# terms

id: MONDO:0015709
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete immunodeficiency syndrome with autoimmunity (obsolete MONDO:0015709)","secondary_identifiers":["icd11.foundation:1902856995","Orphanet:169355"],"termid":"MONDO:0015709","xrefs":{"Monarch":{"xref_id":"0015709"}}}


id: GO:0044761
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont inhibits or disrupts the normal execution of cholinergic synaptic transmission, communication from a neuron to a target (neuron, muscle, or secretory cell) across a synapse via the neurotransmitter choline, in its host organism.","definition_xrefs":["PMID:37157163","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated suppression of host synaptic transmission","termid":"GO:0044759"},{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host cholinergic synaptic transmission","termid":"GO:0044760"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated suppression of host cholinergic synaptic transmission","synonyms":[{"name":"negative regulation by symbiont of host cholinergic synaptic transmission","type":"exact"}],"termid":"GO:0044761"}


id: PBO:0090401
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thiosulfate sulfurtransferase, URM1 activating enzyme E1-type Uba42","termid":"PBO:0090401"}


id: PBO:0081573
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 500","termid":"PBO:0081573"}


id: GO:0070406
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to glutamine, 2,5-diamino-5-oxopentanoic acid.","definition_xrefs":["GOC:ecd","CHEBI:28300"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxylic acid binding","termid":"GO:0031406"}],"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":"glutamine binding","termid":"GO:0070406"}


id: MONDO:0002193
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that affects the Bartholin gland. Representative examples include adenoma, adenomyoma, adenocarcinoma, and squamous cell carcinoma.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vestibular gland benign neoplasm","termid":"MONDO:0000626"},{"relation_name":"is_a","term_name":"integumentary system benign neoplasm","termid":"MONDO:0000652"},{"relation_name":"is_a","term_name":"Bartholin gland neoplasm","termid":"MONDO:0021114"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Bartholin gland benign neoplasm","secondary_identifiers":["NCIT:C6434","DOID:2068","UMLS:C0347500","MEDGEN:83868","SCTID:189130001"],"synonyms":[{"name":"Bartholin gland neoplasm","type":"broad"},{"name":"major vestibular gland benign neoplasm","type":"exact"},{"name":"tumor of Bartholin's gland","type":"broad"},{"name":"tumour of Bartholin's gland","type":"broad"}],"termid":"MONDO:0002193","xrefs":{"Monarch":{"xref_id":"0002193"}}}


id: PBO:0062464
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 155 pseudogene","termid":"PBO:0062464"}


id: GO:0097667
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An SCF ubiquitin ligase complex in which the F-box protein is Rcy1 in S. cerevisiae (Pof6 in S. pombe).","definition_xrefs":["PMID:15147268","GOC:jd","GOC:vw","PMID:14747994"],"direct_ancestors":[{"relation_name":"is_a","term_name":"SCF ubiquitin ligase complex","termid":"GO:0019005"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"SCF-Rcy1/Pof6 ubiquitin ligase complex","termid":"GO:0097667"}


id: PBO:0016042
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by human PTBP3","termid":"PBO:0016042"}


id: GO:0050189
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + phosphoenolpyruvate = phosphate + pyruvate.","definition_xrefs":["EC:3.1.3.60","RHEA:19997"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatase activity","termid":"GO:0016791"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016788","GO:0003674","GO:0016787","GO:0003824"],"is_obsolete":false,"name":"phosphoenolpyruvate phosphatase activity","secondary_identifiers":["MetaCyc:PHOSPHOENOLPYRUVATE-PHOSPHATASE-RXN","KEGG_REACTION:R00208"],"synonyms":[{"name":"PEP phosphatase activity","type":"related"},{"name":"phosphoenolpyruvate phosphohydrolase activity","type":"related"}],"termid":"GO:0050189"}


id: PBO:0034152
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-biomechanically_related_to","termid":"PBO:0034152"}


id: GO:0030838
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of actin polymerization.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of actin filament polymerization","termid":"GO:0030833"},{"relation_name":"is_a","term_name":"positive regulation of protein polymerization","termid":"GO:0032273"},{"relation_name":"is_a","term_name":"positive regulation of cytoskeleton organization","termid":"GO:0051495"},{"relation_name":"is_a","term_name":"positive regulation of supramolecular fiber organization","termid":"GO:1902905"},{"relation_name":"positively_regulates","term_name":"actin filament polymerization","termid":"GO:0030041"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0030036"},{"rel_name":"positively_regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0007010"},{"rel_name":"regulates","termid":"GO:0007010"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"positively_regulates","termid":"GO:0065003"},{"rel_name":"regulates","termid":"GO:0065003"}],"interesting_parent_ids":["GO:0008150","GO:0030036","GO:0044085","GO:0007010","GO:0065003"],"is_obsolete":false,"name":"positive regulation of actin filament polymerization","synonyms":[{"name":"activation of actin filament polymerization","type":"narrow"},{"name":"positive regulation of actin polymerization","type":"exact"},{"name":"positive regulation of actin polymerization and/or depolymerization","type":"broad"},{"name":"stimulation of actin filament polymerization","type":"narrow"},{"name":"up regulation of actin filament polymerization","type":"exact"},{"name":"up-regulation of actin filament polymerization","type":"exact"},{"name":"upregulation of actin filament polymerization","type":"exact"}],"termid":"GO:0030838"}


id: FYPO:0007848
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which microtubules self-assemble into a spindle without the participation of the spindle pole body (SPB) during one or both meiotic nuclear divisions. This phenotype is observed in the absence of both bouquet formation and meiotic SPB insertion into the nuclear envelope.","definition_xrefs":["PMID:34346498","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal meiotic spindle assembly","termid":"FYPO:0000737"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000054"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"part_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000631","FYPO:0000054","FYPO:0000002"],"is_obsolete":false,"name":"meiotic spindle self-assembly","synonyms":[{"name":"SPB-independent meiotic spindle assembly","type":"exact"},{"name":"SPB-independent spindle assembly during meiosis","type":"exact"},{"name":"acentrosomal meiotic spindle assembly","type":"related"},{"name":"acentrosomal spindle assembly during meiosis","type":"related"},{"name":"meiotic SPB-independent spindle","type":"related"},{"name":"spindle pole body-independent meiotic spindle assembly","type":"exact"},{"name":"spindle pole body-independent spindle assembly during meiosis","type":"exact"},{"name":"spindle self-assembly during meiosis","type":"exact"},{"name":"spindle self-assembly during meiotic nuclear division","type":"exact"}],"termid":"FYPO:0007848"}


id: PBO:0074677
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 61","termid":"PBO:0074677"}


id: PBO:0044921
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DiGeorge syndrome critical region gene 6 like","termid":"PBO:0044921"}


id: PATO:0001732
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in a plant by virtue of the bearer's disposition to not shed any body part.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"shedability","termid":"PATO:0001729"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-deciduous (any body part)","termid":"PATO:0001732"}


id: MONDO:0859278
data:
  {"annotated_genes":["SJAG_05194"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87648],"is_not":false,"summary":null,"term":"MONDO:0859278"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05194":null},"genotype_count":0,"is_obsolete":false,"name":"keratoderma-ichthyosis-deafness syndrome, autosomal recessive","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1823973","OMIM:620009","UMLS:C5774200"],"termid":"MONDO:0859278","terms_by_termid":{"MONDO:0859278":null},"xrefs":{"Monarch":{"xref_id":"0859278"}}}


id: GO:0070187
data:
  {"annotated_genes":["SJAG_01864","SJAG_01777","SJAG_03092","SJAG_01378","SJAG_03685","SJAG_02194"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[81600,91578,93653,96903,101535,117799],"is_not":false,"summary":null,"term":"GO:0070187"}]},"cv_name":"cellular_component","definition":"A nuclear telomere cap complex that is formed by the association of telomeric ssDNA- and dsDNA-binding proteins with telomeric DNA, and is involved in telomere protection and recruitment of telomerase. The complex is known to contain TERF1, TERF2, POT1, RAP1, TINF2 and ACD in mammalian cells, and Pot1, Tpz1, Rap1, Rif1, Rif2 and Taz1 in Saccharomyces. Taz1 and Rap1 (or their mammalian equivalents) form a dsDNA-binding subcomplex, Pot1 and Tpz1 form an ssDNA-binding subcomplex, and the two subcomplexes are bridged by Poz1, which acts as an effector molecule along with Ccq1.","definition_xrefs":["GOC:expert_mf","PMID:18828880","GOC:vw","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear telomere cap complex","termid":"GO:0000783"}],"gene_count":6,"genes_by_uniquename":{"SJAG_01378":null,"SJAG_01777":null,"SJAG_01864":null,"SJAG_02194":null,"SJAG_03092":null,"SJAG_03685":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005634","GO:0005694","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"shelterin complex","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"Pot1 complex","type":"exact"},{"name":"Pot1-Tpz1 complex","type":"exact"},{"name":"telosome","type":"exact"}],"termid":"GO:0070187","terms_by_termid":{"GO:0070187":null}}


id: GO:0120154
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of ERBB4 signaling pathway.","definition_xrefs":["PMID:15219672"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of ERBB signaling pathway","termid":"GO:1901185"},{"relation_name":"negatively_regulates","term_name":"ERBB4 signaling pathway","termid":"GO:0038130"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"negative regulation of ERBB4 signaling pathway","termid":"GO:0120154"}


id: PBO:0062289
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 L member 2","termid":"PBO:0062289"}


id: PBO:0117192
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ENHO antisense RNA 1","termid":"PBO:0117192"}


id: PBO:0084127
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Hexaprenyl pyrophosphate synthetase; catalyzes the first step in ubiquinone (coenzyme Q) biosynthesis","termid":"PBO:0084127"}


id: GO:0035099
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a hemocyte within the embryo. Hemocytes are blood cells associated with a hemocoel (the cavity containing most of the major organs of the arthropod body) which are involved in defense and clotting of hemolymph, but not involved in transport of oxygen. In Drosophila, embryonic hemocytes originate from the head mesoderm as a cluster of cells. The cluster splits into two and one group of cells crosses the amnioserosa. Both populations then spread toward the middle of the embryo and then disperse evenly throughout the embryo.","definition_xrefs":["GOC:bf","GOC:mtg_sensu","PMID:12885551"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell migration","termid":"GO:0016477"},{"relation_name":"part_of","term_name":"embryonic hemopoiesis","termid":"GO:0035162"}],"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":"hemocyte migration","synonyms":[{"name":"arthropod blood cell migration","type":"exact"},{"name":"hemocyte cell migration","type":"exact"}],"termid":"GO:0035099"}


id: MONDO:0014783
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Any preimplantation embryonic lethality in which the cause of the disease is a mutation in the TLE6 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"gene_count":0,"genotype_count":0,"name":"obsolete preimplantation embryonic lethality 1 (obsolete MONDO:0014783)","secondary_identifiers":["OMIM:616814"],"synonyms":[{"name":"PREMBL1","type":"exact"},{"name":"Prembl","type":"related"},{"name":"TLE6 preimplantation embryonic lethality","type":"exact"},{"name":"preimplantation embryonic lethality","type":"broad"},{"name":"preimplantation embryonic lethality 1","type":"exact"},{"name":"preimplantation embryonic lethality 1; PREMBL1","type":"exact"},{"name":"preimplantation embryonic lethality caused by mutation in TLE6","type":"exact"},{"name":"preimplantation embryonic lethality type 1","type":"exact"}],"termid":"MONDO:0014783","xrefs":{"Monarch":{"xref_id":"0014783"}}}


id: MONDO:0004927
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A congenital or acquired mucocele that develops in the lacrimal sac. It is usually the result of nasolacrimal duct abnormalities or obstruction.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chronic inflammation of lacrimal passage","termid":"MONDO:0004923"}],"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":"dacryocystocele","secondary_identifiers":["ICD9:375.43","DOID:9939","MEDGEN:472901","UMLS:C0155241"],"synonyms":[{"name":"lacrimal mucocele","type":"exact"}],"termid":"MONDO:0004927","xrefs":{"Monarch":{"xref_id":"0004927"}}}


id: PBO:0029262
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_ammonium","termid":"PBO:0029262"}


id: GO:0043976
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of histone H3 by the addition of an acetyl group to a lysine residue at position 79 of the histone.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete histone H3-K79 acetylation (obsolete GO:0043976)","synonyms":[{"name":"histone H3 acetylation at K79","type":"exact"},{"name":"histone H3K79 acetylation","type":"exact"}],"termid":"GO:0043976"}


id: MONDO:0015400
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Frontonasal arteriovenous malformation is a rare vascular anomaly characterized by abnormal communication between arteries and veins, bypassing the capillary bed, located in the frontonasal area. It may present with intermittent nasal bleeding, blurred vision, pustule formation and/or disfigurement. Overlying skin may be of normal appearance or may manifest a red, pulsatile mass with local rise of temperature. Other features may include pain, ulceration, excessive growth and/or congestive heart failure.","definition_xrefs":["Orphanet:141168"],"direct_ancestors":[{"relation_name":"is_a","term_name":"facial arteriovenous malformation","termid":"MONDO:0015500"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"frontonasal arteriovenous malformation","secondary_identifiers":["icd11.foundation:1779519580","UMLS:C3838993","GARD:19955","MEDGEN:824839"],"termid":"MONDO:0015400","xrefs":{"Monarch":{"xref_id":"0015400"}}}


id: PR:O14328
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ksp1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14328"],"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 ksp1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC16E9.13","synonyms":[{"name":"Spom972h-ksp1","type":"exact"},{"name":"serine/threonine-protein kinase ppk20 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14328"}


id: MONDO:0000285
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete lujo hemorrhagic fever (obsolete MONDO:0000285)","termid":"MONDO:0000285","xrefs":{"Monarch":{"xref_id":"0000285"}}}


id: GO:0110053
data:
  {"annotated_genes":["SJAG_04522","SJAG_02566","SJAG_01894","SJAG_04100","SJAG_04479","SJAG_01993","SJAG_00279","SJAG_00521","SJAG_02700","SJAG_03455","SJAG_03086"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[81936,80885,77285,94137],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051016"},{"annotations":[76246],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034316"},{"annotations":[109448],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032231"},{"annotations":[78478,69537,68641,79119,81183],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030833"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of actin filament organization.","definition_xrefs":["GOC:kmv"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of actin cytoskeleton organization","termid":"GO:0032956"},{"relation_name":"is_a","term_name":"regulation of supramolecular fiber organization","termid":"GO:1902903"},{"relation_name":"regulates","term_name":"actin filament organization","termid":"GO:0007015"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00279":null,"SJAG_00521":null,"SJAG_01894":null,"SJAG_01993":null,"SJAG_02566":null,"SJAG_02700":null,"SJAG_03086":null,"SJAG_03455":null,"SJAG_04100":null,"SJAG_04479":null,"SJAG_04522":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0030036"},{"rel_name":"regulates","termid":"GO:0007010"}],"interesting_parent_ids":["GO:0007010","GO:0008150","GO:0030036"],"is_obsolete":false,"name":"regulation of actin filament organization","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0110053","terms_by_termid":{"GO:0030833":null,"GO:0032231":null,"GO:0034316":null,"GO:0051016":null}}


id: PBO:0065304
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine protease 21","termid":"PBO:0065304"}


id: PBO:0059332
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein S6 pseudogene 1","termid":"PBO:0059332"}


id: GO:0102508
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: cyanidin 3,7-di-O-beta-D-glucoside betaine + H2O = cyanidin 3-O-beta-D-glucoside betaine + beta-D-glucose.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete cyanidin 3,7-diglucoside glucosidase activity (obsolete GO:0102508)","termid":"GO:0102508"}


id: GO:1900893
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of tridecane metabolic process.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of metabolic process","termid":"GO:0019222"},{"relation_name":"regulates","term_name":"tridecane metabolic process","termid":"GO:1900631"}],"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 tridecane metabolic process","synonyms":[{"name":"regulation of tridecane metabolism","type":"exact"}],"termid":"GO:1900893"}


id: GO:0034308
data:
  {"annotated_genes":["SJAG_00381","SJAG_04067","SJAG_04282","SJAG_00240","SJAG_04866","SJAG_00827","SJAG_01742","SJAG_02406","SJAG_02420","SJAG_03743","SJAG_03822","SJAG_02047","SJAG_03362","SJAG_03538","SJAG_05006","SJAG_01970","SJAG_02421","SJAG_01414","SJAG_03370"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[116472,100544,100543,90322,116473],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019655"},{"annotations":[98388],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:2001172"},{"annotations":[90852,115541],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0090180"},{"annotations":[75672,80196,62213,78755,71804,75730],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009228"},{"annotations":[59299,67375],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006772"},{"annotations":[101341,112295,112296],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036172"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving primary alcohols. A primary alcohol is any alcohol in which a hydroxy group, -OH, is attached to a saturated carbon atom which has either three hydrogen atoms attached to it or only one other carbon atom and two hydrogen atoms attached to it.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alcohol metabolic process","termid":"GO:0006066"}],"gene_count":19,"genes_by_uniquename":{"SJAG_00240":null,"SJAG_00381":null,"SJAG_00827":null,"SJAG_01414":null,"SJAG_01742":null,"SJAG_01970":null,"SJAG_02047":null,"SJAG_02406":null,"SJAG_02420":null,"SJAG_02421":null,"SJAG_03362":null,"SJAG_03370":null,"SJAG_03538":null,"SJAG_03743":null,"SJAG_03822":null,"SJAG_04067":null,"SJAG_04282":null,"SJAG_04866":null,"SJAG_05006":null},"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":"primary alcohol metabolic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"monohydric alcohol metabolic process","type":"exact"},{"name":"primary alcohol metabolism","type":"exact"}],"termid":"GO:0034308","terms_by_termid":{"GO:0006772":null,"GO:0009228":null,"GO:0019655":null,"GO:0036172":null,"GO:0090180":null,"GO:2001172":null}}


id: GO:0015188
data:
  {"annotated_genes":["SJAG_02029","SJAG_04725"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[104625,111875],"is_not":false,"summary":null,"term":"GO:0015188"}]},"cv_name":"molecular_function","definition":"Enables the transfer of L-isoleucine from one side of a membrane to the other. L-isoleucine is (2R*,3R*)-2-amino-3-methylpentanoic acid.","definition_xrefs":["GOC:ai","GOC:mtg_transport","ISBN:0815340729"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic cation transmembrane transporter activity","termid":"GO:0015101"},{"relation_name":"is_a","term_name":"neutral L-amino acid transmembrane transporter activity","termid":"GO:0015175"},{"relation_name":"is_a","term_name":"L-amino acid transmembrane transporter activity","termid":"GO:0015179"},{"relation_name":"is_a","term_name":"branched-chain amino acid transmembrane transporter activity","termid":"GO:0015658"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02029":null,"SJAG_04725":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:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"L-isoleucine transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"L-isoleucine transporter activity","type":"broad"},{"name":"isoleucine/valine:sodium symporter activity","type":"narrow"},{"name":"leucine/isoleucine/valine porter activity","type":"narrow"},{"name":"leucine/valine/isoleucine permease activity","type":"narrow"}],"termid":"GO:0015188","terms_by_termid":{"GO:0015188":null}}


id: MONDO:0002786
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cancer involving a diencephalon.","definition_xrefs":["MONDO:patterns/cancer"],"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":"diencephalic cancer","secondary_identifiers":["UMLS:C1334576","DOID:3843","MEDGEN:233659","NCIT:C5126"],"synonyms":[{"name":"cancer of diencephalon","type":"exact"},{"name":"diencephalic neoplasm","type":"related"},{"name":"diencephalon cancer","type":"exact"},{"name":"malignant diencephalic neoplasm","type":"exact"},{"name":"malignant diencephalic neoplasms","type":"exact"},{"name":"malignant diencephalic tumor","type":"exact"},{"name":"malignant diencephalic tumour","type":"exact"},{"name":"malignant diencephalon neoplasm","type":"exact"},{"name":"malignant neoplasm of diencephalon","type":"exact"},{"name":"tumor of diencephalon","type":"exact"},{"name":"tumour of diencephalon","type":"exact"}],"termid":"MONDO:0002786","xrefs":{"Monarch":{"xref_id":"0002786"}}}


id: PBO:0080191
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vascular endothelial growth factor D","termid":"PBO:0080191"}


id: PBO:0041978
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CCDC18 antisense RNA 1","termid":"PBO:0041978"}


id: FYPO:0003876
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell cycle checkpoint phenotype in which the cytokinesis after mitosis checkpoint of a mitotic cell cycle is normal (i.e. indistinguishable from wild type). The cytokinesis after mitosis checkpoint normally delays the G2/M transition of a mitotic cell cycle if cytokinesis was not completed correctly in the previous cell cycle.","definition_xrefs":["PomBase:mah","GO:0044878"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal mitotic cell cycle checkpoint","termid":"FYPO:0001703"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000298","FYPO:0001312","FYPO:0000257","FYPO:0001320","FYPO:0000631"],"is_obsolete":false,"name":"normal cytokinesis checkpoint","synonyms":[{"name":"normal cytokinesis after mitosis checkpoint","type":"exact"},{"name":"normal cytokinesis checkpoint activation","type":"related"},{"name":"normal mitotic cell cycle cytokinesis checkpoint","type":"exact"},{"name":"normally activated cytokinesis checkpoint","type":"related"}],"termid":"FYPO:0003876"}


id: FYPO:0001630
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of L-isoleucine measured in the vacuole is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal level of substance in vacuole","termid":"FYPO:0001603"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001312","FYPO:0001320","FYPO:0000257"],"is_obsolete":false,"name":"normal vacuolar isoleucine level","synonyms":[{"name":"normal level of isoleucine in vacuole","type":"exact"},{"name":"normal vacuolar L-isoleucine level","type":"exact"},{"name":"normal vacuolar isoleucine level during mitotic cell cycle","type":"related"},{"name":"normal vacuolar isoleucine level during vegetative growth","type":"exact"}],"termid":"FYPO:0001630"}


id: PBO:0052790
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 31","termid":"PBO:0052790"}


id: PBO:0030527
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_chromatin","termid":"PBO:0030527"}


id: PBO:0056964
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"miR-23a/27a/24-2 cluster host gene","termid":"PBO:0056964"}


id: FYPO:0004434
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 4-amino-1-methyl-1H-imidazole-5-carboselenoamide. Cells stop growing (and may die) at a concentration of 4-amino-1-methyl-1H-imidazole-5-carboselenoamide that allows wild type cells to grow.","definition_xrefs":["PMID:18204818","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000003","FYPO:0002683","FYPO:0000139","FYPO:0005447"],"is_obsolete":false,"name":"sensitive to 4-amino-1-methyl-1H-imidazole-5-carboselenoamide","synonyms":[{"name":"hypersensitive to 4-amino-1-methyl-1H-imidazole-5-carboselenoamide","type":"exact"},{"name":"sensitive to 4-amino-1-methyl-1H-imidazole-5-carboselenoamide during mitotic cell cycle","type":"related"},{"name":"sensitive to 4-amino-1-methyl-1H-imidazole-5-carboselenoamide during vegetative growth","type":"exact"}],"termid":"FYPO:0004434"}


id: PBO:0029426
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_protein_palmitoylation","termid":"PBO:0029426"}


id: GO:0004275
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the selective cleavage of Lys6-Ile7 bond in trypsinogen.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete enteropeptidase activity (obsolete GO:0004275)","synonyms":[{"name":"enterokinase activity","type":"related"},{"name":"enteropeptidase activity","type":"exact"}],"termid":"GO:0004275"}


id: GO:0008608
data:
  {"annotated_genes":["SJAG_03048","SJAG_04412","SJAG_01370","SJAG_05290","SJAG_00794","SJAG_03220","SJAG_03126","SJAG_00930","SJAG_00678","SJAG_03543","SJAG_03437","SJAG_01371","SJAG_02731","SJAG_01837","SJAG_02624","SJAG_02336","SJAG_04259","SJAG_03683","SJAG_02451","SJAG_00418","SJAG_02761","SJAG_00302","SJAG_04140","SJAG_02346","SJAG_03217","SJAG_00646","SJAG_02045","SJAG_01278","SJAG_04508","SJAG_04040","SJAG_02286","SJAG_01297","SJAG_05266","SJAG_04076","SJAG_01224","SJAG_00918","SJAG_04280","SJAG_01805","SJAG_00082","SJAG_05319","SJAG_02814","SJAG_03327","SJAG_00335","SJAG_01082","SJAG_04884","SJAG_03926","SJAG_03540","SJAG_01601","SJAG_00207","SJAG_05220","SJAG_04623","SJAG_01775","SJAG_00768","SJAG_01211","SJAG_03989"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89683,95642],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051456"},{"annotations":[112206,89817,107300,99717,92804,112160,97375,91853,102196,73754,77460,113536,70180,118385,93196,89569,74680,66733],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051315"},{"annotations":[110093],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0099607"},{"annotations":[91562,110098,64638,90956,114478,96008,92792,102340,95644,100936,104256,111737,114477,105363,115085,115954,116358,100436,118777,109340,120571,110727,105716,91176,79728],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990758"},{"annotations":[104182],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1902424"},{"annotations":[113814,117868,107009],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1902425"},{"annotations":[95618,91815,104202,113054,118539],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0140429"},{"annotations":[118542],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1904967"},{"annotations":[110985],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031134"},{"annotations":[115956,99718,91564,102342,109660,112207,92794,104257,107303,97376,109342,97130,110729,110986,90958,103159,111739,117786,112163,115086,100440,118779,95623],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051455"}]},"cv_name":"biological_process","definition":"The process in which spindle microtubules become physically associated with the proteins making up the kinetochore complex.","definition_xrefs":["GOC:vw","PMID:10322137"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell cycle process","termid":"GO:0022402"},{"relation_name":"part_of","term_name":"metaphase chromosome 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of spindle microtubules to kinetochore","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["GO:0051313"],"synonyms":[{"name":"amphotelic attachment","type":"related"},{"name":"attachment of spindle microtubules to chromosome","type":"exact"},{"name":"bipolar attachment","type":"related"},{"name":"kinetochore microtubule interaction","type":"broad"},{"name":"kinetochore-microtubule attachment","type":"exact"},{"name":"kinetochore-microtubule interaction","type":"broad"},{"name":"microtubule anchoring at kinetochore","type":"exact"},{"name":"microtubule and chromosome interaction","type":"broad"},{"name":"microtubule and kinetochore interaction","type":"related"},{"name":"microtubule capture","type":"narrow"},{"name":"spindle chromosome attachment","type":"exact"},{"name":"spindle kinetochore attachment","type":"exact"},{"name":"spindle-chromosome interaction","type":"broad"}],"termid":"GO:0008608","terms_by_termid":{"GO:0031134":null,"GO:0051315":null,"GO:0051455":null,"GO:0051456":null,"GO:0099607":null,"GO:0140429":null,"GO:1902424":null,"GO:1902425":null,"GO:1904967":null,"GO:1990758":null}}


id: PBO:0000194
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mevalonate kinase Erg12 (predicted)","termid":"PBO:0000194"}


id: PR:O60185
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A methylthioribose-1-phosphate isomerase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03887","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":"methylthioribose-1-phosphate isomerase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC23E6.10c","secondary_identifiers":["UniProtKB:O60185"],"synonyms":[{"name":"M1Pi (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"MTR-1-P isomerase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"S-methyl-5-thioribose-1-phosphate isomerase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-MRI1","type":"exact"},{"name":"translation initiation factor eIF-2B subunit alpha/beta/delta-like protein (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O60185"}


id: SO:0001731
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A kind of histone modification site, whereby the 8th residue (a lysine), from the start of the H4 histone protein is acetylated.","definition_xrefs":["SO:KE"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone_4_acetylation_site","termid":"SO:0001972"}],"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":"H4K8_acetylation_site","synonyms":[{"name":"H4K8 acetylation site","type":"exact"},{"name":"H4K8ac","type":"exact"}],"termid":"SO:0001731"}


id: PBO:0078237
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor beta variable 19","termid":"PBO:0078237"}


id: PBO:0027750
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_localization_to_nucleus_during_nitrogen_starvation","termid":"PBO:0027750"}


id: PBO:0053802
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 1058","termid":"PBO:0053802"}


id: PBO:0068759
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U5F small nuclear 4, pseudogene","termid":"PBO:0068759"}


id: GO:1900383
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates synaptic plasticity, the ability of synapses to change as circumstances require, via receptor localization to the synapse, the junction between a nerve fiber of one neuron and another neuron or muscle fiber or glial cell. Processes may include receptor transport to, and/or maintenance at, the synapse.","definition_xrefs":["GOC:TermGenie","PMID:22464329","GOC:kmv"],"direct_ancestors":[{"relation_name":"is_a","term_name":"receptor localization to synapse","termid":"GO:0097120"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"regulation of synaptic plasticity by receptor localization to synapse","synonyms":[{"name":"regulation of synaptic plasticity by receptor localisation to synapse","type":"exact"}],"termid":"GO:1900383"}


id: PBO:0042749
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"centromere protein U pseudogene 2","termid":"PBO:0042749"}


id: PBO:0063598
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peroxisomal biogenesis factor 11 gamma","termid":"PBO:0063598"}


id: PBO:0081390
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 230","termid":"PBO:0081390"}


id: PBO:0002392
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome P450 regulator Dap1","termid":"PBO:0002392"}


id: MONDO:0012986
data:
  {"annotated_genes":["SJAG_02289"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87264],"is_not":false,"summary":null,"term":"MONDO:0012986"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"bilateral polymicrogyria","termid":"MONDO:0017091"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02289":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"bilateral parasagittal parieto-occipital polymicrogyria","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:208441","MEDGEN:862085","GARD:10785","DOID:0080923","icd11.foundation:293410499","OMIM:612691","MESH:C567201","UMLS:C4013648"],"synonyms":[{"name":"BTOP","type":"related"},{"name":"polymicrogyria, bilateral temporooccipital","type":"related"}],"termid":"MONDO:0012986","terms_by_termid":{"MONDO:0012986":null},"xrefs":{"Monarch":{"xref_id":"0012986"}}}


id: GO:0048363
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving the pectin component of mucilage.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pectin metabolic process","termid":"GO:0045488"},{"relation_name":"part_of","term_name":"mucilage metabolic process","termid":"GO:0010191"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"mucilage pectin metabolic process","synonyms":[{"name":"mucilage pectin metabolism","type":"exact"}],"termid":"GO:0048363"}


id: PBO:0000517
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CLK/STY/LAMMEr subfamily","termid":"PBO:0000517"}


id: GO:0004668
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + L-arginyl-[protein] = L-citrullyl-[protein] + NH4+, resulting in citrullination of the target protein. This reaction is calcium-dependent.","definition_xrefs":["PMID:27393304"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amidines","termid":"GO:0016813"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003674","GO:0016810","GO:0016787","GO:0003824"],"is_obsolete":false,"name":"protein-arginine deiminase activity","secondary_identifiers":["MetaCyc:PROTEIN-ARGININE-DEIMINASE-RXN","RHEA:18089","Reactome:R-HSA-3247569","EC:3.5.3.15","Reactome:R-HSA-1183128"],"synonyms":[{"name":"peptidylarginine deiminase activity","type":"related"},{"name":"protein-L-arginine iminohydrolase activity","type":"related"}],"termid":"GO:0004668"}


id: SO:0002100
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A pseudogenic constant region of an immunoglobulin gene which closely resembles a known functional Imunoglobulin constant gene but in which the coding region has stop codons, frameshift mutations or a mutation that effects the initiation codon.","definition_xrefs":["GENCODE:http://www.gencodegenes.org/gencode_biotypes.html","IGMT:http://www.imgt.org/IMGTScientificChart/SequenceDescription/Keywords.php"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immunoglobulin_pseudogene","termid":"SO:0002098"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IG_C_pseudogene","synonyms":[{"name":"IG C pseudogene","type":"exact"}],"termid":"SO:0002100"}


id: PR:000050399
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A spindle pole body-associated protein cut12 (Schizosaccharomyces pombe) that has been phosphorylated at positions equivalent to Thr-75 and Thr-78 of the amino acid sequence represented by UniProtKB:O59755. Example: UniProtKB:O59755, Thr-75/Thr-78, MOD:00047.","definition_xrefs":["PomBase:VW","PMID:23333317","PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spindle pole body-associated protein cut12 (Schizosaccharomyces pombe)","termid":"PR:000050397"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cut12/Phos(T75,T78)","pombase_gene_id":"SPBC649.05","synonyms":[{"name":"PomBase_original_PRO_term_name: spindle pole body-associated protein cut12 phosphorylated 1 (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-cut12/Phos:1","type":"exact"},{"name":"UniProtKB:O59755, Thr-75/Thr-78, MOD:00047","type":"narrow"},{"name":"cut12/Phos(T75,T78)","type":"exact"}],"termid":"PR:000050399"}


id: GO:0070864
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A cellular structure that includes cytoskeletal components and part of the cell membrane. Forms at the nuclear end of a male germline syncytium, or cyst, and translocates the over the length of the syncytium in the course of sperm individualization. Each complex contains an array of 64 investment cones, one per nucleus, that move synchronously along the spermatogenic cyst.","definition_xrefs":["GOC:sart","PMID:10588662","PMID:9550716"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"}],"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":"sperm individualization complex","termid":"GO:0070864"}


id: PBO:0050103
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group box 1 pseudogene 13","termid":"PBO:0050103"}


id: MONDO:0022651
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete cardiomyopathy dilated with conduction defect type 1 (obsolete MONDO:0022651)","termid":"MONDO:0022651","xrefs":{"Monarch":{"xref_id":"0022651"}}}


id: PBO:0004398
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Golgi transport complex peripheral subunit Cog6 (predicted)","termid":"PBO:0004398"}


id: GO:0046439
data:
  {"annotated_genes":["SJAG_03671"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[115793],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019450"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving L-cysteine, the L-enantiomer of 2-amino-3-mercaptopropanoic acid, i.e. (2R)-2-amino-3-mercaptopropanoic acid.","definition_xrefs":["GOC:mah","GOC:ai","GOC:jsg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cysteine metabolic process","termid":"GO:0006534"},{"relation_name":"is_a","term_name":"serine family amino acid metabolic process","termid":"GO:0009069"},{"relation_name":"is_a","term_name":"L-amino acid metabolic process","termid":"GO:0170033"},{"relation_name":"is_a","term_name":"proteinogenic amino acid metabolic process","termid":"GO:0170039"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03671":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006520","GO:0008150","GO:0006790","GO:0044281"],"is_obsolete":false,"name":"L-cysteine metabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"L-cysteine metabolism","type":"exact"}],"termid":"GO:0046439","terms_by_termid":{"GO:0019450":null}}


id: FYPO:0004544
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 duration of heterochromatin maintenance is longer than normal. Heterochromatin maintenance is the process that preserves heterochromatin in a stable functional or structural state.","definition_xrefs":["PomBase:mah","GO:0070829"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal heterochromatin organization during vegetative growth","termid":"FYPO:0004543"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"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:0005447","FYPO:0000641","FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"increased duration of heterochromatin maintenance","synonyms":[{"name":"increased duration of heterochromatin maintenance during mitotic cell cycle","type":"related"},{"name":"increased duration of heterochromatin maintenance during vegetative growth","type":"exact"},{"name":"prolonged heterochromatin maintenance","type":"exact"}],"termid":"FYPO:0004544"}


id: MONDO:1040010
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Van der Woude syndrome, popliteal pterygium syndrome, cleft lip with or without palate, or a spectrum of one or two of those conditions in which the cause of the disease is a mutation in the IRF6 gene.","definition_xrefs":["PMID:12219090","PMID:20301581"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IRF6-related condition","termid":"MONDO:1040010","xrefs":{"Monarch":{"xref_id":"1040010"}}}


id: PBO:0066220
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA binding motif protein 25","termid":"PBO:0066220"}


id: PBO:0012558
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by H. sapiens XPO1","termid":"PBO:0012558"}


id: SO:0000096
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene from proplastid sequence.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"has_origin","term_name":"proplastid_sequence","termid":"SO:0000748"},{"relation_name":"is_a","term_name":"plastid_gene","termid":"SO:0000090"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proplastid_gene","synonyms":[{"name":"proplastid gene","type":"exact"}],"termid":"SO:0000096"}


id: GO:0051335
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The reformation of the nuclear membrane during meiosis II.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meiotic nuclear membrane reassembly","termid":"GO:0051333"},{"relation_name":"part_of","term_name":"meiosis II","termid":"GO:0007135"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0061024"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0140013"},{"rel_name":"is_a","termid":"GO:0061024"}],"interesting_parent_ids":["GO:0061024","GO:0140013","GO:0007049","GO:0008150","GO:0044085"],"is_obsolete":false,"name":"meiosis II nuclear membrane reassembly","synonyms":[{"name":"meiosis II nuclear envelope reassembly","type":"related"}],"termid":"GO:0051335"}


id: MONDO:0005815
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplasm with neuroendocrine differentiation that arises from the pancreas. It includes neuroendocrine tumors (low and intermediate grade) and neuroendocrine carcinomas (high grade).","definition_xrefs":["NCIT:C27031"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endocrine pancreas disorder","termid":"MONDO:0001933"},{"relation_name":"is_a","term_name":"pancreatic neoplasm","termid":"MONDO:0021040"},{"relation_name":"is_a","term_name":"digestive system neuroendocrine neoplasm","termid":"MONDO:0024503"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"pancreatic neuroendocrine neoplasm","secondary_identifiers":["MEDGEN:1848937","Orphanet:506052","EFO:0007331","icd11.foundation:1421495979","ICDO:8150/1","UMLS:C5848399","SCTID:254611009","GARD:22052","DOID:1799"],"synonyms":[{"name":"Islet cell tumors","type":"narrow"},{"name":"Islet cell tumours","type":"narrow"},{"name":"Islet of Langerhans tumor","type":"related"},{"name":"Islet of Langerhans tumour","type":"related"},{"name":"PNEN","type":"exact"},{"name":"endocrine pancreas cancer","type":"narrow"},{"name":"endocrine pancreas neoplasm","type":"exact"},{"name":"endocrine pancreas neoplasm (disease)","type":"exact"},{"name":"endocrine pancreas tumor","type":"exact"},{"name":"endocrine pancreas tumour","type":"exact"},{"name":"islet cell neoplasm","type":"narrow"},{"name":"islet cell tumor","type":"narrow"},{"name":"islet cell tumour","type":"narrow"},{"name":"malignant pancreatic endocrine tumor","type":"narrow"},{"name":"malignant pancreatic endocrine tumour","type":"narrow"},{"name":"malignant tumor of endocrine pancreas","type":"exact"},{"name":"malignant tumour of endocrine pancreas","type":"exact"},{"name":"neoplasm of endocrine pancreas","type":"exact"},{"name":"neuroendocrine neoplasm of pancreas","type":"related"},{"name":"pancreatic NEN","type":"exact"},{"name":"pancreatic endocrine neoplasm","type":"exact"},{"name":"pancreatic neuroendocrine neoplasm","type":"exact"},{"name":"tumor of endocrine pancreas","type":"exact"},{"name":"tumour of endocrine pancreas","type":"exact"}],"termid":"MONDO:0005815","xrefs":{"Monarch":{"xref_id":"0005815"}}}


id: GO:0007602
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The sequence of reactions within a cell required to convert absorbed photons into a molecular signal.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"signal transduction","termid":"GO:0007165"},{"relation_name":"is_a","term_name":"detection of light stimulus","termid":"GO:0009583"}],"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":"phototransduction","secondary_identifiers":["Wikipedia:Visual_phototransduction"],"synonyms":[{"name":"opsin","type":"related"},{"name":"phototransduction, visible light, light adaptation","type":"narrow"},{"name":"phototrophin mediated phototransduction","type":"narrow"}],"termid":"GO:0007602"}


id: PBO:0048927
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"golgi integral membrane protein 4","termid":"PBO:0048927"}


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


id: MONDO:0016383
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Nephrogenic diabetes insipidus (NDI) is characterized by polyuria with polydipsia, recurrent bouts of fever, constipation, and acute hypernatremic dehydration after birth that may cause neurological sequelae. Polyuria may exceed 10 liters in children.","definition_xrefs":["Orphanet:223"],"direct_ancestors":[{"relation_name":"is_a","term_name":"impaired renal function disease","termid":"MONDO:0001343"},{"relation_name":"is_a","term_name":"diabetes insipidus","termid":"MONDO:0004782"},{"relation_name":"is_a","term_name":"inherited renal tubular disease","termid":"MONDO:0015962"}],"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":"nephrogenic diabetes insipidus","secondary_identifiers":["MedDRA:10029147","MEDGEN:57876","MESH:D018500","DOID:12387","GARD:7178","icd11.foundation:1417669099","NCIT:C84919","NANDO:2200326","ICD9:588.1","NANDO:1200742","NORD:1497","UMLS:C0162283","SCTID:111395007","ICD10CM:N25.1"],"synonyms":[{"name":"ADH resistant diabetes insipidus","type":"related"},{"name":"diabetes insipidus nephrogenic","type":"related"},{"name":"diabetes insipidus nephrogenic X-linked","type":"related"},{"name":"diabetes insipidus nephrogenic type 1","type":"related"},{"name":"vasopressin-resistant diabetes insipidus","type":"related"}],"termid":"MONDO:0016383","xrefs":{"Monarch":{"xref_id":"0016383"}}}


id: PBO:0064159
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phospholipase A2 group IID","termid":"PBO:0064159"}


id: MONDO:0010703
data:
  {"annotated_genes":["SJAG_00635"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88843],"is_not":false,"summary":null,"term":"MONDO:0010703"}]},"cv_name":"mondo","definition":"Ornithine transcarbamylase deficiency (OTCD) is a disorder of urea cycle metabolism and ammonia detoxification characterized by either a severe, neonatal-onset disease found almost exclusively in males, or later-onset (partial) forms of the disease. Both present with episodes of hyperammonemia that can be fatal and which can lead to neurological complications.","definition_xrefs":["Orphanet:664"],"direct_ancestors":[{"relation_name":"is_a","term_name":"urea cycle disorder or inherited hyperammonemia","termid":"MONDO:0800153"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00635":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004736"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0005066"],"is_obsolete":false,"name":"ornithine carbamoyltransferase deficiency","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:9271","MEDGEN:75692","OMIM:311250","EFO:0007409","UMLS:C0268542","MedDRA:10052450","NANDO:1200804","GARD:8391","icd11.foundation:1822444026","MESH:D020163","NANDO:2200479","NCIT:C84957","SCTID:80908008"],"synonyms":[{"name":"OCT deficiency","type":"exact"},{"name":"OTC deficiency","type":"exact"},{"name":"OTCD","type":"exact"},{"name":"deficiency of citrulline phosphorylase","type":"exact"},{"name":"ornithine carbamoyltransferase deficiency","type":"exact"},{"name":"ornithine carbamoyltransferase deficiency disease","type":"exact"},{"name":"ornithine transcarbamylase deficiency","type":"exact"},{"name":"ornithine transcarbamylase deficiency, hyperammonemia due to","type":"related"},{"name":"valproate sensitivity","type":"related"}],"termid":"MONDO:0010703","terms_by_termid":{"MONDO:0010703":null},"xrefs":{"Monarch":{"xref_id":"0010703"}}}


id: PBO:0031023
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_concentration_of_M-factor_in_growth_medium","termid":"PBO:0031023"}


id: FYPO:0001566
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of L-citrulline measured in a cell is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased cellular amino acid level","termid":"FYPO:0003986"}],"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:0001320","FYPO:0000002"],"is_obsolete":false,"name":"increased cellular citrulline level","synonyms":[{"name":"increased cellular L-citrulline level","type":"exact"},{"name":"increased cellular citrulline level during mitotic cell cycle","type":"related"},{"name":"increased cellular citrulline level during vegetative growth","type":"exact"},{"name":"increased citrulline accumulation","type":"related"}],"termid":"FYPO:0001566"}


id: PBO:0053300
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lin-7 homolog B, crumbs cell polarity complex component","termid":"PBO:0053300"}


id: PBO:0089295
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha mannosidase Mnl1","termid":"PBO:0089295"}


id: GO:0070697
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to an activin receptor.","definition_xrefs":["GOC:vk","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane receptor protein serine/threonine kinase binding","termid":"GO:0070696"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"activin receptor binding","termid":"GO:0070697"}


id: FYPO:0004230
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the phosphorylation of one or more specific proteins is normal (i.e. indistinguishable from wild type) during a cellular response to ultraviolet light.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein phosphorylation during vegetative growth","termid":"FYPO:0000776"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001320","FYPO:0000002","FYPO:0001312"],"is_obsolete":false,"name":"normal protein phosphorylation during cellular response to UV","synonyms":[{"name":"normal protein phosphorylation during cellular response to UV during mitotic cell cycle","type":"related"},{"name":"normal protein phosphorylation during cellular response to UV during vegetative growth","type":"exact"},{"name":"normal protein phosphorylation during cellular response to ultraviolet light","type":"related"}],"termid":"FYPO:0004230"}


id: PBO:0055443
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 2874","termid":"PBO:0055443"}


id: GO:0160223
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A specialized membranous structure that extends from the photosynthetic thylakoid membrane into and transverses the matrix of a pyrenoid.","definition_xrefs":["PMID:32428480"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"pyrenoid","termid":"GO:1990732"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005737"],"is_obsolete":false,"name":"pyrenoid tubule","synonyms":[{"name":"thylakoid membrane tubule","type":"exact"}],"termid":"GO:0160223"}


id: PBO:0091048
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dolichol-phosphate mannosyltransferase regulatory subunit Dpm2","termid":"PBO:0091048"}


id: PBO:0090589
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial MIB complex subunit, human DNAJC11 ortholog","termid":"PBO:0090589"}


id: PBO:0032720
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_after_spore_germination,_multiple_cell_divisions,_spherical_cell_with_cell_lysis","termid":"PBO:0032720"}


id: PBO:0116669
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARL6 interacting reticulophagy regulator 1","termid":"PBO:0116669"}


id: MONDO:0016091
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A Krabbe disease that occurs in an adult.","definition_xrefs":["MONDO:design_pattern"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Krabbe disease","termid":"MONDO:0009499"},{"relation_name":"is_a","term_name":"cerebral lipidosis with dementia","termid":"MONDO:0020143"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0002561"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0002525"}],"interesting_parent_ids":["MONDO:0005244","MONDO:0005066","MONDO:0002561","MONDO:0002525","MONDO:0005328","MONDO:0002039","MONDO:0005559"],"is_obsolete":false,"name":"adult Krabbe disease","secondary_identifiers":["icd11.foundation:699668826","Orphanet:206448","MEDGEN:120623","NANDO:1200077","NANDO:2201219","UMLS:C0268252","GARD:20345"],"synonyms":[{"name":"Krabbe disease of adults","type":"exact"}],"termid":"MONDO:0016091","xrefs":{"Monarch":{"xref_id":"0016091"}}}


id: GO:1903278
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of sodium ion export across the plasma membrane.","definition_xrefs":["GOC:rl","PMID:17095720","GOC:BHF","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of sodium ion transmembrane transport","termid":"GO:1902307"},{"relation_name":"is_a","term_name":"regulation of sodium ion export across plasma membrane","termid":"GO:1903276"},{"relation_name":"positively_regulates","term_name":"sodium ion export across plasma membrane","termid":"GO:0036376"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"positively_regulates","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0008150","GO:0055085","GO:0006810"],"is_obsolete":false,"name":"positive regulation of sodium ion export across plasma membrane","secondary_identifiers":["GO:1903275"],"synonyms":[{"name":"activation of sodium export","type":"narrow"},{"name":"activation of sodium ion export","type":"narrow"},{"name":"activation of sodium ion export from cell","type":"narrow"},{"name":"positive regulation of sodium export","type":"related"},{"name":"positive regulation of sodium ion export","type":"related"},{"name":"positive regulation of sodium ion export from cell","type":"exact"},{"name":"up regulation of sodium export","type":"related"},{"name":"up regulation of sodium ion export","type":"related"},{"name":"up regulation of sodium ion export from cell","type":"exact"},{"name":"up-regulation of sodium export","type":"related"},{"name":"up-regulation of sodium ion export","type":"related"},{"name":"up-regulation of sodium ion export from cell","type":"exact"},{"name":"upregulation of sodium export","type":"related"},{"name":"upregulation of sodium ion export","type":"related"},{"name":"upregulation of sodium ion export from cell","type":"exact"}],"termid":"GO:1903278"}


id: MOD:00412
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod artifact. OBSOLETE because Unimod entry 19 is now merged with Unimod 35 remap to MOD:00425 'monohydroxylated residue'.","definition_xrefs":["PubMed:18688235"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE MOD:00412 oxidation (obsolete MOD:00412)","termid":"MOD:00412"}


id: MONDO:0850269
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An acute myeloid leukemia that is characterized by the presence of t(8;21)(q22;q22) or inv(16)(p13q22)/t(16;16)(p13;q22). These cytogenetic abnormalities result in disruption of the transcription factor CBF, which is a regulator of normal hematopoiesis.","definition_xrefs":["DOID:0080796"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute myeloid leukemia","termid":"MONDO:0018874"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046","MONDO:0004992"],"is_obsolete":false,"name":"core binding factor acute myeloid leukemia","secondary_identifiers":["MEDGEN:825586","NCIT:C122688","UMLS:C3839741"],"termid":"MONDO:0850269","xrefs":{"Monarch":{"xref_id":"0850269"}}}


id: PBO:0005478
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"caffeine induced death protein Cid2","termid":"PBO:0005478"}


id: GO:0010334
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: trans,trans-farnesyl diphosphate = a sesquiterpene + diphosphate. Sesquiterpenes are terpenes containing three isoprene units, i.e. 15 carbons.","definition_xrefs":["GOC:tair_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"terpene synthase activity","termid":"GO:0010333"}],"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:0016829"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016829"],"is_obsolete":false,"name":"sesquiterpene synthase activity","termid":"GO:0010334"}


id: PBO:0034219
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-mesoparasite_of","termid":"PBO:0034219"}


id: PBO:0057954
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIR3677 and MIR940 host gene","termid":"PBO:0057954"}


id: PBO:0002304
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"P-TEFb-associated cyclin-dependent protein kinase Lsk1","termid":"PBO:0002304"}


id: PBO:0027603
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_mitotic_spindle_microtubule_depolymerization","termid":"PBO:0027603"}


id: MONDO:0016328
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete fatty acid oxidation and ketogenesis disorder with hypertrophic cardiomyopathy (obsolete MONDO:0016328)","secondary_identifiers":["Orphanet:217591"],"termid":"MONDO:0016328","xrefs":{"Monarch":{"xref_id":"0016328"}}}


id: PBO:0072642
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"regulator of telomere elongation helicase 1","termid":"PBO:0072642"}


id: PBO:0072766
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S100 calcium binding protein B","termid":"PBO:0072766"}


id: PBO:0066591
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ras homolog family member F, filopodia associated","termid":"PBO:0066591"}


id: GO:0016859
data:
  {"annotated_genes":["SJAG_04155","SJAG_03238","SJAG_02413","SJAG_01714","SJAG_00470","SJAG_00602","SJAG_01270","SJAG_02551","SJAG_00950","SJAG_03905","SJAG_02308","SJAG_04352","SJAG_03601","SJAG_01005","SJAG_02620","SJAG_00078","SJAG_01246"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[64859,73573,73452,57901,77573,77194,94580,79695,74341,79686,58268,77697,71901,65900,79729,81890,64720],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003755"}]},"cv_name":"molecular_function","definition":"Catalysis of a reaction that interconverts cis and trans isomers. Atoms or groups are termed cis or trans to one another when they lie respectively on the same or on opposite sides of a reference plane identifiable as common among stereoisomers.","definition_xrefs":["GOC:mah","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isomerase activity","termid":"GO:0016853"}],"gene_count":17,"genes_by_uniquename":{"SJAG_00078":null,"SJAG_00470":null,"SJAG_00602":null,"SJAG_00950":null,"SJAG_01005":null,"SJAG_01246":null,"SJAG_01270":null,"SJAG_01714":null,"SJAG_02308":null,"SJAG_02413":null,"SJAG_02551":null,"SJAG_02620":null,"SJAG_03238":null,"SJAG_03601":null,"SJAG_03905":null,"SJAG_04155":null,"SJAG_04352":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016853"}],"interesting_parent_ids":["GO:0003674","GO:0016853","GO:0003824"],"is_obsolete":false,"name":"cis-trans isomerase activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["EC:5.2.-.-"],"termid":"GO:0016859","terms_by_termid":{"GO:0003755":null}}


id: PR:O42826
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pdh1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O42826"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein pdh1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1235.08c","synonyms":[{"name":"Spom972h-pdh1","type":"exact"}],"termid":"PR:O42826"}


id: FYPO:0007613
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 transcription from a promoter that contains one or more STREP motifs occurs to a lower extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased transcription during vegetative growth","termid":"FYPO:0000781"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0000294","FYPO:0006551","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"decreased transcription from STREP promoter","synonyms":[{"name":"increased transcription from STREP promoter during mitotic cell cycle","type":"related"},{"name":"increased transcription from STREP promoter during vegetative growth","type":"exact"}],"termid":"FYPO:0007613"}


id: GO:1903574
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of a cellular response to amino acid starvation.","definition_xrefs":["PMID:11381086","GOC:TermGenie","GO_REF:0000058","GOC:PARL","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of response to nutrient levels","termid":"GO:0032108"},{"relation_name":"is_a","term_name":"negative regulation of cellular process","termid":"GO:0048523"},{"relation_name":"is_a","term_name":"regulation of cellular response to amino acid starvation","termid":"GO:1903832"},{"relation_name":"negatively_regulates","term_name":"cellular response to amino acid starvation","termid":"GO:0034198"}],"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 cellular response to amino acid starvation","synonyms":[{"name":"down regulation of cellular response to amino acid starvation","type":"exact"},{"name":"down-regulation of cellular response to amino acid starvation","type":"exact"},{"name":"downregulation of cellular response to amino acid starvation","type":"exact"},{"name":"inhibition of cellular response to amino acid starvation","type":"narrow"}],"termid":"GO:1903574"}


id: FYPO:0000706
data:
  {"alleles_by_uniquename":{"SJAG_01458:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01458","name":"acb1delta","uniquename":"SJAG_01458:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[121187],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000719"}]},"cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a specific molecular function is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal phenotype","termid":"FYPO:0000257"},{"relation_name":"is_a","term_name":"molecular function phenotype","termid":"FYPO:0000652"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01458":null},"genotype_count":1,"genotypes_by_uniquename":{"acb1delta":{"display_name":"acb1delta","display_uniquename":"acb1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01458:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000652"],"is_obsolete":false,"name":"normal molecular function","references_by_uniquename":{"PMID:31956022":null},"single_locus_annotated_genes":["SJAG_01458"],"single_locus_genotype_uniquenames":["acb1delta"],"termid":"FYPO:0000706","terms_by_termid":{"FYECO:0000126":null,"FYPO:0000719":null}}


id: PR:P0CT36
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- Tf2-3 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P0CT36"],"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":"transposon Tf2-3 polyprotein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC2E1P3.03c","synonyms":[{"name":"Spom972h-Tf2-3","type":"exact"},{"name":"retrotransposable element Tf2 155 kDa protein (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P0CT36"}


id: PBO:0077579
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trimethyllysine hydroxylase, epsilon","termid":"PBO:0077579"}


id: GO:1900015
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cytokine production involved in inflammatory response.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytokine production","termid":"GO:0001817"},{"relation_name":"regulates","term_name":"cytokine production involved in inflammatory response","termid":"GO:0002534"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"regulation of cytokine production involved in inflammatory response","synonyms":[{"name":"regulation of cytokine production involved in acute inflammatory response","type":"narrow"}],"termid":"GO:1900015"}


id: PBO:0062557
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 10 subfamily A member 4","termid":"PBO:0062557"}


id: PBO:0002065
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KASH domain protein","termid":"PBO:0002065"}


id: GO:1902486
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a protein is transported to, or maintained in, a location within a growing cell tip.","definition_xrefs":["PMID:23041194","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization to cell tip","termid":"GO:1990151"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"protein localization to growing cell tip","synonyms":[{"name":"protein localisation in growing cell tip","type":"exact"},{"name":"protein localisation to growing cell tip","type":"exact"},{"name":"protein localization in growing cell tip","type":"exact"}],"termid":"GO:1902486"}


id: PBO:0089708
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U3 snoRNP-associated WD repeat protein Utp15","termid":"PBO:0089708"}


id: GO:0009590
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events in which a gravitational stimulus is received and converted into a molecular signal.","definition_xrefs":["GOC:dos","GOC:hb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detection of external stimulus","termid":"GO:0009581"},{"relation_name":"is_a","term_name":"detection of abiotic stimulus","termid":"GO:0009582"},{"relation_name":"is_a","term_name":"response to gravity","termid":"GO:0009629"}],"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 gravity","synonyms":[{"name":"perception of gravity","type":"related"}],"termid":"GO:0009590"}


id: PBO:0054133
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 1499","termid":"PBO:0054133"}


id: PBO:0074148
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 35 member D1","termid":"PBO:0074148"}


id: PATO:0001977
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A shape quality inhering in a bearer by virtue of the bearer's having at least one salient angle on the margin.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"shape","termid":"PATO:0000052"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"angular","synonyms":[{"name":"angulate","type":"exact"}],"termid":"PATO:0001977"}


id: MONDO:0009054
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"autosomal recessive cutis laxa type 2A","termid":"MONDO:0018163"},{"relation_name":"is_a","term_name":"inherited cutis laxa","termid":"MONDO:0100237"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autosomal recessive cutis laxa type 2, classic type","secondary_identifiers":["UMLS:C5679922","SCTID:73856006","Orphanet:357074","GARD:17546","MEDGEN:1825992","DOID:0070141","MESH:C562632"],"synonyms":[{"name":"ARCL2, Debre type","type":"exact"},{"name":"ARCL2, Debré type","type":"exact"},{"name":"ARCL2, classic type","type":"exact"},{"name":"ARCL2A","type":"related"},{"name":"Arcl2","type":"related"},{"name":"autosomal recessive cutis laxa type 2, Debre type","type":"exact"},{"name":"autosomal recessive cutis laxa type 2, Debré type","type":"exact"},{"name":"autosomal recessive cutis laxa type II classic type","type":"related"}],"termid":"MONDO:0009054","xrefs":{"Monarch":{"xref_id":"0009054"}}}


id: FYPO:0007603
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate or other property of a microfilament motor activity is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal microfilament motor activity","termid":"FYPO:0006093"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000661","FYPO:0000707","FYPO:0000654","FYPO:0000652"],"is_obsolete":false,"name":"decreased microfilament motor activity","synonyms":[{"name":"decreased actin filament motor activity","type":"exact"},{"name":"decreased microfilament motor (ATPase) activity","type":"exact"},{"name":"decreased myosin ATPase activity","type":"related"},{"name":"reduced microfilament motor activity","type":"exact"}],"termid":"FYPO:0007603"}


id: PBO:0000123
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"expressed during meiosis","termid":"PBO:0000123"}


id: FYPO:0002764
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which tRNA (guanine(9)-N(1))-methyltransferase activity is absent.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished tRNA methyltransferase activity","termid":"FYPO:0001773"},{"relation_name":"is_a","term_name":"abnormal tRNA (guanine(9)-N(1))-methyltransferase activity","termid":"FYPO:0002763"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000707","FYPO:0000661","FYPO:0000654","FYPO:0001985"],"is_obsolete":false,"name":"abolished tRNA (guanine(9)-N(1))-methyltransferase activity","synonyms":[{"name":"tRNA (guanine(9)-N(1))-methyltransferase activity abolished","type":"exact"}],"termid":"FYPO:0002764"}


id: PBO:0067318
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 404, pseudogene","termid":"PBO:0067318"}


id: PBO:0090990
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial carrier, glycine Hem25","termid":"PBO:0090990"}


id: MONDO:0010841
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Waardenburg syndrome type 2","termid":"MONDO:0019517"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"Waardenburg syndrome type 2B","secondary_identifiers":["GARD:5522","MESH:C536465","MEDGEN:373973","DOID:0110947","OMIM:600193","UMLS:C1838447"],"synonyms":[{"name":"WS2B","type":"exact"},{"name":"Waardenburg syndrome type IIB","type":"exact"},{"name":"Waardenburg syndrome, type 2B","type":"related"}],"termid":"MONDO:0010841","xrefs":{"Monarch":{"xref_id":"0010841"}}}


id: PBO:0060464
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NALCN channel auxiliary factor 1","termid":"PBO:0060464"}


id: PBO:0054424
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 1820","termid":"PBO:0054424"}


id: PBO:0061708
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear transport factor 2 pseudogene 3","termid":"PBO:0061708"}


id: PBO:0001924
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA-binding splicing factor (predicted)","termid":"PBO:0001924"}


id: MONDO:0013060
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare neurodegenerative disease usually presenting before the age of 30 and which is characterized by dystonia, L-dopa-responsive parkinsonism, pyramidal signs and rapid cognitive decline.","definition_xrefs":["Orphanet:199351"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete persistent combined dystonia (obsolete MONDO:0018329)","termid":"MONDO:0018329"},{"relation_name":"is_a","term_name":"late-onset Parkinson disease","termid":"MONDO:0008199"},{"relation_name":"is_a","term_name":"PLA2G6-associated neurodegeneration","termid":"MONDO:0017998"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0002039","MONDO:0005559"],"is_obsolete":false,"name":"autosomal recessive Parkinson disease 14","secondary_identifiers":["SCTID:720466001","UMLS:C2751842","GARD:12568","DOID:0060900","MEDGEN:414488","MESH:C567844","OMIM:612953"],"synonyms":[{"name":"PARK14","type":"exact"},{"name":"PLA2G6 hereditary late onset Parkinson disease","type":"exact"},{"name":"PLA2G6-related dystonia-parkinsonism","type":"exact"},{"name":"Parkinson disease 14, autosomal recessive","type":"related"},{"name":"adult-onset dystonia - parkinsonism","type":"related"},{"name":"autosomal recessive Parkinson disease type 14","type":"exact"},{"name":"autosomal recessive Parkinson's disease 14","type":"related"},{"name":"dystonia-Parkinsonism Adult-onset","type":"exact"},{"name":"dystonia-Parkinsonism, adult-onset","type":"related"},{"name":"dystonia-parkinsonism, Paisan-Ruiz type","type":"exact"},{"name":"hereditary late onset Parkinson disease caused by mutation in PLA2G6","type":"exact"}],"termid":"MONDO:0013060","xrefs":{"Monarch":{"xref_id":"0013060"}}}


id: PBO:0080787
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"XK related, Y-linked pseudogene 7","termid":"PBO:0080787"}


id: PR:Q9UTT1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ubp15 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9UTT1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin carboxyl-terminal hydrolase 21 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC713.02c","synonyms":[{"name":"Spom972h-ubp15","type":"exact"},{"name":"deubiquitinating enzyme 21 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"ubiquitin thioesterase 21 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"ubiquitin-specific-processing protease 21 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9UTT1"}


id: MONDO:0014283
data:
  {"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 TNC 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:0019497"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0019497","MONDO:0000426"],"is_obsolete":false,"name":"autosomal dominant nonsyndromic hearing loss 56","secondary_identifiers":["GARD:18137","MEDGEN:816500","OMIM:615629","UMLS:C3810170","DOID:0110581"],"synonyms":[{"name":"DFNA56","type":"narrow"},{"name":"TNC autosomal dominant nonsyndromic deafness","type":"narrow"},{"name":"autosomal dominant deafness 56","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness 56","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness caused by mutation in TNC","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness type 56","type":"narrow"},{"name":"deafness, autosomal dominant 56","type":"narrow"},{"name":"deafness, autosomal dominant type 56","type":"narrow"}],"termid":"MONDO:0014283","xrefs":{"Monarch":{"xref_id":"0014283"}}}


id: GO:0033994
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (1->4)-beta-D-glucuronan = an oligosaccharide with 4-deoxy-beta-D-gluc-4-enuronosyl end + (1->4)-beta-D-glucuronan. This reaction is the eliminative cleavage of (1->4)-beta-D-glucuronans to give oligosaccharides with 4-deoxy-beta-D-gluc-4-enuronosyl groups at their non-reducing ends. Complete degradation of glucuronans results in the formation of tetrasaccharides.","definition_xrefs":["EC:4.2.2.14"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-oxygen lyase activity, acting on polysaccharides","termid":"GO:0016837"}],"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":"glucuronan lyase activity","secondary_identifiers":["MetaCyc:4.2.2.14-RXN"],"synonyms":[{"name":"(1,4)-beta-D-glucuronan lyase activity","type":"related"}],"termid":"GO:0033994"}


id: MONDO:0032723
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"immunodeficiency disease","termid":"MONDO:0021094"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"immunodeficiency 60","secondary_identifiers":["MEDGEN:1681890","OMIM:618394","UMLS:C5193072","DOID:0111954"],"synonyms":[{"name":"IMD60","type":"related"},{"name":"IMMUNODEFICIENCY 60","type":"related"},{"name":"Immunodeficiency and Autoimmunity, Bach2-Related","type":"related"},{"name":"immunodeficiency 60 and autoimmunity","type":"exact"}],"termid":"MONDO:0032723","xrefs":{"Monarch":{"xref_id":"0032723"}}}


id: FYPO:0006491
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of chitin synthase activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal catalytic activity","termid":"FYPO:0000661"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0000654","FYPO:0001985","FYPO:0000661","FYPO:0000707","FYPO:0000652"],"is_obsolete":false,"name":"abnormal chitin synthase activity","termid":"FYPO:0006491"}


id: PBO:0003961
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-directed RNA polymerase I, II and III subunit Rpb8","termid":"PBO:0003961"}


id: GO:0016335
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of a larval imaginal disc epithelium are generated and organized.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"morphogenesis of an epithelium","termid":"GO:0002009"},{"relation_name":"is_a","term_name":"post-embryonic animal morphogenesis","termid":"GO:0009886"},{"relation_name":"part_of","term_name":"instar larval development","termid":"GO:0002168"},{"relation_name":"part_of","term_name":"imaginal disc morphogenesis","termid":"GO:0007560"}],"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":"morphogenesis of larval imaginal disc epithelium","termid":"GO:0016335"}


id: MONDO:0010617
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus.","definition_xrefs":["Orphanet:2234"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome","secondary_identifiers":["OMIM:307500","MEDGEN:334557","MESH:C564406","UMLS:C1843994","SCTID:722459008","GARD:4899"],"synonyms":[{"name":"Sohval-Soffer syndrome","type":"exact"},{"name":"hypogonadism, MALE, with intellectual disability and skeletal anomalies","type":"related"},{"name":"hypogonadism, MALE, with mental retardation and skeletal anomalies","type":"related"}],"termid":"MONDO:0010617","xrefs":{"Monarch":{"xref_id":"0010617"}}}


id: PBO:0052210
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KCNQ5 antisense RNA 1","termid":"PBO:0052210"}


id: PBO:0045896
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation elongation factor 1 gamma pseudogene 8","termid":"PBO:0045896"}


id: GO:0044485
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which an organism initiates, promotes, or enhances fibrinogenolysis in another organism via the action of a venom. Fibrinogenolysis is the degradation of fibrinogen by proteolytic cleavage.","definition_xrefs":["PMID:17433397","GOC:fj","PMID:17544404"],"direct_ancestors":[{"relation_name":"is_a","term_name":"venom-mediated depletion of circulating fibrinogen","termid":"GO:0044536"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"venom-mediated fibrinogenolysis","synonyms":[{"name":"envenomation resulting in fibrinogenolysis in another organism","type":"exact"},{"name":"envenomation resulting in fibrinogenolysis in other organism","type":"exact"}],"termid":"GO:0044485"}


id: PBO:0113466
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the signal peptidase complex (SPC); SPC cleaves the signal sequence from proteins targeted to the endoplasmic reticulum (ER); regulates cellular levels of membrane proteins; homolog of the SPC12 subunit of mammalian signal peptidase complex; protein abundance increases in response to DNA replication stress","termid":"PBO:0113466"}


id: PBO:0076483
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TARBP2 subunit of RISC loading complex","termid":"PBO:0076483"}


id: RO:0002641
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"inverse of intracellular endoparasite of","direct_ancestors":[{"relation_name":"is_a","term_name":"has_endoparasite","termid":"RO:0002635"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_intracellular_endoparasite","termid":"RO:0002641"}


id: MONDO:0700010
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chromosomal disorder in which chromosome 3 is affected.","definition_xrefs":["MONDO:patterns/chromosome_type"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal anomaly","termid":"MONDO:0020049"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 3 disorder","termid":"MONDO:0700010","xrefs":{"Monarch":{"xref_id":"0700010"}}}


id: PBO:0076921
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor B2, mitochondrial","termid":"PBO:0076921"}


id: PBO:0030667
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_27S_rRNA_precursor_level","termid":"PBO:0030667"}


id: PBO:0085441
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Polypeptide release factor (eRF1) in translation termination; mutant form acts as a recessive omnipotent suppressor; methylated by Mtq2p-Trm112p in ternary complex eRF1-eRF3-GTP; mutation of methylation site confers resistance to zymocin; has a role in cytokinesis through interaction with Mlc1p","termid":"PBO:0085441"}


id: MONDO:0000542
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete duodenum adenoma (obsolete MONDO:0000542)","termid":"MONDO:0000542","xrefs":{"Monarch":{"xref_id":"0000542"}}}


id: PBO:0058833
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 8063","termid":"PBO:0058833"}


id: PBO:0073259
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"septin 7 pseudogene 3","termid":"PBO:0073259"}


id: MONDO:0035759
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"coagulation protein disease","termid":"MONDO:0002242"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"factor V atlanta bleeding disorder","secondary_identifiers":["GARD:22415","MEDGEN:1842929","Orphanet:600194","UMLS:C5681543"],"termid":"MONDO:0035759","xrefs":{"Monarch":{"xref_id":"0035759"}}}


id: PBO:0040048
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARPC1A pseudogene 4","termid":"PBO:0040048"}


id: MONDO:0020804
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma involving the basal cells.","definition_xrefs":["NCIT:C156767"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carcinoma","termid":"MONDO:0004993"},{"relation_name":"is_a","term_name":"basal cell neoplasm","termid":"MONDO:0020799"}],"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":"basal cell carcinoma","secondary_identifiers":["NCIT:C7586","MESH:D002280","MEDGEN:2870","UMLS:C0007117","EFO:0004193"],"synonyms":[{"name":"basal cell cancer","type":"exact"},{"name":"epithelioma, basal cell","type":"exact"},{"name":"malignant basal cell neoplasm","type":"exact"}],"termid":"MONDO:0020804","xrefs":{"Monarch":{"xref_id":"0020804"}}}


id: PBO:0000850
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein kinase, RIO family (predicted)","termid":"PBO:0000850"}


id: SO:0001320
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Mannosyl_queuosine 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":"mannosyl_queuosine","secondary_identifiers":["RNAMOD:046"],"synonyms":[{"name":"manQ","type":"exact"},{"name":"mannosyl queuosine","type":"exact"},{"name":"mannosyl-queuosine","type":"exact"}],"termid":"SO:0001320"}


id: GO:1903283
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of glutathione peroxidase activity.","definition_xrefs":["GOC:PARL","GOC:TermGenie","GO_REF:0000059","GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of glutathione peroxidase activity (obsolete GO:1903283)","synonyms":[{"name":"down regulation of GSH peroxidase activity","type":"exact"},{"name":"down regulation of glutathione peroxidase activity","type":"exact"},{"name":"down regulation of glutathione:hydrogen-peroxide oxidoreductase activity","type":"exact"},{"name":"down regulation of non-selenium glutathione peroxidase activity","type":"narrow"},{"name":"down regulation of reduced glutathione peroxidase activity","type":"exact"},{"name":"down regulation of selenium-glutathione peroxidase activity","type":"exact"},{"name":"down-regulation of GSH peroxidase activity","type":"exact"},{"name":"down-regulation of glutathione peroxidase activity","type":"exact"},{"name":"down-regulation of glutathione:hydrogen-peroxide oxidoreductase activity","type":"exact"},{"name":"down-regulation of non-selenium glutathione peroxidase activity","type":"narrow"},{"name":"down-regulation of reduced glutathione peroxidase activity","type":"exact"},{"name":"down-regulation of selenium-glutathione peroxidase activity","type":"exact"},{"name":"downregulation of GSH peroxidase activity","type":"exact"},{"name":"downregulation of glutathione peroxidase activity","type":"exact"},{"name":"downregulation of glutathione:hydrogen-peroxide oxidoreductase activity","type":"exact"},{"name":"downregulation of non-selenium glutathione peroxidase activity","type":"narrow"},{"name":"downregulation of reduced glutathione peroxidase activity","type":"exact"},{"name":"downregulation of selenium-glutathione peroxidase activity","type":"exact"},{"name":"inhibition of GSH peroxidase activity","type":"narrow"},{"name":"inhibition of glutathione peroxidase activity","type":"narrow"},{"name":"inhibition of glutathione:hydrogen-peroxide oxidoreductase activity","type":"narrow"},{"name":"inhibition of non-selenium glutathione peroxidase activity","type":"narrow"},{"name":"inhibition of reduced glutathione peroxidase activity","type":"narrow"},{"name":"inhibition of selenium-glutathione peroxidase activity","type":"narrow"},{"name":"negative regulation of GSH peroxidase activity","type":"exact"},{"name":"negative regulation of glutathione:hydrogen-peroxide oxidoreductase activity","type":"exact"},{"name":"negative regulation of non-selenium glutathione peroxidase activity","type":"narrow"},{"name":"negative regulation of reduced glutathione peroxidase activity","type":"exact"},{"name":"negative regulation of selenium-glutathione peroxidase activity","type":"exact"}],"termid":"GO:1903283"}


id: FYPO:0006273
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which the structure of the glycan moiety of a nascent glycoprotein in the endoplasmic reticulum lumen differs from wild type.","definition_xrefs":["PomBase:mah","PMID:27587357"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal glycoprotein glycan structure","termid":"FYPO:0003290"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0002494"},{"rel_name":"output_of","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0003290"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0003290","FYPO:0002274","FYPO:0001985","FYPO:0005447","FYPO:0001320","FYPO:0002494"],"is_obsolete":false,"name":"abnormal glycoprotein glycan structure in endoplasmic reticulum lumen","synonyms":[{"name":"abnormal glycoprotein glycan structure in ER lumen","type":"exact"},{"name":"abnormal glycoprotein oligosaccharide structure in endoplasmic reticulum lumen","type":"related"}],"termid":"FYPO:0006273"}


id: PBO:0046134
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EIF5 divergent transcript","termid":"PBO:0046134"}


id: GO:0120293
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An aggregation of axonemal dyneins, their specific assembly factors, and broadly-acting chaperones that is located in the cytoplasm.","definition_xrefs":["PMID:32898505","PMID:33263282","GOC:krc","PMID:30561330"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular membraneless organelle","termid":"GO:0043232"},{"relation_name":"part_of","term_name":"cytoplasm","termid":"GO:0005737"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005737","GO:0005575"],"is_obsolete":false,"name":"dynein axonemal particle","synonyms":[{"name":"DynAP","type":"related"}],"termid":"GO:0120293"}


id: PBO:0112851
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"asynchronous replication autosomal RNA 15-1","termid":"PBO:0112851"}


id: PBO:0045039
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DIX domain containing 1","termid":"PBO:0045039"}


id: PBO:0080599
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat domain 33","termid":"PBO:0080599"}


id: MONDO:0016812
data:
  {"annotated_genes":["SJAG_03275","SJAG_03098"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87233],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012994"},{"annotations":[86828],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007495"}]},"cv_name":"mondo","definition":"Dopa-responsive dystonia (DRD) describes a group of neurometabolic disorders characterized by dystonia that typically shows diurnal fluctuations, that responds excellently to levodopa (L-dopa) and that is comprised of autosomal dominant dopa-responsive dystonia (DYT5a), autosomal recessive dopa-responsive dystonia (DYT5b) and dopa responsive dystonia due to sepiapterin reductase (SR) deficiency.","definition_xrefs":["Orphanet:255"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metabolic disease","termid":"MONDO:0005066"},{"relation_name":"is_a","term_name":"nervous system disorder","termid":"MONDO:0005071"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03098":null,"SJAG_03275":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"dopa-responsive dystonia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:C538007","NANDO:1200516","NANDO:2200885","icd11.foundation:1534901505","NCIT:C116719","SCTID:230332007","GARD:12144"],"synonyms":[{"name":"DYT-GCH1 (subtype)","type":"related"},{"name":"DYT-SPR (subtype)","type":"related"},{"name":"DYT-TH (subtype)","type":"related"},{"name":"DYT5","type":"related"},{"name":"DYT5 dystonia","type":"exact"},{"name":"HPD with diurnal fluctuation","type":"exact"},{"name":"Segawa's disease","type":"exact"},{"name":"dopa-responsive dystonia","type":"exact"},{"name":"hereditary progressive dystonia with diurnal fluctuation","type":"exact"}],"termid":"MONDO:0016812","terms_by_termid":{"MONDO:0007495":null,"MONDO:0012994":null},"xrefs":{"Monarch":{"xref_id":"0016812"}}}


id: GO:0070580
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving base J (beta-D-glucosyl-hydroxymethyluracil), a hypermodified thymidine residue found in the genome of kinetoplastid parasites. This modified base is localized primarily to repetitive DNA, namely the telomeres, and is implicated in the regulation of antigenic variation. The base is synthesized in a two-step pathway. Initially, a thymidine residue in DNA is hydroxylated by a thymidine hydroxylase (TH) to form the intermediate hydroxymethyluracil, which is then glucosylated to form base J.","definition_xrefs":["PMID:19114062"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA modification","termid":"GO:0006304"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006259","GO:0008150"],"is_obsolete":false,"name":"base J metabolic process","synonyms":[{"name":"base J metabolism","type":"exact"},{"name":"beta-D-glucosyl-HOMedU metabolic process","type":"exact"},{"name":"beta-D-glucosyl-hydroxymethyluracil metabolism","type":"exact"}],"termid":"GO:0070580"}


id: GO:1902805
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of synaptic vesicle transport.","definition_xrefs":["GO_REF:0000058","PMID:23527112","GOC:TermGenie","GOC:kmv"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cellular process","termid":"GO:0048522"},{"relation_name":"is_a","term_name":"positive regulation of transport","termid":"GO:0051050"},{"relation_name":"is_a","term_name":"regulation of synaptic vesicle transport","termid":"GO:1902803"},{"relation_name":"positively_regulates","term_name":"synaptic vesicle transport","termid":"GO:0048489"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"positive regulation of synaptic vesicle transport","synonyms":[{"name":"activation of synaptic vesicle fission","type":"related"},{"name":"activation of synaptic vesicle fusion","type":"related"},{"name":"activation of synaptic vesicle transport","type":"narrow"},{"name":"positive regulation of synaptic vesicle fission","type":"related"},{"name":"positive regulation of synaptic vesicle fusion","type":"related"},{"name":"up regulation of synaptic vesicle fission","type":"related"},{"name":"up regulation of synaptic vesicle fusion","type":"related"},{"name":"up regulation of synaptic vesicle transport","type":"exact"},{"name":"up-regulation of synaptic vesicle fission","type":"related"},{"name":"up-regulation of synaptic vesicle fusion","type":"related"},{"name":"up-regulation of synaptic vesicle transport","type":"exact"},{"name":"upregulation of synaptic vesicle fission","type":"related"},{"name":"upregulation of synaptic vesicle fusion","type":"related"},{"name":"upregulation of synaptic vesicle transport","type":"exact"}],"termid":"GO:1902805"}


id: PBO:0060787
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase subunit C1","termid":"PBO:0060787"}


id: MONDO:0010480
data:
  {"annotated_genes":["SJAG_02297"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87028],"is_not":false,"summary":null,"term":"MONDO:0010480"}]},"cv_name":"mondo","definition":"Any nonspherocytic hemolytic anemia in which the cause of the disease is a variation in the G6PD gene resulting in severely decreased activity levels of the enzyme glucose-6-phosphate dehydrogenase. Individuals with hemizygous or homozygous G6PD variants associated with chronic nonspherocytic hemolytic anemia (CNSHA) will clinically manifest CNSHA. Individuals with G6PD variants that cause CNSHA are at risk for severe neonatal jaundice and acute exacerbation of their chronic hemolytic anemia in response to certain medication exposures, chemical exposures, infections, or consumption of fava beans.","direct_ancestors":[{"relation_name":"is_a","term_name":"anemia, nonspherocytic hemolytic","termid":"MONDO:0000105"},{"relation_name":"is_a","term_name":"G6PD deficiency","termid":"MONDO:0005775"},{"relation_name":"is_a","term_name":"inborn disorder of pentose phosphate metabolism","termid":"MONDO:0019231"},{"relation_name":"is_a","term_name":"anemia due to erythrocyte enzyme disorder","termid":"MONDO:0020585"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02297":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002280"}],"interesting_parent_ids":["MONDO:0002280","MONDO:0037792","MONDO:0005570","MONDO:0005066"],"is_obsolete":false,"name":"anemia, nonspherocytic hemolytic, due to G6PD deficiency","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:403555","MESH:C567533","GARD:6520","OMIM:300908","Orphanet:466026","UMLS:C2720289"],"synonyms":[{"name":"Class I G6PD deficiency","type":"exact"},{"name":"anemia, congenital, nonspherocytic hemolytic, 1, G6PD deficient","type":"exact"},{"name":"anemia, nonspherocytic hemolytic, due to G6PD deficiency","type":"exact"},{"name":"class I glucose-6-phosphate dehydrogenase deficiency","type":"exact"},{"name":"hemolytic anaemia due to G6PD deficiency","type":"exact"},{"name":"hemolytic anemia due to G6PD deficiency","type":"exact"},{"name":"hemolytic anemia, G6PD deficient (favism), X-linked dominant","type":"exact"},{"name":"severe hemolytic anaemia due to G6PD deficiency","type":"exact"},{"name":"severe hemolytic anemia due to G6PD deficiency","type":"exact"}],"termid":"MONDO:0010480","terms_by_termid":{"MONDO:0010480":null},"xrefs":{"Monarch":{"xref_id":"0010480"}}}


id: PBO:0046151
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endosome-lysosome associated apoptosis and autophagy regulator 1","termid":"PBO:0046151"}


id: PBO:0081790
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 718","termid":"PBO:0081790"}


id: PBO:0117253
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TORC1 inhibitor, Ecl3","termid":"PBO:0117253"}


id: GO:0022603
data:
  {"annotated_genes":["SJAG_00216","SJAG_00661","SJAG_04666","SJAG_00610","SJAG_00333","SJAG_02169","SJAG_00304","SJAG_02392","SJAG_04509","SJAG_00244","SJAG_03486","SJAG_04322","SJAG_02536","SJAG_04724","SJAG_02222","SJAG_00596","SJAG_01212","SJAG_00514","SJAG_01799","SJAG_03581","SJAG_00236","SJAG_01456","SJAG_04461","SJAG_04203","SJAG_00028","SJAG_02022","SJAG_02838","SJAG_03637","SJAG_00855","SJAG_03705","SJAG_00845","SJAG_04522"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[91680,97662,96391],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051519"},{"annotations":[112610,119764,89869,101556,108686,105306,118340],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051523"},{"annotations":[92537],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051517"},{"annotations":[118162],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090258"},{"annotations":[103864,108286],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010637"},{"annotations":[109447,118446],"is_not":false,"rel_names":["regulates","is_a","positively_regulates"],"summary":null,"term":"GO:2000784"},{"annotations":[95553,107184,101997],"is_not":false,"rel_names":["is_a","regulates","positively_regulates"],"summary":null,"term":"GO:2000247"},{"annotations":[105519],"is_not":false,"rel_names":["is_a","regulates","positively_regulates"],"summary":null,"term":"GO:0061361"},{"annotations":[110722],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090141"},{"annotations":[116908],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051516"},{"annotations":[121491,121492],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008360"},{"annotations":[92953,106358,114903,96397,120667,97475],"is_not":false,"rel_names":["is_a","regulates"],"summary":null,"term":"GO:2000100"},{"annotations":[107938,94238,104668,89714],"is_not":false,"rel_names":["regulates","is_a"],"summary":null,"term":"GO:2000769"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of anatomical structure morphogenesis.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of developmental process","termid":"GO:0050793"},{"relation_name":"regulates","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"}],"gene_count":32,"genes_by_uniquename":{"SJAG_00028":null,"SJAG_00216":null,"SJAG_00236":null,"SJAG_00244":null,"SJAG_00304":null,"SJAG_00333":null,"SJAG_00514":null,"SJAG_00596":null,"SJAG_00610":null,"SJAG_00661":null,"SJAG_00845":null,"SJAG_00855":null,"SJAG_01212":null,"SJAG_01456":null,"SJAG_01799":null,"SJAG_02022":null,"SJAG_02169":null,"SJAG_02222":null,"SJAG_02392":null,"SJAG_02536":null,"SJAG_02838":null,"SJAG_03486":null,"SJAG_03581":null,"SJAG_03637":null,"SJAG_03705":null,"SJAG_04203":null,"SJAG_04322":null,"SJAG_04461":null,"SJAG_04509":null,"SJAG_04522":null,"SJAG_04666":null,"SJAG_04724":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of anatomical structure morphogenesis","references_by_uniquename":{"GO_REF:0000107":null,"PMID:30664646":null},"synonyms":[{"name":"regulation of morphogenesis","type":"exact"}],"termid":"GO:0022603","terms_by_termid":{"GO:0008360":null,"GO:0010637":null,"GO:0051516":null,"GO:0051517":null,"GO:0051519":null,"GO:0051523":null,"GO:0061361":null,"GO:0090141":null,"GO:0090258":null,"GO:2000100":null,"GO:2000247":null,"GO:2000769":null,"GO:2000784":null}}


id: GO:0032096
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of a response to a food stimulus.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of response to food","termid":"GO:0032095"},{"relation_name":"is_a","term_name":"negative regulation of response to nutrient levels","termid":"GO:0032108"},{"relation_name":"negatively_regulates","term_name":"response to food","termid":"GO:0032094"}],"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 response to food","synonyms":[{"name":"down regulation of response to food","type":"exact"},{"name":"down-regulation of response to food","type":"exact"},{"name":"downregulation of response to food","type":"exact"},{"name":"inhibition of response to food","type":"narrow"}],"termid":"GO:0032096"}


id: PBO:0058782
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 7151","termid":"PBO:0058782"}


id: MONDO:0014521
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any progressive myoclonic epilepsy in which the cause of the disease is a mutation in the KCNC1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"movement disorder","termid":"MONDO:0005395"},{"relation_name":"is_a","term_name":"progressive myoclonus epilepsy","termid":"MONDO:0020074"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"progressive myoclonic epilepsy type 7","secondary_identifiers":["OMIM:616187","DOID:0111447","GARD:17715","MEDGEN:863857","NCIT:C142804","UMLS:C4015420","Orphanet:435438"],"synonyms":[{"name":"EPM7","type":"exact"},{"name":"KCNC1 progressive myoclonic epilepsy","type":"exact"},{"name":"MEAK","type":"exact"},{"name":"PME type 7","type":"exact"},{"name":"epilepsy, progressive myoclonic 7","type":"related"},{"name":"epilepsy, progressive myoclonic type 7","type":"exact"},{"name":"meak","type":"exact"},{"name":"myoclonus epilepsy and ataxia due to potassium channel mutation","type":"exact"},{"name":"progressive myoclonic epilepsy caused by mutation in KCNC1","type":"exact"},{"name":"progressive myoclonic epilepsy due to KV3.1 deficiency","type":"exact"},{"name":"progressive myoclonus epilepsy type 7","type":"exact"}],"termid":"MONDO:0014521","xrefs":{"Monarch":{"xref_id":"0014521"}}}


id: GO:0003697
data:
  {"annotated_genes":["SJAG_05239","SJAG_04418","SJAG_03832","SJAG_04863","SJAG_01887","SJAG_03722","SJAG_03682","SJAG_02503","SJAG_01076","SJAG_02079","SJAG_01354","SJAG_00327","SJAG_01708","SJAG_02362","SJAG_02031","SJAG_02545","SJAG_03161","SJAG_03855","SJAG_00857","SJAG_04156","SJAG_01762","SJAG_02627","SJAG_05214","SJAG_00871","SJAG_04530","SJAG_04995","SJAG_00757","SJAG_00619","SJAG_02822","SJAG_04933","SJAG_03957","SJAG_04210","SJAG_00796","SJAG_01436","SJAG_00884","SJAG_02667","SJAG_03436","SJAG_04574","SJAG_01771","SJAG_03780","SJAG_02267","SJAG_01410","SJAG_02194","SJAG_01698","SJAG_01049","SJAG_04410","SJAG_00939","SJAG_01677","SJAG_03068","SJAG_00819","SJAG_02828","SJAG_00399","SJAG_02348","SJAG_02556","SJAG_03886","SJAG_00768","SJAG_03495","SJAG_04245"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[64625,66067,66146,66591,66950,66982,71667,71966,72707,73731,73893,74055,74402,74471,75149,75188,75607,76477,76514,76604,76676,76855,77015,77412,77529,78780,78949,79133,80018,81023,91527,91623,98067,107161,109504,110930,112348,113336,113909,114275,115428,116509,118117,118392,118674,120060],"is_not":false,"summary":null,"term":"GO:0003697"},{"annotations":[114385,105004,117776,115248],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990814"},{"annotations":[78796],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098505"},{"annotations":[81966,109959,112221,82028,97885,113387,64278],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043047"}]},"cv_name":"molecular_function","definition":"Binding to single-stranded DNA.","definition_xrefs":["GOC:elh","GOC:vw","PMID:22976174"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA binding","termid":"GO:0003677"}],"gene_count":58,"genes_by_uniquename":{"SJAG_00327":null,"SJAG_00399":null,"SJAG_00619":null,"SJAG_00757":null,"SJAG_00768":null,"SJAG_00796":null,"SJAG_00819":null,"SJAG_00857":null,"SJAG_00871":null,"SJAG_00884":null,"SJAG_00939":null,"SJAG_01049":null,"SJAG_01076":null,"SJAG_01354":null,"SJAG_01410":null,"SJAG_01436":null,"SJAG_01677":null,"SJAG_01698":null,"SJAG_01708":null,"SJAG_01762":null,"SJAG_01771":null,"SJAG_01887":null,"SJAG_02031":null,"SJAG_02079":null,"SJAG_02194":null,"SJAG_02267":null,"SJAG_02348":null,"SJAG_02362":null,"SJAG_02503":null,"SJAG_02545":null,"SJAG_02556":null,"SJAG_02627":null,"SJAG_02667":null,"SJAG_02822":null,"SJAG_02828":null,"SJAG_03068":null,"SJAG_03161":null,"SJAG_03436":null,"SJAG_03495":null,"SJAG_03682":null,"SJAG_03722":null,"SJAG_03780":null,"SJAG_03832":null,"SJAG_03855":null,"SJAG_03886":null,"SJAG_03957":null,"SJAG_04156":null,"SJAG_04210":null,"SJAG_04245":null,"SJAG_04410":null,"SJAG_04418":null,"SJAG_04530":null,"SJAG_04574":null,"SJAG_04863":null,"SJAG_04933":null,"SJAG_04995":null,"SJAG_05214":null,"SJAG_05239":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003677"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0003677","GO:0005488"],"is_obsolete":false,"name":"single-stranded DNA binding","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["GO:0003698","GO:0003699"],"synonyms":[{"name":"ssDNA binding","type":"exact"}],"termid":"GO:0003697","terms_by_termid":{"GO:0003697":null,"GO:0043047":null,"GO:0098505":null,"GO:1990814":null}}


id: PBO:0031019
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_RNA_level","termid":"PBO:0031019"}


id: PBO:0051954
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inositol 1,4,5-trisphosphate receptor type 2","termid":"PBO:0051954"}


id: GO:2000785
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of autophagosome assembly.","definition_xrefs":["GOC:autophagy","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of vacuole organization","termid":"GO:0044088"},{"relation_name":"is_a","term_name":"regulation of organelle assembly","termid":"GO:1902115"},{"relation_name":"regulates","term_name":"autophagosome assembly","termid":"GO:0000045"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044085","GO:0008150"],"is_obsolete":false,"name":"regulation of autophagosome assembly","synonyms":[{"name":"regulation of PAS formation","type":"related"},{"name":"regulation of autophagic vacuole assembly","type":"exact"},{"name":"regulation of autophagic vacuole formation","type":"related"},{"name":"regulation of autophagosome biosynthesis","type":"exact"},{"name":"regulation of autophagosome formation","type":"exact"}],"termid":"GO:2000785"}


id: GO:0035560
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: pheophorbide a + H2O = pyropheophorbide a + methanol + CO2. The reaction occurs in two steps; pheophoridase catalyzes the conversion of pheophorbide a to a precursor of pyropheophorbide a, C-13(2)-carboxylpyropheophorbide a, by demethylation, and then the precursor is decarboxylated non-enzymatically to yield pyropheophorbide a.","definition_xrefs":["PMID:16228561","RHEA:32483"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxylic ester hydrolase activity","termid":"GO:0052689"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016788"}],"interesting_parent_ids":["GO:0016788","GO:0003824","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"pheophorbidase activity","secondary_identifiers":["EC:3.1.1.82"],"synonyms":[{"name":"PPD activity","type":"related"},{"name":"phedase activity","type":"related"},{"name":"pheophoridase activity","type":"related"}],"termid":"GO:0035560"}


id: MONDO:0000534
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A mucoepidermoid carcinoma that involves the trachea.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mucoepidermoid carcinoma","termid":"MONDO:0003036"},{"relation_name":"is_a","term_name":"trachea carcinoma","termid":"MONDO:0003184"}],"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":"trachea mucoepidermoid carcinoma","secondary_identifiers":["MEDGEN:835970","DOID:0050919","SCTID:707379000","UMLS:C3873401"],"synonyms":[{"name":"trachea mucoepidermoid carcinoma","type":"exact"}],"termid":"MONDO:0000534","xrefs":{"Monarch":{"xref_id":"0000534"}}}


id: MONDO:0014303
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An extremely rare and complex form of hereditary spastic paraplegia (see this term), reported in only 4 patients from 2 families to date, characterized by spastic paraplegia (presenting between the ages of 1 to 4 years with abnormal gait) associated with microcephaly, amyotrophy, cerebellar signs (e.g. dysarthria) aggressiveness, delayed puberty and mild to moderate intellectual disability. SPG64 is due to mutations in the ENTPD1 gene (10q24.1), encoding ectonucleoside triphosphate diphosphohydrolase 1.","definition_xrefs":["Orphanet:401810"],"direct_ancestors":[{"relation_name":"is_a","term_name":"complex hereditary spastic paraplegia","termid":"MONDO:0015150"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"hereditary spastic paraplegia 64","secondary_identifiers":["SCTID:726609005","MEDGEN:816619","UMLS:C3810289","DOID:0110815","GARD:17659","OMIM:615683"],"synonyms":[{"name":"ENTPD1 autosomal recessive complex spastic paraplegia","type":"exact"},{"name":"SPG64","type":"exact"},{"name":"autosomal recessive complex spastic paraplegia caused by mutation in ENTPD1","type":"exact"},{"name":"autosomal recessive spastic paraplegia 64","type":"exact"},{"name":"autosomal recessive spastic paraplegia type 64","type":"exact"},{"name":"hereditary spastic paraplegia type 64","type":"exact"},{"name":"spastic paraplegia 64, autosomal recessive","type":"related"}],"termid":"MONDO:0014303","xrefs":{"Monarch":{"xref_id":"0014303"}}}


id: PBO:0005895
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA Glutamine, mitochondrial","termid":"PBO:0005895"}


id: MONDO:0001212
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A otitis media which involves transudation of fluid in the middle ear without pus formation.","definition_xrefs":["DOID:11180"],"direct_ancestors":[{"relation_name":"is_a","term_name":"otitis media","termid":"MONDO:0005441"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-suppurative otitis media","secondary_identifiers":["ICD10CM:H65","MEDGEN:543351","SCTID:275481002","ICD9:381.4","UMLS:C0271446"],"synonyms":[{"name":"nonsuppurative otitis media","type":"exact"}],"termid":"MONDO:0001212","xrefs":{"Monarch":{"xref_id":"0001212"}}}


id: PBO:0060485
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nanog homeobox pseudogene 7","termid":"PBO:0060485"}


id: PBO:0027199
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_mitotic_spindle_orientation_correction","termid":"PBO:0027199"}


id: GO:0051019
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a mitogen-activated protein kinase.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein kinase binding","termid":"GO:0019901"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"mitogen-activated protein kinase binding","synonyms":[{"name":"MAP kinase binding","type":"exact"},{"name":"MAP-kinase anchoring activity","type":"related"},{"name":"MAPK binding","type":"exact"}],"termid":"GO:0051019"}


id: PBO:0056402
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAPT intronic transcript 1","termid":"PBO:0056402"}


id: MONDO:0020315
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Unclassified myelodysplastic syndrome (MDS-U) is a subtype of myelodysplastic syndrome (MDS) with atypical features of uncertain clinical significance.","definition_xrefs":["Orphanet:98827"],"gene_count":0,"genotype_count":0,"name":"obsolete unclassified myelodysplastic syndrome (obsolete MONDO:0020315)","secondary_identifiers":["icd11.foundation:1684468291"],"termid":"MONDO:0020315","xrefs":{"Monarch":{"xref_id":"0020315"}}}


id: GO:0019966
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to interleukin-1.","definition_xrefs":["GOC:jl","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"growth factor binding","termid":"GO:0019838"},{"relation_name":"is_a","term_name":"cytokine binding","termid":"GO:0019955"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"interleukin-1 binding","synonyms":[{"name":"IL-1 binding","type":"exact"}],"termid":"GO:0019966"}


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


id: MONDO:0007923
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, benign familial","secondary_identifiers":["UMLS:C0220690","OMIM:153470","MEDGEN:113101","MESH:C537717"],"synonyms":[{"name":"Cole-Hughes syndrome","type":"related"},{"name":"benign familial macrocephaly","type":"related"},{"name":"benign familial megalencephaly","type":"related"},{"name":"macrocephaly, benign familial","type":"exact"}],"termid":"MONDO:0007923","xrefs":{"Monarch":{"xref_id":"0007923"}}}


id: MONDO:0018988
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Iridocorneal endothelial (ICE) syndrome describes a group of progressive corneal proliferative endotheliopathies comprised of Chandler syndrome, Cogan-Reese syndrome and essential iris atrophy, affecting mainly young adult females and characterized by iris holes and atrophy, papillary distortion, anterior synechiae, corneal edema and often with secondary glaucoma and corneal decompensation as complications","definition_xrefs":["Orphanet:64734"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"excluded_subClassOf","term_name":"obsolete rare acquired eye disease (obsolete MONDO:0015120)","termid":"MONDO:0015120"},{"relation_name":"excluded_subClassOf","term_name":"obsolete secondary glaucoma due to a proliferation and differentiation anomaly (obsolete MONDO:0020221)","termid":"MONDO:0020221"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iridocorneal endothelial syndrome","secondary_identifiers":["MEDGEN:242751","MedDRA:10053678","MESH:D057129","GARD:60","icd11.foundation:265074385","NCIT:C84792","SCTID:129623003","UMLS:C1096100"],"synonyms":[{"name":"ICE syndrome","type":"exact"}],"termid":"MONDO:0018988","xrefs":{"Monarch":{"xref_id":"0018988"}}}


id: MONDO:0006416
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A Burkitt lymphoma that arises from the small intestine.","definition_xrefs":["NCIT:C27409"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune system cancer","termid":"MONDO:0000621"},{"relation_name":"is_a","term_name":"small intestine lymphoma","termid":"MONDO:0001852"},{"relation_name":"is_a","term_name":"Burkitt lymphoma","termid":"MONDO:0007243"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992","MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"small intestinal Burkitt lymphoma","secondary_identifiers":["MEDGEN:277650","UMLS:C1335991"],"synonyms":[{"name":"Burkitt lymphoma of small intestine","type":"exact"},{"name":"Burkitts lymphoma of small intestine","type":"exact"},{"name":"primary small intestinal Burkitt's lymphoma","type":"exact"},{"name":"small intestinal Burkitt lymphoma","type":"exact"},{"name":"small intestinal Burkitt's lymphoma","type":"exact"},{"name":"small intestine Burkitt lymphoma","type":"exact"},{"name":"small intestine Burkitt's lymphoma","type":"exact"},{"name":"small intestine Burkitts lymphoma","type":"exact"}],"termid":"MONDO:0006416","xrefs":{"Monarch":{"xref_id":"0006416"}}}


id: PBO:0001131
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA Lysine","termid":"PBO:0001131"}


id: PR:O13750
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A succinyl-CoA ligase [ADP/GDP-forming] subunit alpha, mitochondrial that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO01475","PANTHER:PTHR11117:SF3","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":"succinyl-CoA ligase [ADP-forming] subunit alpha, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC16E8.17c","secondary_identifiers":["UniProtKB:O13750"],"synonyms":[{"name":"SCS-alpha (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-SUCLG1","type":"exact"},{"name":"succinyl-CoA synthetase subunit alpha (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O13750"}


id: PBO:0041704
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calmodulin 1 pseudogene 2","termid":"PBO:0041704"}


id: GO:0048843
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of axon extension involved in axon guidance.","definition_xrefs":["GOC:devbiol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of axon extension","termid":"GO:0030517"},{"relation_name":"is_a","term_name":"regulation of axon extension involved in axon guidance","termid":"GO:0048841"},{"relation_name":"is_a","term_name":"negative regulation of chemotaxis","termid":"GO:0050922"},{"relation_name":"negatively_regulates","term_name":"axon extension involved in axon guidance","termid":"GO:0048846"}],"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 axon extension involved in axon guidance","synonyms":[{"name":"down regulation of axon extension involved in axon guidance","type":"exact"},{"name":"down-regulation of axon extension involved in axon guidance","type":"exact"},{"name":"downregulation of axon extension involved in axon guidance","type":"exact"},{"name":"inhibition of axon extension involved in axon guidance","type":"narrow"}],"termid":"GO:0048843"}


id: MONDO:0008397
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Aplasia of the lacrimal and salivary glands (ALSG) is a rare autosomal dominant disorder characterized by aplasia, atresia or hypoplasia of the lacrimal and salivary glands leading to varying features since infancy such as recurrent eye infections, irritable eyes, epiphora, xerostomia, dental caries, dental erosion and oral inflammation.","definition_xrefs":["Orphanet:86815"],"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":"aplasia of lacrimal and salivary glands","secondary_identifiers":["GARD:16759","MEDGEN:57641","SCTID:715656004","icd11.foundation:539255304","OMIM:180920","UMLS:C0158667","DOID:0111549"],"synonyms":[{"name":"ALSG","type":"exact"},{"name":"aplasia of lacrimal and salivary glands","type":"exact"},{"name":"congenital absence of lacrimal puncta and salivary glands","type":"exact"},{"name":"parotid aplasia or hypoplasia","type":"related"},{"name":"salivary glands, absence of","type":"related"},{"name":"salivary glands, absence of, include","type":"related"}],"termid":"MONDO:0008397","xrefs":{"Monarch":{"xref_id":"0008397"}}}


id: PBO:0114734
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial GTP dependent ribosome recycling factor Gfm2","termid":"PBO:0114734"}


id: PBO:0085454
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Posttranscriptional regulator of phosphate and glucose metabolism; facilitates PHO4 mRNA degradation by interacting with Pop2p; regulates PHO4 mRNA stability by binding to PHO4's 3'UTR in a phosphate-dependent manner; contains highly conserved YTH (YT521-B Homology) domain that exhibits RNA-binding activity; human homolog YTHDF2 can complement yeast null mutant","termid":"PBO:0085454"}


id: FYPO:0007724
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 ERMES foci in a cell are normal (i.e. indistinguishable from wild type) in number, size, and distribution. An ERMES focus is a site that contains one or more ERMES complex(es).","definition_xrefs":["PomBase:mah","PMID:33483504"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular physical quality phenotype","termid":"FYPO:0007723"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal ERMES foci","synonyms":[{"name":"normal ERMES foci during mitotic cell cycle","type":"related"},{"name":"normal ERMES foci during vegetative growth","type":"exact"}],"termid":"FYPO:0007724"}


id: PBO:0043617
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"COMM domain containing 6","termid":"PBO:0043617"}


id: PBO:0053604
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 636","termid":"PBO:0053604"}


id: GO:0006070
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving octanol, the 8-carbon alcohol with the formula C8H17OH.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary alcohol metabolic process","termid":"GO:0034308"},{"relation_name":"is_a","term_name":"fatty alcohol metabolic process","termid":"GO:1903173"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0006629"],"is_obsolete":false,"name":"octanol metabolic process","synonyms":[{"name":"octanol metabolism","type":"exact"}],"termid":"GO:0006070"}


id: PBO:0069463
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 728, pseudogene","termid":"PBO:0069463"}


id: PBO:0045772
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"extracellular matrix protein 2","termid":"PBO:0045772"}


id: GO:0010906
data:
  {"annotated_genes":["SJAG_05006"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[98388],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001172"}]},"cv_name":"biological_process","definition":"Any process that modulates the rate, frequency or extent of glucose metabolism. Glucose metabolic processes are the chemical reactions and pathways involving glucose, the aldohexose gluco-hexose.","definition_xrefs":["GOC:tb","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of carbohydrate metabolic process","termid":"GO:0006109"},{"relation_name":"is_a","term_name":"regulation of small molecule metabolic process","termid":"GO:0062012"},{"relation_name":"regulates","term_name":"glucose metabolic process","termid":"GO:0006006"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05006":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0005975"},{"rel_name":"regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0005975","GO:0044281"],"is_obsolete":false,"name":"regulation of glucose metabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"regulation of glucose metabolism","type":"exact"}],"termid":"GO:0010906","terms_by_termid":{"GO:2001172":null}}


id: MONDO:0005857
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infections with viruses of the genus morbillivirus, family paramyxoviridae. Infections mainly cause acute disease in their hosts, although in some cases infection is persistent and leads to degenerative conditions.","definition_xrefs":["MESH:D018185"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Paramyxoviridae infectious disease","termid":"MONDO:0005896"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"morbillivirus infectious disease","secondary_identifiers":["EFO:0007377","MEDGEN:61642","UMLS:C0206614"],"synonyms":[{"name":"Morbillivirus caused disease or disorder","type":"exact"},{"name":"Morbillivirus disease or disorder","type":"exact"},{"name":"Morbillivirus infectious disease","type":"exact"}],"termid":"MONDO:0005857","xrefs":{"Monarch":{"xref_id":"0005857"}}}


id: GO:0048575
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A change from vegetative to reproductive phase as a result of detection of, or exposure to, a period of light that falls short of the critical day length. The critical day length varies between species. Although the term is short-day is used, most species actually respond to the duration of the night, so that the response will occur when a period of darkness exceeds the number of hours defined by 24 minus the critical day length.","definition_xrefs":["GOC:pj","ISBN:0582015952","ISBN:0709408862","GOC:jid","ISBN:0697037754"],"direct_ancestors":[{"relation_name":"is_a","term_name":"short-day photoperiodism","termid":"GO:0048572"},{"relation_name":"is_a","term_name":"photoperiodism, flowering","termid":"GO:0048573"}],"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":"short-day photoperiodism, flowering","synonyms":[{"name":"long-night photoperiodism, flowering","type":"exact"},{"name":"response to long-night, flowering","type":"exact"},{"name":"response to short-day, flowering","type":"exact"},{"name":"short-day photoperiodic control of flowering","type":"exact"},{"name":"short-day photoperiodic control of flowering time","type":"exact"},{"name":"short-day photoperiodic control of inflorescence development","type":"exact"}],"termid":"GO:0048575"}


id: GO:0019022
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A viral genome composed of ribonucleic acid. This results in genome replication and expression of genetic information being inextricably linked.","definition_xrefs":["ISBN:0121585336"],"gene_count":0,"genotype_count":0,"name":"obsolete RNA viral genome (obsolete GO:0019022)","termid":"GO:0019022"}


id: MONDO:0016861
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Alagille syndrome","termid":"MONDO:0007318"},{"relation_name":"is_a","term_name":"partial monosomy of the short arm of chromosome 20","termid":"MONDO:0016898"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0004335","MONDO:0005267","MONDO:0002515"],"is_obsolete":false,"name":"Alagille syndrome due to 20p12 microdeletion","secondary_identifiers":["GARD:17250","Orphanet:261600","MEDGEN:1826025","UMLS:C5679679"],"synonyms":[{"name":"Alagille syndrome due to del(20)(p12)","type":"exact"},{"name":"Alagille syndrome due to monosomy 20p12","type":"exact"},{"name":"Alagille-Watson syndrome due to monosomy 20p12","type":"exact"},{"name":"Arteriohepatic dysplasia due to monosomy 20p12","type":"exact"},{"name":"syndromic bile duct paucity due to monosomy 20p12","type":"exact"}],"termid":"MONDO:0016861","xrefs":{"Monarch":{"xref_id":"0016861"}}}


id: GO:0045942
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of phosphorus utilization.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of phosphorus utilization","termid":"GO:0006795"},{"relation_name":"is_a","term_name":"negative regulation of phosphorus metabolic process","termid":"GO:0010563"},{"relation_name":"negatively_regulates","term_name":"phosphorus utilization","termid":"GO:0006794"}],"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 phosphorus utilization","synonyms":[{"name":"down regulation of phosphorus utilization","type":"exact"},{"name":"down-regulation of phosphorus utilization","type":"exact"},{"name":"downregulation of phosphorus utilization","type":"exact"},{"name":"inhibition of phosphorus utilization","type":"narrow"}],"termid":"GO:0045942"}


id: MOD:00919
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that modifies an L-tyrosine residue.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein modification categorized by amino acid modified","termid":"MOD:01157"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"modified L-tyrosine residue","synonyms":[{"name":"ModTyr","type":"exact"}],"termid":"MOD:00919"}


id: PBO:0001618
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase regulatory subunit Sds22","termid":"PBO:0001618"}


id: GO:2000565
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of CD8-positive, alpha-beta T cell proliferation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of alpha-beta T cell proliferation","termid":"GO:0046642"},{"relation_name":"is_a","term_name":"regulation of CD8-positive, alpha-beta T cell proliferation","termid":"GO:2000564"},{"relation_name":"is_a","term_name":"negative regulation of CD8-positive, alpha-beta T cell activation","termid":"GO:2001186"},{"relation_name":"negatively_regulates","term_name":"CD8-positive, alpha-beta T cell proliferation","termid":"GO:0035740"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0007155"},{"rel_name":"regulates","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"negative regulation of CD8-positive, alpha-beta T cell proliferation","termid":"GO:2000565"}


id: PBO:0079524
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tyrosinase related protein 1","termid":"PBO:0079524"}


id: GO:1902018
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of cilium assembly.","definition_xrefs":["GOC:cilia","GOC:dph","GOC:TermGenie","PMID:17719545"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of plasma membrane bounded cell projection assembly","termid":"GO:0120033"},{"relation_name":"is_a","term_name":"regulation of cilium assembly","termid":"GO:1902017"},{"relation_name":"is_a","term_name":"negative regulation of organelle assembly","termid":"GO:1902116"},{"relation_name":"negatively_regulates","term_name":"cilium assembly","termid":"GO:0060271"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"negative regulation of cilium assembly","synonyms":[{"name":"down regulation of ciliogenesis","type":"exact"},{"name":"down regulation of cilium assembly","type":"exact"},{"name":"down regulation of cilium biogenesis","type":"related"},{"name":"down-regulation of ciliogenesis","type":"exact"},{"name":"down-regulation of cilium assembly","type":"exact"},{"name":"down-regulation of cilium biogenesis","type":"related"},{"name":"downregulation of ciliogenesis","type":"exact"},{"name":"downregulation of cilium assembly","type":"exact"},{"name":"downregulation of cilium biogenesis","type":"related"},{"name":"inhibition of ciliogenesis","type":"exact"},{"name":"inhibition of cilium assembly","type":"narrow"},{"name":"inhibition of cilium biogenesis","type":"related"},{"name":"negative regulation of ciliogenesis","type":"exact"},{"name":"negative regulation of cilium biogenesis","type":"related"}],"termid":"GO:1902018"}


id: PBO:0048094
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ferritin light chain pseudogene 15","termid":"PBO:0048094"}


id: FYPO:0000281
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which a cell contains more, but smaller, vacuoles than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"vacuoles present in increased numbers during vegetative growth","termid":"FYPO:0000952"},{"relation_name":"is_a","term_name":"vacuoles present in increased numbers during vegetative growth","termid":"FYPO:0000952"},{"relation_name":"is_a","term_name":"small vacuoles present in increased numbers","termid":"FYPO:0002258"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"small vacuoles present in increased numbers during vegetative growth","synonyms":[{"name":"fragmented vacuoles during vegetative growth","type":"related"},{"name":"small vacuoles present in greater numbers during vegetative growth","type":"exact"},{"name":"small vacuoles present in increased numbers during mitotic cell cycle","type":"related"},{"name":"vacuole fusion defects","type":"related"},{"name":"vacuole organization defects, fragmented vacuoles during vegetative growth","type":"related"},{"name":"vacuoles present in increased numbers, with decreased vacuole size, during vegetative growth","type":"exact"}],"termid":"FYPO:0000281"}


id: PBO:0040401
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPase H+ transporting V1 subunit G1 pseudogene 2","termid":"PBO:0040401"}


id: PBO:0031501
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_fatty_acid_synthase_activity","termid":"PBO:0031501"}


id: GO:0102893
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: UDP-alpha-D-glucose + betanidin = H+ + gomphrenin I + UDP.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete betanidin 6-O-glucosyltransferase activity (obsolete GO:0102893)","termid":"GO:0102893"}


id: MONDO:0044337
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm characterized by the presence of atypical mesenchymal-stromal cells. Representative examples include endometrial stromal sarcoma and prostate stromal sarcoma.","definition_xrefs":["NCIT:C6926"],"direct_ancestors":[{"relation_name":"is_a","term_name":"soft tissue sarcoma","termid":"MONDO:0018078"}],"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":"stromal sarcoma","secondary_identifiers":["ICDO:8935/3","MEDGEN:235091","UMLS:C1370723"],"synonyms":[{"name":"stromal sarcoma","type":"exact"},{"name":"stromal sarcoma, malignant","type":"exact"},{"name":"stromal tumor, malignant","type":"exact"}],"termid":"MONDO:0044337","xrefs":{"Monarch":{"xref_id":"0044337"}}}


id: MONDO:0008232
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"phagocytic cell dysfunction","termid":"MONDO:0024627"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"phagocytosis, plasma-related defect 1N","secondary_identifiers":["MESH:C566808","OMIM:171100","MEDGEN:356965","UMLS:C1868402"],"synonyms":[{"name":"phagocytosis, plasma-RELATED defect IN","type":"related"},{"name":"phagocytosis, plasma-related defect type 1N","type":"exact"}],"termid":"MONDO:0008232","xrefs":{"Monarch":{"xref_id":"0008232"}}}


id: PBO:0062513
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 8 subfamily J member 2 (gene/pseudogene)","termid":"PBO:0062513"}


id: PBO:0051290
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin kappa variable 1D-8","termid":"PBO:0051290"}


id: PBO:0028419
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-resistance_to_nitrogen_starvation","termid":"PBO:0028419"}


id: GO:0102165
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: acetyl-CoA + (Z)-hex-3-en-1-ol = (3Z)-hex-3-en-1-yl acetate + coenzyme A.","definition_xrefs":["GOC:pz","RHEA:28254"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyltransferase activity, transferring groups other than amino-acyl groups","termid":"GO:0016747"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016746","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"(Z)-3-hexen-1-ol acetyltransferase activity","secondary_identifiers":["EC:2.3.1.195","MetaCyc:RXN-11852"],"termid":"GO:0102165"}


id: PBO:0086336
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protoporphyrinogen oxidase; a mitochondrial enzyme that catalyzes the seventh step in the heme biosynthetic pathway, converting protoporphyrinogen IX to protoporphyrin IX; inhibited by diphenyl ether-type herbicides","termid":"PBO:0086336"}


id: MONDO:0003262
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A WHO grade III meningioma characterized by the predominant presence of rhabdoid cells forming sheets.","definition_xrefs":["NCIT:C6909"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meningioma","termid":"MONDO:0016642"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rhabdoid meningioma","secondary_identifiers":["ONCOTREE:RHM","MEDGEN:120445","DOID:5058","UMLS:C0259786"],"synonyms":[{"name":"meningioma, rhabdoid","type":"exact"},{"name":"meningioma, rhabdoid (morphologic abnormality)","type":"exact"},{"name":"papillary meningioma","type":"related"},{"name":"papillary meningioma (morphologic abnormality)","type":"exact"},{"name":"rhabdoid meningioma","type":"exact"}],"termid":"MONDO:0003262","xrefs":{"Monarch":{"xref_id":"0003262"}}}


id: PBO:0057040
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 132","termid":"PBO:0057040"}


id: GO:0004793
data:
  {"annotated_genes":["SJAG_02450"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[73860],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008732"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: L-threonine = glycine + acetaldehyde.","definition_xrefs":["EC:4.1.2.5"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aldehyde-lyase activity","termid":"GO:0016832"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02450":null},"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:0016829"}],"interesting_parent_ids":["GO:0016829","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"threonine aldolase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["RHEA:19625","MetaCyc:THREONINE-ALDOLASE-RXN"],"synonyms":[{"name":"L-threonine acetaldehyde-lyase (glycine-forming)","type":"related"},{"name":"L-threonine acetaldehyde-lyase activity","type":"related"},{"name":"L-threonine aldolase activity","type":"exact"}],"termid":"GO:0004793","terms_by_termid":{"GO:0008732":null}}


id: SO:0000126
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A repressor molecule is required for transcription to stop.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcriptionally_regulated","termid":"SO:0000123"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptionally_repressed","synonyms":[{"name":"transcriptionally repressed","type":"exact"}],"termid":"SO:0000126"}


id: MONDO:0010389
data:
  {"annotated_genes":["SJAG_04743"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88981],"is_not":false,"summary":null,"term":"MONDO:0010389"}]},"cv_name":"mondo","definition":"Any X-linked Mendelian susceptibility to mycobacterial diseases in which the cause of the disease is a mutation in the CYBB gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked Mendelian susceptibility to mycobacterial diseases","termid":"MONDO:0017905"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04743":null},"genotype_count":0,"is_obsolete":false,"name":"X-linked Mendelian susceptibility to mycobacterial diseases due to CYBB deficiency","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:370369","NANDO:2201279","MESH:C567068","OMIM:300645","Orphanet:319623","DOID:0112000","UMLS:C1970859"],"synonyms":[{"name":"CYBB X-linked mendelian susceptibility to mycobacterial diseases","type":"exact"},{"name":"IMD34","type":"related"},{"name":"X-linked MSMD due to CYBB deficiency","type":"exact"},{"name":"X-linked mendelian susceptibility to mycobacterial diseases caused by mutation in CYBB","type":"exact"},{"name":"atypical Mycobacteriosis, familial, X-linked 2","type":"related"},{"name":"immunodeficiency 34","type":"related"},{"name":"immunodeficiency 34, Mycobacteriosis, X-linked","type":"related"},{"name":"immunodeficiency 34, mycobacteriosis, X-linked, X-linked recessive","type":"exact"},{"name":"immunodeficiency type 34","type":"exact"}],"termid":"MONDO:0010389","terms_by_termid":{"MONDO:0010389":null},"xrefs":{"Monarch":{"xref_id":"0010389"}}}


id: PBO:0077710
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"troponin T3, fast skeletal type","termid":"PBO:0077710"}


id: GO:0070046
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A SNARE complex that contains synaptobrevin 2 (VAMP2), SNAP-25, and syntaxin 3 (or orthologs thereof).","definition_xrefs":["PMID:10336434"],"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:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0032991"],"is_obsolete":false,"name":"synaptobrevin 2-SNAP-25-syntaxin-3 complex","synonyms":[{"name":"SNARE complex (Stx3, Snap25, Vamp2)","type":"narrow"},{"name":"Stx3-Snap25-Vamp2 complex","type":"narrow"}],"termid":"GO:0070046"}


id: PR:Q9P6N1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- atg1802 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P6N1"],"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":"autophagy-related protein 21 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC823.16c","synonyms":[{"name":"Spom972h-atg1802","type":"exact"},{"name":"meiotically up-regulated gene 179 protein (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9P6N1"}


id: PBO:0083513
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the verified ORF HEF3/YNL014W","termid":"PBO:0083513"}


id: GO:1901829
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of zeaxanthin bis(beta-D-glucoside).","definition_xrefs":["PMID:20075616","GOC:TermGenie","GOC:yaf","MetaCyc:PWY-6288","UniPathway:UPA00798"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carotenoid catabolic process","termid":"GO:0016118"},{"relation_name":"is_a","term_name":"beta-glucoside catabolic process","termid":"GO:1901805"},{"relation_name":"is_a","term_name":"zeaxanthin bis(beta-D-glucoside) metabolic process","termid":"GO:1901828"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"zeaxanthin bis(beta-D-glucoside) catabolic process","synonyms":[{"name":"zeaxanthin bis(beta-D-glucoside) breakdown","type":"exact"},{"name":"zeaxanthin bis(beta-D-glucoside) catabolism","type":"exact"},{"name":"zeaxanthin bis(beta-D-glucoside) degradation","type":"exact"},{"name":"zeaxanthin diglucoside breakdown","type":"exact"},{"name":"zeaxanthin diglucoside catabolism","type":"exact"},{"name":"zeaxanthin diglucoside degradation","type":"exact"}],"termid":"GO:1901829"}


id: FYPO:0005277
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype in which a cell has two or more nuclei and more than one septum per cell.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multinucleate","termid":"FYPO:0003341"},{"relation_name":"is_a","term_name":"multiseptate cell","termid":"FYPO:0004295"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"multinucleate multiseptate cell","termid":"FYPO:0005277"}


id: FYPO:0002042
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of RNA measured in a cell during a cellular response to iron ion starvation is lower than normal. Total RNA or a specific RNA may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased RNA level during vegetative growth","termid":"FYPO:0001117"},{"relation_name":"is_a","term_name":"altered RNA level during cellular response to iron ion starvation","termid":"FYPO:0003196"}],"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":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0005447","FYPO:0006551","FYPO:0000002"],"is_obsolete":false,"name":"decreased RNA level during cellular response to iron ion starvation","synonyms":[{"name":"decreased RNA accumulation during cellular response to iron ion starvation","type":"related"},{"name":"decreased RNA level during cellular response to iron ion depletion","type":"exact"},{"name":"decreased RNA level during cellular response to iron ion deprivation","type":"exact"},{"name":"decreased RNA level during cellular response to iron ion starvation during mitotic cell cycle","type":"related"},{"name":"decreased RNA level during cellular response to iron ion starvation during vegetative growth","type":"exact"},{"name":"decreased RNA level during cellular response to iron starvation","type":"exact"},{"name":"decreased RNA level during iron ion starvation","type":"exact"},{"name":"decreased mRNA level during cellular response to iron ion starvation","type":"narrow"},{"name":"decreased transcript level during cellular response to iron ion starvation","type":"exact"},{"name":"reduced RNA level during cellular response to iron ion starvation","type":"exact"}],"termid":"FYPO:0002042"}


id: PBO:0038998
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actin filament associated protein 1","termid":"PBO:0038998"}


id: MONDO:0800353
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital disorder of glycosylation","termid":"MONDO:0015286"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0024322"],"is_obsolete":false,"name":"congenital disorder of glycosylation, type Ibb","secondary_identifiers":["MEDGEN:1637983","UMLS:C4693133"],"synonyms":[{"name":"CDG1BB","type":"exact"}],"termid":"MONDO:0800353","xrefs":{"Monarch":{"xref_id":"0800353"}}}


id: GO:0030891
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that possesses ubiquitin ligase activity; the complex is usually pentameric; for example, in mammals the subunits are pVHL, elongin B, elongin C, cullin-2 (Cul2), and Rbx1.","definition_xrefs":["GOC:mah","PMID:11865071"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoplasmic ubiquitin ligase complex","termid":"GO:0000153"}],"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:0032991","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"VCB complex","synonyms":[{"name":"VHL complex","type":"exact"},{"name":"pVHL-elongin C-elongin B complex","type":"exact"},{"name":"von Hippel-Lindau tumor suppressor complex","type":"exact"}],"termid":"GO:0030891"}


id: PBO:0091249
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha-One, Three-Galactosyltransferase","termid":"PBO:0091249"}


id: FYPO:0005627
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell cycle checkpoint phenotype in which the duration of cell cycle arrest or delay due to regulation by any mitotic DNA damage checkpoint is greater than in wild type during a cellular response to ultraviolet (UV) light, when cells are exposed to UV during S phase of the mitotic cell cycle.","definition_xrefs":["PMID:26652183","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased duration of mitotic DNA damage checkpoint during cellular response to UV","termid":"FYPO:0003445"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000298"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000298","FYPO:0000631","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"increased duration of mitotic DNA damage checkpoint during cellular response to UV during mitotic S phase","synonyms":[{"name":"delayed DNA damage checkpoint deactivation during cellular response to UV during mitotic S phase","type":"exact"},{"name":"increased duration of mitotic DNA damage checkpoint after UV irradiation during S phase","type":"exact"},{"name":"increased duration of mitotic DNA damage checkpoint during cellular response to S phase exposure to UV","type":"exact"},{"name":"prolonged DNA damage checkpoint during cellular response to UV during mitotic S phase","type":"exact"}],"termid":"FYPO:0005627"}


id: PBO:0012286
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Golgi membrane protein involved in vesicle-mediated transport (predicted)","termid":"PBO:0012286"}


id: PR:Q9P7D2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein phosphatase methylesterase 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO03467","PANTHER:PTHR14189:SF0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase methylesterase 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBP4H10.17c","secondary_identifiers":["UniProtKB:Q9P7D2"],"synonyms":[{"name":"PME-1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-PPME1","type":"exact"}],"termid":"PR:Q9P7D2"}


id: PBO:0090361
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin-protein ligase E3, unknown specificity","termid":"PBO:0090361"}


id: PBO:0085584
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in apoptosis; variously described as containing a BCL-2 homology (BH3) domain or as a member of the BAX inhibitor family; reported to promote apoptosis under some conditions and to inhibit it in others; localizes to ER and vacuole; may link the unfolded protein response to apoptosis via regulation of calcium-mediated signaling; translocates to mitochondria under apoptosis-inducing conditions in a process involving Mir1p and Cor1p","termid":"PBO:0085584"}


id: GO:0006552
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of L-leucine, 2-amino-4-methylpentanoic acid.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-leucine metabolic process","termid":"GO:0006551"},{"relation_name":"is_a","term_name":"pyruvate family amino acid catabolic process","termid":"GO:0009080"},{"relation_name":"is_a","term_name":"branched-chain amino acid catabolic process","termid":"GO:0009083"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006520"}],"interesting_parent_ids":["GO:0008150","GO:0006520","GO:0044281"],"is_obsolete":false,"name":"L-leucine catabolic process","synonyms":[{"name":"L-leucine breakdown","type":"exact"},{"name":"L-leucine catabolism","type":"exact"},{"name":"L-leucine degradation","type":"exact"},{"name":"leucine catabolic process","type":"broad"}],"termid":"GO:0006552"}


id: PR:Q9Y812
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A histone H3-like centromeric protein cnp1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DAN","UniProtKB:Q9Y812"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"},{"relation_name":"is_a","term_name":"histone H3-like centromeric protein cnp1 (Schizosaccharomyces pombe)","termid":"PR:000041369"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone H3-like centromeric protein cnp1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1105.17","synonyms":[{"name":"CENP-A homolog (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-cnp1","type":"exact"},{"name":"centromere protein 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"silencing in the middle of the centromere protein 2 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9Y812"}


id: GO:0062161
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of a pyocyanine biosynthetic process.","definition_xrefs":["PMID:28715477"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of biosynthetic process","termid":"GO:0009889"},{"relation_name":"regulates","term_name":"pyocyanine biosynthetic process","termid":"GO:0106220"}],"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 pyocyanine biosynthetic process","synonyms":[{"name":"regulation of pyocyanin biosynthetic process","type":"exact"}],"termid":"GO:0062161"}


id: MONDO:0810000
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An eye disorder described by the growth of new blood vessels that originate from the choroid through a break in the Bruch membrane into the sub–retinal pigment epithelium (sub-RPE) or subretinal space. Choroidal neovascularization (CNV) is a major cause of visual loss.","direct_ancestors":[{"relation_name":"is_a","term_name":"eye disorder","termid":"MONDO:0005328"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"choroidal neovascularization","secondary_identifiers":["HP:0011506","UMLS:C0600518","MESH:D020256","MEDGEN:154726"],"termid":"MONDO:0810000","xrefs":{"Monarch":{"xref_id":"0810000"}}}


id: PBO:0085416
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Plasma membrane transporter for choline, ethanolamine, and carnitine; involved in the uptake of nitrogen mustard and the uptake of glycine betaine during hypersaline stress; co-regulated with phospholipid biosynthetic genes and negatively regulated by choline and myo-inositol","termid":"PBO:0085416"}


id: GO:1990712
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex containing at least HFE and a transferrin receptor (either TFR1/TFRC or TFR2), proposed to play a role in the sensing of transferrin-bound Fe (Fe2-Tf) on the plasma membrane to regulate hepcidin transcription.","definition_xrefs":["PMID:25147378","GOC:kom","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane signaling receptor complex","termid":"GO:0098802"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005886","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"HFE-transferrin receptor complex","termid":"GO:1990712"}


id: MONDO:0002197
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, benign neoplasm that arises from the vulva It is characterized by the presence of clusters of small glands lined by mucinous epithelial cells. Bartholin duct structures are not present.","definition_xrefs":["NCIT:C40301"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vestibular gland benign neoplasm","termid":"MONDO:0000626"},{"relation_name":"is_a","term_name":"vulvar glandular neoplasm","termid":"MONDO:0002198"},{"relation_name":"is_a","term_name":"paraurethral gland neoplasm","termid":"MONDO:0002219"},{"relation_name":"is_a","term_name":"benign urethral neoplasm","termid":"MONDO:0004177"},{"relation_name":"is_a","term_name":"adenoma","termid":"MONDO:0004972"},{"relation_name":"is_a","term_name":"benign epithelial neoplasm","termid":"MONDO:0036976"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"minor vestibular glands adenoma","secondary_identifiers":["DOID:2075","MEDGEN:267644","UMLS:C1510791"],"synonyms":[{"name":"adenoma of minor vestibular glands","type":"exact"},{"name":"minor vestibular gland adenoma","type":"exact"}],"termid":"MONDO:0002197","xrefs":{"Monarch":{"xref_id":"0002197"}}}


id: PR:P78890
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC23H3.15c gene.","definition_xrefs":["PRO:DNx","UniProtKB:P78890"],"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 C23H3.15c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC23H3.15c","synonyms":[{"name":"Spom972h-SPAC23H3.15c","type":"exact"}],"termid":"PR:P78890"}


id: MONDO:0001421
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplasm involving a frontal lobe.","definition_xrefs":["MONDO:patterns/neoplasm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neoplasm of cerebral hemisphere","termid":"MONDO:0021374"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"frontal lobe neoplasm","secondary_identifiers":["NCIT:C5572","DOID:12016","UMLS:C1263886","SCTID:126954003","ICD9:191.1","MEDGEN:224730"],"synonyms":[{"name":"frontal lobe neoplasm (disease)","type":"exact"},{"name":"frontal lobe tumor","type":"exact"},{"name":"frontal lobe tumour","type":"exact"},{"name":"malignant neoplasm of frontal lobe","type":"narrow"},{"name":"neoplasm of frontal lobe","type":"exact"},{"name":"neoplasm of the frontal lobe","type":"exact"},{"name":"tumor of frontal lobe","type":"exact"},{"name":"tumor of the frontal lobe","type":"exact"},{"name":"tumour of frontal lobe","type":"exact"},{"name":"tumour of the frontal lobe","type":"exact"}],"termid":"MONDO:0001421","xrefs":{"Monarch":{"xref_id":"0001421"}}}


id: PBO:0050678
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock protein family A (Hsp70) member 8 pseudogene 5","termid":"PBO:0050678"}


id: PBO:0054855
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 2269","termid":"PBO:0054855"}


id: PBO:0071471
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L32 pseudogene 12","termid":"PBO:0071471"}


id: GO:0048808
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of male genitalia are generated and organized.","definition_xrefs":["GOC:ems","ISBN:0140512888"],"direct_ancestors":[{"relation_name":"is_a","term_name":"genitalia morphogenesis","termid":"GO:0035112"},{"relation_name":"is_a","term_name":"male anatomical structure morphogenesis","termid":"GO:0090598"},{"relation_name":"part_of","term_name":"male genitalia development","termid":"GO:0030539"}],"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":"male genitalia morphogenesis","synonyms":[{"name":"male genital morphogenesis","type":"related"}],"termid":"GO:0048808"}


id: PBO:0080568
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat and FYVE domain containing 3","termid":"PBO:0080568"}


id: PBO:0034277
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_end_location","termid":"PBO:0034277"}


id: MOD:00263
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively results from forming an adduct between a cysteine residue and the tetrapyrrole compound phycoviolobilin.","definition_xrefs":["PubMed:3208761","PubMed:2106585","Unimod:387","RESID:AA0258"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tetrapyrrole modified residue","termid":"MOD:00700"},{"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-phycoviolobilin-L-cysteine","synonyms":[{"name":"(4S)-3-[(1R)-1-(((2R)-2-amino-2-carboxy)ethylsulfanyl)ethyl]-8,12-bis(2-carboxyethyl)-18-ethyl-4,5-dihydro-2,7,13,17-tetramethyl-(21H,22H,24H)-biladiene-bc-1,19-dione","type":"exact"},{"name":"BINDING Phycoviolobilin chromophore (covalent; via 1 link)","type":"exact"},{"name":"PBV","type":"exact"},{"name":"PVB","type":"exact"},{"name":"PXB","type":"exact"},{"name":"Phycocyanobilin","type":"related"},{"name":"S-phycobiliviolin-L-cysteine","type":"exact"},{"name":"S-phycoviolobilin-L-cysteine","type":"exact"},{"name":"cryptobiliviolin","type":"exact"},{"name":"cryptoviolin","type":"exact"},{"name":"cryptoviolobilin","type":"exact"},{"name":"phycocyanobilin","type":"related"}],"termid":"MOD:00263"}


id: GO:0016308
data:
  {"annotated_genes":["SJAG_01863"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[81398],"is_not":false,"summary":null,"term":"GO:0016308"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: a 1-phosphatidyl-1D-myo-inositol 4-phosphate + ATP = a 1-phosphatidyl-1D-myo-inositol 4,5-bisphosphate + ADP + H+.","definition_xrefs":["RHEA:14425","EC:2.7.1.68"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatidylinositol kinase activity","termid":"GO:0052742"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01863":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016740","GO:0016301"],"is_obsolete":false,"name":"1-phosphatidylinositol-4-phosphate 5-kinase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-3772436","Reactome:R-HSA-8868066","KEGG_REACTION:R03469","MetaCyc:2.7.1.68-RXN","Reactome:R-HSA-1676082","GO:0004431","GO:0045215"],"synonyms":[{"name":"1-phosphatidylinositol-4-phosphate kinase activity","type":"broad"},{"name":"1-phosphatidylinositol-4-phosphate kinase, class IA","type":"narrow"},{"name":"1-phosphatidylinositol-4-phosphate kinase, class IB","type":"narrow"},{"name":"ATP:1-phosphatidyl-1D-myo-inositol-4-phosphate 5-phosphotransferase activity","type":"related"},{"name":"PI(4)5K","type":"related"},{"name":"PIP kinase activity","type":"broad"},{"name":"PIP5K","type":"exact"},{"name":"PtdIns(4)P-5-kinase activity","type":"related"},{"name":"diphosphoinositide kinase activity","type":"broad"},{"name":"phosphatidylinositol 4-phosphate kinase activity","type":"broad"},{"name":"phosphatidylinositol-4-phosphate 5-kinase activity","type":"related"},{"name":"type I PIP kinase activity","type":"narrow"}],"termid":"GO:0016308","terms_by_termid":{"GO:0016308":null}}


id: GO:0010710
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency or extent of collagen catabolism. Collagen catabolism is the proteolytic chemical reactions and pathways resulting in the breakdown of collagen in the extracellular matrix.","definition_xrefs":["GOC:BHF","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of catabolic process","termid":"GO:0009894"},{"relation_name":"is_a","term_name":"regulation of collagen metabolic process","termid":"GO:0010712"},{"relation_name":"regulates","term_name":"collagen catabolic process","termid":"GO:0030574"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of collagen catabolic process","synonyms":[{"name":"regulation of collagen breakdown","type":"exact"},{"name":"regulation of collagen catabolism","type":"exact"},{"name":"regulation of collagen degradation","type":"exact"}],"termid":"GO:0010710"}


id: PATO:0000172
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000172 relative yield (obsolete PATO:0000172)","termid":"PATO:0000172"}


id: FYPO:0007035
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 5-fluorouracil.","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:0000139"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0002060","FYPO:0000257","FYPO:0000139","FYPO:0002058","FYPO:0002057","FYPO:0000003"],"is_obsolete":false,"name":"normal growth on 5-fluorouracil","synonyms":[{"name":"normal cell population growth in presence of 5-fluorouracil","type":"exact"},{"name":"normal cell population growth on 5-FU","type":"exact"},{"name":"normal cell population growth on 5-fluorouracil","type":"exact"},{"name":"normal vegetative cell population growth on 5-fluorouracil","type":"exact"}],"termid":"FYPO:0007035"}


id: GO:1902138
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of (-)-secoisolariciresinol.","definition_xrefs":["PMID:9872995","GOC:TermGenie","PMID:8910615"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lignan biosynthetic process","termid":"GO:0009807"},{"relation_name":"is_a","term_name":"diol biosynthetic process","termid":"GO:0034312"},{"relation_name":"is_a","term_name":"phenol-containing compound biosynthetic process","termid":"GO:0046189"},{"relation_name":"is_a","term_name":"(-)-secoisolariciresinol metabolic process","termid":"GO:1902136"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0019748","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"(-)-secoisolariciresinol biosynthetic process","synonyms":[{"name":"(-)-secoisolariciresinol anabolism","type":"exact"},{"name":"(-)-secoisolariciresinol biosynthesis","type":"exact"},{"name":"(-)-secoisolariciresinol formation","type":"exact"},{"name":"(-)-secoisolariciresinol synthesis","type":"exact"}],"termid":"GO:1902138"}


id: PBO:0058196
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4489","termid":"PBO:0058196"}


id: PBO:0048708
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycine receptor beta","termid":"PBO:0048708"}


id: PATO:0000460
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in a bearer by virtue of the bearer's deviation from normal or average.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"deviation(from_normal)","termid":"PATO:0000069"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"abnormal","synonyms":[{"name":"aberrant","type":"related"},{"name":"atypia","type":"related"},{"name":"atypical","type":"related"},{"name":"defective","type":"related"}],"termid":"PATO:0000460"}


id: PBO:0035960
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_spatial_extent_of_double-strand_break_processing","termid":"PBO:0035960"}


id: PATO:0000679
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000679 temporal value (obsolete PATO:0000679)","termid":"PATO:0000679"}


id: FYPO:0002849
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype observed in the vegetative growth phase of the life cycle in which a cell is curved when the cell population has been in stationary phase and is then placed in conditions that allow recovery. In a curved cell, the long axis follows a smooth bend rather than a straight line.","definition_xrefs":["PomBase:mah","PomBase:jh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"curved vegetative cell","termid":"FYPO:0000016"}],"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:0000005"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000005","FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"curved cell during recovery from stationary phase","synonyms":[{"name":"comma-shaped cell during recovery from stationary phase","type":"exact"},{"name":"curved cell during recovery from stationary phase during mitotic cell cycle","type":"related"},{"name":"curved cell during vegetative growth following stationary phase","type":"exact"}],"termid":"FYPO:0002849"}


id: PBO:0057381
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 548aw","termid":"PBO:0057381"}


id: PBO:0088174
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Xylose and arabinose reductase; member of the aldo-keto reductase (AKR) family; GFP-fusion protein is induced in response to the DNA-damaging agent MMS","termid":"PBO:0088174"}


id: GO:1901317
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of flagellated sperm motility.","definition_xrefs":["GOC:TermGenie","GOC:cilia","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cilium movement involved in cell motility","termid":"GO:0060295"},{"relation_name":"is_a","term_name":"regulation of reproductive process","termid":"GO:2000241"},{"relation_name":"regulates","term_name":"flagellated sperm motility","termid":"GO:0030317"}],"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 flagellated sperm motility","synonyms":[{"name":"regulation of sperm motility","type":"broad"},{"name":"regulation of sperm movement","type":"broad"}],"termid":"GO:1901317"}


id: MOD:00582
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-lysine residue to 6x(13)C,2x(15)N labeled L-lysine.","definition_xrefs":["PubMed:12716131","Unimod:259","OMSSA:181"],"direct_ancestors":[{"relation_name":"is_a","term_name":"(13)C labeled residue","termid":"MOD:00842"},{"relation_name":"is_a","term_name":"(15)N labeled residue","termid":"MOD:00843"},{"relation_name":"is_a","term_name":"modified L-lysine residue","termid":"MOD:00912"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"6x(13)C,2x(15)N labeled L-lysine","synonyms":[{"name":"13C(6) 15N(2) Silac label","type":"related"},{"name":"Label:13C(6)15N(2)","type":"related"},{"name":"lys-13C615N2","type":"exact"}],"termid":"MOD:00582"}


id: PBO:0077905
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tyrosylprotein sulfotransferase 1","termid":"PBO:0077905"}


id: GO:1904343
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of colon smooth muscle contraction.","definition_xrefs":["PMID:24170253","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of gastro-intestinal system smooth muscle contraction","termid":"GO:1904306"},{"relation_name":"is_a","term_name":"regulation of colon smooth muscle contraction","termid":"GO:1904341"},{"relation_name":"positively_regulates","term_name":"colon smooth muscle contraction","termid":"GO:1990765"}],"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 colon smooth muscle contraction","synonyms":[{"name":"activation of colon smooth muscle contraction","type":"narrow"},{"name":"up regulation of colon smooth muscle contraction","type":"exact"},{"name":"up-regulation of colon smooth muscle contraction","type":"exact"},{"name":"upregulation of colon smooth muscle contraction","type":"exact"}],"termid":"GO:1904343"}


id: PBO:0047295
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fatty acyl-CoA reductase 2 pseudogene 2","termid":"PBO:0047295"}


id: MONDO:0006823
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A sex chromosome disorder caused by the presence of an extra X chromosome in the male karyotype. Affected individuals are infertile and have a small penis and testes. They tend to have tall stature and long legs and may have difficulties with speech and language development. Gynecomastia may be present.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"epilepsy","termid":"MONDO:0005027"},{"relation_name":"is_a","term_name":"sex chromosome disorder of sex development","termid":"MONDO:0017975"},{"relation_name":"is_a","term_name":"chromosome X disorder","termid":"MONDO:0700027"},{"relation_name":"is_a","term_name":"trisomy","termid":"MONDO:0700065"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Klinefelter syndrome","secondary_identifiers":["EFO:1001006","icd11.foundation:1937385304","ICD9:758.7","MEDGEN:44033","DOID:1921","MESH:D007713","NANDO:2200386","NCIT:C34752","UMLS:C0022735","SCTID:405769009","MedDRA:10023463"],"synonyms":[{"name":"47,XXY syndrome","type":"exact"},{"name":"Klinefelter syndrome","type":"exact"},{"name":"Klinefelter's syndrome","type":"exact"},{"name":"Klinefelter's syndrome, XXY","type":"exact"},{"name":"XXY syndrome","type":"exact"},{"name":"XXY syndrome (Klinefelter syndrome)","type":"exact"},{"name":"XXY trisomy","type":"exact"},{"name":"hypogonadotropic hypogonadism","type":"related"}],"termid":"MONDO:0006823","xrefs":{"Monarch":{"xref_id":"0006823"}}}


id: PBO:0034151
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-is_subsequence_of","termid":"PBO:0034151"}


id: PBO:0002048
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by S. cerevisiae YNL102W","termid":"PBO:0002048"}


id: PBO:0011475
data:
  {"annotation_feature_type":"gene","cv_name":"cat_act","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hydrolysis rate of soluble starch to glucose is 8.9 (mM min-1 ml-2)","termid":"PBO:0011475"}


id: GO:0098039
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Process of transposition in which the existing element is replicated and one of the copies is excised and integrated at a new target site. Also referred to as copy-and-paste transposition.","definition_xrefs":["GOC:bm","PMID:1660177","PMID:10540284"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA transposition","termid":"GO:0006313"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006310"},{"rel_name":"is_a","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0008150","GO:0006310","GO:0006259"],"is_obsolete":false,"name":"replicative DNA transposition","synonyms":[{"name":"copy-and-paste transposition","type":"exact"},{"name":"replicative transposition, DNA-mediated","type":"exact"},{"name":"transpositional DNA genome replication","type":"exact"}],"termid":"GO:0098039"}


id: GO:2000657
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of apolipoprotein binding.","definition_xrefs":["GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of apolipoprotein binding (obsolete GO:2000657)","termid":"GO:2000657"}


id: PBO:0074869
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 53","termid":"PBO:0074869"}


id: GO:0036457
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A cytoplasmic, non-membrane bound granule of, at least, keratinocyte. Associated to keratin intermediate filaments and partially crosslinked to the cell envelope.","definition_xrefs":["GOC:krc","PMID:15854042"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"cytoplasm","termid":"GO:0005737"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005737","GO:0005575"],"is_obsolete":false,"name":"keratohyalin granule","termid":"GO:0036457"}


id: MONDO:0003711
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete malignant peripheral nerve sheath tumor (obsolete MONDO:0003711)","termid":"MONDO:0003711","xrefs":{"Monarch":{"xref_id":"0003711"}}}


id: GO:0032304
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the controlled release of an icosanoid from a cell.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of icosanoid secretion","termid":"GO:0032303"},{"relation_name":"is_a","term_name":"negative regulation of secretion","termid":"GO:0051048"},{"relation_name":"is_a","term_name":"negative regulation of fatty acid transport","termid":"GO:2000192"},{"relation_name":"negatively_regulates","term_name":"icosanoid secretion","termid":"GO:0032309"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"negative regulation of icosanoid secretion","synonyms":[{"name":"down regulation of icosanoid secretion","type":"exact"},{"name":"down-regulation of icosanoid secretion","type":"exact"},{"name":"downregulation of icosanoid secretion","type":"exact"},{"name":"inhibition of icosanoid secretion","type":"narrow"},{"name":"negative regulation of eicosanoid secretion","type":"exact"}],"termid":"GO:0032304"}


id: PBO:0087390
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Steryl ester hydrolase; one of three gene products (Yeh1p, Yeh2p, Tgl1p) responsible for steryl ester hydrolase activity and involved in sterol homeostasis; localized to lipid particle membranes","termid":"PBO:0087390"}


id: MONDO:0054770
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Orofaciodigital syndrome 18 (OFD18) is characterized by short stature, brachymesophalangy, pre- and postaxial polysyndactyly, and stocky femoral necks, as well as oral anomalies and dysmorphic facial features.","definition_xrefs":["OMIM:617927"],"direct_ancestors":[{"relation_name":"is_a","term_name":"orofaciodigital syndrome","termid":"MONDO:0015375"}],"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":"orofaciodigital syndrome 18","secondary_identifiers":["MEDGEN:1799326","DOID:0060961","Orphanet:508501","UMLS:C5567903"],"synonyms":[{"name":"OFD18","type":"exact"},{"name":"Ofds 18","type":"exact"},{"name":"oral-facial-digital syndrome type 18","type":"exact"},{"name":"oral-facial-digital syndrome with short stature and brachymesophalangy","type":"exact"},{"name":"orofaciodigital syndrome XVIII","type":"exact"},{"name":"orofaciodigital syndrome type 18","type":"exact"}],"termid":"MONDO:0054770","xrefs":{"Monarch":{"xref_id":"0054770"}}}


id: PBO:0064027
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi-interacting RNA cluster 61","termid":"PBO:0064027"}


id: MONDO:0013602
data:
  {"annotated_genes":["SJAG_01671"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87625],"is_not":false,"summary":null,"term":"MONDO:0013602"}]},"cv_name":"mondo","definition":"Any paraganglioma in which the cause of the disease is a mutation in the SDHA gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"paraganglioma","termid":"MONDO:0000448"},{"relation_name":"is_a","term_name":"central nervous system cancer","termid":"MONDO:0002714"},{"relation_name":"is_a","term_name":"adrenal gland cancer","termid":"MONDO:0002817"},{"relation_name":"is_a","term_name":"malignant urinary system neoplasm","termid":"MONDO:0006295"},{"relation_name":"is_a","term_name":"hereditary pheochromocytoma-paraganglioma","termid":"MONDO:0017366"},{"relation_name":"is_a","term_name":"peripheral nervous system cancer","termid":"MONDO:0021089"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01671":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"paragangliomas 5","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C3279992","OMIM:614165","GARD:15763","MEDGEN:481622"],"synonyms":[{"name":"PGL5","type":"related"},{"name":"SDHA paraganglioma","type":"exact"},{"name":"paraganglioma caused by mutation in SDHA","type":"exact"},{"name":"paragangliomas 5","type":"exact"},{"name":"paragangliomas type 5","type":"exact"}],"termid":"MONDO:0013602","terms_by_termid":{"MONDO:0013602":null},"xrefs":{"Monarch":{"xref_id":"0013602"}}}


id: PBO:0004776
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleoporin Nup120","termid":"PBO:0004776"}


id: PBO:0068381
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring finger protein 182","termid":"PBO:0068381"}


id: PBO:0066381
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RDX pseudogene 1","termid":"PBO:0066381"}


id: GO:0003179
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the structure of a heart valve is generated and organized.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"},{"relation_name":"part_of","term_name":"heart valve development","termid":"GO:0003170"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"heart valve morphogenesis","synonyms":[{"name":"heart valve remodeling","type":"narrow"},{"name":"heart valve remodelling","type":"narrow"}],"termid":"GO:0003179"}


id: PBO:0076409
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TATA-box binding protein associated factor 5 like","termid":"PBO:0076409"}


id: PBO:0038883
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adenylate cyclase 9","termid":"PBO:0038883"}


id: PBO:0082248
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alpha subunit of the F1 sector of mitochondrial F1F0 ATP synthase; which is a large, evolutionarily conserved enzyme complex required for ATP synthesis; F1 translationally regulates ATP6 and ATP8 expression to achieve a balanced output of ATP synthase genes encoded in nucleus and mitochondria; phosphorylated; N-terminally propionylated in vivo","termid":"PBO:0082248"}


id: GO:0010626
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the frequency or extent of the multiplication or reproduction of Schwann cells, resulting in the expansion of their population. Schwann cells are a type of glial cell in the peripheral nervous system.","definition_xrefs":["GOC:sl","GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of Schwann cell proliferation","termid":"GO:0010624"},{"relation_name":"is_a","term_name":"negative regulation of glial cell proliferation","termid":"GO:0060253"},{"relation_name":"negatively_regulates","term_name":"Schwann cell proliferation","termid":"GO:0014010"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of Schwann cell proliferation","termid":"GO:0010626"}


id: GO:1900632
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of tridecane.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alkane biosynthetic process","termid":"GO:0043447"},{"relation_name":"is_a","term_name":"tridecane metabolic process","termid":"GO:1900631"}],"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":"tridecane biosynthetic process","synonyms":[{"name":"tridecane anabolism","type":"exact"},{"name":"tridecane biosynthesis","type":"exact"},{"name":"tridecane formation","type":"exact"},{"name":"tridecane synthesis","type":"exact"}],"termid":"GO:1900632"}


id: PBO:0034439
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_double-strand_break_repair_via_nonhomologous_end_joining","termid":"PBO:0034439"}


id: SO:0001757
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A SL2_acceptor_site which appends the SL12 RNA leader sequence to the 5' end of an mRNA. SL12 acceptor sites occur in genes in internal segments of polycistronic transcripts.","definition_xrefs":["SO:nlw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"SL2_acceptor_site","termid":"SO:0000709"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SL12_acceptor_site","synonyms":[{"name":"SL12 acceptor site","type":"exact"}],"termid":"SO:0001757"}


id: PBO:0048491
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GCSH pseudogene 3","termid":"PBO:0048491"}


id: GO:0110096
data:
  {"annotated_genes":["SJAG_03786","SJAG_02988","SJAG_04404","SJAG_02960","SJAG_04674","SJAG_01457","SJAG_01596","SJAG_02106","SJAG_02010","SJAG_05256","SJAG_04726"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[114589,102684],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0110095"},{"annotations":[79887,97350],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0046294"},{"annotations":[104616,76209,61740,74579],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0019243"},{"annotations":[59690,61490,106879],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061727"}]},"cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an aldehyde stimulus.","definition_xrefs":["GOC:vw","PMID:25656103"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"}],"gene_count":11,"genes_by_uniquename":{"SJAG_01457":null,"SJAG_01596":null,"SJAG_02010":null,"SJAG_02106":null,"SJAG_02960":null,"SJAG_02988":null,"SJAG_03786":null,"SJAG_04404":null,"SJAG_04674":null,"SJAG_04726":null,"SJAG_05256":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to aldehyde","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000108":null},"termid":"GO:0110096","terms_by_termid":{"GO:0019243":null,"GO:0046294":null,"GO:0061727":null,"GO:0110095":null}}


id: MONDO:0022512
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete atrial septal defect coronary sinus (obsolete MONDO:0022512)","termid":"MONDO:0022512","xrefs":{"Monarch":{"xref_id":"0022512"}}}


id: GO:0071009
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A spliceosomal snRNP complex that is formed by the association of the U4atac/U6atac and U5 snRNPs.","definition_xrefs":["GOC:pr","GOC:krc","ISBN:0879695897","PMID:16201866","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spliceosomal tri-snRNP complex","termid":"GO:0097526"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0032991","GO:0005634","GO:0005575"],"is_obsolete":false,"name":"U4atac/U6atac x U5 tri-snRNP complex","synonyms":[{"name":"U4atac/U6atac.U5 snRNP complex","type":"exact"}],"termid":"GO:0071009"}


id: GO:0031071
data:
  {"annotated_genes":["SJAG_00186"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[80607],"is_not":false,"summary":null,"term":"GO:0031071"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: L-cysteine + [enzyme]-cysteine = L-alanine + [enzyme]-S-sulfanylcysteine.","definition_xrefs":["EC:2.8.1.7"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfurtransferase activity","termid":"GO:0016783"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00186":null},"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:0016782"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0003824","GO:0016782"],"is_obsolete":false,"name":"cysteine desulfurase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["RHEA:43892","Reactome:R-HSA-1362408","Reactome:R-HSA-947514"],"synonyms":[{"name":"IscS","type":"related"},{"name":"L-cysteine:enzyme cysteine sulfurtransferase activity","type":"related"},{"name":"NIFS","type":"related"},{"name":"SufS","type":"related"},{"name":"cysteine desulfurylase activity","type":"related"}],"termid":"GO:0031071","terms_by_termid":{"GO:0031071":null}}


id: PBO:0041507
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 14 open reading frame 39","termid":"PBO:0041507"}


id: PBO:0111312
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ThiJ domain protein, glyoxylase III","termid":"PBO:0111312"}


id: GO:2000319
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of T-helper 17 cell differentiation.","definition_xrefs":["GOC:BHF","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of T-helper cell differentiation","termid":"GO:0045622"},{"relation_name":"is_a","term_name":"regulation of T-helper 17 type immune response","termid":"GO:2000316"},{"relation_name":"regulates","term_name":"T-helper 17 cell differentiation","termid":"GO:0072539"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of T-helper 17 cell differentiation","synonyms":[{"name":"regulation of T-helper 17 cell development","type":"related"}],"termid":"GO:2000319"}


id: PBO:0027699
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_rDNA_separation","termid":"PBO:0027699"}


id: GO:0060107
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The extracellular matrix that is a regularly spaced circumferential ridge present in the cortical region of the cuticle. Annuli are delineated by annular furrows and are present throughout the cuticle with the exception of lateral regions where longitudinal alae are present.","definition_xrefs":["GOC:dph","GOC:kmv","ISSN:15518507"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"cortical layer of collagen and cuticulin-based cuticle extracellular matrix","termid":"GO:0060106"}],"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":"annuli extracellular matrix","synonyms":[{"name":"annulae","type":"related"},{"name":"annular rings","type":"related"},{"name":"annule(s)","type":"related"},{"name":"annulus","type":"related"}],"termid":"GO:0060107"}


id: MONDO:0023273
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A morphologic variant of dermatofibrosarcoma protuberans characterized by the presence of melanin-pigmented dendritic cells.","definition_xrefs":["NCIT:C9430"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dermatofibrosarcoma protuberans","termid":"MONDO:0011934"}],"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":"pigmented dermatofibrosarcoma protuberans","secondary_identifiers":["UMLS:C0334464","SCTID:398670003","MEDGEN:90786"],"synonyms":[{"name":"Bednar Tumor","type":"related"},{"name":"Bednar Tumour","type":"related"},{"name":"Bednar's Tumor","type":"related"},{"name":"Bednar's Tumour","type":"related"},{"name":"Bednars Tumor","type":"related"},{"name":"Bednars Tumour","type":"related"},{"name":"DFSP, Pigmented","type":"related"},{"name":"DFSPs, Pigmented","type":"related"},{"name":"Dermatofibrosarcoma Protuberan, Pigmented","type":"related"},{"name":"Dermatofibrosarcoma Protuberans, Pigmented","type":"related"},{"name":"Pigmented DFSP","type":"related"},{"name":"Pigmented DFSPs","type":"related"},{"name":"Pigmented Dermatofibrosarcoma Protuberan","type":"related"},{"name":"Pigmented Dermatofibrosarcoma Protuberans","type":"related"},{"name":"Pigmented Dermatofibrosarcoma Protuberans (Bednar Tumor)","type":"related"},{"name":"Pigmented dermatofibrosarcoma","type":"related"},{"name":"Pigmented dermatofibrosarcoma protuberans","type":"related"},{"name":"Pigmented dermatofibrosarcoma protuberans of skin","type":"related"},{"name":"Pigmented storiform neurofibroma","type":"related"},{"name":"Protuberan, Pigmented Dermatofibrosarcoma","type":"related"},{"name":"Protuberans, Pigmented Dermatofibrosarcoma","type":"related"},{"name":"Tumor, Bednar","type":"related"},{"name":"Tumor, Bednar's","type":"related"},{"name":"bednar tumor","type":"exact"},{"name":"bednar tumour","type":"exact"},{"name":"pigmented dermatofibrosarcoma protuberans","type":"exact"},{"name":"pigmented dermatofibrosarcoma protuberans (bednar tumor)","type":"exact"}],"termid":"MONDO:0023273","xrefs":{"Monarch":{"xref_id":"0023273"}}}


id: GO:0009127
data:
  {"annotated_genes":["SJAG_04634","SJAG_01070","SJAG_02364","SJAG_03140","SJAG_04123","SJAG_01814","SJAG_01081","SJAG_00964","SJAG_01661","SJAG_04681","SJAG_01298","SJAG_03355","SJAG_06634","SJAG_00044","SJAG_02850","SJAG_01859"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[80706,78728],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044208"},{"annotations":[65440,58353,57215,71662,78503,73333,60564,66803],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006189"},{"annotations":[75680,57366],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044209"},{"annotations":[59857,63912],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006177"},{"annotations":[77381,103012],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032263"},{"annotations":[65953,77382],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032264"},{"annotations":[77383,110112],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032265"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of purine nucleoside monophosphate, a compound consisting of a purine base linked to a ribose or deoxyribose sugar esterified with phosphate on the sugar.","definition_xrefs":["GOC:go_curators","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside monophosphate biosynthetic process","termid":"GO:0009124"},{"relation_name":"is_a","term_name":"purine nucleoside monophosphate metabolic process","termid":"GO:0009126"}],"gene_count":16,"genes_by_uniquename":{"SJAG_00044":null,"SJAG_00964":null,"SJAG_01070":null,"SJAG_01081":null,"SJAG_01298":null,"SJAG_01661":null,"SJAG_01814":null,"SJAG_01859":null,"SJAG_02364":null,"SJAG_02850":null,"SJAG_03140":null,"SJAG_03355":null,"SJAG_04123":null,"SJAG_04634":null,"SJAG_04681":null,"SJAG_06634":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"purine nucleoside monophosphate biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000108":null},"synonyms":[{"name":"purine nucleoside monophosphate anabolism","type":"exact"},{"name":"purine nucleoside monophosphate biosynthesis","type":"exact"},{"name":"purine nucleoside monophosphate formation","type":"exact"},{"name":"purine nucleoside monophosphate synthesis","type":"exact"}],"termid":"GO:0009127","terms_by_termid":{"GO:0006177":null,"GO:0006189":null,"GO:0032263":null,"GO:0032264":null,"GO:0032265":null,"GO:0044208":null,"GO:0044209":null}}


id: PBO:0041424
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 8 putative open reading frame 44","termid":"PBO:0041424"}


id: PBO:0018147
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane protein involved in inositol lipid-mediated signaling Sfk1 (predicted)","termid":"PBO:0018147"}


id: PBO:0091715
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by human PSMC1","termid":"PBO:0091715"}


id: PBO:0034385
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_derived_by_descendant","termid":"PBO:0034385"}


id: GO:0031852
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a mu-type opioid receptor.","definition_xrefs":["GOC:nln","GOC:mah","GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"opioid receptor binding","termid":"GO:0031628"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"mu-type opioid receptor binding","synonyms":[{"name":"morphine receptor binding","type":"related"},{"name":"mu-type opioid receptor ligand","type":"narrow"}],"termid":"GO:0031852"}


id: PBO:0001961
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"target genes transcriptionally co-regulated by Mcs6","termid":"PBO:0001961"}


id: PBO:0038505
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP binding cassette subfamily D member 1","termid":"PBO:0038505"}


id: PBO:0011171
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HOPS/CORVET complex subunit, ubiquitin-protein ligase E3 (predicted)","termid":"PBO:0011171"}


id: PBO:0067421
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 539, pseudogene","termid":"PBO:0067421"}


id: PBO:0031546
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_cell_population_growth_at_high_temperature","termid":"PBO:0031546"}


id: PBO:0080876
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"yippee like 2","termid":"PBO:0080876"}


id: PBO:0049434
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GUSB pseudogene 11","termid":"PBO:0049434"}


id: GO:0040006
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Attaching of a protein-based cuticle to the epithelium underlying it.","definition_xrefs":["GOC:jl","GOC:mtg_sensu"],"gene_count":0,"genotype_count":0,"name":"obsolete protein-based cuticle attachment to epithelium (obsolete GO:0040006)","synonyms":[{"name":"cuticular attachment to epithelium","type":"broad"},{"name":"protein-based cuticle attachment to epithelium","type":"exact"}],"termid":"GO:0040006"}


id: GO:0015507
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Permease for hydroxy and aromatic amino acids.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete hydroxy/aromatic amino acid permease activity (obsolete GO:0015507)","synonyms":[{"name":"hydroxy/aromatic amino acid permease activity","type":"exact"}],"termid":"GO:0015507"}


id: MONDO:0003787
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant mixed germ cell neoplasm that arises from the testis during childhood.","definition_xrefs":["NCIT:C6542"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mixed testicular germ cell cancer","termid":"MONDO:0003120"},{"relation_name":"is_a","term_name":"childhood testicular germ cell tumor","termid":"MONDO:0003758"},{"relation_name":"is_a","term_name":"malignant childhood germ cell neoplasm","termid":"MONDO:0004479"}],"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":"childhood testicular mixed germ cell cancer","secondary_identifiers":["MEDGEN:272471","UMLS:C1333009","DOID:6161"],"synonyms":[{"name":"childhood mixed testicular germ cell cancer","type":"exact"},{"name":"childhood testicular mixed germ cell neoplasm","type":"related"},{"name":"childhood testicular mixed germ cell tumor","type":"related"},{"name":"childhood testicular mixed germ cell tumour","type":"related"},{"name":"mixed testicular germ cell cancer of childhood","type":"exact"},{"name":"paediatric mixed testicular germ cell cancer","type":"exact"},{"name":"paediatric testicular mixed germ cell neoplasm","type":"related"},{"name":"paediatric testicular mixed germ cell tumour","type":"related"},{"name":"pediatric mixed testicular germ cell cancer","type":"exact"},{"name":"pediatric testicular mixed germ cell neoplasm","type":"related"},{"name":"pediatric testicular mixed germ cell tumor","type":"related"}],"termid":"MONDO:0003787","xrefs":{"Monarch":{"xref_id":"0003787"}}}


id: GO:0030116
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A growth factor that binds selectively and non-covalently to glial cell-derived neurotrophic factor receptors.","definition_xrefs":["GOC:vw","PMID:11476867"],"direct_ancestors":[{"relation_name":"is_a","term_name":"growth factor receptor binding","termid":"GO:0070851"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"glial cell-derived neurotrophic factor receptor binding","synonyms":[{"name":"glial cell line-derived neurotrophic factor receptor binding","type":"related"},{"name":"glial cell line-derived neurotrophic factor receptor ligand","type":"narrow"}],"termid":"GO:0030116"}


id: MONDO:0007152
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any arrhythmogenic right ventricular cardiomyopathy in which the cause of the disease is a mutation in the TGFB3 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"familial isolated arrhythmogenic ventricular dysplasia, left dominant form","termid":"MONDO:0017401"},{"relation_name":"excluded_subClassOf","term_name":"familial isolated arrhythmogenic ventricular dysplasia, biventricular form","termid":"MONDO:0017402"},{"relation_name":"excluded_subClassOf","term_name":"familial isolated arrhythmogenic ventricular dysplasia, right dominant form","termid":"MONDO:0017403"},{"relation_name":"is_a","term_name":"familial isolated arrhythmogenic right ventricular dysplasia","termid":"MONDO:0016342"}],"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":"arrhythmogenic right ventricular dysplasia 1","secondary_identifiers":["MEDGEN:349530","DOID:0110070","OMIM:107970","UMLS:C1862511"],"synonyms":[{"name":"ARVC1","type":"exact"},{"name":"ARVD1","type":"exact"},{"name":"TGFB3 arrhythmogenic right ventricular cardiomyopathy","type":"exact"},{"name":"Uhl anomaly","type":"related"},{"name":"arrhythmogenic right ventricular cardiomyopathy 1","type":"exact"},{"name":"arrhythmogenic right ventricular cardiomyopathy caused by mutation in TGFB3","type":"exact"},{"name":"arrhythmogenic right ventricular dysplasia type 1","type":"exact"},{"name":"arrhythmogenic right ventricular dysplasia, familial, 1","type":"related"},{"name":"arrhythmogenic right ventricular dysplasia, familial, type 1","type":"exact"},{"name":"cardiomyopathy, right ventricular dilated","type":"related"},{"name":"familial arrhythmogenic right ventricular dysplasia 1","type":"exact"}],"termid":"MONDO:0007152","xrefs":{"Monarch":{"xref_id":"0007152"}}}


id: PBO:0046899
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 21 member F, pseudogene","termid":"PBO:0046899"}


id: PBO:0091342
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by human BCL2","termid":"PBO:0091342"}


id: MONDO:0007757
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hyperkeratosis-hyperpigmentation syndrome describes a very rare hyperpigmentation of the skin characterized by tiny hyperpigmented spots mainly on skin exposed to sunlight, together with mild punctate palmoplantar papular hyperkeratosis as a major feature. There have been no further descriptions in the literature since 1993.","definition_xrefs":["Orphanet:1336"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"hyperpigmentation of the skin","termid":"MONDO:0019289"},{"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:0000426"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0000426"],"is_obsolete":false,"name":"hyperkeratosis-hyperpigmentation syndrome","secondary_identifiers":["UMLS:C1840428","OMIM:144190","GARD:16563","MEDGEN:326735","MESH:C564172"],"synonyms":[{"name":"hyperkeratosis-hyperpigmentation syndrome","type":"exact"}],"termid":"MONDO:0007757","xrefs":{"Monarch":{"xref_id":"0007757"}}}


id: PBO:0040658
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Bardet-Biedl syndrome 2","termid":"PBO:0040658"}


id: PBO:0079198
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TSPY like 1","termid":"PBO:0079198"}


id: FYPO:0000551
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which pseudohyphal growth does not occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal pseudohyphal growth","termid":"FYPO:0000550"},{"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:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"pseudohyphal growth abolished","secondary_identifiers":["FYPO:0000436"],"synonyms":[{"name":"abolished filamentous growth","type":"broad"},{"name":"abolished pseudohyphal growth","type":"exact"},{"name":"absent filamentous growth","type":"broad"},{"name":"absent pseudohyphal growth","type":"exact"},{"name":"filamentous growth abolished","type":"broad"},{"name":"filamentous growth: absent","type":"broad"},{"name":"pseudohyphal growth: absent","type":"related"}],"termid":"FYPO:0000551"}


id: MOD:01616
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively cross-links two L-cysteine residues and adds three sulfur atoms to form trithiocystine.","definition_xrefs":["RESID:AA0513","PubMed:19438211"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polysulfide crosslinked residues","termid":"MOD:01620"}],"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":"trithiocystine","synonyms":[{"name":"(2R,2'R)-3,3'-pentasulfane-1,5-diylbis(2-aminopropanoic acid)","type":"exact"},{"name":"3,3'-pentathiobisalanine","type":"exact"},{"name":"bis(2-amino-2-carboxyethyl)pentasulfide","type":"exact"},{"name":"trithiocystine","type":"exact"}],"termid":"MOD:01616"}


id: PBO:0062188
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 P member 4","termid":"PBO:0062188"}


id: PR:O14276
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- fyv7 gene.","definition_xrefs":["UniProtKB:O14276","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":"rRNA-processing protein fyv7 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC8C9.07","synonyms":[{"name":"Spom972h-fyv7","type":"exact"}],"termid":"PR:O14276"}


id: MONDO:0000042
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hyperprolinemia (obsolete MONDO:0000042)","termid":"MONDO:0000042","xrefs":{"Monarch":{"xref_id":"0000042"}}}


id: GO:0014717
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of satellite cell activation. The satellite cell activation is the process that initiates satellite cell division by causing it to move from quiescence to the G1 stage of the cell cycle. The cell swells and there are a number of other small changes. The cells then start to divide. Following cell division the cells will differentiate.","definition_xrefs":["GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of skeletal muscle tissue regeneration","termid":"GO:0043416"},{"relation_name":"is_a","term_name":"regulation of cell activation","termid":"GO:0050865"},{"relation_name":"regulates","term_name":"satellite cell activation involved in skeletal muscle regeneration","termid":"GO:0014901"}],"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 satellite cell activation involved in skeletal muscle regeneration","termid":"GO:0014717"}


id: PATO:0001490
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A growth quality of a process inhering in an organism, structure, or group of organisms by virtue of the bearer's reduced or increased growth.","definition_xrefs":["PATOC:MAH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"growth quality of occurrent","termid":"PATO:0001433"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterochronic growth","termid":"PATO:0001490"}


id: PBO:0088618
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial respiratory chain complex II assembly factor 4 Sdh8","termid":"PBO:0088618"}


id: GO:1990718
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Part of the 9+2 axoneme, that occurs in most motile cilia, consisting of the projections off of the central pair of single microtubules.","definition_xrefs":["PMID:9295136","GOC:cilia","PMID:21586547"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"axonemal central apparatus","termid":"GO:1990716"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0005737"],"is_obsolete":false,"name":"axonemal central pair projection","termid":"GO:1990718"}


id: PBO:0071046
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 48","termid":"PBO:0071046"}


id: GO:0050452
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: CoA + glutathione + NADP+ = CoA-glutathione + NADPH + H+.","definition_xrefs":["RHEA:14617"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on a sulfur group of donors, NAD(P) as acceptor","termid":"GO:0016668"}],"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":"CoA-glutathione reductase (NADPH) activity","secondary_identifiers":["EC:1.8.1.10","MetaCyc:COA-GLUTATHIONE-REDUCTASE-NADPH-RXN"],"synonyms":[{"name":"CoA-glutathione reductase (NADP) activity","type":"exact"},{"name":"CoA-glutathione reductase activity","type":"broad"},{"name":"NADPH-dependent coenzyme A-SS-glutathione reductase activity","type":"exact"},{"name":"NADPH:CoA-glutathione oxidoreductase activity","type":"exact"},{"name":"coenzyme A disulfide-glutathione reductase activity","type":"broad"},{"name":"coenzyme A glutathione disulfide reductase activity","type":"broad"},{"name":"glutathione:NADP+ oxidoreductase (CoA-acylating)","type":"exact"}],"termid":"GO:0050452"}


id: PBO:0070686
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7 pseudogene 57","termid":"PBO:0070686"}


id: MONDO:0002935
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A basal cell carcinoma of the penis with an indolent clinical course. It is usually superficial and arises from the shaft and rarely the glans.","definition_xrefs":["NCIT:C39961"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skin basal cell carcinoma","termid":"MONDO:0005341"},{"relation_name":"is_a","term_name":"squamous cell carcinoma of penis","termid":"MONDO:0018352"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005093"],"is_obsolete":false,"name":"penis basal cell carcinoma","secondary_identifiers":["UMLS:C1518949","DOID:4277","MEDGEN:275349"],"synonyms":[{"name":"basal cell carcinoma of the penis","type":"exact"},{"name":"penile basal cell cancer","type":"exact"},{"name":"penile basal cell carcinoma","type":"exact"},{"name":"penis skin basal cell carcinoma","type":"exact"},{"name":"skin basal cell carcinoma of penis","type":"exact"},{"name":"skin of penis skin basal cell carcinoma","type":"exact"}],"termid":"MONDO:0002935","xrefs":{"Monarch":{"xref_id":"0002935"}}}


id: PBO:0026736
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_mitotic_cell_cycle_regulation_upon_nitrogen_source_shift","termid":"PBO:0026736"}


id: RO:0002087
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","direct_ancestors":[{"relation_name":"is_a","term_name":"preceded_by","termid":"BFO:0000062"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immediately_preceded_by","termid":"RO:0002087"}


id: MONDO:0011573
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"psoriasis, susceptibility to","termid":"MONDO:0100171"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"psoriasis 7, susceptibility to","secondary_identifiers":["DOID:0111279","OMIM:605606","UMLS:C1854124","MEDGEN:343057"],"synonyms":[{"name":"PSORS7","type":"exact"},{"name":"psoriasis 7, susceptibility to","type":"exact"},{"name":"psoriasis susceptibility 7","type":"exact"},{"name":"psoriasis, protection against","type":"exact"}],"termid":"MONDO:0011573","xrefs":{"Monarch":{"xref_id":"0011573"}}}


id: PBO:0073860
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 9 member A8","termid":"PBO:0073860"}


id: PATO:0002245
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A force which relative high.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"increased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"force","termid":"PATO:0001035"},{"relation_name":"is_a","term_name":"increased object quality","termid":"PATO:0002305"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased force","synonyms":[{"name":"increased force amplitude","type":"exact"}],"termid":"PATO:0002245"}


id: PBO:0060288
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myosin light chain 5","termid":"PBO:0060288"}


id: PATO:0000935
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000935 relative photosensitivity (obsolete PATO:0000935)","termid":"PATO:0000935"}


id: GO:0080049
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-gulono-1,4-lactone + 2 ferricytochrome c = L-ascorbate + 2 ferrocytochrome c.","definition_xrefs":["PMID:18190525","PMID:30112455","RHEA:47248"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-CH group of donors, cytochrome as acceptor","termid":"GO:0016632"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"L-gulono-1,4-lactone dehydrogenase activity","secondary_identifiers":["MetaCyc:RXN-1439"],"termid":"GO:0080049"}


id: PBO:0053658
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 824","termid":"PBO:0053658"}


id: PBO:0061179
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear-encoded mitochondrial tRNA-Gln (TTG) 9-1","termid":"PBO:0061179"}


id: PBO:0113972
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fungal protein, conserved in ascomycetes","termid":"PBO:0113972"}


id: PBO:0066102
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAS and EF-hand domain containing","termid":"PBO:0066102"}


id: GO:1903528
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of dCDP biosynthetic process.","definition_xrefs":["GOC:TermGenie","PMID:16317005","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of pyrimidine nucleotide biosynthetic process","termid":"GO:1900397"},{"relation_name":"regulates","term_name":"dCDP biosynthetic process","termid":"GO:0006240"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0008150","GO:0055086","GO:0044281"],"is_obsolete":false,"name":"regulation of dCDP biosynthetic process","synonyms":[{"name":"regulation of dCDP anabolism","type":"exact"},{"name":"regulation of dCDP biosynthesis","type":"exact"},{"name":"regulation of dCDP formation","type":"exact"},{"name":"regulation of dCDP synthesis","type":"exact"}],"termid":"GO:1903528"}


id: MONDO:0859371
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rhabdomyolysis, susceptibility to, 1","secondary_identifiers":["UMLS:C5774307","MEDGEN:1824080","OMIM:620235"],"termid":"MONDO:0859371","xrefs":{"Monarch":{"xref_id":"0859371"}}}


id: GO:1902079
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of D-valine.","definition_xrefs":["GOC:TermGenie","PMID:23085840"],"direct_ancestors":[{"relation_name":"is_a","term_name":"branched-chain amino acid catabolic process","termid":"GO:0009083"},{"relation_name":"is_a","term_name":"D-amino acid catabolic process","termid":"GO:0019478"},{"relation_name":"is_a","term_name":"D-valine metabolic process","termid":"GO:1902114"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006520","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"D-valine catabolic process","synonyms":[{"name":"D-valine breakdown","type":"exact"},{"name":"D-valine catabolism","type":"exact"},{"name":"D-valine degradation","type":"exact"}],"termid":"GO:1902079"}


id: FYPO:0005261
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A vegetative cell population growth phenotype in which cell growth is increased relative to normal in a medium containing galactose as the carbon source.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased vegetative cell population growth","termid":"FYPO:0004557"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0002058","FYPO:0001985","FYPO:0002057","FYPO:0000003","FYPO:0005447"],"is_obsolete":false,"name":"increased cell population growth on galactose carbon source","synonyms":[{"name":"increased growth on galactose carbon source","type":"broad"},{"name":"increased vegetative cell growth on galactose carbon source","type":"exact"}],"termid":"FYPO:0005261"}


id: MONDO:0021511
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that involves the adrenal gland.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign endocrine neoplasm","termid":"MONDO:0000627"},{"relation_name":"is_a","term_name":"adrenal gland neoplasm","termid":"MONDO:0021227"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign neoplasm of adrenal gland","secondary_identifiers":["NCIT:C3629","ICD10CM:D35.0","SCTID:91967007","MEDGEN:56330","icd11.foundation:2121003176","UMLS:C0154040","ICD9:227.0"],"synonyms":[{"name":"adrenal gland benign neoplasm","type":"exact"},{"name":"benign adrenal gland neoplasm","type":"exact"},{"name":"benign adrenal gland tumor","type":"exact"},{"name":"benign adrenal gland tumour","type":"exact"},{"name":"benign adrenal neoplasm","type":"exact"},{"name":"benign adrenal tumor","type":"exact"},{"name":"benign adrenal tumour","type":"exact"},{"name":"benign neoplasm of the adrenal gland","type":"exact"},{"name":"benign tumor of adrenal gland","type":"exact"},{"name":"benign tumor of the adrenal gland","type":"exact"},{"name":"benign tumour of adrenal gland","type":"exact"},{"name":"benign tumour of the adrenal gland","type":"exact"}],"termid":"MONDO:0021511","xrefs":{"Monarch":{"xref_id":"0021511"}}}


id: PBO:0067780
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 80","termid":"PBO:0067780"}


id: FYPO:0004856
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of glucan endo-1,6-beta-glucosidase activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal catalytic activity","termid":"FYPO:0000661"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000654","FYPO:0001985","FYPO:0000661","FYPO:0000652","FYPO:0000707"],"is_obsolete":false,"name":"abnormal endo-1,6-beta-glucosidase activity","synonyms":[{"name":"abnormal glucan endo-1,6-beta-glucosidase activity","type":"exact"}],"termid":"FYPO:0004856"}


id: PBO:0048343
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 54","termid":"PBO:0048343"}


id: GO:1990793
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The controlled release of substance P by a cell, in which the substance P acts as a neurotransmitter.","definition_xrefs":["PMID:15292051"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neurotransmitter secretion","termid":"GO:0007269"},{"relation_name":"is_a","term_name":"substance P secretion","termid":"GO:1990772"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"substance P secretion, neurotransmission","termid":"GO:1990793"}


id: GO:0000444
data:
  {"annotated_genes":["SJAG_03220","SJAG_02346","SJAG_01228","SJAG_00418"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[60783,71613,76068,81639],"is_not":false,"summary":null,"term":"GO:0000444"}]},"cv_name":"cellular_component","definition":"A multiprotein kinetochore subcomplex that binds to centromeric chromatin and forms part of the outer kinetochore. It helps to recruit outer kinetochore subunits that will bind to microtubules. In humans, it consists of MIS12, DSN1, NSL1 and PMF1.","definition_xrefs":["PMID:16585270","GOC:krc","PMID:14633972"],"direct_ancestors":[{"relation_name":"is_a","term_name":"outer kinetochore","termid":"GO:0000940"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00418":null,"SJAG_01228":null,"SJAG_02346":null,"SJAG_03220":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"part_of","termid":"GO:0000776"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005694","GO:0000776","GO:0005575"],"is_obsolete":false,"name":"MIS12/MIND type complex","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null},"secondary_identifiers":["GO:0000818"],"synonyms":[{"name":"MIND complex","type":"exact"},{"name":"Mis12 complex","type":"narrow"},{"name":"Mtw1p Including Nnf1p-Nsl1p-Dsn1p complex","type":"related"},{"name":"nuclear MIS12/MIND complex","type":"related"}],"termid":"GO:0000444","terms_by_termid":{"GO:0000444":null}}


id: GO:0030955
data:
  {"annotated_genes":["SJAG_02796"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[70421],"is_not":false,"summary":null,"term":"GO:0030955"}]},"cv_name":"molecular_function","definition":"Binding to a potassium ion (K+).","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alkali metal ion binding","termid":"GO:0031420"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02796":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0046872"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0046872","GO:0005488"],"is_obsolete":false,"name":"potassium ion binding","references_by_uniquename":{"GO_REF:0000002":null},"synonyms":[{"name":"K ion binding","type":"exact"}],"termid":"GO:0030955","terms_by_termid":{"GO:0030955":null}}


id: PBO:0056602
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MDM4 regulator of p53","termid":"PBO:0056602"}


id: PBO:0027567
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_centromere_central_core","termid":"PBO:0027567"}


id: FYPO:0007925
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to a combination of sodium chloride and methyl methanesulfonate. Cells stop growing (and may die) at concentrations of sodium chloride and methyl methanesulfonate that allow wild type cells to grow.","definition_xrefs":["PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000003","FYPO:0002683","FYPO:0000139","FYPO:0001985"],"is_obsolete":false,"name":"sensitive to sodium chloride and methyl methanesulfonate","synonyms":[{"name":"sensitive to sodium chloride and methyl methanesulfonate  during vegetative growth","type":"exact"}],"termid":"FYPO:0007925"}


id: PBO:0087568
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of TFIID, TFIIF, INO80, SWI/SNF, and NuA3 complexes; involved in RNA polymerase II transcription initiation and in chromatin modification; contains a YEATS domain","termid":"PBO:0087568"}


id: FYPO:0001245
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 cobalt ions.","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:0001985"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0002683","FYPO:0001985","FYPO:0000139","FYPO:0005447"],"is_obsolete":false,"name":"sensitive to cobalt","synonyms":[{"name":"hypersensitive to cobalt","type":"exact"},{"name":"sensitive to cobalt during mitotic cell cycle","type":"related"},{"name":"sensitive to cobalt during vegetative growth","type":"exact"},{"name":"sensitive to cobalt ions","type":"exact"}],"termid":"FYPO:0001245"}


id: PR:Q9Y7S9
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- aah3 gene.","definition_xrefs":["UniProtKB:Q9Y7S9","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":"alpha-amylase 3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC63.02c","synonyms":[{"name":"1,4-alpha-D-glucan glucanohydrolase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-aah3","type":"exact"}],"termid":"PR:Q9Y7S9"}


id: MONDO:0006665
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Atrophic gastritis that is persistent and long-standing.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chronic gastritis","termid":"MONDO:0005001"}],"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 atrophic gastritis","secondary_identifiers":["ICD9:535.11","MedDRA:10003685","SCTID:84568007","ICD9:535.10","DOID:8929","EFO:1000826","MEDGEN:42157","MESH:D005757","UMLS:C0017154","NCIT:C7405","ICD10CM:K29.4","ICD9:535.1"],"synonyms":[{"name":"Gastritides, atrophic","type":"exact"},{"name":"atrophic Gastritides","type":"exact"},{"name":"atrophic gastritis","type":"exact"},{"name":"gastric atrophy","type":"exact"}],"termid":"MONDO:0006665","xrefs":{"Monarch":{"xref_id":"0006665"}}}


id: PATO:0001693
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A viscosity which relatively high.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"increased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"viscous","termid":"PATO:0000998"},{"relation_name":"is_a","term_name":"increased object quality","termid":"PATO:0002305"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased viscosity","synonyms":[{"name":"high viscosity","type":"exact"}],"termid":"PATO:0001693"}


id: PBO:0060828
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nectin cell adhesion molecule 3","termid":"PBO:0060828"}


id: GO:0050223
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 3,4-dihydroxybenzoate + H+ = catechol + CO2.","definition_xrefs":["RHEA:22416","EC:4.1.1.63"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxy-lyase activity","termid":"GO:0016831"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0003674","GO:0016829","GO:0003824"],"is_obsolete":false,"name":"protocatechuate decarboxylase activity","secondary_identifiers":["MetaCyc:PROTOCATECHUATE-DECARBOXYLASE-RXN","KEGG_REACTION:R00822"],"synonyms":[{"name":"3,4-dihydrobenzoate decarboxylase activity","type":"related"},{"name":"3,4-dihydroxybenzoate carboxy-lyase (catechol-forming)","type":"related"},{"name":"3,4-dihydroxybenzoate decarboxylase activity","type":"related"},{"name":"protocatechuate carboxy-lyase activity","type":"related"}],"termid":"GO:0050223"}


id: SO:0002320
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant that leads to a change in the location of a termination codon in a transcript but allows the transcript to escape nonsense-mediated decay (NMD). The change in location of a termination codon can be caused by several different types of sequence variants, including stop_gained (SO:0001587), frameshift_variant (SO:0001589), splice_donor_variant (SO:0001575), and splice_acceptor_variant (SO:0001574) types of variants.","definition_xrefs":["GenCC:AR"],"direct_ancestors":[{"relation_name":"is_a","term_name":"functionally_abnormal","termid":"SO:0002218"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NMD_escaping_variant","synonyms":[{"name":"NMD escaping variant","type":"exact"},{"name":"nonsense-mediated decay escaping variant","type":"exact"}],"termid":"SO:0002320"}


id: PBO:0078281
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Cys (anticodon GCA) 14-1","termid":"PBO:0078281"}


id: PBO:0030569
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_cellular_glutamine_level","termid":"PBO:0030569"}


id: GO:0000731
data:
  {"annotated_genes":["SJAG_00573","SJAG_04877","SJAG_03906","SJAG_00611","SJAG_05197","SJAG_04791","SJAG_00153","SJAG_04089","SJAG_00406","SJAG_02818","SJAG_02199","SJAG_16460","SJAG_02667","SJAG_00814","SJAG_04190"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[80321],"is_not":false,"summary":null,"term":"GO:0000731"},{"annotations":[104648,78623,110949,97053],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904161"},{"annotations":[104699,68155,61619,101118,58950,72185],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070987"},{"annotations":[104700,97692,74988,79717,106045,76694,79418,72183],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042276"},{"annotations":[113612],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1904332"},{"annotations":[100119],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019985"}]},"cv_name":"biological_process","definition":"Synthesis of DNA that proceeds from the broken 3' single-strand DNA end and uses the homologous intact duplex as the template.","definition_xrefs":["PMID:10357855"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA biosynthetic process","termid":"GO:0071897"},{"relation_name":"part_of","term_name":"DNA repair","termid":"GO:0006281"}],"gene_count":15,"genes_by_uniquename":{"SJAG_00153":null,"SJAG_00406":null,"SJAG_00573":null,"SJAG_00611":null,"SJAG_00814":null,"SJAG_02199":null,"SJAG_02667":null,"SJAG_02818":null,"SJAG_03906":null,"SJAG_04089":null,"SJAG_04190":null,"SJAG_04791":null,"SJAG_04877":null,"SJAG_05197":null,"SJAG_16460":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006259"},{"rel_name":"part_of","termid":"GO:0006281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006281","GO:0008150","GO:0006259"],"is_obsolete":false,"name":"DNA synthesis involved in DNA repair","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"DNA repair synthesis","type":"broad"},{"name":"DNA synthesis during DNA repair","type":"related"},{"name":"mitotic DNA repair synthesis","type":"narrow"}],"termid":"GO:0000731","terms_by_termid":{"GO:0000731":null,"GO:0019985":null,"GO:0042276":null,"GO:0070987":null,"GO:1904161":null,"GO:1904332":null}}


id: GO:0034876
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: isoniazid + H2O = isonicotinate + hydrazine.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete isonicotinic acid hydrazide hydrolase activity (obsolete GO:0034876)","termid":"GO:0034876"}


id: PBO:0018174
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"structure-specific DNA nuclease regulator Pxd1","termid":"PBO:0018174"}


id: PBO:0080966
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger and BTB domain containing 7C","termid":"PBO:0080966"}


id: SO:0001590
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant whereby at least one of the bases in the terminator codon is changed.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"coding_sequence_variant","termid":"SO:0001580"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"terminator_codon_variant","secondary_identifiers":["http://vat.gersteinlab.org/formats.php","SO:0001625","loinc:LA6700-2"],"synonyms":[{"name":"VAT:endOverlap","type":"exact"},{"name":"terminal codon variant","type":"exact"},{"name":"terminal_codon_variant","type":"exact"},{"name":"terminator codon variant","type":"exact"}],"termid":"SO:0001590"}


id: GO:0035784
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process involved in the maintenance of an internal steady state of nickel cations within an organism or cell.","definition_xrefs":["GOC:kmv"],"gene_count":0,"genotype_count":0,"name":"obsolete nickel cation homeostasis (obsolete GO:0035784)","synonyms":[{"name":"nickel homeostasis","type":"exact"}],"termid":"GO:0035784"}


id: GO:1904345
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of gastric mucosal blood circulation.","definition_xrefs":["GOC:TermGenie","PMID:10807413","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of blood circulation","termid":"GO:1903523"},{"relation_name":"is_a","term_name":"regulation of gastric mucosal blood circulation","termid":"GO:1904344"},{"relation_name":"negatively_regulates","term_name":"gastric mucosal blood circulation","termid":"GO:1990768"}],"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 gastric mucosal blood circulation","synonyms":[{"name":"down regulation of gastric mucosal blood circulation","type":"exact"},{"name":"down regulation of stomach mucosal blood circulation","type":"exact"},{"name":"down-regulation of gastric mucosal blood circulation","type":"exact"},{"name":"down-regulation of stomach mucosal blood circulation","type":"exact"},{"name":"downregulation of gastric mucosal blood circulation","type":"exact"},{"name":"downregulation of stomach mucosal blood circulation","type":"exact"},{"name":"inhibition of gastric mucosal blood circulation","type":"narrow"},{"name":"inhibition of stomach mucosal blood circulation","type":"narrow"},{"name":"negative regulation of stomach mucosal blood circulation","type":"exact"}],"termid":"GO:1904345"}


id: MONDO:0033541
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"immunodeficiency disease","termid":"MONDO:0021094"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"immunodeficiency 69","secondary_identifiers":["OMIM:618963","MEDGEN:1735911","UMLS:C5436498","DOID:0112006"],"synonyms":[{"name":"IMD69","type":"related"},{"name":"IMMUNODEFICIENCY 69","type":"related"},{"name":"Ifng Deficiency, Autosomal Recessive","type":"related"},{"name":"Immunodeficiency 69, Mycobacteriosis, Autosomal Recessive","type":"related"},{"name":"immunodeficiency 69, mycobacteriosis","type":"exact"}],"termid":"MONDO:0033541","xrefs":{"Monarch":{"xref_id":"0033541"}}}


id: GO:0002276
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A change in morphology and behavior of a basophil resulting from exposure to a cytokine, chemokine, soluble factor, or to (at least in mammals) an antigen which the basophil has specifically bound via IgE bound to Fc-epsilonRI receptors, leading to the initiation or perpetuation of an immune response.","definition_xrefs":["ISBN:0781735149","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukocyte activation involved in immune response","termid":"GO:0002366"},{"relation_name":"is_a","term_name":"basophil activation","termid":"GO:0045575"},{"relation_name":"part_of","term_name":"myeloid cell activation involved in immune response","termid":"GO:0002275"}],"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":"basophil activation involved in immune response","synonyms":[{"name":"basophil activation during immune response","type":"related"}],"termid":"GO:0002276"}


id: GO:0046375
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving K antigen, a capsular polysaccharide antigen carried on the surface of bacterial capsules that masks somatic (O) antigens.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"macromolecule metabolic process","termid":"GO:0043170"},{"relation_name":"is_a","term_name":"carbohydrate derivative metabolic process","termid":"GO:1901135"}],"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":"K antigen metabolic process","synonyms":[{"name":"K antigen metabolism","type":"exact"}],"termid":"GO:0046375"}


id: PBO:0063381
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"programmed cell death 1 ligand 2","termid":"PBO:0063381"}


id: MOD:00805
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-serine residue to O3-(N-acetylaminoglucosyl)-L-serine.","definition_xrefs":["PubMed:3086323","RESID:AA0398","PubMed:8404891"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-acetylaminoglucosylated residue","termid":"MOD:00448"},{"relation_name":"is_a","term_name":"O-(N-acetylamino)hexosyl-L-serine","termid":"MOD:01675"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00764"}],"interesting_parent_ids":["MOD:00764"],"is_obsolete":false,"name":"O-(N-acetylamino)glucosyl-L-serine","synonyms":[{"name":"(2S)-2-amino-3-(2-acetamido-2-deoxy-beta-D-glucopyranosyloxy)propanoic acid","type":"exact"},{"name":"CARBOHYD O-linked (GlcNAc) serine","type":"exact"},{"name":"CARBOHYD O-linked (HexNAc)","type":"exact"},{"name":"HexNAc","type":"related"},{"name":"O-(2-acetylamino-2-deoxy-beta-D-glucopyranosyl)-L-serine","type":"exact"},{"name":"O-(N-acetylamino)glucosyl-L-serine","type":"exact"},{"name":"O-(N-acetylglucosaminyl)serine","type":"exact"},{"name":"O-glycosylserine","type":"exact"},{"name":"O-seryl-beta-N-acetylglucosaminide","type":"exact"},{"name":"O3-(2-acetamido-2-deoxy-beta-D-glucopyranosyl)-L-serine","type":"exact"},{"name":"O3-(N-acetylglucosaminyl)serine","type":"exact"},{"name":"OGlcNAcSer","type":"exact"}],"termid":"MOD:00805"}


id: PBO:0068290
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribonuclease L","termid":"PBO:0068290"}


id: GO:0003361
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of an noradrenergic neuron that is part of the brainstem.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"noradrenergic neuron differentiation","termid":"GO:0003357"},{"relation_name":"part_of","term_name":"brainstem development","termid":"GO:0003360"}],"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":"noradrenergic neuron differentiation involved in brainstem development","termid":"GO:0003361"}


id: PBO:0084269
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Integral membrane protein; localized to late Golgi vesicles along with the v-SNARE Tlg2p; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm in a punctate pattern","termid":"PBO:0084269"}


id: GO:0062194
data:
  {"annotated_genes":["SJAG_04841"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[99078],"is_not":false,"summary":null,"term":"GO:0062194"}]},"cv_name":"cellular_component","definition":"A microtubule minus end that is part of a cytoplasmic microtubule.","definition_xrefs":["PMID:18061564"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microtubule minus-end","termid":"GO:0036449"},{"relation_name":"part_of","term_name":"cytoplasmic microtubule","termid":"GO:0005881"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04841":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0015630"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0015630"],"is_obsolete":false,"name":"cytoplasmic microtubule minus-end","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0062194","terms_by_termid":{"GO:0062194":null}}


id: PBO:0017849
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fatty acid amide hydrolase Fah1 (predicted)","termid":"PBO:0017849"}


id: PBO:0040912
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BMS1 pseudogene 16","termid":"PBO:0040912"}


id: PBO:0076945
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transferrin receptor","termid":"PBO:0076945"}


id: PBO:0016566
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pombe Unidentified Cyclin","termid":"PBO:0016566"}


id: PR:000044743
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An E3 ubiquitin-protein ligase dma1 (Schizosaccharomyces pombe) that lacks ubiquitinated lysine.","definition_xrefs":["PMID:29975113","PomBase:VW","PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"E3 ubiquitin-protein ligase dma1","termid":"PR:000027845"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dma1/UnUbiq","pombase_gene_id":"SPAC17G8.10c","synonyms":[{"name":"PomBase_original_PRO_term_name: E3 ubiquitin-protein ligase dma1 non-ubiquitinated form (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-dma1/UnUbiq","type":"exact"},{"name":"dma1/UnUbiq","type":"exact"}],"termid":"PR:000044743"}


id: GO:0071687
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The part of the horsetail nucleus where telomeres cluster under the SPB and that leads horsetail movement. The horsetail nucleus is the elongated nucleus which forms during the rapid oscillatory movement at meiotic prophase; characterized in Schizosaccharomyces pombe.","definition_xrefs":["GOC:mah","PMID:15030757","GOC:vw"],"gene_count":0,"genotype_count":0,"name":"obsolete horsetail nucleus leading edge (obsolete GO:0071687)","termid":"GO:0071687"}


id: PBO:0052329
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KIAA1614 antisense RNA 1","termid":"PBO:0052329"}


id: PBO:0082665
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the conserved R2TP complex (Rvb1-Rvb2-Tah1-Pih1); R2TP complex interacts with Hsp90 (Hsp82p and Hsc82p) to mediate assembly large protein complexes such as box C/D snoRNPs and RNA polymerase II","termid":"PBO:0082665"}


id: MONDO:0700130
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A chromosomal disorder consisting of the partial duplication of chromosome 21.","definition_xrefs":["PMID:29218069"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndrome caused by partial chromosomal duplication","termid":"MONDO:0000762"},{"relation_name":"is_a","term_name":"Down syndrome","termid":"MONDO:0008608"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partial segmental duplication","synonyms":[{"name":"partial trisomy 21","type":"exact"},{"name":"segmental duplication","type":"broad"}],"termid":"MONDO:0700130","xrefs":{"Monarch":{"xref_id":"0700130"}}}


id: PBO:0086671
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; identified by fungal homology comparisons and RT-PCR; identified in a screen for mutants with decreased levels of rDNA transcription","termid":"PBO:0086671"}


id: PBO:0065891
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB38, member RAS oncogene family","termid":"PBO:0065891"}


id: PBO:0000063
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"no detectable long open reading frame","termid":"PBO:0000063"}


id: PATO:0002310
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in a bearer by virtue of the bearer's being strong, thick or sturdy.","definition_xrefs":["PATOC:BF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"shape","termid":"PATO:0000052"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"robust","termid":"PATO:0002310"}


id: PBO:0058534
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6079","termid":"PBO:0058534"}


id: MONDO:0002701
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An invasive cystic adenocarcinoma arising from the ovary. It is characterized by the presence of malignant glandular epithelial cells which contain intracytoplasmic mucin. The malignant cells invade the ovarian stroma and the cystic spaces contain mucoid material. In a minority of cases both ovaries are involved by the tumor. The prognosis for stage I tumors is excellent. Patients with metastases usually have a poor prognosis.","definition_xrefs":["NCIT:C4026"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ovarian cystadenocarcinoma","termid":"MONDO:0002702"},{"relation_name":"is_a","term_name":"ovarian mucinous adenocarcinoma","termid":"MONDO:0005601"},{"relation_name":"is_a","term_name":"mucinous cystadenocarcinoma","termid":"MONDO:0005858"}],"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":"ovarian mucinous cystadenocarcinoma","secondary_identifiers":["MEDGEN:76011","SCTID:254851009","DOID:3604","UMLS:C0279665","EFO:1001963"],"synonyms":[{"name":"mucinous cystadenocarcinoma of ovary","type":"exact"},{"name":"mucinous cystadenocarcinoma of the ovary","type":"exact"},{"name":"ovarian mucinous cystadenocarcinoma","type":"exact"},{"name":"ovary mucinous cystadenocarcinoma","type":"exact"}],"termid":"MONDO:0002701","xrefs":{"Monarch":{"xref_id":"0002701"}}}


id: MONDO:0006150
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare Burkitt lymphoma that arises from the colon.","definition_xrefs":["NCIT:C27465"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune system cancer","termid":"MONDO:0000621"},{"relation_name":"is_a","term_name":"colon lymphoma","termid":"MONDO:0002035"},{"relation_name":"is_a","term_name":"Burkitt lymphoma","termid":"MONDO:0007243"},{"relation_name":"is_a","term_name":"familial colorectal cancer","termid":"MONDO:0023113"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005570","MONDO:0004335","MONDO:0005046"],"is_obsolete":false,"name":"colon Burkitt lymphoma","secondary_identifiers":["UMLS:C1333083","MEDGEN:272491"],"synonyms":[{"name":"Burkitt lymphoma of colon","type":"exact"},{"name":"Burkitts lymphoma of colon","type":"exact"},{"name":"colon Burkitt lymphoma","type":"exact"},{"name":"colon Burkitt's lymphoma","type":"exact"},{"name":"colon Burkitts lymphoma","type":"exact"},{"name":"primary colon Burkitt's lymphoma","type":"exact"}],"termid":"MONDO:0006150","xrefs":{"Monarch":{"xref_id":"0006150"}}}


id: PBO:0047404
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box protein 42","termid":"PBO:0047404"}


id: GO:0009341
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that possesses beta-galactosidase activity, i.e. catalyzes the hydrolysis of terminal non-reducing beta-D-galactose residues in beta-D-galactosides. In E. coli, the complex is a homotetramer; dimeric and hexameric beta-galactosidase complexes have been observed in other species.","definition_xrefs":["PMID:15950161"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catalytic complex","termid":"GO:1902494"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"beta-galactosidase complex","termid":"GO:0009341"}


id: GO:0051553
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of flavones, a class of pigmented plant compounds based on 2-phenyl-4H-1-benzopyran-4-one (2-phenylchromone).","definition_xrefs":["GOC:ai","PMID:18567791"],"direct_ancestors":[{"relation_name":"is_a","term_name":"flavonoid biosynthetic process","termid":"GO:0009813"},{"relation_name":"is_a","term_name":"pigment biosynthetic process","termid":"GO:0046148"},{"relation_name":"is_a","term_name":"flavone metabolic process","termid":"GO:0051552"}],"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":"flavone biosynthetic process","synonyms":[{"name":"2-phenyl-4H-1-benzopyran-4-one biosynthesis","type":"narrow"},{"name":"2-phenyl-4H-1-benzopyran-4-one biosynthetic process","type":"narrow"},{"name":"2-phenylchromone biosynthesis","type":"narrow"},{"name":"2-phenylchromone biosynthetic process","type":"narrow"}],"termid":"GO:0051553"}


id: GO:0044239
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of polysaccharides by salivary amylase. Salivary amylase is released by salivary glands, usually in the mouth.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete salivary polysaccharide catabolic process (obsolete GO:0044239)","synonyms":[{"name":"salivary polysaccharide breakdown","type":"exact"},{"name":"salivary polysaccharide catabolism","type":"exact"},{"name":"salivary polysaccharide degradation","type":"exact"}],"termid":"GO:0044239"}


id: GO:0075109
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process by which a symbiont alters or subverts a receptor-mediated signal transduction pathway in its host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host signal transduction pathway","termid":"GO:0052027"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated perturbation of host receptor-mediated signal transduction","synonyms":[{"name":"perturbation of host receptor-mediated signal transduction","type":"exact"}],"termid":"GO:0075109"}


id: GO:0060043
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cardiac muscle cell proliferation.","definition_xrefs":["GOC:rph","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell population proliferation","termid":"GO:0042127"},{"relation_name":"is_a","term_name":"regulation of cardiac muscle tissue growth","termid":"GO:0055021"},{"relation_name":"regulates","term_name":"cardiac muscle cell proliferation","termid":"GO:0060038"}],"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 muscle cell proliferation","synonyms":[{"name":"regulation of cardiomyocyte proliferation","type":"related"},{"name":"regulation of heart muscle cell proliferation","type":"exact"}],"termid":"GO:0060043"}


id: MONDO:0000824
data:
  {"annotated_genes":["SJAG_04049","SJAG_00938","SJAG_03011","SJAG_02463","SJAG_01941","SJAG_04059"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88225,88224],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014375"},{"annotations":[87267,87268],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008964"},{"annotations":[87101,87100],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009635"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"diarrheal disease","termid":"MONDO:0001673"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00938":null,"SJAG_01941":null,"SJAG_02463":null,"SJAG_03011":null,"SJAG_04049":null,"SJAG_04059":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"congenital diarrhea","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIMPS:214700","DOID:0060774"],"synonyms":[{"name":"diarrhea, congenital","type":"exact"}],"termid":"MONDO:0000824","terms_by_termid":{"MONDO:0008964":null,"MONDO:0009635":null,"MONDO:0014375":null},"xrefs":{"Monarch":{"xref_id":"0000824"}}}


id: PBO:0077018
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"THBS4 antisense RNA 1","termid":"PBO:0077018"}


id: PBO:0018150
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autophagy associated sorting nexin Atg20 (predicted)","termid":"PBO:0018150"}


id: PBO:0001201
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell wall protein Psu1, beta-glucosidase (predicted)","termid":"PBO:0001201"}


id: PBO:0072206
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S18 pseudogene 5","termid":"PBO:0072206"}


id: GO:2000896
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving an amylopectin.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"macromolecule metabolic process","termid":"GO:0043170"},{"relation_name":"is_a","term_name":"carbohydrate derivative metabolic process","termid":"GO:1901135"}],"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":"amylopectin metabolic process","synonyms":[{"name":"Amylopectin metabolism","type":"exact"}],"termid":"GO:2000896"}


id: PBO:0003844
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Blt1","termid":"PBO:0003844"}


id: PBO:0046943
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 66 member E","termid":"PBO:0046943"}


id: GO:0043626
data:
  {"annotated_genes":["SJAG_04190"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[72934],"is_not":false,"summary":null,"term":"GO:0043626"}]},"cv_name":"cellular_component","definition":"A protein complex composed of three identical PCNA monomers, each comprising two similar domains, which are joined in a head-to-tail arrangement to form a homotrimer. Forms a ring-like structure in solution, with a central hole sufficiently large to accommodate the double helix of DNA. Originally characterized as a DNA sliding clamp for replicative DNA polymerases and as an essential component of the replisome, and has also been shown to be involved in other processes including Okazaki fragment processing, DNA repair, translesion DNA synthesis, DNA methylation, chromatin remodeling and cell cycle regulation.","definition_xrefs":["PMID:12829735","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA polymerase processivity factor complex","termid":"GO:0044796"},{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04190":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005634","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"PCNA complex","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"PCNA homotrimer","type":"exact"},{"name":"proliferating cell nuclear antigen complex","type":"exact"},{"name":"sliding clamp","type":"broad"}],"termid":"GO:0043626","terms_by_termid":{"GO:0043626":null}}


id: MONDO:0850083
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"craniosynostosis","termid":"MONDO:0015469"}],"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":"non-syndromic bicoronal and sagittal craniosynostosis","secondary_identifiers":["Orphanet:620205","MEDGEN:1842401","UMLS:C5680391","GARD:22480"],"termid":"MONDO:0850083","xrefs":{"Monarch":{"xref_id":"0850083"}}}


id: MONDO:0060777
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A usually solitary polypoid lesion that arises from the cervix. It usually affects women in their reproductive years. It is characterized by the presence of a connective tissue core and overlying epithelium.","definition_xrefs":["NCIT:C40200"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cervical polyp","termid":"MONDO:0000751"},{"relation_name":"is_a","term_name":"fibroepithelial polyp","termid":"MONDO:0060765"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cervical fibroepithelial polyp","secondary_identifiers":["UMLS:C1516413","MEDGEN:308945"],"synonyms":[{"name":"Cervical fibroepithelial polyp","type":"exact"},{"name":"uterine cervix fibroepithelial polyp","type":"exact"}],"termid":"MONDO:0060777","xrefs":{"Monarch":{"xref_id":"0060777"}}}


id: PBO:0071160
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23","termid":"PBO:0071160"}


id: PBO:0035995
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_histone_H2A_phosphorylation_at_subtelomere_during_vegetative_growth","termid":"PBO:0035995"}


id: PBO:0056713
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MEMO1 pseudogene 5","termid":"PBO:0056713"}


id: MONDO:0009270
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Genitopalatocardiac syndrome is a rare, multiple congenital anomalies/dysmorphic syndrome characterized by male, 46,XY gonadal dysgenesis, cleft palate, micrognathia, conotruncal heart defects and unspecific skeletal, brain and kidney anomalies.","definition_xrefs":["Orphanet:2075"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endocrine system disorder","termid":"MONDO:0005151"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"genito-palato-cardiac syndrome","secondary_identifiers":["GARD:2460","icd11.foundation:2011995320","MEDGEN:341558","MESH:C537683","OMIM:231060","UMLS:C1856466"],"synonyms":[{"name":"GENITOPALATOCARDIAC syndrome","type":"related"},{"name":"Gardner-Silengo-Wachtel syndrome","type":"exact"},{"name":"Male pseudohermaphroditism with micrognathia, cleft palate, and conotruncal Cardiac defect","type":"related"},{"name":"genito palato cardiac syndrome","type":"related"}],"termid":"MONDO:0009270","xrefs":{"Monarch":{"xref_id":"0009270"}}}


id: MONDO:0971145
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"peritoneal mesothelioma","termid":"MONDO:0006362"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peritoneal mesothelioma in situ","secondary_identifiers":["MEDGEN:1864253","Orphanet:676036","UMLS:C5925102"],"termid":"MONDO:0971145","xrefs":{"Monarch":{"xref_id":"0971145"}}}


id: GO:0097720
data:
  {"annotated_genes":["SJAG_02858","SJAG_03631","SJAG_03799","SJAG_03793","SJAG_04668","SJAG_03879"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[74796,81306,94211,99918],"is_not":false,"summary":null,"term":"GO:0097720"},{"annotations":[117987,102815],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0106057"}]},"cv_name":"biological_process","definition":"Any intracellular signal transduction in which the signal is passed on within the cell by activation of a transcription factor as a consequence of dephosphorylation by Ca(2+)-activated calcineurin. The process begins with calcium-dependent activation of the phosphatase calcineurin. Calcineurin is a calcium- and calmodulin-dependent serine/threonine protein phosphatase with a conserved function in eukaryotic species from yeast to humans. In yeast and fungi, calcineurin regulates stress signaling and cell cycle, and sporulation and virulence in pathogenic fungi. In metazoans, calcineurin is involved in cell commitment, organogenesis and organ development and immune function of T-lymphocytes. By a conserved mechanism, calcineurin phosphatase activates fungal Crz1 and mammalian NFATc by dephosphorylation and translocation of these transcription factors to the nucleus to regulate gene expression.","definition_xrefs":["PMID:25655284","GOC:di","PMID:25878052","PMID:26851544"],"direct_ancestors":[{"relation_name":"is_a","term_name":"calcium-mediated signaling","termid":"GO:0019722"}],"gene_count":6,"genes_by_uniquename":{"SJAG_02858":null,"SJAG_03631":null,"SJAG_03793":null,"SJAG_03799":null,"SJAG_03879":null,"SJAG_04668":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"calcineurin-mediated signaling","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"calcineurin signaling","type":"related"},{"name":"calcineurin-mediated signalling","type":"exact"}],"termid":"GO:0097720","terms_by_termid":{"GO:0097720":null,"GO:0106057":null}}


id: GO:0010748
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate, frequency or extent of plasma membrane long-chain fatty acid transport. Plasma membrane long-chain fatty acid transport is the directed movement of long-chain fatty acids across the plasma membrane.","definition_xrefs":["GOC:tb","GOC:BHF","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of long-chain fatty acid import across plasma membrane","termid":"GO:0010746"},{"relation_name":"is_a","term_name":"negative regulation of transmembrane transport","termid":"GO:0034763"},{"relation_name":"is_a","term_name":"negative regulation of long-chain fatty acid import into cell","termid":"GO:0140213"},{"relation_name":"negatively_regulates","term_name":"long-chain fatty acid import across plasma membrane","termid":"GO:0015911"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0055085"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0006810","GO:0055085","GO:0008150"],"is_obsolete":false,"name":"negative regulation of long-chain fatty acid import across plasma membrane","synonyms":[{"name":"negative regulation of plasma membrane long-chain fatty acid transport","type":"exact"}],"termid":"GO:0010748"}


id: GO:1904071
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a presynaptic active zone. The presynaptic active zone is a specialized region of the plasma membrane and cell cortex of a presynaptic neuron; encompasses a region of the plasma membrane where synaptic vesicles dock and fuse, and a specialized cortical cytoskeletal matrix.","definition_xrefs":["GO_REF:0000079","GOC:TermGenie","PMID:10769383","GOC:pr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular component assembly","termid":"GO:0022607"},{"relation_name":"is_a","term_name":"presynaptic active zone organization","termid":"GO:1990709"},{"relation_name":"part_of","term_name":"presynapse assembly","termid":"GO:0099054"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"presynaptic active zone assembly","synonyms":[{"name":"pre-synaptic active zone assembly","type":"exact"},{"name":"pre-synaptic active zone component assembly","type":"narrow"},{"name":"pre-synaptic active zone component formation","type":"narrow"},{"name":"pre-synaptic active zone formation","type":"exact"},{"name":"presynaptic active zone formation","type":"exact"}],"termid":"GO:1904071"}


id: PBO:0085743
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in vacuole morphogenesis; acts at an early step of homotypic vacuole fusion that is required for vacuole tethering","termid":"PBO:0085743"}


id: MONDO:0006658
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The thickening of the wall of the small arteries and arterioles. It is caused by deposition of hyaline material in the wall or concentric smooth muscle wall hypertrophy. It results in lumen narrowing and tissue ischemia.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"coronary atherosclerosis","termid":"MONDO:0021661"}],"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":"arteriolosclerosis","secondary_identifiers":["EFO:1000819","UMLS:C0878486","MESH:D050379","NCIT:C35543","DOID:5162","ICD10CM:I70","MEDGEN:209223"],"synonyms":[{"name":"arteriolosclerosis (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0006658","xrefs":{"Monarch":{"xref_id":"0006658"}}}


id: PBO:0015679
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"carboxypeptidase Ecm14 (predicted)","termid":"PBO:0015679"}


id: PBO:0082354
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP sulfurylase; catalyzes the primary step of intracellular sulfate activation, essential for assimilatory reduction of sulfate to sulfide, involved in methionine metabolism; human homolog PAPSS2 complements yeast null mutant","termid":"PBO:0082354"}


id: PBO:0073760
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLC2A13 pseudogene 1","termid":"PBO:0073760"}


id: GO:0005713
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An electron dense structure that is associated with meiotic chromosomes.","definition_xrefs":["GOC:elh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"condensed nuclear chromosome","termid":"GO:0000794"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"part_of","termid":"GO:0005694"}],"interesting_parent_ids":["GO:0005694","GO:0005575","GO:0005634"],"is_obsolete":false,"name":"recombination nodule","termid":"GO:0005713"}


id: GO:0004605
data:
  {"annotated_genes":["SJAG_03563","SJAG_00426"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[81803,121034],"is_not":false,"summary":null,"term":"GO:0004605"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: CTP + phosphatidate = diphosphate + CDP-diacylglycerol.","definition_xrefs":["EC:2.7.7.41"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytidylyltransferase activity","termid":"GO:0070567"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00426":null,"SJAG_03563":null},"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:0016779"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0016779","GO:0003824"],"is_obsolete":false,"name":"phosphatidate cytidylyltransferase activity","references_by_uniquename":{"GO_REF:0000033":null,"PMID:25318672":null},"secondary_identifiers":["RHEA:16229","MetaCyc:CDPDIGLYSYN-RXN","Reactome:R-HSA-1483165","Reactome:R-HSA-1483121"],"synonyms":[{"name":"CDP diglyceride pyrophosphorylase activity","type":"related"},{"name":"CDP-DG","type":"related"},{"name":"CDP-diacylglyceride synthetase activity","type":"related"},{"name":"CDP-diacylglycerol synthase activity","type":"exact"},{"name":"CDP-diglyceride diphosphorylase activity","type":"exact"},{"name":"CDP-diglyceride pyrophosphorylase activity","type":"exact"},{"name":"CDP-diglyceride synthase activity","type":"exact"},{"name":"CDP-diglyceride synthetase activity","type":"related"},{"name":"CTP-diacylglycerol synthetase activity","type":"related"},{"name":"CTP:1,2-diacylglycerophosphate-cytidyl transferase activity","type":"related"},{"name":"CTP:phosphatidate cytidylyltransferase activity","type":"related"},{"name":"DAG synthetase activity","type":"related"},{"name":"cytidine diphosphoglyceride pyrophosphorylase activity","type":"related"},{"name":"phosphatidate cytidyltransferase activity","type":"related"},{"name":"phosphatidic acid cytidylyltransferase activity","type":"related"}],"termid":"GO:0004605","terms_by_termid":{"GO:0004605":null,"GO:0008654":null}}


id: PBO:0047117
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 163 member B","termid":"PBO:0047117"}


id: GO:0004411
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: homogentisate + O2 = 4-maleylacetoacetate + H+.","definition_xrefs":["EC:1.13.11.5","RHEA:15449"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen","termid":"GO:0016702"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"homogentisate 1,2-dioxygenase activity","secondary_identifiers":["KEGG_REACTION:R02519","MetaCyc:HOMOGENTISATE-12-DIOXYGENASE-RXN","UM-BBD_reactionID:r0105","Reactome:R-HSA-71164"],"synonyms":[{"name":"homogentisate dioxygenase activity","type":"related"},{"name":"homogentisate oxidase activity","type":"related"},{"name":"homogentisate oxygenase activity","type":"related"},{"name":"homogentisate:oxygen 1,2-oxidoreductase (decyclizing)","type":"related"},{"name":"homogentisic acid oxidase activity","type":"related"},{"name":"homogentisic acid oxygenase activity","type":"related"},{"name":"homogentisic oxygenase activity","type":"related"},{"name":"homogentisicase activity","type":"related"}],"termid":"GO:0004411"}


id: MONDO:0023067
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Kaposi's sarcoma","termid":"MONDO:0005055"}],"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":"endemic Kaposi sarcoma","secondary_identifiers":["GARD:10431","icd11.foundation:509381237","MEDGEN:698516","UMLS:C1275231"],"synonyms":[{"name":"African Kaposi sarcoma","type":"related"},{"name":"African/endemic Kaposi sarcoma","type":"related"}],"termid":"MONDO:0023067","xrefs":{"Monarch":{"xref_id":"0023067"}}}


id: MONDO:0015231
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Bartter syndrome is a group of rare renal tubular disease characterized by impaired salt reabsorption in the thick ascending limb of Henle's loop and clinically by the association of hypokalemic alkalosis, hypercalciuria/nephrocalcinosis, increased levels of plasma renin and aldosterone, low blood pressure and vascular resistance to angiotensin II.","definition_xrefs":["Orphanet:112"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"renal tubular transport disease","termid":"MONDO:0006510"},{"relation_name":"is_a","term_name":"inherited renal tubular disease","termid":"MONDO:0015962"}],"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":"Bartter syndrome","secondary_identifiers":["NANDO:2200146","UMLS:C0004775","ICD10CM:E26.81","NCIT:C34412","SCTID:707742001","ICD9:255.13","DOID:445","NORD:842","MESH:D001477","icd11.foundation:777233947","NANDO:2100021","OMIMPS:601678","GARD:5893","MEDGEN:2172","MedDRA:10050839"],"synonyms":[{"name":"Bartter disease","type":"exact"},{"name":"Bartter's syndrome","type":"exact"},{"name":"Potassium wasting","type":"related"},{"name":"aldosteronism with hyperplasia of the adrenal cortex","type":"exact"},{"name":"hypokalemic alkalosis","type":"exact"},{"name":"hypokalemic alkalosis with hypercalciuria","type":"related"},{"name":"renal tubular normotensive hypokalemic alkalosis with hypercalciuria","type":"exact"},{"name":"salt-losing tubular disorder, Henle's loop type","type":"exact"},{"name":"salt-wasting tubulopathy, Henle's loop type","type":"exact"}],"termid":"MONDO:0015231","xrefs":{"Monarch":{"xref_id":"0015231"}}}


id: SO:0000577
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region of chromosome where the spindle fibers attach during mitosis and meiosis.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosomal_structural_element","termid":"SO:0000628"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"centromere","secondary_identifiers":["http://en.wikipedia.org/wiki/Centromere"],"synonyms":[{"name":"INSDC_feature:centromere","type":"exact"}],"termid":"SO:0000577"}


id: PR:Q6LA53
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein AAR2 homolog that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO01434"],"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":"A1 cistron-splicing factor aar2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC3H5.04","secondary_identifiers":["UniProtKB:Q6LA53"],"synonyms":[{"name":"Spom972h-AAR2","type":"exact"}],"termid":"PR:Q6LA53"}


id: GO:0015754
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which D-allose is transported across a lipid bilayer, from one side of a membrane to the other. Allose is an aldohexose similar to glucose, differing only in the configuration of the hydroxyl group of C-3.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hexose transmembrane transport","termid":"GO:0008645"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0055085","GO:0051179"],"is_obsolete":false,"name":"D-allose transmembrane transport","synonyms":[{"name":"allose transmembrane transport","type":"narrow"},{"name":"allose transport","type":"related"}],"termid":"GO:0015754"}


id: PBO:0028396
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_27S_rRNA_precursor_level","termid":"PBO:0028396"}


id: PBO:0086598
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; expression is cell-cycle regulated as shown by microarray analysis; potential regulatory target of Mbp1p, which binds to the YJL181W promoter region; contains a PH-like domain; RBH1 has a paralog, RBH2, that arose from the whole genome duplication","termid":"PBO:0086598"}


id: GO:1900879
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of (Z)-nonadeca-1,14-diene.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"olefin biosynthetic process","termid":"GO:1900674"},{"relation_name":"is_a","term_name":"(Z)-nonadeca-1,14-diene metabolic process","termid":"GO:1900878"}],"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":"(Z)-nonadeca-1,14-diene biosynthetic process","synonyms":[{"name":"(Z)-nonadeca-1,14-diene anabolism","type":"exact"},{"name":"(Z)-nonadeca-1,14-diene biosynthesis","type":"exact"},{"name":"(Z)-nonadeca-1,14-diene formation","type":"exact"},{"name":"(Z)-nonadeca-1,14-diene synthesis","type":"exact"}],"termid":"GO:1900879"}


id: PBO:0052693
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 16 pseudogene 1","termid":"PBO:0052693"}


id: GO:0031052
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Regulated cleavage of the developing macronuclear genome at a limited number of chromosome breakage sites (CBS). The macronuclear destined segment (MDS) sequence adjacent to the CBS (or separated from it by a BES) receives a macronuclear telomere following chromosome breakage.","definition_xrefs":["GOC:ns","PMID:32165395","PMID:25303953","PMID:15956677"],"direct_ancestors":[{"relation_name":"is_a","term_name":"programmed DNA elimination","termid":"GO:0031049"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"programmed DNA elimination by chromosome breakage","synonyms":[{"name":"chromosome breakage","type":"related"}],"termid":"GO:0031052"}


id: PATO:0001184
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001184 maturity value (obsolete PATO:0001184)","termid":"PATO:0001184"}


id: PBO:0043907
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CRK like proto-oncogene, adaptor protein","termid":"PBO:0043907"}


id: MONDO:0025622
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Charcot-Marie-Tooth disease","termid":"MONDO:0015626"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"Charcot-Marie-Tooth disease, axonal, mitochondrial form, 1","secondary_identifiers":["UMLS:C5435765","MEDGEN:1731194","OMIM:500013"],"synonyms":[{"name":"CMTMA1","type":"exact"}],"termid":"MONDO:0025622","xrefs":{"Monarch":{"xref_id":"0025622"}}}


id: MONDO:0019346
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Sialidosis type 1 (ST-1) is a very rare lysosomal storage disease, and is the normosomatic form of sialidosis, characterized by gait abnormalities, progressive visual loss, bilateral macular cherry red spots and myoclonic epilepsy and ataxia, that usually presents in the second to third decade of life.","definition_xrefs":["Orphanet:812"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"eye disorder","termid":"MONDO:0005328"},{"relation_name":"is_a","term_name":"sialidosis","termid":"MONDO:0017734"},{"relation_name":"is_a","term_name":"familial mucolipidosis","termid":"MONDO:0031422"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0002561"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0037792","MONDO:0002561"],"is_obsolete":false,"name":"sialidosis type 1","secondary_identifiers":["NANDO:2201191","GARD:7639","MEDGEN:44174","NANDO:1200117","SCTID:723675006","icd11.foundation:1154773192","UMLS:C0023806","SCTID:34960006"],"synonyms":[{"name":"Normomorphic sialidosis","type":"exact"},{"name":"cherry red spot myoclonus syndrome","type":"related"},{"name":"cherry-red spot-myoclonus syndrome","type":"exact"},{"name":"lipomucopolysaccharidosis","type":"exact"},{"name":"myoclonus cherry red spot syndrome","type":"related"},{"name":"normosomatic sialidosis","type":"exact"},{"name":"sialidosis type I","type":"related"}],"termid":"MONDO:0019346","xrefs":{"Monarch":{"xref_id":"0019346"}}}


id: GO:1902770
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of choline O-acetyltransferase activity.","definition_xrefs":["GOC:TermGenie","GO_REF:0000059","PMID:7576634","GOC:mr"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of choline O-acetyltransferase activity (obsolete GO:1902770)","synonyms":[{"name":"down regulation of CHOACTase activity","type":"exact"},{"name":"down regulation of acetyl-CoA:choline O-acetyltransferase activity","type":"exact"},{"name":"down regulation of choline O-acetyltransferase activity","type":"exact"},{"name":"down regulation of choline acetylase activity","type":"exact"},{"name":"down regulation of choline acetyltransferase activity","type":"exact"},{"name":"down-regulation of CHOACTase activity","type":"exact"},{"name":"down-regulation of acetyl-CoA:choline O-acetyltransferase activity","type":"exact"},{"name":"down-regulation of choline O-acetyltransferase activity","type":"exact"},{"name":"down-regulation of choline acetylase activity","type":"exact"},{"name":"down-regulation of choline acetyltransferase activity","type":"exact"},{"name":"downregulation of CHOACTase activity","type":"exact"},{"name":"downregulation of acetyl-CoA:choline O-acetyltransferase activity","type":"exact"},{"name":"downregulation of choline O-acetyltransferase activity","type":"exact"},{"name":"downregulation of choline acetylase activity","type":"exact"},{"name":"downregulation of choline acetyltransferase activity","type":"exact"},{"name":"inhibition of CHOACTase activity","type":"narrow"},{"name":"inhibition of acetyl-CoA:choline O-acetyltransferase activity","type":"narrow"},{"name":"inhibition of choline O-acetyltransferase activity","type":"narrow"},{"name":"inhibition of choline acetylase activity","type":"narrow"},{"name":"inhibition of choline acetyltransferase activity","type":"narrow"},{"name":"negative regulation of CHOACTase activity","type":"exact"},{"name":"negative regulation of acetyl-CoA:choline O-acetyltransferase activity","type":"exact"},{"name":"negative regulation of choline acetylase activity","type":"exact"},{"name":"negative regulation of choline acetyltransferase activity","type":"exact"}],"termid":"GO:1902770"}


id: PATO:0001618
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A tonicity which is relatively high.","definition_xrefs":["PATO:GVG"],"direct_ancestors":[{"relation_name":"increased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"tonicity","termid":"PATO:0001439"},{"relation_name":"is_a","term_name":"increased object quality","termid":"PATO:0002305"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased tonicity","synonyms":[{"name":"high tonicity","type":"exact"}],"termid":"PATO:0001618"}


id: FYPO:0007241
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell polarity phenotype in which the switch from the monopolar to bipolar mode of cell growth (new end take-off; NETO) is abnormal in both of the daughter cells formed as a result of the division of a mother cell in which NETO did not occur, such that NETO is abolished in the daughter cell that inherits the parent cell's old end, and begins earlier than normal in the daughter cell that inherits parent cell's new end. Normally, growth begins at the old end and then becomes bipolar with similar timing in both daughter cells.","definition_xrefs":["PMID:31719163","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal NETO in daughter cells","termid":"FYPO:0007240"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005568"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000002","FYPO:0005568","FYPO:0001320"],"is_obsolete":false,"name":"abolished NETO in cell derived from growing end and premature NETO in cell derived from non-growing end","synonyms":[{"name":"abolished NETO in cell derived from growing end and premature NETO in cell derived from non-growing end during mitotic cell cycle","type":"related"},{"name":"abolished NETO in cell derived from growing end and premature NETO in cell derived from non-growing end during vegetative growth","type":"exact"},{"name":"abolished cell growth mode switching, monopolar to bipolar in cell derived from growing end and premature cell growth mode switching, monopolar to bipolar in cell derived from non-growing end","type":"exact"},{"name":"abolished new end take-off in cell derived from growing end and premature new end take-off in cell derived from non-growing end","type":"exact"},{"name":"abolished switch from monopolar to bipolar cell growth in cell derived from growing end and premature switch from monopolar to bipolar cell growth in cell derived from non-growing end","type":"exact"}],"termid":"FYPO:0007241"}


id: PBO:0073166
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SECIS binding protein 2","termid":"PBO:0073166"}


id: MONDO:0001264
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Kyasanur forest disease (obsolete MONDO:0001264)","termid":"MONDO:0001264","xrefs":{"Monarch":{"xref_id":"0001264"}}}


id: FYPO:0005300
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the kinetochore of a chromosome is decreased during mitotic spindle assembly checkpoint signaling.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein localization to kinetochore during mitotic M phase","termid":"FYPO:0005215"}],"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"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0000138"],"is_obsolete":false,"name":"decreased protein localization to kinetochore during mitotic spindle assembly checkpoint signaling","synonyms":[{"name":"decreased protein localisation to kinetochore during mitotic spindle assembly checkpoint signalling","type":"exact"},{"name":"decreased protein localization to kinetochore during mitotic cell cycle spindle assembly checkpoint signaling","type":"exact"},{"name":"decreased protein localization to kinetochore during signal transduction involved in mitotic spindle assembly checkpoint","type":"exact"},{"name":"decreased protein localization to kinetochore during spindle assembly checkpoint signaling during mitotic cell cycle","type":"exact"},{"name":"defective protein recruitment to unattached kinetochores","type":"exact"},{"name":"reduced protein localization to kinetochore during mitotic spindle assembly checkpoint signaling","type":"exact"}],"termid":"FYPO:0005300"}


id: PBO:0030959
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_outer_repeat","termid":"PBO:0030959"}


id: FYECO:0000111
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which myo-inositol was added to the medium or assay buffers in a limiting quantity compared to standard medium or assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping limited","termid":"FYECO:0000011"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ limited myo-inositol","secondary_identifiers":["PMID:9560432"],"synonyms":[{"name":"limited inositol added","type":"related"}],"termid":"FYECO:0000111"}


id: PBO:0064743
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl isomerase A pseudogene 79","termid":"PBO:0064743"}


id: MONDO:0009121
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Von Voss-Cherstvoy syndrome is a very rare disorder with phocomelia of upper limbs, encephalocele, variable brain anomalies, urogenital abnormalities, and thrombocytopenia.","definition_xrefs":["Orphanet:3439"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"von Voss-Cherstvoy syndrome","secondary_identifiers":["MESH:C565618","SCTID:719021005","OMIM:223340","UMLS:C1857226","MEDGEN:341728","GARD:1894"],"synonyms":[{"name":"DK phocomelia syndrome","type":"exact"},{"name":"Von Voss Cherstvoy syndrome","type":"related"},{"name":"phocomelia thrombocytopenia encephalocele and urogenital malformations","type":"related"},{"name":"phocomelia, thrombocytopenia, encephalocele, urogenital malformations","type":"related"},{"name":"phocomelia-thrombocytopenia-encephalocele-urogenital malformations syndrome","type":"exact"},{"name":"von Voss-Cherstvoy syndrome","type":"exact"}],"termid":"MONDO:0009121","xrefs":{"Monarch":{"xref_id":"0009121"}}}


id: PBO:0088723
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER protein folding protein","termid":"PBO:0088723"}


id: PBO:0002987
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3-oxoacyl-[acyl-carrier-protein]reductase(predicted)","termid":"PBO:0002987"}


id: GO:0035404
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of histones by addition of a phosphate group to a serine residue.","definition_xrefs":["GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete histone-serine phosphorylation (obsolete GO:0035404)","synonyms":[{"name":"histone serine phosphorylation","type":"exact"}],"termid":"GO:0035404"}


id: PATO:0002151
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A curvature quality inhering in a bearer by virtue of the bearer's being curved outwards from the back or upper surface of an organism.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"splayed","termid":"PATO:0001785"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"splayed dorsal","synonyms":[{"name":"splayed posterior (human torso)","type":"related"}],"termid":"PATO:0002151"}


id: PBO:0063209
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"poly(rC) binding protein 3","termid":"PBO:0063209"}


id: GO:0086015
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An action potential that occurs in a sinoatrial node cardiac muscle cell.","definition_xrefs":["GOC:BHF","GOC:mtg_cardiac_conduct_nov11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiac muscle cell action potential","termid":"GO:0086001"},{"relation_name":"part_of","term_name":"SA node cell to atrial cardiac muscle cell signaling","termid":"GO:0086018"}],"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":"SA node cell action potential","synonyms":[{"name":"SA node cardiac muscle cell action potential","type":"exact"},{"name":"SAN cardiac muscle cell action potential","type":"exact"},{"name":"sinoatrial node cardiac muscle cell action potential","type":"exact"},{"name":"sinus node cardiac muscle cell action potential","type":"narrow"}],"termid":"GO:0086015"}


id: GO:0090731
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a very-low-density lipoprotein particle stimulus.","definition_xrefs":["GOC:bc","GOC:aruk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to lipoprotein particle","termid":"GO:0055094"},{"relation_name":"is_a","term_name":"cellular response to lipoprotein particle stimulus","termid":"GO:0071402"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to very-low-density lipoprotein particle stimulus","synonyms":[{"name":"cellular response to VLDL particle stimulus","type":"exact"}],"termid":"GO:0090731"}


id: GO:0070045
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A SNARE complex that contains synaptobrevin 2 (VAMP2), SNAP-25, and syntaxin 2 (or orthologs thereof).","definition_xrefs":["PMID:10336434"],"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:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"synaptobrevin 2-SNAP-25-syntaxin-2 complex","synonyms":[{"name":"SNARE complex (Stx2, Snap25, Vamp2)","type":"narrow"},{"name":"Stx2-Snap25-Vamp2 complex","type":"narrow"}],"termid":"GO:0070045"}


id: MONDO:0100341
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A poisoning that is caused by exposure to a fire ant bite or sting. Fire ants tend to be an aggressive insect that will sting causing very painful reactions. There are two types of fire ants which belong to the Solenopsis species.","definition_xrefs":["PMID:29261949"],"direct_ancestors":[{"relation_name":"is_a","term_name":"poisoning","termid":"MONDO:0029000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fire ant poisoning","synonyms":[{"name":"fire ant allergy","type":"related"},{"name":"fire ant bite","type":"related"},{"name":"fire ant sting","type":"related"}],"termid":"MONDO:0100341","xrefs":{"Monarch":{"xref_id":"0100341"}}}


id: PBO:0080900
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon","termid":"PBO:0080900"}


id: MONDO:0000065
data:
  {"annotated_genes":["SJAG_03303"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89149],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012970"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03303":null},"genotype_count":0,"is_obsolete":false,"name":"microvascular complications of diabetes, susceptibility","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIMPS:603933"],"synonyms":[{"name":"microvascular complications of diabetes","type":"exact"}],"termid":"MONDO:0000065","terms_by_termid":{"MONDO:0012970":null},"xrefs":{"Monarch":{"xref_id":"0000065"}}}


id: PR:O13858
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sle1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O13858"],"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":"eisosome protein sle1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1A6.07","synonyms":[{"name":"SEG1-like eisosome protein 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-sle1","type":"exact"}],"termid":"PR:O13858"}


id: PBO:0040024
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"armadillo repeat containing 12","termid":"PBO:0040024"}


id: SO:0000550
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A chromosome structural variation whereby either a chromosome exists in addition to the normal chromosome complement or is lacking.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome_structure_variation","termid":"SO:1000183"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aneuploid_chromosome","synonyms":[{"name":"aneuploid chromosome","type":"exact"}],"termid":"SO:0000550"}


id: MONDO:0018656
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"eye degenerative disorder","termid":"MONDO:0004884"},{"relation_name":"is_a","term_name":"leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism","termid":"MONDO:0011897"},{"relation_name":"is_a","term_name":"hereditary ataxia","termid":"MONDO:0100309"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0005559"],"is_obsolete":false,"name":"tremor-ataxia-central hypomyelination syndrome","secondary_identifiers":["MEDGEN:1842823","Orphanet:447896","UMLS:C5680067","GARD:17774"],"synonyms":[{"name":"TACH syndrome","type":"exact"}],"termid":"MONDO:0018656","xrefs":{"Monarch":{"xref_id":"0018656"}}}


id: MONDO:0007283
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any early-onset non-syndromic cataract in which the cause of the disease is a mutation in the CRYBA2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"early-onset non-syndromic cataract","termid":"MONDO:0011060"}],"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":"cataract 42","secondary_identifiers":["OMIM:115900","MEDGEN:859891","DOID:0110237","UMLS:C4011454"],"synonyms":[{"name":"A cataract that has_material_basis_in heterozygous mutation in the CRYBA2 gene on chromosome 2q35.","type":"exact"},{"name":"CRYBA2 early-onset non-syndromic cataract","type":"exact"},{"name":"CTRCT42","type":"exact"},{"name":"cataract 42","type":"exact"},{"name":"cataract type 42","type":"exact"},{"name":"early-onset non-syndromic cataract caused by mutation in CRYBA2","type":"exact"}],"termid":"MONDO:0007283","xrefs":{"Monarch":{"xref_id":"0007283"}}}


id: GO:0019483
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of beta-alanine (3-aminopropanoic acid), an achiral amino acid and an isomer of alanine. It occurs free (e.g. in brain) and in combination (e.g. in pantothenate) but it is not a constituent of proteins.","definition_xrefs":["ISBN:0198506732","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid biosynthetic process","termid":"GO:0008652"},{"relation_name":"is_a","term_name":"beta-alanine metabolic process","termid":"GO:0019482"},{"relation_name":"is_a","term_name":"non-proteinogenic amino acid biosynthetic process","termid":"GO:0170043"}],"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:0006520"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0006520"],"is_obsolete":false,"name":"beta-alanine biosynthetic process","synonyms":[{"name":"beta-alanine anabolism","type":"exact"},{"name":"beta-alanine biosynthesis","type":"exact"},{"name":"beta-alanine formation","type":"exact"},{"name":"beta-alanine synthesis","type":"exact"}],"termid":"GO:0019483"}


id: MONDO:0037737
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, usually benign fibroblastic neoplasm that arises from the peritoneum. It is characterized by the presence of prominent hemangiopericytoma-like vessels.","definition_xrefs":["NCIT:C126357"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peritoneal neoplasm","termid":"MONDO:0006901"},{"relation_name":"is_a","term_name":"solitary fibrous tumor","termid":"MONDO:0016238"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peritoneal solitary fibrous tumor","secondary_identifiers":["UMLS:C4288403","MEDGEN:925935"],"synonyms":[{"name":"peritoneal solitary fibrous tumor","type":"exact"}],"termid":"MONDO:0037737","xrefs":{"Monarch":{"xref_id":"0037737"}}}


id: MONDO:1012400
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"dilute coat color with neurological defects, non-human animal","termid":"MONDO:1011883"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dilute coat color with neurological defects, dog","secondary_identifiers":["OMIA:001501-9615"],"termid":"MONDO:1012400","xrefs":{"Monarch":{"xref_id":"1012400"}}}


id: FYPO:0005297
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of 8-oxo-7,8-dihydroguanine DNA N-glycosylase activity is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal catalytic activity","termid":"FYPO:0000660"}],"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:0000257","FYPO:0000654","FYPO:0000652"],"is_obsolete":false,"name":"normal 8-oxo-7,8-dihydroguanine DNA N-glycosylase activity","termid":"FYPO:0005297"}


id: PR:O14349
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC30D10.03c gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14349"],"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":"IMP-specific 5'-nucleotidase 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC30D10.03c","synonyms":[{"name":"Spom972h-SPBC30D10.03c","type":"exact"}],"termid":"PR:O14349"}


id: PBO:0116846
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial translational activator Sls1","termid":"PBO:0116846"}


id: MONDO:0022930
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Dandy-Walker syndrome","termid":"MONDO:0009072"}],"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":"Dandy-Walker malformation with nasopharyngeal teratoma and diaphragmatic hernia","secondary_identifiers":["MEDGEN:419910","UMLS:C2931823","GARD:137","MESH:C538340"],"synonyms":[{"name":"Aughton sloan Milad syndrome","type":"exact"}],"termid":"MONDO:0022930","xrefs":{"Monarch":{"xref_id":"0022930"}}}


id: PBO:0058539
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6084","termid":"PBO:0058539"}


id: PBO:0117078
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PLBD1 antisense RNA 2","termid":"PBO:0117078"}


id: GO:0023020
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of gene expression as a consequence of a process in which a T cell signal is released and/or conveyed from one location to another.","definition_xrefs":["GOC:mtg_signal"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of gene expression as a consequence of T cell signal transmission (obsolete GO:0023020)","synonyms":[{"name":"regulation of gene expression as a consequence of T cell signal transmission","type":"exact"}],"termid":"GO:0023020"}


id: FYPO:0006821
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which cells elongate more slowly than normal in the vegetative growth phase of the life cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell growth rate","termid":"FYPO:0006820"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"slow vegetative cell growth","termid":"FYPO:0006821"}


id: PBO:0075148
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nuclear ribonucleoprotein polypeptide C pseudogene 4","termid":"PBO:0075148"}


id: GO:1990505
data:
  {"annotated_genes":["SJAG_02214","SJAG_00573","SJAG_01410","SJAG_02079","SJAG_01584","SJAG_01677","SJAG_02198","SJAG_01374","SJAG_06022","SJAG_04272","SJAG_02439","SJAG_03780","SJAG_01076","SJAG_01221","SJAG_02822","SJAG_03898","SJAG_03843","SJAG_02992","SJAG_03300","SJAG_01832"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[110966,113611],"is_not":false,"summary":null,"term":"GO:1990505"},{"annotations":[90983,65122,97995,96645,100763,97829,100056,92762,110922,111401,109564,109588,114374,118664,96886],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990426"},{"annotations":[90813,107961,118276],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0120292"}]},"cv_name":"biological_process","definition":"Any maintenance of fidelity that is involved in mitotic cell cycle DNA replication.","definition_xrefs":["PMID:19185548"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell cycle DNA replication maintenance of fidelity","termid":"GO:1902298"},{"relation_name":"is_a","term_name":"mitotic cell cycle process","termid":"GO:1903047"},{"relation_name":"part_of","term_name":"mitotic DNA replication","termid":"GO:1902969"}],"gene_count":20,"genes_by_uniquename":{"SJAG_00573":null,"SJAG_01076":null,"SJAG_01221":null,"SJAG_01374":null,"SJAG_01410":null,"SJAG_01584":null,"SJAG_01677":null,"SJAG_01832":null,"SJAG_02079":null,"SJAG_02198":null,"SJAG_02214":null,"SJAG_02439":null,"SJAG_02822":null,"SJAG_02992":null,"SJAG_03300":null,"SJAG_03780":null,"SJAG_03843":null,"SJAG_03898":null,"SJAG_04272":null,"SJAG_06022":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0006260"},{"rel_name":"part_of","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006259","GO:0006260","GO:0008150","GO:0007049"],"is_obsolete":false,"name":"mitotic DNA replication maintenance of fidelity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:1990510"],"synonyms":[{"name":"maintenance of fidelity involved in mitotic DNA replication","type":"exact"},{"name":"maintenance of fidelity involved in mitotic cell cycle DNA replication","type":"exact"}],"termid":"GO:1990505","terms_by_termid":{"GO:0120292":null,"GO:1990426":null,"GO:1990505":null}}


id: GO:0070832
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The phosphatidylcholine biosynthetic process that begins with three consecutive N-methylation steps that are carried out on phospho-bases, phosphoethanolamine, phospho-N-methylethanolamine, and phospho-N-dimethylethanolamine; the process ends with the conversion of a phosphatidyl-N-dimethylethanolamine to a phosphatidylcholine.","definition_xrefs":["MetaCyc:PWY4FS-2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatidylcholine biosynthetic process","termid":"GO:0006656"},{"relation_name":"is_a","term_name":"primary amino compound metabolic process","termid":"GO:1901160"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"phosphatidylcholine biosynthesis from phosphoryl-ethanolamine via N-dimethylethanolamine phosphate and CDP-choline","termid":"GO:0070832"}


id: PBO:0062198
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 U member 1 pseudogene","termid":"PBO:0062198"}


id: MONDO:0000817
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete MONDO:0000817 (obsolete MONDO:0000817)","termid":"MONDO:0000817","xrefs":{"Monarch":{"xref_id":"0000817"}}}


id: GO:0009831
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events that occur during cell growth that result in chemical or structural changes to existing cell walls of the type composed chiefly of cellulose and pectin. An example of this is found in Arabidopsis thaliana.","definition_xrefs":["GOC:lr","GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plant-type cell wall modification","termid":"GO:0009827"},{"relation_name":"is_a","term_name":"cell wall modification involved in multidimensional cell growth","termid":"GO:0042547"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0071554"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0071554","GO:0008150"],"is_obsolete":false,"name":"plant-type cell wall modification involved in multidimensional cell growth","synonyms":[{"name":"cell wall modification during cell expansion","type":"broad"},{"name":"cellulose and pectin-containing cell wall modification during multidimensional cell growth","type":"related"}],"termid":"GO:0009831"}


id: SO:0001340
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"1_2prime_O_dimethylguanosine 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":"one_two_prime_O_dimethylguanosine","secondary_identifiers":["RNAMOD:096"],"synonyms":[{"name":"1,2'-O-dimethylguanosine","type":"exact"},{"name":"m1Gm","type":"exact"},{"name":"one two prime O dimethylguanosine","type":"exact"}],"termid":"SO:0001340"}


id: GO:0102975
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: versiconol acetate + NADP = versiconal hemiacetal acetate + NADPH.","definition_xrefs":["RHEA:35695"],"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:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"versiconal hemiacetal acetate reductase activity","secondary_identifiers":["MetaCyc:RXN-9490"],"termid":"GO:0102975"}


id: PBO:0061834
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2-oxoglutarate and iron dependent oxygenase domain containing 2","termid":"PBO:0061834"}


id: PBO:0011500
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DUF953 thioredoxin family protein","termid":"PBO:0011500"}


id: FYPO:0002499
data:
  {"alleles_by_uniquename":{"SJAG_01787:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01787","name":"pck1delta","uniquename":"SJAG_01787:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[121115],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001038"}]},"cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the occurrence of protein modification is increased. All modifications may be affected, or only modifications of a certain type, or on specific proteins, or even specific sites within specific proteins.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein modification","termid":"FYPO:0002494"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01787":null,"SJAG_04551":null},"genotype_count":1,"genotypes_by_uniquename":{"pck1delta":{"display_name":"pck1delta","display_uniquename":"pck1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01787:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0002274","FYPO:0002494","FYPO:0001985"],"is_obsolete":false,"name":"increased protein modification","references_by_uniquename":{"PMID:34198697":null},"single_locus_annotated_genes":["SJAG_01787"],"single_locus_genotype_uniquenames":["pck1delta"],"synonyms":[{"name":"increased protein/peptide modification","type":"exact"},{"name":"protein/peptide modification: increased","type":"related"}],"termid":"FYPO:0002499","terms_by_termid":{"FYPO:0001038":null}}


id: PR:G2TRN5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC25B8.20 gene.","definition_xrefs":["PRO:DNx","UniProtKB:G2TRN5"],"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 C25B8.20 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC25B8.20","synonyms":[{"name":"Spom972h-SPAC25B8.20","type":"exact"}],"termid":"PR:G2TRN5"}


id: MONDO:0010104
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Noneruption of teeth - maxillary hypoplasia - genu valgum is an extremely rare syndrome that is characterized by multiple unerupted permanent teeth, hypoplasia of the alveolar process and of the maxillo-zygomatic region, severe genu valgum and deformed ears.","definition_xrefs":["Orphanet:2972"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-eruption of teeth-maxillary hypoplasia-genu valgum syndrome","secondary_identifiers":["GARD:5027","MEDGEN:341331","OMIM:273050","SCTID:723442008","UMLS:C1848903"],"synonyms":[{"name":"Stoelinga de Koomen Davis syndrome","type":"related"},{"name":"Stoelinga-de Koomen-Davis syndrome","type":"exact"},{"name":"multiple non-erupting teeth, maxillo-zygomatical hypoplasia and other congenital defects","type":"related"},{"name":"multiple none-erupting teeth, maxillo-zygomatical hypoplasia and other congenital defects","type":"related"},{"name":"non erupted teeth with maxillary hypoplasia and genu valgum","type":"related"},{"name":"teeth noneruption of with maxillary hypoplasia and genu valgum","type":"related"},{"name":"teeth, noneruption of, with maxillary hypoplasia and genu valgum","type":"related"}],"termid":"MONDO:0010104","xrefs":{"Monarch":{"xref_id":"0010104"}}}


id: PBO:0057984
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3910-2","termid":"PBO:0057984"}


id: GO:0047292
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (6AS,11AS)-3,6A,9-trihydroxypterocarpan + dimethylallyl-pyrophosphate = glyceollin + diphosphate.","definition_xrefs":["EC:2.5.1.36"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity, transferring alkyl or aryl (other than methyl) groups","termid":"GO:0016765"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016765"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016740","GO:0016765","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"trihydroxypterocarpan dimethylallyltransferase activity","synonyms":[{"name":"dimethylallyl-diphosphate:(6aS,11aS)-3,6a,9-trihydroxypterocarpan dimethylallyltransferase activity","type":"related"},{"name":"dimethylallyl-diphosphate:(6aS,11aS)-3,6a,9-trihydroxypterocarpan dimethyltransferase activity","type":"related"},{"name":"dimethylallylpyrophosphate:3,6a,9-trihydroxypterocarpan dimethylallyltransferase activity","type":"related"},{"name":"dimethylallylpyrophosphate:trihydroxypterocarpan dimethylallyl transferase activity","type":"related"}],"termid":"GO:0047292"}


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


id: MONDO:0017285
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Penoscrotal transposition (PST) is a rare congenital genital anomaly in which the scrotum is positioned superior and anterior to the penis. PST may present with a broad spectrum of anomalies ranging from simple shawl scrotum (doughnut scrotum) to very complex extreme transposition with craniofacial, central nervous system, cardiac, gastrointestinal, urological, and other genital (undescended testicles, hypospadias, chordee) malformations. Growth deficiency and intellectual disability may also be noticed (60% of cases).","definition_xrefs":["Orphanet:2842"],"direct_ancestors":[{"relation_name":"is_a","term_name":"male reproductive system disorder","termid":"MONDO:0003150"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"penoscrotal transposition","secondary_identifiers":["MESH:C536650","icd11.foundation:1417779551","NCIT:C99010","MedDRA:10067287","MEDGEN:357036","UMLS:C1868854","HP:0100600","SCTID:312005008","GARD:4273"],"synonyms":[{"name":"Prepenile scrotum","type":"related"},{"name":"congenital penoscrotal transposition","type":"exact"},{"name":"congenital transposition of the penis","type":"related"},{"name":"penoscrotal transposition","type":"exact"},{"name":"penoscrotal transposition (disease)","type":"exact"}],"termid":"MONDO:0017285","xrefs":{"Monarch":{"xref_id":"0017285"}}}


id: PBO:0055935
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat containing 41","termid":"PBO:0055935"}


id: PBO:0078611
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripartite motif containing 64B","termid":"PBO:0078611"}


id: MONDO:0006615
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease involving the sweat gland.","direct_ancestors":[{"relation_name":"is_a","term_name":"skin disorder","termid":"MONDO:0005093"}],"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":"sweat gland disorder","secondary_identifiers":["DOID:1383","ICD9:705.9","SCTID:88232005","ICD9:705.89","MESH:D013543","UMLS:C0262643","ICD9:705","MEDGEN:892310"],"synonyms":[{"name":"disease of sweat gland","type":"exact"},{"name":"disease of sweat glands","type":"related"},{"name":"disease or disorder of sweat gland","type":"exact"},{"name":"disorder of sweat gland","type":"exact"},{"name":"disorder of sweat glands","type":"related"},{"name":"sweat gland disease","type":"exact"},{"name":"sweat gland disease or disorder","type":"exact"}],"termid":"MONDO:0006615","xrefs":{"Monarch":{"xref_id":"0006615"}}}


id: PBO:0046807
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coagulation factor X","termid":"PBO:0046807"}


id: GO:0048838
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the dormant state is broken in a seed. Dormancy is characterized by a suspension of physiological activity that can be reactivated upon release.","definition_xrefs":["GOC:tb","ISBN:9781405139830","GOC:dph","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"seed dormancy process","termid":"GO:0010162"},{"relation_name":"is_a","term_name":"exit from dormancy","termid":"GO:0097438"}],"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":"release of seed from dormancy","termid":"GO:0048838"}


id: PBO:0071913
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPS3A pseudogene 52","termid":"PBO:0071913"}


id: PBO:0030440
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_tRNA_modification","termid":"PBO:0030440"}


id: GO:0140102
data:
  {"annotated_genes":["SJAG_00943","SJAG_03016","SJAG_02821","SJAG_03755","SJAG_02281","SJAG_00722","SJAG_03008","SJAG_02417","SJAG_03877","SJAG_03332","SJAG_03773","SJAG_02350","SJAG_02024","SJAG_03289","SJAG_01958","SJAG_03713"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[70125],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052909"},{"annotations":[80409],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052907"},{"annotations":[78941],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016433"},{"annotations":[100213],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106142"},{"annotations":[59966],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000179"},{"annotations":[80683,97435],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009383"},{"annotations":[96720],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070043"},{"annotations":[91445],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070039"},{"annotations":[77358],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070037"},{"annotations":[77426,77671,80469],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008650"},{"annotations":[81343],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070042"},{"annotations":[75024,112048],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008649"},{"annotations":[57392],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106388"}]},"cv_name":"molecular_function","definition":"Catalytic activity that acts to modify a ribosomal RNA.","definition_xrefs":["GOC:molecular_function_refactoring","GOC:pdt"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catalytic activity, acting on RNA","termid":"GO:0140098"}],"gene_count":16,"genes_by_uniquename":{"SJAG_00722":null,"SJAG_00943":null,"SJAG_01958":null,"SJAG_02024":null,"SJAG_02281":null,"SJAG_02350":null,"SJAG_02417":null,"SJAG_02821":null,"SJAG_03008":null,"SJAG_03016":null,"SJAG_03289":null,"SJAG_03332":null,"SJAG_03713":null,"SJAG_03755":null,"SJAG_03773":null,"SJAG_03877":null},"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:0140098"}],"interesting_parent_ids":["GO:0140098","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"catalytic activity, acting on a rRNA","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000003":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"termid":"GO:0140102","terms_by_termid":{"GO:0000179":null,"GO:0008649":null,"GO:0008650":null,"GO:0009383":null,"GO:0016433":null,"GO:0052907":null,"GO:0052909":null,"GO:0070037":null,"GO:0070039":null,"GO:0070042":null,"GO:0070043":null,"GO:0106142":null,"GO:0106388":null}}


id: GO:0046562
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: beta-D-glucose + O2 = D-glucono-1,5-lactone + H2O2.","definition_xrefs":["RHEA:11428"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hexose oxidase activity","termid":"GO:0047979"}],"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:0003824","GO:0003674"],"is_obsolete":false,"name":"beta-D-glucose oxidase activity","secondary_identifiers":["EC:1.1.3.4","MetaCyc:GLUCOSE-OXIDASE-RXN","KEGG_REACTION:R01522"],"synonyms":[{"name":"D-glucose oxidase activity","type":"related"},{"name":"D-glucose-1-oxidase activity","type":"related"},{"name":"GOD activity","type":"related"},{"name":"beta-D-glucose:oxygen 1-oxido-reductase activity","type":"related"},{"name":"beta-D-glucose:oxygen 1-oxidoreductase activity","type":"related"},{"name":"beta-D-glucose:quinone oxidoreductase activity","type":"related"},{"name":"corylophyline","type":"related"},{"name":"deoxin-1","type":"related"},{"name":"glucose aerodehydrogenase activity","type":"related"},{"name":"glucose oxidase activity","type":"exact"},{"name":"glucose oxyhydrase activity","type":"related"},{"name":"microcid","type":"related"},{"name":"penatin","type":"related"}],"termid":"GO:0046562"}


id: GO:0046794
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a virus, or part of a virus, into, out of, or within a host cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral process","termid":"GO:0016032"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"transport of virus","synonyms":[{"name":"viral transport","type":"exact"},{"name":"virion transport","type":"narrow"}],"termid":"GO:0046794"}


id: PBO:0050839
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ITGB1 adjacent tumor promoting lncRNA","termid":"PBO:0050839"}


id: MONDO:0012781
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"celiac disease","termid":"MONDO:0005130"},{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"celiac disease, susceptibility to, 12","secondary_identifiers":["MEDGEN:436989","UMLS:C2677602","OMIM:612010"],"synonyms":[{"name":"CELIAC12","type":"exact"},{"name":"celiac disease, susceptibility to, 12","type":"exact"},{"name":"gluten-sensitive enteropathy, susceptibility to, 12","type":"related"}],"termid":"MONDO:0012781","xrefs":{"Monarch":{"xref_id":"0012781"}}}


id: FYPO:0007950
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A biological process phenotype in which the observed mating efficiency, as determined by counting zygotes, asci, and sometimes spores, is higher than normal when a cell is subject to nitrogen stress.","definition_xrefs":["PomBase:val"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased mating efficiency","termid":"FYPO:0001043"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000003"],"is_obsolete":false,"name":"increased mating efficency during nitrogen stress","termid":"FYPO:0007950"}


id: FYPO:0005024
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which mitotic sister chromatid separation is abnormal along the chromosome arms. Mitotic sister chromatid separation is the process in which sister chromatids are physically detached from each other during mitosis.","definition_xrefs":["GO:1990891","PMID:21633354","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic sister chromatid separation","termid":"FYPO:0000670"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0000641"},{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000641","FYPO:0001985","FYPO:0000631","FYPO:0005447","FYPO:0001320","FYPO:0000337","FYPO:0000002"],"is_obsolete":false,"name":"abnormal mitotic sister chromatid arm separation","synonyms":[{"name":"abnormal mitotic chromosome arm separation","type":"exact"},{"name":"abnormal sister chromatid arm separation during mitosis","type":"exact"},{"name":"abnormal sister chromatid arm separation during mitotic cell cycle","type":"related"},{"name":"abnormal sister chromatid arm separation during vegetative growth","type":"exact"}],"termid":"FYPO:0005024"}


id: GO:0008934
data:
  {"annotated_genes":["SJAG_03739"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[79025],"is_not":false,"summary":null,"term":"GO:0008934"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 1D-myo-inositol 1-phosphate + H2O = myo-inositol + phosphate.","definition_xrefs":["RHEA:27670"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inositol monophosphate phosphatase activity","termid":"GO:0052834"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03739":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016788"}],"interesting_parent_ids":["GO:0016788","GO:0003674","GO:0016787","GO:0003824"],"is_obsolete":false,"name":"inositol monophosphate 1-phosphatase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-1855154","MetaCyc:RXN0-5408"],"synonyms":[{"name":"L-myo-inositol-1-phosphate phosphatase activity","type":"related"},{"name":"inositol 1-phosphatase activity","type":"related"},{"name":"inositol-1(or 4)-monophosphatase activity","type":"broad"},{"name":"myo-inositol 1-phosphatase activity","type":"related"},{"name":"myo-inositol-1(or 4)-monophosphatase activity","type":"broad"},{"name":"myo-inositol-1(or 4)-phosphate phosphohydrolase activity","type":"broad"},{"name":"myo-inositol-1-phosphatase activity","type":"related"}],"termid":"GO:0008934","terms_by_termid":{"GO:0008934":null}}


id: PBO:0042931
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cingulin like 1","termid":"PBO:0042931"}


id: GO:0097174
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving 1,6-anhydro-N-acetyl-beta-muramic acid, the 1,6-anhydro-derivative of N-acetyl-beta-muramic acid.","definition_xrefs":["PMID:15901686","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monocarboxylic acid metabolic process","termid":"GO:0032787"}],"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":"1,6-anhydro-N-acetyl-beta-muramic acid metabolic process","synonyms":[{"name":"1,6-anhydro-N-acetyl-beta-muramate metabolic process","type":"exact"},{"name":"1,6-anhydro-N-acetyl-beta-muramate metabolism","type":"exact"},{"name":"1,6-anhydro-N-acetyl-beta-muramic acid metabolism","type":"exact"},{"name":"1,6-anhydro-N-acetylmuramic acid metabolic process","type":"exact"},{"name":"1,6-anhydro-N-acetylmuramic acid metabolism","type":"exact"}],"termid":"GO:0097174"}


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


id: PBO:0077350
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 89","termid":"PBO:0077350"}


id: PBO:0055883
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat containing 8 VRAC subunit A","termid":"PBO:0055883"}


id: GO:1990797
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The controlled release of cholecystokinin from a cell. Cholecystokinin is a peptide hormone that participates in pancreatic enzyme release in the gut and is also found in the brain.","definition_xrefs":["PMID:2755938"],"gene_count":0,"genotype_count":0,"name":"obsolete cholecystokinin secretion (obsolete GO:1990797)","synonyms":[{"name":"CCK secretion","type":"exact"}],"termid":"GO:1990797"}


id: PBO:0060976
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuroglobin","termid":"PBO:0060976"}


id: PBO:0030506
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_PPT","termid":"PBO:0030506"}


id: PR:O94512
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC646.08c gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94512"],"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":"oxysterol-binding protein-like protein 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC646.08c","synonyms":[{"name":"Spom972h-SPBC646.08c","type":"exact"}],"termid":"PR:O94512"}


