity","type":"broad"},{"name":"ammonium transmembrane transporter activity","type":"broad"}],"termid":"GO:0008519","terms_by_termid":{"GO:0008519":null}}


id: PBO:0090920
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"guanylate kinase Guk1","termid":"PBO:0090920"}


id: GO:0002846
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of T cell tolerance induction to tumor cell.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of T cell mediated immune response to tumor cell","termid":"GO:0002840"},{"relation_name":"is_a","term_name":"regulation of tolerance induction to tumor cell","termid":"GO:0002843"},{"relation_name":"is_a","term_name":"regulation of peripheral T cell tolerance induction","termid":"GO:0002849"},{"relation_name":"regulates","term_name":"T cell tolerance induction to tumor cell","termid":"GO:0002411"}],"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 T cell tolerance induction to tumor cell","termid":"GO:0002846"}


id: MONDO:0018304
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, underdiagnosed disorder in adults characterized by recurrent febrile rash, bone and/or joint pain, enlarged lymph nodes, fatigue, a monoclonal IgM component, leukocytosis and systemic inflammatory response.","definition_xrefs":["Orphanet:37748"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"type IV hypersensitivity disease","termid":"MONDO:0002459"},{"relation_name":"excluded_subClassOf","term_name":"urticaria","termid":"MONDO:0005492"},{"relation_name":"excluded_subClassOf","term_name":"unexplained periodic fever syndrome","termid":"MONDO:0015158"},{"relation_name":"is_a","term_name":"autoinflammatory syndrome","termid":"MONDO:0019751"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schnitzler syndrome","secondary_identifiers":["SCTID:402415001","MedDRA:10062908","DOID:4371","UMLS:C0524988","NORD:1696","MEDGEN:141892","icd11.foundation:1867840545","ICD9:708.8","MESH:D019873","EFO:1001165","GARD:12390"],"synonyms":[{"name":"chronic urticaria with gammapathy","type":"related"},{"name":"chronic urticaria with gammopathy","type":"exact"},{"name":"chronic urticaria with macroglobulinemia","type":"exact"}],"termid":"MONDO:0018304","xrefs":{"Monarch":{"xref_id":"0018304"}}}


id: GO:0035259
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a nuclear glucocorticoid receptor.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear receptor binding","termid":"GO:0016922"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"nuclear glucocorticoid receptor binding","synonyms":[{"name":"glucocorticoid receptor binding","type":"broad"}],"termid":"GO:0035259"}


id: GO:0050055
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: limonoate D-ring-lactone + H2O = limonoate.","definition_xrefs":["EC:3.1.1.36","MetaCyc:LIMONIN-D-RING-LACTONASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxylic ester hydrolase activity","termid":"GO:0052689"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016788","GO:0016787"],"is_obsolete":false,"name":"limonin-D-ring-lactonase activity","secondary_identifiers":["RHEA:10896"],"synonyms":[{"name":"limonin lactone hydrolase activity","type":"related"},{"name":"limonin-D-ring-lactone hydrolase activity","type":"related"},{"name":"limonoate-D-ring-lactone lactonohydrolase activity","type":"related"}],"termid":"GO:0050055"}


id: GO:0009888
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a tissue over time, from its formation to the mature structure.","definition_xrefs":["ISBN:0471245208"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"}],"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":"tissue development","secondary_identifiers":["Wikipedia:Histogenesis"],"synonyms":[{"name":"histogenesis","type":"exact"},{"name":"histogenesis and organogenesis","type":"broad"}],"termid":"GO:0009888"}


id: PBO:0060570
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NBPF member 6","termid":"PBO:0060570"}


id: MONDO:0012680
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any nephronophthisis in which the cause of the disease is a mutation in the GLIS2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nephronophthisis","termid":"MONDO:0019005"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0005240","MONDO:0006025"],"is_obsolete":false,"name":"nephronophthisis 7","secondary_identifiers":["DOID:0111116","MEDGEN:369409","OMIM:611498","UMLS:C1969092","MESH:C566930"],"synonyms":[{"name":"GLIS2 nephronophthisis (disease)","type":"exact"},{"name":"NPHP7","type":"exact"},{"name":"nephronophthisis (disease) caused by mutation in GLIS2","type":"exact"},{"name":"nephronophthisis 7","type":"exact"},{"name":"nephronophthisis type 7","type":"exact"}],"termid":"MONDO:0012680","xrefs":{"Monarch":{"xref_id":"0012680"}}}


id: GO:0070014
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that possesses oligo-1,6-glucosidase activity; the complex is a heterodimer located in the cell membrane, and is formed by proteolytic cleavage of a single precursor polypeptide. The two subunits have different substrate specificities.","definition_xrefs":["PMID:3366777"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"},{"relation_name":"is_a","term_name":"glucosidase complex","termid":"GO:1902687"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005886","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"sucrase-isomaltase complex","secondary_identifiers":["Wikipedia:Sucrase-isomaltase"],"synonyms":[{"name":"oligo-1,6-glucosidase complex","type":"related"}],"termid":"GO:0070014"}


id: MONDO:0019362
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A gram-negative bacterial infection caused by Rickettsia prowazekii. It is spread by lice infected with the bacteria. Signs and symptoms include sudden headache, generalized muscle pain, malaise, and macular skin lesions. The infection may affect the central nervous system causing encephalitis.","definition_xrefs":["NCIT:C84689"],"direct_ancestors":[{"relation_name":"is_a","term_name":"typhus","termid":"MONDO:0001246"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"epidemic louse-borne typhus","secondary_identifiers":["Orphanet:83314","DOID:0050480","icd11.foundation:295798687","UMLS:C0041473","GARD:19032","MEDGEN:21744","MedDRA:10014979"],"synonyms":[{"name":"epidemic louse-borne typhus","type":"exact"},{"name":"epidemic typhus","type":"exact"},{"name":"epidemic typhus fever","type":"exact"},{"name":"sylvatic typhus","type":"exact"},{"name":"typhus","type":"broad"}],"termid":"MONDO:0019362","xrefs":{"Monarch":{"xref_id":"0019362"}}}


