# terms

id: PBO:0084637
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mevalonate kinase; acts in the biosynthesis of isoprenoids and sterols, including ergosterol, from mevalonate; human MVK functionally complements the lethality of the erg12 null mutation","termid":"PBO:0084637"}


id: PBO:0018033
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nuclear PassenGer=","termid":"PBO:0018033"}


id: PBO:0043003
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chitinase, acidic pseudogene 1","termid":"PBO:0043003"}


id: MONDO:0003820
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An ovarian teratoma which may be cystic, composed entirely of well differentiated, adult-type tissues, without evidence of fetal-type tissues.","definition_xrefs":["NCIT:C8112"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mature teratoma","termid":"MONDO:0003517"},{"relation_name":"is_a","term_name":"ovarian biphasic or triphasic teratoma","termid":"MONDO:0003821"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mature ovarian teratoma","secondary_identifiers":["DOID:6231","UMLS:C1334637","ONCOTREE:OMT","MEDGEN:233672"],"synonyms":[{"name":"mature ovarian teratoma","type":"exact"},{"name":"mature teratoma","type":"related"},{"name":"mature teratoma of ovary","type":"exact"},{"name":"mature teratoma of the ovary","type":"related"},{"name":"ovary mature teratoma","type":"exact"}],"termid":"MONDO:0003820","xrefs":{"Monarch":{"xref_id":"0003820"}}}


id: MONDO:0008404
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Scalp-ear-nipple syndrome is characterized by the following triad: areas of hairless raw skin over the scalp (present at birth and healing during childhood), prominent, hypoplastic ears with almost absent pinnae, and bilateral amastia. Thirty cases have been described so far. Renal and urinary tract abnormalities, as well as cataract, have also been observed. Transmission is autosomal dominant.","definition_xrefs":["Orphanet:2036"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"},{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"},{"relation_name":"is_a","term_name":"mixed dermis disorder","termid":"MONDO:0019294"}],"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":"scalp-ear-nipple syndrome","secondary_identifiers":["UMLS:C1867020","MEDGEN:357183","SCTID:721888002","GARD:159","MESH:C536623","OMIM:181270","DOID:0111550","icd11.foundation:88843032"],"synonyms":[{"name":"Finlay-Marks syndrome","type":"exact"},{"name":"SENS","type":"related"},{"name":"Sen syndrome","type":"related"},{"name":"hereditary syndrome of lumpy scalp, odd ears and rudimentary nipples","type":"related"},{"name":"scalp ear nipple syndrome","type":"related"},{"name":"scalp-EAR-nipple syndrome","type":"related"},{"name":"scalp-ear-nipple syndrome","type":"exact"}],"termid":"MONDO:0008404","xrefs":{"Monarch":{"xref_id":"0008404"}}}


id: FYPO:0009037
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An increased chemical resistance phenotype observed in the vegetative growth phase of the life cycle in which cells grow in the presence of a higher concentration of phloxine B than normal.","definition_xrefs":["PomBase:mlr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"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:0002682"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0000139","FYPO:0002682","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"resistance to phloxine B","synonyms":[{"name":"resistance to phloxine B during mitotic cell cycle","type":"related"},{"name":"resistance to phloxine B during vegetative growth","type":"exact"},{"name":"resistant to phloxine B","type":"exact"}],"termid":"FYPO:0009037"}


id: PBO:0045791
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER degradation enhancing alpha-mannosidase like protein 1","termid":"PBO:0045791"}


id: GO:0047110
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: CoA + NAD+ + phenylglyoxylate = benzoyl-CoA + CO2 + NADH.","definition_xrefs":["RHEA:10372"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor","termid":"GO:0016620"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"phenylglyoxylate dehydrogenase (acylating) activity","secondary_identifiers":["EC:1.2.1.58","MetaCyc:1.2.1.58-RXN","KEGG_REACTION:R02450"],"synonyms":[{"name":"phenylglyoxylate:NAD+ oxidoreductase activity","type":"related"}],"termid":"GO:0047110"}


id: MONDO:0016772
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Annular lichen planus (LP) is a rare variant of cutaneous lichen planus characterized by the development of annular lesions.","definition_xrefs":["Orphanet:254424"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lichen planus","termid":"MONDO:0006572"}],"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":"annular lichen planus","secondary_identifiers":["icd11.foundation:206328727","GARD:12674","SCTID:201000006","MEDGEN:590346","UMLS:C0406363"],"synonyms":[{"name":"annular LP","type":"exact"}],"termid":"MONDO:0016772","xrefs":{"Monarch":{"xref_id":"0016772"}}}


id: PBO:0109374
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis expressed transcript, Y-linked 7B","termid":"PBO:0109374"}


id: MONDO:0010141
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":"tiglic acidemia","secondary_identifiers":["MESH:C536921","OMIM:275190","SCTID:444755001","UMLS:C1848793","MEDGEN:376443","ICD9:270.8"],"synonyms":[{"name":"disorder of isoleucine metabolism","type":"related"},{"name":"tiglic acidemia","type":"exact"}],"termid":"MONDO:0010141","xrefs":{"Monarch":{"xref_id":"0010141"}}}


id: PBO:0065007
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PR/SET domain 11","termid":"PBO:0065007"}


id: RO:0002206
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"x expressed in y if and only if there is a gene expression process (GO:0010467) that occurs in y, and one of the following holds: (i) x is a gene, and x is transcribed into a transcript as part of the gene expression process (ii) x is a transcript, and the transcription of x is part of the gene expression process (iii) x is a mature gene product such as a protein, and x was translated or otherwise processes from a transcript that was transcribed as part of this gene expression process","direct_ancestors":[{"relation_name":"is_a","term_name":"genomically_related_to","termid":"RO:0002330"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"expressed_in","termid":"RO:0002206"}


id: PBO:0075846
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SSU72 pseudogene 1","termid":"PBO:0075846"}


id: PBO:0027305
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_glutathione_transferase_activity","termid":"PBO:0027305"}


id: PBO:0069813
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1099, pseudogene","termid":"PBO:0069813"}


id: MONDO:0008552
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited blood coagulation disease characterized by autosomal dominant inheritance with macrothrombocytopenia, platelet anisocytosis, prolonged bleeding time but only mildly increased bleeding tendency that has material basis in heterozygous mutation in the ITGA2B gene on chromosome 17q21.31 or the ITGB3 gene on chromosome 17q21.32.","definition_xrefs":["PMID:21454453","PMID:9834222","DOID:0060691","PMID:18065693"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited bleeding disorder, platelet-type","termid":"MONDO:0000009"},{"relation_name":"is_a","term_name":"inherited blood coagulation disorder","termid":"MONDO:0021181"}],"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":"platelet-type bleeding disorder 16","secondary_identifiers":["OMIM:187800","UMLS:C5442010","MEDGEN:1781222","MESH:C566061"],"synonyms":[{"name":"BDPLT16","type":"related"},{"name":"Glanzmann thrombasthenia, autosomal dominant","type":"related"},{"name":"autosomal dominant Glanzmann thrombasthenia","type":"exact"},{"name":"autosomal dominant thrombasthenia of Glanzmann and Naegeli","type":"exact"},{"name":"bleeding disorder, platelet-type, 16","type":"related"},{"name":"bleeding disorder, platelet-type, 16, autosomal dominant","type":"exact"},{"name":"platelet-type bleeding disorder 16","type":"exact"},{"name":"thrombasthenia of Glanzmann and Naegeli, autosomal dominant","type":"related"}],"termid":"MONDO:0008552","xrefs":{"Monarch":{"xref_id":"0008552"}}}


id: PBO:0030836
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_guanine_import","termid":"PBO:0030836"}


id: MONDO:0005182
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm characterized by the presence of cystic structures lined by serous epithelial cells in a fibrotic stroma. Most commonly the primary site is the ovary, but serous cystadenofibromas can occur in the pancreas as well.","definition_xrefs":["PMID:16025006"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fibroma","termid":"MONDO:0005167"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serous cystadenofibroma","secondary_identifiers":["NCIT:C40032","EFO:0002510"],"termid":"MONDO:0005182","xrefs":{"Monarch":{"xref_id":"0005182"}}}


id: FYPO:0003539
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which homologous chromosome pairing during meiosis (synapsis) is decreased (i.e. occurs to a lower extent) over the entire length of the chromosomes.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal homologous chromosome pairing","termid":"FYPO:0003024"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000641","FYPO:0000002","FYPO:0000631","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"decreased global homologous chromosome pairing","synonyms":[{"name":"decreased generalised homologous chromosome pairing","type":"exact"},{"name":"decreased global homologous chromosome pairing at meiosis","type":"exact"},{"name":"decreased global synapsis","type":"exact"},{"name":"globally decreased homologous chromosome pairing","type":"exact"},{"name":"reduced global homologous chromosome pairing","type":"exact"}],"termid":"FYPO:0003539"}


id: GO:0070344
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of fat cell proliferation.","definition_xrefs":["GOC:mah","GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell population proliferation","termid":"GO:0042127"},{"relation_name":"regulates","term_name":"fat cell proliferation","termid":"GO:0070341"}],"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 fat cell proliferation","synonyms":[{"name":"regulation of adipocyte proliferation","type":"exact"},{"name":"regulation of adipose cell proliferation","type":"exact"}],"termid":"GO:0070344"}


id: FYPO:0004782
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which spores germinate to a greater extent than wild type following exposure to ionizing radiation.","definition_xrefs":["PomBase:mah","PMID:25533340"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell phenotype","termid":"FYPO:0003037"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"spores resistant to ionizing radiation","synonyms":[{"name":"resistant to ionizing radiation in spore phase","type":"exact"},{"name":"spores resistant to IR","type":"exact"}],"termid":"FYPO:0004782"}


id: PBO:0004589
data:
  {"annotation_feature_type":"gene","cv_name":"sequence_feature","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PIP box","termid":"PBO:0004589"}


id: GO:1900567
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving chanoclavine-I aldehyde.","definition_xrefs":["GOC:TermGenie","GOC:di"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aldehyde metabolic process","termid":"GO:0006081"},{"relation_name":"is_a","term_name":"ergot alkaloid metabolic process","termid":"GO:0035836"},{"relation_name":"is_a","term_name":"olefinic compound metabolic process","termid":"GO:0120254"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0019748","GO:0008150"],"is_obsolete":false,"name":"chanoclavine-I aldehyde metabolic process","synonyms":[{"name":"chanoclavine-I aldehyde metabolism","type":"exact"}],"termid":"GO:1900567"}


id: MONDO:0019870
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Distal trisomy 1p36 is a rare chromosomal anomaly syndrome, resulting from the partial duplication of the short arm of chromosome 1, characterized by borderline to mild intellectual disability, mild developmental delay, metopic craniosynostosis and mild craniofacial dysmorphism (incl. slopping forehead, bitemporal narrowing, blepharophimosis). Other associated abnormalities may include growth retardation, microcephaly, large hands, syndactyly, supernumerary ribs, rectal stenosis and/or anterior displacement of anus. Congenital heart malformations (e.g. atrial septal defect, patent ductus arteriosus) have also been reported.","definition_xrefs":["Orphanet:96069"],"direct_ancestors":[{"relation_name":"is_a","term_name":"partial duplication of the short arm of chromosome 1","termid":"MONDO:0017012"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"distal trisomy 1p36","secondary_identifiers":["UMLS:C4707665","GARD:19303","SCTID:766053003","MEDGEN:1646544"],"synonyms":[{"name":"distal duplication 1p36","type":"exact"},{"name":"distal trisomy type 1p36","type":"exact"},{"name":"telomeric duplication 1p36","type":"exact"},{"name":"trisomy 1pter","type":"exact"}],"termid":"MONDO:0019870","xrefs":{"Monarch":{"xref_id":"0019870"}}}


id: FYPO:0004038
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which an increase in RNA level that occurs as part of a cellular response to hydrogen peroxide begins later than normal. Total RNA or a specific RNA, such as the mRNA transcribed from a gene of interest, may be affected.","definition_xrefs":["PomBase:mah","PMID:9450957"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular response to hydrogen peroxide","termid":"FYPO:0000194"},{"relation_name":"is_a","term_name":"delayed onset of increase in RNA level during cellular response to oxidative stress","termid":"FYPO:0007793"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000298","FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"delayed onset of increase in RNA level during cellular response to hydrogen peroxide","synonyms":[{"name":"delayed increase in RNA level during cellular response to hydrogen peroxide","type":"exact"},{"name":"delayed onset of increase in RNA level during cellular response to H2O2","type":"exact"},{"name":"delayed onset of increase in RNA level during cellular response to hydrogen peroxide during mitotic cell cycle","type":"related"},{"name":"delayed onset of increase in RNA level during cellular response to hydrogen peroxide during vegetative growth","type":"exact"},{"name":"delayed onset of increase in transcript level during cellular response to hydrogen peroxide","type":"exact"}],"termid":"FYPO:0004038"}


id: PBO:0064556
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-)","termid":"PBO:0064556"}


id: GO:0005240
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete glycine receptor-associated protein (obsolete GO:0005240)","synonyms":[{"name":"glycine receptor-associated protein","type":"exact"}],"termid":"GO:0005240"}


id: PBO:0060504
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleosome assembly protein 1 like 4 pseudogene 3","termid":"PBO:0060504"}


id: MONDO:0004090
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A squamous cell carcinoma that arises from the vulva and is characterized by the presence of nests of malignant basaloid cells with a scant amount of cytoplasm.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"basaloid squamous cell carcinoma","termid":"MONDO:0003486"},{"relation_name":"is_a","term_name":"vulvar squamous cell carcinoma","termid":"MONDO:0024609"}],"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":"vulvar basaloid squamous cell carcinoma","secondary_identifiers":["NCIT:C40286","UMLS:C2211850","DOID:7048","MEDGEN:384496"],"synonyms":[{"name":"vulvar basaloid carcinoma","type":"exact"},{"name":"vulvar basaloid squamous cell carcinoma","type":"exact"}],"termid":"MONDO:0004090","xrefs":{"Monarch":{"xref_id":"0004090"}}}


id: PBO:0044143
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CTBP2 pseudogene 9","termid":"PBO:0044143"}


id: GO:0006856
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of eye pigment precursors, the inactive forms of visual pigments, into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transport","termid":"GO:0006810"},{"relation_name":"part_of","term_name":"developmental pigmentation","termid":"GO:0048066"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"eye pigment precursor transport","termid":"GO:0006856"}


id: PBO:0005699
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L27 (predicted)","termid":"PBO:0005699"}


id: PBO:0085105
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nuclear protein with role in transcription, protein quality control; localizes to the intranuclear quality control compartment (INQ) in response to proteasome inhibition or DNA replication stress; INQ likely sequesters proteins involved in DNA metabolism for degradation or re-folding; also localizes to coding regions of transcribed genes; contains three WD domains (WD-40 repeat); human ortholog WDR76 also exhibits perinuclear localization under similar stress conditions","termid":"PBO:0085105"}


id: FYPO:0004653
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 actomyosin contractile ring contraction begins later than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal actomyosin contractile ring contraction","termid":"FYPO:0001364"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000032"},{"rel_name":"is_a","termid":"FYPO:0004803"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000032","FYPO:0004803","FYPO:0001320","FYPO:0000631","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"delayed onset of actomyosin contractile ring contraction","synonyms":[{"name":"delayed actomyosin contractile ring contraction","type":"exact"},{"name":"delayed onset of actomyosin contractile ring contraction during mitotic cell cycle","type":"related"},{"name":"delayed onset of actomyosin contractile ring contraction during vegetative growth","type":"exact"},{"name":"delayed onset of mitotic actomyosin contractile ring contraction","type":"exact"},{"name":"delayed onset of mitotic contractile ring contraction","type":"exact"},{"name":"increased dwell time before actomyosin contractile ring contraction","type":"exact"}],"termid":"FYPO:0004653"}


id: MOD:01965
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-lysine residue to 2xC(13),3x(2)H labeled N6-acetyl-L-lysine.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N6-acetyl-L-lysine","termid":"MOD:00064"},{"relation_name":"is_a","term_name":"(13)C isotope tagged reagent","termid":"MOD:01428"},{"relation_name":"is_a","term_name":"(2)H deuterium tagged reagent","termid":"MOD:01431"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00408"},{"rel_name":"is_a","termid":"MOD:01875"}],"interesting_parent_ids":["MOD:00408","MOD:01875"],"is_obsolete":false,"name":"2xC(13),3x(2)H labeled N6-acetyl-L-lysine","synonyms":[{"name":"Acetate labeling reagent (K) (heavy form, +5amu)","type":"exact"},{"name":"COFRADIC heavy acetyl 13C2 2H3","type":"exact"}],"termid":"MOD:01965"}


id: PR:000027705
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A kinesin-like motor protein klp9/SPBC15D4.01c unmodified form in Schizosaccharomyces pombe.","definition_xrefs":["PomBase:MAH","PMID:18257517","PMID:19686686"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinesin-like motor protein klp9/SPBC15D4.01c","termid":"PR:000027702"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"klp9/UnMod","pombase_gene_id":"SPBC15D4.01c","synonyms":[{"name":"PomBase_original_PRO_term_name: kinesin-like motor protein klp9/SPBC15D4.01c unmodified form (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-klp9/UnMod","type":"exact"},{"name":"klp9/UnMod","type":"exact"}],"termid":"PR:000027705"}


id: GO:0042323
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the duration or quality of non-rapid eye movement (NREM) sleep.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of circadian sleep/wake cycle, sleep","termid":"GO:0042321"},{"relation_name":"is_a","term_name":"regulation of circadian sleep/wake cycle, non-REM sleep","termid":"GO:0045188"},{"relation_name":"negatively_regulates","term_name":"circadian sleep/wake cycle, non-REM sleep","termid":"GO:0042748"}],"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 circadian sleep/wake cycle, non-REM sleep","synonyms":[{"name":"down regulation of circadian sleep/wake cycle, non-REM sleep","type":"exact"},{"name":"down-regulation of circadian sleep/wake cycle, non-REM sleep","type":"exact"},{"name":"downregulation of circadian sleep/wake cycle, non-REM sleep","type":"exact"},{"name":"inhibition of circadian sleep/wake cycle, non-REM sleep","type":"narrow"},{"name":"negative regulation of non-REM sleep","type":"exact"}],"termid":"GO:0042323"}


id: SO:0001454
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A negatively charged, hydorophilic amino acid encoded by the codons GAA and GAG.","direct_ancestors":[{"relation_name":"is_a","term_name":"amino_acid","termid":"SO:0001237"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamic_acid","synonyms":[{"name":"E","type":"exact"},{"name":"Glu","type":"exact"},{"name":"glutamic acid","type":"exact"}],"termid":"SO:0001454"}


id: PBO:0066383
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RDX pseudogene 3","termid":"PBO:0066383"}


id: GO:0106091
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of creating an elongation or projection from a glial cell.","definition_xrefs":["GOC:ha","PMID:27131624"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell projection morphogenesis","termid":"GO:0048858"},{"relation_name":"part_of","term_name":"glial cell development","termid":"GO:0021782"}],"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":"glial cell projection elongation","termid":"GO:0106091"}


id: PR:O43026
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- gpd3 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O43026"],"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":"glyceraldehyde-3-phosphate dehydrogenase 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC354.12","synonyms":[{"name":"GAPDH 2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-gpd3","type":"exact"}],"termid":"PR:O43026"}


id: PBO:0083630
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EH domain-containing protein; involved in regulating phosphatidylinositol 4,5-bisphosphate levels and autophagy; Irs4p and Tax4p bind and activate the PtdIns phosphatase Inp51p; Irs4p and Tax4p are involved in localizing Atg17p to the PAS; IRS4 has a paralog, TAX4, that arose from the whole genome duplication","termid":"PBO:0083630"}


id: GO:0010484
data:
  {"annotated_genes":["SJAG_02990","SJAG_01204","SJAG_02773","SJAG_02165"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[91177,90521],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036408"},{"annotations":[91178],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043993"},{"annotations":[98726],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044016"},{"annotations":[72344],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032931"},{"annotations":[91179],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043992"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: acetyl-CoA + histone H3 = CoA + acetyl-histone H3.","definition_xrefs":["PMID:19056256"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone acetyltransferase activity","termid":"GO:0004402"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01204":null,"SJAG_02165":null,"SJAG_02773":null,"SJAG_02990":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0034212"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0034212","GO:0003674","GO:0016746","GO:0003824","GO:0140096","GO:0016740"],"is_obsolete":false,"name":"histone H3 acetyltransferase activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"H3 histone acetylase activity","type":"exact"},{"name":"H3 histone acetyltransferase activity","type":"exact"}],"termid":"GO:0010484","terms_by_termid":{"GO:0032931":null,"GO:0036408":null,"GO:0043992":null,"GO:0043993":null,"GO:0044016":null}}


id: GO:0045141
data:
  {"annotated_genes":["SJAG_01538","SJAG_01263","SJAG_00756","SJAG_01777","SJAG_03092","SJAG_05196","SJAG_05226","SJAG_03680","SJAG_05260","SJAG_03685","SJAG_03287"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[96474,115687,117303,117439],"is_not":false,"summary":null,"term":"GO:0045141"},{"annotations":[64382,89522],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070197"},{"annotations":[87162,89523,104865,99682,102570],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032121"},{"annotations":[113730],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044821"}]},"cv_name":"biological_process","definition":"The cell cycle process in which the dynamic reorganization of telomeres occurs in early meiotic prophase, during which meiotic chromosome ends are gathered in a bouquet arrangement at the inner surface of the nuclear envelope proximal to the spindle pole body. This plays an important role in progression through meiosis and precedes synapsis.","definition_xrefs":["GOC:vw","PMID:10690419"],"direct_ancestors":[{"relation_name":"is_a","term_name":"telomere localization","termid":"GO:0034397"},{"relation_name":"is_a","term_name":"chromosome organization involved in meiotic cell cycle","termid":"GO:0070192"},{"relation_name":"is_a","term_name":"chromosome localization to nuclear envelope involved in homologous chromosome segregation","termid":"GO:0090220"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00756":null,"SJAG_01263":null,"SJAG_01538":null,"SJAG_01777":null,"SJAG_03092":null,"SJAG_03287":null,"SJAG_03680":null,"SJAG_03685":null,"SJAG_05196":null,"SJAG_05226":null,"SJAG_05260":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"part_of","termid":"GO:0140013"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0140013","GO:0007049"],"is_obsolete":false,"name":"meiotic telomere clustering","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000107":null},"synonyms":[{"name":"bouquet biosynthesis","type":"narrow"},{"name":"bouquet formation","type":"narrow"}],"termid":"GO:0045141","terms_by_termid":{"GO:0032121":null,"GO:0044821":null,"GO:0045141":null,"GO:0070197":null}}


id: PBO:0036318
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L7b involved in cytoplasmic translation","termid":"PBO:0036318"}


id: GO:0050728
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the inflammatory response.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of defense response","termid":"GO:0031348"},{"relation_name":"is_a","term_name":"negative regulation of response to external stimulus","termid":"GO:0032102"},{"relation_name":"is_a","term_name":"regulation of inflammatory response","termid":"GO:0050727"},{"relation_name":"negatively_regulates","term_name":"inflammatory response","termid":"GO:0006954"}],"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 inflammatory response","secondary_identifiers":["GO:0030236","Reactome:R-HSA-9018678"],"synonyms":[{"name":"anti-inflammatory response","type":"exact"},{"name":"down regulation of inflammatory response","type":"exact"},{"name":"down-regulation of inflammatory response","type":"exact"},{"name":"downregulation of inflammatory response","type":"exact"},{"name":"inhibition of inflammatory response","type":"narrow"}],"termid":"GO:0050728"}


id: MONDO:0021297
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A in situ carcinoma that involves the nasopharynx.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pharynx carcinoma in situ","termid":"MONDO:0000372"},{"relation_name":"is_a","term_name":"nasopharyngeal carcinoma","termid":"MONDO:0015459"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992"],"is_obsolete":false,"name":"carcinoma in situ of nasopharynx","secondary_identifiers":["MEDGEN:83850","icd11.foundation:1626158287","SCTID:92664001","NCIT:C9099","UMLS:C0347096"],"synonyms":[{"name":"carcinoma in situ of nasopharynx","type":"exact"},{"name":"carcinoma in situ of the nasopharynx","type":"exact"},{"name":"nasopharyngeal carcinoma in situ","type":"exact"},{"name":"nasopharynx carcinoma in situ","type":"exact"},{"name":"nasopharynx in situ carcinoma","type":"exact"},{"name":"stage 0 carcinoma of nasopharynx","type":"exact"},{"name":"stage 0 carcinoma of the nasopharynx","type":"exact"},{"name":"stage 0 nasopharyngeal cancer","type":"exact"},{"name":"stage 0 nasopharyngeal carcinoma","type":"exact"},{"name":"stage 0 nasopharyngeal carcinoma aJCC v6","type":"exact"},{"name":"stage 0 nasopharyngeal carcinoma aJCC v6, v7, and v8","type":"exact"},{"name":"stage 0 nasopharyngeal carcinoma aJCC v7","type":"exact"},{"name":"stage 0 nasopharyngeal carcinoma aJCC v8","type":"exact"},{"name":"stage 0 nasopharyngeal carcinoma in situ","type":"exact"},{"name":"stage 0 nasopharyngeal throat cancer","type":"exact"},{"name":"stage 0 nasopharynx carcinoma","type":"exact"}],"termid":"MONDO:0021297","xrefs":{"Monarch":{"xref_id":"0021297"}}}


id: FYPO:0000263
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A gene expression phenotype in which regulation of translation in response to stress is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular response to stress","termid":"FYPO:0000162"},{"relation_name":"is_a","term_name":"translation regulation phenotype","termid":"FYPO:0000289"},{"relation_name":"is_a","term_name":"abnormal gene expression","termid":"FYPO:0006551"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0006551","FYPO:0005447","FYPO:0001985","FYPO:0000298","FYPO:0000002"],"is_obsolete":false,"name":"abnormal regulation of translation in response to stress","synonyms":[{"name":"protein synthesis after stress, defective","type":"related"}],"termid":"FYPO:0000263"}


id: GO:0070945
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed killing of a gram-negative bacterium by a neutrophil.","definition_xrefs":["GOC:add","ISBN:0781765196"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neutrophil-mediated killing of bacterium","termid":"GO:0070944"},{"relation_name":"part_of","term_name":"defense response to Gram-negative bacterium","termid":"GO:0050829"}],"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":"neutrophil-mediated killing of gram-negative bacterium","synonyms":[{"name":"neutrophil mediated killing of gram-negative bacterium","type":"exact"}],"termid":"GO:0070945"}


id: MONDO:0017759
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inborn disorder of neurotransmitter metabolism and transport","termid":"MONDO:0019219"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"disorder of catecholamine synthesis","secondary_identifiers":["Orphanet:309830","ICD9:270.8","SCTID:237921002","icd11.foundation:1382276026","MEDGEN:575179","UMLS:C0342685","GARD:21351"],"termid":"MONDO:0017759","xrefs":{"Monarch":{"xref_id":"0017759"}}}


id: GO:1905140
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of apical ectodermal ridge formation.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:18359901"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of anatomical structure morphogenesis","termid":"GO:0022603"},{"relation_name":"regulates","term_name":"apical ectodermal ridge formation","termid":"GO:1905139"}],"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 apical ectodermal ridge formation","synonyms":[{"name":"regulation of AER formation","type":"related"},{"name":"regulation of apical epidermal ridge formation","type":"exact"},{"name":"regulation of crista ectodermalis apicalis formation","type":"related"}],"termid":"GO:1905140"}


id: PBO:0113270
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Phospholipid translocase (flippase); involved in generating phospholipid asymmetry in plasma membrane; involved in endocytosis, vacuolar biogenesis and Golgi-to-ER vesicle-mediated transport; localizes to endosomes and Golgi apparatus; targeted to vacuole via AP-3 pathway","termid":"PBO:0113270"}


id: PR:Q9P6Q5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A deoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","PANTHER:PTHR11241:SF0","OMA:SCHPO01122"],"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":"deoxyuridine 5'-triphosphate nucleotidohydrolase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC644.05c","secondary_identifiers":["UniProtKB:Q9P6Q5"],"synonyms":[{"name":"Spom972h-DUT","type":"exact"},{"name":"dUTP pyrophosphatase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"dUTPase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9P6Q5"}


id: GO:0030719
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of polar granules, cytoplasmic, non-membranous RNA/protein complex aggregates in the primordial germ cells of many higher eukaryotes.","definition_xrefs":["PMID:770367","PMID:10851135"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organelle organization","termid":"GO:0006996"},{"relation_name":"part_of","term_name":"pole plasm assembly","termid":"GO:0007315"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"P granule organization","secondary_identifiers":["GO:0048114"],"synonyms":[{"name":"P granule organization and biogenesis","type":"related"},{"name":"polar granule organisation","type":"exact"},{"name":"polar granule organization and biogenesis","type":"exact"}],"termid":"GO:0030719"}


id: GO:0006602
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of creatinine, 2-amino-1,5-dihydro-1-methyl-4H-imidazol-4-one, an end product of creatine metabolism and a normal constituent of urine.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"creatinine metabolic process","termid":"GO:0046449"},{"relation_name":"is_a","term_name":"lactam catabolic process","termid":"GO:0072340"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"creatinine catabolic process","synonyms":[{"name":"creatinine breakdown","type":"exact"},{"name":"creatinine catabolism","type":"exact"},{"name":"creatinine degradation","type":"exact"}],"termid":"GO:0006602"}


id: GO:1990985
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any biological process that results in permanent cessation of all vital functions of a cell upon exposure to oxidative stress.","definition_xrefs":["GOC:pg","PMID:25950479"],"gene_count":0,"genotype_count":0,"name":"obsolete apoptosis in response to oxidative stress (obsolete GO:1990985)","termid":"GO:1990985"}


id: PR:Q9USM9
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A coenzyme Q-binding protein COQ10 homolog A, mitochondrial that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR12901:SF0","PRO:DNx","OMA:SCHPO04486"],"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":"coenzyme Q-binding protein coq10, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC16A11.07","secondary_identifiers":["UniProtKB:Q9USM9"],"synonyms":[{"name":"Spom972h-COQ10A","type":"exact"}],"termid":"PR:Q9USM9"}


id: PBO:0024483
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sec14 cytosolic factor family, glycerophospholipid-transfer protein Crs103 (predicted)","termid":"PBO:0024483"}


id: PBO:0066540
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RGS5 antisense RNA 1","termid":"PBO:0066540"}


id: MONDO:0018276
data:
  {"annotated_genes":["SJAG_04053","SJAG_00831","SJAG_01491","SJAG_03188","SJAG_05219","SJAG_04316"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84970],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012248"},{"annotations":[86438,86437],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013162"},{"annotations":[85719],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014142"},{"annotations":[85062],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014023"},{"annotations":[84934],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013049"},{"annotations":[85624,85626,85625],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009364"},{"annotations":[85712],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014140"},{"annotations":[86431,86432],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013154"},{"annotations":[85022],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033556"},{"annotations":[86436],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013159"},{"annotations":[85717],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014141"},{"annotations":[86434,86435],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013160"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital muscular dystrophy","termid":"MONDO:0019950"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00831":null,"SJAG_01491":null,"SJAG_03188":null,"SJAG_04053":null,"SJAG_04316":null,"SJAG_05219":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0002320"],"is_obsolete":false,"name":"muscular dystrophy-dystroglycanopathy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0112374","MEDGEN:1842215","UMLS:C5679911","GARD:12584","Orphanet:370953"],"synonyms":[{"name":"CMD due to dystroglycanopathy","type":"exact"},{"name":"congenital muscular dystrophy due to dystroglycanopathy","type":"related"},{"name":"muscular dystrophy-dystroglycanopathy","type":"exact"}],"termid":"MONDO:0018276","terms_by_termid":{"MONDO:0009364":null,"MONDO:0012248":null,"MONDO:0013049":null,"MONDO:0013154":null,"MONDO:0013159":null,"MONDO:0013160":null,"MONDO:0013162":null,"MONDO:0014023":null,"MONDO:0014140":null,"MONDO:0014141":null,"MONDO:0014142":null,"MONDO:0033556":null},"xrefs":{"Monarch":{"xref_id":"0018276"}}}


id: FYPO:0004340
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 mitochondrial fission, the division of a mitochondrion into two or more separate compartments, is abnormal.","definition_xrefs":["PomBase:mah","GO:0000266"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitochondrion organization","termid":"FYPO:0000809"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"abnormal mitochondrial fission","synonyms":[{"name":"abnormal mitochondrial division","type":"exact"},{"name":"abnormal mitochondrial fission during mitotic cell cycle","type":"related"},{"name":"abnormal mitochondrial fission during vegetative growth","type":"exact"},{"name":"abnormal mitochondrial proliferation","type":"related"}],"termid":"FYPO:0004340"}


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


id: PBO:0062939
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"P4HA3 antisense RNA 1","termid":"PBO:0062939"}


id: MONDO:0044406
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"},{"relation_name":"is_a","term_name":"distal arthrogryposis","termid":"MONDO:0019942"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"arthrogryposis-ectodermal dysplasia-other anomalies syndrome","secondary_identifiers":["MEDGEN:1674099","UMLS:C5191837","GARD:5029","Orphanet:3200"],"synonyms":[{"name":"Stoll-Alembik-Finck syndrome","type":"exact"}],"termid":"MONDO:0044406","xrefs":{"Monarch":{"xref_id":"0044406"}}}


id: PBO:0081676
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 597","termid":"PBO:0081676"}


id: MONDO:1012830
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any craniomandibular osteopathy that occurs in dogs due to a mutation in the SLC37A2 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"craniomandibular osteopathy, dog","termid":"MONDO:1012054"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"craniomandibular osteopathy, SLC37A2-related, dog","secondary_identifiers":["OMIA:002244-9615"],"termid":"MONDO:1012830","xrefs":{"Monarch":{"xref_id":"1012830"}}}


id: PBO:0074516
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small NF90 (ILF3) associated RNA A8","termid":"PBO:0074516"}


id: PBO:0061553
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5'-nucleotidase, cytosolic IIIB","termid":"PBO:0061553"}


id: PBO:0088909
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock protein, Hsp70 family,  Ssa-like","termid":"PBO:0088909"}


id: PBO:0065934
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rac family small GTPase 1 pseudogene 8","termid":"PBO:0065934"}


id: MONDO:0003144
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, usually aggressive malignant embryonal neoplasm of the central nervous system occurring in children. It is characterized by the presence of neuroepithelial cells which form papillary, trabecular, or tubular structures and absence of C19MC amplification. Symptoms include headache, nausea, and vomiting.","definition_xrefs":["NCIT:C4327"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"central nervous system primitive neuroectodermal neoplasm","termid":"MONDO:0000640"},{"relation_name":"is_a","term_name":"central nervous system Ewing sarcoma/peripheral primitive neuroectodermal tumor","termid":"MONDO:0016713"}],"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":"medulloepithelioma","secondary_identifiers":["Orphanet:251883","DOID:4790","SCTID:715903004","icd11.foundation:1078680756","UMLS:C5231013","GARD:20721","ONCOTREE:MDEP","MEDGEN:1702218"],"synonyms":[{"name":"Diktyoma, malignant","type":"exact"},{"name":"MDEP","type":"related"},{"name":"central nervous system medulloepithelioma","type":"exact"},{"name":"medulloepithelioma NOS (morphologic abnormality)","type":"exact"},{"name":"medulloepithelioma of the central nervous system","type":"exact"},{"name":"medulloepithelioma, central nervous system","type":"exact"}],"termid":"MONDO:0003144","xrefs":{"Monarch":{"xref_id":"0003144"}}}


id: PBO:0083552
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 verified gene CSE1","termid":"PBO:0083552"}


id: GO:0035311
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a cell in the larval wing imaginal disc becomes capable of differentiating autonomously into a wing cell, if left in its normal environment.","definition_xrefs":["PMID:10860999"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell fate specification involved in pattern specification","termid":"GO:0060573"},{"relation_name":"part_of","term_name":"wing and notum subfield formation","termid":"GO:0035309"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"wing cell fate specification","termid":"GO:0035311"}


id: GO:0070463
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + H2O = ADP + phosphate. This reaction requires the presence of a tubulin dimer to accelerate release of ADP and phosphate.","definition_xrefs":["PMID:16906148","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ATP-dependent activity","termid":"GO:0140657"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674"],"is_obsolete":false,"name":"tubulin-dependent ATPase activity","synonyms":[{"name":"tubulin-activated ATPase activity","type":"exact"}],"termid":"GO:0070463"}


id: FYPO:0003386
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of superoxide dismutase activity is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased catalytic activity","termid":"FYPO:0000662"},{"relation_name":"is_a","term_name":"abnormal superoxide dismutase activity","termid":"FYPO:0003281"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000654","FYPO:0005447","FYPO:0000298","FYPO:0001985","FYPO:0000707","FYPO:0000661","FYPO:0000652","FYPO:0000002"],"is_obsolete":false,"name":"increased superoxide dismutase activity","termid":"FYPO:0003386"}


id: PBO:0088670
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit L23","termid":"PBO:0088670"}


id: GO:0010646
data:
  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process that modulates the frequency, rate or extent of cell communication. 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id: GO:0097560
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A cilium (also called flagellum) found in Giardia species (trophozoite stage). It is nucleated by the left caudal basal body, extending cytoplasmically and exiting at the posterior end of the cell body.","definition_xrefs":["ISBN:9780124260207","GOC:giardia","PMID:5961344","PMID:16607022"],"direct_ancestors":[{"relation_name":"is_a","term_name":"9+2 motile cilium","termid":"GO:0097729"}],"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":"left caudal flagellum","synonyms":[{"name":"left caudal cilium","type":"exact"}],"termid":"GO:0097560"}


id: FYPO:0007483
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which meiotic spindle pole body duplication is abnormal during the first meiotic nuclear division.","definition_xrefs":["PMID:27889481","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal meiotic spindle pole body duplication","termid":"FYPO:0007258"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000054"},{"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:0001985","FYPO:0000002","FYPO:0005447","FYPO:0000631","FYPO:0000054"],"is_obsolete":false,"name":"abnormal meiotic spindle pole body duplication during meiosis I","synonyms":[{"name":"abnormal meiotic SPB duplication during meiosis I","type":"exact"},{"name":"abnormal meiotic spindle pole body duplication during first meiotic nuclear division","type":"exact"},{"name":"abnormal spindle pole body duplication during meiosis I","type":"exact"}],"termid":"FYPO:0007483"}


id: PBO:0053686
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 879","termid":"PBO:0053686"}


id: PBO:0004669
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zf-ZNF_U1","termid":"PBO:0004669"}


id: MONDO:0012428
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":"kyphoscoliosis 1","secondary_identifiers":["MESH:C565711","MEDGEN:347550","OMIM:610170","UMLS:C1857795"],"synonyms":[{"name":"KYPSC1","type":"exact"},{"name":"kyphoscoliosis 1","type":"exact"}],"termid":"MONDO:0012428","xrefs":{"Monarch":{"xref_id":"0012428"}}}


id: GO:0051815
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directional movement of an organism from one place to another within a second organism, where the two organisms are in a symbiotic interaction.","definition_xrefs":["GOC:cc"],"gene_count":0,"genotype_count":0,"name":"obsolete migration in other organism involved in symbiotic interaction (obsolete GO:0051815)","synonyms":[{"name":"migration in other organism during symbiotic interaction","type":"related"},{"name":"migration within other organism during symbiotic interaction","type":"related"}],"termid":"GO:0051815"}


id: GO:0098737
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that results in the incorporation of a protein into a plasma membrane. Incorporation in this context means having some part or covalently attached group that is inserted into the the hydrophobic region of one or both bilayers.","definition_xrefs":["GOC:DOS"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein insertion into membrane","termid":"GO:0051205"},{"relation_name":"is_a","term_name":"protein localization to cell periphery","termid":"GO:1990778"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0061024","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"protein insertion into plasma membrane","termid":"GO:0098737"}


id: GO:0018959
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving a phenol, any compound containing one or more hydroxyl groups directly attached to an aromatic carbon ring, in the presence of oxygen.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenol-containing compound metabolic process","termid":"GO:0018958"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"aerobic phenol-containing compound metabolic process","secondary_identifiers":["UM-BBD_pathwayID:pba"],"synonyms":[{"name":"aerobic phenol-containing compound metabolism","type":"exact"}],"termid":"GO:0018959"}


id: PATO:0001474
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An oriented quality inhering in a bearer by virtue of the bearer's axis being positioned forward.","definition_xrefs":["bdid:bdid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oriented","termid":"PATO:0000614"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anteverted","termid":"PATO:0001474"}


id: PBO:0083015
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Defining member of the SET3 histone deacetylase complex; which is a meiosis-specific repressor of sporulation genes; necessary for efficient transcription by RNAPII; one of two yeast proteins that contains both SET and PHD domains; SET3 has a paralog, SET4, that arose from the whole genome duplication","termid":"PBO:0083015"}


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


id: FYPO:0004561
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An increased chemical resistance phenotype observed in the vegetative growth phase of the life cycle in which cells grow in the presence of a higher concentration of BE49385A (a GPI synthesis inhibitor, also called YW3548) than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002682"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0001985","FYPO:0002682","FYPO:0005447","FYPO:0000139"],"is_obsolete":false,"name":"resistance to BE49385A","synonyms":[{"name":"resistance to BE49385A during mitotic cell cycle","type":"related"},{"name":"resistance to BE49385A during vegetative growth","type":"exact"},{"name":"resistance to YW3548","type":"exact"},{"name":"resistant to BE49385A","type":"exact"}],"termid":"FYPO:0004561"}


id: PBO:0062631
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 11 subfamily H member 12","termid":"PBO:0062631"}


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


id: PBO:0048245
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G antigen 12F","termid":"PBO:0048245"}


id: PBO:0061462
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"negative regulator of antiviral response","termid":"PBO:0061462"}


id: PR:000037300
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein complex composed of two subunits of Schizosaccharomyces pombe serine/threonine-protein kinase cds1 primed by rad3-rad26 complex and activated by autophosphorylation.","definition_xrefs":["PMID:19357077"],"direct_ancestors":[{"relation_name":"is_a","term_name":"serine/threonine-protein kinase cds1 (Schizosaccharomyces pombe)","termid":"PR:000030002"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine-protein kinase cds1 homodimer, phosphorylated 2 (Schizosaccharomyces pombe)","pombase_gene_id":"SPCC18B5.11c","termid":"PR:000037300"}


id: PBO:0066916
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 218","termid":"PBO:0066916"}


id: PBO:0065492
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome assembly chaperone 1","termid":"PBO:0065492"}


id: GO:0048137
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The meiotic divisions undergone by the primary and secondary spermatocytes to produce haploid spermatids.","definition_xrefs":["GOC:pr","GOC:jid","ISBN:0879694238"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell division","termid":"GO:0051301"},{"relation_name":"part_of","term_name":"spermatogenesis","termid":"GO:0007283"}],"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":"spermatocyte division","synonyms":[{"name":"spermatocyte cell division","type":"exact"}],"termid":"GO:0048137"}


id: CHEBI:48607
data:
  {"annotation_feature_type":"gene","cv_name":"chebi_ontology","definition":"A metal chloride salt with a Li(+) counterion.","direct_ancestors":[{"relation_name":"is_a","term_name":"chemical entity","termid":"CHEBI:24431"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lithium chloride","termid":"CHEBI:48607"}


id: PBO:0066375
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RDM1 pseudogene 2","termid":"PBO:0066375"}


id: SO:0001730
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A kind of histone modification site, whereby the 5th residue (a lysine), from the start of the 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":"H4K5_acetylation_site","synonyms":[{"name":"H4K5 acetylation site","type":"exact"},{"name":"H4K5ac","type":"exact"}],"termid":"SO:0001730"}


id: PBO:0044204
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cathepsin L pseudogene 2","termid":"PBO:0044204"}


id: PBO:0039907
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARHGEF7 antisense RNA 2","termid":"PBO:0039907"}


id: PBO:0049661
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H4 clustered histone 15","termid":"PBO:0049661"}


id: MONDO:0013926
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the WDR11 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Kallmann syndrome","termid":"MONDO:0018800"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypogonadotropic hypogonadism 14 with or without anosmia","secondary_identifiers":["UMLS:C3540450","ICD10CM:E23.0","GARD:15857","OMIM:614858","DOID:0090087","MEDGEN:761703"],"synonyms":[{"name":"HH14","type":"related"},{"name":"WDR11 hypogonadotropic hypogonadism","type":"exact"},{"name":"hypogonadotropic hypogonadism 14 with or without anosmia","type":"exact"},{"name":"hypogonadotropic hypogonadism caused by mutation in WDR11","type":"exact"}],"termid":"MONDO:0013926","xrefs":{"Monarch":{"xref_id":"0013926"}}}


id: PBO:0083765
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential membrane protein localized at nuclear envelope and SPBs; required for insertion of the newly duplicated spindle pole body into the nuclear envelope; potentially phosphorylated by Cdc28p; MPS2 has a paralog, CSM4, that arose from the whole genome duplication","termid":"PBO:0083765"}


id: PR:O14080
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPACUNK4.15 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14080"],"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 UNK4,15 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPACUNK4.15","synonyms":[{"name":"Spom972h-SPACUNK4.15","type":"exact"}],"termid":"PR:O14080"}


id: PBO:0069832
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1118, pseudogene","termid":"PBO:0069832"}


id: GO:0072089
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The multiplication or reproduction of stem cells, resulting in the expansion of a stem cell population. A stem cell is a cell that retains the ability to divide and proliferate throughout life to provide progenitor cells that can differentiate into specialized cells.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell population proliferation","termid":"GO:0008283"}],"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":"stem cell proliferation","termid":"GO:0072089"}


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: 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","GOC:vw","PMID:15030757"],"gene_count":0,"genotype_count":0,"name":"obsolete horsetail nucleus leading edge (obsolete GO:0071687)","termid":"GO:0071687"}


id: PBO:0067308
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 394, pseudogene","termid":"PBO:0067308"}


id: PBO:0046876
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 8 member A1","termid":"PBO:0046876"}


id: GO:1903852
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of cristae formation.","definition_xrefs":["GO_REF:0000058","GOC:pad","GOC:PARL","PMID:19279012","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of organelle organization","termid":"GO:0010638"},{"relation_name":"is_a","term_name":"regulation of cristae formation","termid":"GO:1903850"},{"relation_name":"positively_regulates","term_name":"cristae formation","termid":"GO:0042407"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0007005"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0061024"},{"rel_name":"positively_regulates","termid":"GO:0061024"},{"rel_name":"regulates","termid":"GO:0007005"}],"interesting_parent_ids":["GO:0007005","GO:0008150","GO:0061024"],"is_obsolete":false,"name":"positive regulation of cristae formation","synonyms":[{"name":"activation of cristae formation","type":"narrow"},{"name":"up regulation of cristae formation","type":"exact"},{"name":"up-regulation of cristae formation","type":"exact"},{"name":"upregulation of cristae formation","type":"exact"}],"termid":"GO:1903852"}


id: GO:0000142
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A contractile ring, i.e. a cytoskeletal structure composed of actin filaments and myosin, that forms beneath the plasma membrane at the mother-bud neck in mitotic cells that divide by budding in preparation for completing cytokinesis. An example of this structure is found in Saccharomyces cerevisiae.","definition_xrefs":["GOC:krc","PMID:16009555"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitotic actomyosin contractile ring","termid":"GO:0110085"},{"relation_name":"part_of","term_name":"cellular bud neck","termid":"GO:0005935"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0015629"},{"rel_name":"is_a","termid":"GO:0070938"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005938"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0070938","GO:0015629","GO:0005938"],"is_obsolete":false,"name":"cellular bud neck contractile ring","synonyms":[{"name":"neck ring","type":"exact"}],"termid":"GO:0000142"}


id: GO:0080148
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 water deprivation. Response to water deprivation is a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a water deprivation stimulus, prolonged deprivation of water.","definition_xrefs":["PMID:18835996"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of response to stimulus","termid":"GO:0048585"},{"relation_name":"is_a","term_name":"regulation of response to water deprivation","termid":"GO:2000070"},{"relation_name":"negatively_regulates","term_name":"response to water deprivation","termid":"GO:0009414"}],"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 water deprivation","termid":"GO:0080148"}


id: MOD:02007
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-lysine residue to N6-palmitoleyl-L-lysine.","direct_ancestors":[{"relation_name":"is_a","term_name":"N6-acylated L-lysine","termid":"MOD:01875"},{"relation_name":"is_a","term_name":"N-palmitoleylated residue","termid":"MOD:02008"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01875"},{"rel_name":"is_a","termid":"MOD:01155"}],"interesting_parent_ids":["MOD:01875","MOD:01155"],"is_obsolete":false,"name":"N6-palmitoleyl-L-lysine","termid":"MOD:02007"}


id: PBO:0064330
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PLS3 antisense RNA 1","termid":"PBO:0064330"}


id: PBO:0072722
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RXYLT1 antisense RNA 1","termid":"PBO:0072722"}


id: PBO:0027629
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_level_of_histone_H3_in_cell","termid":"PBO:0027629"}


id: GO:0051259
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of creating protein oligomers, compounds composed of a small number, usually between three and ten, of component monomers; protein oligomers may be composed of different or identical monomers. Oligomers may be formed by the polymerization of a number of monomers or the depolymerization of a large protein polymer.","definition_xrefs":["PMID:18293929","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex assembly","termid":"GO:0065003"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0065003","GO:0044085","GO:0008150"],"is_obsolete":false,"name":"protein complex oligomerization","secondary_identifiers":["GO:0035786"],"synonyms":[{"name":"protein multimerization","type":"related"},{"name":"protein oligomer assembly","type":"exact"},{"name":"protein oligomer biosynthesis","type":"broad"},{"name":"protein oligomer biosynthetic process","type":"broad"},{"name":"protein oligomer formation","type":"exact"},{"name":"protein oligomerization","type":"exact"}],"termid":"GO:0051259"}


id: GO:1901801
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving 1,5-anhydro-D-fructose.","definition_xrefs":["PMID:15716041","GOC:TermGenie","MetaCyc:PWY-6992","UniPathway:UPA00738","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monosaccharide metabolic process","termid":"GO:0005996"},{"relation_name":"is_a","term_name":"polyol metabolic process","termid":"GO:0019751"},{"relation_name":"is_a","term_name":"ketone metabolic process","termid":"GO:0042180"},{"relation_name":"is_a","term_name":"epoxide metabolic process","termid":"GO:0097176"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0005975","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"1,5-anhydro-D-fructose metabolic process","synonyms":[{"name":"1,5-anhydro-D-fructose metabolism","type":"exact"}],"termid":"GO:1901801"}


id: MONDO:0007775
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":"hypersecretion of adrenal androgens, familial","secondary_identifiers":["OMIM:145295","MEDGEN:326725","UMLS:C1840387","MESH:C536845"],"synonyms":[{"name":"familial hypersecretion of adrenal androgens","type":"related"},{"name":"hypersecretion of adrenal androgens, familial","type":"exact"}],"termid":"MONDO:0007775","xrefs":{"Monarch":{"xref_id":"0007775"}}}


id: PBO:0116848
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane beta-glucan biosynthesis protein Max1","termid":"PBO:0116848"}


id: GO:0097743
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A de novo centriole assembly process observed in multi-ciliated sperm cells of some primitive land plants, and where centrioles are formed from a blepharoplast, ultimately giving rise to multiple cilia on the sperm surface.","definition_xrefs":["GOC:cilia","PMID:25047614"],"direct_ancestors":[{"relation_name":"is_a","term_name":"de novo centriole assembly","termid":"GO:0097742"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007010"},{"rel_name":"part_of","termid":"GO:0000226"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0000226","GO:0007010","GO:0008150","GO:0044085"],"is_obsolete":false,"name":"de novo centriole assembly via blepharoplast","synonyms":[{"name":"multiciliation","type":"related"},{"name":"multiciliogenesis","type":"related"}],"termid":"GO:0097743"}


id: PBO:0009980
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MCM complex subunit Mcm4/Cdc21","termid":"PBO:0009980"}


id: PBO:0070322
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNY3 pseudogene 11","termid":"PBO:0070322"}


id: PBO:0088270
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit L51-b","termid":"PBO:0088270"}


id: MONDO:0043176
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"inborn disorder of purine or pyrimidine metabolism","termid":"MONDO:0019254"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019254"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0019254","MONDO:0005066"],"is_obsolete":false,"name":"phosphoribosylpyrophosphate synthetase deficiency","secondary_identifiers":["SCTID:124343001","MESH:C537897","HGNC:9462","UMLS:C1291401","MEDGEN:220944","MESH:C535995"],"synonyms":[{"name":"PRPP synthetase deficiency","type":"related"},{"name":"deafness hyperuricemia neurologic ataxia","type":"exact"}],"termid":"MONDO:0043176","xrefs":{"Monarch":{"xref_id":"0043176"}}}


id: FYPO:0001588
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the import of lysine into the cell occurs to a lower extent than normal when the cell is subject to nitrogen starvation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased lysine import","termid":"FYPO:0001650"},{"relation_name":"is_a","term_name":"abnormal lysine import during nitrogen starvation","termid":"FYPO:0001652"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000002","FYPO:0000138"],"is_obsolete":false,"name":"decreased lysine import during nitrogen starvation","synonyms":[{"name":"decreased L-lysine import across plasma membrane during nitrogen starvation","type":"exact"},{"name":"decreased L-lysine import during nitrogen starvation","type":"exact"},{"name":"decreased lysine import during nitrogen depletion","type":"exact"},{"name":"decreased lysine import during nitrogen deprivation","type":"exact"},{"name":"decreased lysine import into cell during nitrogen starvation","type":"exact"},{"name":"decreased lysine transport into cell during nitrogen starvation","type":"exact"},{"name":"decreased lysine uptake during nitrogen starvation","type":"exact"},{"name":"reduced lysine import during nitrogen starvation","type":"exact"}],"termid":"FYPO:0001588"}


id: PBO:0084671
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial aminopeptidase; cleaves the N termini of at least 38 imported proteins after cleavage by the mitochondrial processing peptidase (MPP), thereby increasing their stability; member of the aminopeptidase P family; yeast ortholog of human gene XPNPEP3, which is mutated in rare hereditary kidney disease similar to nephronophthisis","termid":"PBO:0084671"}


id: MONDO:0016621
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Juvenile Huntington disease (JHD) is a form of Huntington disease (HD), characterized by onset of signs and symptoms before 20 years of age.","definition_xrefs":["Orphanet:248111"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Huntington disease","termid":"MONDO:0007739"}],"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":"juvenile Huntington disease","secondary_identifiers":["MEDGEN:155518","GARD:10510","NCIT:C147072","SCTID:230299004","UMLS:C0751208"],"synonyms":[{"name":"Huntington disease, juvenile onset","type":"related"},{"name":"JHD","type":"exact"},{"name":"juvenile Huntington chorea","type":"exact"},{"name":"juvenile onset HD","type":"related"}],"termid":"MONDO:0016621","xrefs":{"Monarch":{"xref_id":"0016621"}}}


id: GO:0045765
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of angiogenesis.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of anatomical structure morphogenesis","termid":"GO:0022603"},{"relation_name":"is_a","term_name":"regulation of vasculature development","termid":"GO:1901342"},{"relation_name":"regulates","term_name":"angiogenesis","termid":"GO:0001525"}],"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 angiogenesis","termid":"GO:0045765"}


id: MONDO:0006991
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete sympathetic ophthalmia (obsolete MONDO:0006991)","termid":"MONDO:0006991","xrefs":{"Monarch":{"xref_id":"0006991"}}}


id: PBO:0079097
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Tyr (GTA) 10-1","termid":"PBO:0079097"}


id: PBO:0056524
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"melanocortin 1 receptor","termid":"PBO:0056524"}


id: MONDO:0013196
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hereditary nonpolyposis colon cancer in which the cause of the disease is a mutation in the EPCAM gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"Lynch syndrome","termid":"MONDO:0005835"},{"relation_name":"is_a","term_name":"hereditary nonpolyposis colon cancer","termid":"MONDO:0018630"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"Lynch syndrome 8","secondary_identifiers":["DOID:0070270","MEDGEN:412966","MESH:C567685","UMLS:C2750471","GARD:15638","OMIM:613244"],"synonyms":[{"name":"EPCAM hereditary nonpolyposis colon cancer","type":"exact"},{"name":"HNPCC8","type":"related"},{"name":"colorectal cancer, hereditary nonpolyposis, type 8","type":"exact"},{"name":"hereditary nonpolyposis colon cancer caused by mutation in EPCAM","type":"exact"}],"termid":"MONDO:0013196","xrefs":{"Monarch":{"xref_id":"0013196"}}}


id: GO:0047329
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: hexose + phosphoramidate = hexose 1-phosphate + NH3.","definition_xrefs":["MetaCyc:2.7.1.62-RXN","EC:2.7.1.62"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinase activity","termid":"GO:0016301"},{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016740","GO:0003824","GO:0003674","GO:0016301"],"is_obsolete":false,"name":"phosphoramidate-hexose phosphotransferase activity","secondary_identifiers":["RHEA:10972"],"synonyms":[{"name":"phosphoramidate-hexose transphosphorylase activity","type":"related"},{"name":"phosphoramidate:hexose 1-phosphotransferase activity","type":"related"},{"name":"phosphoramidic-hexose transphosphorylase activity","type":"related"}],"termid":"GO:0047329"}


id: GO:0061534
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regulated release of gamma-aminobutyric acid by a cell, in which the gamma-aminobutyric acid acts as a neurotransmitter.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neurotransmitter secretion","termid":"GO:0007269"},{"relation_name":"is_a","term_name":"gamma-aminobutyric acid secretion","termid":"GO:0014051"},{"relation_name":"part_of","term_name":"synaptic transmission, GABAergic","termid":"GO:0051932"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810","GO:0023052"],"is_obsolete":false,"name":"gamma-aminobutyric acid secretion, neurotransmission","termid":"GO:0061534"}


id: PBO:0068109
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 416","termid":"PBO:0068109"}


id: PBO:0047524
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"free fatty acid receptor 4","termid":"PBO:0047524"}


id: MONDO:0002527
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A dome-shaped, rapidly growing skin lesion composed of well differentiated squamous cells. It represents a proliferation of the infundibular epithelium of the hair follicle and its morphologic distinction from a well differentiated carcinoma may be difficult or impossible. Keratoacanthomas affect males more frequently than females and the majority tend to regress spontaneously. It has been suggested that keratoacanthoma represents a distinct subtype of squamous cell carcinoma of the skin.","definition_xrefs":["NCIT:C3146"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"skin squamous cell carcinoma","termid":"MONDO:0002529"},{"relation_name":"is_a","term_name":"epithelial skin neoplasm","termid":"MONDO:0021634"}],"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":"keratoacanthoma","secondary_identifiers":["SCTID:254662007","UMLS:C0022572","DOID:3149","MEDGEN:5954","ICDO:8071/1","MESH:D007636","icd11.foundation:516478127"],"termid":"MONDO:0002527","xrefs":{"Monarch":{"xref_id":"0002527"}}}


id: GO:0017021
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete myosin phosphatase myosin binding (obsolete GO:0017021)","synonyms":[{"name":"myosin phosphatase myosin binding","type":"exact"}],"termid":"GO:0017021"}


id: FYPO:0004788
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cellular process phenotype in which the phosphorylation of serine residues in one or more specific proteins, or of specific protein sites, occurs to a greater extent than normal when the cell is subject to glucose starvation.","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete increased protein serine phosphorylation during glucose starvation (obsolete FYPO:0004788)","synonyms":[{"name":"increased peptidyl-serine phosphorylation during glucose starvation","type":"exact"},{"name":"increased protein serine phosphorylation during cellular response to glucose starvation","type":"exact"},{"name":"increased protein serine phosphorylation during glucose depletion","type":"exact"},{"name":"increased protein serine phosphorylation during glucose deprivation","type":"exact"},{"name":"increased protein serine phosphorylation during glucose limitation","type":"related"},{"name":"increased serine phosphorylation during glucose starvation","type":"exact"}],"termid":"FYPO:0004788"}


id: SO:0002316
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant that decreases the level or amount of gene product produced.","definition_xrefs":["GenCC:AR"],"direct_ancestors":[{"relation_name":"is_a","term_name":"altered_gene_product_level","termid":"SO:0002314"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"decreased_gene_product_level","synonyms":[{"name":"decreased gene product level","type":"exact"},{"name":"decreased transcription level","type":"exact"},{"name":"decreased_transcription_level","type":"exact"},{"name":"reduced gene product level","type":"exact"},{"name":"reduced transcription level","type":"exact"},{"name":"reduced_gene_product_level","type":"exact"},{"name":"reduced_transcription_level","type":"exact"}],"termid":"SO:0002316"}


id: PBO:0044572
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DBF4 zinc finger pseudogene 2","termid":"PBO:0044572"}


id: PBO:0040345
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP synthase membrane subunit f pseudogene 2","termid":"PBO:0040345"}


id: PBO:0002293
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial single-stranded DNA binding protein Rim1","termid":"PBO:0002293"}


id: PBO:0066829
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 128","termid":"PBO:0066829"}


id: PBO:0070710
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L9 pseudogene 15","termid":"PBO:0070710"}


id: PBO:0044756
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DEAD-box helicase 39B pseudogene 2","termid":"PBO:0044756"}


id: PBO:0113577
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RQT complex subunit ubiquitin-protein ligase E3 subunit Rqt1","termid":"PBO:0113577"}


id: MONDO:0016582
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital heart malformation","termid":"MONDO:0019512"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital mitral malformation","secondary_identifiers":["GARD:1495","Orphanet:2447","UMLS:C5680882","MEDGEN:1842184"],"termid":"MONDO:0016582","xrefs":{"Monarch":{"xref_id":"0016582"}}}


id: FYPO:0003263
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A sporulation phenotype in which asci that contain more than four, and up to eight, spores form following conjugation and subsequent sporulation.","definition_xrefs":["PomBase:mah","PMID:24196444","PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal sporulation resulting in formation of ascus with more or fewer than four spores","termid":"FYPO:0001894"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000121"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000121","FYPO:0001985","FYPO:0000002","FYPO:0000631","FYPO:0005447"],"is_obsolete":false,"name":"abnormal sporulation resulting in formation of ascus with more than four spores","synonyms":[{"name":"8-spored asci","type":"related"},{"name":"abnormal ascospore formation resulting in formation of asci with more than four spores","type":"exact"},{"name":"abnormal sporulation resulting in formation of asci with more than four spores","type":"exact"},{"name":"asci with increased number of spores","type":"exact"},{"name":"eight-spored asci","type":"related"}],"termid":"FYPO:0003263"}


id: GO:0150018
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a basal dendrite over time, from its formation to the mature structure.","definition_xrefs":["GOC:aruk","PMID:22683681","GOC:bc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dendrite development","termid":"GO:0016358"}],"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":"basal dendrite development","termid":"GO:0150018"}


id: GO:0072100
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The establishment of the ureteric bud such that there is a similar arrangement in form and relationship of parts along its anterior/posterior axis.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"specification of symmetry","termid":"GO:0009799"},{"relation_name":"is_a","term_name":"anterior/posterior pattern specification involved in ureteric bud development","termid":"GO:0072099"}],"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":"specification of ureteric bud anterior/posterior symmetry","synonyms":[{"name":"specification of ureteric bud anterior/posterior asymmetry","type":"exact"}],"termid":"GO:0072100"}


id: PBO:0081194
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein interacting with K protein 1","termid":"PBO:0081194"}


id: PBO:0077776
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TOMM40 pseudogene 3","termid":"PBO:0077776"}


id: MONDO:0001354
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete acute endophthalmitis (obsolete MONDO:0001354)","termid":"MONDO:0001354","xrefs":{"Monarch":{"xref_id":"0001354"}}}


id: PBO:0049001
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycerophosphocholine phosphodiesterase 1","termid":"PBO:0049001"}


id: GO:1990658
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A transferase complex which is capable of transferring nitrogenous groups from one component to another.","definition_xrefs":["GOC:bhm","PMID:25417112"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase complex","termid":"GO:1990234"},{"relation_name":"part_of","term_name":"cytoplasm","termid":"GO:0005737"}],"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":"transnitrosylase complex","synonyms":[{"name":"transferase complex, transferring nitrogenous groups","type":"exact"}],"termid":"GO:1990658"}


id: PBO:0067691
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5.8S ribosomal N3","termid":"PBO:0067691"}


id: PBO:0058186
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4479","termid":"PBO:0058186"}


id: PBO:0040099
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADP-ribosyltransferase 5","termid":"PBO:0040099"}


id: GO:1904877
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of DNA ligase activity.","definition_xrefs":["GOC:BHF","GO_REF:0000059","GOC:BHF_telomere","GOC:TermGenie","GOC:rl","PMID:17389648"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of DNA ligase activity (obsolete GO:1904877)","synonyms":[{"name":"activation of DNA ligase activity","type":"narrow"},{"name":"up regulation of DNA ligase activity","type":"exact"},{"name":"up-regulation of DNA ligase activity","type":"exact"},{"name":"upregulation of DNA ligase activity","type":"exact"}],"termid":"GO:1904877"}


id: PBO:0050803
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HtrA serine peptidase 3","termid":"PBO:0050803"}


id: GO:0070649
data:
  {"annotated_genes":["SJAG_00938","SJAG_03011"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[107887,115921],"is_not":false,"summary":null,"term":"GO:0070649"}]},"cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a formin-nucleated actin cable. A formin-nucleated actin cable is an actin filament bundle that consists of short filaments organized into bundles of uniform polarity, and is nucleated by formins.","definition_xrefs":["PMID:14671023","GOC:mah","PMID:16959963"],"direct_ancestors":[{"relation_name":"is_a","term_name":"parallel actin filament bundle assembly","termid":"GO:0030046"},{"relation_name":"is_a","term_name":"formin-nucleated actin cable organization","termid":"GO:0110009"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00938":null,"SJAG_03011":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007010"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0030036"}],"interesting_parent_ids":["GO:0007010","GO:0030036","GO:0044085","GO:0008150"],"is_obsolete":false,"name":"formin-nucleated actin cable assembly","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"formin-nucleated actin cable formation","type":"exact"}],"termid":"GO:0070649","terms_by_termid":{"GO:0070649":null}}


id: GO:0032133
data:
  {"annotated_genes":["SJAG_01837","SJAG_02807","SJAG_04412","SJAG_00697"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[73116,76875,108961,111634],"is_not":false,"summary":null,"term":"GO:0032133"}]},"cv_name":"cellular_component","definition":"A eukaryotically conserved protein complex that localizes to kinetochores in early mitosis, the spindle mid-zone in anaphase B and to the telophase midbody. It has been proposed that the passenger complex coordinates various events based on its location to different structures during the course of mitosis. Complex members include the BIR-domain-containing protein Survivin, Aurora kinase, INCENP and Borealin.","definition_xrefs":["PMID:16824200","GOC:vw","PMID:19570910"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microtubule associated complex","termid":"GO:0005875"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00697":null,"SJAG_01837":null,"SJAG_02807":null,"SJAG_04412":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0015630"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0015630"],"is_obsolete":false,"name":"chromosome passenger complex","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"CPC","type":"broad"},{"name":"CPC complex","type":"exact"},{"name":"chromosomal passenger complex","type":"exact"}],"termid":"GO:0032133","terms_by_termid":{"GO:0032133":null}}


id: MONDO:0013667
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete myelodysplastic syndrome (obsolete MONDO:0013667)","termid":"MONDO:0013667","xrefs":{"Monarch":{"xref_id":"0013667"}}}


id: PBO:0085396
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Plasma membrane permease; mediates uptake of glycerophosphoinositol and glycerophosphocholine as sources of the nutrients inositol and phosphate; expression and transport rate are regulated by phosphate and inositol availability","termid":"PBO:0085396"}


id: GO:1990225
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Narrow, electron-dense part of the rhoptry that extends through the conoid at the apical tip of an apicomplexan parasite. The rhoptry neck serves as a duct through which the contents of the rhoptry are secreted after attachment to the host has been completed and at the commencement of invasion.","definition_xrefs":["GOC:pr","PMID:23499754","PMID:24002067","PMID:23937520","PMID:24070999","GOC:giardia"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"rhoptry","termid":"GO:0020008"}],"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":"rhoptry neck","termid":"GO:1990225"}


id: MONDO:1010789
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Stiff skin syndrome that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"stiff skin syndrome, non-human animal","termid":"MONDO:1010147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"stiff skin syndrome, dog","secondary_identifiers":["OMIA:002018-9615"],"termid":"MONDO:1010789","xrefs":{"Monarch":{"xref_id":"1010789"}}}


id: PBO:0081940
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger HIT-type containing 3","termid":"PBO:0081940"}


id: MONDO:0850068
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"immune system disorder","termid":"MONDO:0005046"}],"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":"early-onset autoimmunity-autoinflammation-immunodeficiency syndrome","secondary_identifiers":["Orphanet:619948","MEDGEN:1842754","UMLS:C5680416","GARD:22465"],"termid":"MONDO:0850068","xrefs":{"Monarch":{"xref_id":"0850068"}}}


id: GO:0044158
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The rigid or semi-rigid envelope lying outside the host cell membrane of plant, fungal, and most prokaryotic cells, maintaining their shape and protecting them from osmotic lysis. In plants it is made of cellulose and, often, lignin; in fungi it is composed largely of polysaccharides; in bacteria it is composed of peptidoglycan.","definition_xrefs":["GOC:rph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host cell part","termid":"GO:0033643"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"host cell wall","termid":"GO:0044158"}


id: GO:1904969
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The orderly movement of a slow muscle cell from one site to another.","definition_xrefs":["PMID:14667409","GOC:TermGenie","PMID:15572133","PMID:25534553","GO_REF:0000091","GOC:ymb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myotube cell migration","termid":"GO:0110122"}],"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":"slow muscle cell migration","synonyms":[{"name":"slow-twitch muscle cell migration","type":"exact"}],"termid":"GO:1904969"}


id: GO:0085017
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The invasion by a symbiont of a cell of a host organism, forming a vacuole in which the symbiont resides. The vacuole membrane is formed from lipids and proteins derived from both host and symbiont. Begins when the symbiont attaches on to the host cell membrane which invaginates and deepens as the symbiont enters, and ends when the host cell membrane closes behind the newly-formed vacuole.","definition_xrefs":["GOC:jl","PMID:18665841","PMID:8690024","PMID:9580555"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont entry into host cell","termid":"GO:0046718"}],"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":"entry into host cell by a symbiont-containing vacuole","secondary_identifiers":["GO:0052370"],"synonyms":[{"name":"symbiont entry into host cell forming a parasitophorous vacuole","type":"exact"},{"name":"symbiont entry into host cell forming a pathogen-containing vacuole","type":"exact"},{"name":"symbiont entry into host cell forming a symbiont-containing vacuole","type":"related"}],"termid":"GO:0085017"}


id: PBO:0050328
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 30","termid":"PBO:0050328"}


id: GO:0072591
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + citrate + L-glutamate = ADP + phosphate + beta-citryl-L-glutamate.","definition_xrefs":["PMID:20657015"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ligase activity, forming carbon-nitrogen bonds","termid":"GO:0016879"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016874"],"is_obsolete":false,"name":"citrate-L-glutamate ligase activity","termid":"GO:0072591"}


id: MONDO:0001669
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete lung cancer (obsolete MONDO:0001669)","termid":"MONDO:0001669","xrefs":{"Monarch":{"xref_id":"0001669"}}}


id: MONDO:0004052
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma that arises from the transitional zone at the junction of the rectum and anus.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"squamous cell carcinoma of rectum","termid":"MONDO:0018515"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"rectal cloacogenic carcinoma","secondary_identifiers":["UMLS:C1333074","DOID:6959","MEDGEN:234156","NCIT:C5555"],"synonyms":[{"name":"cloacogenic carcinoma of rectum","type":"exact"},{"name":"cloacogenic carcinoma of the rectum","type":"exact"},{"name":"rectal cloacogenic carcinoma","type":"exact"},{"name":"rectal transition zone carcinoma","type":"exact"},{"name":"rectal transitional zone carcinoma","type":"exact"},{"name":"transition zone carcinoma of rectum","type":"exact"},{"name":"transition zone carcinoma of the rectum","type":"exact"},{"name":"transitional zone carcinoma of rectum","type":"exact"},{"name":"transitional zone carcinoma of the rectum","type":"exact"}],"termid":"MONDO:0004052","xrefs":{"Monarch":{"xref_id":"0004052"}}}


id: PBO:0077997
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TNF receptor associated factor 1","termid":"PBO:0077997"}


id: GO:0043032
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stimulates, induces or increases the rate of macrophage activation.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of leukocyte activation","termid":"GO:0002696"},{"relation_name":"is_a","term_name":"regulation of macrophage activation","termid":"GO:0043030"},{"relation_name":"positively_regulates","term_name":"macrophage activation","termid":"GO:0042116"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of macrophage activation","synonyms":[{"name":"activation of macrophage activation","type":"narrow"},{"name":"positive regulation of macrophage polarization","type":"exact"},{"name":"stimulation of macrophage activation","type":"narrow"},{"name":"up regulation of macrophage activation","type":"exact"},{"name":"up-regulation of macrophage activation","type":"exact"},{"name":"upregulation of macrophage activation","type":"exact"}],"termid":"GO:0043032"}


id: PR:B8Y7Y5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- iec5 gene.","definition_xrefs":["UniProtKB:B8Y7Y5","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":"INO80 complex subunit 5 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAPB1E7.14","synonyms":[{"name":"Spom972h-iec5","type":"exact"}],"termid":"PR:B8Y7Y5"}


id: PBO:0089557
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotic tetraspan protein, claudin Dni2","termid":"PBO:0089557"}


id: GO:0009072
data:
  {"annotated_genes":["SJAG_02505","SJAG_00592","SJAG_02408","SJAG_03485","SJAG_03312","SJAG_02734","SJAG_03775","SJAG_03124","SJAG_03167","SJAG_04842","SJAG_00224","SJAG_00248","SJAG_01137","SJAG_00518","SJAG_02400","SJAG_04747","SJAG_01455","SJAG_00493","SJAG_03580","SJAG_00337","SJAG_01346","SJAG_04652","SJAG_03055","SJAG_05007","SJAG_03743"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[72782],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008153"},{"annotations":[59853,77957,76577,72418],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009073"},{"annotations":[76370],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009074"},{"annotations":[71180,73650,70940],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000949"},{"annotations":[76378,60026,70902,79941,57836,64152,75501,78222],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000105"},{"annotations":[77685,98101,63037],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009094"},{"annotations":[73086,74048,79042,76994],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000162"},{"annotations":[63036,78424,76369],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006571"},{"annotations":[106537],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006572"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving aromatic amino acid family, amino acids with aromatic ring (phenylalanine, tyrosine, tryptophan).","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid metabolic process","termid":"GO:0006520"},{"relation_name":"is_a","term_name":"carboxylic acid metabolic process","termid":"GO:0019752"}],"gene_count":25,"genes_by_uniquename":{"SJAG_00224":null,"SJAG_00248":null,"SJAG_00337":null,"SJAG_00493":null,"SJAG_00518":null,"SJAG_00592":null,"SJAG_01137":null,"SJAG_01346":null,"SJAG_01455":null,"SJAG_02400":null,"SJAG_02408":null,"SJAG_02505":null,"SJAG_02734":null,"SJAG_03055":null,"SJAG_03124":null,"SJAG_03167":null,"SJAG_03312":null,"SJAG_03485":null,"SJAG_03580":null,"SJAG_03743":null,"SJAG_03775":null,"SJAG_04652":null,"SJAG_04747":null,"SJAG_04842":null,"SJAG_05007":null},"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:0008150","GO:0044281"],"is_obsolete":false,"name":"aromatic amino acid metabolic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000043":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-8963691"],"synonyms":[{"name":"aromatic amino acid family metabolic process","type":"exact"},{"name":"aromatic amino acid family metabolism","type":"exact"}],"termid":"GO:0009072","terms_by_termid":{"GO:0000105":null,"GO:0000162":null,"GO:0000949":null,"GO:0006571":null,"GO:0006572":null,"GO:0008153":null,"GO:0009073":null,"GO:0009074":null,"GO:0009094":null}}


id: GO:0032595
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a B cell receptor within a lipid bilayer.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein transport within lipid bilayer","termid":"GO:0032594"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0061024"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150","GO:0061024"],"is_obsolete":false,"name":"B cell receptor transport within lipid bilayer","synonyms":[{"name":"B cell receptor translocation within membrane","type":"exact"},{"name":"BCR translocation within membrane","type":"exact"},{"name":"BCR transport within lipid bilayer","type":"exact"}],"termid":"GO:0032595"}


id: GO:0150063
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the visual system over time, from its formation to the mature structure, including the eye, parts of the central nervous system (CNS) involved in processing of visual inputs, and connecting nerve pathways.","definition_xrefs":["GOC:krc","PMID:15004427","PMID:22632727","PMID:20647017","GOC:bc","GOC:aruk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sensory system development","termid":"GO:0048880"}],"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":"visual system development","synonyms":[{"name":"optic pathway development","type":"related"},{"name":"visual pathway development","type":"related"}],"termid":"GO:0150063"}


id: PBO:0044041
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chondroitin sulfate proteoglycan 4 pseudogene 13","termid":"PBO:0044041"}


id: GO:0045859
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of protein kinase activity.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein phosphorylation","termid":"GO:0001932"},{"relation_name":"is_a","term_name":"regulation of kinase activity","termid":"GO:0043549"}],"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 protein kinase activity","termid":"GO:0045859"}


id: PBO:0052625
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 4","termid":"PBO:0052625"}


id: GO:0047534
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-acetolactate = 3-hydroxy-3-methyl-2-oxobutanoate.","definition_xrefs":["EC:5.4.99.3","MetaCyc:2-ACETOLACTATE-MUTASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular transferase activity","termid":"GO:0016866"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016853"}],"interesting_parent_ids":["GO:0016853","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"2-acetolactate mutase activity","secondary_identifiers":["RHEA:16361"],"synonyms":[{"name":"2-acetolactate methylmutase activity","type":"related"},{"name":"acetohydroxy acid isomerase activity","type":"broad"},{"name":"acetolactate mutase activity","type":"related"}],"termid":"GO:0047534"}


id: FYPO:0007527
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the cell tip is increased when the cell is subject to nitrogen starvation.","definition_xrefs":["PMID:27746023","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to cell tip","termid":"FYPO:0005987"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"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:0000138","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"increased protein localization to cell tip during nitrogen starvation","synonyms":[{"name":"increased protein localization to cell tip during nitrogen depletion","type":"exact"},{"name":"increased protein localization to cell tip during nitrogen deprivation","type":"exact"}],"termid":"FYPO:0007527"}


id: GO:0032874
data:
  {"annotated_genes":["SJAG_00610","SJAG_01787","SJAG_03969","SJAG_00424","SJAG_03705","SJAG_04666"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89197,90531,87845,117650,92181,102595],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903139"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of signal transduction mediated by the stress-activated MAPK cascade.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of stress-activated MAPK cascade","termid":"GO:0032872"},{"relation_name":"is_a","term_name":"positive regulation of MAPK cascade","termid":"GO:0043410"},{"relation_name":"is_a","term_name":"positive regulation of stress-activated protein kinase signaling cascade","termid":"GO:0070304"},{"relation_name":"positively_regulates","term_name":"stress-activated MAPK cascade","termid":"GO:0051403"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00424":null,"SJAG_00610":null,"SJAG_01787":null,"SJAG_03705":null,"SJAG_03969":null,"SJAG_04666":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_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":"positive regulation of stress-activated MAPK cascade","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"activation of stress-activated MAPK cascade","type":"narrow"},{"name":"positive regulation of p38 MAPK signaling","type":"exact"},{"name":"positive regulation of p38 MAPK signalling","type":"exact"},{"name":"positive regulation of stress-activated MAPK signaling pathway","type":"exact"},{"name":"positive regulation of stress-activated MAPK signalling pathway","type":"exact"},{"name":"positive regulation of stress-activated MAPKKK cascade","type":"exact"},{"name":"positive regulation of stress-activated MAPKKK signaling pathway","type":"exact"},{"name":"positive regulation of stress-activated MAPKKK signalling pathway","type":"exact"},{"name":"stimulation of stress-activated MAPK cascade","type":"narrow"},{"name":"up regulation of stress-activated MAPK cascade","type":"exact"},{"name":"up-regulation of stress-activated MAPK cascade","type":"exact"},{"name":"upregulation of stress-activated MAPK cascade","type":"exact"}],"termid":"GO:0032874","terms_by_termid":{"GO:1903139":null}}


id: MONDO:0009539
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"acute lymphoblastic leukemia","termid":"MONDO:0004967"}],"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":"lymphoblastic leukemia, acute, with lymphomatous features","secondary_identifiers":["OMIM:247640","MESH:C565429","MEDGEN:340879","UMLS:C1855472"],"synonyms":[{"name":"lall","type":"related"},{"name":"leukemia, acute lymphoblastic","type":"exact"},{"name":"lymphoblastic leukemia, acute, with lymphomatous features","type":"exact"},{"name":"lymphomatous All","type":"related"}],"termid":"MONDO:0009539","xrefs":{"Monarch":{"xref_id":"0009539"}}}


id: MONDO:0008029
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A usually autosomal dominant inherited movement disorder caused by mutations in the COL6A1, COL6A2, and COL6A3 genes. It is characterized by progressive muscle weakness and joint stiffness in the fingers, wrists, elbows, and ankles.","definition_xrefs":["NCIT:C126688"],"direct_ancestors":[{"relation_name":"is_a","term_name":"progressive muscular dystrophy","termid":"MONDO:0016106"},{"relation_name":"is_a","term_name":"congenital muscular dystrophy","termid":"MONDO:0019950"},{"relation_name":"is_a","term_name":"congenital myopathy","termid":"MONDO:0019952"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0005336"],"is_obsolete":false,"name":"Bethlem myopathy","secondary_identifiers":["UMLS:C1834674","MEDGEN:331805","NANDO:1200220","SCTID:718572004","GARD:873","DOID:0050663","Orphanet:610","icd11.foundation:72734329","MESH:C535436","OMIMPS:158810"],"synonyms":[{"name":"BTHLM1","type":"related"},{"name":"Bethlem myopathy 1","type":"related"},{"name":"Bethlem myopathy type 1","type":"exact"},{"name":"benign autosomal dominant myopathy","type":"exact"},{"name":"benign congenital muscular dystrophy","type":"exact"}],"termid":"MONDO:0008029","xrefs":{"Monarch":{"xref_id":"0008029"}}}


id: PATO:0001563
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A mass which is higher than normal or average.","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":"mass","termid":"PATO:0000125"},{"relation_name":"is_a","term_name":"increased object quality","termid":"PATO:0002305"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased mass","secondary_identifiers":["PATO:0000578"],"synonyms":[{"name":"high mass","type":"exact"},{"name":"large mass","type":"exact"}],"termid":"PATO:0001563"}


id: PBO:0110023
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Social Distancing Gene","termid":"PBO:0110023"}


id: MONDO:0957541
data:
  {"annotated_genes":["SJAG_04772"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86134],"is_not":false,"summary":null,"term":"MONDO:0957541"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04772":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with hypotonia and speech delay, with or without seizures","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1841290","DOID:0070512","OMIM:620455","UMLS:C5830654"],"termid":"MONDO:0957541","terms_by_termid":{"MONDO:0957541":null},"xrefs":{"Monarch":{"xref_id":"0957541"}}}


id: MONDO:1012766
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any dwarfism that occurs in cattle due to a mutation in the GON4L gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"dwarfism, non-human animal","termid":"MONDO:1012971"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dwarfism, GON4L-related, cattle","secondary_identifiers":["OMIA:001985-9913"],"synonyms":[{"name":"dwarfism, Fleckvieh cattle","type":"related"}],"termid":"MONDO:1012766","xrefs":{"Monarch":{"xref_id":"1012766"}}}


id: GO:0010310
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways involving hydrogen peroxide.","definition_xrefs":["PMID:14765119"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of reactive oxygen species metabolic process","termid":"GO:2000377"},{"relation_name":"regulates","term_name":"hydrogen peroxide metabolic process","termid":"GO:0042743"}],"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 hydrogen peroxide metabolic process","synonyms":[{"name":"regulation of hydrogen peroxide metabolism","type":"exact"}],"termid":"GO:0010310"}


id: PBO:0074355
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"structural maintenance of chromosomes 3","termid":"PBO:0074355"}


id: FYPO:0008171
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which the nuclear pore complexes are more clustered together than normal.","definition_xrefs":["PMID:35354597"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular physical quality phenotype during vegetative growth","termid":"FYPO:0001321"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"increased nuclear pore complex clustering","termid":"FYPO:0008171"}


id: PBO:0090725
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deoxyuridine 5'-triphosphate nucleotidohydrolase","termid":"PBO:0090725"}


id: PBO:0048819
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein subunit gamma 5 pseudogene 3","termid":"PBO:0048819"}


id: GO:1905016
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of isoleucine-tRNA ligase activity.","definition_xrefs":["PMID:1665486","GO_REF:0000059","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of isoleucine-tRNA ligase activity (obsolete GO:1905016)","synonyms":[{"name":"down regulation of L-isoleucine:tRNAIle ligase (AMP-forming)","type":"exact"},{"name":"down regulation of isoleucine translase activity","type":"exact"},{"name":"down regulation of isoleucine-tRNA ligase activity","type":"exact"},{"name":"down regulation of isoleucine-tRNA synthetase activity","type":"exact"},{"name":"down regulation of isoleucine-transfer RNA ligase activity","type":"exact"},{"name":"down regulation of isoleucyl-tRNA synthetase activity","type":"exact"},{"name":"down regulation of isoleucyl-transfer RNA synthetase activity","type":"exact"},{"name":"down regulation of isoleucyl-transfer ribonucleate synthetase activity","type":"exact"},{"name":"down-regulation of L-isoleucine:tRNAIle ligase (AMP-forming)","type":"exact"},{"name":"down-regulation of isoleucine translase activity","type":"exact"},{"name":"down-regulation of isoleucine-tRNA ligase activity","type":"exact"},{"name":"down-regulation of isoleucine-tRNA synthetase activity","type":"exact"},{"name":"down-regulation of isoleucine-transfer RNA ligase activity","type":"exact"},{"name":"down-regulation of isoleucyl-tRNA synthetase activity","type":"exact"},{"name":"down-regulation of isoleucyl-transfer RNA synthetase activity","type":"exact"},{"name":"down-regulation of isoleucyl-transfer ribonucleate synthetase activity","type":"exact"},{"name":"downregulation of L-isoleucine:tRNAIle ligase (AMP-forming)","type":"exact"},{"name":"downregulation of isoleucine translase activity","type":"exact"},{"name":"downregulation of isoleucine-tRNA ligase activity","type":"exact"},{"name":"downregulation of isoleucine-tRNA synthetase activity","type":"exact"},{"name":"downregulation of isoleucine-transfer RNA ligase activity","type":"exact"},{"name":"downregulation of isoleucyl-tRNA synthetase activity","type":"exact"},{"name":"downregulation of isoleucyl-transfer RNA synthetase activity","type":"exact"},{"name":"downregulation of isoleucyl-transfer ribonucleate synthetase activity","type":"exact"},{"name":"inhibition of L-isoleucine:tRNAIle ligase (AMP-forming)","type":"narrow"},{"name":"inhibition of isoleucine translase activity","type":"narrow"},{"name":"inhibition of isoleucine-tRNA ligase activity","type":"narrow"},{"name":"inhibition of isoleucine-tRNA synthetase activity","type":"narrow"},{"name":"inhibition of isoleucine-transfer RNA ligase activity","type":"narrow"},{"name":"inhibition of isoleucyl-tRNA synthetase activity","type":"narrow"},{"name":"inhibition of isoleucyl-transfer RNA synthetase activity","type":"narrow"},{"name":"inhibition of isoleucyl-transfer ribonucleate synthetase activity","type":"narrow"},{"name":"negative regulation of L-isoleucine:tRNAIle ligase (AMP-forming)","type":"exact"},{"name":"negative regulation of isoleucine translase activity","type":"exact"},{"name":"negative regulation of isoleucine-tRNA synthetase activity","type":"exact"},{"name":"negative regulation of isoleucine-transfer RNA ligase activity","type":"exact"},{"name":"negative regulation of isoleucyl-tRNA synthetase activity","type":"exact"},{"name":"negative regulation of isoleucyl-transfer RNA synthetase activity","type":"exact"},{"name":"negative regulation of isoleucyl-transfer ribonucleate synthetase activity","type":"exact"}],"termid":"GO:1905016"}


id: PBO:0088487
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA translocase/ SUMO-targeted ubiquitin ligase E3","termid":"PBO:0088487"}


id: GO:2000706
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of dense core granule biogenesis.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cellular process","termid":"GO:0048523"},{"relation_name":"is_a","term_name":"regulation of dense core granule biogenesis","termid":"GO:2000705"},{"relation_name":"negatively_regulates","term_name":"dense core granule biogenesis","termid":"GO:0061110"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0044085","GO:0008150"],"is_obsolete":false,"name":"negative regulation of dense core granule biogenesis","termid":"GO:2000706"}


id: GO:0090072
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of the directed movement of sodium ions via the activity of voltage-gated sodium channels.","definition_xrefs":["GOC:dph","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of sodium ion transport via voltage-gated sodium channel activity (obsolete GO:0090072)","synonyms":[{"name":"positive regulation of sodium ion transport via voltage-gated sodium channel activity","type":"exact"}],"termid":"GO:0090072"}


id: GO:0006726
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of eye pigments, any general or particular coloring matter in living organisms, found or utilized in the eye.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eye pigment metabolic process","termid":"GO:0042441"},{"relation_name":"is_a","term_name":"pigment biosynthetic process","termid":"GO:0046148"}],"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":"eye pigment biosynthetic process","synonyms":[{"name":"eye pigment anabolism","type":"exact"},{"name":"eye pigment biosynthesis","type":"exact"},{"name":"eye pigment formation","type":"exact"},{"name":"eye pigment synthesis","type":"exact"}],"termid":"GO:0006726"}


id: MONDO:0032653
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":"cardiac-urogenital syndrome","secondary_identifiers":["OMIM:618280","Orphanet:647811","UMLS:C4748946","MEDGEN:1648333"],"synonyms":[{"name":"CARDIAC-UROGENITAL SYNDROME","type":"exact"},{"name":"CUGS","type":"exact"}],"termid":"MONDO:0032653","xrefs":{"Monarch":{"xref_id":"0032653"}}}


id: GO:0044482
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that begins with venom being forced into an organism by the bite or sting of another organism which causes damage to the extracellular matrix of the blood vessels of the bitten organism, ultimately resulting in hemorrhage in the bitten organism.","definition_xrefs":["GOC:jl","PMID:10441379","PMID:19485419","GOC:fj"],"direct_ancestors":[{"relation_name":"is_a","term_name":"envenomation resulting in hemorrhagic damage in another organism","termid":"GO:0044358"}],"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":"envenomation resulting in blood vessel extracellular matrix damage, causing hemorrhagic damage in another organism","synonyms":[{"name":"envenomation resulting in blood vessel ECM, causing hemorrhagic damage in other organism","type":"exact"},{"name":"envenomation resulting in blood vessel extracellular matrix damage, causing hemorrhagic damage in other organism","type":"exact"}],"termid":"GO:0044482"}


id: GO:0046808
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. Antigenically dense structures located at the periphery of nuclei, close to but not abutting nuclear membranes. Assemblons contain the proteins for immature-capsid assembly; they are located at the periphery of a diffuse structure composed of proteins involved in DNA synthesis, which overlaps only minimally with the assemblons. More than one site can be present simultaneously.","definition_xrefs":["PMID:8676489"],"gene_count":0,"genotype_count":0,"name":"obsolete assemblon (obsolete GO:0046808)","termid":"GO:0046808"}


id: PBO:0051747
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"integrator complex subunit 13","termid":"PBO:0051747"}


id: PBO:0075783
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine and arginine rich splicing factor 7","termid":"PBO:0075783"}


id: GO:0009539
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An integral membrane complex containing P680, the chlorophyll a molecule that functions as a primary electron donor. In the light, functioning as a water-plastoquinone oxidoreductase, it transfers electrons from water to plastoquinone.","definition_xrefs":["GOC:kd","ISBN:0943088399"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane protein complex","termid":"GO:0098796"},{"relation_name":"part_of","term_name":"photosystem II","termid":"GO:0009523"}],"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:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"photosystem II reaction center","synonyms":[{"name":"photosystem II reaction centre","type":"exact"}],"termid":"GO:0009539"}


id: PBO:0001619
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"20S proteasome component beta 5","termid":"PBO:0001619"}


id: GO:0034432
data:
  {"annotated_genes":["SJAG_04870"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[78966],"is_not":false,"summary":null,"term":"GO:0034432"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: P1-P6-bis(5'-adenosyl) pentaphosphate + H2O = AMP + adenosine 5'-tetraphosphate.","definition_xrefs":["PMID:10085096","PMID:9450008"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrophosphatase activity","termid":"GO:0016462"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04870":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"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"bis(5'-adenosyl)-pentaphosphatase activity","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"AP(5)A hydrolase activity","type":"exact"},{"name":"AP-5-A hydrolase activity","type":"exact"},{"name":"AP5A hydrolase activity","type":"exact"},{"name":"Ap5a pyrophosphohydrolase activity","type":"exact"},{"name":"diadenosine 5',5'''-P1,P6-pentaphosphate hydrolase activity","type":"exact"}],"termid":"GO:0034432","terms_by_termid":{"GO:0034432":null}}


id: MONDO:0100323
data:
  {"annotated_genes":["SJAG_04335"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86447],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013782"}]},"cv_name":"mondo","definition":"A form of pseudohypoaldosteronism that is characterized Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology.","direct_ancestors":[{"relation_name":"is_a","term_name":"pseudohypoaldosteronism","termid":"MONDO:0018638"},{"relation_name":"is_a","term_name":"inherited kidney disorder","termid":"MONDO:0100191"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04335":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"inherited pseudohypoaldosteronism","references_by_uniquename":{"PB_REF:0000006":null},"synonyms":[{"name":"hereditary pseudohypoaldosteronism","type":"exact"}],"termid":"MONDO:0100323","terms_by_termid":{"MONDO:0013782":null},"xrefs":{"Monarch":{"xref_id":"0100323"}}}


id: GO:0048442
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the sepal over time, from its formation to the mature structure.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"floral organ development","termid":"GO:0048437"},{"relation_name":"is_a","term_name":"phyllome development","termid":"GO:0048827"},{"relation_name":"part_of","term_name":"flower calyx development","termid":"GO:0048464"}],"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":"sepal development","secondary_identifiers":["GO:0048421"],"termid":"GO:0048442"}


id: PBO:0072706
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RWD domain containing 1 pseudogene 3","termid":"PBO:0072706"}


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


id: PBO:0028849
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_RNA_stability","termid":"PBO:0028849"}


id: PBO:0024802
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_part_structure_that_is_capable_of","termid":"PBO:0024802"}


id: PBO:0060427
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NGFI-A binding protein 2","termid":"PBO:0060427"}


id: GO:0061347
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of molecular signals initiated by binding of a Wnt protein to a receptor on the surface of the target cell where activated receptors signal via downstream effectors including C-Jun N-terminal kinase (JNK) to modulate cytoskeletal elements and control cell polarity that contributes to the shaping of the outflow tract.","definition_xrefs":["GOC:mtg_heart","GOC:dph","PMID:19056682"],"gene_count":0,"genotype_count":0,"name":"obsolete planar cell polarity pathway involved in outflow tract morphogenesis (obsolete GO:0061347)","termid":"GO:0061347"}


id: GO:0002090
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of receptor internalization.","definition_xrefs":["GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of receptor-mediated endocytosis","termid":"GO:0048259"},{"relation_name":"regulates","term_name":"receptor internalization","termid":"GO:0031623"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0016192"],"is_obsolete":false,"name":"regulation of receptor internalization","termid":"GO:0002090"}


id: PBO:0075909
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ST13, Hsp70 interacting protein pseudogene 1","termid":"PBO:0075909"}


id: PBO:0049816
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone deacetylase 8","termid":"PBO:0049816"}


id: PBO:0061234
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NOP14 nucleolar protein","termid":"PBO:0061234"}


id: PBO:0044839
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"defensin beta 127","termid":"PBO:0044839"}


id: GO:0016319
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the mushroom body over time, from its formation to the mature structure. The mushroom body is composed of the prominent neuropil structures of the insect central brain, thought to be crucial for olfactory associated learning. These consist mainly of a bulbous calyx and tightly packaged arrays of thin parallel fibers of the Kenyon cells.","definition_xrefs":["PMID:8790424"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"brain development","termid":"GO:0007420"}],"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":"mushroom body development","termid":"GO:0016319"}


id: PBO:0044044
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cysteine and serine rich nuclear protein 1","termid":"PBO:0044044"}


id: PBO:0064823
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase 1 regulatory subunit 3E","termid":"PBO:0064823"}


id: PBO:0088902
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Golgi UDP-galactose transmembrane transporter Gms2","termid":"PBO:0088902"}


id: PBO:0073706
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SKI8 subunit of superkiller complex","termid":"PBO:0073706"}


id: GO:0080114
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of glycine hydroxymethyltransferase activity, the catalysis of the reaction 5,10-methylenetetrahydrofolate + glycine + H2O = tetrahydrofolate + L-serine.","definition_xrefs":["PMID:19223513"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of glycine hydroxymethyltransferase activity (obsolete GO:0080114)","termid":"GO:0080114"}


id: FYPO:0005460
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 chromatin at promoters that contain MCB sites is abolished.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to chromatin at promoter","termid":"FYPO:0006349"},{"relation_name":"is_a","term_name":"decreased protein localization to chromatin at protein coding gene","termid":"FYPO:0008249"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0000138","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"abolished protein localization to chromatin at MCB promoters","synonyms":[{"name":"abolished protein localisation to chromatin at MCB promoters during vegetative growth","type":"exact"},{"name":"abolished protein localization to chromatin at MCB promoters during mitotic cell cycle","type":"related"},{"name":"abolished protein localization to chromatin at MCB target genes","type":"related"},{"name":"abolished protein localization to chromatin at MCB-containing promoters","type":"exact"},{"name":"protein localization to chromatin at MCB promoters during vegetative growth abolished","type":"exact"}],"termid":"FYPO:0005460"}


id: PBO:0078929
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Arg (anticodon CCG) 1-1","termid":"PBO:0078929"}


id: MONDO:1010640
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Factor XII deficiency that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"factor XII deficiency, non-human animal","termid":"MONDO:1010074"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"factor XII deficiency, domestic cat","secondary_identifiers":["OMIA:000364-9685"],"termid":"MONDO:1010640","xrefs":{"Monarch":{"xref_id":"1010640"}}}


id: PBO:0089363
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hydrolase activity, implicated in cellular detoxification","termid":"PBO:0089363"}


id: GO:0001666
data:
  {"annotated_genes":["SJAG_00642","SJAG_01585","SJAG_03345","SJAG_01150","SJAG_04018","SJAG_00221"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[111458,100976,109599,116726],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071456"},{"annotations":[116134,89022],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1900039"}]},"cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a stimulus indicating lowered oxygen tension. Hypoxia, defined as a decline in O2 levels below normoxic levels of 20.8 - 20.95%, results in metabolic adaptation at both the cellular and organismal level.","definition_xrefs":["GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to stress","termid":"GO:0006950"},{"relation_name":"is_a","term_name":"response to decreased oxygen levels","termid":"GO:0036293"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00221":null,"SJAG_00642":null,"SJAG_01150":null,"SJAG_01585":null,"SJAG_03345":null,"SJAG_04018":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to hypoxia","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"response to hypoxic stress","type":"exact"},{"name":"response to intermittent hypoxia","type":"narrow"},{"name":"response to lowered oxygen tension","type":"exact"},{"name":"response to sustained hypoxia","type":"narrow"}],"termid":"GO:0001666","terms_by_termid":{"GO:0071456":null,"GO:1900039":null}}


id: MONDO:0005337
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete neuropathy (obsolete MONDO:0005337)","termid":"MONDO:0005337","xrefs":{"Monarch":{"xref_id":"0005337"}}}


id: PBO:0066002
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RALGAPA1 pseudogene 1","termid":"PBO:0066002"}


id: PBO:0064001
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi-interacting RNA cluster 35","termid":"PBO:0064001"}


id: GO:0030892
data:
  {"annotated_genes":["SJAG_05019","SJAG_01831","SJAG_01067","SJAG_03418"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[69606,71813,90681,107488],"is_not":false,"summary":null,"term":"GO:0030892"}]},"cv_name":"cellular_component","definition":"A cohesin complex that mediates sister chromatid cohesion during mitosis; has a subunit composition distinct from that of the meiotic cohesin complex.","definition_xrefs":["GOC:mah","PMID:12750522"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cohesin complex","termid":"GO:0008278"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01067":null,"SJAG_01831":null,"SJAG_03418":null,"SJAG_05019":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005694"],"is_obsolete":false,"name":"mitotic cohesin complex","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0034990"],"synonyms":[{"name":"nuclear mitotic cohesin complex","type":"related"}],"termid":"GO:0030892","terms_by_termid":{"GO:0030892":null}}


id: PBO:0070091
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 5 pseudogene","termid":"PBO:0070091"}


id: GO:0062052
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The sequence of events that initiates (or primes) the synthesis of semi-crystalline starch granules within photosynthetic chloroplasts or non-photosynthetic amyloplasts.","definition_xrefs":["PMID:28684429"],"direct_ancestors":[{"relation_name":"is_a","term_name":"starch biosynthetic process","termid":"GO:0019252"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"starch granule initiation","termid":"GO:0062052"}


id: PBO:0041152
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"basic transcription factor 3 pseudogene 7","termid":"PBO:0041152"}


id: GO:0102733
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: typhasterol + O2 + a reduced electron acceptor = castasterone + H2O + an oxidized electron acceptor.","definition_xrefs":["GOC:pz","PMID:17138693"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monooxygenase activity","termid":"GO:0004497"},{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen","termid":"GO:0016705"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"typhasterol C-23 hydroxylase activity","secondary_identifiers":["MetaCyc:RXN-719"],"termid":"GO:0102733"}


id: MONDO:0019015
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Omphalocele is an embryopathy classified in the group of abdominal celosomias and is characterized by a large hernia of the abdominal wall, centered on the umbilical cord, in which the protruding viscera are protected by a sac.","definition_xrefs":["Orphanet:660"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abdominal wall malformation","termid":"MONDO:0100298"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"omphalocele","secondary_identifiers":["NCIT:C98997","SCTID:18735004","MEDGEN:162756","icd11.foundation:1168696429","GARD:16540","DOID:0060327","ICD9:756.72","MedDRA:10030308","MESH:D006554","HP:0001539","SCTID:396347007","UMLS:C0795690"],"synonyms":[{"name":"congenital omphalocele","type":"exact"},{"name":"eventration","type":"broad"},{"name":"exomphalos","type":"exact"},{"name":"omphalocele","type":"exact"},{"name":"omphalocele (disease)","type":"exact"},{"name":"omphalocoele","type":"exact"}],"termid":"MONDO:0019015","xrefs":{"Monarch":{"xref_id":"0019015"}}}


id: GO:0019769
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with low affinity with an immunoglobulin of the IgE isotype via the Fc region, and transmitting the signal from one side of the membrane to the other to initiate a change in cell activity.","definition_xrefs":["ISBN:0781735149","GOC:signaling","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"IgE receptor activity","termid":"GO:0019767"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"low-affinity IgE receptor activity","synonyms":[{"name":"low affinity Fc receptor activity","type":"related"},{"name":"low affinity IgE receptor activity","type":"exact"}],"termid":"GO:0019769"}


id: PBO:0108898
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPL7L1 pseudogene 11","termid":"PBO:0108898"}


id: GO:0008453
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-alanine + glyoxylate = pyruvate + glycine.","definition_xrefs":["EC:2.6.1.44"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transaminase activity","termid":"GO:0008483"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016769"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0016769","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"alanine-glyoxylate transaminase activity","secondary_identifiers":["Reactome:R-HSA-904864","Reactome:R-HSA-389684","MetaCyc:ALANINE--GLYOXYLATE-AMINOTRANSFERASE-RXN","RHEA:24248"],"synonyms":[{"name":"AGT activity","type":"related"},{"name":"L-alanine-glycine transaminase activity","type":"related"},{"name":"L-alanine:glyoxylate aminotransferase activity","type":"related"},{"name":"alanine--glyoxylate aminotransferase activity","type":"related"},{"name":"alanine-glyoxylate aminotransferase activity","type":"exact"},{"name":"alanine-glyoxylic aminotransferase activity","type":"related"}],"termid":"GO:0008453"}


id: GO:0106378
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-hydroxy-dATP + H2O = 2-hydroxy-dAMP + H+ + diphosphate.","definition_xrefs":["PMID:11139615","RHEA:31583"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside triphosphate diphosphatase activity","termid":"GO:0047429"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0047429"}],"interesting_parent_ids":["GO:0047429","GO:0016787","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"2-hydroxy-dATP hydrolase activity","secondary_identifiers":["Reactome:R-HSA-2395818"],"termid":"GO:0106378"}


id: PBO:0069583
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 857, pseudogene","termid":"PBO:0069583"}


id: PBO:0042360
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CD109 molecule","termid":"PBO:0042360"}


id: PBO:0069211
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 466, pseudogene","termid":"PBO:0069211"}


id: MONDO:0013513
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any familial atrial fibrillation in which the cause of the disease is a mutation in the KCNJ2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial atrial fibrillation","termid":"MONDO:0018054"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"atrial fibrillation, familial, 9","secondary_identifiers":["OMIM:613980","UMLS:C3151431","MEDGEN:462781","GARD:15737"],"synonyms":[{"name":"ATFB9","type":"related"},{"name":"KCNJ2 familial atrial fibrillation","type":"exact"},{"name":"atrial fibrillation, familial, 9","type":"exact"},{"name":"atrial fibrillation, familial, type 9","type":"exact"},{"name":"familial atrial fibrillation caused by mutation in KCNJ2","type":"exact"}],"termid":"MONDO:0013513","xrefs":{"Monarch":{"xref_id":"0013513"}}}


id: MONDO:0100272
data:
  {"annotated_genes":["SJAG_00326"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85813],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008972"}]},"cv_name":"mondo","definition":"Any peroxisome biogenesis disorder in which the cause of the disease is a mutation in the PEX7 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"peroxisome biogenesis disorder","termid":"MONDO:0019234"},{"relation_name":"is_a","term_name":"non-Zellweger spectrum disorder","termid":"MONDO:0100322"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00326":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0019053"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005244","MONDO:0019053","MONDO:0006025","MONDO:0005559"],"is_obsolete":false,"name":"peroxisome biogenesis disorder due to PEX7 defect","references_by_uniquename":{"PB_REF:0000006":null},"synonyms":[{"name":"PEX7 related peroxisome biogenesis disorder","type":"exact"},{"name":"adult refsum disease due to PEX7 defect (formerly)","type":"narrow"},{"name":"rhizomelic chondrodysplasia punctata type 1 (formerly)","type":"narrow"}],"termid":"MONDO:0100272","terms_by_termid":{"MONDO:0008972":null},"xrefs":{"Monarch":{"xref_id":"0100272"}}}


id: PBO:0064955
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRAME family member 7","termid":"PBO:0064955"}


id: PBO:0076738
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"t-complex 11","termid":"PBO:0076738"}


id: PBO:0050884
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"indoleamine 2,3-dioxygenase 1","termid":"PBO:0050884"}


id: PBO:0082696
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the kinetochore-associated Ndc80 complex; involved in chromosome segregation, spindle checkpoint activity, and kinetochore clustering; evolutionarily conserved; other members include Ndc80p, Nuf2p, Spc24p, and Spc25p","termid":"PBO:0082696"}


id: GO:0102532
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: genkwanin + O2 + reduced [NADPH--hemoprotein reductase] = H2O + oxidized [NADPH--hemoprotein reductase] + scutellarein 7-methyl ether.","definition_xrefs":["RHEA:73427"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen","termid":"GO:0016709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"genkwanin 6-hydroxylase activity","secondary_identifiers":["MetaCyc:RXN-14748"],"termid":"GO:0102532"}


id: GO:0072131
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of a kidney mesenchymal tissue are generated and organized. Kidney mesenchyme is the tissue made up of loosely connected mesenchymal cells in the kidney.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mesenchyme morphogenesis","termid":"GO:0072132"},{"relation_name":"part_of","term_name":"kidney mesenchyme development","termid":"GO:0072074"}],"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":"kidney mesenchyme morphogenesis","termid":"GO:0072131"}


id: MONDO:0004017
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"malignant pineal area germ cell neoplasm","termid":"MONDO:0002073"},{"relation_name":"is_a","term_name":"malignant teratoma","termid":"MONDO:0003514"},{"relation_name":"is_a","term_name":"extragonadal nonseminomatous germ cell tumor","termid":"MONDO:0003578"},{"relation_name":"is_a","term_name":"central nervous system immature teratoma","termid":"MONDO:0003735"},{"relation_name":"is_a","term_name":"pineal region teratoma","termid":"MONDO:0004015"},{"relation_name":"is_a","term_name":"immature teratoma","termid":"MONDO:0024746"}],"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":"pineal region immature teratoma","secondary_identifiers":["NCIT:C6755","MEDGEN:277516","UMLS:C1335416","DOID:6858"],"synonyms":[{"name":"atypical pineal teratoma","type":"exact"},{"name":"immature teratoma of pineal area","type":"exact"},{"name":"immature teratoma of pineal region","type":"exact"},{"name":"immature teratoma of the pineal area","type":"exact"},{"name":"immature teratoma of the pineal region","type":"exact"},{"name":"pineal area immature teratoma","type":"exact"}],"termid":"MONDO:0004017","xrefs":{"Monarch":{"xref_id":"0004017"}}}


id: PBO:0086494
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative phosphomutase; contains a region homologous to the active site of phosphomutases; overexpression suppresses the histidine auxotrophy of an ade3 ade16 ade17 triple mutant and the temperature sensitivity of a tps2 mutant","termid":"PBO:0086494"}


id: PBO:0051657
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inosine monophosphate dehydrogenase 2","termid":"PBO:0051657"}


id: PBO:0033787
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_level_of_large-Y_replication_intermediates","termid":"PBO:0033787"}


id: PBO:0083481
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the verified gene SYM1, a mitochondrial protein involved in ethanol metabolism","termid":"PBO:0083481"}


id: FYPO:0005514
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 protein that is not normally found in the vacuole is observed there.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein mislocalized to cytoplasm during vegetative growth","termid":"FYPO:0000783"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000138"},{"rel_name":"output_of","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0000138","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"protein mislocalized to vacuole","synonyms":[{"name":"ectopic protein localization to vacuole","type":"exact"},{"name":"protein mislocalised to vacuole","type":"exact"},{"name":"protein mislocalised to vacuole during vegetative growth","type":"exact"},{"name":"protein mislocalized to vacuole during mitotic cell cycle","type":"related"},{"name":"protein mislocalized to vacuole during vegetative growth","type":"exact"}],"termid":"FYPO:0005514"}


id: PBO:0066507
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"regulatory factor X4","termid":"PBO:0066507"}


id: PATO:0000552
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000552 absolute temperature sensitivity value (obsolete PATO:0000552)","termid":"PATO:0000552"}


id: PBO:0072186
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S17 pseudogene 2","termid":"PBO:0072186"}


id: PBO:0055654
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 3094","termid":"PBO:0055654"}


id: PBO:0004006
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1.5.1.12","termid":"PBO:0004006"}


id: GO:0141076
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A process in which a symbiont interferes with, inhibits or disrupts a TRAF-mediated signal transduction in its host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:22407319","PMID:31311877","PMID:20335533"],"gene_count":0,"genotype_count":0,"name":"obsolete suppression of host TRAF-mediated signal transduction (obsolete GO:0141076)","synonyms":[{"name":"disruption of host TRAF-mediated signal transduction","type":"exact"},{"name":"inhibition of host TRAF-mediated signal transduction","type":"exact"},{"name":"inhibition of host TRAFs","type":"narrow"},{"name":"negative regulation of host TRAF-mediated signal transduction","type":"exact"},{"name":"suppression of host TRAF activity","type":"narrow"},{"name":"suppression of host TRAF-mediated signal transduction","type":"exact"},{"name":"suppression of host tumor necrosis factor receptor-associated factor signaling","type":"exact"},{"name":"symbiont-mediated suppression of host TRAF-mediated signal transduction","type":"related"}],"termid":"GO:0141076"}


id: PBO:0076854
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tet methylcytosine dioxygenase 1 pseudogene 1","termid":"PBO:0076854"}


id: PBO:0089698
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BRO1 domain protein Bro1","termid":"PBO:0089698"}


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


id: GO:2001091
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a nigerotrioseacetate into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"trisaccharide transport","termid":"GO:2001088"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"nigerotriose transport","termid":"GO:2001091"}


id: PBO:0069092
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 339, pseudogene","termid":"PBO:0069092"}


id: PBO:0077268
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TMEM9 domain family member B","termid":"PBO:0077268"}


id: PBO:0086111
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein required for biogenesis of the large ribosomal subunit; required for biogenesis of the large ribosomal subunit; interacts with proteins involved in RNA processing, ribosome biogenesis, ubiquitination and demethylation; similar to WDR55, a human WD repeat protein; essential gene","termid":"PBO:0086111"}


id: PR:O94578
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mic26 gene.","definition_xrefs":["UniProtKB:O94578","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C1442.05c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1442.05c","synonyms":[{"name":"Spom972h-mic26","type":"exact"}],"termid":"PR:O94578"}


id: GO:0070303
data:
  {"annotated_genes":["SJAG_03263","SJAG_04522","SJAG_01114","SJAG_04825","SJAG_02392","SJAG_05000"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[118057,107364,103555,95608,99201,106804],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903138"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of signaling via the stress-activated protein kinase signaling cascade.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of stress-activated protein kinase signaling cascade","termid":"GO:0070302"},{"relation_name":"is_a","term_name":"negative regulation of intracellular signal transduction","termid":"GO:1902532"},{"relation_name":"negatively_regulates","term_name":"stress-activated protein kinase signaling cascade","termid":"GO:0031098"}],"gene_count":6,"genes_by_uniquename":{"SJAG_01114":null,"SJAG_02392":null,"SJAG_03263":null,"SJAG_04522":null,"SJAG_04825":null,"SJAG_05000":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of stress-activated protein kinase signaling cascade","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of stress-activated protein kinase signaling pathway","type":"exact"},{"name":"down-regulation of stress-activated protein kinase signaling pathway","type":"exact"},{"name":"downregulation of stress-activated protein kinase signaling pathway","type":"exact"},{"name":"inhibition of stress-activated protein kinase signaling pathway","type":"narrow"},{"name":"negative regulation of SAPK signaling pathway","type":"exact"},{"name":"negative regulation of stress-activated protein kinase signaling pathway","type":"exact"},{"name":"negative regulation of stress-activated protein kinase signalling pathway","type":"exact"}],"termid":"GO:0070303","terms_by_termid":{"GO:1903138":null}}


id: GO:0033048
data:
  {"annotated_genes":["SJAG_04884","SJAG_04259","SJAG_00460","SJAG_01082","SJAG_03681","SJAG_04126","SJAG_02451","SJAG_03126","SJAG_01297","SJAG_03353","SJAG_02169","SJAG_02336","SJAG_00883","SJAG_04999","SJAG_01679","SJAG_01837","SJAG_04699","SJAG_01330"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[99350,115643,108006,103647,111706,113524,114011,90486,106987],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1902426"},{"annotations":[109656,114244,101551,106077,115298,99194],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007094"},{"annotations":[103031],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000816"},{"annotations":[93960],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0140499"},{"annotations":[116417],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0090267"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of sister chromatid segregation during mitosis.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of sister chromatid segregation","termid":"GO:0033046"},{"relation_name":"is_a","term_name":"regulation of mitotic sister chromatid segregation","termid":"GO:0033047"},{"relation_name":"negatively_regulates","term_name":"mitotic sister chromatid segregation","termid":"GO:0000070"}],"gene_count":18,"genes_by_uniquename":{"SJAG_00460":null,"SJAG_00883":null,"SJAG_01082":null,"SJAG_01297":null,"SJAG_01330":null,"SJAG_01679":null,"SJAG_01837":null,"SJAG_02169":null,"SJAG_02336":null,"SJAG_02451":null,"SJAG_03126":null,"SJAG_03353":null,"SJAG_03681":null,"SJAG_04126":null,"SJAG_04259":null,"SJAG_04699":null,"SJAG_04884":null,"SJAG_04999":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0000070"},{"rel_name":"negatively_regulates","termid":"GO:0007049"},{"rel_name":"negatively_regulates","termid":"GO:0000070"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0000070","GO:0008150","GO:0007049"],"is_obsolete":false,"name":"negative regulation of mitotic sister chromatid segregation","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0033048","terms_by_termid":{"GO:0007094":null,"GO:0090267":null,"GO:0140499":null,"GO:1902426":null,"GO:2000816":null}}


id: GO:0030159
data:
  {"annotated_genes":["SJAG_03081"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[75108],"is_not":false,"summary":null,"term":"GO:0030159"}]},"cv_name":"molecular_function","definition":"The binding activity of a molecule that provides a physical support for the assembly of a multiprotein receptor signaling complex.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"signaling adaptor activity","termid":"GO:0035591"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03081":null},"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:0060090"}],"interesting_parent_ids":["GO:0003674","GO:0060090","GO:0030674"],"is_obsolete":false,"name":"signaling receptor complex adaptor activity","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"receptor signaling complex adaptor activity","type":"exact"},{"name":"receptor signaling complex scaffold activity","type":"exact"},{"name":"receptor signaling complex scaffold protein activity","type":"exact"},{"name":"receptor signalling complex adaptor activity","type":"exact"},{"name":"receptor signalling complex scaffold activity","type":"exact"}],"termid":"GO:0030159","terms_by_termid":{"GO:0030159":null}}


id: MONDO:0001432
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete sodoku disease (obsolete MONDO:0001432)","termid":"MONDO:0001432","xrefs":{"Monarch":{"xref_id":"0001432"}}}


id: GO:0097664
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An SCF ubiquitin ligase complex in which the F-box protein is Grr1 in S. cerevisiae (Pof2 in S. pombe).","definition_xrefs":["PMID:10213692","GOC:jd","PMID:15147268","GOC:vw"],"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-Grr1/Pof2 ubiquitin ligase complex","termid":"GO:0097664"}


id: PBO:0078002
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TRAF3IP2 antisense RNA 1","termid":"PBO:0078002"}


id: PBO:0044716
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DEAD/H-box helicase 11 like 3 (pseudogene)","termid":"PBO:0044716"}


id: GO:0034075
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: oxidosqualene + H2O = arabidiol ((13R,14R,17E)-malabarica-17,21-diene-3beta,14-diol).","definition_xrefs":["PMID:16774269","PMID:17474751","GOC:cb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidosqualene cyclase activity","termid":"GO:0031559"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016853","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"arabidiol synthase activity","secondary_identifiers":["EC:4.2.1.124","RHEA:31035","MetaCyc:RXN-9684"],"termid":"GO:0034075"}


id: GO:0071244
data:
  {"annotated_genes":["SJAG_06611"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[77385],"is_not":false,"summary":null,"term":"GO:0071244"}]},"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 carbon dioxide (CO2) stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to carbon dioxide","termid":"GO:0010037"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"}],"gene_count":1,"genes_by_uniquename":{"SJAG_06611":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 carbon dioxide","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0071244","terms_by_termid":{"GO:0071244":null}}


id: PBO:0090456
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER thiol oxidase Erv2","termid":"PBO:0090456"}


id: MONDO:0015554
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"maculopapular cutaneous mastocytosis","termid":"MONDO:0019316"}],"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:0005093"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046","MONDO:0005093"],"is_obsolete":false,"name":"typical urticaria pigmentosa","secondary_identifiers":["GARD:20033","MEDGEN:1843439","Orphanet:158766","UMLS:C5680683"],"termid":"MONDO:0015554","xrefs":{"Monarch":{"xref_id":"0015554"}}}


id: PBO:0080892
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"YTH N6-methyladenosine RNA binding protein F2","termid":"PBO:0080892"}


id: MONDO:0014991
data:
  {"annotated_genes":["SJAG_01776"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86776],"is_not":false,"summary":null,"term":"MONDO:0014991"}]},"cv_name":"mondo","definition":"Any Seckel syndrome in which the cause of the disease is a mutation in the NSMCE2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Seckel syndrome","termid":"MONDO:0019342"},{"relation_name":"is_a","term_name":"primordial dwarfism and slender bone disorder","termid":"MONDO:0800063"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01776":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"Seckel syndrome 10","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:18484","OMIM:617253","UMLS:C4310647","MEDGEN:934614","DOID:0070008"],"synonyms":[{"name":"NSMCE2 Seckel syndrome","type":"exact"},{"name":"SCKL10","type":"exact"},{"name":"Seckel syndrome 10","type":"exact"},{"name":"Seckel syndrome caused by mutation in NSMCE2","type":"exact"},{"name":"Seckel syndrome type 10","type":"exact"}],"termid":"MONDO:0014991","terms_by_termid":{"MONDO:0014991":null},"xrefs":{"Monarch":{"xref_id":"0014991"}}}


id: FYPO:0007668
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which a vegetative cell is elongated and progression through the mitotic cell cycle is arrested in G1 phase.","definition_xrefs":["PomBase:mah","PMID:8121488"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell cycle arrest in mitotic G1 phase","termid":"FYPO:0000445"},{"relation_name":"is_a","term_name":"elongated vegetative cell","termid":"FYPO:0001122"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000005"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0001985","FYPO:0000002","FYPO:0001320","FYPO:0000005"],"is_obsolete":false,"name":"elongated vegetative cell with cell cycle arrest in mitotic G1 phase","synonyms":[{"name":"abnormal cell cycle arrest in mitotic G1 phase with elongated cell","type":"exact"},{"name":"elongated cell with cell cycle arrest in mitotic G1 phase during vegetative growth","type":"exact"},{"name":"elongated vegetative cell with cell cycle arrest in G1 phase of mitotic cell cycle","type":"exact"},{"name":"elongated vegetative cell with mitotic G1 phase cell cycle arrest","type":"exact"}],"termid":"FYPO:0007668"}


id: GO:0010332
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a gamma radiation stimulus. Gamma radiation is a form of electromagnetic radiation (EMR) or light emission of a specific frequency produced from sub-atomic particle interaction, such as electron-positron annihilation and radioactive decay. Gamma rays are generally characterized as EMR having the highest frequency and energy, and also the shortest wavelength, within the electromagnetic radiation spectrum.","definition_xrefs":["GOC:tair_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to ionizing radiation","termid":"GO:0010212"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to gamma radiation","synonyms":[{"name":"response to gamma ray","type":"related"},{"name":"response to gamma-ray photon","type":"related"}],"termid":"GO:0010332"}


id: PBO:0056027
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LSP1 pseudogene 5","termid":"PBO:0056027"}


id: MONDO:0022546
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete basal cell nevus anodontia abnormal bone mineralization (obsolete MONDO:0022546)","termid":"MONDO:0022546","xrefs":{"Monarch":{"xref_id":"0022546"}}}


id: PBO:0048612
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTPase, IMAP family member 4","termid":"PBO:0048612"}


id: PBO:0051854
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iron-sulfur cluster assembly 1","termid":"PBO:0051854"}


id: GO:0098780
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.) in response to the depolarization of one or more mitochondria.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to stress","termid":"GO:0033554"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to mitochondrial depolarisation","secondary_identifiers":["Reactome:R-HSA-9840373"],"termid":"GO:0098780"}


id: PBO:0028760
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_cellular_nitric_oxide_level","termid":"PBO:0028760"}


id: PBO:0040451
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPase phospholipid transporting 11A","termid":"PBO:0040451"}


id: PBO:0073154
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SEC31 homolog B, COPII coat complex component","termid":"PBO:0073154"}


id: PBO:0089735
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"karyopherin/importin-beta family nuclear import receptor Los1","termid":"PBO:0089735"}


id: PBO:0058727
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6855","termid":"PBO:0058727"}


id: GO:0090283
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the rate, frequency, or extent of the addition of a carbohydrate or carbohydrate derivative unit to a protein amino acid in any compartment of the Golgi apparatus.","definition_xrefs":["GOC:pr","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of protein glycosylation in Golgi (obsolete GO:0090283)","synonyms":[{"name":"regulation of protein amino acid glycosylation in Golgi","type":"exact"}],"termid":"GO:0090283"}


id: MONDO:0008450
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A chronic adhesive arachnoiditis in the spinal arachnoid, with root and spinal cord symptoms similar to those caused by pressure from a tumor.","definition_xrefs":["NCIT:C50749"],"direct_ancestors":[{"relation_name":"is_a","term_name":"arachnoiditis","termid":"MONDO:0015304"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spinal arachnoiditis","secondary_identifiers":["GARD:15113","MESH:C531624","SCTID:426055002","OMIM:182950","UMLS:C1710146","MEDGEN:318191","icd11.foundation:1074591848"],"synonyms":[{"name":"arachnoiditis, spinal","type":"exact"},{"name":"spinal arachnoiditis","type":"exact"}],"termid":"MONDO:0008450","xrefs":{"Monarch":{"xref_id":"0008450"}}}


id: FYPO:0003407
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An increased chemical resistance phenotype observed in the vegetative growth phase of the life cycle in which cells grow in the presence of a higher concentration of glyoxal than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002682"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0002682","FYPO:0005447","FYPO:0001985","FYPO:0000003","FYPO:0000139"],"is_obsolete":false,"name":"resistance to glyoxal","synonyms":[{"name":"resistance to GO","type":"broad"},{"name":"resistance to glyoxal during mitotic cell cycle","type":"related"},{"name":"resistance to glyoxal during vegetative growth","type":"exact"},{"name":"resistant to glyoxal","type":"exact"}],"termid":"FYPO:0003407"}


id: PBO:0003636
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha-1,2-mannosyltransferase Omh5 (predicted)","termid":"PBO:0003636"}


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


id: MONDO:0030475
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"visceral heterotaxy","termid":"MONDO:0018677"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterotaxy, visceral, 11, autosomal, with male infertility","secondary_identifiers":["UMLS:C5562019","MEDGEN:1794229","OMIM:619608"],"synonyms":[{"name":"HTX11","type":"exact"}],"termid":"MONDO:0030475","xrefs":{"Monarch":{"xref_id":"0030475"}}}


id: FYPO:0004770
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-glutamine measured in the vacuole is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased level of substance in vacuole","termid":"FYPO:0001730"},{"relation_name":"is_a","term_name":"increased cellular glutamine level","termid":"FYPO:0006955"}],"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:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"increased vacuolar glutamine level","synonyms":[{"name":"increased level of glutamine in vacuole","type":"exact"},{"name":"increased vacuolar L-glutamine level","type":"exact"},{"name":"increased vacuolar glutamine level during mitotic cell cycle","type":"related"},{"name":"increased vacuolar glutamine level during vegetative growth","type":"exact"}],"termid":"FYPO:0004770"}


id: GO:0046572
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: versiconal = versicolorin B + H2O.","definition_xrefs":["MetaCyc:RXN-9494","PMID:8784203"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-oxygen lyase activity","termid":"GO:0016835"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016829"],"is_obsolete":false,"name":"versicolorin B synthase activity","secondary_identifiers":["RHEA:33859","EC:4.2.1.143"],"termid":"GO:0046572"}


id: RO:0002491
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"x existence starts and ends during y if and only if the start of x is part of y and the end of x is part of y. Formally: x existence starts and ends during y iff α(x) >= α(y) & α(x) <= ω(y) & ω(x) <= ω(y) & ω(x) >= α(y)","direct_ancestors":[{"relation_name":"is_a","term_name":"existence_starts_during","termid":"RO:0002488"},{"relation_name":"is_a","term_name":"existence_ends_during","termid":"RO:0002492"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"existence_starts_and_ends_during","termid":"RO:0002491"}


id: MONDO:0011879
data:
  {"annotated_genes":["SJAG_02695"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85966],"is_not":false,"summary":null,"term":"MONDO:0011879"}]},"cv_name":"mondo","definition":"Any neuronopathy, distal hereditary motor in which the cause of the disease is a mutation in the DCTN1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"distal hereditary motor neuropathy type 7","termid":"MONDO:0015355"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02695":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0005559","MONDO:0005244"],"is_obsolete":false,"name":"neuronopathy, distal hereditary motor, type 7B","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:375157","GARD:18270","MESH:C564362","UMLS:C1843315","DOID:0111202","OMIM:607641"],"synonyms":[{"name":"DCTN1 neuronopathy, distal hereditary motor","type":"exact"},{"name":"Dhmn7B","type":"related"},{"name":"HMN 7B","type":"related"},{"name":"HMN7B","type":"related"},{"name":"Lower motor neuron disease, dynactin type","type":"related"},{"name":"neuronopathy, distal hereditary motor caused by mutation in DCTN1","type":"exact"},{"name":"neuronopathy, distal hereditary motor, type VIIB","type":"related"},{"name":"neuropathy, distal hereditary motor, type 7B","type":"related"},{"name":"neuropathy, distal hereditary motor, with vocal cord paralysis, type 7B","type":"related"}],"termid":"MONDO:0011879","terms_by_termid":{"MONDO:0011879":null},"xrefs":{"Monarch":{"xref_id":"0011879"}}}


id: PBO:0085020
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nicotinate phosphoribosyltransferase; acts in the salvage pathway of NAD+ biosynthesis; required for silencing at rDNA and telomeres and has a role in silencing at mating-type loci; localized to the nucleus","termid":"PBO:0085020"}


id: FYPO:0004697
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 1,2-dioctanoyl-sn-glycerol (DiC8 DAG). Cells stop growing (and may die) at a concentration of 1,2-dioctanoyl-sn-glycerol that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO: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:0001985","FYPO:0000139","FYPO:0005447","FYPO:0002683","FYPO:0000003"],"is_obsolete":false,"name":"sensitive to 1,2-dioctanoyl-sn-glycerol","synonyms":[{"name":"hypersensitive to 1,2-dioctanoyl-sn-glycerol","type":"exact"},{"name":"sensitive to 1,2-dioctanoyl-sn-glycerol during mitotic cell cycle","type":"related"},{"name":"sensitive to 1,2-dioctanoyl-sn-glycerol during vegetative growth","type":"exact"},{"name":"sensitive to DiC8 DAG","type":"exact"}],"termid":"FYPO:0004697"}


id: PBO:0050593
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 1","termid":"PBO:0050593"}


id: GO:1902608
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of large conductance calcium-activated potassium channel activity.","definition_xrefs":["GOC:TermGenie","GO_REF:0000059","PMID:23407708"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of potassium ion transmembrane transporter activity","termid":"GO:1901018"},{"relation_name":"is_a","term_name":"positive regulation of cation channel activity","termid":"GO:2001259"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0055085","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"positive regulation of large conductance calcium-activated potassium channel activity","synonyms":[{"name":"activation of BK KCa channels","type":"narrow"},{"name":"activation of BK calcium-activated potassium channel activity","type":"narrow"},{"name":"activation of BK channel activity","type":"related"},{"name":"activation of large conductance KCa channels","type":"narrow"},{"name":"activation of large conductance calcium-activated potassium channel activity","type":"narrow"},{"name":"positive regulation of BK KCa channels","type":"exact"},{"name":"positive regulation of BK calcium-activated potassium channel activity","type":"exact"},{"name":"positive regulation of BK channel activity","type":"related"},{"name":"positive regulation of large conductance KCa channels","type":"exact"},{"name":"up regulation of BK KCa channels","type":"exact"},{"name":"up regulation of BK calcium-activated potassium channel activity","type":"exact"},{"name":"up regulation of BK channel activity","type":"related"},{"name":"up regulation of large conductance KCa channels","type":"exact"},{"name":"up regulation of large conductance calcium-activated potassium channel activity","type":"exact"},{"name":"up-regulation of BK KCa channels","type":"exact"},{"name":"up-regulation of BK calcium-activated potassium channel activity","type":"exact"},{"name":"up-regulation of BK channel activity","type":"related"},{"name":"up-regulation of large conductance KCa channels","type":"exact"},{"name":"up-regulation of large conductance calcium-activated potassium channel activity","type":"exact"},{"name":"upregulation of BK KCa channels","type":"exact"},{"name":"upregulation of BK calcium-activated potassium channel activity","type":"exact"},{"name":"upregulation of BK channel activity","type":"related"},{"name":"upregulation of large conductance KCa channels","type":"exact"},{"name":"upregulation of large conductance calcium-activated potassium channel activity","type":"exact"}],"termid":"GO:1902608"}


id: PBO:0052077
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"katanin regulatory subunit B1 like 1 pseudogene 2","termid":"PBO:0052077"}


id: MONDO:0017918
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"White matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome is a very rare neurological condition. The few patients described in the medical literature were characterized by brain anomalies; an unusual face with broad nasal root, wide spaced eyes (hypertelorism) and a very small chin (micrognathia); failure to thrive; severe intellectual disability ;and lack of muscle tone (hypotonia). Exams of the brain showed a poor development (hypoplasia) of the pale part of the brain known as white matter, and an absent or abnormal corpus callosum (nerve fibers joining the two hemispheres of the brain). Only a few cases have being described. The cause is unknown but may be related to a disorder of axonal development. The described cases seem to be inherited in an autosomal recessive or X-linked way. Corpus callosum agenesis is one of the more frequent congenital malformations. It can be either asymptomatic or associated with intellectual disability, epilepsy, or psychiatric syndromes. It can be part of several genetic syndromes, such as Aicardi syndrome, Andermann syndrome and Apert syndrome, trisomies 13, 18 ; or result from metabolic causes; drugs (cocaine); or viral infection (influenza). Many patients with corpus callosum anomalies have other brain anomalies, including white matter hypoplasia. There is no information on specific treatment for this condition.","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"white matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome","secondary_identifiers":["UMLS:C2931292","MEDGEN:419038","MESH:C536701","GARD:12488","Orphanet:3207"],"synonyms":[{"name":"Curatolo Cilio Pessagno syndrome","type":"related"},{"name":"Curatolo-Cilio-Pessagno syndrome","type":"exact"},{"name":"familial white matter hypoplasia, agenesis of the corpus callosum, intellectual disability and growth deficiency","type":"related"}],"termid":"MONDO:0017918","xrefs":{"Monarch":{"xref_id":"0017918"}}}


id: MONDO:0004317
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Multiple meningiomas that arises from the spinal meninges.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intraspinal meningioma","termid":"MONDO:0001279"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"multiple spinal canal and spinal cord meningioma","secondary_identifiers":["NCIT:C5275","UMLS:C1334825","MEDGEN:235341","DOID:7646"],"synonyms":[{"name":"multiple Meningiomas of spinal canal and spinal cord","type":"exact"},{"name":"multiple intraspinal Meningiomas","type":"exact"},{"name":"multiple meningiomas of the spinal canal and spinal cord","type":"exact"},{"name":"multiple spinal canal and spinal cord Meningiomas","type":"exact"}],"termid":"MONDO:0004317","xrefs":{"Monarch":{"xref_id":"0004317"}}}


id: PBO:0001719
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"telomere length regulator protein Rif1","termid":"PBO:0001719"}


id: PBO:0004607
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA polymerase epsilon catalytic subunit B, Dpb2","termid":"PBO:0004607"}


id: MONDO:0000984
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited blood disorder characterized by a decreased synthesis of one of the polypeptide chains that form hemoglobin. Anemia results from this abnormal hemoglobin formation.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"inherited hemoglobinopathy","termid":"MONDO:0019050"}],"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":"thalassemia","secondary_identifiers":["GARD:7756","ICD9:282.4","DOID:10241","ICD9:282.49","MEDGEN:21121","NANDO:2200626","EFO:1001996","NCIT:C35069","ICD10CM:D56","ICD9:282.40","SCTID:40108008","UMLS:C0039730","MESH:D013789"],"synonyms":[{"name":"sickle-cell thalassemia with crisis","type":"exact"},{"name":"sickle-cell thalassemia without crisis","type":"exact"},{"name":"thalassemia Hb-S disease with crisis","type":"exact"},{"name":"thalassemia Hb-S disease without crisis","type":"exact"}],"termid":"MONDO:0000984","xrefs":{"Monarch":{"xref_id":"0000984"}}}


id: GO:1904225
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of glucuronosyltransferase activity.","definition_xrefs":["GOC:BHF","GOC:TermGenie","GOC:rl","PMID:20610558","GO_REF:0000059"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of glucuronosyltransferase activity (obsolete GO:1904225)","synonyms":[{"name":"activation of 1-naphthol glucuronyltransferase activity","type":"narrow"},{"name":"activation of 1-naphthol-UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"activation of 17-OH steroid UDPGT activity","type":"narrow"},{"name":"activation of 17-beta-hydroxysteroid UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"activation of 17beta-hydroxysteroid UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"activation of 3-OH androgenic UDPGT activity","type":"narrow"},{"name":"activation of 3-alpha-hydroxysteroid UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"activation of 3alpha-hydroxysteroid UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"activation of 4-hydroxybiphenyl UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"activation of 4-methylumbelliferone UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"activation of 4-nitrophenol UDP-glucuronyltransferase activity","type":"narrow"},{"name":"activation of 4-nitrophenol UDPGT activity","type":"narrow"},{"name":"activation of GT activity","type":"narrow"},{"name":"activation of PNP-UDPGT","type":"related"},{"name":"activation of UDP glucuronate-estradiol-glucuronosyltransferase activity","type":"narrow"},{"name":"activation of UDP glucuronate-estriol glucuronosyltransferase activity","type":"narrow"},{"name":"activation of UDP glucuronic acid transferase activity","type":"narrow"},{"name":"activation of UDP glucuronosyltransferase activity","type":"narrow"},{"name":"activation of UDP glucuronyltransferase activity","type":"narrow"},{"name":"activation of UDP-glucuronate beta-D-glucuronosyltransferase (acceptor-unspecific)","type":"narrow"},{"name":"activation of UDP-glucuronate-4-hydroxybiphenyl glucuronosyltransferase activity","type":"narrow"},{"name":"activation of UDP-glucuronate-bilirubin glucuronyltransferase activity","type":"narrow"},{"name":"activation of UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"activation of UDP-glucuronyltransferase activity","type":"narrow"},{"name":"activation of UDPGA transferase activity","type":"narrow"},{"name":"activation of UDPGA-glucuronyltransferase activity","type":"narrow"},{"name":"activation of UDPGT activity","type":"narrow"},{"name":"activation of UDPglucuronate beta-D-glucuronosyltransferase (acceptor-unspecific) activity","type":"narrow"},{"name":"activation of bilirubin UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"activation of bilirubin UDPGT activity","type":"narrow"},{"name":"activation of bilirubin glucuronyltransferase activity","type":"narrow"},{"name":"activation of bilirubin monoglucuronide glucuronyltransferase activity","type":"narrow"},{"name":"activation of bilirubin uridine diphosphoglucuronyltransferase activity","type":"narrow"},{"name":"activation of ciramadol UDP-glucuronyltransferase activity","type":"narrow"},{"name":"activation of estriol UDPglucuronosyltransferase activity","type":"narrow"},{"name":"activation of estrone UDPglucuronosyltransferase activity","type":"narrow"},{"name":"activation of glucuronosyltransferase activity","type":"narrow"},{"name":"activation of morphine glucuronyltransferase activity","type":"narrow"},{"name":"activation of p-hydroxybiphenyl UDP glucuronyltransferase activity","type":"narrow"},{"name":"activation of p-nitrophenol UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"activation of p-nitrophenol UDP-glucuronyltransferase activity","type":"narrow"},{"name":"activation of p-nitrophenylglucuronosyltransferase activity","type":"narrow"},{"name":"activation of p-phenylphenol glucuronyltransferase activity","type":"narrow"},{"name":"activation of phenyl-UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"activation of pnp-UDPGT activity","type":"narrow"},{"name":"activation of uridine 5'-diphosphoglucuronyltransferase activity","type":"narrow"},{"name":"activation of uridine diphosphate glucuronyltransferase activity","type":"narrow"},{"name":"activation of uridine diphosphoglucuronate-1,2-diacylglycerol glucuronosyltransferase activity","type":"narrow"},{"name":"activation of uridine diphosphoglucuronate-4-hydroxybiphenyl glucuronosyltransferase activity","type":"narrow"},{"name":"activation of uridine diphosphoglucuronate-bilirubin glucuronoside glucuronosyltransferase activity","type":"narrow"},{"name":"activation of uridine diphosphoglucuronate-bilirubin glucuronosyltransferase activity","type":"narrow"},{"name":"activation of uridine diphosphoglucuronate-estradiol glucuronosyltransferase activity","type":"narrow"},{"name":"activation of uridine diphosphoglucuronate-estriol 16-alpha-glucuronosyltransferase activity","type":"narrow"},{"name":"activation of uridine diphosphoglucuronate-estriol 16alpha-glucuronosyltransferase activity","type":"narrow"},{"name":"activation of uridine diphosphoglucuronate-estriol glucuronosyltransferase activity","type":"narrow"},{"name":"activation of uridine diphosphoglucuronosyltransferase activity","type":"narrow"},{"name":"activation of uridine diphosphoglucuronyltransferase activity","type":"narrow"},{"name":"positive regulation of 1-naphthol glucuronyltransferase activity","type":"narrow"},{"name":"positive regulation of 1-naphthol-UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"positive regulation of 17-OH steroid UDPGT activity","type":"narrow"},{"name":"positive regulation of 17-beta-hydroxysteroid UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"positive regulation of 17beta-hydroxysteroid UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"positive regulation of 3-OH androgenic UDPGT activity","type":"narrow"},{"name":"positive regulation of 3-alpha-hydroxysteroid UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"positive regulation of 3alpha-hydroxysteroid UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"positive regulation of 4-hydroxybiphenyl UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"positive regulation of 4-methylumbelliferone UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"positive regulation of 4-nitrophenol UDP-glucuronyltransferase activity","type":"narrow"},{"name":"positive regulation of 4-nitrophenol UDPGT activity","type":"narrow"},{"name":"positive regulation of GT activity","type":"exact"},{"name":"positive regulation of PNP-UDPGT","type":"related"},{"name":"positive regulation of UDP glucuronate-estradiol-glucuronosyltransferase activity","type":"narrow"},{"name":"positive regulation of UDP glucuronate-estriol glucuronosyltransferase activity","type":"narrow"},{"name":"positive regulation of UDP glucuronic acid transferase activity","type":"exact"},{"name":"positive regulation of UDP glucuronosyltransferase activity","type":"exact"},{"name":"positive regulation of UDP glucuronyltransferase activity","type":"exact"},{"name":"positive regulation of UDP-glucuronate beta-D-glucuronosyltransferase (acceptor-unspecific)","type":"exact"},{"name":"positive regulation of UDP-glucuronate-4-hydroxybiphenyl glucuronosyltransferase activity","type":"narrow"},{"name":"positive regulation of UDP-glucuronate-bilirubin glucuronyltransferase activity","type":"narrow"},{"name":"positive regulation of UDP-glucuronosyltransferase activity","type":"exact"},{"name":"positive regulation of UDP-glucuronyltransferase activity","type":"exact"},{"name":"positive regulation of UDPGA transferase activity","type":"exact"},{"name":"positive regulation of UDPGA-glucuronyltransferase activity","type":"exact"},{"name":"positive regulation of UDPGT activity","type":"exact"},{"name":"positive regulation of UDPglucuronate beta-D-glucuronosyltransferase (acceptor-unspecific) activity","type":"narrow"},{"name":"positive regulation of bilirubin UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"positive regulation of bilirubin UDPGT activity","type":"narrow"},{"name":"positive regulation of bilirubin glucuronyltransferase activity","type":"narrow"},{"name":"positive regulation of bilirubin monoglucuronide glucuronyltransferase activity","type":"narrow"},{"name":"positive regulation of bilirubin uridine diphosphoglucuronyltransferase activity","type":"narrow"},{"name":"positive regulation of ciramadol UDP-glucuronyltransferase activity","type":"narrow"},{"name":"positive regulation of estriol UDPglucuronosyltransferase activity","type":"narrow"},{"name":"positive regulation of estrone UDPglucuronosyltransferase activity","type":"narrow"},{"name":"positive regulation of morphine glucuronyltransferase activity","type":"narrow"},{"name":"positive regulation of p-hydroxybiphenyl UDP glucuronyltransferase activity","type":"narrow"},{"name":"positive regulation of p-nitrophenol UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"positive regulation of p-nitrophenol UDP-glucuronyltransferase activity","type":"narrow"},{"name":"positive regulation of p-nitrophenylglucuronosyltransferase activity","type":"narrow"},{"name":"positive regulation of p-phenylphenol glucuronyltransferase activity","type":"narrow"},{"name":"positive regulation of phenyl-UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"positive regulation of pnp-UDPGT activity","type":"narrow"},{"name":"positive regulation of uridine 5'-diphosphoglucuronyltransferase activity","type":"exact"},{"name":"positive regulation of uridine diphosphate glucuronyltransferase activity","type":"exact"},{"name":"positive regulation of uridine diphosphoglucuronate-1,2-diacylglycerol glucuronosyltransferase activity","type":"narrow"},{"name":"positive regulation of uridine diphosphoglucuronate-4-hydroxybiphenyl glucuronosyltransferase activity","type":"narrow"},{"name":"positive regulation of uridine diphosphoglucuronate-bilirubin glucuronoside glucuronosyltransferase activity","type":"narrow"},{"name":"positive regulation of uridine diphosphoglucuronate-bilirubin glucuronosyltransferase activity","type":"narrow"},{"name":"positive regulation of uridine diphosphoglucuronate-estradiol glucuronosyltransferase activity","type":"narrow"},{"name":"positive regulation of uridine diphosphoglucuronate-estriol 16-alpha-glucuronosyltransferase activity","type":"narrow"},{"name":"positive regulation of uridine diphosphoglucuronate-estriol 16alpha-glucuronosyltransferase activity","type":"narrow"},{"name":"positive regulation of uridine diphosphoglucuronate-estriol glucuronosyltransferase activity","type":"narrow"},{"name":"positive regulation of uridine diphosphoglucuronosyltransferase activity","type":"exact"},{"name":"positive regulation of uridine diphosphoglucuronyltransferase activity","type":"exact"},{"name":"up regulation of 1-naphthol glucuronyltransferase activity","type":"narrow"},{"name":"up regulation of 1-naphthol-UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"up regulation of 17-OH steroid UDPGT activity","type":"narrow"},{"name":"up regulation of 17-beta-hydroxysteroid UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"up regulation of 17beta-hydroxysteroid UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"up regulation of 3-OH androgenic UDPGT activity","type":"narrow"},{"name":"up regulation of 3-alpha-hydroxysteroid UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"up regulation of 3alpha-hydroxysteroid UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"up regulation of 4-hydroxybiphenyl UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"up regulation of 4-methylumbelliferone UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"up regulation of 4-nitrophenol UDP-glucuronyltransferase activity","type":"narrow"},{"name":"up regulation of 4-nitrophenol UDPGT activity","type":"narrow"},{"name":"up regulation of GT activity","type":"exact"},{"name":"up regulation of PNP-UDPGT","type":"related"},{"name":"up regulation of UDP glucuronate-estradiol-glucuronosyltransferase activity","type":"narrow"},{"name":"up regulation of UDP glucuronate-estriol glucuronosyltransferase activity","type":"narrow"},{"name":"up regulation of UDP glucuronic acid transferase activity","type":"exact"},{"name":"up regulation of UDP glucuronosyltransferase activity","type":"exact"},{"name":"up regulation of UDP glucuronyltransferase activity","type":"exact"},{"name":"up regulation of UDP-glucuronate beta-D-glucuronosyltransferase (acceptor-unspecific)","type":"exact"},{"name":"up regulation of UDP-glucuronate-4-hydroxybiphenyl glucuronosyltransferase activity","type":"narrow"},{"name":"up regulation of UDP-glucuronate-bilirubin glucuronyltransferase activity","type":"narrow"},{"name":"up regulation of UDP-glucuronosyltransferase activity","type":"exact"},{"name":"up regulation of UDP-glucuronyltransferase activity","type":"exact"},{"name":"up regulation of UDPGA transferase activity","type":"exact"},{"name":"up regulation of UDPGA-glucuronyltransferase activity","type":"exact"},{"name":"up regulation of UDPGT activity","type":"exact"},{"name":"up regulation of UDPglucuronate beta-D-glucuronosyltransferase (acceptor-unspecific) activity","type":"narrow"},{"name":"up regulation of bilirubin UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"up regulation of bilirubin UDPGT activity","type":"narrow"},{"name":"up regulation of bilirubin glucuronyltransferase activity","type":"narrow"},{"name":"up regulation of bilirubin monoglucuronide glucuronyltransferase activity","type":"narrow"},{"name":"up regulation of bilirubin uridine diphosphoglucuronyltransferase activity","type":"narrow"},{"name":"up regulation of ciramadol UDP-glucuronyltransferase activity","type":"narrow"},{"name":"up regulation of estriol UDPglucuronosyltransferase activity","type":"narrow"},{"name":"up regulation of estrone UDPglucuronosyltransferase activity","type":"narrow"},{"name":"up regulation of glucuronosyltransferase activity","type":"exact"},{"name":"up regulation of morphine glucuronyltransferase activity","type":"narrow"},{"name":"up regulation of p-hydroxybiphenyl UDP glucuronyltransferase activity","type":"narrow"},{"name":"up regulation of p-nitrophenol UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"up regulation of p-nitrophenol UDP-glucuronyltransferase activity","type":"narrow"},{"name":"up regulation of p-nitrophenylglucuronosyltransferase activity","type":"narrow"},{"name":"up regulation of p-phenylphenol glucuronyltransferase activity","type":"narrow"},{"name":"up regulation of phenyl-UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"up regulation of pnp-UDPGT activity","type":"narrow"},{"name":"up regulation of uridine 5'-diphosphoglucuronyltransferase activity","type":"exact"},{"name":"up regulation of uridine diphosphate glucuronyltransferase activity","type":"exact"},{"name":"up regulation of uridine diphosphoglucuronate-1,2-diacylglycerol glucuronosyltransferase activity","type":"narrow"},{"name":"up regulation of uridine diphosphoglucuronate-4-hydroxybiphenyl glucuronosyltransferase activity","type":"narrow"},{"name":"up regulation of uridine diphosphoglucuronate-bilirubin glucuronoside glucuronosyltransferase activity","type":"narrow"},{"name":"up regulation of uridine diphosphoglucuronate-bilirubin glucuronosyltransferase activity","type":"narrow"},{"name":"up regulation of uridine diphosphoglucuronate-estradiol glucuronosyltransferase activity","type":"narrow"},{"name":"up regulation of uridine diphosphoglucuronate-estriol 16-alpha-glucuronosyltransferase activity","type":"narrow"},{"name":"up regulation of uridine diphosphoglucuronate-estriol 16alpha-glucuronosyltransferase activity","type":"narrow"},{"name":"up regulation of uridine diphosphoglucuronate-estriol glucuronosyltransferase activity","type":"narrow"},{"name":"up regulation of uridine diphosphoglucuronosyltransferase activity","type":"exact"},{"name":"up regulation of uridine diphosphoglucuronyltransferase activity","type":"exact"},{"name":"up-regulation of 1-naphthol glucuronyltransferase activity","type":"narrow"},{"name":"up-regulation of 1-naphthol-UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"up-regulation of 17-OH steroid UDPGT activity","type":"narrow"},{"name":"up-regulation of 17-beta-hydroxysteroid UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"up-regulation of 17beta-hydroxysteroid UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"up-regulation of 3-OH androgenic UDPGT activity","type":"narrow"},{"name":"up-regulation of 3-alpha-hydroxysteroid UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"up-regulation of 3alpha-hydroxysteroid UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"up-regulation of 4-hydroxybiphenyl UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"up-regulation of 4-methylumbelliferone UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"up-regulation of 4-nitrophenol UDP-glucuronyltransferase activity","type":"narrow"},{"name":"up-regulation of 4-nitrophenol UDPGT activity","type":"narrow"},{"name":"up-regulation of GT activity","type":"exact"},{"name":"up-regulation of PNP-UDPGT","type":"related"},{"name":"up-regulation of UDP glucuronate-estradiol-glucuronosyltransferase activity","type":"narrow"},{"name":"up-regulation of UDP glucuronate-estriol glucuronosyltransferase activity","type":"narrow"},{"name":"up-regulation of UDP glucuronic acid transferase activity","type":"exact"},{"name":"up-regulation of UDP glucuronosyltransferase activity","type":"exact"},{"name":"up-regulation of UDP glucuronyltransferase activity","type":"exact"},{"name":"up-regulation of UDP-glucuronate beta-D-glucuronosyltransferase (acceptor-unspecific)","type":"exact"},{"name":"up-regulation of UDP-glucuronate-4-hydroxybiphenyl glucuronosyltransferase activity","type":"narrow"},{"name":"up-regulation of UDP-glucuronate-bilirubin glucuronyltransferase activity","type":"narrow"},{"name":"up-regulation of UDP-glucuronosyltransferase activity","type":"exact"},{"name":"up-regulation of UDP-glucuronyltransferase activity","type":"exact"},{"name":"up-regulation of UDPGA transferase activity","type":"exact"},{"name":"up-regulation of UDPGA-glucuronyltransferase activity","type":"exact"},{"name":"up-regulation of UDPGT activity","type":"exact"},{"name":"up-regulation of UDPglucuronate beta-D-glucuronosyltransferase (acceptor-unspecific) activity","type":"narrow"},{"name":"up-regulation of bilirubin UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"up-regulation of bilirubin UDPGT activity","type":"narrow"},{"name":"up-regulation of bilirubin glucuronyltransferase activity","type":"narrow"},{"name":"up-regulation of bilirubin monoglucuronide glucuronyltransferase activity","type":"narrow"},{"name":"up-regulation of bilirubin uridine diphosphoglucuronyltransferase activity","type":"narrow"},{"name":"up-regulation of ciramadol UDP-glucuronyltransferase activity","type":"narrow"},{"name":"up-regulation of estriol UDPglucuronosyltransferase activity","type":"narrow"},{"name":"up-regulation of estrone UDPglucuronosyltransferase activity","type":"narrow"},{"name":"up-regulation of glucuronosyltransferase activity","type":"exact"},{"name":"up-regulation of morphine glucuronyltransferase activity","type":"narrow"},{"name":"up-regulation of p-hydroxybiphenyl UDP glucuronyltransferase activity","type":"narrow"},{"name":"up-regulation of p-nitrophenol UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"up-regulation of p-nitrophenol UDP-glucuronyltransferase activity","type":"narrow"},{"name":"up-regulation of p-nitrophenylglucuronosyltransferase activity","type":"narrow"},{"name":"up-regulation of p-phenylphenol glucuronyltransferase activity","type":"narrow"},{"name":"up-regulation of phenyl-UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"up-regulation of pnp-UDPGT activity","type":"narrow"},{"name":"up-regulation of uridine 5'-diphosphoglucuronyltransferase activity","type":"exact"},{"name":"up-regulation of uridine diphosphate glucuronyltransferase activity","type":"exact"},{"name":"up-regulation of uridine diphosphoglucuronate-1,2-diacylglycerol glucuronosyltransferase activity","type":"narrow"},{"name":"up-regulation of uridine diphosphoglucuronate-4-hydroxybiphenyl glucuronosyltransferase activity","type":"narrow"},{"name":"up-regulation of uridine diphosphoglucuronate-bilirubin glucuronoside glucuronosyltransferase activity","type":"narrow"},{"name":"up-regulation of uridine diphosphoglucuronate-bilirubin glucuronosyltransferase activity","type":"narrow"},{"name":"up-regulation of uridine diphosphoglucuronate-estradiol glucuronosyltransferase activity","type":"narrow"},{"name":"up-regulation of uridine diphosphoglucuronate-estriol 16-alpha-glucuronosyltransferase activity","type":"narrow"},{"name":"up-regulation of uridine diphosphoglucuronate-estriol 16alpha-glucuronosyltransferase activity","type":"narrow"},{"name":"up-regulation of uridine diphosphoglucuronate-estriol glucuronosyltransferase activity","type":"narrow"},{"name":"up-regulation of uridine diphosphoglucuronosyltransferase activity","type":"exact"},{"name":"up-regulation of uridine diphosphoglucuronyltransferase activity","type":"exact"},{"name":"upregulation of 1-naphthol glucuronyltransferase activity","type":"narrow"},{"name":"upregulation of 1-naphthol-UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"upregulation of 17-OH steroid UDPGT activity","type":"narrow"},{"name":"upregulation of 17-beta-hydroxysteroid UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"upregulation of 17beta-hydroxysteroid UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"upregulation of 3-OH androgenic UDPGT activity","type":"narrow"},{"name":"upregulation of 3-alpha-hydroxysteroid UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"upregulation of 3alpha-hydroxysteroid UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"upregulation of 4-hydroxybiphenyl UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"upregulation of 4-methylumbelliferone UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"upregulation of 4-nitrophenol UDP-glucuronyltransferase activity","type":"narrow"},{"name":"upregulation of 4-nitrophenol UDPGT activity","type":"narrow"},{"name":"upregulation of GT activity","type":"exact"},{"name":"upregulation of PNP-UDPGT","type":"related"},{"name":"upregulation of UDP glucuronate-estradiol-glucuronosyltransferase activity","type":"narrow"},{"name":"upregulation of UDP glucuronate-estriol glucuronosyltransferase activity","type":"narrow"},{"name":"upregulation of UDP glucuronic acid transferase activity","type":"exact"},{"name":"upregulation of UDP glucuronosyltransferase activity","type":"exact"},{"name":"upregulation of UDP glucuronyltransferase activity","type":"exact"},{"name":"upregulation of UDP-glucuronate beta-D-glucuronosyltransferase (acceptor-unspecific)","type":"exact"},{"name":"upregulation of UDP-glucuronate-4-hydroxybiphenyl glucuronosyltransferase activity","type":"narrow"},{"name":"upregulation of UDP-glucuronate-bilirubin glucuronyltransferase activity","type":"narrow"},{"name":"upregulation of UDP-glucuronosyltransferase activity","type":"exact"},{"name":"upregulation of UDP-glucuronyltransferase activity","type":"exact"},{"name":"upregulation of UDPGA transferase activity","type":"exact"},{"name":"upregulation of UDPGA-glucuronyltransferase activity","type":"exact"},{"name":"upregulation of UDPGT activity","type":"exact"},{"name":"upregulation of UDPglucuronate beta-D-glucuronosyltransferase (acceptor-unspecific) activity","type":"narrow"},{"name":"upregulation of bilirubin UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"upregulation of bilirubin UDPGT activity","type":"narrow"},{"name":"upregulation of bilirubin glucuronyltransferase activity","type":"narrow"},{"name":"upregulation of bilirubin monoglucuronide glucuronyltransferase activity","type":"narrow"},{"name":"upregulation of bilirubin uridine diphosphoglucuronyltransferase activity","type":"narrow"},{"name":"upregulation of ciramadol UDP-glucuronyltransferase activity","type":"narrow"},{"name":"upregulation of estriol UDPglucuronosyltransferase activity","type":"narrow"},{"name":"upregulation of estrone UDPglucuronosyltransferase activity","type":"narrow"},{"name":"upregulation of glucuronosyltransferase activity","type":"exact"},{"name":"upregulation of morphine glucuronyltransferase activity","type":"narrow"},{"name":"upregulation of p-hydroxybiphenyl UDP glucuronyltransferase activity","type":"narrow"},{"name":"upregulation of p-nitrophenol UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"upregulation of p-nitrophenol UDP-glucuronyltransferase activity","type":"narrow"},{"name":"upregulation of p-nitrophenylglucuronosyltransferase activity","type":"narrow"},{"name":"upregulation of p-phenylphenol glucuronyltransferase activity","type":"narrow"},{"name":"upregulation of phenyl-UDP-glucuronosyltransferase activity","type":"narrow"},{"name":"upregulation of pnp-UDPGT activity","type":"narrow"},{"name":"upregulation of uridine 5'-diphosphoglucuronyltransferase activity","type":"exact"},{"name":"upregulation of uridine diphosphate glucuronyltransferase activity","type":"exact"},{"name":"upregulation of uridine diphosphoglucuronate-1,2-diacylglycerol glucuronosyltransferase activity","type":"narrow"},{"name":"upregulation of uridine diphosphoglucuronate-4-hydroxybiphenyl glucuronosyltransferase activity","type":"narrow"},{"name":"upregulation of uridine diphosphoglucuronate-bilirubin glucuronoside glucuronosyltransferase activity","type":"narrow"},{"name":"upregulation of uridine diphosphoglucuronate-bilirubin glucuronosyltransferase activity","type":"narrow"},{"name":"upregulation of uridine diphosphoglucuronate-estradiol glucuronosyltransferase activity","type":"narrow"},{"name":"upregulation of uridine diphosphoglucuronate-estriol 16-alpha-glucuronosyltransferase activity","type":"narrow"},{"name":"upregulation of uridine diphosphoglucuronate-estriol 16alpha-glucuronosyltransferase activity","type":"narrow"},{"name":"upregulation of uridine diphosphoglucuronate-estriol glucuronosyltransferase activity","type":"narrow"},{"name":"upregulation of uridine diphosphoglucuronosyltransferase activity","type":"exact"},{"name":"upregulation of uridine diphosphoglucuronyltransferase activity","type":"exact"}],"termid":"GO:1904225"}


id: PBO:0029320
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_histone_H2A_phosphorylation_at_centromere_outer_repeat","termid":"PBO:0029320"}


id: PBO:0074198
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 39 member 8","termid":"PBO:0074198"}


id: PBO:0058757
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6881","termid":"PBO:0058757"}


id: GO:0004653
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-N-acetyl-D-galactosamine + polypeptide = UDP + N-acetyl-D-galactosaminyl-polypeptide. This reaction is the modification of serine or threonine residues in polypeptide chains by the transfer of a N-acetylgalactose from UDP-N-acetylgalactose to the hydroxyl group of the amino acid; it is the first step in O-glycan biosynthesis.","definition_xrefs":["EC:2.4.1.41","ISBN:0879695595"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acetylgalactosaminyltransferase activity","termid":"GO:0008376"},{"relation_name":"is_a","term_name":"catalytic activity, acting on a protein","termid":"GO:0140096"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016757","GO:0016740","GO:0140096"],"is_obsolete":false,"name":"polypeptide N-acetylgalactosaminyltransferase activity","secondary_identifiers":["Reactome:R-HSA-9683760","Reactome:R-HSA-5096537","Reactome:R-HSA-8851619","MetaCyc:2.4.1.41-RXN","Reactome:R-HSA-9694438","Reactome:R-HSA-913675","Reactome:R-HSA-5096532"],"synonyms":[{"name":"UDP-GalNAc:polypeptide N-acetylgalactosaminyl transferase activity","type":"related"},{"name":"UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase activity","type":"related"},{"name":"UDP-N-acetyl-D-galactosamine:polypeptide N-acetylgalactosaminyl-transferase activity","type":"related"},{"name":"UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase activity","type":"related"},{"name":"UDP-N-acetylgalactosamine-glycoprotein N-acetylgalactosaminyltransferase activity","type":"related"},{"name":"UDP-N-acetylgalactosamine-protein N-acetylgalactosaminyltransferase activity","type":"related"},{"name":"UDP-N-acetylgalactosamine:kappa-casein polypeptide N-acetylgalactosaminyltransferase activity","type":"related"},{"name":"UDP-N-acetylgalactosamine:polypeptide N-acetylgalactosaminyltransferase activity","type":"related"},{"name":"UDP-N-acetylgalactosamine:protein N-acetylgalactosaminyl transferase activity","type":"related"},{"name":"UDP-acetylgalactosamine-glycoprotein acetylgalactosaminyltransferase activity","type":"related"},{"name":"UDP-acetylgalactosamine:peptide-N-galactosaminyltransferase activity","type":"related"},{"name":"glycoprotein acetylgalactosaminyltransferase activity","type":"related"},{"name":"polypeptide-N-acetylgalactosamine transferase activity","type":"related"},{"name":"protein-UDP acetylgalactosaminyltransferase activity","type":"related"},{"name":"uridine diphosphoacetylgalactosamine-glycoprotein acetylgalactosaminyltransferase activity","type":"related"}],"termid":"GO:0004653"}


id: MONDO:0044266
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Berg and Bearn (1966, 1966) discovered an X-linked serum protein type by means of heteroantiserum made specific by absorption. Since the group-specific antigen appears to be located in the alpha-2-macroglobulin of serum, the name Xm was assigned to the system. The distribution of phenotypes in families and in populations was consistent with X-linkage.","definition_xrefs":["OMIM:314900"],"gene_count":0,"genotype_count":0,"name":"obsolete xm system (obsolete MONDO:0044266)","secondary_identifiers":["HGNC:12813"],"synonyms":[{"name":"XM system","type":"related"}],"termid":"MONDO:0044266","xrefs":{"Monarch":{"xref_id":"0044266"}}}


id: PBO:0083592
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 protein, based on available experimental and comparative sequence data; partially overlaps the dubious ORF Q0017","termid":"PBO:0083592"}


id: MONDO:0008199
data:
  {"annotated_genes":["SJAG_01039","SJAG_00421","SJAG_01317"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87105,87106],"is_not":false,"summary":null,"term":"MONDO:0008199"},{"annotations":[87069],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013625"}]},"cv_name":"mondo","definition":"A Parkinson disease that begins after around the age of 50.","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"primary orthostatic hypotension","termid":"MONDO:0015914"},{"relation_name":"is_a","term_name":"Parkinson disease","termid":"MONDO:0005180"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00421":null,"SJAG_01039":null,"SJAG_01317":null},"genotype_count":0,"is_obsolete":false,"name":"late-onset Parkinson disease","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C3160718","DOID:0060892","Orphanet:411602","OMIM:168600","SCTID:716662004","MEDGEN:463618","GARD:17684"],"synonyms":[{"name":"LOPD","type":"exact"},{"name":"PARK","type":"exact"},{"name":"PD","type":"exact"},{"name":"Parkinson disease, age of onset, modifier, Multifactorial","type":"exact"},{"name":"Parkinson disease, late-onset","type":"exact"},{"name":"Parkinson disease, late-onset, susceptibility to, Multifactorial","type":"exact"},{"name":"Parkinson disease, susceptibility to, Multifactorial","type":"exact"},{"name":"autosomal dominant late-onset Parkinson disease","type":"exact"},{"name":"hereditary late onset Parkinson disease","type":"exact"},{"name":"hereditary late-onset Parkinson disease","type":"exact"},{"name":"late onset Parkinson disease","type":"exact"},{"name":"late onset Parkinson's disease","type":"exact"},{"name":"late-onset Parkinson disease","type":"exact"}],"termid":"MONDO:0008199","terms_by_termid":{"MONDO:0008199":null,"MONDO:0013625":null},"xrefs":{"Monarch":{"xref_id":"0008199"}}}


id: MONDO:1010211
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Mycosis fungoides that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-hodgkin lymphoma, non-human animal","termid":"MONDO:1010214"},{"relation_name":"is_a","term_name":"integumentary system disorder, non-human animal","termid":"MONDO:1011328"},{"relation_name":"is_a","term_name":"cancer, non-human animal","termid":"MONDO:1011828"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mycosis fungoides, non-human animal","secondary_identifiers":["OMIA:001109"],"termid":"MONDO:1010211","xrefs":{"Monarch":{"xref_id":"1010211"}}}


id: GO:0060818
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Compensating for the two-fold variation in X-chromosome:autosome ratios between sexes by a global inactivation of all, or most of, the genes on the paternal X-chromosome in the XX sex by genomic imprinting.","definition_xrefs":["GOC:dph","PMID:11743158","PMID:23578369","GOC:tb","PMID:16789828","PMID:18425126","GOC:sdb_2009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dosage compensation by inactivation of X chromosome","termid":"GO:0009048"},{"relation_name":"is_a","term_name":"genomic imprinting","termid":"GO:0071514"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006325"},{"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","GO:0006325"],"is_obsolete":false,"name":"inactivation of paternal X chromosome by genomic imprinting","synonyms":[{"name":"iXCI","type":"related"},{"name":"inactivation of paternal X chromosome by genetic imprinting","type":"related"}],"termid":"GO:0060818"}


id: PBO:0059958
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND3 pseudogene 3","termid":"PBO:0059958"}


id: FYPO:0007042
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of alkaline phosphatase activity is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased phosphatase activity","termid":"FYPO:0004304"},{"relation_name":"is_a","term_name":"abnormal alkaline phosphatase activity","termid":"FYPO:0007040"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0000661","FYPO:0000652","FYPO:0000654","FYPO:0001985"],"is_obsolete":false,"name":"decreased alkaline phosphatase activity","synonyms":[{"name":"reduced alkaline phosphatase activity","type":"exact"}],"termid":"FYPO:0007042"}


id: GO:2000335
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of endothelial microparticle formation.","definition_xrefs":["GOC:BHF","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of blood microparticle formation","termid":"GO:2000332"},{"relation_name":"regulates","term_name":"endothelial microparticle formation","termid":"GO:0072565"}],"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 endothelial microparticle formation","synonyms":[{"name":"regulation of endothelial microparticle generation","type":"exact"},{"name":"regulation of endothelial microparticle release","type":"exact"}],"termid":"GO:2000335"}


id: GO:0031774
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a leukotriene receptor.","definition_xrefs":["GOC:mah","GOC:nln"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor binding","termid":"GO:0001664"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"leukotriene receptor binding","synonyms":[{"name":"leukotriene receptor ligand","type":"narrow"}],"termid":"GO:0031774"}


id: PBO:0089332
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HSP chaperone complex subunit Cns1","termid":"PBO:0089332"}


id: MONDO:0008932
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":"premature centromere division","secondary_identifiers":["MEDGEN:349138","OMIM:212790","UMLS:C1859308"],"synonyms":[{"name":"PCD","type":"exact"},{"name":"X-chromosome centromere peculiarity","type":"related"},{"name":"premature centromere division","type":"exact"}],"termid":"MONDO:0008932","xrefs":{"Monarch":{"xref_id":"0008932"}}}


id: PBO:0109466
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DDAH family member 2, ADMA-independent","termid":"PBO:0109466"}


id: PBO:0051771
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inositol-pentakisphosphate 2-kinase","termid":"PBO:0051771"}


id: GO:0032458
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of membrane-bounded vesicles from deep (non-peripheral) compartments endocytic compartments back to the plasma membrane where they are recycled for further rounds of transport.","definition_xrefs":["GOC:ecd","PMID:16473635"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endocytic recycling","termid":"GO:0032456"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0051179","GO:0016192","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"slow endocytic recycling","termid":"GO:0032458"}


id: PBO:0062933
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PIK3R3 upstream open reading frame","termid":"PBO:0062933"}


id: GO:0007435
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the salivary gland are generated and organized.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gland morphogenesis","termid":"GO:0022612"},{"relation_name":"part_of","term_name":"salivary gland development","termid":"GO:0007431"}],"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":"salivary gland morphogenesis","termid":"GO:0007435"}


id: MONDO:0013646
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Heterozygous overlapping microdeletions on chromosome 8q21.11 resulting in intellectual disability, facial dysmorphism comprising a round face, ptosis, short philtrum, Cupid's bow and prominent low-set ears, nasal speech and mild finger and toe anomalies.","definition_xrefs":["Orphanet:284160"],"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"},{"relation_name":"is_a","term_name":"partial deletion of the long arm of chromosome 8","termid":"MONDO:0016907"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 8q21.11 deletion syndrome","secondary_identifiers":["OMIM:614230","MEDGEN:481861","UMLS:C3280231","DOID:0060425","SCTID:718615003","DECIPHER:86","GARD:17310"],"synonyms":[{"name":"8q21.11 microdeletion syndrome","type":"exact"},{"name":"Del(8)(q21.11)","type":"exact"},{"name":"chromosome 8q21.11 deletion syndrome","type":"exact"},{"name":"chromosome 8q21.11 deletion syndrome, isolated cases","type":"exact"},{"name":"deletion 8q21.11","type":"exact"},{"name":"monosomy 8q21.11","type":"exact"}],"termid":"MONDO:0013646","xrefs":{"Monarch":{"xref_id":"0013646"}}}


id: GO:0097099
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"The action of a molecule that contributes to the structural integrity of albumen (also called egg white). Albumen is the clear liquid contained within an egg and consists of water and proteins, among which are ovomucin and ovomucoid. It protects the egg yolk and provides additional nutrition for the growth of the embryo.","definition_xrefs":["GOC:jj","Wikipedia:Albumen"],"direct_ancestors":[{"relation_name":"is_a","term_name":"structural molecule activity","termid":"GO:0005198"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005198"}],"interesting_parent_ids":["GO:0005198","GO:0003674"],"is_obsolete":false,"name":"structural constituent of albumen","synonyms":[{"name":"structural constituent of egg white","type":"exact"}],"termid":"GO:0097099"}


id: SO:0000535
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Genomic DNA of immunoglobulin/T-cell receptor gene in germline configuration including at least one V-gene, one J-gene and one C-gene.","direct_ancestors":[{"relation_name":"has_part","term_name":"V_gene_segment","termid":"SO:0000466"},{"relation_name":"has_part","term_name":"J_gene_segment","termid":"SO:0000470"},{"relation_name":"has_part","term_name":"C_gene_segment","termid":"SO:0000478"},{"relation_name":"is_a","term_name":"vertebrate_immunoglobulin_T_cell_receptor_gene_cluster","termid":"SO:0000482"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"V_J_C_cluster","synonyms":[{"name":"V J C cluster","type":"exact"},{"name":"V-J-C-CLUSTER","type":"exact"}],"termid":"SO:0000535"}


id: GO:1901966
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cellular response to iron ion starvation.","definition_xrefs":["PMID:23115244","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of response to nutrient levels","termid":"GO:0032107"},{"relation_name":"is_a","term_name":"regulation of cellular response to stress","termid":"GO:0080135"},{"relation_name":"regulates","term_name":"cellular response to iron ion starvation","termid":"GO:0010106"}],"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 cellular response to iron ion starvation","termid":"GO:1901966"}


id: MONDO:0013802
data:
  {"annotated_genes":["SJAG_01630","SJAG_03588"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86218,86219],"is_not":false,"summary":null,"term":"MONDO:0013802"}]},"cv_name":"mondo","definition":"Infantile cerebellar retinal degeneration (ICRD) is a genetic condition present from birth (congenital) that involves the brain and eyes. Individuals with this condition usually develop symptoms around six months of age including developmental delays, low muscle tone (hypotonia), and seizures. Other symptoms may include head bobbing, abnormal muscle twitching and movement, and loss of brain cells in the main part of the brain called the cerebellum. Eye findings in individuals with this condition may include retinal degeneration (weakening of the layer of tissue in the back of the eye that senses light), strabismus (crossed eyes), and nystagmus (fast, uncontrollable movements of the eyes). ICRD is caused by mutations in the ACO2 gene and is inherited in an autosomal recessive manner. While there is still no cure for this condition, treatment options will depend on the type and severity of symptoms.","direct_ancestors":[{"relation_name":"is_a","term_name":"eye degenerative disorder","termid":"MONDO:0004884"},{"relation_name":"is_a","term_name":"tricarboxylic acid cycle disorder","termid":"MONDO:0016790"},{"relation_name":"is_a","term_name":"inherited retinal dystrophy","termid":"MONDO:0019118"},{"relation_name":"is_a","term_name":"inherited neurodegenerative disorder","termid":"MONDO:0024237"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01630":null,"SJAG_03588":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0005066","MONDO:0005328"],"is_obsolete":false,"name":"infantile cerebellar-retinal degeneration","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C3281192","MEDGEN:482822","GARD:13264","DOID:0050883","OMIM:614559","Orphanet:313850"],"synonyms":[{"name":"ICRD","type":"related"},{"name":"infantile cerebellar retinal degeneration","type":"related"},{"name":"infantile cerebellar-retinal degeneration","type":"exact"}],"termid":"MONDO:0013802","terms_by_termid":{"MONDO:0013802":null},"xrefs":{"Monarch":{"xref_id":"0013802"}}}


id: PR:000050397
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the cut12 gene in Schizosaccharomyces pombe.","definition_xrefs":["PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein","termid":"PR:000000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spindle pole body-associated protein cut12 (Schizosaccharomyces pombe)","pombase_gene_id":"SPBC649.05","synonyms":[{"name":"SPBC649.05","type":"related"},{"name":"Spom-cut12","type":"exact"},{"name":"cell untimely torn protein 12 (Schizosaccharomyces pombe)","type":"exact"},{"name":"cut12","type":"related"},{"name":"stf1","type":"related"}],"termid":"PR:000050397"}


id: PBO:0001026
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IQ domain","termid":"PBO:0001026"}


id: MONDO:0012898
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"narcolepsy, susceptibility to","termid":"MONDO:0100049"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"narcolepsy 4, susceptibility to","secondary_identifiers":["UMLS:C2676275","MEDGEN:391001","OMIM:612417"],"synonyms":[{"name":"NRCLP4","type":"exact"},{"name":"narcolepsy 4","type":"related"},{"name":"narcolepsy 4, susceptibility to","type":"exact"}],"termid":"MONDO:0012898","xrefs":{"Monarch":{"xref_id":"0012898"}}}


id: PBO:0005514
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3.6.1.19","termid":"PBO:0005514"}


id: FYECO:0000353
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which silver nanoparticles were added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PMID:29294138"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ AgNP","synonyms":[{"name":"+ silver nanoparticles","type":"exact"}],"termid":"FYECO:0000353"}


id: GO:0015937
data:
  {"annotated_genes":["SJAG_04627","SJAG_05277","SJAG_01139","SJAG_04288","SJAG_00427"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[70890,71085,78360,79746,89135],"is_not":false,"summary":null,"term":"GO:0015937"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of coenzyme A, 3'-phosphoadenosine-(5')diphospho(4')pantatheine, an acyl carrier in many acylation and acyl-transfer reactions in which the intermediate is a thiol ester.","definition_xrefs":["ISBN:0198547684"],"direct_ancestors":[{"relation_name":"is_a","term_name":"coenzyme A metabolic process","termid":"GO:0015936"},{"relation_name":"is_a","term_name":"amide biosynthetic process","termid":"GO:0043604"},{"relation_name":"is_a","term_name":"sulfur compound biosynthetic process","termid":"GO:0044272"},{"relation_name":"is_a","term_name":"purine-containing compound biosynthetic process","termid":"GO:0072522"},{"relation_name":"is_a","term_name":"nucleoside phosphate biosynthetic process","termid":"GO:1901293"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00427":null,"SJAG_01139":null,"SJAG_04288":null,"SJAG_04627":null,"SJAG_05277":null},"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:0006790"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0006790","GO:0008150"],"is_obsolete":false,"name":"coenzyme A biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-196783","GO:0006764"],"synonyms":[{"name":"CoA biosynthesis","type":"exact"},{"name":"coenzyme A anabolism","type":"exact"},{"name":"coenzyme A biosynthesis","type":"exact"},{"name":"coenzyme A formation","type":"exact"},{"name":"coenzyme A synthesis","type":"exact"}],"termid":"GO:0015937","terms_by_termid":{"GO:0015937":null}}


id: MONDO:0957560
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":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hearing loss, noise-induced, susceptibility to","secondary_identifiers":["OMIM:613035","MEDGEN:414426","UMLS:C2751629"],"termid":"MONDO:0957560","xrefs":{"Monarch":{"xref_id":"0957560"}}}


id: PBO:0033829
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mannose-6-phosphate isomerase Mpi1 (predicted)","termid":"PBO:0033829"}


id: MONDO:0019254
data:
  {"annotated_genes":["SJAG_03811","SJAG_01859","SJAG_04882","SJAG_02009","SJAG_04192","SJAG_00461","SJAG_04334","SJAG_03247","SJAG_02107","SJAG_02796","SJAG_00839","SJAG_00964","SJAG_03660","SJAG_02369","SJAG_02850","SJAG_03797","SJAG_04495","SJAG_01359","SJAG_00605","SJAG_04681","SJAG_06634"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85925],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013869"},{"annotations":[85237],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007068"},{"annotations":[86373],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012099"},{"annotations":[86833,86834],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011534"},{"annotations":[85958,85957],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010699"},{"annotations":[85786],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014719"},{"annotations":[84889],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014647"},{"annotations":[84930,84931,84929],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013046"},{"annotations":[87005],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010392"},{"annotations":[85615],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009865"},{"annotations":[85452],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009295"},{"annotations":[85956],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013275"},{"annotations":[86264,86265],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011236"},{"annotations":[85939],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010299"},{"annotations":[85938],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010298"},{"annotations":[87037],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014674"},{"annotations":[84914,84915],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007453"},{"annotations":[86239,86238],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009340"},{"annotations":[86185,86184],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100165"},{"annotations":[87013,87012],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010395"},{"annotations":[86258],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013171"},{"annotations":[85373],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009950"},{"annotations":[85565],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014221"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inborn errors of metabolism","termid":"MONDO:0019052"}],"gene_count":21,"genes_by_uniquename":{"SJAG_00461":null,"SJAG_00605":null,"SJAG_00839":null,"SJAG_00964":null,"SJAG_01359":null,"SJAG_01859":null,"SJAG_02009":null,"SJAG_02107":null,"SJAG_02369":null,"SJAG_02796":null,"SJAG_02850":null,"SJAG_03247":null,"SJAG_03660":null,"SJAG_03797":null,"SJAG_03811":null,"SJAG_04192":null,"SJAG_04334":null,"SJAG_04495":null,"SJAG_04681":null,"SJAG_04882":null,"SJAG_06634":null},"genotype_count":0,"in_subsets":["pombe_mondo_slim"],"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"inborn disorder of purine or pyrimidine metabolism","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:D011686","UMLS:C0034139","Orphanet:79224","GARD:18980","MEDGEN:48263","ICD9:277.2","MedDRA:10037546","DOID:653"],"synonyms":[{"name":"disorder of purine or pyrimidine metabolism","type":"related"},{"name":"inborn errors of purine-pyrimidine metabolism","type":"exact"},{"name":"inborn purine-pyrimidine metabolic disorder","type":"exact"},{"name":"purine-pyrimidine metabolic disorder","type":"related"}],"termid":"MONDO:0019254","terms_by_termid":{"MONDO:0007068":null,"MONDO:0007453":null,"MONDO:0009295":null,"MONDO:0009340":null,"MONDO:0009865":null,"MONDO:0009950":null,"MONDO:0010298":null,"MONDO:0010299":null,"MONDO:0010392":null,"MONDO:0010395":null,"MONDO:0010699":null,"MONDO:0011236":null,"MONDO:0011534":null,"MONDO:0012099":null,"MONDO:0013046":null,"MONDO:0013171":null,"MONDO:0013275":null,"MONDO:0013869":null,"MONDO:0014221":null,"MONDO:0014647":null,"MONDO:0014674":null,"MONDO:0014719":null,"MONDO:0100165":null},"xrefs":{"Monarch":{"xref_id":"0019254"}}}


id: PBO:0042722
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"centromere protein B","termid":"PBO:0042722"}


id: GO:0047208
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 7,8-dihydroxycoumarin + UDP-D-glucose = daphnin + H+ + UDP.","definition_xrefs":["EC:2.4.1.104","RHEA:14325"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glucosyltransferase activity","termid":"GO:0035251"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016757"}],"interesting_parent_ids":["GO:0016757","GO:0003674","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"o-dihydroxycoumarin 7-O-glucosyltransferase activity","secondary_identifiers":["KEGG_REACTION:R03548","MetaCyc:2.4.1.104-RXN"],"synonyms":[{"name":"UDP-glucose:7,8-dihydroxycoumarin 7-O-beta-D-glucosyltransferase activity","type":"related"},{"name":"UDP-glucose:o-dihydroxycoumarin glucosyltransferase activity","type":"related"},{"name":"UDPglucose:7,8-dihydroxycoumarin 7-O-beta-D-glucosyltransferase activity","type":"related"},{"name":"uridine diphosphoglucose-o-dihydroxycoumarin 7-O-glucosyltransferase activity","type":"related"}],"termid":"GO:0047208"}


id: MONDO:0022174
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cytogenetic abnormality that refers to the allelic loss of all or part of the short arm of chromosome 12.","definition_xrefs":["NCIT:C36410"],"direct_ancestors":[{"relation_name":"is_a","term_name":"partial deletion of chromosome 12","termid":"MONDO:0017277"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 12p deletion","secondary_identifiers":["GARD:21404","MEDGEN:208640","MESH:C538301","Orphanet:316244","UMLS:C0795844","MESH:C538302"],"synonyms":[{"name":"12p del","type":"related"},{"name":"12p deletion","type":"related"},{"name":"12p monosomy","type":"related"},{"name":"12p-","type":"related"},{"name":"del(12p)","type":"related"},{"name":"deletion 12p","type":"related"},{"name":"loss of chromosome 12p","type":"related"},{"name":"monosomy 12p","type":"related"},{"name":"partial deletion of chromosome 12p","type":"exact"},{"name":"partial deletion of the short arm of chromosome 12","type":"exact"},{"name":"partial deletion of the short arm of chromosome type 12","type":"exact"},{"name":"partial monosomy 12p","type":"related"},{"name":"partial monosomy of chromosome 12p","type":"exact"},{"name":"partial monosomy of the short arm of chromosome 12","type":"exact"}],"termid":"MONDO:0022174","xrefs":{"Monarch":{"xref_id":"0022174"}}}


id: FYPO:0002582
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 mature mitochondrial transfer RNA (tRNA) measured in a cell is normal (i.e. indistinguishable from wild type). Total tRNA or a specific tRNA may be measured.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal mature tRNA level","termid":"FYPO:0002580"},{"relation_name":"is_a","term_name":"normal mitochondrial RNA level","termid":"FYPO:0004960"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0001312","FYPO:0000257"],"is_obsolete":false,"name":"normal mature mitochondrial tRNA level","synonyms":[{"name":"normal mature mitochondrial tRNA accumulation","type":"related"},{"name":"normal mature mitochondrial tRNA level during mitotic cell cycle","type":"related"},{"name":"normal mature mitochondrial tRNA level during vegetative growth","type":"exact"},{"name":"normal mature mitochondrial tRNA transcript level","type":"exact"},{"name":"normal mature mitochondrial transfer RNA level","type":"exact"},{"name":"normal mitochondrial tRNA level","type":"broad"}],"termid":"FYPO:0002582"}


id: PBO:0042640
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromodomain Y-linked 15 pseudogene","termid":"PBO:0042640"}


id: PBO:0051406
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IgLON family member 5","termid":"PBO:0051406"}


id: PBO:0047271
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 247 member C","termid":"PBO:0047271"}


id: GO:0031340
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of vesicle fusion.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of organelle organization","termid":"GO:0010638"},{"relation_name":"is_a","term_name":"regulation of vesicle fusion","termid":"GO:0031338"},{"relation_name":"is_a","term_name":"positive regulation of transport","termid":"GO:0051050"},{"relation_name":"positively_regulates","term_name":"vesicle fusion","termid":"GO:0006906"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0061024"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0061024"},{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0061024","GO:0016192","GO:0006810"],"is_obsolete":false,"name":"positive regulation of vesicle fusion","synonyms":[{"name":"activation of vesicle fusion","type":"narrow"},{"name":"stimulation of vesicle fusion","type":"narrow"},{"name":"up regulation of vesicle fusion","type":"exact"},{"name":"up-regulation of vesicle fusion","type":"exact"},{"name":"upregulation of vesicle fusion","type":"exact"}],"termid":"GO:0031340"}


id: GO:1902650
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of histone H2A-H2B dimer displacement.","definition_xrefs":["GOC:di","GO_REF:0000058","PMID:22199252","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of histone H2A-H2B dimer displacement (obsolete GO:1902650)","synonyms":[{"name":"down regulation of histone H2A-H2B dimer displacement","type":"exact"},{"name":"down-regulation of histone H2A-H2B dimer displacement","type":"exact"},{"name":"downregulation of histone H2A-H2B dimer displacement","type":"exact"},{"name":"inhibition of histone H2A-H2B dimer displacement","type":"narrow"}],"termid":"GO:1902650"}


id: GO:0008758
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + UDP-2,3-bis(3-hydroxymyristoyl)glucosamine = 2,3-bis(3-hydroxymyristoyl)-beta-D-glucosaminyl 1-phosphate + UMP.","definition_xrefs":["MetaCyc:LIPIDXSYNTHESIS-RXN","PMID:12000770"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrophosphatase activity","termid":"GO:0016462"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"UDP-2,3-diacylglucosamine hydrolase activity","secondary_identifiers":["RHEA:25213"],"termid":"GO:0008758"}


id: PBO:0048782
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein subunit alpha 13","termid":"PBO:0048782"}


id: MONDO:0019079
data:
  {"annotated_genes":["SJAG_03894","SJAG_02286"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85621],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008026"},{"annotations":[85959],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009669"},{"annotations":[86215],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009673"},{"annotations":[85821],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009672"},{"annotations":[85981],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010056"}]},"cv_name":"mondo","definition":"Proximal spinal muscular atrophies are a group of neuromuscular disorders characterized by progressive muscle weakness resulting from the degeneration and loss of the lower motor neurons in the spinal cord and the brain stem nuclei.","definition_xrefs":["Orphanet:70"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spinal muscular atrophy","termid":"MONDO:0001516"},{"relation_name":"is_a","term_name":"hereditary peripheral neuropathy","termid":"MONDO:0020127"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02286":null,"SJAG_03894":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0005244"],"is_obsolete":false,"name":"proximal spinal muscular atrophy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NANDO:2100231","MEDGEN:870510","UMLS:C4024957","GARD:4531","NORD:1729"],"synonyms":[{"name":"SMA","type":"exact"},{"name":"Spinal Muscular Atrophy","type":"exact"}],"termid":"MONDO:0019079","terms_by_termid":{"MONDO:0008026":null,"MONDO:0009669":null,"MONDO:0009672":null,"MONDO:0009673":null,"MONDO:0010056":null},"xrefs":{"Monarch":{"xref_id":"0019079"}}}


id: PBO:0057108
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 198","termid":"PBO:0057108"}


id: PBO:0086678
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 gene-trapping, microarray-based expression analysis, and genome-wide homology searching","termid":"PBO:0086678"}


id: PBO:0074519
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small NF90 (ILF3) associated RNA A11","termid":"PBO:0074519"}


id: GO:0047363
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: alpha-D-glucosyl-1,6-alpha-D-glucosyl-1,6-alpha-D-glucosyl-1,3-1-O-alkyl-2-O-acylglycerol + 3'-phosphoadenosine 5'-phosphosulfate = 6-sulfo-alpha-D-glucosyl-1,6-alpha-D-glucosyl-1,6-alpha-D-glucosyl-1,3-1-O-alkyl-2-O-acylglycerol + adenosine 3',5'-bisphosphate.","definition_xrefs":["MetaCyc:2.8.2.19-RXN","EC:2.8.2.19"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfotransferase activity","termid":"GO:0008146"}],"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:0016782"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0016782","GO:0003824"],"is_obsolete":false,"name":"triglucosylalkylacylglycerol sulfotransferase activity","secondary_identifiers":["RHEA:13273"],"synonyms":[{"name":"3'-phosphoadenylyl-sulfate:triglucosyl-1-O-alkyl-2-O-acylglycerol 6-sulfotransferase activity","type":"related"},{"name":"triglucosylalkylacylglycerol sulphotransferase activity","type":"exact"},{"name":"triglucosylmonoalkylmonoacyl sulfotransferase activity","type":"related"}],"termid":"GO:0047363"}


id: MONDO:0002977
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder characterized by the degeneration of the nervous system due to autoimmunity. Representative examples include multiple sclerosis, Guillain-Barre syndrome, and myasthenia gravis.","definition_xrefs":["NCIT:C99383"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder","termid":"MONDO:0005071"},{"relation_name":"is_a","term_name":"autoimmune disease","termid":"MONDO:0007179"}],"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":"autoimmune disorder of the nervous system","secondary_identifiers":["DOID:438","MESH:D020274","MEDGEN:155946","UMLS:C0751871"],"synonyms":[{"name":"autoimmune disease of nervous system","type":"exact"},{"name":"autoimmune disease, neurologic","type":"exact"},{"name":"autoimmune diseases, nervous system","type":"exact"},{"name":"autoimmune diseases, neurologic","type":"exact"},{"name":"autoimmune disorders of the nervous system","type":"exact"},{"name":"autoimmune disorders, nervous system","type":"exact"},{"name":"autoimmune nervous system diseases","type":"exact"},{"name":"autoimmune nervous system disorder","type":"exact"},{"name":"disease, neurologic autoimmune","type":"exact"},{"name":"diseases, neurologic autoimmune","type":"exact"},{"name":"immune diseases, nervous system","type":"exact"},{"name":"immune disorders, nervous system","type":"exact"},{"name":"nervous system autoimmune disease","type":"exact"},{"name":"nervous system autoimmune diseases","type":"exact"},{"name":"nervous system hypersensitivity reaction type II disease","type":"exact"},{"name":"nervous system immune diseases","type":"exact"},{"name":"nervous system immune disorders","type":"exact"},{"name":"neurologic autoimmune disease","type":"exact"},{"name":"neurologic autoimmune diseases","type":"exact"}],"termid":"MONDO:0002977","xrefs":{"Monarch":{"xref_id":"0002977"}}}


id: MONDO:1010923
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Muscular dystrophy, Duchenne type that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscular dystrophy, Duchenne type, non-human animal","termid":"MONDO:1010199"},{"relation_name":"is_a","term_name":"muscular dystrophy, dog","termid":"MONDO:1010911"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"muscular dystrophy, Duchenne type, dog","secondary_identifiers":["OMIA:001081-9615"],"termid":"MONDO:1010923","xrefs":{"Monarch":{"xref_id":"1010923"}}}


id: PBO:0087964
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transporter of the ATP-binding cassette (ABC) family; involved in bile acid transport; negative regulator of vacuole fusion; regulates release of lumenal Ca2+ stores; similar to mammalian bile transporters; YBT1 has a paralog, VMR1, that arose from the whole genome duplication","termid":"PBO:0087964"}


id: PR:O94458
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC1687.17c gene.","definition_xrefs":["UniProtKB:O94458","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized derlin-like protein C1687.17c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1687.17c","synonyms":[{"name":"Spom972h-SPAC1687.17c","type":"exact"}],"termid":"PR:O94458"}


id: FYPO:0005225
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 dimethylation of lysine at position 4 of histone H3 occurs to a greater extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased histone methylation during vegetative growth","termid":"FYPO:0000869"},{"relation_name":"is_a","term_name":"abnormal histone H3-K4 methylation during vegetative growth","termid":"FYPO:0002330"}],"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:0002494"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002274"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0002494","FYPO:0005447","FYPO:0002274","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"increased histone H3-K4 dimethylation during vegetative growth","synonyms":[{"name":"increased histone H3 K4 dimethylation during vegetative growth","type":"exact"},{"name":"increased histone H3-K4 dimethylation during mitotic cell cycle","type":"related"},{"name":"increased histone H3K4 dimethylation during vegetative growth","type":"exact"},{"name":"increased histone H3K4me2 during vegetative growth","type":"exact"},{"name":"increased histone lysine H3 K4 dimethylation during vegetative growth","type":"exact"}],"termid":"FYPO:0005225"}


id: PBO:0041442
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C9orf78 pseudogene 1","termid":"PBO:0041442"}


id: MONDO:1011622
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Wilms tumour that occurs in sheep.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Wilms tumor, non-human animal","termid":"MONDO:1011439"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Wilms tumor, sheep","secondary_identifiers":["OMIA:001142-9940"],"termid":"MONDO:1011622","xrefs":{"Monarch":{"xref_id":"1011622"}}}


id: PBO:0083736
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential component of GPI-mannosyltransferase II; complex is responsible for second mannose addition to GPI precursors as a partner of Gpi18p; required for maturation of Gas1p and Pho8p; has synthetic genetic interactions with secretory pathway genes","termid":"PBO:0083736"}


id: PBO:0030415
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_spindle_pole_body_duplication","termid":"PBO:0030415"}


id: MONDO:0026190
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete genetic malformation syndrome with odontal and/or periodontal component (obsolete MONDO:0026190)","secondary_identifiers":["Orphanet:183580"],"termid":"MONDO:0026190","xrefs":{"Monarch":{"xref_id":"0026190"}}}


id: MONDO:1012119
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hypothalamic dysplasia, non-human animal","termid":"MONDO:1011846"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypothalamic dysplasia, dog","secondary_identifiers":["OMIA:000535-9615"],"termid":"MONDO:1012119","xrefs":{"Monarch":{"xref_id":"1012119"}}}


id: PBO:0062353
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 6 subfamily N member 1","termid":"PBO:0062353"}


id: MONDO:0005482
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A hypomineralisation of systemic origin of one to four permanent first molars frequently associated with affected incisors","definition_xrefs":["EFO:0005321"],"gene_count":0,"genotype_count":0,"name":"obsolete molar-incisor hypomineralization (obsolete MONDO:0005482)","secondary_identifiers":["SCTID:698053001","ICD9:520.5"],"termid":"MONDO:0005482","xrefs":{"Monarch":{"xref_id":"0005482"}}}


id: GO:0090350
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate, frequency or extent of the chemical reactions and pathways involving organofluorine compounds, as carried out by individual cells.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of organofluorine metabolic process","termid":"GO:0090348"},{"relation_name":"is_a","term_name":"negative regulation of organohalogen metabolic process","termid":"GO:0090349"},{"relation_name":"negatively_regulates","term_name":"organofluorine metabolic process","termid":"GO:0090346"}],"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 organofluorine metabolic process","termid":"GO:0090350"}


id: PBO:0000009
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-dependent_on","termid":"PBO:0000009"}


id: MONDO:0013473
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":"Hirschsprung disease, cardiac defects, and autonomic dysfunction","secondary_identifiers":["MESH:C563939","OMIM:613870","UMLS:C3151237","MEDGEN:462587"],"synonyms":[{"name":"HCAD","type":"related"},{"name":"Hirschsprung disease, CARDIAC defects, and autonomic dysfunction","type":"related"},{"name":"Hirschsprung disease, cardiac defects, and autonomic dysfunction","type":"exact"}],"termid":"MONDO:0013473","xrefs":{"Monarch":{"xref_id":"0013473"}}}


id: PBO:0090001
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin-protein ligase E3/SUMO transferase, Topors, possibly associated with DNA damage","termid":"PBO:0090001"}


id: MONDO:1010659
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Thrombocytopenia that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thrombocytopenia, non-human animal","termid":"MONDO:1010080"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thrombocytopenia, dog","secondary_identifiers":["OMIA:001001-9615"],"termid":"MONDO:1010659","xrefs":{"Monarch":{"xref_id":"1010659"}}}


id: PBO:0046131
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation initiation factor 4H pseudogene 1","termid":"PBO:0046131"}


id: GO:0039568
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which a virus stops, prevents, or reduces STAT1-dependent gene transcription, by preventing STAT1 from binding to promoter sites in the nucleus.","definition_xrefs":["PMID:17287281"],"gene_count":0,"genotype_count":0,"name":"obsolete suppression by virus of host STAT1 activity by inhibition of DNA binding (obsolete GO:0039568)","synonyms":[{"name":"inhibition of DNA binding of STAT1","type":"exact"},{"name":"suppression by virus of host STAT1 activity by negative regulation of DNA binding","type":"exact"}],"termid":"GO:0039568"}


id: PR:O94425
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC660.05 gene.","definition_xrefs":["UniProtKB:O94425","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":"WW domain-containing protein C660.05 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC660.05","synonyms":[{"name":"Spom972h-SPBC660.05","type":"exact"}],"termid":"PR:O94425"}


id: GO:0061353
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of molecular signals initiated by the binding of a member of the BMP (bone morphogenetic protein) family to its receptor on the surface of a target cell, which contributes to the directed movement of a Malpighian tubule cell toward a stimulus, thereby contributing to the shaping of the tubule.","definition_xrefs":["PMID:19783135","GOC:dph","GOC:mtg_kidney_jan10"],"gene_count":0,"genotype_count":0,"name":"obsolete BMP signaling pathway involved in Malpighian tubule cell chemotaxis (obsolete GO:0061353)","synonyms":[{"name":"bone morphogenic protein receptor signalling pathway involved in Malpighian tubule cell chemotaxis","type":"exact"}],"termid":"GO:0061353"}


id: MONDO:0013521
data:
  {"annotated_genes":["SJAG_05979"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85245],"is_not":false,"summary":null,"term":"MONDO:0013521"}]},"cv_name":"mondo","definition":"A dyskeratosis congenita that has material basis in an autosomal dominant mutation of TERT on chromosome 5p15.33.","definition_xrefs":["DOID:0070016"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"dyskeratosis congenita","termid":"MONDO:0015780"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05979":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0005093"],"is_obsolete":false,"name":"dyskeratosis congenita, autosomal dominant 2","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:15741","MEDGEN:462793","OMIM:613989","UMLS:C3151443","NCIT:C176922"],"synonyms":[{"name":"DKCA2","type":"exact"},{"name":"autosomal dominant dyskeratosis congenita 2","type":"related"},{"name":"dyskeratosis congenita, autosomal dominant 2","type":"exact"},{"name":"dyskeratosis congenita, autosomal dominant type 2","type":"exact"},{"name":"dyskeratosis congenita, autosomal recessive 4","type":"related"}],"termid":"MONDO:0013521","terms_by_termid":{"MONDO:0013521":null},"xrefs":{"Monarch":{"xref_id":"0013521"}}}


id: MONDO:1012941
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cleft palate that occurs in cattle due to a mutation in the MYH3 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cleft palate, cattle","termid":"MONDO:1010530"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cleft palate, MYH3-related, cattle","secondary_identifiers":["OMIA:002590-9913"],"termid":"MONDO:1012941","xrefs":{"Monarch":{"xref_id":"1012941"}}}


id: PBO:0059680
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO1 pseudogene 46","termid":"PBO:0059680"}


id: FYPO:0007660
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell population phenotype in which cells in a population do not divide at a uniform size, although each cell divides to form equal-size daughter cells, which then subsequently divide at an abnormal size. Within one population, some cells may be larger and others smaller than normal (i.e. compared to wild-type cells under the same conditions) upon each division.","definition_xrefs":["PomBase:jh","PomBase:vw","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"variable cell size at division","termid":"FYPO:0007474"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0000003"],"is_obsolete":false,"name":"variable cell size at division with subsequent division at abnormal size","synonyms":[{"name":"increased variability of cell size in a vegetative population, with subsequent division at abnormal size","type":"exact"},{"name":"variable cell length at entry into mitosis followed by unequal cell division","type":"exact"},{"name":"variable cell size at division with abnormal cell size homeostasis","type":"exact"},{"name":"variable cell size at division with loss of cell size homeostasis","type":"exact"},{"name":"variable cell size at division with subsequent division at abnormal size during mitotic cell cycle","type":"related"},{"name":"variable cell size at division with subsequent division at abnormal size during vegetative growth","type":"exact"},{"name":"variable vegetative cell size at division with subsequent division at abnormal size","type":"exact"}],"termid":"FYPO:0007660"}


id: GO:1900463
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents, or reduces the frequency, rate or extent of cellular response to alkalinity by stopping, preventing, or reducing the frequency, rate or extent of transcription from an RNA polymerase II promoter.","definition_xrefs":["PMID:17023428","GOC:dgf","PMID:12509465","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of cellular response to alkaline pH by negative regulation of transcription from RNA polymerase II promoter (obsolete GO:1900463)","synonyms":[{"name":"negative regulation of cellular response to alkalinity by negative regulation of transcription from RNA polymerase II promoter","type":"broad"},{"name":"negative regulation of cellular response to basic pH by negative regulation of transcription from RNA polymerase II promoter","type":"exact"}],"termid":"GO:1900463"}


id: SO:0001105
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Residues which interact with a ligand.","definition_xrefs":["EBIBS:GAR"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ligand_binding_site","termid":"SO:0001657"},{"relation_name":"is_a","term_name":"molecular_contact_region","termid":"SO:0100002"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"SO:0000839"}],"interesting_parent_ids":["SO:0000839"],"is_obsolete":false,"name":"polypeptide_ligand_contact","secondary_identifiers":["BS:00157"],"synonyms":[{"name":"polypeptide ligand contact","type":"exact"},{"name":"protein-ligand interaction","type":"related"}],"termid":"SO:0001105"}


id: MONDO:1011309
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Connective tissue disorder that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-human animal disease","termid":"MONDO:0005583"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"connective tissue disorder, non-human animal","termid":"MONDO:1011309","xrefs":{"Monarch":{"xref_id":"1011309"}}}


id: PBO:0114279
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"orthologus to S. cerevisiae YOR350C","termid":"PBO:0114279"}


id: PATO:0000617
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A shape quality inhering in a bearer by virtue of the bearer's having one or more angle(s) in its length.","definition_xrefs":["PATOC:MAH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"shape","termid":"PATO:0000052"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bent","termid":"PATO:0000617"}


id: MONDO:0013056
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare mitochondrial substrate carrier disorder characterized by severe muscular hypotonia, seizures (with or without episodic apnea) beginning in the first year of life, and arrested psychomotor development (affecting mainly motor skills). Severe spasticity with hyperreflexia has also been reported. Global cerebral hypomyelination is a characteristic imaging feature of this disease.","definition_xrefs":["Orphanet:353217"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial substrate carrier disorder","termid":"MONDO:0016801"},{"relation_name":"is_a","term_name":"neonatal-onset developmental and epileptic encephalopathy","termid":"MONDO:0100455"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005027"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092","MONDO:0005066","MONDO:0004069","MONDO:0005027"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy, 39","secondary_identifiers":["MESH:C567847","GARD:17532","OMIM:612949","SCTID:726702005","UMLS:C2751855","DOID:0080349","MEDGEN:414492"],"synonyms":[{"name":"AGC1 deficiency","type":"exact"},{"name":"DEE39","type":"exact"},{"name":"EIEE39","type":"exact"},{"name":"SLC25A12 early infantile epileptic encephalopathy","type":"exact"},{"name":"aspartate-glutamate carrier 1 deficiency","type":"related"},{"name":"developmental and epileptic encephalopathy 39","type":"exact"},{"name":"early infantile epileptic encephalopathy caused by mutation in SLC25A12","type":"exact"},{"name":"epileptic encephalopathy with global cerebral demyelination","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 39","type":"exact"},{"name":"hypomyelination, global cerebral","type":"related"},{"name":"mitochondrial aspartate-glutamate carrier 1 deficiency","type":"exact"}],"termid":"MONDO:0013056","xrefs":{"Monarch":{"xref_id":"0013056"}}}


id: GO:0009149
data:
  {"annotated_genes":["SJAG_04487"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[79241],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046081"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of pyrimidine nucleoside triphosphate, a compound consisting of a pyrimidine base linked to a ribose or deoxyribose sugar esterified with triphosphate on the sugar.","definition_xrefs":["GOC:go_curators","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside triphosphate catabolic process","termid":"GO:0009143"},{"relation_name":"is_a","term_name":"pyrimidine nucleoside triphosphate metabolic process","termid":"GO:0009147"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04487":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"pyrimidine nucleoside triphosphate catabolic process","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"pyrimidine nucleoside triphosphate breakdown","type":"exact"},{"name":"pyrimidine nucleoside triphosphate catabolism","type":"exact"},{"name":"pyrimidine nucleoside triphosphate degradation","type":"exact"}],"termid":"GO:0009149","terms_by_termid":{"GO:0046081":null}}


id: GO:0034070
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: acetyl-CoA + aminoglycoside = CoA + 1-N-acetylaminoglycoside. This is acetylation of the 1-amino group of the central deoxystreptamine ring.","definition_xrefs":["GOC:cb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aminoglycoside N-acetyltransferase activity","termid":"GO:0034069"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016746","GO:0016740","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"aminoglycoside 1-N-acetyltransferase activity","termid":"GO:0034070"}


id: MONDO:0016548
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Megacystic-megaureter syndrome is an urinary tract malformation characterized by the presence of a massive primary non-obstructive vesicoureteral reflux and a large capacity, smooth, thin walled bladder due to the continual recycling of refluxed urine. Recurrent urinary infections are commonly associated with this condition.","definition_xrefs":["Orphanet:238637"],"direct_ancestors":[{"relation_name":"is_a","term_name":"urinary system disorder","termid":"MONDO:0002118"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"megacystis-megaureter syndrome","secondary_identifiers":["icd11.foundation:1872503107","MEDGEN:609133","GARD:20638","UMLS:C0431752","SCTID:253904001"],"synonyms":[{"name":"megaureter-megacystis syndrome","type":"exact"}],"termid":"MONDO:0016548","xrefs":{"Monarch":{"xref_id":"0016548"}}}


id: PBO:0064035
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi-interacting RNA cluster 69","termid":"PBO:0064035"}


id: MONDO:0005752
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Circumscribed collections of suppurative material occurring in the spinal or intracranial epidural space. The majority of epidural abscesses occur in the spinal canal and are associated with osteomyelitis of a vertebral body; analgesia, epidural; and other conditions. Clinical manifestations include local and radicular pain, weakness, sensory loss, urinary incontinence, and fecal incontinence. Cranial epidural abscesses are usually associated with osteomyelitis of a cranial bone, sinusitis, or otitis media. (From Adams et al., Principles of Neurology, 6th ed, p710 and pp1240-1; J Neurol Neurosurg Psychiatry 1998 Aug;65(2):209-12)","definition_xrefs":["MESH:D020802"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abscess","termid":"MONDO:0005227"},{"relation_name":"is_a","term_name":"central nervous system neoplasm","termid":"MONDO:0006130"},{"relation_name":"is_a","term_name":"central nervous system infectious disorder","termid":"MONDO:0024619"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"epidural abscess","secondary_identifiers":["MEDGEN:82848","DOID:11387","EFO:0007260","SCTID:61974008","UMLS:C0270629"],"synonyms":[{"name":"abscess epidural","type":"exact"},{"name":"extradural intraspinal abscess","type":"exact"},{"name":"intraspinal epidural abscess","type":"exact"},{"name":"intraspinal extradural abscess","type":"exact"},{"name":"spinal epidural abscess","type":"exact"},{"name":"spinal epidural abscess (disorder)","type":"exact"},{"name":"spinal extradural abscess","type":"exact"}],"termid":"MONDO:0005752","xrefs":{"Monarch":{"xref_id":"0005752"}}}


id: GO:0051667
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a plastid to a specific location in the cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plastid localization","termid":"GO:0051644"},{"relation_name":"is_a","term_name":"establishment of localization in cell","termid":"GO:0051649"},{"relation_name":"is_a","term_name":"establishment of organelle localization","termid":"GO:0051656"}],"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":"establishment of plastid localization","synonyms":[{"name":"establishment of plastid localisation","type":"exact"}],"termid":"GO:0051667"}


id: PBO:0059127
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-methylpurine DNA glycosylase","termid":"PBO:0059127"}


id: PBO:0065769
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"quinoid dihydropteridine reductase","termid":"PBO:0065769"}


id: PBO:0045171
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DnaJ heat shock protein family (Hsp40) member A1 pseudogene 5","termid":"PBO:0045171"}


id: GO:0001987
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that is triggered by vasomotor excitation and results in a decrease in the diameter of an artery during the baroreceptor response to decreased blood pressure.","definition_xrefs":["ISBN:0721643949"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vasoconstriction","termid":"GO:0042310"},{"relation_name":"part_of","term_name":"baroreceptor response to decreased systemic arterial blood pressure","termid":"GO:0001982"}],"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":"vasoconstriction of artery involved in baroreceptor response to lowering of systemic arterial blood pressure","termid":"GO:0001987"}


id: MOD:01118
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from DeltaMass","definition_xrefs":["DeltaMass:275"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DeltaMass","termid":"MOD:00947"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha-N-6-phosphogluconoylation (His Tagged proteins)","termid":"MOD:01118"}


id: PBO:0028428
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-growth_auxotrophic_for_pyridoxine","termid":"PBO:0028428"}


id: MONDO:0013792
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Bleeding into one or both cerebral hemispheres including the basal ganglia and the cerebral cortex. It is often associated with hypertension and craniocerebral trauma.","definition_xrefs":["MESH:D002543"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerebrovascular disorder","termid":"MONDO:0011057"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intracerebral hemorrhage","secondary_identifiers":["EFO:0005669","SCTID:274100004","UMLS:C2937358","ICD9:431","MEDGEN:423648"],"synonyms":[{"name":"stroke, hemorrhagic","type":"exact"}],"termid":"MONDO:0013792","xrefs":{"Monarch":{"xref_id":"0013792"}}}


id: MONDO:0010096
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":"tardive dyskinesia","secondary_identifiers":["SCTID:102449007","HP:0040141","MEDGEN:151939","MESH:D000071057","OMIM:272620","UMLS:C0686347"],"synonyms":[{"name":"tardive dyskinesia","type":"exact"},{"name":"tardive dyskinesia (disease)","type":"exact"}],"termid":"MONDO:0010096","xrefs":{"Monarch":{"xref_id":"0010096"}}}


id: MONDO:0007735
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital Horner syndrome is a rare neurological disorder characterized by relative pupillary miosis and blepharoptosis, evident at birth, caused by interruption of the oculosympathetic innervation at any point along the neural pathway from the hypothalamus to the orbit. Often additional symptoms, such as enophthalmos, facial anhidrosis, iris heterochromia, conjunctival congestion, transient hypotonia and/or pupillary dilation lag, may be present. Association with birth trauma, neoplasms or vascular malformations has been reported.","definition_xrefs":["Orphanet:91413"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Horner syndrome","termid":"MONDO:0001294"}],"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":"congenital Horner syndrome","secondary_identifiers":["MEDGEN:327111","OMIM:143000","HP:0006837","GARD:6670","MESH:C564178","UMLS:C1840475"],"synonyms":[{"name":"HORNER syndrome, congenital","type":"related"},{"name":"congenital Claude-Bernard-Horner syndrome","type":"exact"},{"name":"congenital Horner syndrome","type":"exact"},{"name":"congenital Horner syndrome (disease)","type":"exact"}],"termid":"MONDO:0007735","xrefs":{"Monarch":{"xref_id":"0007735"}}}


id: PBO:0083148
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; almost completely overlaps ORF PCI8/YIL071C","termid":"PBO:0083148"}


id: PR:O74985
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- naa15 gene.","definition_xrefs":["UniProtKB:O74985","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-terminal acetyltransferase A complex subunit nat1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC338.07c","synonyms":[{"name":"NatA complex subunit nat1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-naa15","type":"exact"}],"termid":"PR:O74985"}


id: FYPO:0002627
data:
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id: PBO:0068922
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 165, pseudogene","termid":"PBO:0068922"}


id: MONDO:0000332
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease caused by infection with Neorickettsia sennetsu.","definition_xrefs":["MONDO:patterns/infectious_disease_by_agent"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"ehrlichiosis","termid":"MONDO:0016003"},{"relation_name":"is_a","term_name":"primary bacterial infectious disease","termid":"MONDO:0000314"},{"relation_name":"is_a","term_name":"Neorickettsia infectious disease","termid":"MONDO:0024416"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sennetsu fever","secondary_identifiers":["ICD9:088.89","GARD:120","MESH:C537582","DOID:0050485","MEDGEN:105459","NORD:1703","SCTID:21013006","UMLS:C0520779"],"synonyms":[{"name":"Human Ehrlichial infection, sennetsu type","type":"related"},{"name":"Neorickettsia sennetsu caused disease or disorder","type":"exact"},{"name":"Neorickettsia sennetsu disease or disorder","type":"exact"},{"name":"Neorickettsia sennetsu infectious disease","type":"exact"},{"name":"sennetsu ehrlichiosis","type":"related"},{"name":"sennetsu fever","type":"exact"}],"termid":"MONDO:0000332","xrefs":{"Monarch":{"xref_id":"0000332"}}}


id: GO:0004924
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  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with oncostatin-M and transmitting the signal from one side of the membrane to the other to initiate a change in cell activity.","definition_xrefs":["GOC:signaling","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine receptor activity","termid":"GO:0004896"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0038023","GO:0003674"],"is_obsolete":false,"name":"oncostatin-M receptor activity","termid":"GO:0004924"}


id: PBO:0054534
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  {"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 1934","termid":"PBO:0054534"}


id: MONDO:0000509
data:
  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intellectual disability","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0050889"],"synonyms":[{"name":"isolated intellectual disability","type":"exact"},{"name":"nonsyndromic intellectual 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id: PBO:0088868
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein P2","termid":"PBO:0088868"}


id: GO:0003339
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency or extent of the transition where a mesenchymal cell establishes apical/basolateral polarity,forms intercellular adhesive junctions, synthesizes basement membrane components and becomes an epithelial cell that will contribute to the shaping of the metanephros.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of epithelial cell differentiation involved in kidney development","termid":"GO:2000696"},{"relation_name":"regulates","term_name":"mesenchymal to epithelial transition involved in metanephros morphogenesis","termid":"GO:0003337"}],"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 mesenchymal to epithelial transition involved in metanephros morphogenesis","termid":"GO:0003339"}


id: PBO:0004303
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin conjugating enzyme Ubc1 (predicted)","termid":"PBO:0004303"}


id: GO:0042361
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of menaquinones, any of the quinone-derived compounds synthesized by intestinal bacteria. Structurally, menaquinones consist of a methylated naphthoquinone ring structure and side chains composed of a variable number of unsaturated isoprenoid residues. Menaquinones have vitamin K activity and are known as vitamin K2.","definition_xrefs":["GOC:jl","PMID:37938463"],"direct_ancestors":[{"relation_name":"is_a","term_name":"menaquinone metabolic process","termid":"GO:0009233"},{"relation_name":"is_a","term_name":"ketone catabolic process","termid":"GO:0042182"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"menaquinone catabolic process","synonyms":[{"name":"menaquinone breakdown","type":"exact"},{"name":"menaquinone catabolism","type":"exact"},{"name":"menaquinone degradation","type":"exact"},{"name":"menatetrenone catabolic process","type":"exact"},{"name":"menatetrenone catabolism","type":"exact"},{"name":"multiprenylmenaquinone catabolic process","type":"exact"},{"name":"multiprenylmenaquinone catabolism","type":"exact"},{"name":"vitamin K2 catabolic process","type":"exact"},{"name":"vitamin K2 catabolism","type":"exact"}],"termid":"GO:0042361"}


id: PBO:0086982
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Regulatory subunit of the vacuolar transporter chaperone (VTC) complex; VTC complex is involved in membrane trafficking, vacuolar polyphosphate accumulation, microautophagy and non-autophagic vacuolar fusion; also has mRNA binding activity; protein abundance increases in response to DNA replication stress","termid":"PBO:0086982"}


id: PBO:0086390
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative checkpoint factor in transcription; binds to U2 snRNA and Prp11p; regulates toggling of the U2 snRNA stem II region between different structures; contains two RNA recognition motifs (RRMs)","termid":"PBO:0086390"}


id: PBO:0084073
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTPase with similarity to translation release factors; together with binding partner Dom34p, facilitates ribosomal subunit dissociation and peptidyl-tRNA release when translation is stalled, particularly in 3' UTRs; genetically implicated in mRNA no-go decay; HBS1 has a paralog, SKI7, that arose from the whole genome duplication","termid":"PBO:0084073"}


id: PBO:0045583
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deoxyuridine triphosphatase pseudogene 5","termid":"PBO:0045583"}


id: MOD:02052
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that contains an L-methionine residue crosslinked to one or more amino acid residues.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-methionine residue","termid":"MOD:00913"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"crosslinked L-methionine residue","synonyms":[{"name":"XlnkMet","type":"exact"}],"termid":"MOD:02052"}


id: GO:0036377
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A form of mutualism between a fungus and the roots of a vascular plant, where hyphae of the fungus penetrate the plant cell wall and invaginate its cell membrane. Once inside, the fungus forms highly branched structures for nutrient exchange with the plant called arbuscules. Aids in the acquisition by the plant of nutrients such as phosphorus from the soil.","definition_xrefs":["Wikipedia:Arbuscular_mycorrhiza","GOC:sk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biological process involved in symbiotic interaction","termid":"GO:0044403"}],"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":"arbuscular mycorrhizal association","synonyms":[{"name":"arbuscular mycorrhizae formation","type":"exact"},{"name":"arbuscular mycorrhizal symbiosis","type":"related"},{"name":"arbuscular mycorrhizas formation","type":"exact"}],"termid":"GO:0036377"}


id: PBO:0065111
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRKCE antisense RNA 1","termid":"PBO:0065111"}


id: PR:000027564
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A histone H2A-alpha phosphorylated 1 in Schizosaccharomyces pombe. Phosphorylation motif is SQE. Example: UniProtKB:P04909-1, Ser-129, MOD:00046.","definition_xrefs":["PMID:15226425","PMID:21516229","PomBase:MAH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H2A-alpha (Schizosaccharomyces pombe 972h-)","termid":"PR:P04909"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hta1/Phos(S128)","pombase_gene_id":"SPCC622.08c","synonyms":[{"name":"PomBase_original_PRO_term_name: histone H2A-alpha phosphorylated 1 (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-hta1/Phos:1","type":"exact"},{"name":"gamma-H2A (Schizosaccharomyces pombe)","type":"related"},{"name":"histone H2A.1 phosphorylated 1 (Schizosaccharomyces pombe)","type":"exact"},{"name":"hta1/Phos(S128)","type":"exact"},{"name":"hta1/Phos:(S129)","type":"exact"}],"termid":"PR:000027564"}


id: GO:0051766
data:
  {"annotated_genes":["SJAG_03409","SJAG_02321"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[70992,75547],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008440"},{"annotations":[98561],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000823"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: inositol trisphosphate + ATP = inositol tetrakisphosphate + ADP + H+.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"},{"relation_name":"is_a","term_name":"inositol phosphate kinase activity","termid":"GO:0180030"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02321":null,"SJAG_03409":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016301","GO:0003674","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"inositol trisphosphate kinase activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"IP3K","type":"broad"}],"termid":"GO:0051766","terms_by_termid":{"GO:0000823":null,"GO:0008440":null}}


id: PBO:0002198
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ethanolamine-phosphate cytidylyltransferase (predicted)","termid":"PBO:0002198"}


id: PBO:0081473
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZNF346 intronic transcript 1","termid":"PBO:0081473"}


id: GO:0031082
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Any of several protein complexes required for the biogenesis of specialized organelles of the endosomal-lysosomal system, such as melanosomes, platelet dense granules, and other related organelles; acronym for biogenesis of lysosomal-related organelles complex.","definition_xrefs":["PMID:15261680","PMID:15102850"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular protein-containing complex","termid":"GO:0140535"}],"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":"BLOC complex","synonyms":[{"name":"BLOC-1 related complex","type":"exact"}],"termid":"GO:0031082"}


id: MONDO:0015861
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare uterine adnexal tumor (obsolete MONDO:0015861)","secondary_identifiers":["Orphanet:180220"],"synonyms":[{"name":"syn: Rare tumor of ovaries and fallopian tubes","type":"exact"}],"termid":"MONDO:0015861","xrefs":{"Monarch":{"xref_id":"0015861"}}}


id: GO:0102028
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: L-cysteine + O-phosphonato-L-homoserine = L-cystathionine + hydrogenphosphate.","definition_xrefs":["GOC:pz","PMID:5922970","PMID:9531508"],"gene_count":0,"genotype_count":0,"name":"obsolete cystathionine gamma-synthase activity (acts on O-phosphohomoserine) (obsolete GO:0102028)","termid":"GO:0102028"}


id: GO:2000807
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of synaptic vesicle clustering.","definition_xrefs":["PMID:21513708"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of localization","termid":"GO:0032879"},{"relation_name":"regulates","term_name":"synaptic vesicle clustering","termid":"GO:0097091"}],"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 synaptic vesicle clustering","termid":"GO:2000807"}


id: GO:0071028
data:
  {"annotated_genes":["SJAG_04153","SJAG_04824","SJAG_03745","SJAG_04025","SJAG_03883","SJAG_02879","SJAG_04006","SJAG_03448","SJAG_04601","SJAG_00854","SJAG_02622","SJAG_02382","SJAG_00961","SJAG_01818","SJAG_01331","SJAG_04818","SJAG_00425","SJAG_02720","SJAG_01867","SJAG_02005","SJAG_01412","SJAG_02275","SJAG_01529","SJAG_00456","SJAG_04321","SJAG_05243","SJAG_04500","SJAG_03454","SJAG_03984","SJAG_04198","SJAG_02723","SJAG_04084","SJAG_04768","SJAG_01540","SJAG_00452","SJAG_01521","SJAG_03179","SJAG_01191","SJAG_01431"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[71019,71383,72187,72992,74230,88842,89206,92841,94719,95671,96287,100793,115186,115627],"is_not":false,"summary":null,"term":"GO:0071028"},{"annotations":[89545],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0120271"},{"annotations":[107208,108991,109010,90632,92008,98853,111049,90556,117854,87257,91626,104055,96485],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033621"},{"annotations":[93212,74385,70018,117855,97002],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071031"},{"annotations":[116072],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071032"},{"annotations":[87258,94760,88599,106067,109535,90557,115291,92129,117856,109011],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071030"},{"annotations":[106414],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0120272"}]},"cv_name":"biological_process","definition":"A process that identifies and degrades defective or aberrant mRNAs within the nucleus.","definition_xrefs":["PMID:11586364","PMID:12417728","GOC:dgf","GOC:krc","PMID:14718167","PMID:18644474"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear-transcribed mRNA catabolic process","termid":"GO:0000956"},{"relation_name":"is_a","term_name":"nuclear RNA surveillance","termid":"GO:0071027"}],"gene_count":39,"genes_by_uniquename":{"SJAG_00425":null,"SJAG_00452":null,"SJAG_00456":null,"SJAG_00854":null,"SJAG_00961":null,"SJAG_01191":null,"SJAG_01331":null,"SJAG_01412":null,"SJAG_01431":null,"SJAG_01521":null,"SJAG_01529":null,"SJAG_01540":null,"SJAG_01818":null,"SJAG_01867":null,"SJAG_02005":null,"SJAG_02275":null,"SJAG_02382":null,"SJAG_02622":null,"SJAG_02720":null,"SJAG_02723":null,"SJAG_02879":null,"SJAG_03179":null,"SJAG_03448":null,"SJAG_03454":null,"SJAG_03745":null,"SJAG_03883":null,"SJAG_03984":null,"SJAG_04006":null,"SJAG_04025":null,"SJAG_04084":null,"SJAG_04153":null,"SJAG_04198":null,"SJAG_04321":null,"SJAG_04500":null,"SJAG_04601":null,"SJAG_04768":null,"SJAG_04818":null,"SJAG_04824":null,"SJAG_05243":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016071"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"negatively_regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0016071","GO:0010467","GO:0008150"],"is_obsolete":false,"name":"nuclear mRNA surveillance","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0071048","GO:0071049","GO:0071033"],"synonyms":[{"name":"nuclear aberrant mRNA catabolic process","type":"exact"},{"name":"nuclear mRNA quality control","type":"exact"},{"name":"nuclear retention of pre-mRNA at the site of transcription","type":"narrow"},{"name":"nuclear retention of pre-mRNA with aberrant 3'-ends at the site of transcription","type":"narrow"},{"name":"nuclear retention of unspliced pre-mRNA at the site of transcription","type":"narrow"}],"termid":"GO:0071028","terms_by_termid":{"GO:0033621":null,"GO:0071028":null,"GO:0071030":null,"GO:0071031":null,"GO:0071032":null,"GO:0120271":null,"GO:0120272":null}}


id: MONDO:0015925
data:
  {"annotated_genes":["SJAG_03855","SJAG_00570","SJAG_00566","SJAG_02206","SJAG_05979","SJAG_03125","SJAG_02805","SJAG_01836","SJAG_03626","SJAG_02194"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85249],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010926"},{"annotations":[84838],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0800029"},{"annotations":[85974],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011871"},{"annotations":[86335],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957261"},{"annotations":[86334],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957263"},{"annotations":[86103],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957294"},{"annotations":[85934],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013878"},{"annotations":[85063],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014612"},{"annotations":[86897],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030690"},{"annotations":[86820],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100215"},{"annotations":[85636],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100220"}]},"cv_name":"mondo","definition":"A diverse group of lung diseases that affect the lung parenchyma. They are characterized by an initial inflammation of pulmonary alveoli that extends to the interstitium and beyond leading to diffuse pulmonary fibrosis. Interstitial lung diseases are classified by their etiology (known or unknown causes), and radiological-pathological features.","definition_xrefs":["MESH:D017563"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lung disorder","termid":"MONDO:0005275"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00566":null,"SJAG_00570":null,"SJAG_01836":null,"SJAG_02194":null,"SJAG_02206":null,"SJAG_02805":null,"SJAG_03125":null,"SJAG_03626":null,"SJAG_03855":null,"SJAG_05979":null},"genotype_count":0,"is_obsolete":false,"name":"interstitial lung disease","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:3082","Orphanet:182095","SCTID:233703007","UMLS:C5441745","MEDGEN:1788738","EFO:0004244","ICD10CM:J80-J84","MedDRA:10022611","NCIT:C164315"],"synonyms":[{"name":"ILD","type":"exact"},{"name":"interstitial lung disease","type":"exact"}],"termid":"MONDO:0015925","terms_by_termid":{"MONDO:0010926":null,"MONDO:0011871":null,"MONDO:0013878":null,"MONDO:0014612":null,"MONDO:0030690":null,"MONDO:0100215":null,"MONDO:0100220":null,"MONDO:0800029":null,"MONDO:0957261":null,"MONDO:0957263":null,"MONDO:0957294":null},"xrefs":{"Monarch":{"xref_id":"0015925"}}}


id: PBO:0057344
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 532","termid":"PBO:0057344"}


id: GO:0140887
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the controlled breakdown of nucleosomes, the beadlike structural units of eukaryotic chromatin composed of histones and DNA.","definition_xrefs":["PMID:34471130","PMID:35308047"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein-containing complex assembly","termid":"GO:0031334"},{"relation_name":"is_a","term_name":"positive regulation of chromatin organization","termid":"GO:1905269"},{"relation_name":"positively_regulates","term_name":"nucleosome assembly","termid":"GO:0006334"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"positively_regulates","termid":"GO:0006325"},{"rel_name":"positively_regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006325"},{"rel_name":"positively_regulates","termid":"GO:0065003"},{"rel_name":"regulates","termid":"GO:0065003"}],"interesting_parent_ids":["GO:0006325","GO:0008150","GO:0065003","GO:0044085"],"is_obsolete":false,"name":"positive regulation of nucleosome disassembly","termid":"GO:0140887"}


id: GO:0070022
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A homodimeric receptor complex that consists of two TGF-beta receptor monomers.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete transforming growth factor beta receptor complex (obsolete GO:0070022)","synonyms":[{"name":"TGF-beta receptor complex","type":"broad"},{"name":"transforming growth factor beta receptor complex","type":"exact"}],"termid":"GO:0070022"}


id: PBO:0017854
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ABC transmembrane transporter Abc3, unknown specificity","termid":"PBO:0017854"}


id: MONDO:0958190
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"bradyopsia","termid":"MONDO:0012033"}],"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":"prolonged electroretinal response suppression 2","secondary_identifiers":["UMLS:C5830452","MEDGEN:1841088","OMIM:620344","DOID:0070364"],"termid":"MONDO:0958190","xrefs":{"Monarch":{"xref_id":"0958190"}}}


id: PR:Q10214
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC4H3.06 gene.","definition_xrefs":["UniProtKB:Q10214","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C4H3.06 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4H3.06","synonyms":[{"name":"Spom972h-SPAC4H3.06","type":"exact"}],"termid":"PR:Q10214"}


id: MONDO:0100565
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An instance of alpha thalessemia spectrum that is caused by an inherited monogenomic modification in an individual.","definition_xrefs":["MONDO:patterns/hereditary"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alpha thalassemia spectrum","termid":"MONDO:0011399"}],"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":"monogenic alpha thalassemia spectrum","termid":"MONDO:0100565","xrefs":{"Monarch":{"xref_id":"0100565"}}}


id: MONDO:0016349
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hydrocephalus that is present at birth.","definition_xrefs":["NCIT:C98876"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete non-syndromic central nervous system malformation (obsolete MONDO:0015219)","termid":"MONDO:0015219"},{"relation_name":"is_a","term_name":"hydrocephalus","termid":"MONDO:0001150"},{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"congenital hydrocephalus","secondary_identifiers":["icd11.foundation:1878746673","MedDRA:10010506","ICD10CM:Q03","MEDGEN:9336","NANDO:2200822","GARD:6682","Orphanet:2185","SCTID:47032000","UMLS:C0020256","OMIMPS:236600"],"synonyms":[{"name":"HYC3","type":"related"},{"name":"congenital hydrocephalus","type":"exact"}],"termid":"MONDO:0016349","xrefs":{"Monarch":{"xref_id":"0016349"}}}


id: MONDO:1012319
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"high-frequency tremor, non-human animal","termid":"MONDO:1011796"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high-frequency tremor, macaques","secondary_identifiers":["OMIA:001200-9539"],"termid":"MONDO:1012319","xrefs":{"Monarch":{"xref_id":"1012319"}}}


id: PBO:0080313
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vomeronasal 1 receptor 77 pseudogene","termid":"PBO:0080313"}


id: PBO:0110415
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SSBP3 pseudogene 5","termid":"PBO:0110415"}


id: GO:0045325
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The hydroxylation of peptidyl-tryptophan, to form peptidyl-L-3-hydroxytryptophan.","definition_xrefs":["RESID:AA0322"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-tryptophan hydroxylation (obsolete GO:0045325)","termid":"GO:0045325"}


id: PBO:0038632
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acyl-CoA:amino acid N-acyltransferase pseudogene","termid":"PBO:0038632"}


id: GO:0015930
data:
  {"annotated_genes":["SJAG_04054"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[71859],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016040"}]},"cv_name":"molecular_function","definition":"Catalysis of the formation of L-glutamine and 2-oxoglutarate from L-glutamate, using NADH, NADPH or ferredoxin as hydrogen acceptors.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-NH2 group of donors","termid":"GO:0016638"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04054":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:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"glutamate synthase activity","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0015930","terms_by_termid":{"GO:0016040":null}}


id: PBO:0042366
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CD164 molecule","termid":"PBO:0042366"}


id: MONDO:0008103
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":"noduli Cutanei, multiple, with urinary tract abnormalities","secondary_identifiers":["MESH:C563512","MEDGEN:371746","UMLS:C1834143","OMIM:163850"],"synonyms":[{"name":"noduli Cutanei, multiple, with urinary tract abnormalities","type":"exact"}],"termid":"MONDO:0008103","xrefs":{"Monarch":{"xref_id":"0008103"}}}


id: GO:1905386
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of protein localization to presynapse.","definition_xrefs":["GO_REF:0000058","GOC:PARL","GOC:TermGenie","PMID:24449494","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein localization to synapse","termid":"GO:1902474"},{"relation_name":"is_a","term_name":"regulation of protein localization to presynapse","termid":"GO:1905384"},{"relation_name":"positively_regulates","term_name":"protein localization to presynapse","termid":"GO:1905383"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of protein localization to presynapse","synonyms":[{"name":"activation of protein localisation in presynapse","type":"narrow"},{"name":"activation of protein localisation to presynapse","type":"narrow"},{"name":"activation of protein localization in presynapse","type":"narrow"},{"name":"activation of protein localization to presynapse","type":"narrow"},{"name":"activation of recruitment of presynaptic proteins","type":"narrow"},{"name":"positive regulation of protein localisation in presynapse","type":"exact"},{"name":"positive regulation of protein localisation to presynapse","type":"exact"},{"name":"positive regulation of protein localization in presynapse","type":"exact"},{"name":"positive regulation of recruitment of presynaptic proteins","type":"exact"},{"name":"up regulation of protein localisation in presynapse","type":"exact"},{"name":"up regulation of protein localisation to presynapse","type":"exact"},{"name":"up regulation of protein localization in presynapse","type":"exact"},{"name":"up regulation of protein localization to presynapse","type":"exact"},{"name":"up regulation of recruitment of presynaptic proteins","type":"exact"},{"name":"up-regulation of protein localisation in presynapse","type":"exact"},{"name":"up-regulation of protein localisation to presynapse","type":"exact"},{"name":"up-regulation of protein localization in presynapse","type":"exact"},{"name":"up-regulation of protein localization to presynapse","type":"exact"},{"name":"up-regulation of recruitment of presynaptic proteins","type":"exact"},{"name":"upregulation of protein localisation in presynapse","type":"exact"},{"name":"upregulation of protein localisation to presynapse","type":"exact"},{"name":"upregulation of protein localization in presynapse","type":"exact"},{"name":"upregulation of protein localization to presynapse","type":"exact"},{"name":"upregulation of recruitment of presynaptic proteins","type":"exact"}],"termid":"GO:1905386"}


id: PBO:0075404
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sperm acrosome associated 1","termid":"PBO:0075404"}


id: PBO:0059307
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein L50 pseudogene 3","termid":"PBO:0059307"}


id: GO:0090597
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the nematode male tail mating organ are generated and organized. The male tail is a sensory organ required for mating and, in C. elegans, consists of ray sensilla, an acellular cuticular fan, a sensory hook, and protracting, copulatory spicules.","definition_xrefs":["GOC:kmv","PMID:7409314","PMID:1782863","PMID:18050419"],"direct_ancestors":[{"relation_name":"is_a","term_name":"male genitalia morphogenesis","termid":"GO:0048808"},{"relation_name":"is_a","term_name":"sensory organ morphogenesis","termid":"GO:0090596"}],"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":"nematode male tail mating organ morphogenesis","termid":"GO:0090597"}


id: PBO:0081113
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger AN1-type containing 3","termid":"PBO:0081113"}


id: PR:O14073
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPACUNK4.08 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14073"],"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":"dipeptidyl aminopeptidase C2E11.08 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPACUNK4.08","synonyms":[{"name":"Spom972h-SPACUNK4.08","type":"exact"}],"termid":"PR:O14073"}


id: PBO:0087069
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribosomal 60S subunit protein L34A; homologous to mammalian ribosomal protein L34, no bacterial homolog; RPL34A has a paralog, RPL34B, that arose from the whole genome duplication","termid":"PBO:0087069"}


id: MONDO:0030519
data:
  {"annotated_genes":["SJAG_00222"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85878],"is_not":false,"summary":null,"term":"MONDO:0030519"}]},"cv_name":"mondo","definition":"An autosomal recessive primary immunodeficiency characterized by recurrent bacterial infections associated with agammaglobulinemia and absence of circulating B cells. Additional features include failure to thrive and skin involvement. The severity is variable: more severe cases may require hematopoietic stem cell transplantation, whereas others can be treated effectively with Ig replacement therapy.","definition_xrefs":["OMIM:619693"],"direct_ancestors":[{"relation_name":"is_a","term_name":"agammaglobulinemia","termid":"MONDO:0015977"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00222":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"agammaglobulinemia 9, autosomal recessive","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1794269","DOID:0081141","UMLS:C5562059"],"synonyms":[{"name":"AGM9","type":"exact"}],"termid":"MONDO:0030519","terms_by_termid":{"MONDO:0030519":null},"xrefs":{"Monarch":{"xref_id":"0030519"}}}


id: PBO:0042680
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CCAAT enhancer binding protein beta","termid":"PBO:0042680"}


id: PBO:0059490
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MSS51 mitochondrial translational activator","termid":"PBO:0059490"}


id: PBO:0038874
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adenylate cyclase 1","termid":"PBO:0038874"}


id: GO:0034183
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the extent to which the association between sister chromatids of a replicated chromosome is maintained during a mitotic cell cycle.","definition_xrefs":["GOC:mah","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of maintenance of sister chromatid cohesion","termid":"GO:0034092"},{"relation_name":"is_a","term_name":"regulation of maintenance of mitotic sister chromatid cohesion","termid":"GO:0034182"},{"relation_name":"negatively_regulates","term_name":"maintenance of mitotic sister chromatid cohesion","termid":"GO:0034088"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"negative regulation of maintenance of mitotic sister chromatid cohesion","termid":"GO:0034183"}


id: PBO:0032707
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_error-prone_translesion_synthesis_of_pyrimidine-pyrimidone_6-4_photoproducts","termid":"PBO:0032707"}


id: GO:0099178
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of retrograde trans-synaptic signaling by an endocannabinoid.","definition_xrefs":["PMID:15664177","GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of trans-synaptic signaling","termid":"GO:0099177"},{"relation_name":"regulates","term_name":"retrograde trans-synaptic signaling by endocannabinoid","termid":"GO:0098921"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"regulation of retrograde trans-synaptic signaling by endocanabinoid","synonyms":[{"name":"regulation of endocannabinoid-mediated retrograde trans-synaptic signaling","type":"related"}],"termid":"GO:0099178"}


id: GO:1902298
data:
  {"annotated_genes":["SJAG_03300","SJAG_00573","SJAG_01644","SJAG_02214","SJAG_01374","SJAG_02992","SJAG_03780","SJAG_03843","SJAG_02079","SJAG_04272","SJAG_01076","SJAG_02439","SJAG_02610","SJAG_02198","SJAG_01832","SJAG_06022","SJAG_01677","SJAG_02822","SJAG_03898","SJAG_01221","SJAG_01410","SJAG_01584"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[96909,112485],"is_not":false,"summary":null,"term":"GO:1902298"},{"annotations":[111505,108877],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990505"},{"annotations":[95769,112264,94586,116545,95934,107507,88927,94829,63930,98001,98707,108833,109306,107483,90714],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990426"},{"annotations":[105892,88759,116161],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0120292"}]},"cv_name":"biological_process","definition":"Any maintenance of fidelity that is involved in cell cycle DNA replication.","definition_xrefs":["GOC:mtg_cell_cycle","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell cycle process","termid":"GO:0022402"},{"relation_name":"is_a","term_name":"DNA-templated DNA replication maintenance of fidelity","termid":"GO:0045005"},{"relation_name":"part_of","term_name":"cell cycle DNA replication","termid":"GO:0044786"}],"gene_count":22,"genes_by_uniquename":{"SJAG_00573":null,"SJAG_01076":null,"SJAG_01221":null,"SJAG_01374":null,"SJAG_01410":null,"SJAG_01584":null,"SJAG_01644":null,"SJAG_01677":null,"SJAG_01832":null,"SJAG_02079":null,"SJAG_02198":null,"SJAG_02214":null,"SJAG_02439":null,"SJAG_02610":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":"part_of","termid":"GO:0006260"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0007049","GO:0006260","GO:0006259","GO:0008150"],"is_obsolete":false,"name":"cell cycle DNA replication maintenance of fidelity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000107":null},"synonyms":[{"name":"maintenance of fidelity during DNA-dependent DNA replication involved in cell cycle DNA replication","type":"related"},{"name":"maintenance of fidelity involved in cell cycle DNA replication","type":"exact"}],"termid":"GO:1902298","terms_by_termid":{"GO:0120292":null,"GO:1902298":null,"GO:1990426":null,"GO:1990505":null}}


id: GO:0004575
data:
  {"annotated_genes":["SJAG_04301"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[76451],"is_not":false,"summary":null,"term":"GO:0004575"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: sucrose + H2O = alpha-D-glucose + beta-D-fructose.","definition_xrefs":["RHEA:33795"],"direct_ancestors":[{"relation_name":"is_a","term_name":"beta-fructofuranosidase activity","termid":"GO:0004564"},{"relation_name":"is_a","term_name":"alpha-glucosidase activity","termid":"GO:0090599"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04301":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016787","GO:0016798","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"sucrose alpha-glucosidase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-189069","Reactome:R-HSA-5659926","KEGG_REACTION:R00802","EC:3.2.1.48","MetaCyc:3.2.1.48-RXN"],"synonyms":[{"name":"alpha-D-glucopyranosyl beta-D-fructofuranoside hydrolysis","type":"broad"},{"name":"beta-D-fructofuranosyl alpha-D-glucopyranoside hydrolysis","type":"broad"},{"name":"intestinal sucrase activity","type":"related"},{"name":"sucrase activity","type":"related"},{"name":"sucrase(invertase)","type":"related"},{"name":"sucrase-isomaltase activity","type":"related"},{"name":"sucrose alpha-D-glucohydrolase activity","type":"exact"},{"name":"sucrose alpha-glucohydrolase activity","type":"related"},{"name":"sucrose hydrolysis","type":"broad"},{"name":"sucrose-alpha-D-glucohydrolase activity","type":"related"}],"termid":"GO:0004575","terms_by_termid":{"GO:0004575":null}}


id: MONDO:0009232
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Fuhrmann syndrome is mainly characterized by bowing of the femora, aplasia or hypoplasia of the fibulae and poly-, oligo-, and syndactyly.","definition_xrefs":["Orphanet:2854"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dysostosis","termid":"MONDO:0018234"},{"relation_name":"is_a","term_name":"congenital limb malformation","termid":"MONDO:0019054"},{"relation_name":"is_a","term_name":"non-syndromic limb reduction defect","termid":"MONDO:0019713"}],"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":"Fuhrmann syndrome","secondary_identifiers":["MEDGEN:346429","MESH:C538189","OMIM:228930","SCTID:721296004","UMLS:C1856728","DOID:0090067","GARD:2410"],"synonyms":[{"name":"Fuhrmann syndrome","type":"exact"},{"name":"Fuhrmann-Rieger-de Sousa syndrome","type":"exact"},{"name":"bowing of the femurs, aplasia or hypoplasia of the fibula, and digital anomalies","type":"related"},{"name":"fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly","type":"related"},{"name":"fibular hypoplasia or aplasia-femoral bowing-oligodactyly syndrome","type":"exact"}],"termid":"MONDO:0009232","xrefs":{"Monarch":{"xref_id":"0009232"}}}


id: PBO:0052713
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 18 pseudogene 5","termid":"PBO:0052713"}


id: GO:0140244
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that regulates translation occurring at the presynapse.","definition_xrefs":["PMID:20427644"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of translation at synapse","termid":"GO:0140243"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"regulation of translation at presynapse","termid":"GO:0140244"}


id: PBO:0079208
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis specific serine kinase 1A (pseudogene)","termid":"PBO:0079208"}


id: SO:0000786
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:0000786 reagent_attribute (obsolete SO:0000786)","synonyms":[{"name":"reagent attribute","type":"exact"}],"termid":"SO:0000786"}


id: GO:0019648
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The pathway in which formaldehyde is used as a carbon source in the xylulose monophosphate cycle. Methylotrophic yeasts, but not bacteria, utilize the xylulose monophosphate cycle to fix formaldehyde and convert it into metabolically useful organic compounds.","definition_xrefs":["MetaCyc:P185-PWY"],"direct_ancestors":[{"relation_name":"is_a","term_name":"formaldehyde assimilation","termid":"GO:0019649"},{"relation_name":"is_a","term_name":"xylulose 5-phosphate metabolic process","termid":"GO:0051167"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"formaldehyde assimilation via xylulose monophosphate cycle","synonyms":[{"name":"formaldehyde assimilation via xylulose-5-phosphate cycle","type":"exact"},{"name":"formaldehyde fixation cycle","type":"exact"}],"termid":"GO:0019648"}


id: MONDO:0006159
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A gastrointestinal stromal tumor that arises from the colon or rectum. The majority of cases have spindle cell morphology. Gastrointestinal stromal tumors of the colon are usually advanced upon detection and tend to have a poor prognosis; gastrointestinal stromal tumors of the rectum usually have an aggressive clinical course.","definition_xrefs":["NCIT:C27735"],"direct_ancestors":[{"relation_name":"is_a","term_name":"colorectal neoplasm","termid":"MONDO:0005335"}],"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":"colorectal gastrointestinal stromal tumor","secondary_identifiers":["EFO:1000192","MEDGEN:272496","UMLS:C1333109"],"synonyms":[{"name":"colorectal (colon or rectal) gastrointestinal stromal tumor (gist)","type":"exact"},{"name":"colorectal (colon or rectal) gastrointestinal stromal tumour (gist)","type":"exact"},{"name":"colorectal gastrointestinal stromal tumor","type":"exact"},{"name":"colorectal gastrointestinal stromal tumor (gist)","type":"exact"},{"name":"colorectal gastrointestinal stromal tumour (gist)","type":"exact"},{"name":"colorectal gist","type":"exact"}],"termid":"MONDO:0006159","xrefs":{"Monarch":{"xref_id":"0006159"}}}


id: PBO:0066548
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"regulator of G protein signaling 11","termid":"PBO:0066548"}


id: PBO:0051025
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"insulin like growth factor binding protein 5","termid":"PBO:0051025"}


id: MONDO:0032668
data:
  {"annotated_genes":["SJAG_02597","SJAG_03335"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85822,85823],"is_not":false,"summary":null,"term":"MONDO:0032668"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Diamond-Blackfan anemia","termid":"MONDO:0015253"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02597":null,"SJAG_03335":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0002280"],"is_obsolete":false,"name":"Diamond-Blackfan anemia 18","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:618310","UMLS:C5193020","MEDGEN:1681154","DOID:0111896","GARD:16338"],"synonyms":[{"name":"DBA18","type":"related"},{"name":"DIAMOND-BLACKFAN ANEMIA 18","type":"related"}],"termid":"MONDO:0032668","terms_by_termid":{"MONDO:0032668":null},"xrefs":{"Monarch":{"xref_id":"0032668"}}}


id: PATO:0001367
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A surface feature shape quality inhering in a bearer by virtue of the bearer's having deeply undulating edges forming lobes.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"surface feature shape","termid":"PATO:0001925"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lobate","termid":"PATO:0001367"}


id: PR:O94637
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A tRNA threonylcarbamoyladenosine biosynthesis protein OSGEP that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03775","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":"tRNA N6-adenosine threonylcarbamoyltransferase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC16D10.03","secondary_identifiers":["UniProtKB:O94637"],"synonyms":[{"name":"N6-L-threonylcarbamoyladenine synthase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-OSGEP","type":"exact"},{"name":"pombe glycoprotease 2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"t(6)A synthase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"t(6)A37 threonylcarbamoyladenosine biosynthesis protein kae1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"tRNA threonylcarbamoyladenosine biosynthesis protein kae1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94637"}


id: PBO:0090115
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nebulin-family actin filament anchoring protein Cyk3","termid":"PBO:0090115"}


id: PR:O94479
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC1919.12c gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94479"],"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":"vacuolar membrane protease (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1919.12c","synonyms":[{"name":"FXNA-related family protease 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-SPCC1919.12c","type":"exact"}],"termid":"PR:O94479"}


id: PBO:0108506
data:
  {"annotation_feature_type":"gene","cv_name":"feature_cvtermprop_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eco_evidence","termid":"PBO:0108506"}


id: PBO:0046913
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity E5","termid":"PBO:0046913"}


id: MONDO:0700115
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Vitreoretinal membrane shrinkage or contraction secondary to the proliferation of primarily retinal pigment epithelial cells and glial cells, particularly fibrous astrocytes, followed by membrane formation. The formation of fibrillar collagen and cellular proliferation appear to be the basis for the contractile properties of the epiretinal and vitreous membranes.","definition_xrefs":["MESH:D018630"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinal disorder","termid":"MONDO:0005283"}],"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":"proliferative vitreoretinopathy","secondary_identifiers":["icd11.foundation:1908429642","MEDGEN:66167","SCTID:232016005","UMLS:C0242852"],"termid":"MONDO:0700115","xrefs":{"Monarch":{"xref_id":"0700115"}}}


id: PBO:0069283
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 539, pseudogene","termid":"PBO:0069283"}


id: GO:0046834
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of introducing one or more phosphate groups into a lipid, any member of a group of substances soluble in lipid solvents but only sparingly soluble in aqueous solvents.","definition_xrefs":["ISBN:0198506732","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphorylation","termid":"GO:0016310"},{"relation_name":"is_a","term_name":"lipid modification","termid":"GO:0030258"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"lipid phosphorylation","termid":"GO:0046834"}


id: PBO:0029994
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-premature_actomyosin_contractile_ring_disassembly","termid":"PBO:0029994"}


id: MONDO:0700190
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant lymphoma that arises in the bursa of Fabricius in a chicken.","definition_xrefs":["NCIT:C134556"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chicken lymphoma","termid":"MONDO:0700194"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chicken bursal lymphoma","termid":"MONDO:0700190","xrefs":{"Monarch":{"xref_id":"0700190"}}}


id: PBO:0064072
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi-interacting RNA cluster 106","termid":"PBO:0064072"}


id: MONDO:0016705
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Angiocentric glioma (AG) is an extremely rare slow-growing glial neoplasm of the central nervous system, usually arising in a superficial location in the cerebrum, affecting all ages and both sexes, and characterized by intractable seizures and headaches, with most cases being cured by surgical incision alone and therefore having a good prognosis.","definition_xrefs":["Orphanet:251671"],"direct_ancestors":[{"relation_name":"is_a","term_name":"low grade glioma","termid":"MONDO:0021637"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"angiocentric glioma","secondary_identifiers":["ONCOTREE:ANGL","GARD:20714","DOID:0081261","ICDO:9431/1","MEDGEN:453267","NCIT:C92552","UMLS:C2363903"],"synonyms":[{"name":"ANGL","type":"related"},{"name":"Monomorphus angiocentric glioma","type":"exact"},{"name":"angiocentric glioma (WHO grade I)","type":"exact"},{"name":"angiocentric neuroepithelial tumor","type":"exact"},{"name":"angiocentric neuroepithelial tumour","type":"exact"}],"termid":"MONDO:0016705","xrefs":{"Monarch":{"xref_id":"0016705"}}}


