# terms

id: PBO:0054722
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 2131","termid":"PBO:0054722"}


id: FYPO:0000431
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 does not occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal fermentation","termid":"FYPO:0000430"},{"relation_name":"is_a","term_name":"abolished cellular process","termid":"FYPO:0005449"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"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:0000002","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"abolished fermentation","synonyms":[{"name":"abolished fermentation during mitotic cell cycle","type":"related"},{"name":"absent fermentative metabolism","type":"exact"},{"name":"fermentation abolished","type":"exact"},{"name":"fermentation abolished during vegetative growth","type":"exact"},{"name":"fermentative metabolism abolished","type":"exact"},{"name":"fermentative metabolism: absent","type":"related"}],"termid":"FYPO:0000431"}


id: PBO:0026669
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_meiotic_cell_cycle_phase_transition","termid":"PBO:0026669"}


id: PATO:0001004
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001004 absolute alternation value (obsolete PATO:0001004)","termid":"PATO:0001004"}


id: GO:0030887
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stimulates, induces or increases the rate of myeloid dendritic cell activation.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of leukocyte activation","termid":"GO:0002696"},{"relation_name":"is_a","term_name":"regulation of myeloid dendritic cell activation","termid":"GO:0030885"},{"relation_name":"positively_regulates","term_name":"myeloid dendritic cell activation","termid":"GO:0001773"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of myeloid dendritic cell activation","synonyms":[{"name":"activation of myeloid dendritic cell activation","type":"narrow"},{"name":"stimulation of myeloid dendritic cell activation","type":"narrow"},{"name":"up regulation of myeloid dendritic cell activation","type":"exact"},{"name":"up-regulation of myeloid dendritic cell activation","type":"exact"},{"name":"upregulation of myeloid dendritic cell activation","type":"exact"}],"termid":"GO:0030887"}


id: PBO:0056221
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAGE family member D1","termid":"PBO:0056221"}


id: PBO:0080215
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vimentin","termid":"PBO:0080215"}


id: PBO:0061836
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"opioid growth factor receptor","termid":"PBO:0061836"}


id: GO:0050680
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the rate or extent of epithelial cell proliferation.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell population proliferation","termid":"GO:0008285"},{"relation_name":"is_a","term_name":"regulation of epithelial cell proliferation","termid":"GO:0050678"},{"relation_name":"negatively_regulates","term_name":"epithelial cell proliferation","termid":"GO:0050673"}],"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 epithelial cell proliferation","synonyms":[{"name":"down regulation of epithelial cell proliferation","type":"exact"},{"name":"down-regulation of epithelial cell proliferation","type":"exact"},{"name":"downregulation of epithelial cell proliferation","type":"exact"},{"name":"inhibition of epithelial cell proliferation","type":"narrow"}],"termid":"GO:0050680"}


id: GO:1904942
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cardiac ventricle formation.","definition_xrefs":["PMID:23575307","GO_REF:0000058","GOC:TermGenie","GOC:bc","GOC:BHF","GOC:BHF_miRNA"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cardiac chamber formation","termid":"GO:1901210"},{"relation_name":"regulates","term_name":"cardiac ventricle formation","termid":"GO:0003211"}],"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 cardiac ventricle formation","termid":"GO:1904942"}


id: PBO:0054451
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 1848","termid":"PBO:0054451"}


id: PBO:0086493
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative phosphatidylinositol/phosphatidylcholine transfer protein; possibly involved in lipid metabolism; localizes to the nucleus; contains a CRAL/TRIO domain and binds several lipids in a large-scale study; YKL091C has a paralog, SEC14, that arose from the whole genome duplication","termid":"PBO:0086493"}


id: PBO:0028701
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_level_during_meiosis","termid":"PBO:0028701"}


id: MONDO:1010963
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cystic hygroma that occurs in pig.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cystic hygroma, non-human animal","termid":"MONDO:1010225"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cystic hygroma, pig","secondary_identifiers":["OMIA:002369-9823"],"termid":"MONDO:1010963","xrefs":{"Monarch":{"xref_id":"1010963"}}}


id: MONDO:0014020
data:
  {"annotated_genes":["SJAG_00308"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87117],"is_not":false,"summary":null,"term":"MONDO:0014020"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"complex hereditary spastic paraplegia","termid":"MONDO:0015150"},{"relation_name":"is_a","term_name":"mitochondrial oxidative phosphorylation disorder","termid":"MONDO:0016387"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00308":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0005066","MONDO:0004069"],"is_obsolete":false,"name":"hereditary spastic paraplegia 55","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:320375","MEDGEN:761342","OMIM:615035","GARD:17474","SCTID:723825006","DOID:0110807","UMLS:C3539506"],"synonyms":[{"name":"SPG55","type":"exact"},{"name":"autosomal recessive spastic paraplegia 55","type":"exact"},{"name":"autosomal recessive spastic paraplegia type 55","type":"exact"},{"name":"hereditary spastic paraplegia type 55","type":"exact"},{"name":"spastic paraplegia 55, autosomal recessive","type":"related"}],"termid":"MONDO:0014020","terms_by_termid":{"MONDO:0014020":null},"xrefs":{"Monarch":{"xref_id":"0014020"}}}


id: PBO:0069901
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1192, pseudogene","termid":"PBO:0069901"}


id: GO:0106146
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of sideretin.","definition_xrefs":["PMID:29581584","GOC:lr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"coumarin biosynthetic process","termid":"GO:0009805"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0019748","GO:0008150"],"is_obsolete":false,"name":"sideretin biosynthesis","termid":"GO:0106146"}


id: MONDO:0020497
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Turcot syndrome with polyposis or Turcot syndrome type 2 is a form of familial adematous polyposis, characterized by the concurrence of thousands of colonic adenomatous polyposis or colorectal cancer (CRC) and a primary central nervous system tumor (principally medulloblastoma). It is also associated with pigmented ocular fundus lesions.","definition_xrefs":["Orphanet:99818"],"direct_ancestors":[{"relation_name":"is_a","term_name":"classic familial adenomatous polyposis","termid":"MONDO:0021055"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Turcot syndrome with polyposis","secondary_identifiers":["icd11.foundation:813602368","MEDGEN:1826134","NCIT:C40464","GARD:16912","UMLS:C5681818"],"termid":"MONDO:0020497","xrefs":{"Monarch":{"xref_id":"0020497"}}}


id: GO:0055114
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A metabolic process that results in the removal or addition of one or more electrons to or from a substance, with or without the concomitant removal or addition of a proton or protons.","definition_xrefs":["GOC:rph","GOC:dhl","GOC:mlg","GOC:ecd","GOC:jh2","GOC:jid"],"gene_count":0,"genotype_count":0,"name":"obsolete oxidation-reduction process (obsolete GO:0055114)","synonyms":[{"name":"oxidation reduction","type":"exact"},{"name":"oxidoreductase process","type":"exact"}],"termid":"GO:0055114"}


id: MONDO:0009334
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary elliptocytosis","termid":"MONDO:0017319"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0002280"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0002280"],"is_obsolete":false,"name":"hemolytic anemia with thermal sensitivity of red cells","secondary_identifiers":["GARD:15179","OMIM:235370","MEDGEN:343488","UMLS:C1856158","MESH:C565522"],"synonyms":[{"name":"hemolytic anemia with thermal sensitivity of red cells","type":"exact"}],"termid":"MONDO:0009334","xrefs":{"Monarch":{"xref_id":"0009334"}}}


id: GO:0019389
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways involving glucuronosides, any compound formed by combination in glycosidic linkage of a hydroxy compound with the anomeric carbon atom of a glucuronate.","definition_xrefs":["ISBN:0198506732"],"gene_count":0,"genotype_count":0,"name":"obsolete glucuronoside metabolic process (obsolete GO:0019389)","synonyms":[{"name":"glucuronide metabolic process","type":"exact"},{"name":"glucuronide metabolism","type":"exact"},{"name":"glucuronoside metabolism","type":"exact"}],"termid":"GO:0019389"}


id: GO:0047910
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-galactose + NADP+ = D-galactonolactone + NADPH.","definition_xrefs":["EC:1.1.1.120","MetaCyc:GALACTOSE-1-DEHYDROGENASE-NADP+-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"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:0003824","GO:0003674"],"is_obsolete":false,"name":"galactose 1-dehydrogenase (NADP+) activity","secondary_identifiers":["RHEA:18625"],"synonyms":[{"name":"D-galactose dehydrogenase (NADP+)","type":"related"},{"name":"D-galactose:NADP+ 1-oxidoreductase activity","type":"related"}],"termid":"GO:0047910"}


id: PBO:0041143
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"basic transcription factor 3 like 4 pseudogene 2","termid":"PBO:0041143"}


id: GO:0032391
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The portion of the photoreceptor cell cilium linking the photoreceptor inner and outer segments. It's considered to be equivalent to the ciliary transition zone.","definition_xrefs":["PMID:22653444","PMID:8718680","GOC:cilia","PMID:15917207"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ciliary transition zone","termid":"GO:0035869"},{"relation_name":"part_of","term_name":"photoreceptor cell cilium","termid":"GO:0097733"}],"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":"photoreceptor connecting cilium","synonyms":[{"name":"photoreceptor cilium","type":"related"}],"termid":"GO:0032391"}


id: MONDO:0859295
data:
  {"annotated_genes":["SJAG_02467"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87605],"is_not":false,"summary":null,"term":"MONDO:0859295"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02467":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1824001","UMLS:C5774228","DOID:0070479","OMIM:620070"],"termid":"MONDO:0859295","terms_by_termid":{"MONDO:0859295":null},"xrefs":{"Monarch":{"xref_id":"0859295"}}}


id: PBO:0036434
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Counteracter of CENP-A loading Protein","termid":"PBO:0036434"}


id: MONDO:0019782
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"synostosis","termid":"MONDO:0001411"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"humero-ulnar synostosis","secondary_identifiers":["Orphanet:94056","icd11.foundation:2144695561","UMLS:C0431799","MEDGEN:451053","GARD:19244"],"synonyms":[{"name":"humero-ulnar fusion","type":"exact"}],"termid":"MONDO:0019782","xrefs":{"Monarch":{"xref_id":"0019782"}}}


id: PBO:0087681
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the mitochondrial (mt) i-AAA protease supercomplex; i-AAA degrades misfolded mitochondrial proteins; forms a subcomplex with Mgr3p that binds to substrates to facilitate proteolysis; required for growth of cells lacking mtDNA","termid":"PBO:0087681"}


id: PBO:0031738
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_mating_type_switching","termid":"PBO:0031738"}


id: PBO:0075130
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nuclear ribonucleoprotein U11/U12 subunit 35","termid":"PBO:0075130"}


id: MONDO:0012660
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"visceral leishmaniasis","termid":"MONDO:0005445"},{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"susceptibility to visceral leishmaniasis, 2","secondary_identifiers":["UMLS:C1969649","MEDGEN:409879","OMIM:611381"],"synonyms":[{"name":"KAZA2","type":"related"},{"name":"kala-AZAR, susceptibility to, 2","type":"related"},{"name":"leishmaniasis, visceral, susceptibility to, 2","type":"related"}],"termid":"MONDO:0012660","xrefs":{"Monarch":{"xref_id":"0012660"}}}


id: GO:0050967
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events that contribute to the perception of pain in which an electrical stimulus is received and converted into a molecular signal.","definition_xrefs":["GOC:ai","GOC:dos","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detection of electrical stimulus involved in sensory perception","termid":"GO:0050963"},{"relation_name":"is_a","term_name":"detection of stimulus involved in sensory perception of pain","termid":"GO:0062149"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"detection of electrical stimulus involved in sensory perception of pain","synonyms":[{"name":"detection of electrical stimulus during sensory perception of pain","type":"related"},{"name":"perception of pain, detection of electrical stimulus","type":"exact"},{"name":"perception of pain, sensory detection of electrical stimulus","type":"exact"},{"name":"perception of pain, sensory transduction of electrical stimulus","type":"exact"},{"name":"sensory detection of electrical stimulus during perception of pain","type":"related"},{"name":"sensory transduction of electrical stimulus during perception of pain","type":"related"}],"termid":"GO:0050967"}


id: PBO:0015680
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translation initiation factor eIF4E, 4F complex E subunit isoform 2, stress response factor","termid":"PBO:0015680"}


id: SO:0002164
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A kind of histone modification site, whereby the 5th residue (a lysine), from the start of the H2B histone protein is acetylated.","definition_xrefs":["PMID:18552846"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone_2B_acetylation_site","termid":"SO:0002143"}],"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":"H2BK5_acetylation_site","synonyms":[{"name":"H2BK5 acetylation site","type":"exact"},{"name":"H2BK5ac","type":"exact"}],"termid":"SO:0002164"}


id: GO:0150077
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of neuroinflammatory response.","definition_xrefs":["PMID:18164423","GOC:bc","GOC:aruk","PMID:11099416","PMID:10981966"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of inflammatory response","termid":"GO:0050727"},{"relation_name":"regulates","term_name":"neuroinflammatory response","termid":"GO:0150076"}],"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 neuroinflammatory response","termid":"GO:0150077"}


id: GO:1901220
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of cardiac chamber morphogenesis.","definition_xrefs":["GOC:TermGenie","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of developmental process","termid":"GO:0051093"},{"relation_name":"is_a","term_name":"regulation of cardiac chamber morphogenesis","termid":"GO:1901219"},{"relation_name":"negatively_regulates","term_name":"cardiac chamber morphogenesis","termid":"GO:0003206"}],"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 cardiac chamber morphogenesis","synonyms":[{"name":"down regulation of cardiac chamber morphogenesis","type":"exact"},{"name":"down regulation of heart chamber morphogenesis","type":"exact"},{"name":"down-regulation of cardiac chamber morphogenesis","type":"exact"},{"name":"down-regulation of heart chamber morphogenesis","type":"exact"},{"name":"downregulation of cardiac chamber morphogenesis","type":"exact"},{"name":"downregulation of heart chamber morphogenesis","type":"exact"},{"name":"inhibition of cardiac chamber morphogenesis","type":"narrow"},{"name":"inhibition of heart chamber morphogenesis","type":"narrow"},{"name":"negative regulation of heart chamber morphogenesis","type":"exact"}],"termid":"GO:1901220"}


id: PBO:0034586
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_protein_localization_to_cell_tip_during_mitosis","termid":"PBO:0034586"}


id: PBO:0048947
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GOT1 divergent transcript","termid":"PBO:0048947"}


id: MONDO:0023696
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease with similar features to Marinesco-Sjogren syndrome.","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Marinesco-Sjogren-like syndrome","secondary_identifiers":["OMIM:248810","MEDGEN:163207","MESH:C535913","UMLS:C0796036"],"synonyms":[{"name":"Marinesco-Sjogren-like syndrome (MSLS)","type":"related"},{"name":"juvenile cataract, cerebellar atrophy, intellectual disability, and myopathy","type":"related"},{"name":"juvenile cataract, cerebellar atrophy, mental retardation, and myopathy","type":"related"}],"termid":"MONDO:0023696","xrefs":{"Monarch":{"xref_id":"0023696"}}}


id: PR:O74801
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC2D10.08c gene.","definition_xrefs":["UniProtKB:O74801","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 yml6, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC2D10.08c","synonyms":[{"name":"Spom972h-SPBC2D10.08c","type":"exact"}],"termid":"PR:O74801"}


id: GO:0033916
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of (1->4)-beta-D-galactosidic linkages in agarose, giving the tetramer as the predominant product.","definition_xrefs":["EC:3.2.1.81"],"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:0016798"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016798","GO:0003824","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"beta-agarase activity","synonyms":[{"name":"AgaA","type":"related"},{"name":"AgaB","type":"related"},{"name":"agarase activity","type":"broad"},{"name":"agarose 3-glycanohydrolase activity","type":"broad"},{"name":"agarose 4-glycanohydrolase activity","type":"related"}],"termid":"GO:0033916"}


id: FYPO:0004466
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 number of sites at which the protein Rad52 (also called Rad22) accumulates is greater than normal during a cellular response to camptothecin.","definition_xrefs":["PMID:22064477","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased number of Rad52 foci during vegetative growth","termid":"FYPO:0000972"}],"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"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"increased number of Rad52 foci during cellular response to camptothecin","synonyms":[{"name":"increased number of Rad22 foci during cellular response to camptothecin","type":"exact"},{"name":"increased number of Rad52 foci during cellular response to CPT","type":"exact"},{"name":"increased number of Rad52 foci during cellular response to camptothecin during mitotic cell cycle","type":"related"},{"name":"increased number of Rad52 foci during cellular response to camptothecin during vegetative growth","type":"exact"}],"termid":"FYPO:0004466"}


id: PBO:0050157
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group box 3 pseudogene 13","termid":"PBO:0050157"}


id: MONDO:0019023
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cutaneous mastocytosis is a term referring to a group of diseases characterized by abnormal accumulation and proliferation of skin mastocytes. In some cases (most commonly in adults), cutaneous mastocytosis may occur in association with mast cell infiltration of various extracutaneous organs, in which case the disorder is referred to as systemic mastocytosis.","definition_xrefs":["Orphanet:66646"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dermis tumor","termid":"MONDO:0002300"},{"relation_name":"is_a","term_name":"urticaria","termid":"MONDO:0005492"},{"relation_name":"is_a","term_name":"mastocytosis","termid":"MONDO:0007950"},{"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:0005046"},{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005093","MONDO:0005570"],"is_obsolete":false,"name":"cutaneous mastocytosis","secondary_identifiers":["icd11.foundation:1300710062","ICDO:9740/1","NCIT:C7137","HP:0200151","OMIM:154800","SCTID:397012002","ONCOTREE:CMCD","GARD:7842","MESH:D034701","DOID:3663","EFO:1000886","MEDGEN:210143","UMLS:C1136033"],"synonyms":[{"name":"CM","type":"exact"},{"name":"CMCD","type":"related"},{"name":"cutaneous (skin) mastocytosis","type":"exact"},{"name":"cutaneous mastocytosis","type":"exact"},{"name":"cutaneous mastocytosis (disease)","type":"exact"},{"name":"mastocytosis, cutaneous","type":"exact"},{"name":"mastocytosis, systemic, somatic","type":"exact"}],"termid":"MONDO:0019023","xrefs":{"Monarch":{"xref_id":"0019023"}}}


id: PBO:0085899
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; may be involved in chitin biosynthesis by regulation of Chs3p export from the ER; relocalizes from bud neck to ER upon DNA replication stress","termid":"PBO:0085899"}


id: GO:2000981
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of inner ear receptor cell differentiation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of mechanoreceptor differentiation","termid":"GO:0045632"},{"relation_name":"is_a","term_name":"regulation of inner ear receptor cell differentiation","termid":"GO:2000980"},{"relation_name":"negatively_regulates","term_name":"inner ear receptor cell differentiation","termid":"GO:0060113"}],"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 inner ear receptor cell differentiation","synonyms":[{"name":"negative regulation of inner ear hair cell differentiation","type":"exact"}],"termid":"GO:2000981"}


id: PBO:0089590
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G1 cyclin Puc1","termid":"PBO:0089590"}


id: PBO:0001046
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptionally represses genes involved in cell surface adhesion","termid":"PBO:0001046"}


id: PBO:0085952
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; null mutant is resistant to 2-deoxy-D-glucose and displays abnormally elongated buds; DGR2 has a paralog, YMR102C, that arose from the whole genome duplication","termid":"PBO:0085952"}


id: PBO:0082093
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"6-phosphogluconate dehydrogenase (decarboxylating); catalyzes an NADPH regenerating reaction in the pentose phosphate pathway; required for growth on D-glucono-delta-lactone and adaptation to oxidative stress; GND1 has a paralog, GND2, that arose from the whole genome duplication","termid":"PBO:0082093"}


id: MONDO:0010944
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":"mitochondrial import-stimulating factor","secondary_identifiers":["UMLS:C1833246","MEDGEN:331468","OMIM:600851"],"synonyms":[{"name":"MSF","type":"related"},{"name":"mitochondrial import-stimulating factor","type":"exact"}],"termid":"MONDO:0010944","xrefs":{"Monarch":{"xref_id":"0010944"}}}


id: PBO:0083803
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential protein that associates with contractile actomyosin ring; required for ingression of the plasma membrane into the bud neck during cytokinesis; C2 domain, a membrane targeting module, is required for function; activates chitin synthase activity of Chs2p during cytokinesis","termid":"PBO:0083803"}


id: GO:0005500
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a juvenile hormone, a sesquiterpenoid derivative that function to maintain the larval state of insects at molting and that may be required for other processes, e.g. oogenesis.","definition_xrefs":["ISBN:0198506732","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isoprenoid binding","termid":"GO:0019840"},{"relation_name":"is_a","term_name":"hormone binding","termid":"GO:0042562"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0008289"}],"interesting_parent_ids":["GO:0005488","GO:0008289","GO:0003674"],"is_obsolete":false,"name":"juvenile hormone binding","termid":"GO:0005500"}


id: PBO:0063153
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pro-apoptotic WT1 regulator pseudogene 1","termid":"PBO:0063153"}


id: MONDO:0001969
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A type of defective gonadal development in patients with a wide spectrum of chromosomal mosaic variants. Their karyotypes are of partial sex chromosome monosomy resulting from an absence or an abnormal second sex chromosome (X or Y). Karyotypes include 45,X/46,xx; 45,X/46,xx/47,xxx; 46,xxp-; 45,X/46,xy; 45,X/47,xyy; 46,xypi; etc. The spectrum of phenotypes may range from phenotypic female to phenotypic male including variations in gonads and internal and external genitalia, depending on the ratio in each gonad of 45,X primordial germ cells to those with normal 46,xx or 46,xy constitution.","definition_xrefs":["MESH:D006060"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Turner syndrome","termid":"MONDO:0019499"}],"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":"mixed gonadal dysgenesis","secondary_identifiers":["NANDO:2200388","GARD:2539","MEDGEN:6654","UMLS:C0018055","DOID:14449","SCTID:83579008"],"synonyms":[{"name":"gonadal dysgenesis mixed","type":"related"}],"termid":"MONDO:0001969","xrefs":{"Monarch":{"xref_id":"0001969"}}}


id: GO:1904152
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of retrograde protein transport, ER to cytosol.","definition_xrefs":["GO_REF:0000058","GOC:bf","GOC:PARL","PMID:18555783","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein exit from endoplasmic reticulum","termid":"GO:0070861"},{"relation_name":"regulates","term_name":"retrograde protein transport, ER to cytosol","termid":"GO:0030970"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"regulation of retrograde protein transport, ER to cytosol","synonyms":[{"name":"regulation of protein dislocation from ER","type":"exact"},{"name":"regulation of protein retrotranslocation from ER","type":"exact"},{"name":"regulation of retrograde protein transport, endoplasmic reticulum to cytosol","type":"exact"}],"termid":"GO:1904152"}


id: GO:0102826
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: UDP-alpha-D-glucose + kaempferol 3-O-glucoside = kaempferol 3,7-O-diglucoside + UDP.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete kaempferol-3-glucoside-glucosyltransferase activity (obsolete GO:0102826)","termid":"GO:0102826"}


id: MONDO:0014026
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any congenital stationary night blindness in which the cause of the disease is a mutation in the LRIT3 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital stationary night blindness","termid":"MONDO:0016293"},{"relation_name":"is_a","term_name":"LRIT3-related retinopathy","termid":"MONDO:1040035"}],"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":"congenital stationary night blindness 1F","secondary_identifiers":["OMIM:615058","UMLS:C3554399","MEDGEN:767313","GARD:15899","DOID:0110864"],"synonyms":[{"name":"CSNB1F","type":"exact"},{"name":"LRIT3 congenital stationary night blindness","type":"exact"},{"name":"congenital stationary night blindness 1F autosomal recessive","type":"exact"},{"name":"congenital stationary night blindness caused by mutation in LRIT3","type":"exact"},{"name":"congenital stationary night blindness type 1F","type":"exact"},{"name":"night blindness, congenital stationary (complete), 1F, autosomal recessive","type":"exact"},{"name":"night blindness, congenital stationary, type 1F","type":"related"}],"termid":"MONDO:0014026","xrefs":{"Monarch":{"xref_id":"0014026"}}}


id: GO:1990526
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A multiprotein complex that is involved in the transcription regulation of mating genes in the yeast S. cerevisiae.","definition_xrefs":["GOC:rb","PMID:16782869"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"Ste12p-Dig1p-Dig2p complex","termid":"GO:1990526"}


id: PBO:0056448
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microtubule affinity regulating kinase 3","termid":"PBO:0056448"}


id: FYPO:0001881
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 cells form actin filaments that are longer than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal actin cytoskeleton morphology during vegetative growth","termid":"FYPO:0000350"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0004803"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0004803","FYPO:0005447","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"elongated actin filaments","synonyms":[{"name":"elongated actin filaments during mitotic cell cycle","type":"exact"},{"name":"elongated actin filaments during vegetative growth","type":"exact"},{"name":"elongated microfilaments","type":"related"},{"name":"increased actin filament length during vegetative growth","type":"exact"},{"name":"long actin filaments during vegetative growth","type":"exact"}],"termid":"FYPO:0001881"}


id: PBO:0061991
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 2 subfamily C member 1","termid":"PBO:0061991"}


id: PBO:0060051
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND4 pseudogene 39","termid":"PBO:0060051"}


id: PBO:0016120
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"silenced P-specific polypeptide Pi","termid":"PBO:0016120"}


id: MONDO:0017734
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Sialidosis is a lysosomal storage disease, belonging to the group of oligosaccharidoses or glycoproteinoses, with a wide clinical spectrum that is divided into two main clinical subtypes: sialidosis type I, the milder, non dysmorphic form of the disease characterized by gait abnormalities, progressive visual loss, bilateral macular cherry red spots and myoclonus, that presents in adolescence or adulthood (second or third decade of life); and sialidosis type II the more severe, early onset form, characterized by a progressive and severe mucopolysaccharidosis-like phenotype with coarse facies, visceromegaly, dysostosis multiplex, and developmental delay. Bilateral macular cherry red spots are also present. Sialidosis type II has been further divided into congenital (with hydrops fetalis), infantile and juvenile presentations.","definition_xrefs":["Orphanet:309294"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oligosaccharidosis","termid":"MONDO:0019251"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0002561"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0002561","MONDO:0037792"],"is_obsolete":false,"name":"sialidosis","secondary_identifiers":["NANDO:2200556","NORD:1713","GARD:21331","icd11.foundation:1180347697","MedDRA:10058800","NANDO:1200116","SCTID:38795005","MEDGEN:120621","UMLS:C0268226"],"termid":"MONDO:0017734","xrefs":{"Monarch":{"xref_id":"0017734"}}}


id: MONDO:0014621
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Brugada syndrome in which the cause of the disease is a mutation in the KCND3 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Brugada syndrome","termid":"MONDO:0015263"}],"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":"Brugada syndrome 9","secondary_identifiers":["OMIM:616399","UMLS:C4225340","DOID:0110226","GARD:16104","MEDGEN:903155"],"synonyms":[{"name":"BRGDA9","type":"exact"},{"name":"Brugada syndrome 9","type":"exact"},{"name":"Brugada syndrome caused by mutation in KCND3","type":"exact"},{"name":"Brugada syndrome type 9","type":"exact"},{"name":"KCND3 Brugada syndrome","type":"exact"}],"termid":"MONDO:0014621","xrefs":{"Monarch":{"xref_id":"0014621"}}}


id: MONDO:0016198
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"qualitative or quantitative protein defects in neuromuscular diseases","termid":"MONDO:0016139"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"qualitative or quantitative defects of plectin","secondary_identifiers":["GARD:20437","UMLS:C5680835","Orphanet:209196","MEDGEN:1842345"],"termid":"MONDO:0016198","xrefs":{"Monarch":{"xref_id":"0016198"}}}


id: PBO:0017480
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-causally_related_to","termid":"PBO:0017480"}


id: PBO:0066403
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"REL proto-oncogene, NF-kB subunit","termid":"PBO:0066403"}


id: PBO:0065095
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRKAG2 antisense RNA 2","termid":"PBO:0065095"}


id: MONDO:0009082
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"High myopia-sensorineural deafness syndrome is a rare genetic disease characterized by high myopia, typically ranging from -6.0 to -11.0 diopters, and moderate to profound, bilateral, progressive sensorineural hearing loss with prelingual-onset. Affected individuals do not present other systemic, ocular or connective tissue manifestations.","definition_xrefs":["Orphanet:363396"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high myopia-sensorineural deafness syndrome","secondary_identifiers":["MEDGEN:812605","UMLS:C3806275","SCTID:720506002","DOID:0111628","GARD:12844","OMIM:221200"],"synonyms":[{"name":"DFNMYP","type":"related"},{"name":"deafness and myopia","type":"related"},{"name":"deafness and myopia syndrome","type":"related"},{"name":"high myopia-sensorineural deafness syndrome","type":"exact"}],"termid":"MONDO:0009082","xrefs":{"Monarch":{"xref_id":"0009082"}}}


id: GO:0070521
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of an alpha4-beta1 integrin complex bound to membrane protein CD82, a member of the tetraspan family.","definition_xrefs":["PMID:8757325"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005886"],"is_obsolete":false,"name":"alpha4-beta1 integrin-CD82 complex","termid":"GO:0070521"}


id: PR:O13894
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mug103 gene.","definition_xrefs":["UniProtKB:O13894","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotically up-regulated gene 103 protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC22A12.02c","synonyms":[{"name":"Spom972h-mug103","type":"exact"}],"termid":"PR:O13894"}


id: MONDO:0019502
data:
  {"annotated_genes":["SJAG_03333","SJAG_00898","SJAG_01570","SJAG_01702","SJAG_04321","SJAG_04084","SJAG_04119","SJAG_03032","SJAG_03448","SJAG_02042","SJAG_04358","SJAG_00886","SJAG_01070","SJAG_01826","SJAG_01536","SJAG_02099","SJAG_04704","SJAG_04654","SJAG_00325","SJAG_02717","SJAG_04640","SJAG_03635","SJAG_04645","SJAG_03286","SJAG_01625","SJAG_03147","SJAG_01991","SJAG_01465"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87467],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100255"},{"annotations":[86953],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014648"},{"annotations":[86914],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0040500"},{"annotations":[88107],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032662"},{"annotations":[87885],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032665"},{"annotations":[88812],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032789"},{"annotations":[88954],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030533"},{"annotations":[88242],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957288"},{"annotations":[88955],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0958204"},{"annotations":[88327],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013173"},{"annotations":[87779],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013528"},{"annotations":[88237],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014348"},{"annotations":[88126],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014409"},{"annotations":[88947,88946],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012613"},{"annotations":[86954],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014649"},{"annotations":[87650],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014815"},{"annotations":[89010],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014930"},{"annotations":[88874],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014996"},{"annotations":[88708],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0015020"},{"annotations":[88538],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0044313"},{"annotations":[88180,88181,88179],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0020850"},{"annotations":[88948],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012615"},{"annotations":[88149],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013853"},{"annotations":[88755],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014485"},{"annotations":[87637],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013624"}]},"cv_name":"mondo","definition":"Autosomal recessive form of non-syndromic intellectual disability.","definition_xrefs":["MONDO:patterns/autosomal_recessive"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-syndromic intellectual disability","termid":"MONDO:0000509"},{"relation_name":"is_a","term_name":"disorder of carbohydrate transmembrane transport and absorption","termid":"MONDO:0017706"},{"relation_name":"is_a","term_name":"intellectual disability, autosomal 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disability","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0060308","OMIMPS:249500","GARD:18643","Orphanet:88616","MEDGEN:1826073","UMLS:C5680181"],"synonyms":[{"name":"AR-NSID","type":"exact"},{"name":"NS-ARID","type":"exact"},{"name":"autosomal recessive intellectual disability","type":"broad"},{"name":"autosomal recessive mental retardation","type":"exact"},{"name":"autosomal recessive non-syndromic intellectual disability","type":"exact"},{"name":"autosomal recessive non-syndromic mental retardation","type":"exact"},{"name":"intellectual disability, autosomal recessive","type":"broad"},{"name":"mental retardation, autosomal recessive","type":"exact"},{"name":"non-syndromic intellectual disability, autosomal recessive","type":"exact"}],"termid":"MONDO:0019502","terms_by_termid":{"MONDO:0012613":null,"MONDO:0012615":null,"MONDO:0013173":null,"MONDO:0013528":null,"MONDO:0013624":null,"MONDO:0013853":null,"MONDO:0014348":null,"MONDO:0014409":null,"MONDO:0014485":null,"MONDO:0014648":null,"MONDO:0014649":null,"MONDO:0014815":null,"MONDO:0014930":null,"MONDO:0014996":null,"MONDO:0015020":null,"MONDO:0020850":null,"MONDO:0030533":null,"MONDO:0032662":null,"MONDO:0032665":null,"MONDO:0032789":null,"MONDO:0040500":null,"MONDO:0044313":null,"MONDO:0100255":null,"MONDO:0957288":null,"MONDO:0958204":null},"xrefs":{"Monarch":{"xref_id":"0019502"}}}


id: PATO:0000684
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000684 absolute incidence value (obsolete PATO:0000684)","termid":"PATO:0000684"}


id: PBO:0025490
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"APC ubiquitin conjugating enzyme E2 Ubc4/UbcP1","termid":"PBO:0025490"}


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


id: MONDO:0015680
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Rare pervasive developmental disorder.","gene_count":0,"genotype_count":0,"name":"obsolete rare pervasive developmental disorder (obsolete MONDO:0015680)","secondary_identifiers":["Orphanet:168778","MedDRA:10061345"],"synonyms":[{"name":"rare ASD","type":"narrow"},{"name":"rare PDD","type":"narrow"},{"name":"rare autism spectrum disorder","type":"narrow"},{"name":"rare pervasive developmental disorder","type":"narrow"}],"termid":"MONDO:0015680","xrefs":{"Monarch":{"xref_id":"0015680"}}}


id: GO:0030585
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: diphosphate + oxaloacetate = CO2 + phosphate + phosphoenolpyruvate.","definition_xrefs":["EC:4.1.1.38","RHEA:22356"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphoenolpyruvate carboxykinase activity","termid":"GO:0004611"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016829","GO:0003824"],"is_obsolete":false,"name":"phosphoenolpyruvate carboxykinase (diphosphate) activity","secondary_identifiers":["KEGG_REACTION:R00346","MetaCyc:4.1.1.38-RXN"],"synonyms":[{"name":"PEP carboxyphosphotransferase activity","type":"related"},{"name":"PEPCTrP","type":"related"},{"name":"diphosphate:oxaloacetate carboxy-lyase (transphosphorylating)","type":"related"},{"name":"diphosphate:oxaloacetate carboxy-lyase (transphosphorylating; phosphoenolpyruvate-forming)","type":"related"},{"name":"phosphoenolpyruvate carboxykinase (pyrophosphate) activity","type":"related"},{"name":"phosphoenolpyruvate carboxylase (pyrophosphate)","type":"related"},{"name":"phosphoenolpyruvate carboxyphosphotransferase activity","type":"related"},{"name":"phosphoenolpyruvate carboxytransphosphorylase activity","type":"related"},{"name":"phosphoenolpyruvic carboxykinase","type":"broad"},{"name":"phosphoenolpyruvic carboxykinase (pyrophosphate)","type":"related"},{"name":"phosphoenolpyruvic carboxylase (pyrophosphate)","type":"related"},{"name":"phosphoenolpyruvic carboxytransphosphorylase activity","type":"related"},{"name":"phosphopyruvate carboxykinase","type":"broad"},{"name":"phosphopyruvate carboxykinase (pyrophosphate)","type":"related"},{"name":"phosphopyruvate carboxylase (pyrophosphate)","type":"related"}],"termid":"GO:0030585"}


id: MONDO:0010862
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited susceptibility or predisposition to developing type 1 diabetes mellitus that has material basis in mutation of the locus at chromosome 11q13.","definition_xrefs":["MONDO:patterns/inherited_susceptibility","DOID:0110743","PMID:9683605"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"type 1 diabetes mellitus","termid":"MONDO:0005147"},{"relation_name":"is_a","term_name":"diabetes mellitus, insulin-dependent, X-linked, susceptibility to","termid":"MONDO:0010255"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"type 1 diabetes mellitus 4","secondary_identifiers":["OMIM:600319","MESH:C563959","MEDGEN:373925","UMLS:C1838261"],"synonyms":[{"name":"IDDM4","type":"exact"},{"name":"diabetes mellitus, insulin-dependent, 4","type":"related"},{"name":"insulin-dependent diabetes mellitus 4","type":"exact"}],"termid":"MONDO:0010862","xrefs":{"Monarch":{"xref_id":"0010862"}}}


id: PBO:0000367
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptionally represses frp1","termid":"PBO:0000367"}


id: MONDO:0003118
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An uncommon usually benign neoplasm that arises from the testis. It is characterized by the presence of cysts lined by transitional cells and solid nests of transitional cells in a spindle cell stroma.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neoplasm of testis","termid":"MONDO:0021348"},{"relation_name":"is_a","term_name":"Brenner tumor","termid":"MONDO:0024235"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testicular Brenner tumor","secondary_identifiers":["MEDGEN:273631","UMLS:C1515281","DOID:4739","NCIT:C39953"],"synonyms":[{"name":"testes, rudimentary Brenner tumor","type":"exact"},{"name":"testes, rudimentary Brenner tumour","type":"exact"},{"name":"testis Brenner tumor","type":"exact"},{"name":"testis Brenner tumour","type":"exact"}],"termid":"MONDO:0003118","xrefs":{"Monarch":{"xref_id":"0003118"}}}


id: MONDO:0010416
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":"deafness, cataract, retinitis pigmentosa, and sperm abnormalities","secondary_identifiers":["MEDGEN:395517","OMIM:300719","MESH:C567467","UMLS:C2678011"],"synonyms":[{"name":"deafness, cataract, retinitis pigmentosa, and sperm abnormalities","type":"exact"},{"name":"deafness, cataract, retinitis pigmentosa, and sperm abnormalities, X-linked recessive","type":"exact"}],"termid":"MONDO:0010416","xrefs":{"Monarch":{"xref_id":"0010416"}}}


id: PBO:0069726
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1007, pseudogene","termid":"PBO:0069726"}


id: MONDO:0009836
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":"pancreatitis, sclerosing cholangitis, and sicca complex","secondary_identifiers":["MEDGEN:340461","MESH:C564906","UMLS:C1850080","OMIM:260480"],"synonyms":[{"name":"pancreatitis, sclerosing cholangitis, and sicca complex","type":"exact"}],"termid":"MONDO:0009836","xrefs":{"Monarch":{"xref_id":"0009836"}}}


id: PBO:0039324
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arachidonate 12-lipoxygenase pseudogene 1","termid":"PBO:0039324"}


id: PBO:0059361
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein S17 pseudogene 7","termid":"PBO:0059361"}


id: MONDO:0011335
data:
  {"annotated_genes":["SJAG_00851"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87512],"is_not":false,"summary":null,"term":"MONDO:0011335"}]},"cv_name":"mondo","definition":"A rare disorder caused by mutation in the KIF22 gene. It is characterized by short stature, midface retrusion, progressive knee malalignment, generalized ligamentous laxity, and mild spinal deformity.","definition_xrefs":["NCIT:C125419"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"spondyloepimetaphyseal dysplasia with joint laxity","termid":"MONDO:0019675"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00851":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0005497"],"is_obsolete":false,"name":"spondyloepimetaphyseal dysplasia with multiple dislocations","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0112199","MEDGEN:350960","OMIM:603546","MESH:C535784","Orphanet:93360","SCTID:766820007","GARD:9866","UMLS:C1863732"],"synonyms":[{"name":"SEMD-MD","type":"exact"},{"name":"SEMDJL2","type":"exact"},{"name":"spondyloepimetaphyseal dysplasia with JOINT laxity type 2","type":"related"},{"name":"spondyloepimetaphyseal dysplasia with JOINT laxity, type 2","type":"related"},{"name":"spondyloepimetaphyseal dysplasia with Joint laxity, Hall type","type":"related"},{"name":"spondyloepimetaphyseal dysplasia with Joint laxity, leptodactylic type","type":"related"},{"name":"spondyloepimetaphyseal dysplasia with Joint laxity, type 2","type":"related"},{"name":"spondyloepimetaphyseal dysplasia with joint laxicity, Hall type","type":"exact"},{"name":"spondyloepimetaphyseal dysplasia with joint laxity type 2","type":"exact"},{"name":"spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type","type":"exact"},{"name":"spondyloepimetaphyseal dysplasia with multiple dislocations Hall type","type":"related"},{"name":"spondyloepimetaphyseal dysplasia with multiple dislocations leptodactylic type","type":"related"},{"name":"spondyloepimetaphyseal dysplasia with multiple dislocations, Hall type","type":"exact"}],"termid":"MONDO:0011335","terms_by_termid":{"MONDO:0011335":null},"xrefs":{"Monarch":{"xref_id":"0011335"}}}


id: PBO:0003194
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"argininosuccinate synthase (predicted)","termid":"PBO:0003194"}


id: GO:1901955
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of retrograde dense core granule transport.","definition_xrefs":["GOC:TermGenie","PMID:23358451","GOC:kmv"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of vesicle transport along microtubule","termid":"GO:1901609"},{"relation_name":"is_a","term_name":"regulation of retrograde dense core granule transport","termid":"GO:1901954"},{"relation_name":"is_a","term_name":"negative regulation of dense core granule transport","termid":"GO:1904810"},{"relation_name":"is_a","term_name":"negative regulation of retrograde axon cargo transport","termid":"GO:2001018"},{"relation_name":"negatively_regulates","term_name":"retrograde neuronal dense core vesicle transport","termid":"GO:1990049"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"negative regulation of retrograde dense core granule transport","synonyms":[{"name":"down regulation of retrograde dense core granule transport","type":"exact"},{"name":"down-regulation of retrograde dense core granule transport","type":"exact"},{"name":"downregulation of retrograde dense core granule transport","type":"exact"},{"name":"inhibition of retrograde dense core granule transport","type":"narrow"}],"termid":"GO:1901955"}


id: MOD:01895
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a residue alpha-amino- or alpha-imino-hydrogen with a 3x(12)C-labeled propanoyl group.","definition_xrefs":["Unimod:58#N-term","PubMed:12175151","PubMed:11857757","PubMed:11999733"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alpha-amino propanoylated residue","termid":"MOD:00451"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha-amino 3x(12)C-labeled propanoylated residue","synonyms":[{"name":"Propionate labeling reagent light form (N-term & K)","type":"related"},{"name":"Propionyl","type":"related"}],"termid":"MOD:01895"}


id: GO:0102731
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 1D-myo-inositol 1,3,4,6-tetrakisphosphate + ATP = 1D-myo-inositol 1,2,3,4,6-pentakisphosphate + ADP + H+.","definition_xrefs":["MetaCyc:RXN-7185","PMID:16107538"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inositol tetrakisphosphate kinase activity","termid":"GO:0051765"}],"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:0016301"}],"interesting_parent_ids":["GO:0003824","GO:0016301","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"inositol-1,3,4,6-tetrakisphosphate 2-kinase activity","synonyms":[{"name":"D-myo-inositol (1,3,4,6)-tetrakisphosphate 2-kinase activity","type":"exact"}],"termid":"GO:0102731"}


id: FYPO:0002769
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the spindle pole body is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to microtubule cytoskeleton","termid":"FYPO:0004090"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0000138"],"is_obsolete":false,"name":"abnormal protein localization to spindle pole body","synonyms":[{"name":"abnormal protein localisation to spindle pole body","type":"exact"},{"name":"abnormal protein localization to SPB","type":"exact"}],"termid":"FYPO:0002769"}


id: GO:0140296
data:
  {"annotated_genes":["SJAG_00692","SJAG_00650","SJAG_02458","SJAG_01523","SJAG_02174","SJAG_00095","SJAG_03095","SJAG_03007","SJAG_00202","SJAG_03120","SJAG_00159","SJAG_03900"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[81668],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001179"},{"annotations":[73807,77499,58333,78619,72244,72394,79049,67561],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017025"},{"annotations":[80996],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001096"},{"annotations":[77938],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001097"},{"annotations":[73569],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001156"}]},"cv_name":"molecular_function","definition":"Binding to a general transcription initiation factor, a protein that contributes to transcription start site selection and transcription initiation.","definition_xrefs":["GOC:txnOH-2018"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcription factor binding","termid":"GO:0008134"}],"gene_count":12,"genes_by_uniquename":{"SJAG_00095":null,"SJAG_00159":null,"SJAG_00202":null,"SJAG_00650":null,"SJAG_00692":null,"SJAG_01523":null,"SJAG_02174":null,"SJAG_02458":null,"SJAG_03007":null,"SJAG_03095":null,"SJAG_03120":null,"SJAG_03900":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"general transcription initiation factor binding","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null},"termid":"GO:0140296","terms_by_termid":{"GO:0001096":null,"GO:0001097":null,"GO:0001156":null,"GO:0001179":null,"GO:0017025":null}}


id: MONDO:0012126
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Avascular necrosis of femoral head (ANFH) is a severely disabling disease characterized by progressive groin pain, a limping gait, leg length discrepancy, collapse of the subchondral bone, limitation of hip function and eventual degeneration of the hip joint requiring total hip arthroplasty.","definition_xrefs":["Orphanet:86820"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete type 2 collagen-related bone disorder (obsolete MONDO:0019686)","termid":"MONDO:0019686"},{"relation_name":"is_a","term_name":"primary avascular necrosis","termid":"MONDO:0018379"},{"relation_name":"is_a","term_name":"osteonecrosis of genetic origin","termid":"MONDO:0018383"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"familial avascular necrosis of femoral head","secondary_identifiers":["UMLS:C4275066","MESH:D005271","OMIMPS:608805","SCTID:715657008","icd11.foundation:1216860745","GARD:10914","NANDO:1200373","MEDGEN:909851","NCIT:C35480"],"synonyms":[{"name":"ANFH","type":"related"},{"name":"ANFH1","type":"related"},{"name":"aseptic Necrosis of femoral head","type":"exact"},{"name":"aseptic Necrosis of head of femur","type":"exact"},{"name":"avascular NECROSIS of femoral head, primary","type":"related"},{"name":"avascular NECROSIS of femoral head, primary, 1","type":"related"},{"name":"avascular Necrosis of femoral head, primary, 1","type":"related"},{"name":"familial avascular necrosis of the femoral head","type":"related"},{"name":"familial osteonecrosis of the femoral head","type":"exact"},{"name":"femoral head, aseptic Necrosis of","type":"related"},{"name":"femoral head, avascular Necrosis of","type":"related"},{"name":"ischaemic Necrosis of femoral head","type":"related"},{"name":"ischemic Necrosis of femoral head","type":"related"},{"name":"osteonecrosis of femoral head","type":"related"},{"name":"primary avascular necrosis of the femoral head","type":"related"}],"termid":"MONDO:0012126","xrefs":{"Monarch":{"xref_id":"0012126"}}}


id: MONDO:0019520
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A lymphedema that is part of a larger syndrome.","definition_xrefs":["MONDO:patterns/syndromic"],"gene_count":0,"genotype_count":0,"name":"obsolete syndromic lymphedema (obsolete MONDO:0019520)","secondary_identifiers":["Orphanet:89832"],"synonyms":[{"name":"syndrome associated with lymphedema","type":"exact"},{"name":"syndromic lymphedema","type":"exact"}],"termid":"MONDO:0019520","xrefs":{"Monarch":{"xref_id":"0019520"}}}


id: PBO:0063579
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PERP pseudogene 2","termid":"PBO:0063579"}


id: GO:0005571
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete untranslated RNA (obsolete GO:0005571)","synonyms":[{"name":"untranslated RNA","type":"exact"}],"termid":"GO:0005571"}


id: MONDO:0021553
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"myelitis","termid":"MONDO:0002565"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transverse myelitis","secondary_identifiers":["ICD9:323.9","icd11.foundation:1328350091","MedDRA:10028527","UMLS:C0026976","MEDGEN:6488","DOID:0080743","SCTID:16631009"],"synonyms":[{"name":"Myelitis, Transverse","type":"related"},{"name":"Transverse Myelitis","type":"related"},{"name":"Transverse Myelopathy Syndrome","type":"related"},{"name":"Transverse Myelopathy Syndromes","type":"related"},{"name":"Transverse myelitis","type":"related"},{"name":"Transverse myelopathy syndrome","type":"related"},{"name":"transverse myelitis","type":"exact"},{"name":"transverse myelopathy syndrome","type":"exact"}],"termid":"MONDO:0021553","xrefs":{"Monarch":{"xref_id":"0021553"}}}


id: PBO:0070327
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNY3 pseudogene 16","termid":"PBO:0070327"}


id: PBO:0047012
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 90 member A15, pseudogene","termid":"PBO:0047012"}


id: PR:Q10482
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A lysosomal amino acid transporter 1 homolog that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO01857"],"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":"seven transmembrane protein 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC17C9.10","secondary_identifiers":["UniProtKB:Q10482"],"synonyms":[{"name":"Spom972h-PQLC2","type":"exact"}],"termid":"PR:Q10482"}


id: GO:1901388
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of transforming growth factor beta activation.","definition_xrefs":["GOC:TermGenie","GOC:sl"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of transforming growth factor beta activation (obsolete GO:1901388)","synonyms":[{"name":"regulation of L-TGF-beta activation","type":"exact"},{"name":"regulation of TGF-B activation","type":"exact"},{"name":"regulation of TGF-beta activation","type":"exact"},{"name":"regulation of TGFB activation","type":"exact"},{"name":"regulation of TGFbeta activation","type":"exact"},{"name":"regulation of latent TGF-beta activation","type":"exact"}],"termid":"GO:1901388"}


id: MONDO:0005982
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A skin infection caused by a fungus.","definition_xrefs":["NCIT:C112181"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cutaneous mycosis","termid":"MONDO:0000254"},{"relation_name":"is_a","term_name":"skin infection","termid":"MONDO:0021201"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"tinea infection","secondary_identifiers":["UMLS:C0040247","EFO:0007510","DOID:12404","MEDGEN:52757"],"synonyms":[{"name":"Tinea","type":"exact"},{"name":"Tinea caused disease or disorder","type":"exact"},{"name":"Tinea disease or disorder","type":"exact"},{"name":"Tinea infection","type":"exact"},{"name":"Tinea infectious disease","type":"exact"},{"name":"ringworm","type":"related"}],"termid":"MONDO:0005982","xrefs":{"Monarch":{"xref_id":"0005982"}}}


id: PBO:0070151
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 65 pseudogene","termid":"PBO:0070151"}


id: GO:0120197
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The respiratory system process driven by motile cilia on epithelial cells of the respiratory tract by which mucus and associated inhaled particles and pathogens trapped within it are moved out of the airways.","definition_xrefs":["GOC:krc","PMID:24119105","PMID:27864314"],"direct_ancestors":[{"relation_name":"is_a","term_name":"respiratory system process","termid":"GO:0003016"},{"relation_name":"is_a","term_name":"epithelial cilium movement involved in extracellular fluid movement","termid":"GO:0003351"}],"gene_count":0,"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":"mucociliary clearance","synonyms":[{"name":"MCC","type":"related"},{"name":"MCT","type":"related"},{"name":"mucociliary transport","type":"exact"}],"termid":"GO:0120197"}


id: PBO:0058244
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4531","termid":"PBO:0058244"}


id: MONDO:0054804
data:
  {"annotated_genes":["SJAG_03161"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87851],"is_not":false,"summary":null,"term":"MONDO:0054804"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive primary microcephaly","termid":"MONDO:0016660"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03161":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0700092"],"is_obsolete":false,"name":"microcephaly 21, primary, autosomal recessive","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:16278","UMLS:C4693831","OMIM:617983","MEDGEN:1646916"],"synonyms":[{"name":"MCPH21","type":"related"},{"name":"microcephaly 21, PRIMARY, autosomal recessive","type":"related"}],"termid":"MONDO:0054804","terms_by_termid":{"MONDO:0054804":null},"xrefs":{"Monarch":{"xref_id":"0054804"}}}


id: MONDO:0017609
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Renal tubular dysgenesis is a rare disorder of the fetus characterized by absent or poorly developed proximal tubules of the kidneys, persistent oligohydramnios, leading to Potter sequence (facial dysmorphism with large and flat low-set ears, lung hypoplasia arthrogryposis and limb positioning defects), and skull ossification defects. It can be acquired during fetal development due to drugs taken by the mother or certain disorders (twin-twin transfusion syndrome, TTTS) or inherited in an autosomal recessive manner.","definition_xrefs":["Orphanet:3033"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kidney disorder","termid":"MONDO:0005240"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"renal tubular dysgenesis","secondary_identifiers":["GARD:379","SCTID:702397002","icd11.foundation:191424358","UMLS:C0266313","MEDGEN:82738"],"synonyms":[{"name":"primitive renal tubule syndrome","type":"exact"},{"name":"renotubular dysgenesis","type":"exact"}],"termid":"MONDO:0017609","xrefs":{"Monarch":{"xref_id":"0017609"}}}


id: GO:0061742
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A lysosomal membrane protein complex that enables the translocation of a target protein across the lysosomal membrane as part of chaperone-mediated autophagy.","definition_xrefs":["GOC:pad","GOC:PARL","GOC:dph","PMID:20797626"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane protein complex","termid":"GO:0098796"},{"relation_name":"part_of","term_name":"lysosomal membrane","termid":"GO:0005765"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005773"}],"interesting_parent_ids":["GO:0005773","GO:0005575","GO:0032991","GO:0005737"],"is_obsolete":false,"name":"chaperone-mediated autophagy translocation complex","synonyms":[{"name":"CMA receptor complex","type":"related"},{"name":"CMA translocation complex","type":"exact"},{"name":"chaperone-mediated autophagy receptor complex","type":"related"}],"termid":"GO:0061742"}


id: MONDO:0004185
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm of the ovary characterized by the presence of cystic structures lined by serous epithelial cells in a fibrotic stroma.","definition_xrefs":["NCIT:C40032"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cystadenofibroma","termid":"MONDO:0003464"},{"relation_name":"is_a","term_name":"serous cystadenofibroma","termid":"MONDO:0005182"},{"relation_name":"is_a","term_name":"ovarian serous adenofibroma","termid":"MONDO:0006340"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ovarian serous cystadenofibroma","secondary_identifiers":["DOID:7320","MEDGEN:167919","UMLS:C0877572"],"synonyms":[{"name":"ovarian serous cystadenofibroma","type":"exact"},{"name":"ovary serous cystadenofibroma","type":"exact"}],"termid":"MONDO:0004185","xrefs":{"Monarch":{"xref_id":"0004185"}}}


id: PBO:0017770
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NMS complex subunit Nuf2","termid":"PBO:0017770"}


id: GO:0022016
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The division of a glioblast in the pallium. A glioblast is a dividing precursor cell that gives rise to glial cells.","definition_xrefs":["GO_REF:0000021","GOC:dgh","GOC:cls","GOC:dph","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glioblast division","termid":"GO:0048860"},{"relation_name":"part_of","term_name":"pallium cell proliferation in forebrain","termid":"GO:0022013"}],"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":"pallium glioblast division","synonyms":[{"name":"glioblast cell division in pallium","type":"exact"}],"termid":"GO:0022016"}


id: PBO:0029196
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_threonine_phosphorylation_during_mitotic_M_phase","termid":"PBO:0029196"}


id: PBO:0002063
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotic spindle pole body protein Kms1","termid":"PBO:0002063"}


id: GO:0006301
data:
  {"annotated_genes":["SJAG_02667","SJAG_02918","SJAG_00573","SJAG_00611","SJAG_04089","SJAG_00819","SJAG_16460","SJAG_02521","SJAG_03906","SJAG_00153","SJAG_01221","SJAG_00208","SJAG_01044","SJAG_04816","SJAG_04791","SJAG_04190","SJAG_00406","SJAG_03898"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[61155,78906,89877,90503,97927,100169,106379,119135],"is_not":false,"summary":null,"term":"GO:0006301"},{"annotations":[101233,68147,104826,72201,58863,61555],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070987"},{"annotations":[75012,72199,97789,79457,79758,76722,104827,106175],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042276"},{"annotations":[113761],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1904332"},{"annotations":[100231],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019985"}]},"cv_name":"biological_process","definition":"The conversion of DNA-damage induced single-stranded gaps into large molecular weight DNA after replication. Includes pathways that remove replication-blocking lesions in conjunction with DNA replication.","definition_xrefs":["GOC:elh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA repair","termid":"GO:0006281"}],"gene_count":18,"genes_by_uniquename":{"SJAG_00153":null,"SJAG_00208":null,"SJAG_00406":null,"SJAG_00573":null,"SJAG_00611":null,"SJAG_00819":null,"SJAG_01044":null,"SJAG_01221":null,"SJAG_02521":null,"SJAG_02667":null,"SJAG_02918":null,"SJAG_03898":null,"SJAG_03906":null,"SJAG_04089":null,"SJAG_04190":null,"SJAG_04791":null,"SJAG_04816":null,"SJAG_16460":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006281"},{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006281","GO:0006259","GO:0008150"],"is_obsolete":false,"name":"postreplication repair","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["Wikipedia:Postreplication_repair"],"synonyms":[{"name":"postreplication DNA repair","type":"exact"}],"termid":"GO:0006301","terms_by_termid":{"GO:0006301":null,"GO:0019985":null,"GO:0042276":null,"GO:0070987":null,"GO:1904332":null}}


id: GO:0009971
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form the anastral spindle in male meiotic cells.","definition_xrefs":["PMID:11973272","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spindle assembly involved in male meiosis","termid":"GO:0007053"},{"relation_name":"is_a","term_name":"anastral spindle assembly","termid":"GO:0055048"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0000226"},{"rel_name":"is_a","termid":"GO:0007010"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0140013"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0140013","GO:0007049","GO:0007010","GO:0008150","GO:0000226","GO:0044085"],"is_obsolete":false,"name":"anastral spindle assembly involved in male meiosis","termid":"GO:0009971"}


id: GO:0047915
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-galactose + N-acetyl-D-galactosaminyl-(N-acetylneuraminyl)-D-galactosyl-1,4-beta-D-glucosyl-N-acylsphingosine = UDP + D-galactosyl-1,3-beta-N-acetyl-D-galactosaminyl-(N-acetylneuraminyl)-D-galactosyl-D-glucosyl-N-acylsphingosine.","definition_xrefs":["MetaCyc:GANGLIOSIDE-GALACTOSYLTRANSFERASE-RXN","EC:2.4.1.62"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-galactosyltransferase activity","termid":"GO:0035250"}],"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:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0003824","GO:0016757"],"is_obsolete":false,"name":"ganglioside galactosyltransferase activity","secondary_identifiers":["RHEA:16773"],"synonyms":[{"name":"GM1-synthase activity","type":"related"},{"name":"UDP galactose-LAC Tet-ceramide alpha-galactosyltransferase activity","type":"related"},{"name":"UDP-galactose-GM2 galactosyltransferase activity","type":"related"},{"name":"UDP-galactose-GM2 ganglioside galactosyltransferase activity","type":"related"},{"name":"UDP-galactose:N-acetyl-D-galactosaminyl-(N-acetylneuraminyl)-D-galactosyl-D-glucosyl-N-acylsphingosine beta-1,3-D-galactosyltransferase activity","type":"related"},{"name":"UDP-galactose:N-acetylgalactosaminyl-(N-acetylneuraminyl) galactosyl-glucosyl-ceramide galactosyltransferase activity","type":"related"},{"name":"UDPgalactose-ceramide galactosyltransferase activity","type":"related"},{"name":"UDPgalactose:N-acetyl-D-galactosaminyl-(N-acetylneuraminyl)-D-galactosyl-D-glucosyl-N-acylsphingosine beta-1,3-D-galactosyltransferase activity","type":"related"},{"name":"uridine diphosphate D-galactose:glycolipid galactosyltransferase activity","type":"related"},{"name":"uridine diphosphogalactose-GM2 galactosyltransferase activity","type":"related"},{"name":"uridine diphosphogalactose-ceramide galactosyltransferase activity","type":"related"}],"termid":"GO:0047915"}


id: PBO:0081537
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 446","termid":"PBO:0081537"}


id: GO:0090137
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The attachment of an epithelial cell to another epithelial cell via adhesion molecules that contributes to epithelium migration.","definition_xrefs":["GOC:tb","GOC:dph","GOC:ascb_2009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial cell-cell adhesion","termid":"GO:0090136"},{"relation_name":"part_of","term_name":"epithelium migration","termid":"GO:0090132"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"epithelial cell-cell adhesion involved in epithelium migration","termid":"GO:0090137"}


id: PBO:0015655
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glyoxylase III Hsp3102","termid":"PBO:0015655"}


id: PR:O74864
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A 60S acidic ribosomal protein P0 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO04894"],"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":"60S acidic ribosomal protein P0 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC18.14c","secondary_identifiers":["UniProtKB:O74864"],"synonyms":[{"name":"Spom972h-RPLP0","type":"exact"}],"termid":"PR:O74864"}


id: GO:0010313
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a phytochrome.","definition_xrefs":["PMID:15486102"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein binding","termid":"GO:0005515"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"phytochrome binding","termid":"GO:0010313"}


id: PBO:0086318
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein with similarity to Emp24p and Erv25p; member of the p24 family involved in ER to Golgi transport","termid":"PBO:0086318"}


id: GO:0038026
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by the binding of reelin (a secreted glycoprotein) to a receptor on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["PMID:12827279","PMID:20223215","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell surface receptor signaling pathway","termid":"GO:0007166"}],"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":"reelin-mediated signaling pathway","synonyms":[{"name":"reeler-mediated signaling pathway","type":"exact"},{"name":"reelin-mediated signal transduction pathway","type":"exact"},{"name":"reelin-mediated signalling pathway","type":"exact"}],"termid":"GO:0038026"}


id: PBO:0058855
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 8084","termid":"PBO:0058855"}


id: PBO:0060525
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"asparaginyl-tRNA synthetase 2, mitochondrial","termid":"PBO:0060525"}


id: FYPO:0000284
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A mitosis phenotype observed in the vegetative growth phase of the life cycle in which a cell undergoes unequal mitotic sister chromatid segregation, and as a result the nucleus divides unequally to produce one daughter nucleus that is larger than the other.","definition_xrefs":["PMID:8769419","PomBase:jh","PomBase:vw","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"large and small daughter nuclei","termid":"FYPO:0006715"},{"relation_name":"output_of","term_name":"complete but unequal mitotic sister chromatid segregation","termid":"FYPO:0001270"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0002403"},{"rel_name":"output_of","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0002403","FYPO:0000631","FYPO:0001985","FYPO:0000337","FYPO:0000641","FYPO:0000002","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"large and small daughter nuclei, with unequal mitotic sister chromatid segregation","synonyms":[{"name":"complete but unequal mitotic sister chromatid segregation forming large and small daughter nuclei","type":"exact"},{"name":"large and small daughter nuclei resulting from unequal mitotic sister chromatid segregation","type":"related"},{"name":"large and small daughter nuclei, with complete but unequal mitotic sister chromatid segregation","type":"exact"},{"name":"large and small daughter nuclei, with unequal mitotic chromosome segregation","type":"exact"},{"name":"large and small daughter nuclei, with unequal mitotic sister chromatid segregation, during mitotic cell cycle","type":"related"},{"name":"large and small daughter nuclei, with unequal mitotic sister chromatid segregation, during vegetative growth","type":"exact"}],"termid":"FYPO:0000284"}


id: MONDO:0011691
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial amyotrophic lateral sclerosis","termid":"MONDO:0005144"}],"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":"amyotrophic lateral sclerosis type 3","secondary_identifiers":["GARD:10501","OMIM:606640","UMLS:C1847735","DOID:0060195","MEDGEN:339829","MESH:C564688"],"synonyms":[{"name":"ALS3","type":"related"},{"name":"amyotrophic lateral sclerosis 3","type":"exact"}],"termid":"MONDO:0011691","xrefs":{"Monarch":{"xref_id":"0011691"}}}


id: PBO:0074689
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, H/ACA box 68B","termid":"PBO:0074689"}


id: MONDO:0010591
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Fingerprint body myopathy is a congenital benign muscle disorder characterized by congenital hypotonia and weakness and by the presence of numerous fingerprint bodies located at the periphery of the muscle fibers. Prevalence is unknown. Less than 20 patients have been described. Few sporadic cases have been observed, as well as cases of recessive transmission.","definition_xrefs":["Orphanet:97232"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital myopathy","termid":"MONDO:0019952"}],"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":"fingerprint body myopathy","secondary_identifiers":["MEDGEN:337026","OMIM:305550","MESH:C564425","icd11.foundation:1251733531","GARD:12720","UMLS:C1844560"],"synonyms":[{"name":"fingerprint body myopathy","type":"exact"}],"termid":"MONDO:0010591","xrefs":{"Monarch":{"xref_id":"0010591"}}}


id: GO:0070920
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of regulatory non-coding RNA processing.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of gene silencing by regulatory ncRNA","termid":"GO:0060966"},{"relation_name":"is_a","term_name":"regulation of primary metabolic process","termid":"GO:0080090"},{"relation_name":"regulates","term_name":"regulatory ncRNA processing","termid":"GO:0070918"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"regulation of regulatory ncRNA processing","synonyms":[{"name":"regulation of gene silencing by RNA, production of guide RNA","type":"exact"},{"name":"regulation of gene silencing by RNA, production of small RNA","type":"exact"},{"name":"regulation of production of small RNA involved in gene silencing by RNA","type":"narrow"}],"termid":"GO:0070920"}


id: GO:0006741
data:
  {"annotated_genes":["SJAG_03946","SJAG_01566","SJAG_01582"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[72876,79744,81652],"is_not":false,"summary":null,"term":"GO:0006741"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of nicotinamide adenine dinucleotide phosphate (NADP+), a coenzyme that interconverts with its reduced form, NADPH, in many redox and biosynthetic reactions.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine nucleotide biosynthetic process","termid":"GO:0006164"},{"relation_name":"is_a","term_name":"NADP+ metabolic process","termid":"GO:0006739"},{"relation_name":"is_a","term_name":"nicotinamide nucleotide biosynthetic process","termid":"GO:0019359"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01566":null,"SJAG_01582":null,"SJAG_03946":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0055086","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"NADP+ biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"NADP (oxidized) biosynthesis","type":"exact"},{"name":"NADP (oxidized) biosynthetic process","type":"exact"},{"name":"NADP (reduced) biosynthesis","type":"exact"},{"name":"NADP (reduced) biosynthetic process","type":"exact"},{"name":"NADP anabolism","type":"exact"},{"name":"NADP biosynthesis","type":"exact"},{"name":"NADP biosynthetic process","type":"exact"},{"name":"NADP formation","type":"exact"},{"name":"NADP synthesis","type":"exact"},{"name":"NADPH biosynthesis","type":"exact"},{"name":"NADPH biosynthetic process","type":"exact"},{"name":"nicotinamide adenine dinucleotide phosphate biosynthesis","type":"exact"},{"name":"nicotinamide adenine dinucleotide phosphate biosynthetic process","type":"exact"},{"name":"oxidized NADP biosynthesis","type":"exact"},{"name":"oxidized NADP biosynthetic process","type":"exact"},{"name":"oxidized nicotinamide adenine dinucleotide phosphate biosynthesis","type":"exact"},{"name":"oxidized nicotinamide adenine dinucleotide phosphate biosynthetic process","type":"exact"},{"name":"reduced NADP biosynthesis","type":"exact"},{"name":"reduced NADP biosynthetic process","type":"exact"},{"name":"reduced nicotinamide adenine dinucleotide phosphate biosynthesis","type":"exact"},{"name":"reduced nicotinamide adenine dinucleotide phosphate biosynthetic process","type":"exact"}],"termid":"GO:0006741","terms_by_termid":{"GO:0006741":null}}


id: GO:1904994
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of leukocyte adhesion to vascular endothelial cell.","definition_xrefs":["PMID:23897866","GOC:BHF_miRNA","GOC:BHF","GOC:TermGenie","GO_REF:0000058","GOC:bc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of leukocyte cell-cell adhesion","termid":"GO:1903037"},{"relation_name":"regulates","term_name":"leukocyte adhesion to vascular endothelial cell","termid":"GO:0061756"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"regulation of leukocyte adhesion to vascular endothelial cell","termid":"GO:1904994"}


id: PBO:0087756
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the tRNA splicing endonuclease; tRNA splicing endonuclease (Sen complex) is composed of Sen2p, Sen15p, Sen34p, and Sen54p; Sen complex also cleaves the CBP1 mRNA at the mitochondrial surface","termid":"PBO:0087756"}


id: GO:0043329
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process of directing proteins towards a membrane using signals contained within the protein, occurring that contributes to ubiquitin-dependent protein catabolism via the MVB pathway; the destruction of a protein or peptide covalently tagged with a ubiquitin, via the multivesicular body (MVB) sorting pathway.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete protein targeting to membrane involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway (obsolete GO:0043329)","synonyms":[{"name":"protein membrane targeting during ubiquitin-dependent protein catabolic process via the MVB pathway","type":"exact"},{"name":"protein membrane targeting during ubiquitin-dependent protein catabolism via the MVB pathway","type":"exact"},{"name":"protein targeting to membrane during ubiquitin-dependent protein breakdown via the MVB pathway","type":"exact"},{"name":"protein targeting to membrane during ubiquitin-dependent protein catabolic process via the MVB pathway","type":"related"},{"name":"protein targeting to membrane during ubiquitin-dependent protein degradation via the MVB pathway","type":"exact"},{"name":"protein-membrane targeting during ubiquitin-dependent protein breakdown via the MVB pathway","type":"exact"},{"name":"protein-membrane targeting during ubiquitin-dependent protein catabolic process via the MVB pathway","type":"exact"},{"name":"protein-membrane targeting during ubiquitin-dependent protein catabolism via the MVB pathway","type":"exact"},{"name":"protein-membrane targeting during ubiquitin-dependent protein degradation via the MVB pathway","type":"exact"}],"termid":"GO:0043329"}


id: GO:0032900
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of production of a neurotrophin.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of neurotrophin production","termid":"GO:0032899"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"negatively_regulates","term_name":"neurotrophin production","termid":"GO:0032898"}],"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 neurotrophin production","synonyms":[{"name":"down regulation of neurotrophin production","type":"exact"},{"name":"down-regulation of neurotrophin production","type":"exact"},{"name":"downregulation of neurotrophin production","type":"exact"},{"name":"inhibition of neurotrophin production","type":"narrow"}],"termid":"GO:0032900"}


id: PBO:0041220
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C1GALT1 specific chaperone 1 like","termid":"PBO:0041220"}


id: GO:0051841
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which an organism activates or increases the frequency, rate or extent of cytolysis by that organism of cells in its symbiont organism. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:add"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation by host of cytolysis of symbiont cells (obsolete GO:0051841)","synonyms":[{"name":"activation by host of cytolysis of symbiont cells","type":"narrow"},{"name":"stimulation by host of cytolysis of symbiont cells","type":"narrow"},{"name":"up regulation by host of cytolysis of symbiont cells","type":"exact"},{"name":"up-regulation by host of cytolysis of symbiont cells","type":"exact"},{"name":"upregulation by host of cytolysis of symbiont cells","type":"exact"}],"termid":"GO:0051841"}


id: GO:0004938
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with epinephrine or norepinephrine to initiate a change in cell activity via activation of a G protein, with pharmacological characteristics of alpha2-adrenergic receptors; the activity involves transmitting the signal to the Gi alpha subunit of a heterotrimeric G protein.","definition_xrefs":["GOC:cb","IUPHAR_GPCR:1274","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alpha-adrenergic receptor activity","termid":"GO:0004936"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"alpha2-adrenergic receptor activity","secondary_identifiers":["Reactome:R-HSA-400071"],"synonyms":[{"name":"alpha2 adrenoceptor","type":"exact"}],"termid":"GO:0004938"}


id: MONDO:0011041
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ectodermal dysplasia with natal teeth, Turnpenny type is characterized by hypo- or oligodontia and acanthosis nigricans. It has been described in four generations of one family. Onset generally occurs during adolescence. Some patients were born with multiple teeth. Hair anomalies (sparse body and scalp hair) were also reported. Inheritance is autosomal dominant.","definition_xrefs":["Orphanet:69083"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"}],"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":"ectodermal dysplasia with natal teeth, Turnpenny type","secondary_identifiers":["MESH:C563347","UMLS:C1832444","GARD:10526","MEDGEN:371331","SCTID:715576000","icd11.foundation:612149960","OMIM:601345"],"synonyms":[{"name":"ectodermal dysplasia with natal teeth Turnpenny type","type":"related"},{"name":"ectodermal dysplasia with natal teeth, Turnpenny type","type":"exact"},{"name":"ectodermal dysplasia, hair/Tooth type","type":"related"}],"termid":"MONDO:0011041","xrefs":{"Monarch":{"xref_id":"0011041"}}}


id: PBO:0063071
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polyamine oxidase","termid":"PBO:0063071"}


id: MONDO:0002679
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An ischemic condition of the brain, producing a persistent focal neurological deficit in the area of distribution of the cerebral arteries.","definition_xrefs":["NCIT:C50486"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brain infarction","termid":"MONDO:0005394"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cerebral infarction","secondary_identifiers":["ICD9:433.21","MESH:D002544","ICD9:433.81","DOID:3526","ICD9:433.01","SCTID:432504007","UMLS:C0007785","ICD9:434.91","ICD9:433.31","MEDGEN:3321","SCTID:20059004"],"synonyms":[{"name":"CVA - cerebral infarction","type":"exact"},{"name":"brain infarction of telencephalon","type":"exact"},{"name":"cerebral infarct","type":"exact"},{"name":"cerebral infarction","type":"exact"},{"name":"cerebral ischemia","type":"exact"},{"name":"cerebral, infarction","type":"exact"},{"name":"infarction, cerebral","type":"exact"},{"name":"telencephalon brain infarction","type":"exact"}],"termid":"MONDO:0002679","xrefs":{"Monarch":{"xref_id":"0002679"}}}


id: PBO:0066184
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RBM7 pseudogene 1","termid":"PBO:0066184"}


id: PBO:0081889
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 839 pseudogene 1","termid":"PBO:0081889"}


id: PBO:0040870
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BMI1 proto-oncogene, polycomb ring finger","termid":"PBO:0040870"}


id: GO:0015111
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of iodide ions from one side of a membrane to the other.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monoatomic anion transmembrane transporter activity","termid":"GO:0008509"},{"relation_name":"is_a","term_name":"inorganic anion transmembrane transporter activity","termid":"GO:0015103"}],"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:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"iodide transmembrane transporter activity","secondary_identifiers":["Reactome:R-HSA-209910","Reactome:R-HSA-5627802","Reactome:R-HSA-5627870"],"termid":"GO:0015111"}


id: GO:0008691
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (S)-3-hydroxybutanoyl-CoA + NADP+ = 3-acetoacetyl-CoA + NADPH + H+.","definition_xrefs":["EC:1.1.1.157"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"3-hydroxybutyryl-CoA dehydrogenase activity","secondary_identifiers":["MetaCyc:3-HYDROXYBUTYRYL-COA-DEHYDROGENASE-RXN","RHEA:16197"],"synonyms":[{"name":"(S)-3-hydroxybutanoyl-CoA:NADP+ oxidoreductase activity","type":"related"},{"name":"BHBD activity","type":"related"},{"name":"L(+)-3-hydroxybutyryl-CoA dehydrogenase activity","type":"related"},{"name":"L-(+)-3-hydroxybutyryl-CoA dehydrogenase activity","type":"related"},{"name":"beta-hydroxybutyryl coenzyme A dehydrogenase activity","type":"related"},{"name":"beta-hydroxybutyryl-CoA dehydrogenase activity","type":"related"},{"name":"dehydrogenase, L-3-hydroxybutyryl coenzyme A (nicotinamide adenine dinucleotide phosphate)","type":"related"}],"termid":"GO:0008691"}


id: PBO:0049356
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"general transcription factor IIi pseudogene 14","termid":"PBO:0049356"}


id: PBO:0081112
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger AN1-type containing 2B","termid":"PBO:0081112"}


id: MONDO:0002602
data:
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id: MONDO:0014738
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  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the KITLG gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant nonsyndromic hearing loss","termid":"MONDO:0019587"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0019497"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0019497"],"is_obsolete":false,"name":"autosomal dominant nonsyndromic hearing loss 69","secondary_identifiers":["GARD:18143","OMIM:616697","MEDGEN:905882","UMLS:C4225241","DOID:0110590"],"synonyms":[{"name":"DCUA","type":"narrow"},{"name":"DFNA69","type":"narrow"},{"name":"KITLG autosomal dominant nonsyndromic deafness","type":"narrow"},{"name":"autosomal dominant deafness 69","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness 69","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness caused by mutation in KITLG","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness type 69","type":"narrow"},{"name":"deafness, autosomal dominant 69","type":"narrow"},{"name":"deafness, autosomal dominant 69, unilateral or asymmetric","type":"narrow"},{"name":"deafness, congenital, unilateral or asymmetric","type":"narrow"},{"name":"unilateral or asymmetric congenital deafness","type":"narrow"}],"termid":"MONDO:0014738","xrefs":{"Monarch":{"xref_id":"0014738"}}}


id: PBO:0077783
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA topoisomerase I pseudogene 1","termid":"PBO:0077783"}


id: GO:0008842
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: diphosphate + a purine nucleoside = monophosphate + a purine mononucleotide.","definition_xrefs":["GOC:rynl"],"gene_count":0,"genotype_count":0,"name":"obsolete diphosphate-purine nucleoside kinase activity (obsolete GO:0008842)","termid":"GO:0008842"}


id: GO:0046538
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: (2R)-2-phosphoglycerate = (2R)-3-phosphoglycerate; this reaction mechanism uses 2,3-bisphosphoglycerate as a phosphate donor.","definition_xrefs":["GOC:rynl"],"gene_count":0,"genotype_count":0,"name":"obsolete 2,3-bisphosphoglycerate-dependent phosphoglycerate mutase activity (obsolete GO:0046538)","termid":"GO:0046538"}


id: RO:0002500
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"A relationship between a material entity and a process where the material entity has some causal role that influences the process","direct_ancestors":[{"relation_name":"is_a","term_name":"causal_relation_between_material_entity_and_a_process","termid":"RO:0002595"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"causal_agent_in","termid":"RO:0002500"}


id: PBO:0016940
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schizosaccharomyces specific protein Mug74","termid":"PBO:0016940"}


id: MONDO:0006176
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma characterized by the presence of a cribriform architectural pattern. Representative examples include the intraductal cribriform breast carcinoma and invasive cribriform breast carcinoma.","definition_xrefs":["NCIT:C3680"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carcinoma","termid":"MONDO:0004993"}],"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":"cribriform carcinoma","secondary_identifiers":["ICDO:8201/3","UMLS:C0205643","EFO:1000210","MEDGEN:104694"],"synonyms":[{"name":"cribriform carcinoma","type":"exact"}],"termid":"MONDO:0006176","xrefs":{"Monarch":{"xref_id":"0006176"}}}


id: PR:000050510
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the rec8 gene in Schizosaccharomyces pombe.","definition_xrefs":["PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein","termid":"PR:000000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotic recombination protein rec8 (Schizosaccharomyces pombe)","pombase_gene_id":"SPBC29A10.14","synonyms":[{"name":"SPBC29A10.14","type":"related"},{"name":"Spom-rec8","type":"exact"},{"name":"cohesin rec8 (Schizosaccharomyces pombe)","type":"exact"},{"name":"rec8","type":"related"}],"termid":"PR:000050510"}


id: MONDO:0014607
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the KCNA2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"undetermined early-onset epileptic encephalopathy","termid":"MONDO:0018614"},{"relation_name":"is_a","term_name":"neonatal-onset developmental and epileptic encephalopathy","termid":"MONDO:0100455"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005027","MONDO:0004736","MONDO:0700092"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy, 32","secondary_identifiers":["OMIM:616366","DOID:0080416","GARD:16096","MEDGEN:909501","UMLS:C4225350"],"synonyms":[{"name":"DEE32","type":"exact"},{"name":"EIEE32","type":"exact"},{"name":"KCNA2 early infantile epileptic encephalopathy","type":"exact"},{"name":"developmental and epileptic encephalopathy 32","type":"exact"},{"name":"early infantile epileptic encephalopathy caused by mutation in KCNA2","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 32","type":"exact"},{"name":"epileptic encephalopathy, early infantile, type 32","type":"exact"}],"termid":"MONDO:0014607","xrefs":{"Monarch":{"xref_id":"0014607"}}}


id: PBO:0054246
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 1628","termid":"PBO:0054246"}


id: FYPO:0004501
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the rate and occurrence of DNA polymerase processivity factor activity are normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal molecular function","termid":"FYPO:0000706"},{"relation_name":"is_a","term_name":"binding phenotype","termid":"FYPO:0001092"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000257"],"is_obsolete":false,"name":"normal DNA polymerase processivity factor activity","termid":"FYPO:0004501"}


id: PBO:0060307
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MYL12B pseudogene 2","termid":"PBO:0060307"}


id: GO:0000335
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents, or reduces the frequency, rate or extent of DNA transposition.","definition_xrefs":["GOC:dph","GOC:tb","GOC:krc"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of transposition, DNA-mediated (obsolete GO:0000335)","synonyms":[{"name":"down regulation of DNA transposition","type":"exact"},{"name":"down-regulation of DNA transposition","type":"exact"},{"name":"downregulation of DNA transposition","type":"exact"},{"name":"inhibition of DNA transposition","type":"narrow"},{"name":"negative regulation of DNA transposition","type":"exact"}],"termid":"GO:0000335"}


id: PBO:0039795
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARAP1 antisense RNA 2","termid":"PBO:0039795"}


id: MONDO:0957876
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"neuronopathy, distal hereditary motor, autosomal recessive","termid":"MONDO:0015363"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0006025","MONDO:0005244"],"is_obsolete":false,"name":"neuronopathy, distal hereditary motor, autosomal recessive 10","secondary_identifiers":["MEDGEN:1846713","OMIM:620542","UMLS:C5882703","DOID:0081429"],"termid":"MONDO:0957876","xrefs":{"Monarch":{"xref_id":"0957876"}}}


id: GO:0006863
data:
  {"annotated_genes":["SJAG_04717","SJAG_03777","SJAG_00760"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[114554],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098702"},{"annotations":[114555],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098710"},{"annotations":[117170],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140140"},{"annotations":[81734],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042906"}]},"cv_name":"biological_process","definition":"The directed movement of purine bases, one of the two classes of nitrogen-containing ring compounds found in DNA and RNA, into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleobase transport","termid":"GO:0015851"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00760":null,"SJAG_03777":null,"SJAG_04717":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:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"purine nucleobase transport","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0015852"],"synonyms":[{"name":"purine base transmembrane transport","type":"exact"},{"name":"purine base transport","type":"exact"},{"name":"purine transmembrane transport","type":"related"},{"name":"purine transport","type":"related"}],"termid":"GO:0006863","terms_by_termid":{"GO:0042906":null,"GO:0098702":null,"GO:0098710":null,"GO:0140140":null}}


id: GO:0099557
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Cell-cell signaling between presynapse and postsynapse, mediated by transynaptic protein complexes, that modulates the synaptic transmission properties of the synapse.","definition_xrefs":["GOC:dos","PMID:19029886"],"direct_ancestors":[{"relation_name":"is_a","term_name":"trans-synaptic signaling by trans-synaptic complex","termid":"GO:0099545"},{"relation_name":"is_a","term_name":"trans-synaptic signaling, modulating synaptic transmission","termid":"GO:0099550"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"trans-synaptic signaling by trans-synaptic complex, modulating synaptic transmission","termid":"GO:0099557"}


id: MOD:01819
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-lysine residue to N6-succinyl-L-lysine.","definition_xrefs":["PubMed:21151122","RESID:AA0545","PubMed:16582421"],"direct_ancestors":[{"relation_name":"is_a","term_name":"succinylated residue","termid":"MOD:01029"},{"relation_name":"is_a","term_name":"N6-acylated L-lysine","termid":"MOD:01875"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01875"}],"interesting_parent_ids":["MOD:01875"],"is_obsolete":false,"name":"N6-succinyl-L-lysine","synonyms":[{"name":"(2S)-2-amino-6-[(3-carboxypropanoyl)amino]hexanoic acid","type":"exact"},{"name":"2-azanyl-6-[(3-carboxypropanoyl)azanyl]hexanoic acid","type":"exact"},{"name":"4-[[(5S)-5-amino-6-hydroxy-6-oxohexyl]amino]-4-oxobutanoate","type":"exact"},{"name":"MOD_RES N6-succinyllysine","type":"exact"},{"name":"N(epsilon)-(succinyl)lysine","type":"exact"},{"name":"N6-succinyl-L-lysine","type":"exact"},{"name":"succinyllysine","type":"exact"}],"termid":"MOD:01819"}


id: PBO:0063006
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"platelet activating factor acetylhydrolase 1b catalytic subunit 2","termid":"PBO:0063006"}


id: MONDO:0005406
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Carbohydrate intolerance first diagnosed during pregnancy.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diabetes mellitus","termid":"MONDO:0005015"},{"relation_name":"is_a","term_name":"pregnancy disorder","termid":"MONDO:0024575"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005015"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005015","MONDO:0005066","MONDO:0004335"],"is_obsolete":false,"name":"gestational diabetes","secondary_identifiers":["DOID:11714","MESH:D016640","SCTID:11687002","EFO:0004593","MEDGEN:38815","NCIT:C34942","UMLS:C0085207"],"synonyms":[{"name":"GDM","type":"exact"},{"name":"diabetes in pregnancy","type":"exact"},{"name":"gestational diabetes mellitus","type":"exact"},{"name":"maternal gestational diabetes mellitus","type":"exact"}],"termid":"MONDO:0005406","xrefs":{"Monarch":{"xref_id":"0005406"}}}


id: PBO:0084862
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial ribosomal protein of the small subunit","termid":"PBO:0084862"}


id: PBO:0029713
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_phenotype","termid":"PBO:0029713"}


id: PBO:0003814
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AP-1 adaptor complex mu subunit Apm1","termid":"PBO:0003814"}


id: PBO:0111380
data:
  {"annotation_feature_type":"gene","cv_name":"species_dist","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schizosaccharomyces specific, implicated in rRNA processing","termid":"PBO:0111380"}


id: FYPO:0004488
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 methylation of one or more lysine residues in specific proteins, or at specific protein sites, does not occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein modification during vegetative growth","termid":"FYPO:0000544"},{"relation_name":"is_a","term_name":"abnormal protein acetylation during vegetative growth","termid":"FYPO:0002392"},{"relation_name":"is_a","term_name":"abolished cellular process","termid":"FYPO:0005449"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002274"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000002","FYPO:0002494","FYPO:0001320","FYPO:0002274"],"is_obsolete":false,"name":"abolished protein lysine methylation during vegetative growth","synonyms":[{"name":"abolished peptidyl-lysine methylation during vegetative growth","type":"exact"},{"name":"abolished protein acetylation during mitotic cell cycle","type":"related"},{"name":"protein lysine methylation abolished during vegetative growth","type":"exact"},{"name":"protein lysine methylation absent during vegetative growth","type":"exact"}],"termid":"FYPO:0004488"}


id: MONDO:0013248
data:
  {"annotated_genes":["SJAG_02708"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88157],"is_not":false,"summary":null,"term":"MONDO:0013248"}]},"cv_name":"mondo","definition":"Any Fanconi anemia in which the cause of the disease is a mutation in the RAD51C gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Fanconi anemia","termid":"MONDO:0019391"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02708":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0021190"}],"interesting_parent_ids":["MONDO:0021190","MONDO:0005066","MONDO:0002280","MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"Fanconi anemia complementation group O","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:15656","UMLS:C3150653","MEDGEN:462003","DOID:0111096","OMIM:613390"],"synonyms":[{"name":"FANCO","type":"exact"},{"name":"Fanconi Anemia, complementation group type O","type":"exact"},{"name":"Fanconi anaemia caused by mutation in RAD51C","type":"exact"},{"name":"Fanconi anaemia caused by mutation in Rad51C","type":"exact"},{"name":"Fanconi anaemia complementation group type O","type":"exact"},{"name":"Fanconi anemia caused by mutation in RAD51C","type":"exact"},{"name":"Fanconi anemia caused by mutation in Rad51C","type":"exact"},{"name":"Fanconi anemia complementation group type O","type":"exact"},{"name":"Fanconi anemia, complementation group O","type":"related"},{"name":"RAD51C Fanconi anaemia","type":"exact"},{"name":"RAD51C Fanconi anemia","type":"exact"},{"name":"Rad51C Fanconi anaemia","type":"exact"},{"name":"Rad51C Fanconi anemia","type":"exact"}],"termid":"MONDO:0013248","terms_by_termid":{"MONDO:0013248":null},"xrefs":{"Monarch":{"xref_id":"0013248"}}}


id: PBO:0040117
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin repeat and SOCS box containing 4","termid":"PBO:0040117"}


id: PBO:0017952
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anaphase-promoting complex substrate recognition subunit Apc10","termid":"PBO:0017952"}


id: PBO:0031018
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-premature_cell_cycle_phase_transition","termid":"PBO:0031018"}


id: GO:0036063
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A cone-shaped structure in the head of a spermatozoon, which is formed by the coalescence of Golgi fragments following the completion of meiosis. The acroblast is situated adjacent to the acrosomal vesicle.","definition_xrefs":["GOC:sart","PMID:19934220"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"Golgi apparatus","termid":"GO:0005794"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005794"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005737","GO:0005794","GO:0005575"],"is_obsolete":false,"name":"acroblast","synonyms":[{"name":"spermatid acroblast","type":"exact"}],"termid":"GO:0036063"}


id: PBO:0071152
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L22 pseudogene 17","termid":"PBO:0071152"}


id: GO:0051733
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: NTP + 5'-dephospho-DNA = NDP + 5'-phospho-DNA.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete polydeoxyribonucleotide kinase activity (obsolete GO:0051733)","synonyms":[{"name":"DNA 5'-hydroxyl kinase activity","type":"exact"},{"name":"DNA kinase activity","type":"exact"}],"termid":"GO:0051733"}


id: PBO:0017993
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"M-factor transmembrane transporter Mam1","termid":"PBO:0017993"}


id: PBO:0003378
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"squalene monooxygenase Erg1 (predicted)","termid":"PBO:0003378"}


id: PBO:0074316
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SMAD5 antisense RNA 1","termid":"PBO:0074316"}


id: MONDO:0007434
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":"primary failure of tooth eruption","secondary_identifiers":["GARD:17692","OMIM:125350","MESH:C565114","MEDGEN:338882","UMLS:C1852222","Orphanet:412206","DOID:0111341"],"synonyms":[{"name":"PFE","type":"exact"},{"name":"dental noneruption","type":"related"},{"name":"failure of tooth eruption, primary","type":"related"},{"name":"posterior Openbite malocclusion, familial","type":"related"},{"name":"primary failure of eruption, nonsyndromic","type":"related"},{"name":"primary retention of teeth","type":"exact"},{"name":"unerupted second primary molar","type":"related"}],"termid":"MONDO:0007434","xrefs":{"Monarch":{"xref_id":"0007434"}}}


id: PBO:0066621
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RIC1 homolog, RAB6A GEF complex partner 1","termid":"PBO:0066621"}


id: GO:0019351
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of dethiobiotin, a derivative of biotin in which the sulfur atom has been replaced by two hydrogen atoms.","definition_xrefs":["GOC:ai","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amide biosynthetic process","termid":"GO:0043604"},{"relation_name":"is_a","term_name":"dethiobiotin metabolic process","termid":"GO:0046450"},{"relation_name":"is_a","term_name":"monocarboxylic acid biosynthetic process","termid":"GO:0072330"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"dethiobiotin biosynthetic process","synonyms":[{"name":"desthiobiotin biosynthesis","type":"exact"},{"name":"desthiobiotin biosynthetic process","type":"exact"},{"name":"dethiobiotin anabolism","type":"exact"},{"name":"dethiobiotin biosynthesis","type":"exact"},{"name":"dethiobiotin formation","type":"exact"},{"name":"dethiobiotin synthesis","type":"exact"}],"termid":"GO:0019351"}


id: GO:0045874
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the sevenless signaling pathway.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of signal transduction","termid":"GO:0009967"},{"relation_name":"is_a","term_name":"regulation of sevenless signaling pathway","termid":"GO:0045501"},{"relation_name":"positively_regulates","term_name":"sevenless signaling pathway","termid":"GO:0045500"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"positive regulation of sevenless signaling pathway","synonyms":[{"name":"activation of sevenless signaling pathway","type":"narrow"},{"name":"positive regulation of sev signaling pathway","type":"exact"},{"name":"positive regulation of sevenless signalling pathway","type":"exact"},{"name":"stimulation of sevenless signaling pathway","type":"narrow"},{"name":"up regulation of sevenless signaling pathway","type":"exact"},{"name":"up-regulation of sevenless signaling pathway","type":"exact"},{"name":"upregulation of sevenless signaling pathway","type":"exact"}],"termid":"GO:0045874"}


id: PATO:0001337
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A yeast mating type.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mating type","termid":"PATO:0001895"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"yeast mating type","termid":"PATO:0001337"}


id: PBO:0062210
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 AK member 1 pseudogene","termid":"PBO:0062210"}


id: FYPO:0006538
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype in which a cell is shaped in the form of a spheroid during a cellular response to a pheromone. In spheroid cells, there is much less difference between the long and short axes of the cell than in wild type. Spheroid cells may shorter than normal, with approximately the same diameter as normal, or they may be enlarged.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spheroid cell","termid":"FYPO:0001955"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000005","FYPO:0000002"],"is_obsolete":false,"name":"spheroid cell during cellular response to pheromone","synonyms":[{"name":"cell morphology, round cells during cellular response to pheromone","type":"related"},{"name":"cell morphology, rounded cells during cellular response to pheromone","type":"related"},{"name":"rounded cell during cellular response to pheromone","type":"exact"}],"termid":"FYPO:0006538"}


id: PBO:0041146
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BTF3 pseudogene 1","termid":"PBO:0041146"}


id: PR:Q9UTH3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ppk6 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9UTH3"],"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":"serine/threonine-protein kinase ppk6 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1805.01c","synonyms":[{"name":"Spom972h-ppk6","type":"exact"}],"termid":"PR:Q9UTH3"}


id: PBO:0063873
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphatidylinositol glycan anchor biosynthesis class C pseudogene 2","termid":"PBO:0063873"}


id: PBO:0039557
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ANKRD49 pseudogene 4","termid":"PBO:0039557"}


id: PBO:0028308
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_protein_localization_to_nucleus_during_cellular_response_to_methylglyoxal","termid":"PBO:0028308"}


id: PBO:0005176
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial conserved eukaryotic protein (predicted)","termid":"PBO:0005176"}


id: PBO:0077459
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 184B","termid":"PBO:0077459"}


id: PBO:0069549
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 820, pseudogene","termid":"PBO:0069549"}


id: GO:0061949
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency or extent of the discharge, by sperm, of a single, anterior secretory granule before the sperm reaches to the zona pellucida of the oocyte. The process begins with the fusion of the outer acrosomal membrane with the sperm plasma membrane and ends with the exocytosis of the acrosomal contents.","definition_xrefs":["PMID:23430248","PMID:22228629"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of reproductive process","termid":"GO:2000241"},{"relation_name":"regulates","term_name":"premature acrosome loss","termid":"GO:0061948"}],"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 premature acrosome loss","termid":"GO:0061949"}


id: GO:0097618
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A dinoflagellate sulcus that extends all the way to the posterior end of the cell (also known as antapex). The presence of a sulcal notch makes the dinoflagellate hypocone appear bilobed.","definition_xrefs":["PMID:7002229","GOC:at","Wikipedia:Dinoflagellate#Morphology"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dinoflagellate sulcus","termid":"GO:0097612"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0009986"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0009986"],"is_obsolete":false,"name":"dinoflagellate sulcal notch","synonyms":[{"name":"dinoflagellate sulcus notch","type":"exact"},{"name":"sulcal notch","type":"related"}],"termid":"GO:0097618"}


id: MONDO:0015967
data:
  {"annotated_genes":["SJAG_04495","SJAG_03247","SJAG_04334"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89134],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014674"},{"annotations":[86974,86975],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007453"},{"annotations":[88252,88251],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100165"}]},"cv_name":"mondo","definition":"Diabetes mellitus that is caused by mutations in a single gene.","direct_ancestors":[{"relation_name":"is_a","term_name":"diabetes mellitus","termid":"MONDO:0005015"},{"relation_name":"is_a","term_name":"inborn errors of metabolism","termid":"MONDO:0019052"}],"gene_count":3,"genes_by_uniquename":{"SJAG_03247":null,"SJAG_04334":null,"SJAG_04495":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005015"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005015","MONDO:0004335"],"is_obsolete":false,"name":"monogenic diabetes","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1392102","EFO:1001511","NCIT:C129739","Orphanet:183625","UMLS:C3888631"],"synonyms":[{"name":"monogenic diabetes","type":"exact"},{"name":"rare genetic diabetes mellitus","type":"exact"}],"termid":"MONDO:0015967","terms_by_termid":{"MONDO:0007453":null,"MONDO:0014674":null,"MONDO:0100165":null},"xrefs":{"Monarch":{"xref_id":"0015967"}}}


id: MONDO:0016043
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Isolated cleft lip is a fissure type embryopathy extending from the upper lip to the nasal base.","definition_xrefs":["Orphanet:199302"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cleft lip","termid":"MONDO:0004747"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"isolated cleft lip","secondary_identifiers":["MEDGEN:40327","UMLS:C0008924","GARD:17091","icd11.foundation:172183323","MedDRA:10009259"],"synonyms":[{"name":"isolated cleft lip (disease)","type":"exact"},{"name":"nonsyndromic cleft lip (disease)","type":"exact"}],"termid":"MONDO:0016043","xrefs":{"Monarch":{"xref_id":"0016043"}}}


id: PBO:0075377
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SRY-box transcription factor 14","termid":"PBO:0075377"}


id: MONDO:0011576
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Familial hyperaldosteronism type II (FH-II) is a heritable form of primary aldosteronism (PA) characterized by hypertension of varying severity, and non glucocticoid remediable hyperaldosteronism.","definition_xrefs":["Orphanet:404"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial hyperaldosteronism","termid":"MONDO:0016525"},{"relation_name":"is_a","term_name":"adrenal cortex neoplasm","termid":"MONDO:0036591"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"familial hyperaldosteronism type II","secondary_identifiers":["OMIM:605635","UMLS:C1854107","SCTID:703233008","GARD:2789","NCIT:C127162","MEDGEN:340137","MESH:C565312"],"synonyms":[{"name":"FH 2","type":"related"},{"name":"FH-II","type":"exact"},{"name":"FH2","type":"exact"},{"name":"FHII","type":"related"},{"name":"HALD2","type":"related"},{"name":"familial adrenal adenoma","type":"exact"},{"name":"familial hyperaldosteronism type 2","type":"exact"},{"name":"hyperaldosteronism, familial, type II","type":"related"}],"termid":"MONDO:0011576","xrefs":{"Monarch":{"xref_id":"0011576"}}}


id: PBO:0074446
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small integral membrane protein 47","termid":"PBO:0074446"}


id: GO:0030128
data:
  {"annotated_genes":["SJAG_02805","SJAG_01167","SJAG_00800","SJAG_00104"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[76225,80052,58571,110313],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030122"}]},"cv_name":"cellular_component","definition":"A clathrin coat found on an endocytic vesicle.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"clathrin vesicle coat","termid":"GO:0030125"},{"relation_name":"part_of","term_name":"clathrin-coated endocytic vesicle membrane","termid":"GO:0030669"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00104":null,"SJAG_00800":null,"SJAG_01167":null,"SJAG_02805":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0031410"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0031410","GO:0032991"],"is_obsolete":false,"name":"clathrin coat of endocytic vesicle","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"clathrin coat of endocytotic vesicle","type":"exact"}],"termid":"GO:0030128","terms_by_termid":{"GO:0030122":null}}


id: GO:0035911
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the descending aorta are generated and organized. The descending aorta is the portion of the aorta in a two-pass circulatory system from the arch of aorta to the point where it divides into the common iliac arteries. In a two-pass circulatory system blood passes twice through the heart to supply the body once.","definition_xrefs":["GOC:dgh","MA:0002571","UBERON:0001514","GOC:bf","Wikipedia:Descending_aorta"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"},{"relation_name":"part_of","term_name":"descending aorta development","termid":"GO:0035906"},{"relation_name":"part_of","term_name":"aorta morphogenesis","termid":"GO:0035909"}],"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":"descending aorta morphogenesis","termid":"GO:0035911"}


id: GO:0060656
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency, or extent of branching of the mammary gland cord as a result of a signal being created by a mammary fat precursor cell and its subsequent reception and interpretation by a mammary cord epithelial cell.","definition_xrefs":["GOC:dph","PMID:12558599"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-cell signaling","termid":"GO:0007267"},{"relation_name":"is_a","term_name":"regulation of branching involved in mammary gland duct morphogenesis","termid":"GO:0060762"},{"relation_name":"regulates","term_name":"branching involved in mammary gland cord morphogenesis","termid":"GO:0060655"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"regulation of branching involved in mammary cord morphogenesis by fat precursor cell-epithelial cell signaling","synonyms":[{"name":"regulation of branching involved in mammary cord morphogenesis by fat precursor cell-epithelial cell signalling","type":"exact"}],"termid":"GO:0060656"}


id: PBO:0005012
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"4.1.1.23","termid":"PBO:0005012"}


id: GO:0006219
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of deoxyuridine, 2-deoxyribosyluracil, one of the four major nucleosides of DNA.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"deoxyuridine metabolic process","termid":"GO:0046096"},{"relation_name":"is_a","term_name":"pyrimidine deoxyribonucleoside catabolic process","termid":"GO:0046127"}],"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:0055086"}],"interesting_parent_ids":["GO:0008150","GO:0055086","GO:0044281"],"is_obsolete":false,"name":"deoxyuridine catabolic process","synonyms":[{"name":"deoxyuridine breakdown","type":"exact"},{"name":"deoxyuridine catabolism","type":"exact"},{"name":"deoxyuridine degradation","type":"exact"}],"termid":"GO:0006219"}


id: MONDO:0013216
data:
  {"annotated_genes":["SJAG_02904","SJAG_04695"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88133,88134],"is_not":false,"summary":null,"term":"MONDO:0013216"}]},"cv_name":"mondo","definition":"Any Diamond-Blackfan anemia in which the cause of the disease is a mutation in the RPS10 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Diamond-Blackfan anemia","termid":"MONDO:0015253"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02904":null,"SJAG_04695":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0002280"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0002280"],"is_obsolete":false,"name":"Diamond-Blackfan anemia 9","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:C567650","GARD:15644","DOID:0111884","MEDGEN:412874","NCIT:C176918","OMIM:613308","UMLS:C2750081"],"synonyms":[{"name":"DBA9","type":"related"},{"name":"Diamond-Blackfan Anaemia type 9","type":"exact"},{"name":"Diamond-Blackfan Anemia type 9","type":"exact"},{"name":"Diamond-Blackfan anaemia caused by mutation in RPS10","type":"exact"},{"name":"Diamond-Blackfan anemia 9","type":"exact"},{"name":"Diamond-Blackfan anemia caused by mutation in RPS10","type":"exact"},{"name":"RPS10 Diamond-Blackfan anaemia","type":"exact"},{"name":"RPS10 Diamond-Blackfan anemia","type":"exact"}],"termid":"MONDO:0013216","terms_by_termid":{"MONDO:0013216":null},"xrefs":{"Monarch":{"xref_id":"0013216"}}}


id: MONDO:0017418
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chronic intestinal failure (CIF) is a chronic type of intestinal failure characterized by a nonfunctioning small bowel (that may be reversible or irreversal) where the body is unable to maintain energy and nutritional needs through absorption of food or nutrients via the intestinal tract (despite being metabolically stable) and which therefore necessitates long-term parenteral feeding. CIF may be the result of congenital digestive diseases (such as gastroschisis, atresia of small intestine), short bowel syndrome, intra-abdominal or pelvic cancer, or progressive and devastating gastrointestinal or systemic benign diseases (such as Crohn disease).","definition_xrefs":["Orphanet:294422"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intestinal disorder","termid":"MONDO:0005020"}],"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":"chronic intestinal failure","secondary_identifiers":["GARD:21178","UMLS:C4274352","MEDGEN:909276","SCTID:716665002"],"synonyms":[{"name":"CIF","type":"exact"}],"termid":"MONDO:0017418","xrefs":{"Monarch":{"xref_id":"0017418"}}}


id: GO:0033362
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of lysine, via the intermediate diaminopimelate; in this pathway tetrahydrodipicolinate is converted to meso-diaminopimelate in two enzymatic steps.","definition_xrefs":["GOC:pr","MetaCyc:PWY-5097","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lysine biosynthetic process via diaminopimelate","termid":"GO:0009089"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006520","GO:0044281","GO:0006629","GO:0008150"],"is_obsolete":false,"name":"lysine biosynthetic process via diaminopimelate, diaminopimelate-aminotransferase pathway","synonyms":[{"name":"lysine anabolism via diaminopimelate, diaminopimelate-aminotransferase pathway","type":"exact"},{"name":"lysine biosynthesis via diaminopimelate, diaminopimelate-aminotransferase pathway","type":"exact"},{"name":"lysine formation via diaminopimelate, diaminopimelate-aminotransferase pathway","type":"exact"},{"name":"lysine synthesis via diaminopimelate, diaminopimelate-aminotransferase pathway","type":"exact"}],"termid":"GO:0033362"}


id: PBO:0055253
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 2680","termid":"PBO:0055253"}


id: PBO:0058626
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6758","termid":"PBO:0058626"}


id: PATO:0001013
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001013 absolute intensity value (obsolete PATO:0001013)","termid":"PATO:0001013"}


id: GO:0047209
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: coniferyl alcohol + UDP-D-glucose = coniferin + UDP.","definition_xrefs":["EC:2.4.1.111","MetaCyc:2.4.1.111-RXN"],"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:0016757"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016757","GO:0016740"],"is_obsolete":false,"name":"coniferyl-alcohol glucosyltransferase activity","secondary_identifiers":["RHEA:23944"],"synonyms":[{"name":"UDP-glucose coniferyl alcohol glucosyltransferase activity","type":"related"},{"name":"UDP-glucose:coniferyl-alcohol 4'-beta-D-glucosyltransferase activity","type":"related"},{"name":"UDPglucose:coniferyl-alcohol 4'-beta-D-glucosyltransferase activity","type":"related"},{"name":"uridine diphosphoglucose-coniferyl alcohol glucosyltransferase activity","type":"related"}],"termid":"GO:0047209"}


id: MONDO:0859231
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin","secondary_identifiers":["UMLS:C5676928","OMIM:619769","MEDGEN:1802903"],"termid":"MONDO:0859231","xrefs":{"Monarch":{"xref_id":"0859231"}}}


id: PBO:0039294
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ALG9 intronic transcript 1","termid":"PBO:0039294"}


id: MOD:00676
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively adds oxygen atoms to a residue with or without the removal of hydrogen atoms.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidized residue","termid":"MOD:00675"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oxygenated residue","synonyms":[{"name":"OxyRes","type":"exact"}],"termid":"MOD:00676"}


id: PBO:0051632
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inner mitochondrial membrane peptidase subunit 1 pseudogene 2","termid":"PBO:0051632"}


id: PBO:0002021
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1.1.1.289","termid":"PBO:0002021"}


id: MONDO:1012865
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hearing loss that occurs in dogs due to a mutation in the KLF7 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss disorder, non-human animal","termid":"MONDO:1012969"},{"relation_name":"is_a","term_name":"inherited auditory system disease, non-human animal","termid":"MONDO:1012970"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deafness, KLF7-related, dog","secondary_identifiers":["OMIA:002326-9615"],"synonyms":[{"name":"congenital deafness, dog","type":"related"}],"termid":"MONDO:1012865","xrefs":{"Monarch":{"xref_id":"1012865"}}}


id: PBO:0090470
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial [4Fe-4S] cluster assembly and transfer protein Isa2","termid":"PBO:0090470"}


id: PBO:0013452
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AceTaldehyde Dehydrogenase","termid":"PBO:0013452"}


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


id: PBO:0071934
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S4X pseudogene 11","termid":"PBO:0071934"}


id: MONDO:0007473
data:
  {"annotated_genes":["SJAG_01114","SJAG_04522","SJAG_04765","SJAG_02278"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87205,87206,87207,87208],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011444"}]},"cv_name":"mondo","definition":"Duane retraction syndrome (DRS) is a congenital form of strabismus characterized by horizontal eye movement limitation, globe retraction and palpebral fissure narrowing in attempted adduction. It is caused by a failure of development of the abducens nerve and can lead to amblyopia.","definition_xrefs":["Orphanet:233"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"strabismus","termid":"MONDO:0003432"},{"relation_name":"excluded_subClassOf","term_name":"obsolete neuro-ophthalmological disease (obsolete MONDO:0015368)","termid":"MONDO:0015368"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"nuclear oculomotor paralysis","termid":"MONDO:0015083"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01114":null,"SJAG_02278":null,"SJAG_04522":null,"SJAG_04765":null},"genotype_count":0,"is_obsolete":false,"name":"Duane retraction syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MedDRA:10013799","NCIT:C84678","GARD:6288","SCTID:60318001","OMIMPS:126800","UMLS:C0013261","MESH:D004370","NORD:1062","MEDGEN:4413","ICD9:378.71","DOID:12557"],"synonyms":[{"name":"DRS","type":"exact"},{"name":"DURS","type":"exact"},{"name":"Duane anomaly","type":"related"},{"name":"Duane retraction syndrome","type":"exact"},{"name":"Duane syndrome","type":"exact"},{"name":"Duane's syndrome","type":"exact"},{"name":"Stilling-Turk-Duane syndrome","type":"exact"},{"name":"retraction syndrome","type":"related"}],"termid":"MONDO:0007473","terms_by_termid":{"MONDO:0011444":null},"xrefs":{"Monarch":{"xref_id":"0007473"}}}


id: GO:0015216
data:
  {"annotated_genes":["SJAG_00760","SJAG_02050","SJAG_00612","SJAG_04328","SJAG_03334"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[103307],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046964"},{"annotations":[103308],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902557"},{"annotations":[59110],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005471"},{"annotations":[104805],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140987"},{"annotations":[77244],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001409"},{"annotations":[77544],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051724"}]},"cv_name":"molecular_function","definition":"Enables the transfer of a purine nucleotide, any compound consisting of a purine nucleoside esterified with (ortho)phosphate, from one side of a membrane to the other.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide transmembrane transporter activity","termid":"GO:0015215"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00612":null,"SJAG_00760":null,"SJAG_02050":null,"SJAG_03334":null,"SJAG_04328":null},"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:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"purine nucleotide transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0015216","terms_by_termid":{"GO:0001409":null,"GO:0005471":null,"GO:0046964":null,"GO:0051724":null,"GO:0140987":null,"GO:1902557":null}}


id: _global:relation_between_physical_entity_and_a_process_or_stage
data:
  {"annotation_feature_type":"gene","cv_name":"external","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"relation_between_physical_entity_and_a_process_or_stage","secondary_identifiers":["RO:0002487"],"termid":"_global:relation_between_physical_entity_and_a_process_or_stage"}


id: PBO:0081249
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 20","termid":"PBO:0081249"}


id: GO:0042166
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to acetylcholine, an acetic acid ester of the organic base choline that functions as a neurotransmitter, released at the synapses of parasympathetic nerves and at neuromuscular junctions.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cation binding","termid":"GO:0043169"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"acetylcholine binding","termid":"GO:0042166"}


id: internal:cv_version
data:
  {"annotation_feature_type":"gene","cv_name":"cv_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cv_version","termid":"internal:cv_version"}


id: GO:0007240
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete nuclear translocation of Hog1 (obsolete GO:0007240)","synonyms":[{"name":"nuclear translocation of Hog1","type":"exact"}],"termid":"GO:0007240"}


id: PBO:0057292
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 510","termid":"PBO:0057292"}


id: GO:0071716
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of leukotrienes into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. Leukotrienes are linear C20 endogenous metabolites of arachidonic acid (icosa-5,8,11,14-tetraenoic acid) containing a terminal carboxy function and four or more double bonds (three or more of which are conjugated) as well as other functional groups.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"icosanoid transport","termid":"GO:0071715"}],"gene_count":0,"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:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"leukotriene transport","termid":"GO:0071716"}


id: MONDO:0002449
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"corneal degeneration","termid":"MONDO:0001515"}],"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":"nodular degeneration of cornea","secondary_identifiers":["UMLS:C0155122","ICD9:371.46","DOID:2879","SCTID:72620002","MEDGEN:509799"],"termid":"MONDO:0002449","xrefs":{"Monarch":{"xref_id":"0002449"}}}


id: GO:0030544
data:
  {"annotated_genes":["SJAG_03955","SJAG_00403","SJAG_03094","SJAG_01914","SJAG_00436","SJAG_03135","SJAG_01160"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[59412,67972,68263,72630,79683,81579,81686],"is_not":false,"summary":null,"term":"GO:0030544"}]},"cv_name":"molecular_function","definition":"Binding to a Hsp70 protein, heat shock proteins around 70kDa in size.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heat shock protein binding","termid":"GO:0031072"},{"relation_name":"is_a","term_name":"protein-folding chaperone binding","termid":"GO:0051087"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00403":null,"SJAG_00436":null,"SJAG_01160":null,"SJAG_01914":null,"SJAG_03094":null,"SJAG_03135":null,"SJAG_03955":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"Hsp70 protein binding","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null},"termid":"GO:0030544","terms_by_termid":{"GO:0030544":null}}


id: PBO:0017762
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase assembly protein Rcf1","termid":"PBO:0017762"}


id: PBO:0001657
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retinitis pigmentosa","termid":"PBO:0001657"}


id: MONDO:1010745
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Dermatomyositis that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dermatomyositis, non-human animal","termid":"MONDO:1010127"},{"relation_name":"is_a","term_name":"polymyositis, dog","termid":"MONDO:1010931"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dermatomyositis, dog","secondary_identifiers":["OMIA:000270-9615"],"termid":"MONDO:1010745","xrefs":{"Monarch":{"xref_id":"1010745"}}}


id: GO:0090562
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the PEP-dependent, phosphoryl transfer-driven transport of substances across a membrane. The transport happens by catalysis of the reaction: protein N-phosphohistidine + N,N'-diacetylchitobiose(out) = protein histidine + N,N'-diacetylchitobiose phosphate(in).","definition_xrefs":["GOC:am","PMID:10913119"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-N(PI)-phosphohistidine-sugar phosphotransferase activity","termid":"GO:0008982"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0022857","GO:0016740","GO:0005215"],"is_obsolete":false,"name":"protein-N(PI)-phosphohistidine-N,N'-diacetylchitobiose phosphotransferase system transporter activity","termid":"GO:0090562"}


id: PATO:0001966
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A curled quality inhering in a bearer by virtue of the bearer's one edge of its surface being wholly rolled up in another.","definition_xrefs":["ISBN:0881923214"],"direct_ancestors":[{"relation_name":"is_a","term_name":"curled","termid":"PATO:0000405"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"convolute","termid":"PATO:0001966"}


id: PR:000050474
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A myosin light chain kinase 2, skeletal/cardiac muscle that is encoded in the genome of Schizosaccharomyces pombe.","definition_xrefs":["PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein kinase wis1 (Schizosaccharomyces pombe 972h-)","termid":"PR:P33886"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein kinase wis1 (Schizosaccharomyces pombe)","pombase_gene_id":"SPBC409.07c","synonyms":[{"name":"SPBC409.07c","type":"related"},{"name":"Spom-MYLK2","type":"exact"},{"name":"protein kinase sty2 (Schizosaccharomyces pombe)","type":"exact"},{"name":"spc2","type":"related"},{"name":"sty2","type":"related"},{"name":"wis1","type":"related"}],"termid":"PR:000050474"}


id: PBO:0029600
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_sodium:hydrogen_antiporter_activity","termid":"PBO:0029600"}


id: GO:0061630
data:
  {"annotated_genes":["SJAG_02347","SJAG_00173","SJAG_02371","SJAG_02685","SJAG_04783","SJAG_01772","SJAG_03615","SJAG_04915","SJAG_03613","SJAG_01900","SJAG_05323","SJAG_01165","SJAG_02169","SJAG_02521","SJAG_01535","SJAG_02308","SJAG_02668","SJAG_03112","SJAG_02575","SJAG_00475","SJAG_00819","SJAG_05264","SJAG_02746","SJAG_02319","SJAG_04619","SJAG_03657","SJAG_01637","SJAG_00209","SJAG_01253","SJAG_02851","SJAG_04966","SJAG_00188","SJAG_02299","SJAG_03831","SJAG_00208","SJAG_03970","SJAG_04309","SJAG_01212","SJAG_04600","SJAG_01533","SJAG_03005","SJAG_00341","SJAG_03324","SJAG_00111","SJAG_03618","SJAG_01360","SJAG_03191","SJAG_01992","SJAG_03006","SJAG_03860","SJAG_05274","SJAG_00500","SJAG_03175","SJAG_05236","SJAG_03302","SJAG_00561","SJAG_04990","SJAG_01593","SJAG_03883","SJAG_00435","SJAG_05012","SJAG_04151","SJAG_00509","SJAG_03968","SJAG_00552","SJAG_04429","SJAG_01507","SJAG_01854"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[57065,58583,61845,63136,64187,65597,66877,66930,70918,71032,73253,73600,73697,74513,74726,74927,75333,76052,76055,76151,77111,77143,77404,78099,78402,79212,79247,79986,80492,80566,80948,81312,81790,89881,89891,90182,90508,90863,91603,92085,92611,93432,95462,98708,100461,101323,103254,104975,105357,105372,106314,107207,108926,109986,111631,111961,114092,114829,115407,116347,118727,118728,119233,120486],"is_not":false,"summary":null,"term":"GO:0061630"},{"annotations":[118234,120896],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140850"},{"annotations":[96249],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140851"},{"annotations":[76562],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034450"}]},"cv_name":"molecular_function","definition":"Catalysis of the transfer of ubiquitin to a substrate protein via the reaction X-ubiquitin + S = X + S-ubiquitin, where X is either an E2 or E3 enzyme, the X-ubiquitin linkage is a thioester bond, and the S-ubiquitin linkage is an amide bond: an isopeptide bond between the C-terminal glycine of ubiquitin and the epsilon-amino group of lysine residues in the substrate or, in the linear extension of ubiquitin chains, a peptide bond the between the C-terminal glycine and N-terminal methionine of ubiquitin residues.","definition_xrefs":["GOC:BioGRID","GOC:mah","GOC:tb","GOC:dph","PMID:22863777"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ubiquitin-protein transferase activity","termid":"GO:0004842"},{"relation_name":"is_a","term_name":"ubiquitin-like protein ligase 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protein ligase activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000003":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["Reactome:R-HSA-8867288","Reactome:R-HSA-5687081","Reactome:R-HSA-68946","Reactome:R-HSA-8875431","Reactome:R-HSA-3322429","Reactome:R-HSA-5654672","Reactome:R-HSA-9759172","Reactome:R-HSA-5246693","Reactome:R-HSA-9733316","Reactome:R-HSA-990526","Reactome:R-HSA-5654677","Reactome:R-HSA-69015","Reactome:R-HSA-8939706","Reactome:R-HSA-8956684","Reactome:R-HSA-1504190","Reactome:R-HSA-5682858","Reactome:R-HSA-9011300","Reactome:R-HSA-5635864","Reactome:R-HSA-6785361","Reactome:R-HSA-8953946","Reactome:R-HSA-5654679","Reactome:R-HSA-8854041","Reactome:R-HSA-8942101","Reactome:R-HSA-9009308","Reactome:R-HSA-5674022","Reactome:R-HSA-9033485","Reactome:R-HSA-8866546","Reactome:R-HSA-936462","Reactome:R-HSA-8938815","Reactome:R-HSA-9705738","Reactome:R-HSA-9755505","Reactome:R-HSA-8943080","Reactome:R-HSA-5658424","Reactome:R-HSA-5654684","Reactome:R-HSA-8956026","Reactome:R-HSA-4641253","Reactome:R-HSA-936475","Reactome:R-HSA-5689111","Reactome:R-HSA-5690827","Reactome:R-HSA-6807134","Reactome:R-HSA-8875183","Reactome:R-HSA-8943040","Reactome:R-HSA-6790487","Reactome:R-HSA-9009403","Reactome:R-HSA-6804879","Reactome:R-HSA-8854628","Reactome:R-HSA-934604","Reactome:R-HSA-8848829","Reactome:R-HSA-9766645","Reactome:R-HSA-9604629","Reactome:R-HSA-1225956","Reactome:R-HSA-8952382","Reactome:R-HSA-6804724","GO:0090302","Reactome:R-HSA-8866856","Reactome:R-HSA-9706356","Reactome:R-HSA-8876258","Reactome:R-HSA-8948832","Reactome:R-HSA-5635856","Reactome:R-HSA-6804253","Reactome:R-HSA-6782943","Reactome:R-HSA-8938773","Reactome:R-HSA-9021523","Reactome:R-HSA-9759154","Reactome:R-HSA-9686920","Reactome:R-HSA-4641129","Reactome:R-HSA-8943003","Reactome:R-HSA-8948775","Reactome:R-HSA-5632648","Reactome:R-HSA-6781867","Reactome:R-HSA-9686969","GO:1904264","Reactome:R-HSA-9685195","Reactome:R-HSA-9755304","GO:0090622","Reactome:R-HSA-8851011","Reactome:R-HSA-9762091","Reactome:R-HSA-6804942","Reactome:R-HSA-9706354","Reactome:R-HSA-9708517","Reactome:R-HSA-6807106","GO:1904822","Reactome:R-HSA-183036","Reactome:R-HSA-6804441","Reactome:R-HSA-8854051","Reactome:R-HSA-4608852","Reactome:R-HSA-9008076","Reactome:R-HSA-5610737","Reactome:R-HSA-8877003","Reactome:R-HSA-3640861","Reactome:R-HSA-8939335","Reactome:R-HSA-4641246","Reactome:R-HSA-8952419","Reactome:R-HSA-201445","Reactome:R-HSA-6798373","Reactome:R-HSA-4641159","Reactome:R-HSA-5684071"],"synonyms":[{"name":"E3","type":"broad"},{"name":"ER-associated E3 ligase","type":"related"},{"name":"protein ubiquitination activity","type":"exact"},{"name":"ubiquitin ligase activity","type":"exact"}],"termid":"GO:0061630","terms_by_termid":{"GO:0034450":null,"GO:0061630":null,"GO:0140850":null,"GO:0140851":null}}


id: PBO:0027117
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_premeiotic_DNA_replication_during_azygotic_meiosis","termid":"PBO:0027117"}


id: PBO:0045070
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DLGAP1 antisense RNA 2","termid":"PBO:0045070"}


id: PBO:0052944
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin associated like protein 29-1","termid":"PBO:0052944"}


id: GO:0046501
data:
  {"annotated_genes":["SJAG_02876","SJAG_03961","SJAG_04944","SJAG_00097","SJAG_02896","SJAG_01372","SJAG_05283","SJAG_04109"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[65884,59470,81834,57225,63905,68920,63892,60622],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006782"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving protoporphyrinogen IX, the specific substrate for the enzyme ferrochelatase, which catalyzes the insertion of iron to form protoheme. It is probably also the substrate for chlorophyll formation.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"porphyrin-containing compound metabolic process","termid":"GO:0006778"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00097":null,"SJAG_01372":null,"SJAG_02876":null,"SJAG_02896":null,"SJAG_03961":null,"SJAG_04109":null,"SJAG_04944":null,"SJAG_05283":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0033013"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0033013","GO:0008150"],"is_obsolete":false,"name":"protoporphyrinogen IX metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000041":null},"synonyms":[{"name":"protoporphyrinogen IX metabolism","type":"exact"}],"termid":"GO:0046501","terms_by_termid":{"GO:0006782":null}}


id: FYPO:0002110
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype in which a vegetatively growing cell is viable, and tapers at one end to a diameter smaller than the other. The cell diameter at the narrow end is smaller than that of a wild-type cell.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viable tapered cell","termid":"FYPO:0002108"},{"relation_name":"is_a","term_name":"viable vegetative cell with abnormal cell shape","termid":"FYPO:0002197"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000005","FYPO:0000004","FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"viable tapered vegetative cell","synonyms":[{"name":"viable bottle-shaped vegetative cell","type":"exact"},{"name":"viable bottle-shaped vegetative cell during mitotic cell cycle","type":"related"},{"name":"viable bottle/skittle vegetative cell","type":"exact"},{"name":"viable skittle-shaped vegetative cell","type":"exact"},{"name":"viable tapered cell during vegetative growth","type":"exact"}],"termid":"FYPO:0002110"}


id: PBO:0062467
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 158 pseudogene","termid":"PBO:0062467"}


id: FYPO:0003932
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 an exonucleolytic RNA catabolic process that proceeds in the 5' to 3' direction to degrade mRNA encoded in the nucleus is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah","GO:0034428"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular process during vegetative growth","termid":"FYPO:0001319"},{"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:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001312","FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal nuclear 5'-3' exonucleolytic mRNA catabolic process","synonyms":[{"name":"normal 5'-3' exonucleolytic nuclear-transcribed mRNA catabolic process","type":"exact"},{"name":"normal nuclear 5'-3' exonucleolytic mRNA catabolic process during mitotic cell cycle","type":"related"},{"name":"normal nuclear 5'-3' exonucleolytic mRNA catabolic process during vegetative growth","type":"exact"},{"name":"normal nuclear-transcribed mRNA catabolic process, exonucleolytic, 5'-3'","type":"exact"}],"termid":"FYPO:0003932"}


id: PBO:0062348
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 6 subfamily L member 1 pseudogene","termid":"PBO:0062348"}


id: PATO:0001710
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A size quality inhering in an bearer by virtue of the bearer's extension in three dimensions.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"size","termid":"PATO:0000117"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3-D extent","synonyms":[{"name":"3D size","type":"exact"}],"termid":"PATO:0001710"}


id: MONDO:0003145
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A central nervous system embryonal tumor, not otherwise specified arising from the supratentorial region.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"supratentorial cancer","termid":"MONDO:0002071"}],"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":"supratentorial primitive neuroectodermal tumor","secondary_identifiers":["MEDGEN:234914","DOID:4791","ICD9:209.30","UMLS:C1336538","SCTID:699318007","NCIT:C6968"],"synonyms":[{"name":"CNS/supratentorial PNET","type":"exact"},{"name":"supratent. primitive neuro. tumor","type":"exact"},{"name":"supratent. primitive neuro. tumour","type":"exact"},{"name":"supratentorial PNET","type":"exact"},{"name":"supratentorial primitive neuroectodermal tumor","type":"exact"}],"termid":"MONDO:0003145","xrefs":{"Monarch":{"xref_id":"0003145"}}}


id: GO:0034203
data:
  {"annotated_genes":["SJAG_03774","SJAG_02897"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[78834,96322],"is_not":false,"summary":null,"term":"GO:0034203"}]},"cv_name":"biological_process","definition":"The translocation, or flipping, of glycolipid molecules from one monolayer of a membrane bilayer to the opposite monolayer.","definition_xrefs":["GOC:go_curators","PMID:11807558"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipid translocation","termid":"GO:0034204"},{"relation_name":"is_a","term_name":"glycolipid transport","termid":"GO:0046836"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02897":null,"SJAG_03774":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0061024","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"glycolipid translocation","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0034203","terms_by_termid":{"GO:0034203":null}}


id: PBO:0047383
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box protein 17","termid":"PBO:0047383"}


id: GO:0048250
data:
  {"annotated_genes":["SJAG_02473","SJAG_04737","SJAG_04260"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[72023,100003,115805],"is_not":false,"summary":null,"term":"GO:0048250"}]},"cv_name":"biological_process","definition":"The process in which iron is transported from the cytosol into the mitochondrial matrix.","definition_xrefs":["PMID:12006577","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iron ion transmembrane transport","termid":"GO:0034755"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02473":null,"SJAG_04260":null,"SJAG_04737":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0055085","GO:0051179"],"is_obsolete":false,"name":"iron import into the mitochondrion","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:1990925"],"synonyms":[{"name":"mitochondrial iron cation transmembrane transport","type":"exact"},{"name":"mitochondrial iron ion transmembrane transport","type":"related"},{"name":"mitochondrial iron ion transport","type":"related"},{"name":"mitochondrial iron transport","type":"exact"}],"termid":"GO:0048250","terms_by_termid":{"GO:0048250":null}}


id: GO:0052247
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of a motile cell or organism within a second organism towards a higher level of a physical stimulus involved in energy generation, such as light, oxygen, and oxidizable substrates, where the two organisms are in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete positive energy taxis in other organism involved in symbiotic interaction (obsolete GO:0052247)","synonyms":[{"name":"positive energy taxis in other organism during symbiotic interaction","type":"related"},{"name":"positive energy taxis within other organism during symbiotic interaction","type":"related"}],"termid":"GO:0052247"}


id: PBO:0087280
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Short open reading frame, shows evidence of translation; may be new protein-coding gene that originated de novo from noncoding sequence; same allele found in at least 33 other S. cerevisiae strains; at least 3 strains have a second allele with three nucleotide substitutions leading to two amino acid differences","termid":"PBO:0087280"}


id: PBO:0053151
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lactate dehydrogenase B","termid":"PBO:0053151"}


id: PBO:0039022
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AGA divergent transcript","termid":"PBO:0039022"}


id: MONDO:0024549
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"microphthalmia, isolated, with coloboma","termid":"MONDO:0000170"}],"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":"microphthalmia with coloboma 1","secondary_identifiers":["MEDGEN:337338","OMIM:300345","UMLS:C1845877"],"synonyms":[{"name":"MCOPCB1","type":"exact"},{"name":"microphthalmia, colobomatous, isolated 1","type":"related"},{"name":"microphthalmia, isolated, with coloboma 1","type":"related"}],"termid":"MONDO:0024549","xrefs":{"Monarch":{"xref_id":"0024549"}}}


id: PBO:0000878
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SMN family protein Yip12","termid":"PBO:0000878"}


id: PR:000085733
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A histone H3.2, initiator methionine removed form (Schizosaccharomyces pombe) that has been phosphorylated on Ser-10. Example: UniProtKB:P09988, 2-136, Ser-11, MOD:00046.","definition_xrefs":["PRO:DAN","PomBase:VW"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H3.2, initiator methionine removed form (Schizosaccharomyces pombe)","termid":"PR:000027580"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hht2/Phos(S10)","pombase_gene_id":"SPBC8D2.04","synonyms":[{"name":"PRO_0000221366, Ser-11, MOD:00046","type":"related"},{"name":"PomBase_original_PRO_term_name: histone H3.2, initiator methionine removed phosphorylated 1 (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-hht2/InitMet-/Phos:1","type":"exact"},{"name":"UniProtKB:P09988, 2-136, Ser-11, MOD:00046","type":"related"},{"name":"hht2/Phos(S10)","type":"exact"}],"termid":"PR:000085733"}


id: MONDO:0957988
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"osteogenesis imperfecta","termid":"MONDO:0019019"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"osteogenesis imperfecta, type 23","secondary_identifiers":["UMLS:C5882757","MEDGEN:1846121","OMIM:620639"],"termid":"MONDO:0957988","xrefs":{"Monarch":{"xref_id":"0957988"}}}


id: PBO:0067855
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 157","termid":"PBO:0067855"}


id: PBO:0027762
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_protein_localization_to_prospore_membrane_during_meiosis_II_with_protein_mislocalized_to_plasma_membrane","termid":"PBO:0027762"}


id: PBO:0088834
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial [2Fe-2S] cluster assembly NADPH-ferredoxin reductase Arh1","termid":"PBO:0088834"}


id: FYPO:0001661
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of cyclic AMP measured in a cell is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased level of substance in cell during vegetative growth","termid":"FYPO:0001330"},{"relation_name":"is_a","term_name":"altered cellular cAMP level","termid":"FYPO:0001659"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"increased cellular cAMP level","synonyms":[{"name":"increased cAMP accumulation","type":"related"},{"name":"increased cellular cAMP level during mitotic cell cycle","type":"related"},{"name":"increased cellular cAMP level during vegetative growth","type":"exact"},{"name":"increased cellular cyclic AMP level","type":"exact"}],"termid":"FYPO:0001661"}


id: GO:0002529
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of the plasma kallikrein-kinin cascade.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of kinin cascade","termid":"GO:0002256"},{"relation_name":"regulates","term_name":"plasma kallikrein-kinin cascade","termid":"GO:0002353"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0051604"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0051604"],"is_obsolete":false,"name":"regulation of plasma kallikrein-kinin cascade","termid":"GO:0002529"}


id: PBO:0004707
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin activating enzyme E1","termid":"PBO:0004707"}


id: PBO:0017443
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-regulated_by","termid":"PBO:0017443"}


id: PBO:0062730
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 52 subfamily B member 4","termid":"PBO:0062730"}


id: MOD:01122
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from DeltaMass","definition_xrefs":["DeltaMass:0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DeltaMass","termid":"MOD:00947"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5'phos dCytidinyl","termid":"MOD:01122"}


id: PBO:0080664
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WAP four-disulfide core domain 10A","termid":"PBO:0080664"}


id: GO:0018419
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a protein structure comprising two or more rings that are interlocked but not covalently joined; resembling the links of a chain.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex assembly","termid":"GO:0065003"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0065003","GO:0008150","GO:0044085"],"is_obsolete":false,"name":"protein catenane formation","termid":"GO:0018419"}


id: PBO:0055591
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 3027","termid":"PBO:0055591"}


id: GO:0050034
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-rhamnofuranose + NAD+ = L-rhamnono-1,4-lactone + H+ + NADH.","definition_xrefs":["RHEA:12649","EC:1.1.1.173"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"L-rhamnose 1-dehydrogenase activity","secondary_identifiers":["KEGG_REACTION:R03942","MetaCyc:L-RHAMNOSE-1-DEHYDROGENASE-RXN"],"synonyms":[{"name":"L-rhamnofuranose:NAD+ 1-oxidoreductase activity","type":"related"}],"termid":"GO:0050034"}


id: GO:0180015
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of nucleoside from outside of a cell, across the plasma membrane and into the cytosol.","definition_xrefs":["PMID:30658162","PMID:21998139"],"direct_ancestors":[{"relation_name":"is_a","term_name":"import across plasma membrane","termid":"GO:0098739"},{"relation_name":"is_a","term_name":"nucleoside transmembrane transport","termid":"GO:1901642"}],"gene_count":0,"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:0008150","GO:0006810","GO:0055085","GO:0051179"],"is_obsolete":false,"name":"nucleoside import across plasma membrane","termid":"GO:0180015"}


id: PBO:0003214
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT organizer Mto2","termid":"PBO:0003214"}


id: PBO:0079095
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Tyr (anticodon GTA) 8-1","termid":"PBO:0079095"}


id: FYPO:0004231
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which occurrence of methylated histone binding by a gene product (usually a protein) in a mutant is abnormal. The affected gene product may be encoded by the mutated gene, or by a different gene.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone binding","termid":"FYPO:0007157"}],"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:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000702","FYPO:0000707","FYPO:0000652","FYPO:0001985"],"is_obsolete":false,"name":"abnormal methylated histone binding","termid":"FYPO:0004231"}


id: GO:0070811
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which glycerol-2-phosphate is transported across a membrane. Glycerol-2-phosphate is a phosphoric monoester of glycerol.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic anion transport","termid":"GO:0015711"},{"relation_name":"is_a","term_name":"organophosphate ester transport","termid":"GO:0015748"},{"relation_name":"is_a","term_name":"transmembrane transport","termid":"GO:0055085"},{"relation_name":"is_a","term_name":"carbohydrate derivative transport","termid":"GO:1901264"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179","GO:0055085"],"is_obsolete":false,"name":"glycerol-2-phosphate transmembrane transport","synonyms":[{"name":"glycerol-2-phosphate transport","type":"related"}],"termid":"GO:0070811"}


id: GO:0070766
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A SNARE complex that contains endobrevin (VAMP8), synaptobrevin 2 (VAMP2), alpha-SNAP, NSF, and syntaxin 4 (or orthologs thereof).","definition_xrefs":["PMID:8973549"],"direct_ancestors":[{"relation_name":"is_a","term_name":"SNARE complex","termid":"GO:0031201"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005737"],"is_obsolete":false,"name":"endobrevin-synaptobrevin 2-alpha-SNAP-NSF-syntaxin-4 complex","synonyms":[{"name":"SNARE complex (Stx4, Napa, Vamp3, Nsf, Vamp2)","type":"narrow"},{"name":"Stx4-Napa-Vamp3-Nsf-Vamp2 complex","type":"narrow"}],"termid":"GO:0070766"}


id: PBO:0056707
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MELTF antisense RNA 1","termid":"PBO:0056707"}


id: FYPO:0002712
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the occurrence of DNA recombination is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal DNA recombination","termid":"FYPO:0000063"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0000293"],"is_obsolete":false,"name":"decreased DNA recombination","synonyms":[{"name":"decreased DNA recombination frequency","type":"exact"},{"name":"decreased DNA recombination rate","type":"related"},{"name":"decreased recombination","type":"exact"},{"name":"reduced DNA recombination","type":"exact"}],"termid":"FYPO:0002712"}


id: MONDO:0006190
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An aggressive epithelial neoplasm arising from the temporal bone. It is characterized by the presence of a papillary pattern, and has been described as an adenoma or carcinoma in the literature. There is disagreement regarding its relationship to endolymphatic sac tumor.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"papillary epithelial neoplasm","termid":"MONDO:0021096"},{"relation_name":"is_a","term_name":"inner ear neoplasm","termid":"MONDO:0024320"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endolymphatic sac tumor","secondary_identifiers":["ICDO:8260/1","HP:0030393","ICD9:212.0","MEDGEN:389657","SCTID:699817008","UMLS:C2348239","EFO:1000230","NCIT:C67560"],"synonyms":[{"name":"ELST","type":"exact"},{"name":"aggressive papillary tumor of the temporal bone","type":"exact"},{"name":"aggressive papillary tumour of the temporal bone","type":"exact"},{"name":"endolymphatic sac neoplasm","type":"exact"},{"name":"endolymphatic sac neoplasm (disease)","type":"exact"},{"name":"endolymphatic sac tumor","type":"exact"},{"name":"endolymphatic sac tumor (disease)","type":"exact"},{"name":"endolymphatic sac tumour (disease)","type":"exact"},{"name":"neoplasm of endolymphatic sac","type":"exact"},{"name":"tumor of endolymphatic sac","type":"exact"},{"name":"tumour of endolymphatic sac","type":"exact"}],"termid":"MONDO:0006190","xrefs":{"Monarch":{"xref_id":"0006190"}}}


id: MONDO:0035447
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare neoplastic disease characterized by the presence of ten or more hepatocellular adenomas in a background of normal appearing hepatic parenchyma. The majority of reported cases are female. There is no association with steroid use. The condition is considered benign, although the risk of complications (such as malignant transformation or spontaneous rupture with intraperitoneal hemorrhage) is much higher than in isolated hepatic adenoma. Hepatocellular carcinoma develops in less than 10% of cases.","definition_xrefs":["Orphanet:566841"],"direct_ancestors":[{"relation_name":"is_a","term_name":"liver and intrahepatic bile duct neoplasm","termid":"MONDO:0024477"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0002515"],"is_obsolete":false,"name":"liver adenomatosis","secondary_identifiers":["GARD:22278","UMLS:C5680136","ICD10CM:D13.4","MEDGEN:1803906"],"synonyms":[{"name":"Hepatic adenomatosis","type":"exact"}],"termid":"MONDO:0035447","xrefs":{"Monarch":{"xref_id":"0035447"}}}


id: PBO:0062168
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 4 subfamily K member 11 pseudogene","termid":"PBO:0062168"}


id: PR:000037078
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that includes at least one sumoylated lysine.","definition_xrefs":["PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein","termid":"PR:000000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sumoylated protein","synonyms":[{"name":"Prot/SumoLys+","type":"exact"}],"termid":"PR:000037078"}


id: PBO:0079762
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin-fold modifier conjugating enzyme 1","termid":"PBO:0079762"}


id: MONDO:0002100
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A primary or metastatic malignant neoplasm involving the cardiovascular system.","definition_xrefs":["NCIT:C114940"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cancer","termid":"MONDO:0004992"},{"relation_name":"is_a","term_name":"cardiovascular neoplasm","termid":"MONDO:0024757"}],"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":"cardiovascular cancer","secondary_identifiers":["MEDGEN:858066","DOID:176","UMLS:C3898472"],"synonyms":[{"name":"cancer of cardiovascular system","type":"exact"},{"name":"cardiovascular neoplasm","type":"broad"},{"name":"cardiovascular system cancer","type":"exact"},{"name":"cardiovascular tumors","type":"exact"},{"name":"cardiovascular tumours","type":"exact"},{"name":"malignant cardiovascular neoplasm","type":"exact"},{"name":"malignant cardiovascular system neoplasm","type":"exact"},{"name":"malignant neoplasm of cardiovascular system","type":"exact"}],"termid":"MONDO:0002100","xrefs":{"Monarch":{"xref_id":"0002100"}}}


id: MONDO:0006295
data:
  {"annotated_genes":["SJAG_00440","SJAG_03453","SJAG_01895","SJAG_01671","SJAG_03787","SJAG_02231","SJAG_03677","SJAG_01144","SJAG_00260"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89034],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014937"},{"annotations":[87998],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0003789"},{"annotations":[88626,88627,88625],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007763"},{"annotations":[88885],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011121"},{"annotations":[87466],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007273"},{"annotations":[87675],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013602"},{"annotations":[88127],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0001187"}]},"cv_name":"mondo","definition":"A primary or metastatic malignant tumor involving the urinary system. Common tumor types include carcinomas, lymphomas, and sarcomas.","definition_xrefs":["NCIT:C9297"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cancer","termid":"MONDO:0004992"},{"relation_name":"is_a","term_name":"urinary system neoplasm","termid":"MONDO:0021066"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00260":null,"SJAG_00440":null,"SJAG_01144":null,"SJAG_01671":null,"SJAG_01895":null,"SJAG_02231":null,"SJAG_03453":null,"SJAG_03677":null,"SJAG_03787":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"malignant urinary system neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:3996","UMLS:C1644719","NCIT:C192668","EFO:1000363","ICD10CM:C64-C68","ICD9:189.9","SCTID:448233000","MEDGEN:738719"],"synonyms":[{"name":"cancer of renal system","type":"exact"},{"name":"malignant neoplasm of renal system","type":"exact"},{"name":"malignant renal system neoplasm","type":"exact"},{"name":"malignant urinary system neoplasm","type":"exact"},{"name":"malignant urinary tract neoplasm","type":"exact"},{"name":"renal system cancer","type":"exact"},{"name":"urinary system cancer","type":"exact"}],"termid":"MONDO:0006295","terms_by_termid":{"MONDO:0001187":null,"MONDO:0003789":null,"MONDO:0007273":null,"MONDO:0007763":null,"MONDO:0011121":null,"MONDO:0013602":null,"MONDO:0014937":null},"xrefs":{"Monarch":{"xref_id":"0006295"}}}


id: PBO:0064565
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paraoxonase 3","termid":"PBO:0064565"}


id: PBO:0066078
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retinoic acid receptor responder 2 pseudogene 6","termid":"PBO:0066078"}


id: MONDO:0011800
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"glioma susceptibility","termid":"MONDO:0100242"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glioma susceptibility 4","secondary_identifiers":["MEDGEN:416425","OMIM:607248","UMLS:C2750944"],"synonyms":[{"name":"GLM4","type":"exact"},{"name":"glioma susceptibility 4","type":"exact"}],"termid":"MONDO:0011800","xrefs":{"Monarch":{"xref_id":"0011800"}}}


id: MONDO:1010171
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lysosomal storage disease that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inborn errors of metabolism, non-human animal","termid":"MONDO:1012979"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lysosomal storage disease, non-human animal","secondary_identifiers":["OMIA:000616"],"termid":"MONDO:1010171","xrefs":{"Monarch":{"xref_id":"1010171"}}}


id: GO:1901340
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of store-operated calcium channel activity.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of calcium ion transmembrane transporter activity","termid":"GO:1901020"},{"relation_name":"is_a","term_name":"regulation of store-operated calcium channel activity","termid":"GO:1901339"},{"relation_name":"is_a","term_name":"negative regulation of cation channel activity","termid":"GO:2001258"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"negatively_regulates","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0055085"],"is_obsolete":false,"name":"negative regulation of store-operated calcium channel activity","synonyms":[{"name":"down regulation of store-operated calcium channel activity","type":"exact"},{"name":"down-regulation of store-operated calcium channel activity","type":"exact"},{"name":"downregulation of store-operated calcium channel activity","type":"exact"},{"name":"inhibition of store-operated calcium channel activity","type":"narrow"}],"termid":"GO:1901340"}


id: PBO:0050201
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group nucleosome binding domain 1 pseudogene 18","termid":"PBO:0050201"}


id: SO:0001269
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene that encodes a signal recognition particle (SRP) RNA.","direct_ancestors":[{"relation_name":"has_quality","term_name":"SRP_RNA_encoding","termid":"SO:0000642"},{"relation_name":"is_a","term_name":"ncRNA_gene","termid":"SO:0001263"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SRP_RNA_gene","synonyms":[{"name":"SRP RNA gene","type":"exact"}],"termid":"SO:0001269"}


id: MONDO:0010448
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Moyamoya angiopathy - short stature - facial dysmorphism - hypergonadotropic hypogonadism is a very rare, hereditary, neurological, dysmorphic syndrome characterized by moyamoya disease, short stature of postnatal onset, and stereotyped facial dysmorphism.","definition_xrefs":["Orphanet:280679"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome","termid":"MONDO:0015160"},{"relation_name":"is_a","term_name":"Moyamoya disease","termid":"MONDO:0016820"}],"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":"moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome","secondary_identifiers":["GARD:17301","MEDGEN:463207","icd11.foundation:673174743","OMIM:300845","UMLS:C3151857"],"synonyms":[{"name":"MYMY4","type":"related"},{"name":"Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism, and facial dysmorphism","type":"related"},{"name":"Moyamoya disease-short stature-facial dysmorphism-hypergonadotropic hypogonadism","type":"exact"},{"name":"chromosome Xq28 deletion syndrome, 3.4-Kb","type":"related"},{"name":"moyamoya disease 4, X-linked recessive","type":"exact"},{"name":"syndromic Moyamoya disease","type":"related"}],"termid":"MONDO:0010448","xrefs":{"Monarch":{"xref_id":"0010448"}}}


id: PBO:0035805
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_acetylation_during_vegetative_growth","termid":"PBO:0035805"}


id: GO:0003019
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The neurological process in which nerve impulses arising in the aorta or the carotid sinuses travel to the medulla and reach the nucleus of tractus solaris.","definition_xrefs":["ISBN:0323031951","GOC:mtg_cardio"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system process involved in regulation of systemic arterial blood pressure","termid":"GO:0001976"},{"relation_name":"part_of","term_name":"regulation of systemic arterial blood pressure by carotid sinus baroreceptor feedback","termid":"GO:0001978"}],"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":"central nervous system control of baroreceptor feedback","termid":"GO:0003019"}


id: FYPO:0000087
data:
  {"alleles_by_uniquename":{"SJAG_04312:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04312","name":"pka1delta","uniquename":"SJAG_04312:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[121307],"is_not":false,"summary":null,"term":"FYPO:0000087"}]},"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 hydrogen peroxide. Cells stop growing (and may die) at a concentration of hydrogen peroxide that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sensitive to DNA damaging agents","termid":"FYPO:0000266"},{"relation_name":"is_a","term_name":"sensitive to oxidative stress","termid":"FYPO:0000726"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04312":null},"genotype_count":1,"genotypes_by_uniquename":{"pka1delta":{"display_name":"pka1delta","display_uniquename":"pka1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04312:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002683"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0002683","FYPO:0000139","FYPO:0001985","FYPO:0000003"],"is_obsolete":false,"name":"sensitive to hydrogen peroxide","references_by_uniquename":{"PMID:27678009":null},"single_locus_annotated_genes":["SJAG_04312"],"single_locus_genotype_uniquenames":["pka1delta"],"synonyms":[{"name":"hypersensitive to hydrogen peroxide","type":"exact"},{"name":"sensitive to H2O2","type":"exact"},{"name":"sensitive to hydrogen peroxide during mitotic cell cycle","type":"related"},{"name":"sensitive to hydrogen peroxide during vegetative growth","type":"exact"}],"termid":"FYPO:0000087","terms_by_termid":{"FYPO:0000087":null}}


id: MONDO:0002735
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An anal adenocarcinoma arising from the anal canal mucosa. Morphologically, it resembles the adenocarcinoma which arises from the colorectal glandular epithelium. Symptoms include anal pruritus, discomfort when sitting, pain, change in bowel habit, and bleeding.","definition_xrefs":["NCIT:C7471"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anus adenocarcinoma","termid":"MONDO:0002652"},{"relation_name":"is_a","term_name":"anal canal carcinoma","termid":"MONDO:0007108"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"anal canal adenocarcinoma","secondary_identifiers":["MEDGEN:233977","UMLS:C1332259","GARD:21773","Orphanet:424016","HP:0030439","icd11.foundation:168138050","SCTID:764845008","DOID:3692"],"synonyms":[{"name":"adenocarcinoma arising in anal mucosa","type":"exact"},{"name":"adenocarcinoma arising in the anal mucosa","type":"exact"},{"name":"adenocarcinoma of anal canal","type":"exact"},{"name":"adenocarcinoma of the anal canal","type":"exact"},{"name":"anal canal adenocarcinoma","type":"exact"},{"name":"anal canal adenocarcinoma (disease)","type":"exact"}],"termid":"MONDO:0002735","xrefs":{"Monarch":{"xref_id":"0002735"}}}


id: PR:O14197
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC5D6.04 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14197"],"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 C5D6.04 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC5D6.04","synonyms":[{"name":"Spom972h-SPAC5D6.04","type":"exact"}],"termid":"PR:O14197"}


id: PBO:0001913
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pombe iNhibitor of Growth","termid":"PBO:0001913"}


id: PBO:0079958
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin specific peptidase 8","termid":"PBO:0079958"}


id: MONDO:0017174
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Machado-Joseph disease type 1 is a rare, usually severe subtype of Machado-Joseph disease (SCA3/MJD) characterized by the presence of marked pyramidal and extrapyramidal signs.","definition_xrefs":["Orphanet:276238"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Machado-Joseph disease","termid":"MONDO:0007182"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0002039"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0002039","MONDO:0000426"],"is_obsolete":false,"name":"Machado-Joseph disease type 1","secondary_identifiers":["UMLS:C0751668","GARD:21048","SCTID:91953003","MEDGEN:155610","icd11.foundation:1094680019"],"synonyms":[{"name":"SCA3, Joseph type","type":"exact"},{"name":"azorean disease, type i","type":"exact"},{"name":"spinocerebellar ataxia type 3, Joseph type","type":"exact"}],"termid":"MONDO:0017174","xrefs":{"Monarch":{"xref_id":"0017174"}}}


id: PBO:0109611
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glioma stem cell association long noncoding RNA","termid":"PBO:0109611"}


id: MONDO:0000040
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hyperphenylalaninemia, BH4-deficient (obsolete MONDO:0000040)","termid":"MONDO:0000040","xrefs":{"Monarch":{"xref_id":"0000040"}}}


id: PBO:0060155
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-RNR2 like 3 (pseudogene)","termid":"PBO:0060155"}


id: PBO:0045206
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DnaJ heat shock protein family (Hsp40) member C2","termid":"PBO:0045206"}


id: MONDO:0024465
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary pulmonary alveolar proteinosis","termid":"MONDO:0012580"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"surfactant metabolism dysfunction, pulmonary, 2","secondary_identifiers":["MEDGEN:410078","UMLS:C1970470","OMIM:610913","MESH:C567048"],"synonyms":[{"name":"SMDP2","type":"exact"},{"name":"desquamative interstitial pneumonitis due to surfactant Protein C deficiency","type":"exact"},{"name":"interstitial lung disease due to surfactant Protein C deficiency","type":"exact"},{"name":"pulmonary alveolar proteinosis, congenital, 2","type":"exact"},{"name":"surfactant metabolism dysfunction, pulmonary, 2","type":"exact"}],"termid":"MONDO:0024465","xrefs":{"Monarch":{"xref_id":"0024465"}}}


id: MONDO:0013436
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any retinitis pigmentosa in which the cause of the disease is a mutation in the USH2A gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinitis pigmentosa","termid":"MONDO:0019200"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005328","MONDO:0004736"],"is_obsolete":false,"name":"retinitis pigmentosa 39","secondary_identifiers":["MEDGEN:462488","OMIM:613809","DOID:0110360","ICD10CM:H35.5","GARD:15715","UMLS:C3151138"],"synonyms":[{"name":"RP39","type":"exact"},{"name":"USH2A retinitis pigmentosa","type":"exact"},{"name":"retinitis pigmentosa 39","type":"exact"},{"name":"retinitis pigmentosa caused by mutation in USH2A","type":"exact"},{"name":"retinitis pigmentosa type 39","type":"exact"}],"termid":"MONDO:0013436","xrefs":{"Monarch":{"xref_id":"0013436"}}}


id: PBO:0116801
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DEAD/H-box helicase 11 like 12","termid":"PBO:0116801"}


id: MONDO:0001457
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"peripheral retinal degeneration","termid":"MONDO:0001451"}],"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":"secondary vitreoretinal degeneration","secondary_identifiers":["MEDGEN:509689","UMLS:C0154859","icd11.foundation:345348088","ICD9:362.66","SCTID:60676002","DOID:12167"],"termid":"MONDO:0001457","xrefs":{"Monarch":{"xref_id":"0001457"}}}


id: PBO:0051580
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 17 receptor D","termid":"PBO:0051580"}


id: PBO:0087968
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transportin or cytosolic karyopherin beta 2; functions in the rg-nuclear localization signal-mediated nuclear import/reimport of mRNA-binding proteins Nab2p and Hrp1p; regulates asymmetric protein synthesis in daughter cells during mitosis","termid":"PBO:0087968"}


id: GO:0001163
data:
  {"annotated_genes":["SJAG_02747","SJAG_00202","SJAG_02813","SJAG_00692","SJAG_05253"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[81667,105299],"is_not":false,"summary":null,"term":"GO:0001163"},{"annotations":[80971],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001165"},{"annotations":[81034,77502],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001164"}]},"cv_name":"molecular_function","definition":"Binding to a specific sequence of DNA that is part of a regulatory region that controls the transcription of a gene or cistron by RNA polymerase I.","definition_xrefs":["GOC:txnOH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcription cis-regulatory region binding","termid":"GO:0000976"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00202":null,"SJAG_00692":null,"SJAG_02747":null,"SJAG_02813":null,"SJAG_05253":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003677"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0000976"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003677","GO:0000976","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"RNA polymerase I transcription regulatory region sequence-specific DNA binding","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0001013"],"synonyms":[{"name":"RNA polymerase I regulatory region DNA binding","type":"related"}],"termid":"GO:0001163","terms_by_termid":{"GO:0001163":null,"GO:0001164":null,"GO:0001165":null}}


id: PBO:0049837
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"highly divergent homeobox","termid":"PBO:0049837"}


id: MONDO:0009612
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Vitamin B12-unresponsive methylmalonic acidemia is an inborn error of vitamin B12 (cobalamin) metabolism characterized by recurrent ketoacidotic crises or transient vomiting, dehydration, hypotonia and intellectual deficit, which does not respond to administration of vitamin B12. There are two types of vitamin B12-unresponsive methylmalonic acidemia: mut0 and mut-.","definition_xrefs":["Orphanet:27"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methylmalonic acidemia","termid":"MONDO:0002012"},{"relation_name":"is_a","term_name":"classic organic aciduria","termid":"MONDO:0019215"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004736"],"is_obsolete":false,"name":"methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency","secondary_identifiers":["DOID:0060740","NANDO:1200794","UMLS:C1855114","NCIT:C148366","GARD:3586","MESH:C565390","OMIM:251000","MEDGEN:344424"],"synonyms":[{"name":"MCM deficiency","type":"related"},{"name":"methylmalonic acidemia due to methylmalonyl-CoA mutase deficiency","type":"exact"},{"name":"methylmalonic acidemia due to methylmalonyl-Coa mutase deficiency MMA due to MCM deficiency","type":"related"},{"name":"methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency","type":"exact"},{"name":"methylmalonic aciduria mut type","type":"exact"},{"name":"methylmalonic aciduria, mut type","type":"related"},{"name":"methylmalonic aciduria, mut(-) type","type":"related"},{"name":"methylmalonic aciduria, mut(0) type","type":"related"},{"name":"methylmalonyl-CoA mutase deficiency","type":"exact"},{"name":"methylmalonyl-Coenzyme A mutase deficiency","type":"exact"},{"name":"vitamin B12-unresponsive methylmalonic acidemia","type":"related"},{"name":"vitamin B12-unresponsive methylmalonic aciduria","type":"exact"}],"termid":"MONDO:0009612","xrefs":{"Monarch":{"xref_id":"0009612"}}}


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: PBO:0004154
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNAJ protein Caj1/Djp1-type (predicted)","termid":"PBO:0004154"}


id: FYPO:0007816
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 polyphosphate measured in a cell (total or free) is higher than normal.","definition_xrefs":["PMID:34147496","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased level of substance in cell during vegetative growth","termid":"FYPO:0001330"}],"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:0000002","FYPO:0001320"],"is_obsolete":false,"name":"increased cellular polyphosphate level","synonyms":[{"name":"increased cellular polyphosphate level during mitotic cell cycle","type":"related"},{"name":"increased cellular polyphosphate level during vegetative growth","type":"exact"},{"name":"increased polyphosphate accumulation","type":"related"}],"termid":"FYPO:0007816"}


id: MONDO:0012140
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete pulmonary function (obsolete MONDO:0012140)","secondary_identifiers":["OMIM:608852"],"synonyms":[{"name":"Plf","type":"related"},{"name":"lung function, accelerated rate of decline In, smoking-related","type":"related"},{"name":"pulmonary function","type":"related"}],"termid":"MONDO:0012140","xrefs":{"Monarch":{"xref_id":"0012140"}}}


id: PBO:0001567
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U3 snoRNP-associated protein Imp4 (predicted)","termid":"PBO:0001567"}


id: GO:0048695
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of collateral sprouting of an injured axon.","definition_xrefs":["GOC:jid","GOC:lm","GOC:dgh","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of collateral sprouting","termid":"GO:0048671"},{"relation_name":"is_a","term_name":"negative regulation of sprouting of injured axon","termid":"GO:0048688"},{"relation_name":"is_a","term_name":"regulation of collateral sprouting of injured axon","termid":"GO:0048693"},{"relation_name":"negatively_regulates","term_name":"collateral sprouting of injured axon","termid":"GO:0048674"}],"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 collateral sprouting of injured axon","synonyms":[{"name":"down regulation of collateral sprouting of injured axon","type":"exact"},{"name":"down-regulation of collateral sprouting of injured axon","type":"exact"},{"name":"downregulation of collateral sprouting of injured axon","type":"exact"},{"name":"inhibition of collateral sprouting of injured axon","type":"narrow"}],"termid":"GO:0048695"}


id: GO:0060470
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that increases the concentration of calcium ions in the cytosol after fertilization or the physiological activation of an egg.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cytosolic calcium ion concentration","termid":"GO:0007204"},{"relation_name":"part_of","term_name":"egg activation","termid":"GO:0007343"}],"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 cytosolic calcium ion concentration involved in egg activation","synonyms":[{"name":"elevation of cytosolic calcium ion concentration involved in egg activation","type":"exact"}],"termid":"GO:0060470"}


id: MOD:00435
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"Covalent modification of a peptide or protein amino acid phosphorylated serine with a secondary loss of a neutral trihydrogen phosphate molecular fragment.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"derives_from","term_name":"O-phospho-L-serine","termid":"MOD:00046"},{"relation_name":"is_a","term_name":"phosphorylated residue with neutral loss of phosphate","termid":"MOD:01151"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"O-phospho-L-serine with neutral loss of phosphate","synonyms":[{"name":"dPhosOPhosSer","type":"exact"}],"termid":"MOD:00435"}


id: SO:0001953
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region of DNA sequence formed from the ligation of two sticky ends where the palindrome is broken and no longer comprises the recognition site and thus cannot be re-cut by the restriction enzymes used to create the sticky ends.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"restriction_enzyme_region","termid":"SO:0001954"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"restriction_enzyme_assembly_scar","termid":"SO:0001953"}


id: PBO:0030636
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_proton_transport","termid":"PBO:0030636"}


id: MONDO:0044033
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An acute or subacute reversible condition characterized by headaches, mental status changes, visual disturbances, and seizures associated with imaging findings of posterior leukoencephalopathy. It has been observed in association with hypertensive encephalopathy, eclampsia, and immunosuppressive and cytotoxic drug treatment.","definition_xrefs":["NCIT:C78598"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hypertensive encephalopathy","termid":"MONDO:0006796"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"posterior leukoencephalopathy syndrome","secondary_identifiers":["UMLS:C0878576","MESH:D054038","SCTID:450886002","MEDGEN:163898"],"synonyms":[{"name":"PRES","type":"exact"},{"name":"Posterior reversible encephalopathy syndrome","type":"exact"},{"name":"RPLE","type":"exact"},{"name":"leukoencephalopathy syndrome, Posterior","type":"related"},{"name":"leukoencephalopathy syndromes, Posterior","type":"related"},{"name":"posterior reversible encephalopathy syndrome","type":"exact"},{"name":"reversible Posterior cerebral edema syndrome","type":"exact"},{"name":"reversible Posterior cerebral oedema syndrome","type":"exact"},{"name":"reversible Posterior leukoencephalopathy syndrome","type":"exact"},{"name":"reversible occipital parietal encephalopathy","type":"exact"},{"name":"reversible posterior leukoencephalopathy syndrome","type":"exact"},{"name":"syndrome, Posterior leukoencephalopathy","type":"related"},{"name":"syndromes, Posterior leukoencephalopathy","type":"related"}],"termid":"MONDO:0044033","xrefs":{"Monarch":{"xref_id":"0044033"}}}


id: GO:0090551
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 starvation stimulus, deprivation of manganese.","definition_xrefs":["GOC:tair_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to metal ion starvation","termid":"GO:0180055"}],"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 manganese ion starvation","termid":"GO:0090551"}


id: PBO:0075424
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sperm associated antigen 11A","termid":"PBO:0075424"}


id: PBO:0012837
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mature peptide sequence is YTPKVPYM","termid":"PBO:0012837"}


id: GO:0016743
data:
  {"annotated_genes":["SJAG_00964","SJAG_00635"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[73663],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004070"},{"annotations":[80275],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004585"}]},"cv_name":"molecular_function","definition":"Catalysis of the transfer of a carboxyl- or carbamoyl group from one compound (donor) to another (acceptor).","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity, transferring one-carbon groups","termid":"GO:0016741"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00635":null,"SJAG_00964":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016741","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"carboxyl- or carbamoyltransferase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["EC:2.1.3.-"],"synonyms":[{"name":"carboxyl- and carbamoyltransferase activity","type":"exact"}],"termid":"GO:0016743","terms_by_termid":{"GO:0004070":null,"GO:0004585":null}}


id: PBO:0085433
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Polyamine transporter of the major facilitator superfamily; member of the 12-spanner drug:H(+) antiporter DHA1 family; specific for spermine; localizes to the plasma membrane; TPO3 has a paralog, TPO2, that arose from the whole genome duplication","termid":"PBO:0085433"}


id: PBO:0027532
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_ribonuclease_activity","termid":"PBO:0027532"}


id: PBO:0052988
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lactalbumin alpha","termid":"PBO:0052988"}


id: PBO:0085413
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Plasma membrane sterol transporter of the ATP-binding cassette family; required, along with Pdr11p, for uptake of exogenous sterols and their incorporation into the plasma membrane; activity is stimulated by phosphatidylserine; sterol uptake is required for anaerobic growth because sterol biosynthesis requires oxygen; AUS1 has a paralog, PDR11, that arose from the whole genome duplication","termid":"PBO:0085413"}


id: PBO:0072271
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S23","termid":"PBO:0072271"}


id: PBO:0048838
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein nucleolar 3 like pseudogene 1","termid":"PBO:0048838"}


id: GO:0016073
data:
  {"annotated_genes":["SJAG_01958","SJAG_00566","SJAG_03257","SJAG_02156","SJAG_01176","SJAG_01234","SJAG_04586","SJAG_01521","SJAG_03984","SJAG_01191","SJAG_00081","SJAG_04153","SJAG_00319","SJAG_00088","SJAG_03572","SJAG_00083","SJAG_04527","SJAG_04754","SJAG_02993","SJAG_04321","SJAG_03745","SJAG_03179","SJAG_00854","SJAG_00559","SJAG_04824","SJAG_04286","SJAG_01798","SJAG_04818","SJAG_04084"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[72375,72030],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071037"},{"annotations":[97104],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120049"},{"annotations":[105774,117470],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034472"},{"annotations":[92515,118073,110015],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016180"},{"annotations":[108198,59458,108261,79401,61119,64927,82091],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031120"},{"annotations":[73370,74199,73075],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034473"},{"annotations":[104117],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034474"},{"annotations":[73371,73076,76840,78017,79462,90251,75314,78468,74200,74967,76086],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034475"},{"annotations":[91859,74201,100870,73077,73372],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034476"},{"annotations":[81202],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034477"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving snRNA, small nuclear RNA, any of various low-molecular-mass RNA molecules found in the eukaryotic nucleus as components of the small nuclear ribonucleoprotein.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA metabolic process","termid":"GO:0016070"}],"gene_count":29,"genes_by_uniquename":{"SJAG_00081":null,"SJAG_00083":null,"SJAG_00088":null,"SJAG_00319":null,"SJAG_00559":null,"SJAG_00566":null,"SJAG_00854":null,"SJAG_01176":null,"SJAG_01191":null,"SJAG_01234":null,"SJAG_01521":null,"SJAG_01798":null,"SJAG_01958":null,"SJAG_02156":null,"SJAG_02993":null,"SJAG_03179":null,"SJAG_03257":null,"SJAG_03572":null,"SJAG_03745":null,"SJAG_03984":null,"SJAG_04084":null,"SJAG_04153":null,"SJAG_04286":null,"SJAG_04321":null,"SJAG_04527":null,"SJAG_04586":null,"SJAG_04754":null,"SJAG_04818":null,"SJAG_04824":null},"genotype_count":0,"in_subsets":["bp_goslim_japonicus"],"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"snRNA metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"snRNA metabolism","type":"exact"}],"termid":"GO:0016073","terms_by_termid":{"GO:0016180":null,"GO:0031120":null,"GO:0034472":null,"GO:0034473":null,"GO:0034474":null,"GO:0034475":null,"GO:0034476":null,"GO:0034477":null,"GO:0071037":null,"GO:0120049":null}}


id: MONDO:0003547
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete histiocytic and dendritic cell cancer (obsolete MONDO:0003547)","secondary_identifiers":["NCIT:C9294"],"termid":"MONDO:0003547","xrefs":{"Monarch":{"xref_id":"0003547"}}}


id: GO:0033466
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of trans-zeatin, (2E)-2-methyl-4-(9H-purin-6-ylamino)but-2-en-1-ol.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"zeatin biosynthetic process","termid":"GO:0033398"},{"relation_name":"is_a","term_name":"trans-zeatin metabolic process","termid":"GO:0033400"}],"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":"trans-zeatin biosynthetic process","secondary_identifiers":["MetaCyc:PWY-2681"],"synonyms":[{"name":"trans-zeatin anabolism","type":"exact"},{"name":"trans-zeatin biosynthesis","type":"exact"},{"name":"trans-zeatin formation","type":"exact"},{"name":"trans-zeatin synthesis","type":"exact"}],"termid":"GO:0033466"}


id: PATO:0001599
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An oriented quality inhering in a bearer by virtue of the bearer's being relocated around an axis.","definition_xrefs":["answers.com:answers.com"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oriented","termid":"PATO:0000614"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rotated","synonyms":[{"name":"rotation","type":"exact"}],"termid":"PATO:0001599"}


id: SO:0001318
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Epoxyqueuosine is a modified 7-deazoguanosine.","direct_ancestors":[{"relation_name":"is_a","term_name":"seven_deazaguanosine","termid":"SO:0001316"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"epoxyqueuosine","secondary_identifiers":["RNAMOD:044"],"synonyms":[{"name":"eQ","type":"exact"}],"termid":"SO:0001318"}


id: PBO:0040439
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPase phospholipid transporting 8B1","termid":"PBO:0040439"}


id: MONDO:0010913
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Caroli disease (CD) is a rare congenital liver disease characterized by non-obstructive cystic dilatations of the intra-hepatic and rarely extra-hepatic bile ducts.","definition_xrefs":["Orphanet:53035"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete hereditary biliary tract disease (obsolete MONDO:0015509)","termid":"MONDO:0015509"},{"relation_name":"is_a","term_name":"non-neoplastic bile duct disorder","termid":"MONDO:0006322"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0002515","MONDO:0004335"],"is_obsolete":false,"name":"Caroli disease","secondary_identifiers":["MEDGEN:57924","UMLS:C0162510","MESH:D016767","MedDRA:10013003","OMIM:600643","icd11.foundation:1757434239","EFO:1001286","NCIT:C84619","NORD:896","SCTID:717232005","GARD:6002","NANDO:2200934","DOID:0050876"],"synonyms":[{"name":"CAROLI disease, isolated","type":"related"},{"name":"Caroli disease isolated","type":"related"},{"name":"congenital polycystic dilatation of intrahepatic bile ducts","type":"related"},{"name":"cystic dilatation of the intrahepatic biliary tree","type":"related"}],"termid":"MONDO:0010913","xrefs":{"Monarch":{"xref_id":"0010913"}}}


id: PBO:0004932
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anthranilate synthase component II (predicted)","termid":"PBO:0004932"}


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


id: PBO:0001005
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPAF2 deficiency","termid":"PBO:0001005"}


id: PATO:0002219
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in a bearer that is shaped in the form of a fan.","definition_xrefs":["thefreedictionary:http://www.thefreedictionary.com/fan-shaped"],"direct_ancestors":[{"relation_name":"is_a","term_name":"2-D shape","termid":"PATO:0002006"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fan-shaped","synonyms":[{"name":"fan-like","type":"exact"}],"termid":"PATO:0002219"}


id: GO:0001680
data:
  {"annotated_genes":["SJAG_01704","SJAG_02288"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[72085,76596],"is_not":false,"summary":null,"term":"GO:0001680"}]},"cv_name":"biological_process","definition":"Post-transcriptional addition of the terminal 3' CCA sequence to a tRNA which does not encode this sequence within the primary transcript. CCA addition proceeds by the sequential addition of CTP, CTP, and then ATP to the 3' end of the tRNA, yielding a diphosphate with each nucleotide addition.","definition_xrefs":["PMID:2247609","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA 3'-end processing","termid":"GO:0042780"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01704":null,"SJAG_02288":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0006399"}],"interesting_parent_ids":["GO:0010467","GO:0006399","GO:0008150"],"is_obsolete":false,"name":"tRNA 3'-terminal CCA addition","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0001680","terms_by_termid":{"GO:0001680":null}}


id: PBO:0026813
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_level_of_early_meiotic_gene_mRNA_during_meiotic_cell_cycle","termid":"PBO:0026813"}


id: GO:0019622
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of 3-(3-hydroxy)phenylpropionate, a hydroxylated derivative of phenylpropionate.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alcohol catabolic process","termid":"GO:0046164"},{"relation_name":"is_a","term_name":"3-(3-hydroxy)phenylpropionate metabolic process","termid":"GO:0046435"},{"relation_name":"is_a","term_name":"monocarboxylic acid catabolic process","termid":"GO:0072329"}],"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":"3-(3-hydroxy)phenylpropionate catabolic process","synonyms":[{"name":"3-(3-hydroxy)phenylpropionate breakdown","type":"exact"},{"name":"3-(3-hydroxy)phenylpropionate catabolism","type":"exact"},{"name":"3-(3-hydroxy)phenylpropionate degradation","type":"exact"}],"termid":"GO:0019622"}


id: PBO:0055490
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 2924","termid":"PBO:0055490"}


id: PBO:0083450
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 COX20/YDR231C","termid":"PBO:0083450"}


id: PBO:0064101
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PIWIL2 divergent transcript","termid":"PBO:0064101"}


id: PBO:0054340
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 1733","termid":"PBO:0054340"}


id: GO:0019854
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of L-ascorbic acid; L-ascorbic acid ionizes to give L-ascorbate, (2R)-2-[(1S)-1,2-dihydroxyethyl]-4-hydroxy-5-oxo-2,5-dihydrofuran-3-olate, which is required as a cofactor in the oxidation of prolyl residues to hydroxyprolyl, and other reactions.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-ascorbic acid metabolic process","termid":"GO:0019852"},{"relation_name":"is_a","term_name":"water-soluble vitamin catabolic process","termid":"GO:0042365"},{"relation_name":"is_a","term_name":"monosaccharide catabolic process","termid":"GO:0046365"},{"relation_name":"is_a","term_name":"carboxylic acid catabolic process","termid":"GO:0046395"},{"relation_name":"is_a","term_name":"lactone catabolic process","termid":"GO:1901335"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006766"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0005975","GO:0006766"],"is_obsolete":false,"name":"L-ascorbic acid catabolic process","secondary_identifiers":["MetaCyc:PWY0-301"],"synonyms":[{"name":"L-ascorbic acid breakdown","type":"exact"},{"name":"L-ascorbic acid catabolism","type":"exact"},{"name":"L-ascorbic acid degradation","type":"exact"},{"name":"ascorbate catabolic process","type":"exact"},{"name":"ascorbate catabolism","type":"exact"},{"name":"vitamin C catabolic process","type":"exact"},{"name":"vitamin C catabolism","type":"exact"}],"termid":"GO:0019854"}


id: PATO:0001055
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An angular placement quality inhering in a bearer by virtue of the bearer's placement at an angle that is greater than 180 degrees but less than 360 degrees to another entity.","definition_xrefs":["thesaurus.maths:thesaurus.maths"],"direct_ancestors":[{"relation_name":"is_a","term_name":"angle","termid":"PATO:0002326"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"reflex angle to","termid":"PATO:0001055"}


id: PBO:0038729
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actin gamma 1 pseudogene 24","termid":"PBO:0038729"}


id: PBO:0011519
data:
  {"annotation_feature_type":"gene","cv_name":"species_dist","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved in prokaryotes","termid":"PBO:0011519"}


id: PBO:0087777
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit Vb of cytochrome c oxidase; cytochrome c oxidase is the terminal member of the mitochondrial inner membrane electron transport chain; Cox5Bp is predominantly expressed during anaerobic growth while its isoform Va (Cox5Ap) is expressed during aerobic growth; COX5B has a paralog, COX5A, that arose from the whole genome duplication","termid":"PBO:0087777"}


id: GO:0047123
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: A + H2O + quinoline-4-carboxylate = 2-oxo-1,2-dihydroquinoline-4-carboxylate + AH(2).","definition_xrefs":["RHEA:14949","EC:1.3.99.19"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-CH group of donors","termid":"GO:0016627"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"quinoline-4-carboxylate 2-oxidoreductase activity","secondary_identifiers":["KEGG_REACTION:R05183","MetaCyc:1.3.99.19-RXN"],"synonyms":[{"name":"quinoline-4-carboxylate:acceptor 2-oxidoreductase (hydroxylating)","type":"related"},{"name":"quinoline-4-carboxylic acid 2-oxidoreductase activity","type":"related"}],"termid":"GO:0047123"}


id: PR:P87244
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- alp16 gene.","definition_xrefs":["UniProtKB:P87244","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":"spindle pole body component alp16 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC4G3.19","synonyms":[{"name":"Spom972h-alp16","type":"exact"},{"name":"altered polarity protein 16 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P87244"}


id: PBO:0119996
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SSBP3 antisense RNA 2","termid":"PBO:0119996"}


id: GO:0046579
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of Ras protein signal transduction.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of Ras protein signal transduction","termid":"GO:0046578"},{"relation_name":"is_a","term_name":"positive regulation of small GTPase mediated signal transduction","termid":"GO:0051057"},{"relation_name":"positively_regulates","term_name":"Ras protein signal transduction","termid":"GO:0007265"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of Ras protein signal transduction","secondary_identifiers":["Reactome:R-HSA-9026519","Reactome:R-HSA-9034864","Reactome:R-HSA-9027284"],"synonyms":[{"name":"activation of Ras protein signal transduction","type":"narrow"},{"name":"stimulation of Ras protein signal transduction","type":"narrow"},{"name":"up regulation of Ras protein signal transduction","type":"exact"},{"name":"up-regulation of Ras protein signal transduction","type":"exact"},{"name":"upregulation of Ras protein signal transduction","type":"exact"}],"termid":"GO:0046579"}


id: FYPO:0002651
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the attachment of spindle microtubules to the kinetochore during a mitotic or meiotic nuclear division results in the connection of a single kinetochore to both spindle poles.","definition_xrefs":["PMID:21306900","PMID:17426725"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal attachment of spindle microtubules to kinetochore","termid":"FYPO:0000325"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000631","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"merotelic kinetochore attachment","synonyms":[{"name":"merotelic attachment of spindle microtubules to kinetochore","type":"exact"}],"termid":"FYPO:0002651"}


id: PBO:0072193
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S17 pseudogene 10","termid":"PBO:0072193"}


id: PBO:0038761
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ACTR3B pseudogene 6","termid":"PBO:0038761"}


id: MONDO:1010413
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Epilepsy that occurs in horse.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epilepsy, non-human animal","termid":"MONDO:1010001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"epilepsy, horse","secondary_identifiers":["OMIA:000344-9796"],"termid":"MONDO:1010413","xrefs":{"Monarch":{"xref_id":"1010413"}}}


id: FYPO:0001016
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which vegetative cell population growth is normal (i.e. indistinguishable from wild type) in a medium containing actinomycin D.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal vegetative cell population growth","termid":"FYPO:0001357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0002057"}],"interesting_parent_ids":["FYPO:0002060","FYPO:0002057","FYPO:0000139","FYPO:0002058","FYPO:0000257","FYPO:0000003"],"is_obsolete":false,"name":"normal growth on actinomycin D","synonyms":[{"name":"normal cell population growth in presence of actinomycin D","type":"exact"},{"name":"normal cell population growth on actinomycin D","type":"exact"},{"name":"normal cellular response to actinomycin D","type":"related"},{"name":"normal vegetative cell population growth on actinomycin D","type":"exact"}],"termid":"FYPO:0001016"}


id: GO:0048561
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that determines the orientation of an animal organ or tissue with reference to an axis.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment of anatomical structure orientation","termid":"GO:0048560"},{"relation_name":"part_of","term_name":"animal organ morphogenesis","termid":"GO:0009887"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"establishment of animal organ orientation","termid":"GO:0048561"}


id: FYPO:0000626
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the initiation of premeiotic DNA replication is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal DNA replication initiation","termid":"FYPO:0000176"},{"relation_name":"is_a","term_name":"abnormal premeiotic DNA replication","termid":"FYPO:0000625"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000293"},{"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:0005447"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0000293","FYPO:0005447","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"abnormal initiation of premeiotic DNA replication","synonyms":[{"name":"abnormal initiation of meiotic DNA synthesis","type":"related"},{"name":"abnormal initiation of premeiotic DNA synthesis","type":"related"},{"name":"abnormal meiotic DNA replication initiation","type":"related"},{"name":"abnormal premeiotic DNA replication initiation","type":"exact"}],"termid":"FYPO:0000626"}


id: PBO:0027246
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-polyadenylated_25S_rRNA_absent_from_cell","termid":"PBO:0027246"}


id: MONDO:0010545
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A syndrome characterized by the association in male patients of congenital cataracts with microcornea, dental anomalies and facial dysmorphism.","definition_xrefs":["Orphanet:627"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome","termid":"MONDO:0015160"},{"relation_name":"excluded_subClassOf","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nance-Horan syndrome","secondary_identifiers":["icd11.foundation:938299000","OMIM:302350","NORD:1489","SCTID:445257004","MEDGEN:208665","DOID:0060599","ICD9:759.89","MESH:C538336","UMLS:C0796085","GARD:7161"],"synonyms":[{"name":"Mesiodens cataract syndrome","type":"related"},{"name":"Mesiodens-cataract syndrome","type":"related"},{"name":"NHS","type":"related"},{"name":"Nance-Horan syndrome","type":"exact"},{"name":"cataract X-linked with Hutchinsonian teeth","type":"related"},{"name":"cataract dental syndrome","type":"related"},{"name":"cataract, X-linked, with Hutchinsonian teeth","type":"related"},{"name":"cataract-dental syndrome","type":"related"},{"name":"nance-horan syndrome, X-linked dominant","type":"exact"}],"termid":"MONDO:0010545","xrefs":{"Monarch":{"xref_id":"0010545"}}}


id: PBO:0077832
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tumor protein p73","termid":"PBO:0077832"}


id: GO:0098557
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The side (leaflet) of the smooth endoplasmic reticulum membrane that faces the cytoplasm.","definition_xrefs":["GOC:dos","GOC:ab"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoplasmic side of endoplasmic reticulum membrane","termid":"GO:0098554"},{"relation_name":"part_of","term_name":"smooth endoplasmic reticulum membrane","termid":"GO:0030868"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005783"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005789"}],"interesting_parent_ids":["GO:0005789","GO:0005783","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"cytoplasmic side of smooth endoplasmic reticulum membrane","termid":"GO:0098557"}


id: GO:0031053
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process involved in the conversion of a primary microRNA transcript into a pre-microRNA molecule.","definition_xrefs":["GOC:sl","PMID:15211354","PMID:25799998"],"direct_ancestors":[{"relation_name":"is_a","term_name":"miRNA processing","termid":"GO:0035196"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"primary miRNA processing","secondary_identifiers":["GO:1990729","GO:1990744"],"synonyms":[{"name":"pri-miRNA processing","type":"exact"},{"name":"primary miRNA methylation","type":"narrow"},{"name":"primary miRNA modification","type":"exact"},{"name":"primary microRNA processing","type":"exact"}],"termid":"GO:0031053"}


id: PBO:0026921
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_histone_H4-K5_acetylation","termid":"PBO:0026921"}


id: GO:0034532
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2-hydroxy-7-hydroxymethylchromene-2-carboxylate = 2-hydroxy-4-hydroxymethylbenzalpyruvate.","definition_xrefs":["UM-BBD_reactionID:r0765"],"gene_count":0,"genotype_count":0,"name":"obsolete 2-hydroxy-7-hydroxymethylchromene-2-carboxylate isomerase activity (obsolete GO:0034532)","termid":"GO:0034532"}


id: GO:0019471
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving 4-hydroxyproline, C5H9NO3, a derivative of the amino acid proline. The presence of hydroxyproline is essential to produce stable triple helical tropocollagen, hence the problems caused by ascorbate deficiency in scurvy. This unusual amino acid is also present in considerable amounts in the major glycoprotein of primary plant cell walls.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified amino acid metabolic process","termid":"GO:0006575"},{"relation_name":"is_a","term_name":"non-proteinogenic amino acid metabolic process","termid":"GO:0170041"},{"relation_name":"is_a","term_name":"alpha-amino acid metabolic process","termid":"GO:1901605"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006520","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"4-hydroxyproline metabolic process","synonyms":[{"name":"4-hydroxyproline metabolism","type":"exact"}],"termid":"GO:0019471"}


id: PBO:0034376
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_potential_to_developmentally_contribute_to","termid":"PBO:0034376"}


id: PBO:0065485
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome activator subunit 2 pseudogene 4","termid":"PBO:0065485"}


id: PBO:0116475
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA/tRNA cytidine N-acetyltransferase adaptor Tan1","termid":"PBO:0116475"}


id: GO:2000967
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of cell wall polysaccharide catabolic process.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of catabolic process","termid":"GO:0009895"},{"relation_name":"is_a","term_name":"negative regulation of macromolecule metabolic process","termid":"GO:0010605"},{"relation_name":"is_a","term_name":"negative regulation of carbohydrate metabolic process","termid":"GO:0045912"},{"relation_name":"is_a","term_name":"regulation of cell wall polysaccharide catabolic process","termid":"GO:2000966"},{"relation_name":"negatively_regulates","term_name":"cell wall polysaccharide catabolic process","termid":"GO:0044347"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0005975"},{"rel_name":"negatively_regulates","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0008150","GO:0005975"],"is_obsolete":false,"name":"negative regulation of cell wall polysaccharide catabolic process","synonyms":[{"name":"negative regulation of cell wall polysaccharide breakdown","type":"exact"}],"termid":"GO:2000967"}


id: GO:0019141
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (R)-pantolactone + NADP+ = 2-dehydropantolactone + NADPH + H+. The reaction is B-specific (i.e. the pro-S hydrogen is transferred from the 4-position of reduced nicotinamide cofactor) with respect to NADP+.","definition_xrefs":["EC:1.1.1.214"],"direct_ancestors":[{"relation_name":"is_a","term_name":"2-dehydropantolactone reductase activity","termid":"GO:0036441"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"2-dehydropantolactone reductase (B-specific) activity","synonyms":[{"name":"(R)-pantolactone:NADP+ oxidoreductase (B-specific)","type":"related"},{"name":"2-dehydropantoyl-lactone reductase (B-specific) activity","type":"exact"},{"name":"2-ketopantoyl lactone reductase activity","type":"broad"},{"name":"2-oxopantoyl lactone reductase","type":"broad"},{"name":"ketopantoyl lactone reductase activity","type":"broad"}],"termid":"GO:0019141"}


id: GO:1904510
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of protein localization to basolateral plasma membrane.","definition_xrefs":["GOC:kmv","GO_REF:0000058","PMID:26115433","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein localization to cell periphery","termid":"GO:1904377"},{"relation_name":"is_a","term_name":"regulation of protein localization to basolateral plasma membrane","termid":"GO:1904508"},{"relation_name":"is_a","term_name":"positive regulation of protein localization to membrane","termid":"GO:1905477"},{"relation_name":"positively_regulates","term_name":"protein localization to basolateral plasma membrane","termid":"GO:1903361"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of protein localization to basolateral plasma membrane","synonyms":[{"name":"activation of protein localisation in basolateral plasma membrane","type":"narrow"},{"name":"activation of protein localisation to basolateral plasma membrane","type":"narrow"},{"name":"activation of protein localization in basolateral plasma membrane","type":"narrow"},{"name":"activation of protein localization to basolateral plasma membrane","type":"narrow"},{"name":"positive regulation of protein localisation in basolateral plasma membrane","type":"exact"},{"name":"positive regulation of protein localisation to basolateral plasma membrane","type":"exact"},{"name":"positive regulation of protein localization in basolateral plasma membrane","type":"exact"},{"name":"up regulation of protein localisation in basolateral plasma membrane","type":"exact"},{"name":"up regulation of protein localisation to basolateral plasma membrane","type":"exact"},{"name":"up regulation of protein localization in basolateral plasma membrane","type":"exact"},{"name":"up regulation of protein localization to basolateral plasma membrane","type":"exact"},{"name":"up-regulation of protein localisation in basolateral plasma membrane","type":"exact"},{"name":"up-regulation of protein localisation to basolateral plasma membrane","type":"exact"},{"name":"up-regulation of protein localization in basolateral plasma membrane","type":"exact"},{"name":"up-regulation of protein localization to basolateral plasma membrane","type":"exact"},{"name":"upregulation of protein localisation in basolateral plasma membrane","type":"exact"},{"name":"upregulation of protein localisation to basolateral plasma membrane","type":"exact"},{"name":"upregulation of protein localization in basolateral plasma membrane","type":"exact"},{"name":"upregulation of protein localization to basolateral plasma membrane","type":"exact"}],"termid":"GO:1904510"}


id: MONDO:0013925
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"methylmalonic aciduria and homocystinuria","termid":"MONDO:0016826"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0002280","MONDO:0005066","MONDO:0005570","MONDO:0004736"],"is_obsolete":false,"name":"methylmalonic acidemia with homocystinuria, type cblJ","secondary_identifiers":["Orphanet:369955","UMLS:C3553915","OMIM:614857","GARD:12621","MEDGEN:766829"],"synonyms":[{"name":"MAHCJ","type":"related"},{"name":"cblJ defects","type":"exact"},{"name":"cobalamin J defect","type":"exact"},{"name":"combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblJ","type":"exact"},{"name":"methylmalonic acidemia with homocystinuria type cblJ","type":"related"},{"name":"methylmalonic aciduria and homocystinuria, cblJ type","type":"related"},{"name":"methylmalonic aciduria with homocystinuria, type cblJ","type":"exact"}],"termid":"MONDO:0013925","xrefs":{"Monarch":{"xref_id":"0013925"}}}


id: PBO:0053603
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 635","termid":"PBO:0053603"}


id: GO:0014068
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of signal transduction mediated by the phosphatidylinositol 3-kinase cascade.","definition_xrefs":["GOC:ef"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of phosphatidylinositol 3-kinase signaling (obsolete GO:0014068)","synonyms":[{"name":"activation of phosphoinositide 3-kinase cascade","type":"narrow"},{"name":"positive regulation of PI 3-kinase cascade","type":"exact"},{"name":"positive regulation of PI3K cascade","type":"exact"},{"name":"positive regulation of phosphatidylinositol 3-kinase cascade","type":"related"},{"name":"positive regulation of phosphoinositide 3-kinase cascade","type":"exact"},{"name":"stimulation of phosphatidylinositol 3-kinase cascade","type":"narrow"},{"name":"up regulation of phosphatidylinositol 3-kinase cascade","type":"exact"},{"name":"up-regulation of phosphatidylinositol 3-kinase cascade","type":"exact"},{"name":"upregulation of phosphatidylinositol 3-kinase cascade","type":"exact"}],"termid":"GO:0014068"}


id: PBO:0028638
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-meiotic_spindle_absent_from_cell_during_meiosis_II","termid":"PBO:0028638"}


id: PBO:0113424
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Saccharopine dehydrogenase (NAD+, L-lysine-forming); catalyzes the conversion of saccharopine to L-lysine, which is the final step in the lysine biosynthesis pathway; contains mRNA binding activity; required for targeting of Pls1p to the peroxisomal matrix in the absence of lysine","termid":"PBO:0113424"}


id: FYPO:0004893
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of 1,3-beta-D-glucan synthase activity is normal (i.e. indistinguishable from wild type) during the vegetative growth phase of the life cycle.","definition_xrefs":["PMID:11069657","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal 1,3-beta-D-glucan synthase activity","termid":"FYPO:0002157"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000654","FYPO:0000257","FYPO:0000652"],"is_obsolete":false,"name":"normal 1,3-beta-D-glucan synthase activity during vegetative growth","synonyms":[{"name":"normal 1,3-beta-D-glucan synthase activity during vegetative growth during mitotic cell cycle","type":"related"}],"termid":"FYPO:0004893"}


id: MONDO:0030527
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"epidermolysis bullosa simplex","termid":"MONDO:0017610"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"epidermolysis bullosa simplex 2C, localized","secondary_identifiers":["MEDGEN:1794221","OMIM:619594","UMLS:C5562011"],"synonyms":[{"name":"EBS2C","type":"exact"}],"termid":"MONDO:0030527","xrefs":{"Monarch":{"xref_id":"0030527"}}}


id: PBO:0005121
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rab GTPase binding involved in ER to Golgi vesicle transport (predicted)","termid":"PBO:0005121"}


id: GO:0031607
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The subunits forming the inner ring of the core complex of a proteasome located in the nucleus of a cell.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proteasome core complex, beta-subunit complex","termid":"GO:0019774"},{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"},{"relation_name":"part_of","term_name":"nuclear proteasome core complex","termid":"GO:0031601"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005634","GO:0005575"],"is_obsolete":false,"name":"nuclear proteasome core complex, beta-subunit complex","termid":"GO:0031607"}


id: PBO:0055601
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 3037","termid":"PBO:0055601"}


id: PBO:0091965
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"wtf antidote-like meiotic drive suppressor Wtf16","termid":"PBO:0091965"}


id: GO:0180000
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binds to and stops, prevents or reduces the activity of a histone methyltransferase.","definition_xrefs":["PMID:30923826"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme inhibitor activity","termid":"GO:0004857"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140678"},{"rel_name":"is_a","termid":"GO:0004857"},{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0098772","GO:0140678","GO:0004857","GO:0003674","GO:0030234"],"is_obsolete":false,"name":"histone methyltransferase inhibitor activity","termid":"GO:0180000"}


id: PBO:0030648
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-altered_effect_on_growth_medium","termid":"PBO:0030648"}


id: GO:0140065
data:
  {"annotated_genes":["SJAG_02990"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[100897],"is_not":false,"summary":null,"term":"GO:0140065"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: butyryl-CoA + lysine in peptide = CoA + N-butyryl-lysine-peptide.","definition_xrefs":["PMID:27105113"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-acyltransferase activity","termid":"GO:0016410"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02990":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016746","GO:0016740"],"is_obsolete":false,"name":"peptide butyryltransferase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["RHEA:53912"],"synonyms":[{"name":"protein butyryltransferase activity","type":"related"}],"termid":"GO:0140065","terms_by_termid":{"GO:0140065":null}}


id: PBO:0057600
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 937","termid":"PBO:0057600"}


id: GO:0021518
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a cell becomes capable of differentiating autonomously into a commissural neuron in an environment that is neutral with respect to the developmental pathway.","definition_xrefs":["GOC:dph","GO_REF:0000021","GOC:cls","GOC:dgh","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuron fate specification","termid":"GO:0048665"},{"relation_name":"part_of","term_name":"commissural neuron differentiation in spinal cord","termid":"GO:0021528"}],"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 commissural neuron specification","termid":"GO:0021518"}


id: MONDO:0016421
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Toxic oil syndrome is a rare intoxication, due to consumption of a rapeseed oil denatured with aniline 2%, characterized by generalized vascular lesions affecting all organs and vessels (including veins and arteries) and presenting with severe incapacitating myalgias, marked peripheral eosinophilia and pulmonary infiltrates.","definition_xrefs":["Orphanet:227972"],"direct_ancestors":[{"relation_name":"is_a","term_name":"poisoning","termid":"MONDO:0029000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"toxic oil syndrome","secondary_identifiers":["SCTID:239910001","MedDRA:10051222","GARD:20566"],"termid":"MONDO:0016421","xrefs":{"Monarch":{"xref_id":"0016421"}}}


id: MONDO:0015306
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lemierre syndrome is a rare, potentially lethal, oropharyngeal infectious disease occurring in immunocompetent adolescents and young adults that is mainly due to Fusobacterium necrophorum and that is characterized by septic thrombophlebitis of the internal jugular vein that leads to septic, usually pulmonary, embolism, associated with ENT (ear, nose, and throat) infection that manifests with fever, neck pain, and tonsillopharyngitis.","definition_xrefs":["Orphanet:137839"],"direct_ancestors":[{"relation_name":"is_a","term_name":"commensal bacterial infectious disease","termid":"MONDO:0000315"},{"relation_name":"is_a","term_name":"bacterial infectious disease with sepsis","termid":"MONDO:0005229"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Lemierre syndrome","secondary_identifiers":["MESH:D057831","DOID:11337","UMLS:C0027537","MEDGEN:6541","SCTID:52542005","GARD:6882","ICD9:040.3","MedDRA:10065552"],"synonyms":[{"name":"Lemierre postanginal sepsis","type":"exact"},{"name":"Lemierre syndrome","type":"exact"},{"name":"Lemierre's syndrome","type":"related"},{"name":"acute sore throat","type":"related"},{"name":"human necrobacillosis","type":"exact"},{"name":"necrobacillosis","type":"related"},{"name":"oropharyngeal infection leading to secondary septic thrombophlebitis of the internal jugular vein","type":"related"},{"name":"postanginal sepsis","type":"exact"},{"name":"postanginal sepsis secondary to orophyngeal infection","type":"exact"},{"name":"septic phlebitis of the internal jugular vein","type":"exact"}],"termid":"MONDO:0015306","xrefs":{"Monarch":{"xref_id":"0015306"}}}


id: MONDO:1010101
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Galactosemia that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of orbital region, non-human animal","termid":"MONDO:1011315"},{"relation_name":"is_a","term_name":"disorder of visual system, non-human animal","termid":"MONDO:1011316"},{"relation_name":"is_a","term_name":"inborn errors of metabolism, non-human animal","termid":"MONDO:1012979"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"galactosemia, non-human animal","secondary_identifiers":["OMIA:001144"],"termid":"MONDO:1010101","xrefs":{"Monarch":{"xref_id":"1010101"}}}


id: PBO:0048979
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G-patch domain containing 2 like","termid":"PBO:0048979"}


id: PBO:0045248
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNAJC27 antisense RNA 1","termid":"PBO:0045248"}


id: GO:1902131
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of (+)-lariciresinol.","definition_xrefs":["PMID:8910615","PMID:9872995","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenol-containing compound catabolic process","termid":"GO:0019336"},{"relation_name":"is_a","term_name":"primary alcohol catabolic process","termid":"GO:0034310"},{"relation_name":"is_a","term_name":"lignan catabolic process","termid":"GO:0046273"},{"relation_name":"is_a","term_name":"ether catabolic process","termid":"GO:1901502"},{"relation_name":"is_a","term_name":"(+)-lariciresinol metabolic process","termid":"GO:1902130"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0019748","GO:0044281"],"is_obsolete":false,"name":"(+)-lariciresinol catabolic process","synonyms":[{"name":"(+)-lariciresinol breakdown","type":"exact"},{"name":"(+)-lariciresinol catabolism","type":"exact"},{"name":"(+)-lariciresinol degradation","type":"exact"}],"termid":"GO:1902131"}


id: PBO:0073104
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"stress responsive DNAJB4 interacting membrane protein 1","termid":"PBO:0073104"}


id: PBO:0070855
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L13 pseudogene 8","termid":"PBO:0070855"}


id: MONDO:0003019
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any disorder caused by an insufficient amount or availability of potassium, which generally manifests with myalgia, tetany, hypotension, polyuria, and polydipsia.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mineral metabolism disease","termid":"MONDO:0000226"},{"relation_name":"is_a","term_name":"nutritional disorder","termid":"MONDO:0005137"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"potassium deficiency disease","secondary_identifiers":["HP:0002900","UMLS:C1514284","ICD10CM:E87.6","MEDGEN:271346","NCIT:C34939","ICD9:276.8","DOID:4500","MESH:D007008","SCTID:43339004"],"synonyms":[{"name":"hypokalemia","type":"exact"},{"name":"hypopotassemia","type":"related"},{"name":"potassium deficiency disorder","type":"related"}],"termid":"MONDO:0003019","xrefs":{"Monarch":{"xref_id":"0003019"}}}


id: PBO:0057782
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 2909","termid":"PBO:0057782"}


id: PBO:0076517
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"taste 2 receptor member 19","termid":"PBO:0076517"}


id: PBO:0051577
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 17 receptor A","termid":"PBO:0051577"}


id: MONDO:0002111
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete peritoneal mesothelioma (obsolete MONDO:0002111)","termid":"MONDO:0002111","xrefs":{"Monarch":{"xref_id":"0002111"}}}


id: PBO:0004996
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UCS-domain protein Rng3","termid":"PBO:0004996"}


id: PBO:0110302
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial and nuclear tRNA (guanine-N2-)-methyltransferase Trm1.2","termid":"PBO:0110302"}


id: MONDO:0043125
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"ptosis","termid":"MONDO:0000728"}],"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":"mcpherson robertson cammarano syndrome","secondary_identifiers":["MESH:C538161","MEDGEN:419888","UMLS:C2931751"],"synonyms":[{"name":"dominantly inherited ptosis, strabismus and ectopic pupils","type":"related"}],"termid":"MONDO:0043125","xrefs":{"Monarch":{"xref_id":"0043125"}}}


id: MONDO:0017674
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A disease in which focal palmoplantar keratoderma is a major feature..","gene_count":0,"genotype_count":0,"name":"obsolete disease with focal palmoplantar keratoderma as a major feature (obsolete MONDO:0017674)","secondary_identifiers":["Orphanet:307871"],"synonyms":[{"name":"disease with focal palmoplantar hyperkeratosis as a major feature","type":"exact"}],"termid":"MONDO:0017674","xrefs":{"Monarch":{"xref_id":"0017674"}}}


id: MONDO:0008373
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"arterial disorder","termid":"MONDO:0000473"},{"relation_name":"is_a","term_name":"COL4A1-related disorder","termid":"MONDO:0800461"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retinal arterial tortuosity","secondary_identifiers":["OMIM:180000","HP:0001136","DOID:0111547","MEDGEN:140840","GARD:16693","Orphanet:75326","UMLS:C0423401"],"synonyms":[{"name":"RATOR","type":"related"},{"name":"retinal arterial tortuosity","type":"exact"},{"name":"retinal arterial tortuosity (disease)","type":"exact"},{"name":"retinal arteries, tortuosity OF","type":"related"},{"name":"retinal arteriolar tortuosity","type":"exact"},{"name":"retinal haemorrhage with vascular tortuosity","type":"exact"},{"name":"retinal hemorrhage with vascular tortuosity","type":"exact"},{"name":"tortuosity of retinal arteries","type":"exact"}],"termid":"MONDO:0008373","xrefs":{"Monarch":{"xref_id":"0008373"}}}


id: PBO:0055166
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 2587","termid":"PBO:0055166"}


id: FYPO:0000858
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 nucleosome positioning in regions of heterochromatin is normal (i.e. indistinguishable from wild type). Nucleosome positioning is the ordering of successions of nucleosomes into regular arrays so that nucleosomes are positioned at defined distances from one another.","definition_xrefs":["PomBase:mah","GO:0016584"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal nucleosome positioning","termid":"FYPO:0000856"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0001312","FYPO:0000257"],"is_obsolete":false,"name":"normal nucleosome positioning in heterochromatin","synonyms":[{"name":"normal nucleosome occupancy in heterochromatin","type":"related"},{"name":"normal nucleosome positioning in heterochromatin during mitotic cell cycle","type":"related"},{"name":"normal nucleosome positioning in heterochromatin during vegetative growth","type":"exact"},{"name":"normal nucleosome spacing in heterochromatin","type":"exact"}],"termid":"FYPO:0000858"}


id: PBO:0057711
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1297","termid":"PBO:0057711"}


id: PBO:0113080
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cysteine aminopeptidase with homocysteine-thiolactonase activity; protects cells against homocysteine toxicity; cytosolic protein, selectively transported to vacuole during nitrogen starvation; targeted to vacuole via CVT pathway; has bleomycin hydrolase activity in vitro; transcription is regulated by galactose via Gal4p; orthologous to human BLMH","termid":"PBO:0113080"}


id: GO:0075300
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of zygospore formation, a process in which a thick-walled spore of some algae and fungi is formed by union of two similar sexual cells, usually serves as a resting spore, and produces the sporophytic phase.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of sexual sporulation resulting in formation of a cellular spore","termid":"GO:0043942"},{"relation_name":"is_a","term_name":"regulation of zygospore formation","termid":"GO:0075298"},{"relation_name":"negatively_regulates","term_name":"zygospore formation","termid":"GO:0034296"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"negative regulation of zygospore formation","termid":"GO:0075300"}


id: PATO:0000417
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000417 absolute number value (obsolete PATO:0000417)","termid":"PATO:0000417"}


id: PBO:0067350
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 447, pseudogene","termid":"PBO:0067350"}


id: PBO:0063781
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PHD finger protein 6","termid":"PBO:0063781"}


id: GO:0100008
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any prostaglandin biosynthetic process process that regulates fever generation.","definition_xrefs":["GOC:cjm","GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prostaglandin biosynthetic process","termid":"GO:0001516"},{"relation_name":"regulates","term_name":"fever generation","termid":"GO:0001660"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006629","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"regulation of fever generation by prostaglandin biosynthetic process","termid":"GO:0100008"}


id: PBO:0034205
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-is_model_of","termid":"PBO:0034205"}


id: MOD:00028
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts a source amino acid residue to L-tyrosine.","definition_xrefs":["DeltaMass:0","PubMed:5550972","ChEBI:29975","PubMed:6061414","PubMed:6120171","PubMed:6692818","PubMed:2190093","PubMed:2542938","RESID:AA0019"],"direct_ancestors":[{"relation_name":"is_a","term_name":"natural, standard, encoded residue","termid":"MOD:01441"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-tyrosine residue","synonyms":[{"name":"(2S)-2-amino-3-(4-hydoxyphenyl)propanoic acid","type":"exact"},{"name":"2-azanyl-3-(4-hydoxyphenyl)propanoic acid","type":"exact"},{"name":"L-tyrosine","type":"exact"},{"name":"Tyr","type":"exact"},{"name":"alpha-amino-beta-(para-hydroxyphenyl)propionic acid","type":"exact"},{"name":"p-tyrosine","type":"exact"},{"name":"para-hydroxyphenylalanine","type":"exact"}],"termid":"MOD:00028"}


id: PBO:0005338
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IMPcyclohydrolase/phosphoribosylaminoimidazolecarboxamideformyltransferase","termid":"PBO:0005338"}


id: PBO:0074082
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 25 member 53","termid":"PBO:0074082"}


id: PBO:0076347
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"synaptotagmin 14","termid":"PBO:0076347"}


id: PBO:0047146
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 180 member B","termid":"PBO:0047146"}


id: PBO:0069305
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 561, pseudogene","termid":"PBO:0069305"}


id: PBO:0060228
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myeloid associated differentiation marker","termid":"PBO:0060228"}


id: PBO:0055995
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"large 60S subunit nuclear export GTPase 1","termid":"PBO:0055995"}


id: MONDO:0018280
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Muscle-eye-brain (MEB) disease with bilateral multicystic leucodystrophy is a form of congenital muscular alpha-dystroglycanopathy with brain and eye anomaly characterized by severe muscle-eye-brain disease-like phenotype associated with macrocephaly and extended bilateral multicystic white matter disease, overlapping with the cerebral findings in patients with megalencephalic leukoencephalopathy with subcortical cysts.","definition_xrefs":["Orphanet:370997"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscular dystrophy-dystroglycanopathy","termid":"MONDO:0018276"},{"relation_name":"is_a","term_name":"cobblestone lissencephaly","termid":"MONDO:0018869"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0002320"],"is_obsolete":false,"name":"muscle-eye-brain disease with bilateral multicystic leucodystrophy","secondary_identifiers":["UMLS:C5191414","GARD:17608","MEDGEN:1675257"],"synonyms":[{"name":"MEB disease with bilateral multicystic leucodystrophy","type":"exact"}],"termid":"MONDO:0018280","xrefs":{"Monarch":{"xref_id":"0018280"}}}


id: GO:1905117
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of ribonucleoside-diphosphate reductase activity.","definition_xrefs":["PMID:24733891","GO_REF:0000059","GOC:TermGenie","GOC:bhm"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of ribonucleoside-diphosphate reductase activity (obsolete GO:1905117)","synonyms":[{"name":"regulation of RNR","type":"related"},{"name":"regulation of adenosylcobalamin-dependent ribonucleotide reductase activity","type":"related"},{"name":"regulation of aerobic non-heme iron-dependent ribonucleotide reductase activity","type":"related"},{"name":"regulation of anaerobic iron-sulfur-dependent ribonucleotide reductase activity","type":"related"},{"name":"regulation of class I ribonucleotide reductase activity","type":"related"},{"name":"regulation of class II ribonucleoside-diphosphate reductase activity","type":"related"},{"name":"regulation of class II ribonucleotide reductase activity","type":"related"},{"name":"regulation of class III ribonucleotide reductase activity","type":"related"},{"name":"regulation of nucleoside diphosphate reductase activity","type":"related"},{"name":"regulation of purine/pyrimidine nucleoside diphosphate reduction","type":"related"},{"name":"regulation of ribonucleoside 5'-diphosphate reductase activity","type":"related"},{"name":"regulation of ribonucleotide diphosphate reductase activity","type":"exact"},{"name":"regulation of ribonucleotide reductase activity","type":"broad"}],"termid":"GO:1905117"}


id: GO:0018228
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of peptidyl-cysteine to form peptidyl-S-geranylgeranylcysteine; formation of S-geranylgeranyl-L-cysteine may be coupled with subsequent cleavage of a carboxy-terminal tripeptide for the CAAX motif and methyl esterification of the geranylgeranylated cysteine; methyl esterification but not cleavage occurs for the CXC motif. For the type II geranylgeranyltransferase the residue may be found at the first and final positions in the sequence motif C-X-C* or at the final position in the sequence motif C-C*. These motifs are necessary but not sufficient for modification.","definition_xrefs":["RESID:AA0104"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-S-geranylgeranyl-L-cysteine biosynthetic process from peptidyl-cysteine (obsolete GO:0018228)","synonyms":[{"name":"peptidyl-S-geranylgeranyl-L-cysteine anabolism from peptidyl-cysteine","type":"exact"},{"name":"peptidyl-S-geranylgeranyl-L-cysteine formation from peptidyl-cysteine","type":"exact"},{"name":"peptidyl-S-geranylgeranyl-L-cysteine synthesis from peptidyl-cysteine","type":"exact"}],"termid":"GO:0018228"}


id: GO:0070775
data:
  {"annotated_genes":["SJAG_00411","SJAG_04815","SJAG_00545","SJAG_01385","SJAG_01009","SJAG_02165","SJAG_02629"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[101602,92632,107273,106384],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036410"},{"annotations":[95846,108485,107274,109897],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033100"},{"annotations":[79641],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990467"}]},"cv_name":"cellular_component","definition":"A multisubunit complex that catalyzes the acetylation of histone H3.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone acetyltransferase complex","termid":"GO:0000123"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00411":null,"SJAG_00545":null,"SJAG_01009":null,"SJAG_01385":null,"SJAG_02165":null,"SJAG_02629":null,"SJAG_04815":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005694","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"H3 histone acetyltransferase complex","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"H3 HAT complex","type":"exact"}],"termid":"GO:0070775","terms_by_termid":{"GO:0033100":null,"GO:0036410":null,"GO:1990467":null}}


id: PBO:0091326
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"I:g.1424709delA","termid":"PBO:0091326"}


id: GO:0061077
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process of inhibiting aggregation and assisting in the covalent and noncovalent assembly of single chain polypeptides or multisubunit complexes into the correct tertiary structure that is dependent on interaction with a chaperone.","definition_xrefs":["GOC:dph","GOC:vw"],"gene_count":0,"genotype_count":0,"name":"obsolete chaperone-mediated protein folding (obsolete GO:0061077)","termid":"GO:0061077"}


id: GO:0018679
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: dibenzothiophene 5,5-dioxide + FMNH2 + NADH + O2 = 2'-hydroxybiphenyl-2-sulfinate + FMN + H+ + H2O + NAD+.","definition_xrefs":["RHEA:12312"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen","termid":"GO:0016712"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"dibenzothiophene sulfone monooxygenase (NADH) activity","secondary_identifiers":["UM-BBD_reactionID:r0235","MetaCyc:RXN-20709","EC:1.14.14.22"],"synonyms":[{"name":"dibenzothiophene-5,5-dioxide monooxygenase activity","type":"narrow"}],"termid":"GO:0018679"}


id: GO:0106258
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a 1,2-diacyl-sn-glycero-3-phosphocholine + L-serine = 1,2-diacyl-sn-glycero-3-phospho-L-serine + choline.","definition_xrefs":["PMID:19014349","RHEA:45088"],"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:0003824","GO:0003674","GO:0016740","GO:0016780"],"is_obsolete":false,"name":"L-serine-phosphatidylcholine phosphatidyltransferase activity","termid":"GO:0106258"}


id: PBO:0085071
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nonhistone component of centromeric chromatin; binds to histone H3 variant, Cse4p, and recruits it to centromeres; involved in the assembly and maintenance of Cse4-H4 at centromeres; required for kinetochore assembly and G2/M progression; may protect Cse4p from ubiquitination; homolog of mammalian HJURP","termid":"PBO:0085071"}


id: PBO:0057190
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 362","termid":"PBO:0057190"}


id: MOD:00890
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-histidine residue to a phosphorylated L-histidine, such as pros-phosphohistidine, or tele-phosphohistidine.","definition_xrefs":["OMSSA:192","Unimod:21#H"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-histidine residue","termid":"MOD:00909"},{"relation_name":"is_a","term_name":"N-phosphorylated residue","termid":"MOD:01456"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00696"}],"interesting_parent_ids":["MOD:00696"],"is_obsolete":false,"name":"phosphorylated L-histidine","synonyms":[{"name":"NPhosHis","type":"exact"},{"name":"Phospho","type":"related"},{"name":"mod192","type":"exact"},{"name":"phosphohistidine","type":"exact"}],"termid":"MOD:00890"}


id: PBO:0065448
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome 26S subunit, ATPase 5","termid":"PBO:0065448"}


id: PBO:0031736
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_mitotic_recombination","termid":"PBO:0031736"}


id: GO:0090378
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a seed trichome irreversibly increases in size in one [spatial] dimension or along one axis, resulting in the morphogenesis of the cell.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"is_a","term_name":"unidimensional cell growth","termid":"GO:0009826"},{"relation_name":"is_a","term_name":"cellular process involved in reproduction in multicellular organism","termid":"GO:0022412"},{"relation_name":"part_of","term_name":"seed trichome differentiation","termid":"GO:0090376"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"seed trichome elongation","termid":"GO:0090378"}


id: GO:0061763
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The organelle membrane fusion process in which the membrane of a multivesicular body fuses with a lysosome to create a hybrid organelle.","definition_xrefs":["GOC:pad","PMID:21118109","GOC:dph","GOC:PARL"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle fusion","termid":"GO:0006906"},{"relation_name":"is_a","term_name":"lysosomal membrane organization","termid":"GO:0097212"},{"relation_name":"part_of","term_name":"endosome to lysosome transport via multivesicular body sorting pathway","termid":"GO:0032510"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0008150","GO:0016192","GO:0006810","GO:0061024"],"is_obsolete":false,"name":"multivesicular body-lysosome fusion","synonyms":[{"name":"MVB-lysosome fusion","type":"exact"},{"name":"endosome-lysosome fusion","type":"related"},{"name":"fusion of MVB to lysosome","type":"exact"},{"name":"fusion of multivesicular body to lysosome","type":"exact"},{"name":"late endosome-lysosome fusion","type":"related"}],"termid":"GO:0061763"}


id: GO:0050308
data:
  {"annotated_genes":["SJAG_00685","SJAG_05314","SJAG_00039","SJAG_01862","SJAG_01646","SJAG_02713"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[77915,74847,76783,80603],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004331"},{"annotations":[81694,75713],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004805"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: sugar phosphate + H2O = sugar + phosphate.","definition_xrefs":["EC:3.1.3.23","MetaCyc:SUGAR-PHOSPHATASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbohydrate phosphatase activity","termid":"GO:0019203"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00039":null,"SJAG_00685":null,"SJAG_01646":null,"SJAG_01862":null,"SJAG_02713":null,"SJAG_05314":null},"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:0003674","GO:0016787","GO:0016788","GO:0003824"],"is_obsolete":false,"name":"sugar-phosphatase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["KEGG_REACTION:R00804"],"synonyms":[{"name":"sugar-phosphate phosphatase activity","type":"exact"},{"name":"sugar-phosphate phosphohydrolase activity","type":"exact"}],"termid":"GO:0050308","terms_by_termid":{"GO:0004331":null,"GO:0004805":null}}


id: PBO:0087329
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sorting nexin; involved in retrieval of late-Golgi SNAREs from post-Golgi endosomes to the trans-Golgi network and in cytoplasm to vacuole transport; contains a PX phosphoinositide-binding domain; forms complexes with Snx41p and with Atg20p","termid":"PBO:0087329"}


id: GO:0035957
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of the breakdown of starch, by activating or increasing the frequency, rate or extent of transcription from an RNA polymerase II promoter.","definition_xrefs":["GOC:dgf"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of starch catabolic process by positive regulation of transcription from RNA polymerase II promoter (obsolete GO:0035957)","synonyms":[{"name":"positive regulation of starch breakdown by regulation of transcription from Pol II promoter","type":"exact"},{"name":"positive regulation of starch breakdown by regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of starch catabolic process by regulation of transcription from Pol II promoter","type":"exact"},{"name":"positive regulation of starch catabolism by regulation of transcription from Pol II promoter","type":"exact"},{"name":"positive regulation of starch catabolism by regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of starch degradation by regulation of transcription from Pol II promoter","type":"exact"},{"name":"positive regulation of starch degradation by regulation of transcription from RNA polymerase II promoter","type":"related"}],"termid":"GO:0035957"}


id: GO:1903804
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of glycine from outside of a cell, across the plasma membrane and into the cytosol.","definition_xrefs":["GO_REF:0000075","PMID:23895341","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycine transport","termid":"GO:0015816"},{"relation_name":"is_a","term_name":"amino acid import across plasma membrane","termid":"GO:0089718"},{"relation_name":"is_a","term_name":"carboxylic acid transmembrane transport","termid":"GO:1905039"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810","GO:0055085"],"is_obsolete":false,"name":"glycine import across plasma membrane","secondary_identifiers":["GO:0036233"],"synonyms":[{"name":"glycine import","type":"broad"},{"name":"glycine import into cell","type":"exact"}],"termid":"GO:1903804"}


id: GO:0015439
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + H2O + heme(in) = ADP + phosphate + heme(out).","definition_xrefs":["RHEA:19261"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heme transmembrane transporter activity","termid":"GO:0015232"},{"relation_name":"is_a","term_name":"ABC-type transporter activity","termid":"GO:0140359"}],"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:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"ABC-type heme transporter activity","secondary_identifiers":["EC:7.6.2.5","Reactome:R-HSA-382560","Reactome:R-HSA-917979","MetaCyc:3.6.3.41-RXN","Reactome:R-HSA-5683355","Reactome:R-HSA-1369065","GO:0103115"],"synonyms":[{"name":"ATP-dependent heme transmembrane transporter activity","type":"exact"},{"name":"ATPase-coupled heme transmembrane transporter activity","type":"related"},{"name":"ATPase-coupled heme transporter activity","type":"related"},{"name":"haem-transporting ATPase activity","type":"exact"},{"name":"heme ABC transporter","type":"narrow"},{"name":"heme-transporting ATPase activity","type":"exact"},{"name":"protoheme IX ABC transporter activity","type":"related"}],"termid":"GO:0015439"}


id: FYPO:0007714
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 phosphatidylethanolamine measured in the mitochondrion differs from normal.","definition_xrefs":["PomBase:mah","PMID:33483504"],"direct_ancestors":[{"relation_name":"is_a","term_name":"altered level of substance in mitochondrion","termid":"FYPO:0004957"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"decreased mitochondrial phosphatidylethanolamine level","synonyms":[{"name":"decreased mitochondrial PE level","type":"exact"},{"name":"decreased mitochondrial phosphatidylethanolamine level during mitotic cell cycle","type":"related"},{"name":"decreased mitochondrial phosphatidylethanolamine level during vegetative growth","type":"exact"},{"name":"decreased phosphatidylethanolamine in mitochondria","type":"exact"},{"name":"decreased phosphatidylethanolamine level in mitochondria","type":"exact"},{"name":"reduced mitochondrial phosphatidylethanolamine level","type":"exact"}],"termid":"FYPO:0007714"}


id: GO:0031598
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The regulatory subcomplex of a proteasome located in the nucleus of a cell.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proteasome regulatory particle","termid":"GO:0005838"},{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"},{"relation_name":"part_of","term_name":"nuclear proteasome complex","termid":"GO:0031595"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"part_of","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005634","GO:0005575"],"is_obsolete":false,"name":"nuclear proteasome regulatory particle","termid":"GO:0031598"}


id: GO:0060543
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate, frequency or extent of strand invasion. Strand invasion is the process in which the nucleoprotein complex (composed of the broken single-strand DNA and the recombinase) searches and identifies a region of homology in intact duplex DNA. The broken single-strand DNA displaces the like strand and forms Watson-Crick base pairs with its complement, forming a duplex in which each strand is from one of the two recombining DNA molecules.","definition_xrefs":["GOC:tb","GOC:dph","GOC:elh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of DNA recombination","termid":"GO:0045910"},{"relation_name":"is_a","term_name":"regulation of strand invasion","termid":"GO:0060542"},{"relation_name":"negatively_regulates","term_name":"DNA strand invasion","termid":"GO:0042148"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006310"},{"rel_name":"regulates","termid":"GO:0006310"},{"rel_name":"regulates","termid":"GO:0006259"},{"rel_name":"negatively_regulates","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006259","GO:0008150","GO:0006310"],"is_obsolete":false,"name":"negative regulation of strand invasion","synonyms":[{"name":"negative regulation of D-loop biosynthesis","type":"related"},{"name":"negative regulation of D-loop formation","type":"related"},{"name":"negative regulation of Rad51-mediated strand invasion","type":"exact"}],"termid":"GO:0060543"}


id: SO:0001342
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Isowyosine is a modified guanosine base feature.","direct_ancestors":[{"relation_name":"is_a","term_name":"modified_guanosine","termid":"SO:0001276"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"isowyosine","secondary_identifiers":["RNAMOD:101"],"synonyms":[{"name":"imG2","type":"exact"}],"termid":"SO:0001342"}


id: PBO:0063482
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PDK1 and ITGA6 antisense RNA 1","termid":"PBO:0063482"}


id: GO:0061062
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency, or extent of nematode larval development, the process whose specific outcome is the progression of the nematode larva over time, from its formation to the mature structure. Nematode larval development begins with the newly hatched first-stage larva (L1) and ends with the end of the last larval stage (for example the fourth larval stage (L4) in C. elegans). Each stage of nematode larval development is characterized by proliferation of specific cell lineages and an increase in body size without alteration of the basic body plan. Nematode larval stages are separated by molts in which each stage-specific exoskeleton, or cuticle, is shed and replaced anew.","definition_xrefs":["GOC:kmv","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of post-embryonic development","termid":"GO:0048580"},{"relation_name":"regulates","term_name":"nematode larval development","termid":"GO:0002119"}],"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 nematode larval development","termid":"GO:0061062"}


