# terms

id: GO:0150037
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of calcium-dependent activation of synaptic vesicle fusion.","definition_xrefs":["PMID:27052163","GOC:aruk","GOC:bc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of synaptic vesicle fusion to presynaptic active zone membrane","termid":"GO:0031630"},{"relation_name":"regulates","term_name":"calcium-dependent activation of synaptic vesicle fusion","termid":"GO:0099502"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"regulates","termid":"GO:0061024"}],"interesting_parent_ids":["GO:0061024","GO:0006810","GO:0016192","GO:0008150"],"is_obsolete":false,"name":"regulation of calcium-dependent activation of synaptic vesicle fusion","termid":"GO:0150037"}


id: PBO:0050730
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock protein family D (Hsp60) member 1 pseudogene 16","termid":"PBO:0050730"}


id: PBO:0003219
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"poly(A) polymerase Cid11 (predicted)","termid":"PBO:0003219"}


id: GO:0047059
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: polyvinyl alcohol + ferricytochrome c = oxidized polyvinyl alcohol + ferrocytochrome c + H+.","definition_xrefs":["EC:1.1.2.6"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, cytochrome as acceptor","termid":"GO:0016898"}],"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:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"polyvinyl alcohol dehydrogenase (cytochrome) activity","secondary_identifiers":["MetaCyc:RXN-11316","KEGG_REACTION:R03136","RHEA:20157"],"synonyms":[{"name":"PVA dehydrogenase activity","type":"broad"},{"name":"polyvinyl alcohol:ferricytochrome-c oxidoreductase activity","type":"exact"},{"name":"polyvinyl-alcohol:(acceptor) oxidoreductase activity","type":"broad"},{"name":"polyvinyl-alcohol:acceptor oxidoreductase activity","type":"broad"}],"termid":"GO:0047059"}


id: PBO:0082032
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"17-kDa component of the U4/U6aU5 tri-snRNP; plays an essential role in pre-mRNA splicing; human ortholog TXNL4A (the human U5-specific 15-kDa protein) complements yeast dib1 null mutant","termid":"PBO:0082032"}


id: PBO:0087019
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribose-5-phosphate ketol-isomerase; catalyzes the interconversion of ribose 5-phosphate and ribulose 5-phosphate in the pentose phosphate pathway; participates in pyridoxine biosynthesis","termid":"PBO:0087019"}


id: MONDO:0008164
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"otosclerosis","termid":"MONDO:0005349"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"otosclerosis 1","secondary_identifiers":["DOID:0060920","UMLS:C4551901","MEDGEN:1639517","OMIM:166800"],"synonyms":[{"name":"OTS","type":"related"},{"name":"OTSC1","type":"exact"},{"name":"otosclerosis 1","type":"exact"}],"termid":"MONDO:0008164","xrefs":{"Monarch":{"xref_id":"0008164"}}}


id: MONDO:0007208
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Boomerang dysplasia (BD) is a rare lethal skeletal dysplasia characterized by severe short-limbed dwarfism, dislocated joints, club feet, distinctive facies and diagnostic x-ray findings of underossified and dysplastic long tubular bones, with a boomerang-like bowing.","definition_xrefs":["Orphanet:1263"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with multiple joint dislocations (obsolete MONDO:0019700)","termid":"MONDO:0019700"},{"relation_name":"is_a","term_name":"osteochondrodysplasia","termid":"MONDO:0005516"},{"relation_name":"is_a","term_name":"filamin-related bone disorder","termid":"MONDO:0019690"}],"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":"Boomerang dysplasia","secondary_identifiers":["GARD:933","MESH:C536573","MEDGEN:96579","ICD9:756.9","SCTID:254054000","DOID:0050680","icd11.foundation:423736259","UMLS:C0432201","OMIM:112310"],"synonyms":[{"name":"Boomerang dysplasia","type":"exact"},{"name":"Boomerang-like skeletal dysplasia","type":"related"},{"name":"dwarfism with short, bowed, rigid limbs and characteristic facies","type":"related"}],"termid":"MONDO:0007208","xrefs":{"Monarch":{"xref_id":"0007208"}}}


id: FYPO:0007599
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A transcription regulation phenotype observed in the vegetative growth phase of the life cycle in which chromatin silencing is increased at a site where silencing can be triggered by the ectopic tethering of a protein.","definition_xrefs":["PMID:23613586","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal chromatin silencing","termid":"FYPO:0000144"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0006551","FYPO:0005447","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"increased chromatin silencing at ectopic tethering site","synonyms":[{"name":"increased chromatin silencing at ectopic tethering site","type":"related"},{"name":"increased chromatin silencing at ectopic tethering site during vegetative growth","type":"exact"}],"termid":"FYPO:0007599"}


id: PBO:0002975
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"human WW domain binding protein-2 ortholog","termid":"PBO:0002975"}


id: GO:0106195
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the translocation of inorganic anions linked to oxidoreductase reactions.","definition_xrefs":["GOC:hjd"],"gene_count":0,"genotype_count":0,"name":"obsolete translocase activity acting on inorganic anions linked to oxidoreductase reactions (obsolete GO:0106195)","termid":"GO:0106195"}


id: PBO:0068255
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 45S pre-ribosomal 2","termid":"PBO:0068255"}


id: GO:0048161
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The stage in oogenesis when a double layer of distinct follicle cells surrounds the oocyte. An example of this process is found in Mus musculus.","definition_xrefs":["ISBN:0198542771","GOC:jid","GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mammalian oogenesis stage","termid":"GO:0022605"}],"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":"double layer follicle stage","synonyms":[{"name":"mammalian oogenesis stage 4","type":"exact"}],"termid":"GO:0048161"}


id: GO:0031406
data:
  {"annotated_genes":["SJAG_03861"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[75855],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016594"}]},"cv_name":"molecular_function","definition":"Binding to a carboxylic acid, an organic acid containing one or more carboxyl (COOH) groups or anions (COO-).","definition_xrefs":["ISBN:0198506732","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anion binding","termid":"GO:0043168"},{"relation_name":"is_a","term_name":"organic acid binding","termid":"GO:0043177"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03861":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"carboxylic acid binding","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0031406","terms_by_termid":{"GO:0016594":null}}


id: PBO:0001420
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTPase Ypt3","termid":"PBO:0001420"}


id: GO:0047537
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-2-aminohexanoate + 2-oxoglutarate = 2-oxohexanoate + L-glutamate.","definition_xrefs":["MetaCyc:2-AMINOHEXANOATE-AMINOTRANSFERASE-RXN","EC:2.6.1.67"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transaminase activity","termid":"GO:0008483"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016769"},{"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:0003674","GO:0016740","GO:0016769","GO:0003824"],"is_obsolete":false,"name":"2-aminohexanoate transaminase activity","secondary_identifiers":["RHEA:23600"],"synonyms":[{"name":"2-aminohexanoate aminotransferase activity","type":"exact"},{"name":"L-2-aminohexanoate:2-oxoglutarate aminotransferase activity","type":"related"},{"name":"leucine L-norleucine: 2-oxoglutarate aminotransferase activity","type":"related"},{"name":"norleucine (leucine) aminotransferase activity","type":"related"},{"name":"norleucine aminotransferase activity","type":"related"},{"name":"norleucine transaminase activity","type":"related"}],"termid":"GO:0047537"}


id: MONDO:0009147
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive hypohidrotic ectodermal dysplasia","termid":"MONDO:0016619"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005093"],"is_obsolete":false,"name":"ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive","secondary_identifiers":["DOID:0111665","OMIM:224900","GARD:15163","MEDGEN:854356","UMLS:C3887494"],"synonyms":[{"name":"ECTD10B","type":"related"},{"name":"ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive","type":"exact"},{"name":"ectodermal dysplasia, anhidrotic","type":"related"},{"name":"ectodermal dysplasia, hypohidrotic","type":"related"}],"termid":"MONDO:0009147","xrefs":{"Monarch":{"xref_id":"0009147"}}}


id: PBO:0042559
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclin dependent kinase like 1","termid":"PBO:0042559"}


id: PBO:0060179
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metaxin 3","termid":"PBO:0060179"}


id: PBO:0041634
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CACNA1C antisense RNA 4","termid":"PBO:0041634"}


id: PBO:0042835
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CFAP20DC antisense RNA 1","termid":"PBO:0042835"}


id: MONDO:0012046
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"otosclerosis","termid":"MONDO:0005349"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital corneal opacities, cornea guttata, and corectopia","secondary_identifiers":["OMIM:608484","MEDGEN:324911","MESH:C563921","UMLS:C1837970"],"synonyms":[{"name":"congenital corneal opacities, cornea guttata, and corectopia","type":"exact"},{"name":"corneal opacities, congenital, with cornea guttata and corectopia","type":"related"}],"termid":"MONDO:0012046","xrefs":{"Monarch":{"xref_id":"0012046"}}}


id: FYPO:0004582
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which cell cycle arrest in response to nitrogen starvation occurs in G1 phase, but its occurrence is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cell cycle arrest in mitotic G1 phase during nitrogen starvation","termid":"FYPO:0001000"}],"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:0000298"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0000298","FYPO:0000257","FYPO:0001320","FYPO:0000631"],"is_obsolete":false,"name":"increased cell cycle arrest in mitotic G1 phase in response to nitrogen starvation","synonyms":[{"name":"increased cell cycle arrest in mitotic G1 phase during cellular response to nitrogen starvation","type":"exact"},{"name":"increased cell cycle arrest in mitotic G1 phase in response to nitrogen depletion","type":"exact"},{"name":"increased cell cycle arrest in mitotic G1 phase in response to nitrogen deprivation","type":"exact"},{"name":"increased mitotic G1 arrest in response to nitrogen starvation","type":"exact"},{"name":"increased mitotic cell cycle arrest in G1 phase in response to nitrogen starvation","type":"exact"},{"name":"increased nitrogen deprivation-induced G1 arrest","type":"exact"}],"termid":"FYPO:0004582"}


id: GO:0009120
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving any one of a family of organic molecules consisting of a purine or pyrimidine base covalently bonded to a sugar deoxyribose (a deoxyribonucleoside).","definition_xrefs":["ISBN:0140512713","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside metabolic process","termid":"GO:0009116"}],"gene_count":0,"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:0008150","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"deoxyribonucleoside metabolic process","synonyms":[{"name":"deoxyribonucleoside metabolism","type":"exact"}],"termid":"GO:0009120"}


id: GO:0060620
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency or extent of cholesterol import. Cholesterol import is the directed movement of cholesterol into a cell or organelle.","definition_xrefs":["GOC:dph","GOC:tb","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cholesterol transport","termid":"GO:0032374"},{"relation_name":"regulates","term_name":"cholesterol import","termid":"GO:0070508"}],"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 cholesterol import","termid":"GO:0060620"}


id: MONDO:0017088
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"neural tube defect","termid":"MONDO:0018075"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0020022"}],"interesting_parent_ids":["MONDO:0020022"],"is_obsolete":false,"name":"isolated amyelia","secondary_identifiers":["Orphanet:268868","icd11.foundation:1787577133","GARD:20976"],"termid":"MONDO:0017088","xrefs":{"Monarch":{"xref_id":"0017088"}}}


id: MONDO:0032579
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":"warburg-cinotti syndrome","secondary_identifiers":["OMIM:618175","UMLS:C5193019","MEDGEN:1677486"],"synonyms":[{"name":"WARBURG-CINOTTI SYNDROME","type":"related"},{"name":"WRCN","type":"related"}],"termid":"MONDO:0032579","xrefs":{"Monarch":{"xref_id":"0032579"}}}


id: GO:0018649
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: tetrahydrofuran + O2 + 2 H+ + 2 e- = H2O + 2-hydroxytetrahydrofuran.","definition_xrefs":["UM-BBD_reactionID:r0017"],"gene_count":0,"genotype_count":0,"name":"obsolete tetrahydrofuran hydroxylase activity (obsolete GO:0018649)","termid":"GO:0018649"}


id: MONDO:1011590
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Portosystemic shunt that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"portosystemic shunt, non-human animal","termid":"MONDO:1011409"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"portosystemic shunt, dog","secondary_identifiers":["OMIA:000817-9615"],"termid":"MONDO:1011590","xrefs":{"Monarch":{"xref_id":"1011590"}}}


id: MONDO:0015951
data:
  {"annotated_genes":["SJAG_01841","SJAG_03898","SJAG_02896","SJAG_04183","SJAG_04944","SJAG_02200","SJAG_03206","SJAG_01887","SJAG_04109","SJAG_01049","SJAG_00995","SJAG_02556","SJAG_02031","SJAG_05283","SJAG_04540","SJAG_02876","SJAG_01372","SJAG_04995","SJAG_04791","SJAG_05329","SJAG_04114","SJAG_03961","SJAG_02334"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87051],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008294"},{"annotations":[88752],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008876"},{"annotations":[87195],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009902"},{"annotations":[87451],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008296"},{"annotations":[87150],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030048"},{"annotations":[87604],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007369"},{"annotations":[87196],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013000"},{"annotations":[86887],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008319"},{"annotations":[88582],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0016368"},{"annotations":[86783,86784],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0016369"},{"annotations":[88707],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0970950"},{"annotations":[88513],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010909"},{"annotations":[88030],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013829"},{"annotations":[87470],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008297"},{"annotations":[88123],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957577"},{"annotations":[88467],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010420"},{"annotations":[88396],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010210"},{"annotations":[87593],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012531"},{"annotations":[88417,88416],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010211"},{"annotations":[88425],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010212"},{"annotations":[88384],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010215"},{"annotations":[88332],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010216"},{"annotations":[88369],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010214"}]},"cv_name":"mondo","definition":"Hereditary photodermatoses are a spectrum of rare photosensitive disorders that are often caused by genetic deficiency or malfunction of various components of the DNA repair pathway. This results clinically in extreme photosensitivity, with many syndromes exhibiting an increased risk of cutaneous malignancies.","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary skin disorder","termid":"MONDO:0100118"}],"gene_count":23,"genes_by_uniquename":{"SJAG_00995":null,"SJAG_01049":null,"SJAG_01372":null,"SJAG_01841":null,"SJAG_01887":null,"SJAG_02031":null,"SJAG_02200":null,"SJAG_02334":null,"SJAG_02556":null,"SJAG_02876":null,"SJAG_02896":null,"SJAG_03206":null,"SJAG_03898":null,"SJAG_03961":null,"SJAG_04109":null,"SJAG_04114":null,"SJAG_04183":null,"SJAG_04540":null,"SJAG_04791":null,"SJAG_04944":null,"SJAG_04995":null,"SJAG_05283":null,"SJAG_05329":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"hereditary photodermatosis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:183490","MEDGEN:1842494","UMLS:C5679594","GARD:20277"],"synonyms":[{"name":"genetic photosensitivity","type":"exact"},{"name":"genetic skin photosensitivity","type":"exact"},{"name":"photogenodermatosis","type":"broad"},{"name":"photogénodermatose","type":"broad"}],"termid":"MONDO:0015951","terms_by_termid":{"MONDO:0007369":null,"MONDO:0008294":null,"MONDO:0008296":null,"MONDO:0008297":null,"MONDO:0008319":null,"MONDO:0008876":null,"MONDO:0009902":null,"MONDO:0010210":null,"MONDO:0010211":null,"MONDO:0010212":null,"MONDO:0010214":null,"MONDO:0010215":null,"MONDO:0010216":null,"MONDO:0010420":null,"MONDO:0010909":null,"MONDO:0012531":null,"MONDO:0013000":null,"MONDO:0013829":null,"MONDO:0016368":null,"MONDO:0016369":null,"MONDO:0030048":null,"MONDO:0957577":null,"MONDO:0970950":null},"xrefs":{"Monarch":{"xref_id":"0015951"}}}


id: FYECO:0000323
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"Cells were cold shocked followed by recovery at a temperature range higher than normal for standard pombe growth.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping sequential growth conditions","termid":"FYECO:0000094"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cold shock and recovery at high temperature","termid":"FYECO:0000323"}


id: PBO:0073740
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 1 member 7","termid":"PBO:0073740"}


id: PBO:0028751
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-excess_plasma_membrane_present","termid":"PBO:0028751"}


id: GO:0043084
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The hardening, enlarging and rising of the penis which often occurs in the sexually aroused male and enables sexual intercourse. Achieved by increased inflow of blood into the vessels of erectile tissue, and decreased outflow.","definition_xrefs":["GOC:jl","Wikipedia:Penile_erection"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multicellular organismal reproductive process","termid":"GO:0048609"},{"relation_name":"part_of","term_name":"copulation","termid":"GO:0007620"}],"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":"penile erection","secondary_identifiers":["Wikipedia:Erection#Penile_erection"],"termid":"GO:0043084"}


id: FYPO:0003255
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 import of proline into the cell is abolished.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished amino acid import during vegetative growth","termid":"FYPO:0003253"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0000138","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"abolished proline import","synonyms":[{"name":"abolished L-proline import across plasma membrane","type":"exact"},{"name":"abolished L-proline import into cell","type":"narrow"},{"name":"abolished proline import during mitotic cell cycle","type":"related"},{"name":"abolished proline import during vegetative growth","type":"exact"},{"name":"abolished proline import into cell","type":"exact"},{"name":"abolished proline uptake","type":"exact"},{"name":"proline import abolished","type":"exact"}],"termid":"FYPO:0003255"}


id: MOD:00552
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts a residue containing common isotopes to a 4x(2)H labeled dimethylated residue.","definition_xrefs":["PubMed:14670044","Unimod:199"],"direct_ancestors":[{"relation_name":"is_a","term_name":"(2)H deuterium labeled residue","termid":"MOD:00839"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"4x(2)H labeled dimethylated residue","synonyms":[{"name":"DiMethyl-CHD2","type":"related"},{"name":"Dimethyl:2H(4)","type":"related"}],"termid":"MOD:00552"}


id: MONDO:0009286
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":"gluteal muscles, absence of","secondary_identifiers":["UMLS:C1856398","MEDGEN:383902","MESH:C535561","OMIM:231970"],"synonyms":[{"name":"absence of gluteal muscle","type":"related"},{"name":"congenital absence of gluteal muscles","type":"related"},{"name":"gluteal muscle, absence of","type":"related"},{"name":"gluteal muscles, absence of","type":"exact"}],"termid":"MONDO:0009286","xrefs":{"Monarch":{"xref_id":"0009286"}}}


id: MONDO:0013111
data:
  {"annotated_genes":["SJAG_00358"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87267],"is_not":false,"summary":null,"term":"MONDO:0013111"}]},"cv_name":"mondo","definition":"Acute infantile liver failure due to mtDNA-encoded proteins synthesis defect is a very rare mitochondrial respiratory chain deficiency described in fewer than 10 infants, primarily of middle Eastern descent, and characterized clinically by transient but life-threatening liver failure with elevated liver enzymes, jaundice, vomiting, coagulopathy, hyperbilirubinemia, and lactic acidemia.","definition_xrefs":["Orphanet:217371"],"direct_ancestors":[{"relation_name":"is_a","term_name":"infantile liver failure","termid":"MONDO:0000023"},{"relation_name":"is_a","term_name":"mitochondrial oxidative phosphorylation disorder","termid":"MONDO:0016387"},{"relation_name":"is_a","term_name":"acute liver failure","termid":"MONDO:0019542"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00358":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:0002515"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0002515","MONDO:0004069","MONDO:0005066","MONDO:0004335"],"is_obsolete":false,"name":"acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0080778","MEDGEN:480294","GARD:10593","OMIM:613070","UMLS:C3278664"],"synonyms":[{"name":"LFIT","type":"exact"},{"name":"TRMU infantile liver failure","type":"exact"},{"name":"acute infantile liver failure","type":"broad"},{"name":"acute infantile liver failure due to synthesis defect of mitochondrial DNA-encoded proteins","type":"exact"},{"name":"acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins","type":"exact"},{"name":"infantile liver failure caused by mutation in TRMU","type":"exact"},{"name":"liver failure, infantile, transient","type":"exact"},{"name":"liver failure, transient infantile","type":"exact"},{"name":"transient infantile liver failure","type":"exact"}],"termid":"MONDO:0013111","terms_by_termid":{"MONDO:0013111":null},"xrefs":{"Monarch":{"xref_id":"0013111"}}}


id: GO:0050371
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-tyrosine + H2O = NH4 + phenol + pyruvate.","definition_xrefs":["RHEA:21704","EC:4.1.99.2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-carbon lyase activity","termid":"GO:0016830"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016829"],"is_obsolete":false,"name":"tyrosine phenol-lyase activity","secondary_identifiers":["MetaCyc:TYROSINE-PHENOL-LYASE-RXN","KEGG_REACTION:R00728"],"synonyms":[{"name":"L-tyrosine phenol-lyase (deaminating)","type":"related"},{"name":"L-tyrosine phenol-lyase (deaminating; pyruvate-forming)","type":"related"},{"name":"beta-tyrosinase activity","type":"related"}],"termid":"GO:0050371"}


id: PBO:0012607
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae ADR1","termid":"PBO:0012607"}


id: PBO:0049769
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HLA complex group 4 pseudogene 7","termid":"PBO:0049769"}


id: PBO:0045112
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dentin matrix acidic phosphoprotein 1","termid":"PBO:0045112"}


id: FYPO:0004409
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to tetraplatin. Cells stop growing (and may die) at a concentration of tetraplatin that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0005447","FYPO:0002683","FYPO:0000003","FYPO:0001985"],"is_obsolete":false,"name":"sensitive to tetraplatin","synonyms":[{"name":"hypersensitive to tetraplatin","type":"exact"},{"name":"sensitive to tetraplatin during mitotic cell cycle","type":"related"},{"name":"sensitive to tetraplatin during vegetative growth","type":"exact"}],"termid":"FYPO:0004409"}


id: GO:0045898
data:
  {"annotated_genes":["SJAG_00766","SJAG_01771"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[91483,81264],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045899"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of RNA polymerase II transcriptional preinitiation complex assembly.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein-containing complex assembly","termid":"GO:0043254"},{"relation_name":"is_a","term_name":"regulation of transcription initiation by RNA polymerase II","termid":"GO:0060260"},{"relation_name":"regulates","term_name":"RNA polymerase II preinitiation complex assembly","termid":"GO:0051123"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00766":null,"SJAG_01771":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0065003"},{"rel_name":"regulates","termid":"GO:0006351"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006355"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0044085","GO:0006355","GO:0006351","GO:0065003"],"is_obsolete":false,"name":"regulation of RNA polymerase II transcription preinitiation complex assembly","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"regulation of RNA polymerase II transcriptional pre-initiation complex assembly","type":"exact"},{"name":"regulation of RNA polymerase II transcriptional pre-initiation complex biosynthesis","type":"exact"},{"name":"regulation of RNA polymerase II transcriptional preinitiation complex assembly","type":"exact"},{"name":"regulation of RNA polymerase II transcriptional preinitiation complex formation","type":"related"}],"termid":"GO:0045898","terms_by_termid":{"GO:0045899":null}}


id: PBO:0013020
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA recombination protein Rad52 (previously Rad22)","termid":"PBO:0013020"}


id: PBO:0000304
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rRNA processing protein, unnamed (predicted)","termid":"PBO:0000304"}


id: GO:0050927
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the directed movement of a motile cell or organism towards a higher concentration in a concentration gradient of a specific chemical.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of chemotaxis","termid":"GO:0050921"},{"relation_name":"is_a","term_name":"regulation of positive chemotaxis","termid":"GO:0050926"},{"relation_name":"positively_regulates","term_name":"positive chemotaxis","termid":"GO:0050918"}],"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 positive chemotaxis","synonyms":[{"name":"activation of positive chemotaxis","type":"narrow"},{"name":"stimulation of positive chemotaxis","type":"narrow"},{"name":"up regulation of positive chemotaxis","type":"exact"},{"name":"up-regulation of positive chemotaxis","type":"exact"},{"name":"upregulation of positive chemotaxis","type":"exact"}],"termid":"GO:0050927"}


id: MONDO:0032752
data:
  {"annotated_genes":["SJAG_02236"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88895],"is_not":false,"summary":null,"term":"MONDO:0032752"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"genetic developmental and epileptic encephalopathy","termid":"MONDO:0100062"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02236":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"},{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0005027","MONDO:0700092"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy, 75","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5193099","OMIM:618437","GARD:16352","DOID:0112211","MEDGEN:1684253"],"synonyms":[{"name":"DEE75","type":"exact"},{"name":"EIEE75","type":"exact"},{"name":"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 75","type":"exact"},{"name":"developmental and epileptic encephalopathy 75","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 75","type":"exact"}],"termid":"MONDO:0032752","terms_by_termid":{"MONDO:0032752":null},"xrefs":{"Monarch":{"xref_id":"0032752"}}}


id: PBO:0049714
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HAUS augmin like complex subunit 1 pseudogene 2","termid":"PBO:0049714"}


id: PBO:0046646
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endogenous retrovirus group W member 27","termid":"PBO:0046646"}


id: GO:0032286
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the structure and material content of mature central nervous system myelin is kept in a functional state.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myelin maintenance","termid":"GO:0043217"},{"relation_name":"part_of","term_name":"central nervous system myelination","termid":"GO:0022010"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0061024"],"is_obsolete":false,"name":"central nervous system myelin maintenance","synonyms":[{"name":"central nervous system myelin sheath maintenance","type":"exact"},{"name":"myelin maintenance in central nervous system","type":"exact"}],"termid":"GO:0032286"}


id: PATO:0002175
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A spatial quality inhering in a bearer by virtue of the bearer's changed direction of position towards another entity.","definition_xrefs":["PATO:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spatial pattern","termid":"PATO:0000060"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deviation","termid":"PATO:0002175"}


id: GO:1905128
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of axo-dendritic protein transport.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:20694152"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of intracellular protein transport","termid":"GO:0090316"},{"relation_name":"is_a","term_name":"regulation of axo-dendritic protein transport","termid":"GO:1905126"},{"relation_name":"positively_regulates","term_name":"axo-dendritic protein transport","termid":"GO:0099640"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"positive regulation of axo-dendritic protein transport","synonyms":[{"name":"activation of axo-dendritic protein transport","type":"narrow"},{"name":"activation of axonal protein transport","type":"narrow"},{"name":"positive regulation of axonal protein transport","type":"narrow"},{"name":"up regulation of axo-dendritic protein transport","type":"exact"},{"name":"up regulation of axonal protein transport","type":"narrow"},{"name":"up-regulation of axo-dendritic protein transport","type":"exact"},{"name":"up-regulation of axonal protein transport","type":"narrow"},{"name":"upregulation of axo-dendritic protein transport","type":"exact"},{"name":"upregulation of axonal protein transport","type":"narrow"}],"termid":"GO:1905128"}


id: PBO:0039705
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"apelin receptor","termid":"PBO:0039705"}


id: GO:0031695
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to an alpha-2B adrenergic receptor.","definition_xrefs":["GOC:mah","GOC:nln"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adrenergic receptor binding","termid":"GO:0031690"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"alpha-2B adrenergic receptor binding","synonyms":[{"name":"alpha-2B adrenergic receptor ligand","type":"narrow"}],"termid":"GO:0031695"}


id: GO:0098550
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The side (leaflet) of the early endosome membrane that faces the lumen.","definition_xrefs":["GOC:lr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lumenal side of endosome membrane","termid":"GO:0098565"},{"relation_name":"part_of","term_name":"early endosome membrane","termid":"GO:0031901"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005768"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0031410"}],"interesting_parent_ids":["GO:0031410","GO:0005768","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"lumenal side of early endosome membrane","synonyms":[{"name":"internal leaflet of early endosome membrane","type":"exact"},{"name":"internal side of early endosome membrane","type":"exact"}],"termid":"GO:0098550"}


id: GO:0050460
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: NH3 + NAD+ + H2O = hydroxylamine + NADH + H+.","definition_xrefs":["MetaCyc:HYDROXYLAMINE-REDUCTASE-NADH-RXN","EC:1.7.1.10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on other nitrogenous compounds as donors, with NAD or NADP as acceptor","termid":"GO:0046857"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"hydroxylamine reductase (NADH) activity","secondary_identifiers":["RHEA:20581"],"synonyms":[{"name":"N-hydroxy amine reductase activity","type":"related"},{"name":"NADH-hydroxylamine reductase activity","type":"related"},{"name":"NADH2:hydroxylamine oxidoreductase activity","type":"related"},{"name":"NADH:hydroxylamine oxidoreductase activity","type":"related"},{"name":"ammonium dehydrogenase activity","type":"related"},{"name":"ammonium:NAD+ oxidoreductase activity","type":"related"},{"name":"hydroxylamine reductase (NADH2)","type":"related"}],"termid":"GO:0050460"}


id: GO:0046181
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of ketogluconate, the anion of ketogluconic acid, an aldonic acid derived from glucose containing a ketonic carbonyl group.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ketogluconate metabolic process","termid":"GO:0019522"},{"relation_name":"is_a","term_name":"aldonic acid catabolic process","termid":"GO:0046176"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0005975"],"is_obsolete":false,"name":"ketogluconate catabolic process","synonyms":[{"name":"ketogluconate breakdown","type":"exact"},{"name":"ketogluconate catabolism","type":"exact"},{"name":"ketogluconate degradation","type":"exact"}],"termid":"GO:0046181"}


id: PBO:0030978
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_histone_H3-K9_dimethylation_at_centromere","termid":"PBO:0030978"}


id: PBO:0017899
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphatidyl-N-dimethylethanolamine N-methyltransferase","termid":"PBO:0017899"}


id: MONDO:1010052
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Diabetes mellitus that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"digestive system disorder, non-human animal","termid":"MONDO:1011311"},{"relation_name":"is_a","term_name":"endocrine system disorder, non-human animal","termid":"MONDO:1011317"},{"relation_name":"is_a","term_name":"metabolic disease, non-human animal","termid":"MONDO:1011331"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diabetes mellitus, non-human animal","secondary_identifiers":["OMIA:000279"],"termid":"MONDO:1010052","xrefs":{"Monarch":{"xref_id":"1010052"}}}


id: MONDO:0032821
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","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":"myopathy, congenital, progressive, with scoliosis","secondary_identifiers":["MEDGEN:1684769","UMLS:C5231417","DOID:0081351","OMIM:618578"],"synonyms":[{"name":"MYOSCO","type":"exact"},{"name":"myopathy, congenital, progressive, with scoliosis","type":"exact"}],"termid":"MONDO:0032821","xrefs":{"Monarch":{"xref_id":"0032821"}}}


id: PBO:0082585
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Chromatin-binding ATPase that regulates histone gene expression; only bromodomain-containing AAA-ATPase in yeast; bromodomain interacts with N-terminal tail of histone H3; relocalizes to cytosol in response to hypoxia; human ortholog ANCCA is coactivator of both estrogen and androgen receptors, and increased expression of ANCCA is associated with breast and prostate cancers with poor prognoses","termid":"PBO:0082585"}


id: PBO:0036331
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"not functionally complemented by human COQ9","termid":"PBO:0036331"}


id: GO:0042077
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The glycosylation of peptidyl-serine through a phosphoester bond forming, for example, GlcNAc-alpha-1-P-Ser residues.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete protein phosphate-linked glycosylation via serine (obsolete GO:0042077)","synonyms":[{"name":"protein amino acid phosphate-linked glycosylation via serine","type":"exact"}],"termid":"GO:0042077"}


id: MONDO:0005055
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm characterized by a vascular proliferation which usually contains blunt endothelial cells. Erythrocyte extravasation and hemosiderin deposition are frequently present. The most frequent site of involvement is the skin; however it may also occur internally. It generally develops in people with compromised immune systems including those with acquired immune deficiency syndrome (AIDS).","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete connective tissue cancer (obsolete MONDO:0002176)","termid":"MONDO:0002176"},{"relation_name":"is_a","term_name":"viral infectious disease","termid":"MONDO:0005108"},{"relation_name":"is_a","term_name":"human herpesvirus 8-related tumor","termid":"MONDO:0015157"},{"relation_name":"is_a","term_name":"angiosarcoma","termid":"MONDO:0016982"}],"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":"Kaposi's sarcoma","secondary_identifiers":["EFO:0000558","GARD:6814","HP:0100726","MedDRA:10023284","NCIT:C9087","ICD9:176","DOID:8632","ICD9:176.9","MEDGEN:11321","Orphanet:33276","SCTID:109385007","ICD10CM:C46","UMLS:C0036220","ICDO:9140/3","ICD9:176.8","MESH:D012514"],"synonyms":[{"name":"African lymphadenopathic Kaposi's sarcoma","type":"related"},{"name":"HHV8","type":"related"},{"name":"KS","type":"exact"},{"name":"KSHV","type":"related"},{"name":"Kaposi sarcoma","type":"exact"},{"name":"Kaposi sarcoma herpesvirus","type":"related"},{"name":"Kaposi's sarcoma","type":"exact"},{"name":"Kaposi's sarcoma (disease)","type":"exact"},{"name":"Kaposi's sarcoma of anus","type":"narrow"},{"name":"Kaposi's sarcoma of central nervous system","type":"narrow"},{"name":"Kaposi's sarcoma of conjunctiva","type":"exact"},{"name":"Kaposi's sarcoma of cornea","type":"exact"},{"name":"Kaposi's sarcoma of esophagus","type":"narrow"},{"name":"Kaposi's sarcoma of gastrointestinal sites","type":"narrow"},{"name":"Kaposi's sarcoma of heart","type":"narrow"},{"name":"Kaposi's sarcoma of lung","type":"exact"},{"name":"Kaposi's sarcoma of lymph nodes","type":"narrow"},{"name":"Kaposi's sarcoma of oesophagus","type":"narrow"},{"name":"Kaposi's sarcoma of palate","type":"exact"},{"name":"Kaposi's sarcoma of penis","type":"narrow"},{"name":"Kaposi's sarcoma of skin","type":"narrow"},{"name":"Kaposi's sarcoma of soft tissue","type":"exact"},{"name":"Kaposi's sarcoma of soft tissues","type":"exact"},{"name":"Kaposi's sarcoma of the CNS","type":"narrow"},{"name":"Kaposi's sarcoma of the gallbladder","type":"narrow"},{"name":"Kaposi's sarcoma of the prostate","type":"narrow"},{"name":"Kaposi's sarcoma, lung","type":"narrow"},{"name":"Kaposi's sarcoma, skin","type":"narrow"},{"name":"Kaposi's sarcoma-associated herpesvirus (KSHV)","type":"related"},{"name":"Mediterranean Kaposi sarcoma","type":"related"},{"name":"anal Kaposi's sarcoma","type":"narrow"},{"name":"cardiac Kaposi's sarcoma","type":"narrow"},{"name":"central nervous system Kaposi's sarcoma","type":"narrow"},{"name":"conjunctival Kaposi's sarcoma","type":"narrow"},{"name":"corneal Kaposi's sarcoma","type":"narrow"},{"name":"cutaneous Kaposi's sarcoma","type":"narrow"},{"name":"esophageal Kaposi's sarcoma","type":"narrow"},{"name":"gallbladder Kaposi's sarcoma","type":"narrow"},{"name":"gastric Kaposi's sarcoma","type":"narrow"},{"name":"human herpesvirus 8","type":"related"},{"name":"intestinal Kaposi's sarcoma","type":"narrow"},{"name":"lymph node Kaposi's sarcoma","type":"narrow"},{"name":"lymphadenopathic Kaposi's sarcoma","type":"narrow"},{"name":"multiple hemorrhagic sarcoma","type":"narrow"},{"name":"non AIDS related Kaposi sarcoma","type":"related"},{"name":"palate Kaposi's sarcoma","type":"narrow"},{"name":"penis Kaposi's sarcoma","type":"narrow"},{"name":"prostate Kaposi's sarcoma","type":"narrow"},{"name":"pulmonary Kaposi's sarcoma","type":"narrow"},{"name":"soft tissue Kaposi's sarcoma","type":"narrow"}],"termid":"MONDO:0005055","xrefs":{"Monarch":{"xref_id":"0005055"}}}


id: PBO:0001802
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dehydrogenase (predicted)","termid":"PBO:0001802"}


id: PBO:0072283
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S24 pseudogene 1","termid":"PBO:0072283"}


id: PBO:0084701
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial glycine transporter; required for the transport of glycine into mitochondria for initiation of heme biosynthesis, with YMC1 acting as a secondary transporter; homolog of human SLC25A38, a mitochondrial glycine transporter associated with nonsyndromic autosomal recessive congenital sideroblastic anemia; human SLC25A38 can complement the heme deficiency associated with the null mutant; GFP-fusion protein is induced in response to the DNA-damaging agent MMS","termid":"PBO:0084701"}


id: GO:0031975
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A multilayered structure surrounding all or part of a cell; encompasses one or more lipid bilayers, and may include a cell wall layer; also includes the space between layers.","definition_xrefs":["GOC:mah","GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete envelope (obsolete GO:0031975)","termid":"GO:0031975"}


id: PBO:0084709
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial inner membrane carnitine transporter; required for carnitine-dependent transport of acetyl-CoA from peroxisomes to mitochondria during fatty acid beta-oxidation; human homolog SLC25A20 complements yeast null mutant","termid":"PBO:0084709"}


id: GO:0060773
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The radial pattern formation process that results in the formation of floral organ primordia around a central axis in a flower primordium.","definition_xrefs":["GOC:dph","GOC:sdb_2009","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phyllotactic patterning","termid":"GO:0060771"}],"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":"flower phyllotactic patterning","termid":"GO:0060773"}


id: PBO:0070584
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7a pseudogene 50","termid":"PBO:0070584"}


id: GO:1903799
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of microRNA processing.","definition_xrefs":["GO_REF:0000058","GOC:rph","GOC:TermGenie","GOC:BHF_miRNA","GOC:BHF","PMID:22269326"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of gene expression","termid":"GO:0010629"},{"relation_name":"is_a","term_name":"negative regulation of miRNA-mediated gene silencing","termid":"GO:0060965"},{"relation_name":"is_a","term_name":"regulation of miRNA processing","termid":"GO:1903798"},{"relation_name":"negatively_regulates","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":"positively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"negatively_regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"negative regulation of miRNA processing","synonyms":[{"name":"down regulation of gene silencing by miRNA, production of miRNAs","type":"exact"},{"name":"down regulation of miRNA biogenesis","type":"related"},{"name":"down regulation of miRNA processing","type":"exact"},{"name":"down regulation of miRNA-mediated gene silencing, production of miRNAs","type":"exact"},{"name":"down regulation of microRNA biogenesis","type":"related"},{"name":"down regulation of microRNA biosynthesis","type":"related"},{"name":"down regulation of microRNA biosynthetic process","type":"related"},{"name":"down regulation of microRNA metabolic process","type":"related"},{"name":"down regulation of microRNA metabolism","type":"related"},{"name":"down regulation of microRNA-mediated gene silencing, production of microRNAs","type":"exact"},{"name":"down regulation of production of miRNAs involved in gene silencing by miRNA","type":"exact"},{"name":"down regulation of production of microRNAs involved in gene silencing by microRNA","type":"exact"},{"name":"down-regulation of gene silencing by miRNA, production of miRNAs","type":"exact"},{"name":"down-regulation of miRNA biogenesis","type":"related"},{"name":"down-regulation of miRNA processing","type":"exact"},{"name":"down-regulation of miRNA-mediated gene silencing, production of miRNAs","type":"exact"},{"name":"down-regulation of microRNA biogenesis","type":"related"},{"name":"down-regulation of microRNA biosynthesis","type":"related"},{"name":"down-regulation of microRNA biosynthetic process","type":"related"},{"name":"down-regulation of microRNA metabolic process","type":"related"},{"name":"down-regulation of microRNA metabolism","type":"related"},{"name":"down-regulation of microRNA-mediated gene silencing, production of microRNAs","type":"exact"},{"name":"down-regulation of production of miRNAs involved in gene silencing by miRNA","type":"exact"},{"name":"down-regulation of production of microRNAs involved in gene silencing by microRNA","type":"exact"},{"name":"downregulation of gene silencing by miRNA, production of miRNAs","type":"exact"},{"name":"downregulation of miRNA biogenesis","type":"related"},{"name":"downregulation of miRNA processing","type":"exact"},{"name":"downregulation of miRNA-mediated gene silencing, production of miRNAs","type":"exact"},{"name":"downregulation of microRNA biogenesis","type":"related"},{"name":"downregulation of microRNA biosynthesis","type":"related"},{"name":"downregulation of microRNA biosynthetic process","type":"related"},{"name":"downregulation of microRNA metabolic process","type":"related"},{"name":"downregulation of microRNA metabolism","type":"related"},{"name":"downregulation of microRNA-mediated gene silencing, production of microRNAs","type":"exact"},{"name":"downregulation of production of miRNAs involved in gene silencing by miRNA","type":"exact"},{"name":"downregulation of production of microRNAs involved in gene silencing by microRNA","type":"exact"},{"name":"inhibition of gene silencing by miRNA, production of miRNAs","type":"narrow"},{"name":"inhibition of miRNA biogenesis","type":"related"},{"name":"inhibition of miRNA processing","type":"narrow"},{"name":"inhibition of miRNA-mediated gene silencing, production of miRNAs","type":"narrow"},{"name":"inhibition of microRNA biogenesis","type":"related"},{"name":"inhibition of microRNA biosynthesis","type":"related"},{"name":"inhibition of microRNA biosynthetic process","type":"related"},{"name":"inhibition of microRNA metabolic process","type":"related"},{"name":"inhibition of microRNA metabolism","type":"related"},{"name":"inhibition of microRNA-mediated gene silencing, production of microRNAs","type":"narrow"},{"name":"inhibition of production of miRNAs involved in gene silencing by miRNA","type":"narrow"},{"name":"inhibition of production of microRNAs involved in gene silencing by microRNA","type":"narrow"},{"name":"negative regulation of gene silencing by miRNA, production of miRNAs","type":"exact"},{"name":"negative regulation of miRNA biogenesis","type":"related"},{"name":"negative regulation of miRNA maturation","type":"narrow"},{"name":"negative regulation of miRNA-mediated gene silencing, production of miRNAs","type":"exact"},{"name":"negative regulation of microRNA biogenesis","type":"related"},{"name":"negative regulation of microRNA biosynthesis","type":"related"},{"name":"negative regulation of microRNA biosynthetic process","type":"related"},{"name":"negative regulation of microRNA metabolic process","type":"related"},{"name":"negative regulation of microRNA metabolism","type":"related"},{"name":"negative regulation of microRNA-mediated gene silencing, production of microRNAs","type":"exact"},{"name":"negative regulation of production of miRNAs involved in gene silencing by miRNA","type":"related"},{"name":"negative regulation of production of microRNAs involved in gene silencing by microRNA","type":"exact"}],"termid":"GO:1903799"}


id: GO:0102872
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 1-palmitoyl-2-linoleoyl-phosphatidylcholine + O2 + a reduced electron acceptor = 1-16:0-2-18:3-phosphatidylcholine + 2 H2O + an oxidized electron acceptor.","definition_xrefs":["PMID:15538555","PMID:8102138","GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 1-16:0-2-18:2-phosphatidylcholine desaturase activity (obsolete GO:0102872)","termid":"GO:0102872"}


id: PBO:0084800
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial protein of unknown function","termid":"PBO:0084800"}


id: PBO:0061301
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neural proliferation, differentiation and control 1","termid":"PBO:0061301"}


id: FYPO:0007195
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 mitochondria are larger than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitochondrial morphology","termid":"FYPO:0000359"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"large mitochondria","synonyms":[{"name":"enlarged mitochondria","type":"exact"},{"name":"large mitochondria during mitotic cell cycle","type":"related"},{"name":"large mitochondria during vegetative growth","type":"exact"}],"termid":"FYPO:0007195"}


id: MONDO:1011512
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Glaucoma that occurs in horse.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glaucoma, non-human animal","termid":"MONDO:1011457"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glaucoma, horse","secondary_identifiers":["OMIA:000411-9796"],"termid":"MONDO:1011512","xrefs":{"Monarch":{"xref_id":"1011512"}}}


id: PBO:0043430
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cornichon family AMPA receptor auxiliary protein 2","termid":"PBO:0043430"}


id: PBO:0052246
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"potassium channel tetramerization domain containing 15","termid":"PBO:0052246"}


id: PBO:0046035
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation initiation factor 2 subunit 2 beta pseudogene 3","termid":"PBO:0046035"}


id: MOD:01889
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue to S-(2-succinyl)-L-cysteine, by addition of either fumaric acid or maleic acid.","definition_xrefs":["Unimod:957","PubMed:18448829","PubMed:20677745","PubMed:16624247","RESID:AA0561"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alkylated residue","termid":"MOD:00001"},{"relation_name":"is_a","term_name":"modified L-cysteine residue","termid":"MOD:00905"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"S-(2-succinyl)-L-cysteine","synonyms":[{"name":"(2R)-2-amino-3-([(1R)-1,2-dicarboxyethyl]sulfanyl)propanoic acid","type":"exact"},{"name":"(2R)-2-{[(2R)-2-amino-2-carboxyethyl]sulfanyl}butanedioic acid","type":"exact"},{"name":"2-((2-amino-2-carboxyethyl)thio)butanedioic acid","type":"exact"},{"name":"2-amino-3-(1,2-dicarboxyethylthio)propanoic acid","type":"exact"},{"name":"MOD_RES S-(2-succinyl)cysteine","type":"exact"},{"name":"S-(1,2-dicarboxyethyl)cysteine","type":"exact"},{"name":"S-(2-succinyl)-L-cysteine","type":"exact"},{"name":"S-(2-succinyl)cysteine","type":"exact"},{"name":"S-[(2R)-2-succinyl]-L-cysteine","type":"exact"}],"termid":"MOD:01889"}


id: MONDO:0976130
data:
  {"annotated_genes":["SJAG_04345","SJAG_01709"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86810,86811],"is_not":false,"summary":null,"term":"MONDO:0976130"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"neurodevelopmental disorder","termid":"MONDO:0700092"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01709":null,"SJAG_04345":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 poor growth, absent speech, progressive ataxia, and dysmorphic facies","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:621067"],"termid":"MONDO:0976130","terms_by_termid":{"MONDO:0976130":null},"xrefs":{"Monarch":{"xref_id":"0976130"}}}


id: PR:Q09787
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC13G6.09 gene.","definition_xrefs":["UniProtKB:Q09787","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C13G6.09 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC13G6.09","synonyms":[{"name":"Spom972h-SPAC13G6.09","type":"exact"}],"termid":"PR:Q09787"}


id: GO:0003674
data:
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