# terms

id: PBO:0068311
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNF13 pseudogene 1","termid":"PBO:0068311"}


id: PBO:0044850
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"defensin beta 131E (pseudogene)","termid":"PBO:0044850"}


id: PBO:0108619
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IGBP1 pseudogene 1","termid":"PBO:0108619"}


id: MONDO:0019203
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute interstitial pneumonia (AIP), also referred to as Hamman-Rich syndrome, is a rapidly progressive and histologically distinct form of idiopathic interstitial pneumonia.","definition_xrefs":["Orphanet:79126"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete idiopathic pulmonary fibrosis (obsolete MONDO:0008345)","termid":"MONDO:0008345"},{"relation_name":"is_a","term_name":"idiopathic interstitial pneumonia","termid":"MONDO:0002429"},{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acute interstitial pneumonia","secondary_identifiers":["icd11.foundation:2116884221","NCIT:C35806","MedDRA:10066728","ICD9:516.33","NANDO:1200420","SCTID:236302005","DOID:2800","MEDGEN:224822","GARD:12835","UMLS:C1279945"],"synonyms":[{"name":"AIP","type":"exact"},{"name":"Hamman-rich disease","type":"exact"},{"name":"Hamman-rich syndrome","type":"exact"},{"name":"accelerated interstitial pneumonia","type":"exact"},{"name":"acute interstitial pneumonitis","type":"exact"},{"name":"idiopathic pulmonary fibrosis, acute fatal form","type":"exact"}],"termid":"MONDO:0019203","xrefs":{"Monarch":{"xref_id":"0019203"}}}


id: PBO:0062261
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 5 subfamily D member 17 pseudogene","termid":"PBO:0062261"}


id: GO:1904550
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an arachidonic acid stimulus.","definition_xrefs":["GOC:TermGenie","PMID:16382163","GO_REF:0000071"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to fatty acid","termid":"GO:0070542"}],"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 arachidonate","synonyms":[{"name":"response to arachidonic acid","type":"exact"}],"termid":"GO:1904550"}


id: MONDO:0000453
data:
  {"annotated_genes":["SJAG_01183"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84799],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859368"}]},"cv_name":"mondo","definition":"A genetic disease of the electrical system of the heart that consists of a constellation of signs and symptoms, consisting of a short QT interval on an EKG (< 300 ms) that does not significantly change with heart rate, tall and peaked T waves, and a structurally normal heart. Short QT syndrome appears to be inherited in an autosomal dominant pattern, and a few affected families have been identified","definition_xrefs":["Wikipedia:Short_QT_syndrome"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heart conduction disease","termid":"MONDO:0000992"},{"relation_name":"is_a","term_name":"cardiogenetic disease","termid":"MONDO:0100547"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01183":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"short QT syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIMPS:609620","icd11.foundation:553392015","Orphanet:51083","SCTID:698272007","UMLS:C2348199","NCIT:C71060","ICD9:426.89","MEDGEN:378835","MESH:C580439","NORD:2019","DOID:0050793","GARD:16650"],"synonyms":[{"name":"familial short QT syndrome","type":"related"},{"name":"short QT syndrome","type":"exact"},{"name":"ventricular arrhythmia associated with short QT syndrome","type":"exact"}],"termid":"MONDO:0000453","terms_by_termid":{"MONDO:0859368":null},"xrefs":{"Monarch":{"xref_id":"0000453"}}}


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


id: FYPO:0001672
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of a GTPase activity is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal catalytic activity","termid":"FYPO:0000660"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000654","FYPO:0000652","FYPO:0000257"],"is_obsolete":false,"name":"normal GTPase activity","termid":"FYPO:0001672"}


id: PBO:0071115
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 117","termid":"PBO:0071115"}


id: PBO:0047841
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibroblast proliferation associated lncRNA","termid":"PBO:0047841"}


id: MONDO:0030330
data:
  {"annotated_genes":["SJAG_00930"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85564],"is_not":false,"summary":null,"term":"MONDO:0030330"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial restrictive cardiomyopathy","termid":"MONDO:0016340"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00930":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"cardiomyopathy, familial restrictive, 6","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:619433","MEDGEN:1780781","UMLS:C5543638"],"synonyms":[{"name":"RCM6","type":"exact"},{"name":"cardiomyopathy, familial restrictive, 6","type":"exact"}],"termid":"MONDO:0030330","terms_by_termid":{"MONDO:0030330":null},"xrefs":{"Monarch":{"xref_id":"0030330"}}}


id: GO:0075165
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which the symbiont organism modulates the frequency, rate or extent of its G-protein gamma subunit-mediated signal transduction as a result of detecting molecules of its host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of G-protein gamma subunit-mediated signal transduction in response to host (obsolete GO:0075165)","synonyms":[{"name":"regulation of symbiont G-protein gamma subunit-mediated signal transduction in response to host","type":"exact"}],"termid":"GO:0075165"}


id: _global:function_of
data:
  {"annotation_feature_type":"gene","cv_name":"external","definition":"a relation between a function and an independent continuant (the bearer), in which the function specifically depends on the bearer for its existence","direct_ancestors":[{"relation_name":"is_a","term_name":"characteristic_of","termid":"_global:characteristic_of"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"function_of","secondary_identifiers":["RO:0000079"],"termid":"_global:function_of"}


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: MONDO:0011810
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Horizontal gaze palsy with progressive scoliosis (HGPPS) is a rare congenital autosomal recessive disease, presenting in children and adolescents, and characterized by progressive scoliosis along with the absence of conjugate horizontal eye movements and associated with failure of the somatosensory and corticospinal neuronal tracts to decussate in the medulla.","definition_xrefs":["Orphanet:2744"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete neuro-ophthalmological disease (obsolete MONDO:0015368)","termid":"MONDO:0015368"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"horizontal gaze palsy with progressive scoliosis","secondary_identifiers":["GARD:12682","OMIMPS:607313","ICD9:737.43","ICD10CM:H49.4","MESH:C564593","icd11.foundation:226403142","MEDGEN:1683615","UMLS:C4760875","SCTID:702381007"],"synonyms":[{"name":"HGPPS","type":"exact"},{"name":"gaze palsy, familial horizontal, with progressive scoliosis","type":"related"},{"name":"gaze palsy, horizontal, with progressive scoliosis","type":"related"},{"name":"ophthalmoplegia, progressive external, and scoliosis","type":"related"},{"name":"progressive external ophthalmoplegia and scoliosis","type":"exact"}],"termid":"MONDO:0011810","xrefs":{"Monarch":{"xref_id":"0011810"}}}


id: GO:1901304
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of spermidine biosynthetic process.","definition_xrefs":["GOC:pm","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of polyamine biosynthetic process","termid":"GO:0010967"},{"relation_name":"regulates","term_name":"spermidine biosynthetic process","termid":"GO:0008295"}],"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 spermidine biosynthetic process","synonyms":[{"name":"regulation of spermidine anabolism","type":"exact"},{"name":"regulation of spermidine biosynthesis","type":"exact"},{"name":"regulation of spermidine formation","type":"exact"},{"name":"regulation of spermidine synthesis","type":"exact"}],"termid":"GO:1901304"}


id: MONDO:0004930
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"glaucoma","termid":"MONDO:0005041"}],"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":"steroid-induced glaucoma","secondary_identifiers":["ICD9:365.89","SCTID:1654001","UMLS:C0339578","DOID:9946","ICD9:365.3","MEDGEN:573238"],"synonyms":[{"name":"corticosteroid-induced glaucoma","type":"exact"}],"termid":"MONDO:0004930","xrefs":{"Monarch":{"xref_id":"0004930"}}}


id: GO:1902675
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Any ciliary basal body that is part of a left ventral flagellum found in Giardia species (trophozoite stage).","definition_xrefs":["GOC:TermGenie","GO_REF:0000064","ISBN:9780124260207","PMID:5961344","GOC:giardia","PMID:16607022"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ciliary basal body","termid":"GO:0036064"},{"relation_name":"part_of","term_name":"left ventral flagellum","termid":"GO:0097558"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0015630"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0015630","GO:0005575"],"is_obsolete":false,"name":"left ventral basal body","synonyms":[{"name":"cilial basal body of left ventral cilium","type":"exact"},{"name":"cilial basal body of left ventral flagellum","type":"exact"},{"name":"ciliary basal body of left ventral cilium","type":"exact"},{"name":"ciliary basal body of left ventral flagellum","type":"exact"},{"name":"cilium basal body of left ventral cilium","type":"exact"},{"name":"cilium basal body of left ventral flagellum","type":"exact"},{"name":"left ventral flagellum ciliary basal body","type":"exact"},{"name":"microtubule basal body of left ventral cilium","type":"exact"},{"name":"microtubule basal body of left ventral flagellum","type":"exact"}],"termid":"GO:1902675"}


id: MOD:00337
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue to S-carbamoyl-L-cysteine.","definition_xrefs":["RESID:AA0332","Unimod:5#C","PubMed:240389","PubMed:12586941"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbamoylated residue","termid":"MOD:00398"},{"relation_name":"is_a","term_name":"modified L-cysteine residue","termid":"MOD:00905"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"S-carbamoyl-L-cysteine","synonyms":[{"name":"(R)-2-amino-3-(carbamoylsulfanyl)propanoic acid","type":"exact"},{"name":"2-amino-3-(aminocarbonyl)sulfanylpropanoic acid","type":"exact"},{"name":"2-amino-3-(aminocarbonyl)thiopropanoic acid","type":"exact"},{"name":"MOD_RES S-carbamoylcysteine","type":"exact"},{"name":"S-(aminocarbonyl)cysteine","type":"exact"},{"name":"S-carbamoyl-L-cysteine","type":"exact"},{"name":"S-carbamoylcysteine","type":"exact"},{"name":"S-carbamylcysteine","type":"exact"},{"name":"S-cysteinyl carbamate ester","type":"exact"},{"name":"SCbmCys","type":"exact"},{"name":"alpha-amino-beta-carbamylthiopropionic acid","type":"exact"},{"name":"beta-carbamylthioalanine","type":"exact"}],"termid":"MOD:00337"}


id: PBO:0046999
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 90 member A2, pseudogene","termid":"PBO:0046999"}


id: FYPO:0004228
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the phosphorylation of one or more specific proteins, or of specific protein sites, occurs to a lower extent than normal during a cellular response to ultraviolet light.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein phosphorylation during vegetative growth","termid":"FYPO:0001838"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0002494","FYPO:0005447","FYPO:0001985","FYPO:0001320","FYPO:0000002","FYPO:0002274"],"is_obsolete":false,"name":"decreased protein phosphorylation during cellular response to UV","synonyms":[{"name":"decreased protein phosphorylation during cellular response to UV during mitotic cell cycle","type":"related"},{"name":"decreased protein phosphorylation during cellular response to UV during vegetative growth","type":"exact"},{"name":"decreased protein phosphorylation during cellular response to ultraviolet light","type":"exact"},{"name":"reduced protein phosphorylation during cellular response to UV","type":"exact"}],"termid":"FYPO:0004228"}


id: GO:1903055
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of extracellular matrix organization.","definition_xrefs":["PMID:22357537","GO_REF:0000058","GOC:BHF","GOC:rl","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cellular component organization","termid":"GO:0051130"},{"relation_name":"is_a","term_name":"regulation of extracellular matrix organization","termid":"GO:1903053"},{"relation_name":"positively_regulates","term_name":"extracellular matrix organization","termid":"GO:0030198"}],"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 extracellular matrix organization","synonyms":[{"name":"activation of extracellular matrix organisation","type":"narrow"},{"name":"activation of extracellular matrix organization","type":"narrow"},{"name":"activation of extracellular matrix organization and biogenesis","type":"related"},{"name":"positive regulation of extracellular matrix organisation","type":"exact"},{"name":"positive regulation of extracellular matrix organization and biogenesis","type":"related"},{"name":"up regulation of extracellular matrix organisation","type":"exact"},{"name":"up regulation of extracellular matrix organization","type":"exact"},{"name":"up regulation of extracellular matrix organization and biogenesis","type":"related"},{"name":"up-regulation of extracellular matrix organisation","type":"exact"},{"name":"up-regulation of extracellular matrix organization","type":"exact"},{"name":"up-regulation of extracellular matrix organization and biogenesis","type":"related"},{"name":"upregulation of extracellular matrix organisation","type":"exact"},{"name":"upregulation of extracellular matrix organization","type":"exact"},{"name":"upregulation of extracellular matrix organization and biogenesis","type":"related"}],"termid":"GO:1903055"}


id: PBO:0082728
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the Rix1 complex and pre-replicative complexes (pre-RCs); required for processing of ITS2 sequences from 35S pre-rRNA; component of the pre-60S ribosomal particle with the dynein-related AAA-type ATPase Mdn1p; required for pre-RC formation and maintenance during DNA replication licensing; highly conserved protein which contains several WD40 motifs; IPI3 is an essential gene; other members include Rix1p, Ipi1p, and Ipi3p","termid":"PBO:0082728"}


id: GO:0061755
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the quantity of fibrinogen circulating in the bloodstream.","definition_xrefs":["GOC:bf","GOC:BHF","GOC:BHF_miRNA","PMID:20570858"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of circulating fibrinogen levels","termid":"GO:0044537"}],"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 circulating fibrinogen levels","termid":"GO:0061755"}


id: PBO:0063993
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi-interacting RNA cluster 27","termid":"PBO:0063993"}


id: PBO:0036129
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_histone_H3-K9_dimethylation_at_centromere_outer_repeat_during_vegetative_growth","termid":"PBO:0036129"}


id: PBO:0050395
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein C","termid":"PBO:0050395"}


id: PR:O14268
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC7D4.13c gene.","definition_xrefs":["UniProtKB:O14268","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 C7D4.13c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC7D4.13c","synonyms":[{"name":"Spom972h-SPAC7D4.13c","type":"exact"}],"termid":"PR:O14268"}


id: PBO:0080910
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"YWHAH antisense RNA 1","termid":"PBO:0080910"}


id: PBO:0041024
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BPI fold containing family B member 9, pseudogene","termid":"PBO:0041024"}


id: PBO:0051965
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intersectin 1","termid":"PBO:0051965"}


id: PBO:0090729
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit L40","termid":"PBO:0090729"}


id: MONDO:0022772
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A vascular sarcoma that commonly occurs in the lower extremities. It occurs predominantly in elderly male patients of southern European ancestry. It is characterized by the presence of purple, red-blue, or dark brown macular lesions, plaques and nodules. This disease is usually slow growing, although it can spread to the lungs and the gastrointestinal tract. If necessary, cutaneous lesions can be treated with radiation.","definition_xrefs":["NCIT:C9112"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Kaposi's sarcoma","termid":"MONDO:0005055"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"classic Kaposi sarcoma","secondary_identifiers":["icd11.foundation:1595913346","MEDGEN:78931","UMLS:C0279084"],"synonyms":[{"name":"Kaposi sarcoma classical type","type":"exact"},{"name":"Kaposi sarcoma, classic","type":"exact"},{"name":"Kaposi's sarcoma, classical type","type":"exact"},{"name":"classic Kaposi sarcoma","type":"exact"},{"name":"classic Kaposi's sarcoma","type":"exact"}],"termid":"MONDO:0022772","xrefs":{"Monarch":{"xref_id":"0022772"}}}


id: PBO:0113292
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Probable catalytic subunit of Nem1p-Spo7p phosphatase holoenzyme; regulates nuclear/ER membrane association and activation of Pah1p, a phosphatidate phosphatase involved in the production of diacylglycerol DAG for lipid droplet biogenesis; regulates nuclear growth by controlling phospholipid biosynthesis; required for normal nuclear envelope morphology and sporulation; phosphatase activity of the Nem1p-Spo7p complex is inhibited by Ice2p; homolog of the human protein Dullard","termid":"PBO:0113292"}


id: GO:0034458
data:
  {"annotated_genes":["SJAG_01152"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[104022],"is_not":false,"summary":null,"term":"GO:0034458"}]},"cv_name":"molecular_function","definition":"Unwinding of an RNA helix in the 3' to 5' direction, driven by ATP hydrolysis.","definition_xrefs":["GOC:jp"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA helicase activity","termid":"GO:0003724"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01152":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0140098"],"is_obsolete":false,"name":"3'-5' RNA helicase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["EC:5.6.2.6","GO:0034459","Reactome:R-HSA-9836927"],"synonyms":[{"name":"3' to 5' RNA helicase activity","type":"exact"},{"name":"ATP-dependent 3' to 5' RNA helicase activity","type":"exact"},{"name":"ATP-dependent 3'-5' RNA helicase activity","type":"exact"}],"termid":"GO:0034458","terms_by_termid":{"GO:0034458":null}}


id: PBO:0058806
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 7848","termid":"PBO:0058806"}


id: PBO:0046443
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EPN2 intronic transcript 1","termid":"PBO:0046443"}


id: PBO:0081460
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 329","termid":"PBO:0081460"}


id: GO:0060167
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the adenosine receptor signaling pathway. The adenosine receptor pathway is the series of molecular signals generated as a consequence of an adenosine receptor binding to one of its physiological ligands.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of G protein-coupled receptor signaling pathway","termid":"GO:0008277"},{"relation_name":"regulates","term_name":"G protein-coupled adenosine receptor signaling pathway","termid":"GO:0001973"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"regulation of adenosine receptor signaling pathway","synonyms":[{"name":"regulation of adenosine receptor signalling pathway","type":"exact"}],"termid":"GO:0060167"}


id: PBO:0039549
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ANKRD44 divergent transcript","termid":"PBO:0039549"}


id: MONDO:0003631
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare adenocarcinoma that arises from the cervix. It is characterized by the presence of papillary patterns and cellular budding. Psammoma bodies are often seen.","definition_xrefs":["NCIT:C40201"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cervical adenocarcinoma","termid":"MONDO:0005153"},{"relation_name":"is_a","term_name":"serous adenocarcinoma","termid":"MONDO:0005278"}],"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":"cervical serous adenocarcinoma","secondary_identifiers":["UMLS:C1516431","MEDGEN:308950","DOID:5752"],"synonyms":[{"name":"cervical serous adenocarcinoma","type":"exact"}],"termid":"MONDO:0003631","xrefs":{"Monarch":{"xref_id":"0003631"}}}


id: PBO:0072397
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S27 pseudogene 2","termid":"PBO:0072397"}


id: FYPO:0004413
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of a phosphatase activity is decreased during a cellular response to phosphate starvation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased phosphatase activity","termid":"FYPO:0004304"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000654","FYPO:0001985","FYPO:0000652","FYPO:0000661","FYPO:0000707"],"is_obsolete":false,"name":"decreased phosphatase activity during cellular response to phosphate starvation","synonyms":[{"name":"decreased phosphatase activity during phosphate starvation","type":"exact"},{"name":"reduced phosphatase activity during cellular response to phosphate starvation","type":"exact"}],"termid":"FYPO:0004413"}


id: GO:0052886
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 9,9'-di-cis-zeta-carotene + a quinone = 7,9,9'-tri-cis-neurosporene + a quinol.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete 9,9'-dicis-carotene:quinone oxidoreductase activity (obsolete GO:0052886)","termid":"GO:0052886"}


id: PBO:0063830
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PHD and ring finger domains 1","termid":"PBO:0063830"}


id: MOD:01305
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-tryptophan residue to N1'-hexosaminyl-L-tryptophan.","definition_xrefs":["Unimod:454#W"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hexosaminylated residue","termid":"MOD:00876"},{"relation_name":"is_a","term_name":"modified L-tryptophan residue","termid":"MOD:00918"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00764"}],"interesting_parent_ids":["MOD:00764"],"is_obsolete":false,"name":"N1'-hexosaminylated tryptophan","synonyms":[{"name":"HexN","type":"related"},{"name":"Hexosamine","type":"related"}],"termid":"MOD:01305"}


id: MOD:00685
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-glutamine residue to L-glutamic acid.","definition_xrefs":["PubMed:6692818","PubMed:957425","PubMed:4922541","PubMed:9192900","Unimod:7#Q","RESID:AA0006#GLN","PubMed:4565668","PubMed:1881881"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-glutamic acid residue","termid":"MOD:00015"},{"relation_name":"is_a","term_name":"deamidated residue","termid":"MOD:00400"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deamidated L-glutamine","synonyms":[{"name":"(2S)-2-aminopentanedioic acid","type":"exact"},{"name":"1-aminopropane-1,3-dicarboxylic acid","type":"exact"},{"name":"2-aminoglutaric acid","type":"exact"},{"name":"2-azanylpentanedioic acid","type":"exact"},{"name":"L-glutamic acid","type":"exact"},{"name":"MOD_RES Deamidated glutamine","type":"exact"},{"name":"alpha-aminoglutaric acid","type":"exact"},{"name":"dNGln","type":"exact"},{"name":"glutaminic acid","type":"exact"}],"termid":"MOD:00685"}


id: MONDO:0012946
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the CDH15 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intellectual disability, autosomal dominant","termid":"MONDO:0100172"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"intellectual disability, autosomal dominant 3","secondary_identifiers":["UMLS:C2675488","DOID:0070033","GARD:16454","MEDGEN:436447","MESH:C567241","OMIM:612580"],"synonyms":[{"name":"CDH15 autosomal dominant non-syndromic intellectual disability","type":"exact"},{"name":"MRD3","type":"exact"},{"name":"autosomal dominant intellectual disability 3","type":"exact"},{"name":"autosomal dominant mental retardation 3","type":"exact"},{"name":"autosomal dominant non-syndromic intellectual disability 3","type":"related"},{"name":"autosomal dominant non-syndromic intellectual disability caused by mutation in CDH15","type":"exact"},{"name":"intellectual disability, autosomal dominant 3","type":"exact"},{"name":"intellectual disability, autosomal dominant type 3","type":"exact"},{"name":"mental retardation, autosomal dominant 3","type":"related"},{"name":"mental retardation, autosomal dominant type 3","type":"exact"}],"termid":"MONDO:0012946","xrefs":{"Monarch":{"xref_id":"0012946"}}}


id: PBO:0079227
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tetratricopeptide repeat domain 4 pseudogene 1","termid":"PBO:0079227"}


id: MONDO:0012648
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inborn error of valine metabolism. The prevalence is unknown. Only one symptomatic patient (with anemia, failure to thrive, dilated cardiomyopathy and plasma carnitine deficiency) has been described so far, but several series of patients have been identified through newborn screening programs relying on detection of increased C(4)-carnitine levels by tandem mass spectrometry. The disorder is caused by mutations in the ACAD8 gene (11q25).","definition_xrefs":["Orphanet:79159"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete syndrome associated with dilated cardiomyopathy (obsolete MONDO:0016337)","termid":"MONDO:0016337"},{"relation_name":"is_a","term_name":"classic organic aciduria","termid":"MONDO:0019215"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0005066"],"is_obsolete":false,"name":"isobutyryl-CoA dehydrogenase deficiency","secondary_identifiers":["NCIT:C129975","UMLS:C1969809","GARD:10223","OMIM:611283","MEDGEN:370754","MESH:C535541"],"synonyms":[{"name":"Acad8 deficiency","type":"related"},{"name":"IBD deficiency","type":"related"},{"name":"acyl-Coa dehydrogenase family, member 8, deficiency of","type":"related"},{"name":"acyl-CoaA dehydrogenase family, member 8, deficiency of","type":"related"},{"name":"isobutyric aciduria","type":"exact"},{"name":"isobutyryl-CoA dehydrogenase deficiency","type":"exact"}],"termid":"MONDO:0012648","xrefs":{"Monarch":{"xref_id":"0012648"}}}


id: PBO:0085021
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nicotinic acid mononucleotide adenylyltransferase; catalyzes the transfer of the adenylyl moiety of ATP to nicotinamide mononucleotide to form NAD; involved in de novo and salvage synthesis of NAD(+); homolog of human NMNAT; NMA2 has a paralog, NMA1, that arose from the whole genome duplication","termid":"PBO:0085021"}


id: GO:0042701
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regulated release of progesterone, a steroid hormone, by the corpus luteum of the ovary and by the placenta.","definition_xrefs":["GOC:jl","ISBN:0395825172"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular process involved in reproduction in multicellular organism","termid":"GO:0022412"},{"relation_name":"is_a","term_name":"ovulation cycle process","termid":"GO:0022602"},{"relation_name":"is_a","term_name":"steroid hormone secretion","termid":"GO:0035929"},{"relation_name":"part_of","term_name":"luteinization","termid":"GO:0001553"}],"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":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"progesterone secretion","termid":"GO:0042701"}


id: PBO:0071795
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribonuclease P/MRP subunit p40 pseudogene 1","termid":"PBO:0071795"}


id: PBO:0057079
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIR181A1 host gene","termid":"PBO:0057079"}


id: GO:0102522
data:
  {"annotated_genes":["SJAG_04735"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[97265],"is_not":false,"summary":null,"term":"GO:0102522"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + 4-demethylwyosine37 in tRNAPhe = 5'-S-methyl-5'-thioadenosine + H+ + 7-[(3S)-3-amino-3-carboxypropyl]-4-demethylwyosine37 in tRNAPhe.","definition_xrefs":["EC:2.5.1.114","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity, transferring alkyl or aryl (other than methyl) groups","termid":"GO:0016765"},{"relation_name":"is_a","term_name":"catalytic activity, acting on a tRNA","termid":"GO:0140101"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04735":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016765"},{"rel_name":"is_a","termid":"GO:0140101"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016765","GO:0003824","GO:0140101","GO:0003674","GO:0140098","GO:0016740"],"is_obsolete":false,"name":"tRNA 4-demethylwyosine alpha-amino-alpha-carboxypropyltransferase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["RHEA:36355","MetaCyc:RXN-14518"],"termid":"GO:0102522","terms_by_termid":{"GO:0102522":null}}


id: PBO:0029511
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_microcolony,_stubby_cells_(obsolete_FYPO:0002203)","termid":"PBO:0029511"}


id: PBO:0064726
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl isomerase A pseudogene 62","termid":"PBO:0064726"}


id: MONDO:1011044
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Glomerulonephritis that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glomerulonephritis, non-human animal","termid":"MONDO:1010258"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glomerulonephritis, domestic cat","secondary_identifiers":["OMIA:000413-9685"],"termid":"MONDO:1011044","xrefs":{"Monarch":{"xref_id":"1011044"}}}


id: MONDO:1011276
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any retinitis pigmentosa that occurs in cattle due to a mutation in RP1 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinitis pigmentosa, cattle","termid":"MONDO:1011259"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retinitis pigmentosa, RP1-related, cattle","secondary_identifiers":["OMIA:002029-9913"],"synonyms":[{"name":"retinitis pigmentosa 1, cattle","type":"related"}],"termid":"MONDO:1011276","xrefs":{"Monarch":{"xref_id":"1011276"}}}


id: MONDO:0020143
data:
  {"annotated_genes":["SJAG_02716","SJAG_03052","SJAG_02518"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85659,85660],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008083"},{"annotations":[85070],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008767"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"brain disorder","termid":"MONDO:0005560"},{"relation_name":"is_a","term_name":"hereditary dementia","termid":"MONDO:0015547"},{"relation_name":"is_a","term_name":"lysosomal lipid storage disorder","termid":"MONDO:0019245"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02518":null,"SJAG_02716":null,"SJAG_03052":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0002561"}],"interesting_parent_ids":["MONDO:0002039","MONDO:0005066","MONDO:0002525","MONDO:0002561"],"is_obsolete":false,"name":"cerebral lipidosis with dementia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:98544","GARD:19491","SCTID:16517004","MEDGEN:1825994","UMLS:C5681730","ICD9:330.1","DOID:10742"],"synonyms":[{"name":"cerebral lipidosis","type":"exact"}],"termid":"MONDO:0020143","terms_by_termid":{"MONDO:0008083":null,"MONDO:0008767":null},"xrefs":{"Monarch":{"xref_id":"0020143"}}}


id: PBO:0089060
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger, MIZ-type","termid":"PBO:0089060"}


id: GO:0015262
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. This term was not defined before being made obsolete.","definition_xrefs":["GOC:mtg_transport","ISBN:0815340729"],"gene_count":0,"genotype_count":0,"name":"obsolete taurine channel activity (obsolete GO:0015262)","synonyms":[{"name":"taurine channel activity","type":"exact"}],"termid":"GO:0015262"}


id: GO:0099054
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a presynapse.","definition_xrefs":["PMID:24449494","GOC:dos","GOC:PARL","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular component assembly","termid":"GO:0022607"},{"relation_name":"is_a","term_name":"presynapse organization","termid":"GO:0099172"},{"relation_name":"part_of","term_name":"synapse assembly","termid":"GO:0007416"}],"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:0044085","GO:0008150"],"is_obsolete":false,"name":"presynapse assembly","synonyms":[{"name":"presynapse biogenesis","type":"exact"},{"name":"presynaptic terminal assembly","type":"exact"}],"termid":"GO:0099054"}


id: PBO:0051515
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IKAROS family zinc finger 5","termid":"PBO:0051515"}


id: MONDO:0032931
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":"pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal","secondary_identifiers":["GARD:18034","DOID:0081396","MEDGEN:1716458","OMIM:618810","Orphanet:615954","UMLS:C5394137"],"synonyms":[{"name":"Chromosome 1P36.33 Deletion Syndrome, Atad3 Gene Cluster, Autosomal Recessive","type":"related"},{"name":"PHRINL","type":"related"},{"name":"PONTOCEREBELLAR HYPOPLASIA, HYPOTONIA, AND RESPIRATORY INSUFFICIENCY SYNDROME, NEONATAL LETHAL","type":"related"},{"name":"Phrinl Syndrome","type":"related"},{"name":"fatal pontocerebellar hypoplasia-hypotonia-respiratory distress syndrome","type":"exact"},{"name":"fatal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome","type":"exact"}],"termid":"MONDO:0032931","xrefs":{"Monarch":{"xref_id":"0032931"}}}


id: GO:0086014
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An action potential that occurs in an atrial cardiac muscle cell.","definition_xrefs":["GOC:BHF","GOC:mtg_cardiac_conduct_nov11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiac muscle cell action potential involved in contraction","termid":"GO:0086002"},{"relation_name":"part_of","term_name":"atrial cardiac muscle cell to AV node cell signaling","termid":"GO:0086026"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"atrial cardiac muscle cell action potential","termid":"GO:0086014"}


id: PBO:0030048
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_ferric_iron_import","termid":"PBO:0030048"}


id: GO:0052536
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process by which an organism activates, maintains or increases the frequency, rate or extent of systemic acquired resistance in the symbiont organism; systemic acquired resistance is a salicylic acid-mediated response that confers broad spectrum systemic resistance. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation by organism of systemic acquired resistance in symbiont (obsolete GO:0052536)","synonyms":[{"name":"positive regulation by organism of systemic acquired resistance in symbiont","type":"exact"}],"termid":"GO:0052536"}


id: PBO:0072497
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein SA pseudogene 26","termid":"PBO:0072497"}


id: GO:2000345
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of hepatocyte proliferation.","definition_xrefs":["GOC:BHF","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of epithelial cell proliferation","termid":"GO:0050678"},{"relation_name":"regulates","term_name":"hepatocyte proliferation","termid":"GO:0072574"}],"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 hepatocyte proliferation","termid":"GO:2000345"}


id: PBO:0035843
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-aggregated_filamentous_actin_in_cytoplasm","termid":"PBO:0035843"}


id: PBO:0083634
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eIF3b subunit of the eukaryotic translation initiation factor 3 (eIF3); subunit of the core complex of eIF3; essential for translation; part of a subcomplex (Prt1p-Rpg1p-Nip1p) that stimulates binding of mRNA and tRNA(i)Met to ribosomes; eIF3 is also involved in programmed stop codon readthrough","termid":"PBO:0083634"}


id: PBO:0000047
data:
  {"annotation_feature_type":"gene","cv_name":"feature_cvtermprop_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"evidence","termid":"PBO:0000047"}


id: PBO:0070628
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7 like 1 pseudogene 12","termid":"PBO:0070628"}


id: GO:0009851
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of auxins, plant hormones that regulate aspects of plant growth.","definition_xrefs":["GOC:lm","GOC:lr","ISBN:0122146743"],"direct_ancestors":[{"relation_name":"is_a","term_name":"auxin metabolic process","termid":"GO:0009850"},{"relation_name":"is_a","term_name":"hormone biosynthetic process","termid":"GO:0042446"}],"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":"auxin biosynthetic process","synonyms":[{"name":"auxin anabolism","type":"exact"},{"name":"auxin biosynthesis","type":"exact"},{"name":"auxin formation","type":"exact"},{"name":"auxin synthesis","type":"exact"}],"termid":"GO:0009851"}


id: PBO:0030054
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_rhizoxin","termid":"PBO:0030054"}


id: PBO:0086995
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Reticulon protein; involved in nuclear pore assembly and maintenance of tubular ER morphology; promotes membrane curvature; regulates the ER asymmetry-induced inheritance block during ER stress; role in ER-derived peroxisomal biogenesis; interacts with Sec6p, Yip3p, and Sbh1p; less abundant than RTN1; member of RTNLA (reticulon-like A) subfamily; protein increases in abundance and relocalizes to plasma membrane upon DNA replication stress","termid":"PBO:0086995"}


id: PBO:0087078
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribosomal 60S subunit protein L39; required for ribosome biogenesis; loss of both Rpl31p and Rpl39p confers lethality; also exhibits genetic interactions with SIS1 and PAB1; homologous to mammalian ribosomal protein L39, no bacterial homolog","termid":"PBO:0087078"}


id: FYECO:0000279
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which manganese chloride was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ MnCl2","synonyms":[{"name":"manganese chloride added","type":"exact"}],"termid":"FYECO:0000279"}


id: PBO:0035833
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_histone_H4-K20_dimethylation_during_vegetative_growth","termid":"PBO:0035833"}


id: GO:2000476
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of opioid receptor signaling pathway.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of G protein-coupled receptor signaling pathway","termid":"GO:0045745"},{"relation_name":"is_a","term_name":"regulation of opioid receptor signaling pathway","termid":"GO:2000474"},{"relation_name":"positively_regulates","term_name":"G protein-coupled opioid receptor signaling pathway","termid":"GO:0038003"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of opioid receptor signaling pathway","synonyms":[{"name":"positive regulation of opioid receptor signalling pathway","type":"exact"}],"termid":"GO:2000476"}


id: MONDO:0008990
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"laryngotracheoesophageal cleft","termid":"MONDO:0016060"}],"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":"cleft larynx, posterior","secondary_identifiers":["OMIM:215800","GARD:4015","Orphanet:2005","UMLS:C1859083","MEDGEN:349091"],"synonyms":[{"name":"Novak syndrome","type":"related"},{"name":"cleft larynx, posterior","type":"exact"},{"name":"laryngotracheoesophageal cleft pulmonary hypoplasia","type":"related"},{"name":"stridor, congenital","type":"related"}],"termid":"MONDO:0008990","xrefs":{"Monarch":{"xref_id":"0008990"}}}


id: PBO:0074809
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 14A","termid":"PBO:0074809"}


id: PBO:0064474
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"POLE4 pseudogene 1","termid":"PBO:0064474"}


id: PBO:0025459
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial superoxide dismutase Sod2","termid":"PBO:0025459"}


id: GO:0050596
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H+ + NADPH + O2 + vinorine = H2O + NADP+ + vomilenine.","definition_xrefs":["RHEA:17257","EC:1.14.14.104"],"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:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"vinorine hydroxylase activity","secondary_identifiers":["MetaCyc:1.14.13.75-RXN","KEGG_REACTION:R05877"],"synonyms":[{"name":"vinorine,NADPH:oxygen oxidoreductase (21alpha-hydroxylating)","type":"related"}],"termid":"GO:0050596"}


id: PBO:0038428
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha 1,3-galactosyltransferase 2","termid":"PBO:0038428"}


id: GO:0032727
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of interferon-alpha production.","definition_xrefs":["GOC:mah","PMID:15546383"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of type I interferon production","termid":"GO:0032481"},{"relation_name":"is_a","term_name":"regulation of interferon-alpha production","termid":"GO:0032647"},{"relation_name":"positively_regulates","term_name":"interferon-alpha production","termid":"GO:0032607"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"positive regulation of interferon-alpha production","secondary_identifiers":["GO:1902741","GO:0045356"],"synonyms":[{"name":"activation of interferon-alpha production","type":"narrow"},{"name":"positive regulation of interferon-alpha biosynthetic process","type":"narrow"},{"name":"positive regulation of interferon-alpha secretion","type":"narrow"},{"name":"stimulation of interferon-alpha production","type":"narrow"},{"name":"up regulation of interferon-alpha production","type":"exact"},{"name":"up-regulation of interferon-alpha production","type":"exact"},{"name":"upregulation of interferon-alpha production","type":"exact"}],"termid":"GO:0032727"}


id: PBO:0086545
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; conserved among S. cerevisiae strains; YDR102C is not an essential gene; homozygous diploid deletion strain exhibits high budding index","termid":"PBO:0086545"}


id: PBO:0002010
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rho-type GTPase activating protein Rga2 (predicted)","termid":"PBO:0002010"}


id: PBO:0070735
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L10a pseudogene 5","termid":"PBO:0070735"}


id: GO:1904254
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of an iron transmembrane transporter activity.","definition_xrefs":["GO_REF:0000059","GOC:BHF","GOC:kom","PMID:15514116","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of monoatomic ion transmembrane transporter activity","termid":"GO:0032412"},{"relation_name":"is_a","term_name":"regulation of iron ion transmembrane transport","termid":"GO:0034759"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0055085"],"is_obsolete":false,"name":"regulation of iron ion transmembrane transporter activity","synonyms":[{"name":"regulation of iron cation channel activity","type":"exact"},{"name":"regulation of iron channel activity","type":"exact"},{"name":"regulation of iron-specific channel activity","type":"exact"}],"termid":"GO:1904254"}


id: MONDO:1011667
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"digestive system disorder, non-human animal","termid":"MONDO:1011311"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Lundehund syndrome, non-human animal","secondary_identifiers":["OMIA:002031"],"termid":"MONDO:1011667","xrefs":{"Monarch":{"xref_id":"1011667"}}}


id: GO:0080016
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-trans,6-trans-farnesyl diphosphate = (-)-E-beta-caryophyllene + diphosphate.","definition_xrefs":["PMID:9442047","MetaCyc:RXN-8414","PMID:12566586"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cyclase activity","termid":"GO:0009975"},{"relation_name":"is_a","term_name":"sesquiterpene synthase activity","termid":"GO:0010334"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0009975"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016829","GO:0009975"],"is_obsolete":false,"name":"(-)-E-beta-caryophyllene synthase activity","secondary_identifiers":["EC:4.2.3.57","RHEA:28294"],"termid":"GO:0080016"}


id: GO:0002778
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The synthesis or release of an antibacterial peptide during an immune response, resulting in an increase in intracellular or extracellular levels.","definition_xrefs":["ISBN:0781735149","PMID:11807545","PMID:15638771","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"antimicrobial peptide production","termid":"GO:0002775"},{"relation_name":"part_of","term_name":"antibacterial humoral response","termid":"GO:0019731"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"antibacterial peptide production","termid":"GO:0002778"}


id: MONDO:0015947
data:
  {"annotated_genes":["SJAG_02085","SJAG_02842","SJAG_01307","SJAG_02326"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84502,84503],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014010"},{"annotations":[85088,85089],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100221"}]},"cv_name":"mondo","definition":"Mendelian disorders of cornification affecting all or most of integument characterized by hyperkeratosis and/or scaling, caused by an inherited modification of the individual's genome.","definition_xrefs":["MONDO:patterns/hereditary","PMID:20643494"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ichthyosis","termid":"MONDO:0019269"},{"relation_name":"is_a","term_name":"hereditary skin disorder","termid":"MONDO:0100118"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01307":null,"SJAG_02085":null,"SJAG_02326":null,"SJAG_02842":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"inherited ichthyosis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:13059002","ICD9:757.1","MedDRA:10021202","GARD:20261","NANDO:2100283","Orphanet:183435","UMLS:C0856562","NANDO:1200609","ICD10CM:Q80","MEDGEN:797407"],"synonyms":[{"name":"congenital ichthyosis","type":"related"},{"name":"congenital ichthyosis of skin","type":"exact"},{"name":"fish scale disease","type":"related"},{"name":"fish skin","type":"related"},{"name":"genetic ichthyosis","type":"exact"},{"name":"hereditary ichthyosis (disease)","type":"exact"},{"name":"ichthyosis congenita","type":"related"},{"name":"inherited genetic ichthyosis","type":"exact"}],"termid":"MONDO:0015947","terms_by_termid":{"MONDO:0014010":null,"MONDO:0100221":null},"xrefs":{"Monarch":{"xref_id":"0015947"}}}


id: PBO:0061464
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear receptor subfamily 0 group B member 2","termid":"PBO:0061464"}


id: MONDO:0005993
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A sexually transmitted parasitic infection caused by Trichomonas vaginalis. Symptoms include vaginal discharge, vaginal odor, vaginal itching, and discomfort during intercourse.","definition_xrefs":["NCIT:C35083"],"direct_ancestors":[{"relation_name":"is_a","term_name":"trichomoniasis","termid":"MONDO:0002154"},{"relation_name":"is_a","term_name":"sexually transmitted disease","termid":"MONDO:0021681"},{"relation_name":"is_a","term_name":"urinary tract infection","termid":"MONDO:0100338"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Trichomonas vaginitis urogenital infection","secondary_identifiers":["DOID:0050269","ICD9:131.00","ICD9:131.09","MESH:D014247","ICD10CM:A59.0","SCTID:35089004"],"synonyms":[{"name":"Trichomonas vaginalis caused disease of genitourinary system","type":"exact"},{"name":"Trichomonas vaginalis disease of genitourinary system","type":"exact"},{"name":"Trichomonas vaginalis trichomoniasis","type":"related"},{"name":"Trichomonas vaginitis","type":"exact"},{"name":"urogenital Trichomonas","type":"exact"},{"name":"urogenital infection by Trichomonas vaginalis","type":"exact"},{"name":"urogenital infection caused by Trichomonas vaginalis","type":"related"},{"name":"urogenital trichomoniasis","type":"related"}],"termid":"MONDO:0005993","xrefs":{"Monarch":{"xref_id":"0005993"}}}


id: PBO:0081397
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 236","termid":"PBO:0081397"}


id: FYPO:0003414
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the cell septum is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to cell division site","termid":"FYPO:0002442"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0000002","FYPO:0001312","FYPO:0000257","FYPO:0001320"],"is_obsolete":false,"name":"normal protein localization to septum","synonyms":[{"name":"normal protein localisation to septum","type":"exact"},{"name":"normal protein localization to cell septum","type":"exact"},{"name":"normal protein localization to division septum","type":"exact"},{"name":"normal protein localization to septum during mitotic cell cycle","type":"related"},{"name":"normal protein localization to septum during vegetative growth","type":"exact"}],"termid":"FYPO:0003414"}


id: PBO:0044258
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CXADR Ig-like cell adhesion molecule","termid":"PBO:0044258"}


id: PBO:0064332
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phospholipid scramblase 2","termid":"PBO:0064332"}


id: FYPO:0006863
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell population phenotype in which a smaller than normal proportion of cells in the population remains viable after exposure to bleomycin.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal phenotype","termid":"FYPO:0001985"},{"relation_name":"is_a","term_name":"cell population viability","termid":"FYPO:0002057"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0002057","FYPO:0001985","FYPO:0000003"],"is_obsolete":false,"name":"loss of viability following cellular response to bleomycin","synonyms":[{"name":"decreased viability following cellular response to bleomycin","type":"exact"},{"name":"loss of cell population viability following cellular response to bleomycin","type":"exact"},{"name":"loss of viability following bleomycin exposure","type":"exact"},{"name":"reduced viability following cellular response to bleomycin","type":"related"}],"termid":"FYPO:0006863"}


id: FYPO:0000057
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 mitochondrial nucleoid is larger than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal subcellular component during vegetative growth","termid":"FYPO:0001322"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"mitochondrial nucleoid enlarged","synonyms":[{"name":"mitochondrial nucleoid enlarged during mitotic cell cycle","type":"related"},{"name":"mitochondrial nucleoid enlarged during vegetative growth","type":"exact"}],"termid":"FYPO:0000057"}


id: PBO:0060659
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"natural cytotoxicity triggering receptor 3","termid":"PBO:0060659"}


id: PBO:0027537
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_histidine_or_lysine","termid":"PBO:0027537"}


id: FYPO:0006937
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which lipid binding by a gene product does not occur. The affected gene product may be encoded by the mutated gene, or by a different gene.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished molecular function","termid":"FYPO:0005446"},{"relation_name":"is_a","term_name":"abnormal lipid binding","termid":"FYPO:0007250"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000652","FYPO:0000707"],"is_obsolete":false,"name":"abolished lipid binding","synonyms":[{"name":"lipid binding abolished","type":"exact"}],"termid":"FYPO:0006937"}


id: MONDO:0010795
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A usually benign neoplasm composed of large cells with abundant eosinophilic granular cytoplasm. Representative examples include oncocytic neoplasms of the thyroid gland, and kidney. (NCI05)","definition_xrefs":["NCIT:C7072"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glandular cell neoplasm","termid":"MONDO:0024276"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oncocytic neoplasm","secondary_identifiers":["UMLS:C1378050","MEDGEN:237181","OMIM:553000"],"synonyms":[{"name":"oncocytic neoplasm","type":"exact"},{"name":"oncocytic tumor","type":"exact"},{"name":"oncocytic tumour","type":"exact"},{"name":"oncocytoma","type":"broad"},{"name":"oncocytoma, benign","type":"exact"}],"termid":"MONDO:0010795","xrefs":{"Monarch":{"xref_id":"0010795"}}}


id: GO:0009933
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Organization of a region of tissue in a plant that is composed of one or more undifferentiated cells capable of undergoing mitosis and differentiation, thereby effecting growth and development of a plant by giving rise to more meristem or specialized tissue.","definition_xrefs":["ISBN:0198547684","GOC:sm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure arrangement","termid":"GO:0048532"},{"relation_name":"part_of","term_name":"meristem development","termid":"GO:0048507"}],"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":"meristem structural organization","synonyms":[{"name":"meristem organisation","type":"broad"},{"name":"meristem organization","type":"broad"}],"termid":"GO:0009933"}


id: MONDO:0018643
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"functional neutrophil defect","termid":"MONDO:0015978"},{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"susceptibility to localized juvenile periodontitis","secondary_identifiers":["MEDGEN:1812489","Orphanet:447740","UMLS:C5681199"],"termid":"MONDO:0018643","xrefs":{"Monarch":{"xref_id":"0018643"}}}


id: GO:0075512
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any clathrin-mediated endocytosis that is involved in the uptake of a virus into a host cell. Begins by invagination of a specific region of the host cell plasma membrane around the bound virus to form a clathrin-coated pit, which then pinches off to form a clathrin-coated endocytic vesicle containing the virus.","definition_xrefs":["GOC:jl","VZ:957","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"receptor-mediated endocytosis of virus by host cell","termid":"GO:0019065"},{"relation_name":"is_a","term_name":"clathrin-dependent endocytosis","termid":"GO:0072583"}],"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":"is_a","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0006810","GO:0016192","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"clathrin-dependent endocytosis of virus by host cell","secondary_identifiers":["GO:0075516"],"synonyms":[{"name":"clathrin-mediated endocytosis of virus by host cell","type":"exact"},{"name":"viral entry into host cell via clathrin-mediated endocytosis","type":"related"},{"name":"viral entry into host cell via clathrin-mediated endocytosis followed by endosome lysis","type":"narrow"},{"name":"viral penetration via clathrin-mediated endocytosis","type":"exact"}],"termid":"GO:0075512"}


id: FYPO:0000429
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the G0 to G1 transition begins later than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal G0 to G1 transition","termid":"FYPO:0002955"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0000631"],"is_obsolete":false,"name":"delayed G0 to G1 transition","synonyms":[{"name":"delayed G0/G1 transition","type":"exact"},{"name":"delayed exit from G0","type":"exact"},{"name":"delayed exit from cell quiescence","type":"exact"},{"name":"slow cell population growth following nitrogen starvation","type":"related"}],"termid":"FYPO:0000429"}


id: PBO:0077481
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 201","termid":"PBO:0077481"}


id: FYPO:0003553
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the occurrence of an RNA catabolic process is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_output","term_name":"decreased RNA level","termid":"FYPO:0000826"},{"relation_name":"is_a","term_name":"abnormal RNA catabolic process","termid":"FYPO:0003551"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000294","FYPO:0000002","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"increased RNA catabolic process","synonyms":[{"name":"increased RNA breakdown","type":"exact"},{"name":"increased RNA catabolism","type":"exact"},{"name":"increased RNA degradation","type":"exact"}],"termid":"FYPO:0003553"}


id: PBO:0039693
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acylaminoacyl-peptide hydrolase","termid":"PBO:0039693"}


id: MONDO:0003594
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm characterized by the presence of a combination of liposarcomatous morphologic subtypes: myxoid/round cell and well differentiated/dedifferentiated liposarcoma or myxoid/round cell and pleomorphic liposarcoma.","definition_xrefs":["NCIT:C4253"],"direct_ancestors":[{"relation_name":"is_a","term_name":"liposarcoma","termid":"MONDO:0005060"}],"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":"mixed liposarcoma","secondary_identifiers":["MEDGEN:87249","DOID:5703","UMLS:C0334472","ICDO:8855/3"],"synonyms":[{"name":"mixed liposarcoma","type":"exact"},{"name":"mixed liposarcoma (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0003594","xrefs":{"Monarch":{"xref_id":"0003594"}}}


id: PBO:0055320
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 2748","termid":"PBO:0055320"}


id: GO:0007219
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by an extracellular ligand binding to the receptor Notch on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["GOC:go_curators","GOC:signaling"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell surface receptor signaling pathway","termid":"GO:0007166"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"Notch signaling pathway","secondary_identifiers":["Wikipedia:Notch_signaling_pathway","GO:0030179"],"synonyms":[{"name":"N signaling pathway","type":"exact"},{"name":"N signalling pathway","type":"exact"},{"name":"Notch receptor signaling pathway","type":"exact"},{"name":"Notch receptor signalling pathway","type":"exact"},{"name":"Notch signalling pathway","type":"exact"},{"name":"Notch-receptor signaling pathway","type":"exact"},{"name":"Notch-receptor signalling pathway","type":"exact"}],"termid":"GO:0007219"}


id: PBO:0046501
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ERI1 exoribonuclease family member 2","termid":"PBO:0046501"}


id: PATO:0001220
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001220 angle_unit (obsolete PATO:0001220)","termid":"PATO:0001220"}


id: FYPO:0005094
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell cycle checkpoint phenotype in which the duration of cell cycle arrest or delay due to regulation by the S-phase DNA damage checkpoint is lower than in wild type during a cellular response to hydroxyurea.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic cell cycle regulation during cellular response to hydroxyurea","termid":"FYPO:0001933"},{"relation_name":"is_a","term_name":"decreased duration of S-phase DNA damage checkpoint","termid":"FYPO:0004371"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000298"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000298","FYPO:0000002","FYPO:0001320","FYPO:0005447","FYPO:0000631"],"is_obsolete":false,"name":"decreased duration of S-phase DNA damage checkpoint during cellular response to hydroxyurea","synonyms":[{"name":"decreased duration of S-phase DNA damage checkpoint activation during cellular response to hydroxyurea","type":"exact"},{"name":"decreased duration of S-phase DNA damage checkpoint during cellular response to HU","type":"exact"},{"name":"decreased duration of S-phase DNA damage checkpoint during cellular response to hydroxyurea during mitotic cell cycle","type":"exact"},{"name":"decreased duration of S-phase DNA damage checkpoint during cellular response to hydroxyurea during vegetative growth","type":"exact"},{"name":"decreased duration of intra-S DNA damage checkpoint during cellular response to hydroxyurea","type":"exact"},{"name":"decreased duration of mitotic S-phase DNA damage checkpoint during cellular response to hydroxyurea","type":"exact"},{"name":"premature S-phase DNA damage checkpoint deactivation during cellular response to hydroxyurea","type":"related"},{"name":"reduced duration of S-phase DNA damage checkpoint during cellular response to hydroxyurea","type":"exact"}],"termid":"FYPO:0005094"}


id: PBO:0041523
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 16 open reading frame 78","termid":"PBO:0041523"}


id: PBO:0003064
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dipeptidase Dug1 (predicted)","termid":"PBO:0003064"}


id: PBO:0068907
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 150, pseudogene","termid":"PBO:0068907"}


id: PR:Q9P7J1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- swt1 gene.","definition_xrefs":["UniProtKB:Q9P7J1","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":"transcriptional protein swt1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC24B10.15","synonyms":[{"name":"Spom972h-swt1","type":"exact"}],"termid":"PR:Q9P7J1"}


id: SO:0002254
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The loop portion of a stem loop, which is not folded back upon itself. ","direct_ancestors":[{"relation_name":"is_a","term_name":"stem_loop_region","termid":"SO:0002253"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"loop","synonyms":[{"name":"loop portion of stem loop","type":"exact"}],"termid":"SO:0002254"}


id: GO:0010108
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of events in which a glutamine stimulus is received by a cell and converted into a molecular signal.","definition_xrefs":["GOC:sm"],"gene_count":0,"genotype_count":0,"name":"obsolete detection of glutamine (obsolete GO:0010108)","synonyms":[{"name":"glutamine detection","type":"exact"},{"name":"glutamine perception","type":"related"},{"name":"glutamine sensing","type":"related"}],"termid":"GO:0010108"}


id: MONDO:0060670
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"excluded_subClassOf","term_name":"familial amyotrophic lateral sclerosis","termid":"MONDO:0005144"},{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amyotrophic lateral sclerosis, susceptibility to, 25","secondary_identifiers":["UMLS:C4693609","OMIM:617921","MEDGEN:1633917","DOID:0081379"],"synonyms":[{"name":"ALS25","type":"related"},{"name":"amyotrophic lateral sclerosis, susceptibility to, 25","type":"exact"}],"termid":"MONDO:0060670","xrefs":{"Monarch":{"xref_id":"0060670"}}}


id: GO:0031860
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation of the single stranded telomeric 3' overhang, a conserved feature that ranges in length from 12 nt in budding yeast to approximately 500 nt in humans.","definition_xrefs":["PMID:16096639"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA strand elongation","termid":"GO:0022616"},{"relation_name":"part_of","term_name":"telomere capping","termid":"GO:0016233"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"part_of","termid":"GO:0006259"},{"rel_name":"part_of","termid":"GO:0032200"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006259","GO:0032200","GO:0008150"],"is_obsolete":false,"name":"telomeric 3' overhang formation","synonyms":[{"name":"telomere 3'-end processing","type":"exact"},{"name":"telomere end processing","type":"related"}],"termid":"GO:0031860"}


id: MONDO:0008056
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Steinert disease, also known as myotonic dystrophy type 1, is a muscle disease characterized by myotonia and by multiorgan damage that combines various degrees of muscle weakness, arrhythmia and/or cardiac conduction disorders, cataract, endocrine damage, sleep disorders and baldness.","definition_xrefs":["Orphanet:273"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete neuro-ophthalmological disease (obsolete MONDO:0015368)","termid":"MONDO:0015368"},{"relation_name":"is_a","term_name":"myotonic dystrophy","termid":"MONDO:0016107"},{"relation_name":"is_a","term_name":"familial hypertrophic cardiomyopathy","termid":"MONDO:0024573"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0005267"],"is_obsolete":false,"name":"myotonic dystrophy type 1","secondary_identifiers":["NORD:1075","GARD:8310","ICD9:359.21","OMIM:160900","DOID:11722","icd11.foundation:557405480","MEDGEN:886881","NCIT:C84679","UMLS:C3250443"],"synonyms":[{"name":"DM1","type":"exact"},{"name":"DMPK myotonic dystrophy","type":"exact"},{"name":"MD1","type":"exact"},{"name":"Myotonic Dystrophy","type":"exact"},{"name":"Steinert disease","type":"exact"},{"name":"Steinert myotonic dystrophy","type":"related"},{"name":"Steinert myotonic dystrophy syndrome","type":"exact"},{"name":"Steinert syndrome","type":"exact"},{"name":"Steinert's disease","type":"related"},{"name":"dystrophia myotonica","type":"exact"},{"name":"dystrophia myotonica 1","type":"related"},{"name":"dystrophia myotonica type 1","type":"related"},{"name":"myotonic dystrophy 1","type":"related"},{"name":"myotonic dystrophy caused by mutation in DMPK","type":"exact"},{"name":"myotonic dystrophy of Steinert","type":"exact"},{"name":"myotonic dystrophy type 1","type":"exact"}],"termid":"MONDO:0008056","xrefs":{"Monarch":{"xref_id":"0008056"}}}


id: GO:1904747
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of apoptotic process involved in development.","definition_xrefs":["PMID:22801495","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of apoptotic process","termid":"GO:0043065"},{"relation_name":"is_a","term_name":"positive regulation of developmental process","termid":"GO:0051094"},{"relation_name":"is_a","term_name":"regulation of apoptotic process involved in development","termid":"GO:1904748"},{"relation_name":"positively_regulates","term_name":"apoptotic process involved in development","termid":"GO:1902742"}],"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 apoptotic process involved in development","synonyms":[{"name":"activation of activation of apoptosis involved in anatomical structure development","type":"narrow"},{"name":"activation of activation of apoptosis involved in development of an anatomical structure","type":"narrow"},{"name":"activation of apoptosis activator activity involved in anatomical structure development","type":"related"},{"name":"activation of apoptosis activator activity involved in development of an anatomical structure","type":"related"},{"name":"activation of apoptosis involved in anatomical structure development","type":"narrow"},{"name":"activation of apoptosis involved in development of an anatomical structure","type":"narrow"},{"name":"activation of apoptosis signaling involved in anatomical structure development","type":"narrow"},{"name":"activation of apoptosis signaling involved in development of an anatomical structure","type":"narrow"},{"name":"activation of apoptotic cell death involved in anatomical structure development","type":"narrow"},{"name":"activation of apoptotic cell death involved in development of an anatomical structure","type":"narrow"},{"name":"activation of apoptotic process involved in anatomical structure development","type":"narrow"},{"name":"activation of apoptotic process involved in development","type":"narrow"},{"name":"activation of apoptotic process involved in development of an anatomical structure","type":"narrow"},{"name":"activation of apoptotic program involved in anatomical structure development","type":"narrow"},{"name":"activation of apoptotic program involved in development of an anatomical structure","type":"narrow"},{"name":"activation of apoptotic programmed cell death involved in anatomical structure development","type":"narrow"},{"name":"activation of apoptotic programmed cell death involved in development of an anatomical structure","type":"narrow"},{"name":"activation of commitment to apoptosis involved in anatomical structure development","type":"related"},{"name":"activation of commitment to apoptosis involved in development of an anatomical structure","type":"related"},{"name":"activation of induction of apoptosis by p53 involved in anatomical structure development","type":"related"},{"name":"activation of induction of apoptosis by p53 involved in development of an anatomical structure","type":"related"},{"name":"activation of induction of apoptosis involved in anatomical structure development","type":"related"},{"name":"activation of induction of apoptosis involved in development of an anatomical structure","type":"related"},{"name":"activation of programmed cell death by apoptosis involved in anatomical structure development","type":"narrow"},{"name":"activation of programmed cell death by apoptosis involved in development of an anatomical structure","type":"narrow"},{"name":"activation of signaling (initiator) caspase activity involved in anatomical structure development","type":"related"},{"name":"activation of signaling (initiator) caspase activity involved in development of an anatomical structure","type":"related"},{"name":"activation of type I programmed cell death involved in anatomical structure development","type":"narrow"},{"name":"activation of type I programmed cell death involved in development of an anatomical structure","type":"narrow"},{"name":"positive regulation of activation of apoptosis involved in anatomical structure development","type":"narrow"},{"name":"positive regulation of activation of apoptosis involved in development of an anatomical structure","type":"narrow"},{"name":"positive regulation of apoptosis activator activity involved in anatomical structure development","type":"related"},{"name":"positive regulation of apoptosis activator activity involved in development of an anatomical structure","type":"related"},{"name":"positive regulation of apoptosis involved in anatomical structure development","type":"narrow"},{"name":"positive regulation of apoptosis involved in development of an anatomical structure","type":"narrow"},{"name":"positive regulation of apoptosis signaling involved in anatomical structure development","type":"narrow"},{"name":"positive regulation of apoptosis signaling involved in development of an anatomical structure","type":"narrow"},{"name":"positive regulation of apoptotic cell death involved in anatomical structure development","type":"exact"},{"name":"positive regulation of apoptotic cell death involved in development of an anatomical structure","type":"exact"},{"name":"positive regulation of apoptotic process involved in anatomical structure development","type":"exact"},{"name":"positive regulation of apoptotic process involved in development of an anatomical structure","type":"exact"},{"name":"positive regulation of apoptotic program involved in anatomical structure development","type":"narrow"},{"name":"positive regulation of apoptotic program involved in development of an anatomical structure","type":"narrow"},{"name":"positive regulation of apoptotic programmed cell death involved in anatomical structure development","type":"exact"},{"name":"positive regulation of apoptotic programmed cell death involved in development of an anatomical structure","type":"exact"},{"name":"positive regulation of commitment to apoptosis involved in anatomical structure development","type":"related"},{"name":"positive regulation of commitment to apoptosis involved in development of an anatomical structure","type":"related"},{"name":"positive regulation of induction of apoptosis by p53 involved in anatomical structure development","type":"related"},{"name":"positive regulation of induction of apoptosis by p53 involved in development of an anatomical structure","type":"related"},{"name":"positive regulation of induction of apoptosis involved in anatomical structure development","type":"related"},{"name":"positive regulation of induction of apoptosis involved in development of an anatomical structure","type":"related"},{"name":"positive regulation of programmed cell death by apoptosis involved in anatomical structure development","type":"exact"},{"name":"positive regulation of programmed cell death by apoptosis involved in development of an anatomical structure","type":"exact"},{"name":"positive regulation of signaling (initiator) caspase activity involved in anatomical structure development","type":"related"},{"name":"positive regulation of signaling (initiator) caspase activity involved in development of an anatomical structure","type":"related"},{"name":"positive regulation of type I programmed cell death involved in anatomical structure development","type":"narrow"},{"name":"positive regulation of type I programmed cell death involved in development of an anatomical structure","type":"narrow"},{"name":"up regulation of activation of apoptosis involved in anatomical structure development","type":"narrow"},{"name":"up regulation of activation of apoptosis involved in development of an anatomical structure","type":"narrow"},{"name":"up regulation of apoptosis activator activity involved in anatomical structure development","type":"related"},{"name":"up regulation of apoptosis activator activity involved in development of an anatomical structure","type":"related"},{"name":"up regulation of apoptosis involved in anatomical structure development","type":"narrow"},{"name":"up regulation of apoptosis involved in development of an anatomical structure","type":"narrow"},{"name":"up regulation of apoptosis signaling involved in anatomical structure development","type":"narrow"},{"name":"up regulation of apoptosis signaling involved in development of an anatomical structure","type":"narrow"},{"name":"up regulation of apoptotic cell death involved in anatomical structure development","type":"exact"},{"name":"up regulation of apoptotic cell death involved in development of an anatomical structure","type":"exact"},{"name":"up regulation of apoptotic process involved in anatomical structure development","type":"exact"},{"name":"up regulation of apoptotic process involved in development","type":"exact"},{"name":"up regulation of apoptotic process involved in development of an anatomical structure","type":"exact"},{"name":"up regulation of apoptotic program involved in anatomical structure development","type":"narrow"},{"name":"up regulation of apoptotic program involved in development of an anatomical structure","type":"narrow"},{"name":"up regulation of apoptotic programmed cell death involved in anatomical structure development","type":"exact"},{"name":"up regulation of apoptotic programmed cell death involved in development of an anatomical structure","type":"exact"},{"name":"up regulation of commitment to apoptosis involved in anatomical structure development","type":"related"},{"name":"up regulation of commitment to apoptosis involved in development of an anatomical structure","type":"related"},{"name":"up regulation of induction of apoptosis by p53 involved in anatomical structure development","type":"related"},{"name":"up regulation of induction of apoptosis by p53 involved in development of an anatomical structure","type":"related"},{"name":"up regulation of induction of apoptosis involved in anatomical structure development","type":"related"},{"name":"up regulation of induction of apoptosis involved in development of an anatomical structure","type":"related"},{"name":"up regulation of programmed cell death by apoptosis involved in anatomical structure development","type":"exact"},{"name":"up regulation of programmed cell death by apoptosis involved in development of an anatomical structure","type":"exact"},{"name":"up regulation of signaling (initiator) caspase activity involved in anatomical structure development","type":"related"},{"name":"up regulation of signaling (initiator) caspase activity involved in development of an anatomical structure","type":"related"},{"name":"up regulation of type I programmed cell death involved in anatomical structure development","type":"narrow"},{"name":"up regulation of type I programmed cell death involved in development of an anatomical structure","type":"narrow"},{"name":"up-regulation of activation of apoptosis involved in anatomical structure development","type":"narrow"},{"name":"up-regulation of activation of apoptosis involved in development of an anatomical structure","type":"narrow"},{"name":"up-regulation of apoptosis activator activity involved in anatomical structure development","type":"related"},{"name":"up-regulation of apoptosis activator activity involved in development of an anatomical structure","type":"related"},{"name":"up-regulation of apoptosis involved in anatomical structure development","type":"narrow"},{"name":"up-regulation of apoptosis involved in development of an anatomical structure","type":"narrow"},{"name":"up-regulation of apoptosis signaling involved in anatomical structure development","type":"narrow"},{"name":"up-regulation of apoptosis signaling involved in development of an anatomical structure","type":"narrow"},{"name":"up-regulation of apoptotic cell death involved in anatomical structure development","type":"exact"},{"name":"up-regulation of apoptotic cell death involved in development of an anatomical structure","type":"exact"},{"name":"up-regulation of apoptotic process involved in anatomical structure development","type":"exact"},{"name":"up-regulation of apoptotic process involved in development","type":"exact"},{"name":"up-regulation of apoptotic process involved in development of an anatomical structure","type":"exact"},{"name":"up-regulation of apoptotic program involved in anatomical structure development","type":"narrow"},{"name":"up-regulation of apoptotic program involved in development of an anatomical structure","type":"narrow"},{"name":"up-regulation of apoptotic programmed cell death involved in anatomical structure development","type":"exact"},{"name":"up-regulation of apoptotic programmed cell death involved in development of an anatomical structure","type":"exact"},{"name":"up-regulation of commitment to apoptosis involved in anatomical structure development","type":"related"},{"name":"up-regulation of commitment to apoptosis involved in development of an anatomical structure","type":"related"},{"name":"up-regulation of induction of apoptosis by p53 involved in anatomical structure development","type":"related"},{"name":"up-regulation of induction of apoptosis by p53 involved in development of an anatomical structure","type":"related"},{"name":"up-regulation of induction of apoptosis involved in anatomical structure development","type":"related"},{"name":"up-regulation of induction of apoptosis involved in development of an anatomical structure","type":"related"},{"name":"up-regulation of programmed cell death by apoptosis involved in anatomical structure development","type":"exact"},{"name":"up-regulation of programmed cell death by apoptosis involved in development of an anatomical structure","type":"exact"},{"name":"up-regulation of signaling (initiator) caspase activity involved in anatomical structure development","type":"related"},{"name":"up-regulation of signaling (initiator) caspase activity involved in development of an anatomical structure","type":"related"},{"name":"up-regulation of type I programmed cell death involved in anatomical structure development","type":"narrow"},{"name":"up-regulation of type I programmed cell death involved in development of an anatomical structure","type":"narrow"},{"name":"upregulation of activation of apoptosis involved in anatomical structure development","type":"narrow"},{"name":"upregulation of activation of apoptosis involved in development of an anatomical structure","type":"narrow"},{"name":"upregulation of apoptosis activator activity involved in anatomical structure development","type":"related"},{"name":"upregulation of apoptosis activator activity involved in development of an anatomical structure","type":"related"},{"name":"upregulation of apoptosis involved in anatomical structure development","type":"narrow"},{"name":"upregulation of apoptosis involved in development of an anatomical structure","type":"narrow"},{"name":"upregulation of apoptosis signaling involved in anatomical structure development","type":"narrow"},{"name":"upregulation of apoptosis signaling involved in development of an anatomical structure","type":"narrow"},{"name":"upregulation of apoptotic cell death involved in anatomical structure development","type":"exact"},{"name":"upregulation of apoptotic cell death involved in development of an anatomical structure","type":"exact"},{"name":"upregulation of apoptotic process involved in anatomical structure development","type":"exact"},{"name":"upregulation of apoptotic process involved in development","type":"exact"},{"name":"upregulation of apoptotic process involved in development of an anatomical structure","type":"exact"},{"name":"upregulation of apoptotic program involved in anatomical structure development","type":"narrow"},{"name":"upregulation of apoptotic program involved in development of an anatomical structure","type":"narrow"},{"name":"upregulation of apoptotic programmed cell death involved in anatomical structure development","type":"exact"},{"name":"upregulation of apoptotic programmed cell death involved in development of an anatomical structure","type":"exact"},{"name":"upregulation of commitment to apoptosis involved in anatomical structure development","type":"related"},{"name":"upregulation of commitment to apoptosis involved in development of an anatomical structure","type":"related"},{"name":"upregulation of induction of apoptosis by p53 involved in anatomical structure development","type":"related"},{"name":"upregulation of induction of apoptosis by p53 involved in development of an anatomical structure","type":"related"},{"name":"upregulation of induction of apoptosis involved in anatomical structure development","type":"related"},{"name":"upregulation of induction of apoptosis involved in development of an anatomical structure","type":"related"},{"name":"upregulation of programmed cell death by apoptosis involved in anatomical structure development","type":"exact"},{"name":"upregulation of programmed cell death by apoptosis involved in development of an anatomical structure","type":"exact"},{"name":"upregulation of signaling (initiator) caspase activity involved in anatomical structure development","type":"related"},{"name":"upregulation of signaling (initiator) caspase activity involved in development of an anatomical structure","type":"related"},{"name":"upregulation of type I programmed cell death involved in anatomical structure development","type":"narrow"},{"name":"upregulation of type I programmed cell death involved in development of an anatomical structure","type":"narrow"}],"termid":"GO:1904747"}


id: MONDO:0005694
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign or malignant neoplasm that affects the cecum. Representative examples of benign neoplasms include lipoma and leiomyoma. Representative examples of malignant neoplasms include carcinoma, lymphoma, and sarcoma. Cecal adenomas always exhibit epithelial dysplasia and are considered premalignant neoplasms.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cecal disorder","termid":"MONDO:0002031"},{"relation_name":"is_a","term_name":"colonic neoplasm","termid":"MONDO:0005401"}],"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":"cecal neoplasm","secondary_identifiers":["MEDGEN:2922","NCIT:C4433","MESH:D002430","SCTID:126839008","EFO:0009255","DOID:1517","UMLS:C0007528"],"synonyms":[{"name":"caecum neoplasm","type":"exact"},{"name":"caecum neoplasm (disease)","type":"exact"},{"name":"caecum tumor","type":"exact"},{"name":"caecum tumour","type":"exact"},{"name":"cecal benign neoplasm","type":"related"},{"name":"cecum neoplasm","type":"exact"},{"name":"cecum tumor","type":"exact"},{"name":"cecum tumour","type":"exact"},{"name":"neoplasm of caecum","type":"exact"},{"name":"neoplasm of cecum","type":"exact"},{"name":"neoplasm of the cecum","type":"exact"},{"name":"tumor of caecum","type":"exact"},{"name":"tumor of cecum","type":"exact"},{"name":"tumor of the cecum","type":"exact"},{"name":"tumour of caecum","type":"exact"},{"name":"tumour of cecum","type":"exact"},{"name":"tumour of the cecum","type":"exact"}],"termid":"MONDO:0005694","xrefs":{"Monarch":{"xref_id":"0005694"}}}


id: GO:0000485
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Endonucleolytic cleavage between the LSU-rRNA and the 2S rRNA of an rRNA molecule originally produced as a tetracistronic rRNA transcript that contained the Small SubUnit (SSU) rRNA, the 5.8S rRNA, 2S rRNA, and the Large SubUnit (LSU) rRNA, in that order, from 5' to 3' along the primary transcript.","definition_xrefs":["GOC:curators","PMID:768488"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endonucleolytic cleavage of tetracistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, 2S rRNA, LSU-rRNA)","termid":"GO:0000483"},{"relation_name":"part_of","term_name":"maturation of LSU-rRNA from tetracistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, 2S rRNA, LSU-rRNA)","termid":"GO:0000473"},{"relation_name":"part_of","term_name":"maturation of 2S rRNA","termid":"GO:0000475"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0042254"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0042254","GO:0044085","GO:0010467","GO:0008150"],"is_obsolete":false,"name":"cleavage between 2S rRNA and LSU-rRNA of tetracistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, 2S rRNA, LSU-rRNA)","termid":"GO:0000485"}


id: PBO:0054622
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 2027","termid":"PBO:0054622"}


id: PBO:0031770
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_fermentation","termid":"PBO:0031770"}


id: MONDO:0011688
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A congenital muscular dystrophy characterized by autosomal recessive inheritance of muscular dystrophy with variable penetrance of intellectual disability and structural brain abnormalities that has material basis in homozygous or compound heterozygous mutation in the FKRP gene on chromosome 19q13.3.","definition_xrefs":["DOID:0110635","PMID:11592034","PMID:14652796"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscular dystrophy-dystroglycanopathy, type B","termid":"MONDO:0000172"},{"relation_name":"is_a","term_name":"myopathy caused by variation in FKRP","termid":"MONDO:0700066"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0024322","MONDO:0005066","MONDO:0005336"],"is_obsolete":false,"name":"muscular dystrophy-dystroglycanopathy type B5","secondary_identifiers":["MEDGEN:335764","MESH:C564691","Orphanet:52428","OMIM:606612","UMLS:C1847759"],"synonyms":[{"name":"FKRP-related congenital muscular dystrophy","type":"exact"},{"name":"MDC1C","type":"exact"},{"name":"MDDGB5","type":"exact"},{"name":"congenital muscular dystrophy 1C","type":"exact"},{"name":"congenital muscular dystrophy-FKRP related","type":"exact"},{"name":"muscular dystrophy, congenital, 1C","type":"related"},{"name":"muscular dystrophy, congenital, FKRP-related","type":"related"},{"name":"muscular dystrophy-dystroglycanopathy (congenital with or without intellectual disability), type B, 5","type":"exact"},{"name":"muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type B, 5","type":"exact"}],"termid":"MONDO:0011688","xrefs":{"Monarch":{"xref_id":"0011688"}}}


id: MONDO:0016947
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"partial duplication of chromosome 10","termid":"MONDO:0016931"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partial duplication of the short arm of chromosome 10","secondary_identifiers":["Orphanet:262776","UMLS:C5679712","icd11.foundation:1720386511","MEDGEN:1826038","GARD:20867"],"synonyms":[{"name":"partial duplication of chromosome 10p","type":"exact"},{"name":"partial trisomy of chromosome 10p","type":"exact"},{"name":"partial trisomy of the short arm of chromosome 10","type":"exact"}],"termid":"MONDO:0016947","xrefs":{"Monarch":{"xref_id":"0016947"}}}


id: PATO:0001303
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in a bearer by virtue of the bearer's disposition to varying or changing.","definition_xrefs":["Dictionary:http://dictionary.reference.com/"],"direct_ancestors":[{"relation_name":"is_a","term_name":"process quality","termid":"PATO:0001236"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"variability","synonyms":[{"name":"variability of a physical quality","type":"related"}],"termid":"PATO:0001303"}


id: PR:G2TRN7
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC212.06c gene.","definition_xrefs":["UniProtKB:G2TRN7","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":"RecQ DNA helicase-like protein C212.06c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC212.06c","synonyms":[{"name":"Spom972h-SPAC212.06c","type":"exact"}],"termid":"PR:G2TRN7"}


id: GO:0006273
data:
  {"annotated_genes":["SJAG_05232","SJAG_04190","SJAG_02294","SJAG_02690","SJAG_02818","SJAG_04183","SJAG_05197","SJAG_03495","SJAG_00618","SJAG_00814","SJAG_05239","SJAG_04877","SJAG_02199","SJAG_00198"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[96622],"is_not":false,"summary":null,"term":"GO:0006273"},{"annotations":[94431,108261,104095,102008,103403,117309],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903459"},{"annotations":[94253,91762,99796,99832,103329,100687,91851],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1903461"}]},"cv_name":"biological_process","definition":"The process in which an existing DNA strand is extended in a net 3' to 5' direction by activities including the addition of nucleotides to the 3' end of the strand, complementary to an existing template, as part of DNA replication. Lagging strand DNA elongation proceeds by discontinuous synthesis of short stretches of DNA, known as Okazaki fragments, from RNA primers; these fragments are then joined by DNA ligase. Although each segment of nascent DNA is synthesized in the 5' to 3' direction, the overall direction of lagging strand synthesis is 3' to 5', mirroring the progress of the replication fork.","definition_xrefs":["GOC:mah","ISBN:071673706X","ISBN:0815316194"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA strand elongation involved in DNA replication","termid":"GO:0006271"}],"gene_count":14,"genes_by_uniquename":{"SJAG_00198":null,"SJAG_00618":null,"SJAG_00814":null,"SJAG_02199":null,"SJAG_02294":null,"SJAG_02690":null,"SJAG_02818":null,"SJAG_03495":null,"SJAG_04183":null,"SJAG_04190":null,"SJAG_04877":null,"SJAG_05197":null,"SJAG_05232":null,"SJAG_05239":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006260"},{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006259","GO:0006260","GO:0008150"],"is_obsolete":false,"name":"lagging strand elongation","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0006273","terms_by_termid":{"GO:0006273":null,"GO:1903459":null,"GO:1903461":null}}


id: GO:0047299
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: keto-phenylpyruvate + L-tryptophan = 3-(indol-3-yl)pyruvate + L-phenylalanine.","definition_xrefs":["EC:2.6.1.28","RHEA:13741"],"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:0003674"},{"rel_name":"is_a","termid":"GO:0016769"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016769","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"tryptophan-phenylpyruvate transaminase activity","secondary_identifiers":["MetaCyc:2.6.1.28-RXN","KEGG_REACTION:R01376"],"synonyms":[{"name":"L-tryptophan-alpha-ketoisocaproate aminotransferase activity","type":"related"},{"name":"L-tryptophan:phenylpyruvate aminotransferase activity","type":"related"},{"name":"tryptophan--phenylpyruvate aminotransferase activity","type":"related"},{"name":"tryptophan-phenylpyruvate aminotransferase activity","type":"exact"}],"termid":"GO:0047299"}


id: GO:0032808
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the lacrimal gland over time, from its formation to the mature structure. The lacrimal gland produces secretions that lubricate and protect the cornea of the eye.","definition_xrefs":["GOC:ln"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gland development","termid":"GO:0048732"},{"relation_name":"part_of","term_name":"exocrine system development","termid":"GO:0035272"}],"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":"lacrimal gland development","termid":"GO:0032808"}


id: GO:0034685
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An integrin complex that comprises one alphav subunit and one beta6 subunit.","definition_xrefs":["PMID:12297042"],"direct_ancestors":[{"relation_name":"is_a","term_name":"integrin complex","termid":"GO:0008305"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005886","GO:0005575"],"is_obsolete":false,"name":"integrin alphav-beta6 complex","synonyms":[{"name":"ITGAV-ITGB6 complex","type":"narrow"},{"name":"alphav-beta6 integrin complex","type":"exact"}],"termid":"GO:0034685"}


id: MONDO:0013469
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any retinitis pigmentosa in which the cause of the disease is a mutation in the MERTK gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinitis pigmentosa","termid":"MONDO:0019200"},{"relation_name":"is_a","term_name":"MERTK-related retinopathy","termid":"MONDO:0800394"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0004736"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0004736","MONDO:0005066"],"is_obsolete":false,"name":"retinitis pigmentosa 38","secondary_identifiers":["UMLS:C3151228","GARD:15725","ICD10CM:H35.5","DOID:0110367","MEDGEN:462578","OMIM:613862"],"synonyms":[{"name":"MERTK retinitis pigmentosa","type":"exact"},{"name":"RP38","type":"exact"},{"name":"Rod-cone dystrophy, childhood-onset","type":"related"},{"name":"retinitis pigmentosa 38","type":"exact"},{"name":"retinitis pigmentosa caused by mutation in MERTK","type":"exact"},{"name":"retinitis pigmentosa type 38","type":"exact"}],"termid":"MONDO:0013469","xrefs":{"Monarch":{"xref_id":"0013469"}}}


id: MONDO:0010411
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited hypertrophic pyloric stenosis","termid":"MONDO:0100239"}],"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":"pyloric stenosis, infantile hypertrophic, 4","secondary_identifiers":["OMIM:300711","UMLS:C2678037","MEDGEN:395521","MESH:C567472"],"synonyms":[{"name":"IHPS4","type":"exact"},{"name":"pyloric stenosis, infantile hypertrophic, 4","type":"exact"}],"termid":"MONDO:0010411","xrefs":{"Monarch":{"xref_id":"0010411"}}}


id: MONDO:0009526
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","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":"fibular aplasia, tibial campomelia, and oligosyndactyly syndrome","secondary_identifiers":["UMLS:C1855499","Orphanet:480773","MEDGEN:340887","GARD:2622","MESH:C565436","OMIM:246570"],"synonyms":[{"name":"FATCO syndrome","type":"exact"},{"name":"fibular aplasia, tibial campomelia, and oligosyndactyly syndrome","type":"exact"},{"name":"fibular aplasia-tibial campomelia-oligosyndactyly syndrome","type":"exact"},{"name":"limb deficiency-heart malformation syndrome","type":"related"},{"name":"terminal transverse defects of the limbs associated with congenital heart malformations","type":"exact"}],"termid":"MONDO:0009526","xrefs":{"Monarch":{"xref_id":"0009526"}}}


id: MONDO:0020701
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"brachydactyly","termid":"MONDO:0021004"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"brachydactyly type A1A","synonyms":[{"name":"BDA1","type":"related"},{"name":"BRACHYDACTYLY, type A1","type":"related"},{"name":"Farabee-type Brachydactyly","type":"related"}],"termid":"MONDO:0020701","xrefs":{"Monarch":{"xref_id":"0020701"}}}


id: GO:0060329
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The actin filament-based movement by which cytoplasmic actin filaments slide past one another resulting in a contraction that propels the cell in the direction that has been defined as the rear of the cell.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoplasmic actin-based contraction involved in cell motility","termid":"GO:0060327"}],"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":"cytoplasmic actin-based contraction involved in rearward cell motility","synonyms":[{"name":"cytoplasmic actin-based contraction involved in rearward cell locomotion","type":"related"}],"termid":"GO:0060329"}


id: PBO:0088183
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Zinc cluster transcription factor that regulates respiratory growth; binds to promoters of genes involved in respiration, gluconeogenesis, and the glyoxylate shunt; required for normal carbon source utilization and adaptation to pH, osmotic and ethanol stress especially during non-fermentative metabolism","termid":"PBO:0088183"}


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


id: PBO:0064445
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"POC1B-GALNT4 readthrough","termid":"PBO:0064445"}


id: PBO:0086386
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative calcium channel involved in calcium release under hypotonic stress; required for uptake of FAD into endoplasmic reticulum; involved in cell wall maintenance; FLC2 has a paralog, YOR365C, that arose from the whole genome duplication","termid":"PBO:0086386"}


id: PBO:0071726
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L39 pseudogene 24","termid":"PBO:0071726"}


id: PBO:0082508
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Catalytic subunit of protein phosphatase 2A, PP2A; functionally redundant with Pph22p; C-terminally methylated; forms alternate complexes with several regulatory subunits; involved in signal transduction and regulation of mitosis; forms nuclear foci upon DNA replication stress; PPH21 has a paralog, PPH22, that arose from the whole genome duplication","termid":"PBO:0082508"}


id: GO:0039661
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The outer, i.e. cytoplasm-facing in a cellular organelle, lipid bilayer of an organelle envelope, occurring in a host cell.","definition_xrefs":["GOC:bf","GOC:ch"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host outer membrane","termid":"GO:0044384"}],"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 organelle outer membrane","termid":"GO:0039661"}


id: GO:0046867
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of carotenoids into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. Carotenoids are tetraterpenoid compounds in which two units of 4 isoprenoid residues joined head-to-tail are themselves joined tail-to-tail.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tetraterpenoid transport","termid":"GO:0046866"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"carotenoid transport","termid":"GO:0046867"}


id: GO:0030730
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of binding or confining any triester of glycerol such that it is separated from other components of a biological system.","definition_xrefs":["GOC:mah","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipid storage","termid":"GO:0019915"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"triglyceride storage","synonyms":[{"name":"retention of triacylglycerol","type":"exact"},{"name":"retention of triglyceride","type":"exact"},{"name":"sequestering of triacylglycerol","type":"exact"},{"name":"sequestering of triglyceride","type":"exact"},{"name":"sequestration of triacylglycerol","type":"exact"},{"name":"sequestration of triglyceride","type":"exact"},{"name":"storage of triacylglycerol","type":"exact"},{"name":"storage of triglyceride","type":"exact"},{"name":"triacylglycerol retention","type":"exact"},{"name":"triacylglycerol sequestering","type":"exact"},{"name":"triacylglycerol sequestration","type":"exact"},{"name":"triacylglycerol storage","type":"exact"},{"name":"triglyceride retention","type":"exact"},{"name":"triglyceride sequestering","type":"exact"},{"name":"triglyceride sequestration","type":"exact"}],"termid":"GO:0030730"}


id: PBO:0028582
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-RNA_absent_from_cell_during_cellular_response_to_salt_stress","termid":"PBO:0028582"}


id: MONDO:0017418
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chronic intestinal failure (CIF) is a chronic type of intestinal failure characterized by a nonfunctioning small bowel (that may be reversible or irreversal) where the body is unable to maintain energy and nutritional needs through absorption of food or nutrients via the intestinal tract (despite being metabolically stable) and which therefore necessitates long-term parenteral feeding. CIF may be the result of congenital digestive diseases (such as gastroschisis, atresia of small intestine), short bowel syndrome, intra-abdominal or pelvic cancer, or progressive and devastating gastrointestinal or systemic benign diseases (such as Crohn disease).","definition_xrefs":["Orphanet:294422"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intestinal disorder","termid":"MONDO:0005020"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"chronic intestinal failure","secondary_identifiers":["MEDGEN:909276","UMLS:C4274352","GARD:21178","SCTID:716665002"],"synonyms":[{"name":"CIF","type":"exact"}],"termid":"MONDO:0017418","xrefs":{"Monarch":{"xref_id":"0017418"}}}


id: PBO:0088472
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein N-terminal glutamine amidohydrolase, alpha beta roll superfamily","termid":"PBO:0088472"}


id: FYPO:0002307
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which occurrence of 5-phosphoribose 1-diphosphate binding by a gene product (usually a protein) in a mutant is increased. The affected gene product may be encoded by the mutated gene, or by a different gene.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal 5-phosphoribose 1-diphosphate binding","termid":"FYPO:0002306"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0000652","FYPO:0001985"],"is_obsolete":false,"name":"increased 5-phosphoribose 1-diphosphate binding","synonyms":[{"name":"increased 5-O-phosphono-alpha-D-ribofuranosyl diphosphate binding","type":"exact"},{"name":"increased phosphoribosylpyrophosphate binding","type":"exact"}],"termid":"FYPO:0002307"}


id: PBO:0071990
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S6 pseudogene 19","termid":"PBO:0071990"}


id: GO:0032448
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a DNA region containing a hairpin. A hairpin structure forms when a DNA strand folds back on itself and intrachain base pairing occurs between inverted repeat sequences.","definition_xrefs":["GOC:mah","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA secondary structure binding","termid":"GO:0000217"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003677"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003677","GO:0003674"],"is_obsolete":false,"name":"DNA hairpin binding","termid":"GO:0032448"}


id: PBO:0012292
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FACT complex subunit Pob3","termid":"PBO:0012292"}


id: MONDO:0021836
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A syndrome characterized by a malformations of the neck due to a branchial arch defect. In the neonatal period the following signs were noted: symmetrical preauricular pits, retroauricular additional rudimentary auricles, a blindly ending coccygeal groove, microstomia and papillomata of the hypopharynx. This is an n-of-1 use case where only one patient or family has been described with this disorder.","definition_xrefs":["PMID:6468450"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Aksu von Stockhausen syndrome","secondary_identifiers":["MEDGEN:419676","UMLS:C2930949","MESH:C535611"],"synonyms":[{"name":"aksu von stockhausen syndrome","type":"exact"},{"name":"hereditary branchial arch defects","type":"related"}],"termid":"MONDO:0021836","xrefs":{"Monarch":{"xref_id":"0021836"}}}


id: GO:0050501
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-D-glucuronate + UDP-N-acetyl-D-glucosamine = [beta-N-acetyl-D-glucosaminyl-(1->4)-beta-D-glucuronosyl-(1->3)](n) + 2n UDP.","definition_xrefs":["EC:2.4.1.212","MetaCyc:2.4.1.212-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glycosyltransferase activity","termid":"GO:0008194"},{"relation_name":"is_a","term_name":"hexosyltransferase activity","termid":"GO:0016758"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016740","GO:0003824","GO:0016757","GO:0003674"],"is_obsolete":false,"name":"hyaluronan synthase activity","secondary_identifiers":["Reactome:R-HSA-2160851","RHEA:12528"],"synonyms":[{"name":"HAS activity","type":"broad"},{"name":"alternating UDP-alpha-N-acetyl-D-glucosamine:beta-D-glucuronosyl-(1,3)-[nascent hyaluronan] 4-N-acetyl-beta-D-glucosaminyltransferase and UDP-alpha-D-glucuronate:N-acetyl-beta-D-glucosaminyl-(1,4)-[nascent hyaluronan] 3-beta-D-glucuronosyltransferase activity","type":"related"},{"name":"alternating UDP-alpha-N-acetyl-D-glucosamine:beta-D-glucuronosyl-(1->3)-[nascent hyaluronan] 4-N-acetyl-beta-D-glucosaminyltransferase and UDP-alpha-D-glucuronate:N-acetyl-beta-D-glucosaminyl-(1->4)-[nascent hyaluronan] 3-beta-D-glucuronosyltransferase activity","type":"related"},{"name":"seHAS","type":"related"},{"name":"spHAS","type":"related"}],"termid":"GO:0050501"}


id: PBO:0084807
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial protein of unknown function; green fluorescent protein (GFP)-fusion protein localizes to mitochondria; YLR281C is not an essential gene","termid":"PBO:0084807"}


id: GO:0015087
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of cobalt (Co2+) ions from one side of a membrane to the other.","definition_xrefs":["GOC:dgf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transition metal ion transmembrane transporter activity","termid":"GO:0046915"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0003674","GO:0022857","GO:0005215"],"is_obsolete":false,"name":"cobalt ion transmembrane transporter activity","secondary_identifiers":["MetaCyc:TRANS-RXN-141A"],"synonyms":[{"name":"cobalt, zinc uptake permease activity","type":"related"},{"name":"zinc, cadmium, cobalt, nickel, lead-efflux ATPase activity","type":"related"}],"termid":"GO:0015087"}


id: PBO:0082168
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AdoMet-dependent methyltransferase; involved in a novel 3-methylhistidine modification of multiple proteins, including ribosomal protein Rpl3p; seven beta-strand MTase family member; null mutant exhibits a weak vacuolar protein sorting defect and caspofungin resistance","termid":"PBO:0082168"}


id: PBO:0090304
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chaperone activator Sti1","termid":"PBO:0090304"}


id: PBO:0043886
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cAMP responsive element modulator","termid":"PBO:0043886"}


id: GO:0003861
data:
  {"annotated_genes":["SJAG_03243"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[100012],"is_not":false,"summary":null,"term":"GO:0003861"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: (2R,3S)-3-isopropylmalate = (2S)-2-isopropylmalate.","definition_xrefs":["EC:4.2.1.33"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydro-lyase activity","termid":"GO:0016836"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03243":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:0016829"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016829"],"is_obsolete":false,"name":"3-isopropylmalate dehydratase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["RHEA:32287","MetaCyc:3-ISOPROPYLMALISOM-RXN"],"synonyms":[{"name":"(2R,3S)-3-isopropylmalate hydro-lyase (2-isopropylmaleate-forming)","type":"related"},{"name":"(2R,3S)-3-isopropylmalate hydro-lyase activity","type":"related"},{"name":"alpha-IPM isomerase activity","type":"related"},{"name":"alpha-isopropylmalate isomerase activity","type":"related"},{"name":"beta-isopropylmalate dehydratase activity","type":"related"},{"name":"isopropylmalate isomerase activity","type":"related"}],"termid":"GO:0003861","terms_by_termid":{"GO:0003861":null}}


id: MONDO:0003080
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete indolent systemic mastocytosis (obsolete MONDO:0003080)","termid":"MONDO:0003080","xrefs":{"Monarch":{"xref_id":"0003080"}}}


id: PBO:0084804
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial protein of unknown function; GFP-fusion protein is induced in response to the DNA-damaging agent MMS; the authentic, non-tagged protein is detected in highly purified mitochondria in high-throughput studies; protein abundance increases in response to DNA replication stress","termid":"PBO:0084804"}


id: GO:0044706
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A multicellular organism process which involves another multicellular organism of the same or different species.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multicellular organismal process","termid":"GO:0032501"}],"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":"multi-multicellular organism process","termid":"GO:0044706"}


id: GO:0071220
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a bacterial lipoprotein stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to bacterial lipoprotein","termid":"GO:0032493"},{"relation_name":"is_a","term_name":"cellular response to molecule of bacterial origin","termid":"GO:0071219"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to bacterial lipoprotein","termid":"GO:0071220"}


id: FYPO:0004464
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the phosphorylation of one or more specific proteins, or of specific protein sites, occurs to a lower extent than normal during a cellular response to camptothecin.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein phosphorylation during vegetative growth","termid":"FYPO:0001838"}],"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:0001985"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002274"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0005447","FYPO:0002494","FYPO:0000002","FYPO:0002274"],"is_obsolete":false,"name":"decreased protein phosphorylation during cellular response to camptothecin","synonyms":[{"name":"decreased protein phosphorylation during cellular response to CPT","type":"exact"},{"name":"decreased protein phosphorylation during cellular response to camptothecin during mitotic cell cycle","type":"related"},{"name":"decreased protein phosphorylation during cellular response to camptothecin during vegetative growth","type":"exact"},{"name":"reduced protein phosphorylation during cellular response to camptothecin","type":"exact"}],"termid":"FYPO:0004464"}


id: GO:1900159
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of bone mineralization involved in bone maturation.","definition_xrefs":["GOC:BHF","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of bone mineralization","termid":"GO:0030501"},{"relation_name":"is_a","term_name":"regulation of bone mineralization involved in bone maturation","termid":"GO:1900157"},{"relation_name":"positively_regulates","term_name":"bone mineralization involved in bone maturation","termid":"GO:0035630"}],"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 bone mineralization involved in bone maturation","synonyms":[{"name":"activation of bone mineralization involved in bone maturation","type":"narrow"},{"name":"up regulation of bone mineralization involved in bone maturation","type":"exact"},{"name":"up-regulation of bone mineralization involved in bone maturation","type":"exact"},{"name":"upregulation of bone mineralization involved in bone maturation","type":"exact"}],"termid":"GO:1900159"}


id: GO:1901481
data:
  {"annotated_genes":["SJAG_03256"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[103010],"is_not":false,"summary":null,"term":"GO:1901481"}]},"cv_name":"biological_process","definition":"Any L-glutamate import that is involved in cellular response to nitrogen starvation.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-glutamate import","termid":"GO:0051938"},{"relation_name":"part_of","term_name":"cellular response to nitrogen starvation","termid":"GO:0006995"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03256":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"L-glutamate import involved in cellular response to nitrogen starvation","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"L-glutamate uptake involved in cellular response to nitrogen starvation","type":"exact"}],"termid":"GO:1901481","terms_by_termid":{"GO:1901481":null}}


id: PBO:0067161
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 214, pseudogene","termid":"PBO:0067161"}


id: PBO:0001905
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rRNA processing protein Fcf2 (predicted)","termid":"PBO:0001905"}


id: MONDO:0018443
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome","secondary_identifiers":["Orphanet:404451","GARD:21717","MEDGEN:1650412","UMLS:C4751506"],"termid":"MONDO:0018443","xrefs":{"Monarch":{"xref_id":"0018443"}}}


id: PBO:0087728
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the Set3 complex; complex is a meiotic-specific repressor of sporulation specific genes that contains deacetylase activity; potential Cdc28p substrate","termid":"PBO:0087728"}


id: GO:0042842
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of D-xylose, a naturally occurring plant polysaccharide.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pentose biosynthetic process","termid":"GO:0019322"},{"relation_name":"is_a","term_name":"D-xylose metabolic process","termid":"GO:0042732"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0005975","GO:0008150"],"is_obsolete":false,"name":"D-xylose biosynthetic process","synonyms":[{"name":"D-xylose anabolism","type":"exact"},{"name":"D-xylose biosynthesis","type":"exact"},{"name":"D-xylose formation","type":"exact"},{"name":"D-xylose synthesis","type":"exact"}],"termid":"GO:0042842"}


id: PBO:0027401
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_triglyceride_biosynthetic_process","termid":"PBO:0027401"}


id: PR:G2TRU0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ost5 gene.","definition_xrefs":["PRO:DNx","UniProtKB:G2TRU0"],"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":"dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit ost5 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC18.19c","synonyms":[{"name":"Spom972h-ost5","type":"exact"},{"name":"oligosaccharyl transferase subunit ost5 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"oligosaccharyl transferase subunit zeta (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:G2TRU0"}


id: PBO:0083402
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 3' end of essential gene CDC13","termid":"PBO:0083402"}


id: PBO:0057676
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1267","termid":"PBO:0057676"}


id: PBO:0045822
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 12","termid":"PBO:0045822"}


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


id: MONDO:0016366
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Maternal phenylketonuria (PKU) is a rare disorder of phenylalanine metabolism, an inborn error of amino acid metabolism, characterized by the development of microcephaly, growth retardation, congenital heart disease, facial dysmorphism and intellectual disability in nonphenylketonuric offspring of mothers with excess phenylalanine (Phe) concentrations.","definition_xrefs":["Orphanet:2209"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenylketonuria","termid":"MONDO:0009861"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0004736"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0004736","MONDO:0005066"],"is_obsolete":false,"name":"maternal phenylketonuria","secondary_identifiers":["icd11.foundation:1509230254","MESH:D017042","GARD:3413","UMLS:C0085547","MEDGEN:88435"],"synonyms":[{"name":"hyperphenylalaninemic embryopathy","type":"exact"},{"name":"maternal PKU","type":"exact"},{"name":"maternal hyperphenylalaninemia","type":"exact"},{"name":"phenylketonuric embryopathy","type":"exact"}],"termid":"MONDO:0016366","xrefs":{"Monarch":{"xref_id":"0016366"}}}


id: GO:0072484
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of events in which information about spindle assembly is received and converted into a molecular signal, contributing to a spindle assembly checkpoint.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete detection of stimulus involved in spindle assembly checkpoint (obsolete GO:0072484)","synonyms":[{"name":"sensing involved in spindle assembly checkpoint","type":"related"},{"name":"spindle assembly checkpoint sensor mechanism","type":"related"},{"name":"spindle assembly checkpoint sensor process","type":"related"}],"termid":"GO:0072484"}


id: GO:1902169
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a catechin stimulus.","definition_xrefs":["GOC:TermGenie","GOC:rjd","PMID:23516620"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to catechin","termid":"GO:1902168"},{"relation_name":"is_a","term_name":"cellular response to flavonoid","termid":"GO:1905396"},{"relation_name":"is_a","term_name":"cellular response to phenylpropanoid","termid":"GO:1905546"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to catechin","termid":"GO:1902169"}


id: GO:0016688
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-ascorbate + hydrogen peroxide = dehydroascorbate + 2 H2O.","definition_xrefs":["EC:1.11.1.11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peroxidase activity","termid":"GO:0004601"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"L-ascorbate peroxidase activity","secondary_identifiers":["MetaCyc:RXN-12440","RHEA:22996"],"synonyms":[{"name":"L-ascorbate:hydrogen-peroxide oxidoreductase activity","type":"related"},{"name":"L-ascorbic acid peroxidase activity","type":"related"},{"name":"L-ascorbic acid-specific peroxidase activity","type":"related"},{"name":"ascorbate peroxidase activity","type":"related"},{"name":"ascorbic acid peroxidase activity","type":"related"}],"termid":"GO:0016688"}


id: PBO:0025510
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"galactosemia","termid":"PBO:0025510"}


id: PBO:0075307
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"suppressor of cytokine signaling 4","termid":"PBO:0075307"}


id: MONDO:0003572
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A nonkeratinizing carcinoma which occurs predominantly in the nasopharynx but also in the tonsils and rarely in other anatomic sites. It is characterized by the presence of large malignant cells with vesicular nuclei, prominent nucleoli, syncytial growth pattern, and a lymphoplasmacytic infiltrate.","definition_xrefs":["NCIT:C4107"],"direct_ancestors":[{"relation_name":"is_a","term_name":"large cell carcinoma","termid":"MONDO:0005232"}],"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":"nasopharyngeal type undifferentiated carcinoma","secondary_identifiers":["UMLS:C0334254","DOID:5660","ICDO:8082/3","MEDGEN:87199"],"synonyms":[{"name":"Schmincke tumor","type":"exact"},{"name":"Schmincke tumour","type":"exact"},{"name":"Schminke tumor","type":"exact"},{"name":"Schminke tumour","type":"exact"},{"name":"lymphoepithelial carcinoma","type":"exact"},{"name":"lymphoepithelioma","type":"exact"},{"name":"lymphoepithelioma-like carcinoma","type":"exact"},{"name":"nasopharyngeal type undifferentiated carcinoma","type":"exact"}],"termid":"MONDO:0003572","xrefs":{"Monarch":{"xref_id":"0003572"}}}


id: GO:0016338
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The attachment of one cell to another cell via adhesion molecules that do not require the presence of calcium for the interaction.","definition_xrefs":["GOC:hb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-cell adhesion via plasma-membrane adhesion molecules","termid":"GO:0098742"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"calcium-independent cell-cell adhesion via plasma membrane cell-adhesion molecules","synonyms":[{"name":"calcium-independent cell adhesion molecule activity","type":"related"}],"termid":"GO:0016338"}


id: GO:1990730
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex between the ATPase VCP (p97) and its cofactor p47 (NSFL1C). In human, the protein complex consists of one homotrimer of NSFL1C/p47 per homohexamer of VCP/p97.","definition_xrefs":["GOC:bf","GOC:PARL","PMID:9214505"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"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:0032991"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"VCP-NSFL1C complex","synonyms":[{"name":"p97-p47 complex","type":"exact"}],"termid":"GO:1990730"}


id: PBO:0066145
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RBBP4 pseudogene 1","termid":"PBO:0066145"}


id: GO:0050325
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + NAD+ + tauropine = H+ + NADH + pyruvate + taurine.","definition_xrefs":["RHEA:12580","EC:1.5.1.23"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-NH group of donors, NAD or NADP as acceptor","termid":"GO:0016646"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"tauropine dehydrogenase activity","secondary_identifiers":["MetaCyc:TAUROPINE-DEHYDROGENASE-RXN","KEGG_REACTION:R01683"],"synonyms":[{"name":"2-N-(D-1-carboxyethyl)taurine:NAD+ oxidoreductase (taurine-forming)","type":"related"},{"name":"N2-(D-1-carboxyethyl)taurine:NAD+ oxidoreductase (taurine-forming)","type":"related"}],"termid":"GO:0050325"}


id: GO:1905840
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of telomeric D-loop disassembly.","definition_xrefs":["PMID:15200954","GOC:nc","GOC:BHF_telomere","GOC:TermGenie","GOC:BHF","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of telomeric loop disassembly","termid":"GO:1904535"},{"relation_name":"is_a","term_name":"regulation of telomeric D-loop disassembly","termid":"GO:1905838"},{"relation_name":"positively_regulates","term_name":"telomeric D-loop disassembly","termid":"GO:0061820"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006259"},{"rel_name":"positively_regulates","termid":"GO:0032200"},{"rel_name":"regulates","termid":"GO:0032200"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006259","GO:0032200","GO:0008150"],"is_obsolete":false,"name":"positive regulation of telomeric D-loop disassembly","synonyms":[{"name":"activation of telomeric D-loop disassembly","type":"narrow"},{"name":"up regulation of telomeric D-loop disassembly","type":"exact"},{"name":"up-regulation of telomeric D-loop disassembly","type":"exact"},{"name":"upregulation of telomeric D-loop disassembly","type":"exact"}],"termid":"GO:1905840"}


id: PR:O59738
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC530.02 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O59738"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized transporter C530.02 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC530.02","synonyms":[{"name":"Spom972h-SPBC530.02","type":"exact"}],"termid":"PR:O59738"}


id: GO:0009047
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 hyperactivation of all, or most of, the genes on the X-chromosome in the heterogametic sex, leading to a two-fold increase in gene expression from this chromosome. An example of this is found in Drosophila melanogaster.","definition_xrefs":["PMID:11498577","GOC:mr","GOC:jl","PMID:1568251"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sex-chromosome dosage compensation","termid":"GO:0007549"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006325"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0006325","GO:0010467","GO:0008150"],"is_obsolete":false,"name":"dosage compensation by hyperactivation of X chromosome","secondary_identifiers":["Wikipedia:XY_sex-determination_system"],"termid":"GO:0009047"}


id: PBO:0053600
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 629","termid":"PBO:0053600"}


id: GO:0004217
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the hydrolysis of peptide bonds. Specificity close to that of papain. As compared to cathepsin B, cathepsin L exhibits higher activity towards protein substrates, but has little activity on Z-Arg-Arg-NHMec, and no peptidyl-dipeptidase activity.","definition_xrefs":["EC:3.4.22.15"],"gene_count":0,"genotype_count":0,"name":"obsolete cathepsin L activity (obsolete GO:0004217)","synonyms":[{"name":"Aldrichina grahami cysteine proteinase","type":"narrow"},{"name":"cathepsin L activity","type":"exact"}],"termid":"GO:0004217"}


id: PBO:0083562
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 VID21/YDR359C","termid":"PBO:0083562"}


id: PBO:0088945
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclophilin-type peptidyl-prolyl cis-trans isomerase","termid":"PBO:0088945"}


id: GO:0035072
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process induced by ecdysone that directly activates salivary gland programmed cell death during salivary gland histolysis.","definition_xrefs":["GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete ecdysone-mediated induction of salivary gland cell autophagic cell death (obsolete GO:0035072)","termid":"GO:0035072"}


id: SO:0000204
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region at the 5' end of a mature transcript (preceding the initiation codon) that is not translated into a protein.","direct_ancestors":[{"relation_name":"is_a","term_name":"UTR","termid":"SO:0000203"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"five_prime_UTR","secondary_identifiers":["http://en.wikipedia.org/wiki/5'_UTR"],"synonyms":[{"name":"5' UTR","type":"exact"},{"name":"INSDC_feature:5'UTR","type":"exact"},{"name":"five prime UTR","type":"exact"},{"name":"five_prime_untranslated_region","type":"exact"}],"termid":"SO:0000204"}


id: PR:Q9UUB0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mrps17 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9UUB0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"37S ribosomal protein S17, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC409.14c","synonyms":[{"name":"Spom972h-mrps17","type":"exact"}],"termid":"PR:Q9UUB0"}


id: PBO:0029706
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_elongated_mononucleate_vegetative_cell_with_mislocalized_septum","termid":"PBO:0029706"}


id: PBO:0048977
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G-patch domain containing 1","termid":"PBO:0048977"}


id: PBO:0049364
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"general transcription factor IIi pseudogene 23","termid":"PBO:0049364"}


id: MONDO:0014310
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hereditary fibrosing poikiloderma-tendon contractures-myopathy-pulmonary fibrosis syndrome is a rare, genetic, hereditary poikiloderma syndrome characterized by early-onset poikiloderma (mainly on the face), hypotrichosis, hypohidrosis, muscle and tendon contractures with varus foot deformity, progressive proximal and distal muscle weakness in all extremities, and progressive pulmonary fibrosis. Mild lymphedema of the extremities, growth retardation, liver impairment, exocrine pancreatic insufficiency and hematologic abnormalities are additional variable features.","definition_xrefs":["Orphanet:221043"],"direct_ancestors":[{"relation_name":"is_a","term_name":"respiratory system disorder","termid":"MONDO:0005087"},{"relation_name":"is_a","term_name":"hereditary poikiloderma","termid":"MONDO:0016382"},{"relation_name":"is_a","term_name":"hereditary skin disorder","termid":"MONDO:0100118"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"hereditary sclerosing poikiloderma with tendon and pulmonary involvement","secondary_identifiers":["OMIM:615704","GARD:13218","MEDGEN:816655","icd11.foundation:1585528459","UMLS:C3810325"],"synonyms":[{"name":"POIKTMP","type":"related"},{"name":"POIKTMP syndrome","type":"exact"},{"name":"hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis","type":"related"},{"name":"hereditary fibrosing poikiloderma-tendon contractures-myopathy-pulmonary fibrosis syndrome","type":"related"},{"name":"poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis","type":"related"},{"name":"poikiloderma, hereditary sclerosing, with tendon and pulmonary involvement","type":"related"}],"termid":"MONDO:0014310","xrefs":{"Monarch":{"xref_id":"0014310"}}}


id: GO:0019129
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The racemization of peptidyl-leucine.","definition_xrefs":["RESID:AA0197"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-leucine racemization (obsolete GO:0019129)","termid":"GO:0019129"}


id: PBO:0087819
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TFIID subunit (40 kDa); involved in RNA polymerase II transcription initiation, similar to histone H3 with atypical histone fold motif of Spt3-like transcription factors","termid":"PBO:0087819"}


id: PBO:0090984
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP-dependent RNA helicase Rrp3","termid":"PBO:0090984"}


id: GO:0070453
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of heme.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of tetrapyrrole biosynthetic process","termid":"GO:1901463"},{"relation_name":"regulates","term_name":"heme biosynthetic process","termid":"GO:0006783"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0033013"}],"interesting_parent_ids":["GO:0008150","GO:0033013"],"is_obsolete":false,"name":"regulation of heme biosynthetic process","synonyms":[{"name":"regulation of haem biosynthesis","type":"exact"},{"name":"regulation of haem biosynthetic process","type":"exact"},{"name":"regulation of heme anabolism","type":"exact"},{"name":"regulation of heme biosynthesis","type":"exact"},{"name":"regulation of heme formation","type":"exact"},{"name":"regulation of heme synthesis","type":"exact"}],"termid":"GO:0070453"}


id: MONDO:0014050
data:
  {"annotated_genes":["SJAG_03786"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84337],"is_not":false,"summary":null,"term":"MONDO:0014050"}]},"cv_name":"mondo","definition":"Any isolated microphthalmia in which the cause of the disease is a mutation in the ALDH1A3 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isolated microphthalmia","termid":"MONDO:0000062"},{"relation_name":"is_a","term_name":"isolated anophthalmia-microphthalmia syndrome","termid":"MONDO:0016764"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03786":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"isolated microphthalmia 8","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0060841","OMIM:615113","MEDGEN:767438","UMLS:C3554524"],"synonyms":[{"name":"ALDH1A3 isolated microphthalmia","type":"exact"},{"name":"MCOP8","type":"exact"},{"name":"isolated microphthalmia 8","type":"exact"},{"name":"isolated microphthalmia caused by mutation in ALDH1A3","type":"exact"},{"name":"isolated microphthalmia type 8","type":"exact"},{"name":"microphthalmia, isolated 8","type":"related"},{"name":"microphthalmia, isolated type 8","type":"exact"}],"termid":"MONDO:0014050","terms_by_termid":{"MONDO:0014050":null},"xrefs":{"Monarch":{"xref_id":"0014050"}}}


id: PBO:0071202
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23a pseudogene 43","termid":"PBO:0071202"}


id: PBO:0069634
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 911, pseudogene","termid":"PBO:0069634"}


id: MONDO:0033615
data:
  {"annotated_genes":["SJAG_01043"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85097],"is_not":false,"summary":null,"term":"MONDO:0033615"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"coenzyme Q10 deficiency","termid":"MONDO:0018151"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01043":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005066","MONDO:0005244"],"is_obsolete":false,"name":"coenzyme q10 deficiency, primary, 9","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0112138","UMLS:C5436638","OMIM:619028","MEDGEN:1740444","GARD:16403"],"synonyms":[{"name":"COQ10D9","type":"exact"}],"termid":"MONDO:0033615","terms_by_termid":{"MONDO:0033615":null},"xrefs":{"Monarch":{"xref_id":"0033615"}}}


id: PBO:0052324
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KIAA1522","termid":"PBO:0052324"}


id: MONDO:0018936
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare benign bone-forming neoplasm usually arising from the spine. It is a well-circumscribed lytic tumor that varies in size. The tumor is composed of woven bone trabeculae and shares similar histologic characteristics with the osteoid osteoma. Surgical curettage is the treatment of choice. The prognosis is excellent.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bone benign neoplasm","termid":"MONDO:0000631"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"osteoblastoma","secondary_identifiers":["icd11.foundation:1948326341","MESH:D018215","ICD10CM:D16.5","ICDO:9200/0","GARD:18854","MedDRA:10004430","DOID:0060098","NCIT:C3294","Orphanet:58040","UMLS:C0029417","HP:0011846","MEDGEN:18212"],"synonyms":[{"name":"giant osteoid osteoma","type":"exact"},{"name":"ossifying giant cell tumor","type":"exact"},{"name":"ossifying giant cell tumour","type":"exact"},{"name":"osteoblastoma","type":"exact"},{"name":"osteoblastoma (disease)","type":"exact"},{"name":"osteoblastoma, benign","type":"exact"}],"termid":"MONDO:0018936","xrefs":{"Monarch":{"xref_id":"0018936"}}}


id: PBO:0079477
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TWSG1 divergent transcript","termid":"PBO:0079477"}


id: GO:0097488
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The lipid bilayer surrounding a multivesicular body internal vesicle.","definition_xrefs":["PMID:21183070","GOC:pde"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoplasmic vesicle membrane","termid":"GO:0030659"},{"relation_name":"is_a","term_name":"bounding membrane of organelle","termid":"GO:0098588"},{"relation_name":"part_of","term_name":"multivesicular body, internal vesicle","termid":"GO:0097487"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005768"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0031410"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005737","GO:0005768","GO:0005575","GO:0031410"],"is_obsolete":false,"name":"multivesicular body, internal vesicle membrane","termid":"GO:0097488"}


id: GO:0061979
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of femoral head articular cartilage over time, from its formation to the mature structure.","definition_xrefs":["PMID:20097540"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hip joint articular cartilage development","termid":"GO:0061977"}],"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":"femoral head articular cartilage development","termid":"GO:0061979"}


id: PBO:0001479
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"membrane anchored protein Mac1","termid":"PBO:0001479"}


id: PBO:0084450
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mannose-6-phosphate isomerase; catalyzes the interconversion of fructose-6-P and mannose-6-P; required for early steps in protein mannosylation","termid":"PBO:0084450"}


id: PBO:0070336
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNY4 pseudogene 8","termid":"PBO:0070336"}


id: PBO:0047007
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 90 member A10","termid":"PBO:0047007"}


id: PBO:0004612
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin C-terminal hydrolase Ubp3","termid":"PBO:0004612"}


id: PBO:0065815
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB4A, member RAS oncogene family","termid":"PBO:0065815"}


id: PR:P0CT56
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rps1401 gene.","definition_xrefs":["UniProtKB:P0CT56","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":"40S ribosomal protein S14-A (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC3H5.05c","synonyms":[{"name":"Spom972h-rps1401","type":"exact"}],"termid":"PR:P0CT56"}


id: MONDO:0003091
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A mucoepidermoid carcinoma that involves the zone of skin.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skin carcinoma","termid":"MONDO:0002656"},{"relation_name":"is_a","term_name":"mucoepidermoid carcinoma","termid":"MONDO:0003036"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005093"],"is_obsolete":false,"name":"cutaneous mucoepidermoid carcinoma","secondary_identifiers":["NCIT:C4472","SCTID:254713002","UMLS:C0346019","DOID:4683","MEDGEN:91072"],"synonyms":[{"name":"mucoepidermoid skin carcinoma","type":"exact"},{"name":"zone of skin mucoepidermoid carcinoma","type":"exact"}],"termid":"MONDO:0003091","xrefs":{"Monarch":{"xref_id":"0003091"}}}


id: PBO:0059570
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metallothionein 1 pseudogene 1","termid":"PBO:0059570"}


id: PBO:0065762
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyridine nucleotide-disulphide oxidoreductase domain 2","termid":"PBO:0065762"}


id: PBO:0013831
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"threonine ammonia-lyase","termid":"PBO:0013831"}


id: GO:0048521
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of behavior, the internally coordinated responses (actions or inactions) of whole living organisms (individuals or groups) to internal or external stimuli.","definition_xrefs":["GOC:jid","GOC:pr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of behavior","termid":"GO:0050795"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"negatively_regulates","term_name":"behavior","termid":"GO:0007610"}],"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 behavior","synonyms":[{"name":"down regulation of behavior","type":"exact"},{"name":"down-regulation of behavior","type":"exact"},{"name":"downregulation of behavior","type":"exact"},{"name":"inhibition of behavior","type":"narrow"}],"termid":"GO:0048521"}


id: FYPO:0000856
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which nucleosome positioning is normal (i.e. indistinguishable from wild type). Nucleosome positioning is the ordering of successions of nucleosomes into regular arrays so that nucleosomes are positioned at defined distances from one another.","definition_xrefs":["PomBase:mah","GO:0016584"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular process during vegetative growth","termid":"FYPO:0001319"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0000002","FYPO:0001320","FYPO:0000257"],"is_obsolete":false,"name":"normal nucleosome positioning","synonyms":[{"name":"normal nucleosome occupancy","type":"related"},{"name":"normal nucleosome positioning during mitotic cell cycle","type":"related"},{"name":"normal nucleosome positioning during vegetative growth","type":"exact"},{"name":"normal nucleosome spacing","type":"exact"}],"termid":"FYPO:0000856"}


id: PBO:0086201
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein that associates with mitochondrial ribosome; likely functions in cristae junction formation; the authentic, non-tagged protein is detected in highly purified mitochondria in high-throughput studies","termid":"PBO:0086201"}


id: GO:1900829
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of D-tyrosine.","definition_xrefs":["GOC:TermGenie","PMID:10766779"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aromatic amino acid family catabolic process","termid":"GO:0009074"},{"relation_name":"is_a","term_name":"D-amino acid catabolic process","termid":"GO:0019478"},{"relation_name":"is_a","term_name":"D-tyrosine metabolic process","termid":"GO:1900828"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0044248"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044248","GO:0006520","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"D-tyrosine catabolic process","synonyms":[{"name":"D-tyrosine breakdown","type":"exact"},{"name":"D-tyrosine catabolism","type":"exact"},{"name":"D-tyrosine degradation","type":"exact"}],"termid":"GO:1900829"}


id: PBO:0045674
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynein cytoplasmic 1 light intermediate chain 2","termid":"PBO:0045674"}


id: MONDO:0007500
data:
  {"annotated_genes":["SJAG_00321"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85530],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013845"},{"annotations":[85586],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957544"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00321":null},"genotype_count":0,"is_obsolete":false,"name":"ear malformation","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:128600","SCTID:275259005","UMLS:C0266589","ICD9:744.29","ICD9:744.3","MEDGEN:75618"],"synonyms":[{"name":"cup Ear","type":"related"},{"name":"ear malformation","type":"exact"}],"termid":"MONDO:0007500","terms_by_termid":{"MONDO:0013845":null,"MONDO:0957544":null},"xrefs":{"Monarch":{"xref_id":"0007500"}}}


id: GO:0052666
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: S-adenosyl-L-methionine + tRNA = S-adenosyl-L-homocysteine + tRNA containing 2'-O-methylcytosine.","definition_xrefs":["GOC:hjd"],"gene_count":0,"genotype_count":0,"name":"obsolete tRNA (cytosine-2'-O-)-methyltransferase activity (obsolete GO:0052666)","synonyms":[{"name":"S-adenosyl-L-methionine:tRNA (cytosine-2'-O-)-methyltransferase activity","type":"exact"},{"name":"S-adenosyl-L-methionine:tRNA cytosine-2'-O-methyltransferase activity","type":"exact"},{"name":"tRNA (cytosine 2')-methyltransferase activity","type":"exact"},{"name":"tRNA cytosine 2'-methyltransferase activity","type":"exact"},{"name":"tRNA cytosine-2'-O-methyltransferase activity","type":"exact"},{"name":"transfer ribonucleate cytosine 2'-methyltransferase activity","type":"exact"}],"termid":"GO:0052666"}


id: FYPO:0004610
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the duration of prophase of the first meiotic nuclear division is longer than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal meiosis","termid":"FYPO:0000051"},{"relation_name":"is_a","term_name":"increased duration of meiotic cell cycle phase","termid":"FYPO:0002220"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000631","FYPO:0000002"],"is_obsolete":false,"name":"increased duration of meiotic prophase I","synonyms":[{"name":"long meiotic prophase I","type":"exact"},{"name":"prolonged meiotic prophase I","type":"exact"}],"termid":"FYPO:0004610"}


id: PBO:0003139
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iron/zinc ion transporter (predicted)","termid":"PBO:0003139"}


id: PBO:0056613
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"male-enhanced antigen 1","termid":"PBO:0056613"}


id: FYPO:0004529
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A metabolism phenotype observed in the vegetative growth phase of the life cycle in which mitochondrial translation is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal metabolic process during vegetative growth","termid":"FYPO:0000859"}],"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:0000002","FYPO:0000257","FYPO:0001312","FYPO:0001320"],"is_obsolete":false,"name":"normal mitochondrial translation","synonyms":[{"name":"normal mitochondrial protein biosynthesis","type":"exact"},{"name":"normal mitochondrial protein synthesis","type":"exact"},{"name":"normal mitochondrial translation during mitotic cell cycle","type":"related"},{"name":"normal mitochondrial translation during vegetative growth","type":"exact"}],"termid":"FYPO:0004529"}


id: PATO:0001340
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A biological sex quality inhering in an organism or a population with both male and female sexual organs in one individual.","definition_xrefs":["MGED:MGED"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenotypic sex","termid":"PATO:0001894"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hermaphrodite","synonyms":[{"name":"intersex","type":"exact"}],"termid":"PATO:0001340"}


id: SO:0001678
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A promoter element that is not part of the core promoter, but provides the promoter with a specific regulatory region.","definition_xrefs":["PMID:12381659"],"direct_ancestors":[{"relation_name":"is_a","term_name":"promoter_element","termid":"SO:0001659"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"regulatory_promoter_element","synonyms":[{"name":"regulatory promoter element","type":"related"}],"termid":"SO:0001678"}


id: PBO:0109221
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tubulin gamma complex component 2","termid":"PBO:0109221"}


id: FYPO:0006627
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 phosphatidylinositol-4,5-bisphosphate measured in the plasma membrane is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular phosphatidylinositol level","termid":"FYPO:0001507"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000257","FYPO:0000002","FYPO:0001312"],"is_obsolete":false,"name":"normal phosphatidylinositol-4,5-bisphosphate level in plasma membrane","synonyms":[{"name":"normal 1-phosphatidyl-1D-myo-inositol 4,5-bisphosphate level in plasma membrane","type":"exact"},{"name":"normal phosphatidylinositol-4,5-bisphosphate level in cell membrane","type":"exact"},{"name":"normal phosphatidylinositol-4,5-bisphosphate level in plasma membrane during mitotic cell cycle","type":"related"},{"name":"normal phosphatidylinositol-4,5-bisphosphate level in plasma membrane during vegetative growth","type":"exact"},{"name":"normal plasma membrane PI(4,5)P2 level","type":"exact"},{"name":"normal plasma membrane phosphatidylinositol-4,5-bisphosphate level","type":"exact"}],"termid":"FYPO:0006627"}


id: PBO:0091853
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"equivalent function in S. cerevisiae is performed by STE12, but this is STE-like, not HMG","termid":"PBO:0091853"}


id: GO:0000448
data:
  {"annotated_genes":["SJAG_02275","SJAG_03789","SJAG_01581","SJAG_02374"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90895,94153,103290,117682],"is_not":false,"summary":null,"term":"GO:0000448"}]},"cv_name":"biological_process","definition":"Endonucleolytic cleavage within ITS2 between the 5.8S rRNA and the LSU-rRNA of an rRNA molecule originally produced as a tricistronic rRNA transcript that contained the Small SubUnit (SSU) rRNA, the 5.8S rRNA, and the Large SubUnit (LSU) rRNA, in that order, from 5' to 3' along the primary transcript.","definition_xrefs":["PMID:10690410","GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endonucleolytic cleavage of tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA)","termid":"GO:0000479"},{"relation_name":"part_of","term_name":"maturation of LSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA)","termid":"GO:0000463"},{"relation_name":"part_of","term_name":"maturation of 5.8S rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA)","termid":"GO:0000466"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01581":null,"SJAG_02275":null,"SJAG_02374":null,"SJAG_03789":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"part_of","termid":"GO:0042254"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0042254","GO:0044085"],"is_obsolete":false,"name":"cleavage in ITS2 between 5.8S rRNA and LSU-rRNA of tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA)","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0000490"],"synonyms":[{"name":"cleavage at C2","type":"related"},{"name":"cleavage in ITS2 of tricistronic rRNA transcript to separate 5.8S and LSU rRNAs (SSU-rRNA, 5.8S rRNA, LSU-rRNA)","type":"exact"}],"termid":"GO:0000448","terms_by_termid":{"GO:0000448":null}}


id: GO:0000248
data:
  {"annotated_genes":["SJAG_03509","SJAG_00717"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[88867,106689],"is_not":false,"summary":null,"term":"GO:0000248"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 5,7,24(28)-ergostatrienol + O2 + NADPH = 5,7,22,24(28)-ergostatetraenol + 2 H2O + NADP+.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sterol desaturase activity","termid":"GO:0070704"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00717":null,"SJAG_03509":null},"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:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"C-5 sterol desaturase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-6807053","Reactome:R-HSA-195664"],"synonyms":[{"name":"sterol-C5-desaturase activity","type":"exact"}],"termid":"GO:0000248","terms_by_termid":{"GO:0000248":null}}


id: PBO:0062506
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 8 subfamily H member 1","termid":"PBO:0062506"}


id: GO:0034337
data:
  {"annotated_genes":["SJAG_00886","SJAG_00195","SJAG_04266"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[60760,112956],"is_not":false,"summary":null,"term":"GO:0034337"},{"annotations":[97681],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061818"}]},"cv_name":"biological_process","definition":"The process of assisting in the covalent and noncovalent assembly of single or multimeric RNAs into the correct tertiary structure.","definition_xrefs":["GOC:mah","PMID:10393192"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular process","termid":"GO:0009987"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00195":null,"SJAG_00886":null,"SJAG_04266":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"RNA folding","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000108":null},"synonyms":[{"name":"RNA chaperone","type":"related"}],"termid":"GO:0034337","terms_by_termid":{"GO:0034337":null,"GO:0061818":null}}


id: PBO:0054389
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 1785","termid":"PBO:0054389"}


id: GO:0016847
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine(1+) = 1-aminocyclopropane-1-carboxylate + S-methyl-5'-thioadenosine + H+.","definition_xrefs":["EC:4.4.1.14","RHEA:21744"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-sulfur lyase activity","termid":"GO:0016846"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016829","GO:0003824"],"is_obsolete":false,"name":"1-aminocyclopropane-1-carboxylate synthase activity","secondary_identifiers":["GO:0034100","MetaCyc:4.4.1.14-RXN","KEGG_REACTION:R00179"],"synonyms":[{"name":"1-aminocyclopropane-1-carboxylate synthetase activity","type":"related"},{"name":"1-aminocyclopropane-1-carboxylic acid synthase activity","type":"related"},{"name":"1-aminocyclopropanecarboxylate synthase activity","type":"related"},{"name":"ACC synthase activity","type":"related"},{"name":"L-VG deaminase activity","type":"related"},{"name":"L-vinylglycine deaminase activity","type":"related"},{"name":"S-adenosyl-L-methionine methylthioadenosine-lyase (1-aminocyclopropane-1-carboxylate-forming)","type":"related"},{"name":"S-adenosyl-L-methionine methylthioadenosine-lyase activity","type":"related"},{"name":"aminocyclopropanecarboxylate synthase activity","type":"related"},{"name":"aminocyclopropanecarboxylic acid synthase activity","type":"related"}],"termid":"GO:0016847"}


id: PBO:0072749
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S100 calcium binding protein A10","termid":"PBO:0072749"}


id: PBO:0044927
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diacylglycerol kinase epsilon","termid":"PBO:0044927"}


id: FYPO:0006386
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which a protein that normally localizes to a compact region at the tip of a shmoo, or mating projection, is more dispersed than normal.","definition_xrefs":["PomBase:mah","PMID:19627505"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to shmoo tip","termid":"FYPO:0004802"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001985","FYPO:0000138"],"is_obsolete":false,"name":"protein abnormally dispersed at shmoo tip","synonyms":[{"name":"abnormally dispersed protein localization at shmoo tip","type":"exact"},{"name":"protein abnormally dispersed at mating projection tip","type":"exact"},{"name":"protein abnormally dispersed at shmoo projection","type":"related"}],"termid":"FYPO:0006386"}


id: GO:0048278
data:
  {"annotated_genes":["SJAG_03552","SJAG_03848","SJAG_00380","SJAG_04966","SJAG_02320","SJAG_02587","SJAG_00280","SJAG_00171","SJAG_01598","SJAG_01633","SJAG_04023","SJAG_03536","SJAG_03347","SJAG_04978","SJAG_01324","SJAG_01697","SJAG_01772","SJAG_03499","SJAG_03005"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[98709,99401,99501,100309,107837,108809,108962,111817,116681,117661],"is_not":false,"summary":null,"term":"GO:0048278"},{"annotations":[94748],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048211"},{"annotations":[88928,91534,116637,117339,99441,117962,117558,89786],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006904"}]},"cv_name":"biological_process","definition":"The initial attachment of a transport vesicle membrane to the target membrane, mediated by proteins protruding from the membrane of the vesicle and the target membrane. Docking requires only that the two membranes come close enough for these proteins to interact and adhere.","definition_xrefs":["GOC:ai","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organelle localization by membrane tethering","termid":"GO:0140056"},{"relation_name":"part_of","term_name":"vesicle-mediated transport","termid":"GO:0016192"}],"gene_count":19,"genes_by_uniquename":{"SJAG_00171":null,"SJAG_00280":null,"SJAG_00380":null,"SJAG_01324":null,"SJAG_01598":null,"SJAG_01633":null,"SJAG_01697":null,"SJAG_01772":null,"SJAG_02320":null,"SJAG_02587":null,"SJAG_03005":null,"SJAG_03347":null,"SJAG_03499":null,"SJAG_03536":null,"SJAG_03552":null,"SJAG_03848":null,"SJAG_04023":null,"SJAG_04966":null,"SJAG_04978":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0140056"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"part_of","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0140056","GO:0051179","GO:0016192","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"vesicle docking","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"vesicle to membrane docking","type":"exact"}],"termid":"GO:0048278","terms_by_termid":{"GO:0006904":null,"GO:0048211":null,"GO:0048278":null}}


id: MONDO:0008633
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An intermediate form of cryopyrin-associated periodic syndrome (CAPS) and is characterized by recurrent fever (with malaise and chills), recurrent urticaria-like skin rash, sensorineural deafness, general signs of inflammation (eye redness, headaches, arthralgia/myalgia) and potentially life-threatening secondary amyloidosis (AA type).","definition_xrefs":["Orphanet:575"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete secondary glomerular disease (obsolete MONDO:0019724)","termid":"MONDO:0019724"},{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"cryopyrin-associated periodic syndrome","termid":"MONDO:0016168"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0000426"],"is_obsolete":false,"name":"Muckle-Wells syndrome","secondary_identifiers":["NCIT:C119054","MEDGEN:120634","SCTID:402417009","UMLS:C0268390","GARD:8472","NANDO:1200467","icd11.foundation:1983358487","NORD:1459","DOID:0050854","NANDO:2201067","OMIM:191900","ICD9:708.8","MedDRA:10064569"],"synonyms":[{"name":"Cryopyrin-associated periodic syndrome 2","type":"related"},{"name":"MUCKLE-Wells syndrome","type":"related"},{"name":"MWS","type":"related"},{"name":"Muckle Wells syndrome","type":"related"},{"name":"Muckle-Wells syndrome","type":"exact"},{"name":"Uda syndrome","type":"related"},{"name":"neutrophilic urticaria","type":"exact"},{"name":"urticaria, deafness and amyloidosis","type":"related"},{"name":"urticaria-deafness-amyloidosis syndrome","type":"related"}],"termid":"MONDO:0008633","xrefs":{"Monarch":{"xref_id":"0008633"}}}


id: MONDO:0000505
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete small cell neuroendocrine carcinoma (obsolete MONDO:0000505)","termid":"MONDO:0000505","xrefs":{"Monarch":{"xref_id":"0000505"}}}


id: PBO:0089059
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"V-type ATPase V1 domain subunit G","termid":"PBO:0089059"}


id: PBO:0034740
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"greatwall kinase Ppk18","termid":"PBO:0034740"}


id: PBO:0030094
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_bipolar_mitotic_spindle","termid":"PBO:0030094"}


id: PBO:0084072
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTPase that associates with nuclear 60S pre-ribosomes; required for export of 60S ribosomal subunits from the nucleus","termid":"PBO:0084072"}


id: PBO:0004261
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP citrate synthase subunit 1 (predicted)","termid":"PBO:0004261"}


id: MONDO:1012106
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"internal hydrocephalus, non-human animal","termid":"MONDO:1011843"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"internal hydrocephalus, cattle","secondary_identifiers":["OMIA:000489-9913"],"termid":"MONDO:1012106","xrefs":{"Monarch":{"xref_id":"1012106"}}}


id: MONDO:0000998
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete parotid disease (obsolete MONDO:0000998)","termid":"MONDO:0000998","xrefs":{"Monarch":{"xref_id":"0000998"}}}


id: PBO:0082492
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Catalytic core subunit, Anaphase-Promoting Complex/Cyclosome (APC/C); which is a ubiquitin-protein ligase required for degradation of anaphase inhibitors, including mitotic cyclins, during the metaphase/anaphase transition; contains a RING-H2 domain that is required for activity","termid":"PBO:0082492"}


id: MONDO:1011221
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Retinal detachment that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinal detachment, non-human animal","termid":"MONDO:1010321"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retinal detachment, dog","secondary_identifiers":["OMIA:000275-9615"],"termid":"MONDO:1011221","xrefs":{"Monarch":{"xref_id":"1011221"}}}


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


id: PBO:0042318
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CD37 molecule","termid":"PBO:0042318"}


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


id: PR:O60081
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- trm72 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O60081"],"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 C1494.07 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1494.07","synonyms":[{"name":"Spom972h-trm72","type":"exact"}],"termid":"PR:O60081"}


id: PR:000027517
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ase1 gene or a 1:1 ortholog thereof.","definition_xrefs":["PRO:CNA"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein","termid":"PR:000000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anaphase spindle elongation protein 1","pombase_gene_id":"SPAPB1A10.09","synonyms":[{"name":"Ase1p","type":"exact"},{"name":"ase1","type":"exact"}],"termid":"PR:000027517"}


id: FYPO:0006014
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which one cell forms multiple mating projections that engage multiple partner cells.","definition_xrefs":["PomBase:mah","PMID:28410370"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mating","termid":"FYPO:0000031"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000301"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000301"],"is_obsolete":false,"name":"promiscuous mating","synonyms":[{"name":"conjugation with multiple partner cells","type":"exact"},{"name":"formation of multiple mating projections","type":"related"},{"name":"formation of multiple shmoos","type":"related"},{"name":"mating with multiple partner cells","type":"exact"},{"name":"promiscuous conjugation","type":"exact"}],"termid":"FYPO:0006014"}


id: MONDO:0041755
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"twin to twin transfusion syndrome","termid":"MONDO:0019805"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0002280","MONDO:0005570"],"is_obsolete":false,"name":"twin reversal arterial perfusion syndrome","secondary_identifiers":["SCTID:417006004","UMLS:C1562817","MEDGEN:736778"],"synonyms":[{"name":"twin reversal arterial perfusion syndrome","type":"exact"}],"termid":"MONDO:0041755","xrefs":{"Monarch":{"xref_id":"0041755"}}}


id: GO:0008733
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-arabinose = L-ribulose.","definition_xrefs":["RHEA:14821","EC:5.3.1.4"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular oxidoreductase activity, interconverting aldoses and ketoses","termid":"GO:0016861"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016853"}],"interesting_parent_ids":["GO:0003824","GO:0016853","GO:0003674"],"is_obsolete":false,"name":"L-arabinose isomerase activity","secondary_identifiers":["KEGG_REACTION:R01761","MetaCyc:ARABISOM-RXN"],"synonyms":[{"name":"L-arabinose aldose-ketose-isomerase activity","type":"related"},{"name":"L-arabinose ketol-isomerase activity","type":"related"}],"termid":"GO:0008733"}


id: GO:0003143
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the embryonic heart tube are generated and organized. The embryonic heart tube is an epithelial tube that will give rise to the mature heart.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"embryonic morphogenesis","termid":"GO:0048598"},{"relation_name":"is_a","term_name":"epithelial tube morphogenesis","termid":"GO:0060562"},{"relation_name":"part_of","term_name":"heart morphogenesis","termid":"GO:0003007"},{"relation_name":"part_of","term_name":"embryonic heart tube development","termid":"GO:0035050"},{"relation_name":"part_of","term_name":"embryonic organ morphogenesis","termid":"GO:0048562"}],"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":"embryonic heart tube morphogenesis","termid":"GO:0003143"}


id: MONDO:0005309
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Traumatic or pathological injury to the spine in which the continuity of a vertebral bone is broken. Symptoms include back pain and difficulty bending and twisting.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bone fracture","termid":"MONDO:0005315"},{"relation_name":"is_a","term_name":"spinal injury","termid":"MONDO:0037747"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spinal fracture","secondary_identifiers":["EFO:0003902","MESH:D016103","SCTID:50448004"],"synonyms":[{"name":"bone fracture of vertebral column","type":"exact"},{"name":"vertebral column bone fracture","type":"exact"}],"termid":"MONDO:0005309","xrefs":{"Monarch":{"xref_id":"0005309"}}}


id: PBO:0085208
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Oxalyl-CoA synthetase; capable of catalyzing conversion of oxalate to oxalyl-CoA; catalyzes first step in pathway of oxalate degradation that functions to protect yeast from inhibitory effects of oxalate; peroxisomal protein that binds mRNA; localizes to both peroxisomal peripheral membrane and matrix, expression is highly inducible by oleic acid; similar to E. coli long chain acyl-CoA synthetase","termid":"PBO:0085208"}


id: PBO:0034778
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small RNA 2'-O-methyltransferase Hen1 (predicted)","termid":"PBO:0034778"}


id: GO:0034505
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which calcium salts are deposited into calcareous tooth structures such as dental enamel, dentin and cementum.","definition_xrefs":["GOC:mah","MP:0002817","MSH:D014074"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biomineral tissue development","termid":"GO:0031214"},{"relation_name":"part_of","term_name":"odontogenesis","termid":"GO:0042476"}],"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":"tooth mineralization","synonyms":[{"name":"tooth calcification","type":"exact"}],"termid":"GO:0034505"}


id: MONDO:0011906
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital bile acid synthesis defect type 1 (BAS defect type 1) is the most common anomaly of bile acid synthesis characterized by variable manifestations of progressive cholestatic liver disease, and fat malabsorption.","definition_xrefs":["Orphanet:79301"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital bile acid synthesis defect","termid":"MONDO:0018841"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0002525"],"is_obsolete":false,"name":"congenital bile acid synthesis defect 1","secondary_identifiers":["GARD:9813","OMIM:607765","UMLS:C1843116","MEDGEN:335883","MESH:C535442","DOID:0111071"],"synonyms":[{"name":"3-Beta-hydroxy-Delta-5-C27-steroid oxidoreductase deficiency","type":"related"},{"name":"3-alpha beta-hydroxy-delta-5-C27-steroid oxidoreductase, deficiency of","type":"related"},{"name":"3-beta-hydroxy-delta-5-C27-steroid oxidoreductase deficiency type 1","type":"exact"},{"name":"BASD1","type":"exact"},{"name":"CBAS1","type":"exact"},{"name":"HSD3B7 congenital bile acid synthesis defect","type":"exact"},{"name":"bile acid synthesis defect, congenital, 1","type":"related"},{"name":"bile acid synthesis defect, congenital, type 1","type":"exact"},{"name":"congenital bile acid synthesis defect 1","type":"exact"},{"name":"congenital bile acid synthesis defect caused by mutation in HSD3B7","type":"exact"},{"name":"congenital bile acid synthesis defect type 1","type":"exact"},{"name":"congenital bile acid synthesis defect, type 1","type":"related"}],"termid":"MONDO:0011906","xrefs":{"Monarch":{"xref_id":"0011906"}}}


id: GO:0047597
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 6-oxocineole + H+ + NADPH + O2 = 1,6,6-trimethyl-2,7-dioxabicyclo[3.2.2]nonan-3-one + H2O + NADP+.","definition_xrefs":["EC:1.14.13.51","RHEA:24324"],"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:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"6-oxocineole dehydrogenase activity","secondary_identifiers":["MetaCyc:6-OXOCINEOLE-DEHYDROGENASE-RXN","KEGG_REACTION:R02995"],"synonyms":[{"name":"6-oxocineole oxygenase activity","type":"related"},{"name":"6-oxocineole,NADPH:oxygen oxidoreductase activity","type":"related"}],"termid":"GO:0047597"}


id: PR:O14190
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A bifunctional UDP-N-acetylglucosamine transferase and deubiquitinase ALG13 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00502","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":"UDP-N-acetylglucosamine transferase subunit alg13 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC56E4.02c","secondary_identifiers":["UniProtKB:O14190"],"synonyms":[{"name":"Spom972h-ALG13","type":"exact"},{"name":"asparagine-linked glycosylation protein 13 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14190"}


id: MONDO:0010517
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any primary ciliary dyskinesia in which the cause of the disease is a mutation in the PIH1D3 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary ciliary dyskinesia","termid":"MONDO:0016575"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ciliary dyskinesia, primary, 36, X-linked","secondary_identifiers":["UMLS:C4478372","OMIM:300991","DOID:0111850","MEDGEN:1393107","GARD:15280"],"synonyms":[{"name":"CILD36","type":"exact"},{"name":"PIH1D3 primary ciliary dyskinesia","type":"exact"},{"name":"ciliary dyskinesia, primary, 36, X-linked","type":"exact"},{"name":"ciliary dyskinesia, primary, 36, X-linked, X-linked recessive","type":"exact"},{"name":"ciliary dyskinesia, primary, 36, X-linked; CILD36","type":"exact"},{"name":"ciliary dyskinesia, primary, 36, with or without situs inversus","type":"related"},{"name":"primary ciliary dyskinesia caused by mutation in PIH1D3","type":"exact"}],"termid":"MONDO:0010517","xrefs":{"Monarch":{"xref_id":"0010517"}}}


id: PBO:0089112
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microtubule severing ATPase Spg4","termid":"PBO:0089112"}


id: MONDO:0000172
data:
  {"annotated_genes":["SJAG_03188","SJAG_04316","SJAG_00831","SJAG_04053","SJAG_01491"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84475],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033556"},{"annotations":[85890],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013159"},{"annotations":[85171],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014141"},{"annotations":[85889,85888],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013160"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"muscular dystrophy-dystroglycanopathy","termid":"MONDO:0018276"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00831":null,"SJAG_01491":null,"SJAG_03188":null,"SJAG_04053":null,"SJAG_04316":null},"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":"muscular dystrophy-dystroglycanopathy, type B","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0112375","OMIMPS:613155"],"termid":"MONDO:0000172","terms_by_termid":{"MONDO:0013159":null,"MONDO:0013160":null,"MONDO:0014141":null,"MONDO:0033556":null},"xrefs":{"Monarch":{"xref_id":"0000172"}}}


id: GO:0072270
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a short nephron in the metanephros over time, from its formation to the mature structure. Short nephrons are associated with mid-cortical and superficial glomeruli, are situated entirely in the outer medulla, and have no thin ascending limb.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"short nephron development","termid":"GO:0072030"},{"relation_name":"is_a","term_name":"metanephric nephron development","termid":"GO:0072210"}],"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":"metanephric short nephron development","termid":"GO:0072270"}


id: GO:0000345
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The eubacterial DNA-directed RNA polymerase is a multisubunit complex with a core composed of the essential subunits beta-prime, beta, and two copies of alpha and a fifth nonessential subunit called omega. An additional subunit, a sigma factor, is required for promoter recognition and specificity.","definition_xrefs":["PMID:11158566"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA-directed RNA polymerase complex","termid":"GO:0000428"},{"relation_name":"part_of","term_name":"cytosol","termid":"GO:0005829"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005829"}],"interesting_parent_ids":["GO:0032991","GO:0005737","GO:0005575","GO:0005829"],"is_obsolete":false,"name":"cytosolic DNA-directed RNA polymerase complex","termid":"GO:0000345"}


id: PBO:0062948
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proliferation-associated 2G4 pseudogene 6","termid":"PBO:0062948"}


id: MONDO:0100451
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A ciliopathy caused by biallelic variants in the CEP290 gene.","direct_ancestors":[{"relation_name":"is_a","term_name":"ciliopathy","termid":"MONDO:0005308"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CEP290-related ciliopathy","synonyms":[{"name":"BBS14","type":"narrow"},{"name":"Bardet-Biedl syndrome 14","type":"narrow"},{"name":"Bardet-Biedl syndrome type 14","type":"narrow"},{"name":"CEP290 Joubert syndrome","type":"narrow"},{"name":"CEP290 Leber congenital amaurosis","type":"narrow"},{"name":"CEP290 Meckel syndrome","type":"narrow"},{"name":"CEP290 Senior-Loken syndrome","type":"narrow"},{"name":"CEP290 ciliopathy","type":"exact"},{"name":"JBTS5","type":"narrow"},{"name":"Joubert syndrome 5","type":"narrow"},{"name":"Joubert syndrome caused by mutation in CEP290","type":"narrow"},{"name":"Joubert syndrome type 5","type":"narrow"},{"name":"LCA10","type":"narrow"},{"name":"Leber congenital amaurosis 10","type":"narrow"},{"name":"Leber congenital amaurosis caused by mutation in CEP290","type":"narrow"},{"name":"Leber congenital amaurosis type 10","type":"narrow"},{"name":"MKS4","type":"narrow"},{"name":"Meckel syndrome 4","type":"narrow"},{"name":"Meckel syndrome caused by mutation in CEP290","type":"narrow"},{"name":"Meckel syndrome, type 4","type":"narrow"},{"name":"Meckel-Gruber syndrome, type 4","type":"narrow"},{"name":"Meckel-like Cerebrorenodigital syndrome","type":"narrow"},{"name":"SENIOR-Loken syndrome 6","type":"narrow"},{"name":"SLSN6","type":"narrow"},{"name":"Senior-Loken syndrome 6","type":"narrow"},{"name":"Senior-Loken syndrome caused by mutation in CEP290","type":"narrow"},{"name":"Senior-Loken syndrome type 6","type":"narrow"},{"name":"amaurosis congenita of Leber, type 10","type":"narrow"}],"termid":"MONDO:0100451","xrefs":{"Monarch":{"xref_id":"0100451"}}}


id: GO:0061883
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A clathrin-mediated endocytosis process whereby yolk proteins are internalized and trafficked through the endocytic pathway for yolk deposition.","definition_xrefs":["PMID:26265702"],"direct_ancestors":[{"relation_name":"is_a","term_name":"clathrin-dependent endocytosis","termid":"GO:0072583"},{"relation_name":"part_of","term_name":"vitellogenesis","termid":"GO:0007296"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150","GO:0016192"],"is_obsolete":false,"name":"clathrin-dependent endocytosis involved in vitellogenesis","synonyms":[{"name":"clathrin-dependent endocytosis involved in yolk formation","type":"exact"}],"termid":"GO:0061883"}


id: MONDO:0000549
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A relatively uncommon neuroblastoma that is found in the neck.","definition_xrefs":["PMID:23120455"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extracranial neuroblastoma","termid":"MONDO:0002749"},{"relation_name":"is_a","term_name":"neoplasm of neck","termid":"MONDO:0021351"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cervical neuroblastoma","secondary_identifiers":["DOID:0050935"],"synonyms":[{"name":"neck neuroblastoma","type":"exact"},{"name":"neuroblastoma of neck","type":"exact"}],"termid":"MONDO:0000549","xrefs":{"Monarch":{"xref_id":"0000549"}}}


id: MOD:00544
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts a residue containing common isotopes to a 6x(13)C labeled residue.","definition_xrefs":["Unimod:188","PubMed:12716131"],"direct_ancestors":[{"relation_name":"is_a","term_name":"(13)C labeled residue","termid":"MOD:00842"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"6x(13)C labeled residue","synonyms":[{"name":"13C(6) Silac label","type":"related"},{"name":"Label:13C(6)","type":"related"}],"termid":"MOD:00544"}


id: MONDO:0001845
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare morphologic variant of uterine corpus leiomyoma characterized by the presence of scattered islands of mature adipocytes within the smooth muscle neoplasm.","definition_xrefs":["NCIT:C40168"],"direct_ancestors":[{"relation_name":"is_a","term_name":"uterine corpus leiomyoma","termid":"MONDO:0007886"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uterine corpus lipoleiomyoma","secondary_identifiers":["DOID:13957","MEDGEN:311424","UMLS:C1519856"],"synonyms":[{"name":"uterine corpus lipomatous leiomyoma","type":"exact"}],"termid":"MONDO:0001845","xrefs":{"Monarch":{"xref_id":"0001845"}}}


id: MONDO:0032749
data:
  {"annotated_genes":["SJAG_04856"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86349],"is_not":false,"summary":null,"term":"MONDO:0032749"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04856":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0019497","MONDO:0006025"],"is_obsolete":false,"name":"hearing loss, autosomal recessive 94","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0111641","GARD:22661","UMLS:C5193096","MEDGEN:1679077","OMIM:618434"],"synonyms":[{"name":"DFNB94","type":"narrow"},{"name":"deafness, autosomal recessive 94","type":"narrow"}],"termid":"MONDO:0032749","terms_by_termid":{"MONDO:0032749":null},"xrefs":{"Monarch":{"xref_id":"0032749"}}}


id: MONDO:0015609
data:
  {"annotated_genes":["SJAG_02104","SJAG_02724","SJAG_04457"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85098],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0031044"},{"annotations":[84334,84335],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014088"}]},"cv_name":"mondo","definition":"A very rare circadian rhythm sleep disorder characterized by very early sleep onset and offset possibly resulting in emotional and physical disruptions.","definition_xrefs":["Orphanet:164736"],"direct_ancestors":[{"relation_name":"is_a","term_name":"circadian rhythm sleep disorder","termid":"MONDO:0024361"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02104":null,"SJAG_02724":null,"SJAG_04457":null},"genotype_count":0,"is_obsolete":false,"name":"advanced sleep phase syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C1858496","DOID:0050628","SCTID:715829003","GARD:9242","ICD10CM:G47.2","MEDGEN:348956","OMIMPS:604348"],"synonyms":[{"name":"FASPS","type":"exact"},{"name":"advanced sleep phase syndrome, familial","type":"related"},{"name":"familial advanced sleep phase syndrome","type":"related"},{"name":"familial advanced sleep-phase syndrome","type":"exact"}],"termid":"MONDO:0015609","terms_by_termid":{"MONDO:0014088":null,"MONDO:0031044":null},"xrefs":{"Monarch":{"xref_id":"0015609"}}}


id: PBO:0090819
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cortical variant C2 domain protein, human FAM102A and FAM102B ortholog, implicated in signalling or endocytosis","termid":"PBO:0090819"}


id: PBO:0080466
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vesicle trafficking 1 pseudogene 2","termid":"PBO:0080466"}


id: GO:1900234
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of Kit signaling pathway.","definition_xrefs":["GOC:signaling","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytokine-mediated signaling pathway","termid":"GO:0001959"},{"relation_name":"regulates","term_name":"Kit signaling pathway","termid":"GO:0038109"}],"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 Kit signaling pathway","synonyms":[{"name":"regulation of Kit signalling pathway","type":"exact"},{"name":"regulation of stem cell factor receptor signaling pathway","type":"exact"},{"name":"regulation of stem cell factor signaling pathway","type":"exact"}],"termid":"GO:1900234"}


id: PBO:0049622
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H3 histone pseudogene 25","termid":"PBO:0049622"}


id: GO:0003415
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The growth of a chondrocyte, where growth contributes to the progression of the chondrocyte over time.","definition_xrefs":["GOC:tb","GOC:dph","GOC:ascb_2009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental cell growth","termid":"GO:0048588"},{"relation_name":"part_of","term_name":"chondrocyte development","termid":"GO:0002063"}],"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":"chondrocyte hypertrophy","termid":"GO:0003415"}


id: PBO:0061522
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-ethylmaleimide sensitive factor, vesicle fusing ATPase","termid":"PBO:0061522"}


id: MONDO:0013966
data:
  {"annotated_genes":["SJAG_04901","SJAG_04781"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86415,86416],"is_not":false,"summary":null,"term":"MONDO:0013966"}]},"cv_name":"mondo","definition":"Any catecholaminergic polymorphic ventricular tachycardia in which the cause of the disease is a mutation in the CALM1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catecholaminergic polymorphic ventricular tachycardia","termid":"MONDO:0017990"}],"gene_count":2,"genes_by_uniquename":{"SJAG_04781":null,"SJAG_04901":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"catecholaminergic polymorphic ventricular tachycardia 4","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C3554047","DOID:0060678","GARD:15880","ICD10CM:I47.2","MEDGEN:766961","OMIM:614916"],"synonyms":[{"name":"CALM1 catecholaminergic polymorphic ventricular tachycardia","type":"exact"},{"name":"CPVT4","type":"related"},{"name":"CVPT4","type":"exact"},{"name":"catecholaminergic polymorphic ventricular tachycardia 4","type":"exact"},{"name":"catecholaminergic polymorphic ventricular tachycardia caused by mutation in CALM1","type":"exact"},{"name":"catecholaminergic polymorphic ventricular tachycardia type 4","type":"exact"},{"name":"ventricular tachycardia, catecholaminergic polymorphic, 4","type":"related"},{"name":"ventricular tachycardia, catecholaminergic polymorphic, type 4","type":"exact"}],"termid":"MONDO:0013966","terms_by_termid":{"MONDO:0013966":null},"xrefs":{"Monarch":{"xref_id":"0013966"}}}


id: PBO:0069631
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 908, pseudogene","termid":"PBO:0069631"}


id: MONDO:0010715
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete pseudohermaphroditism, incomplete male, type 1 (obsolete MONDO:0010715)","termid":"MONDO:0010715","xrefs":{"Monarch":{"xref_id":"0010715"}}}


id: MONDO:0008602
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"triglyceride storage disease","termid":"MONDO:0000155"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0002561"}],"interesting_parent_ids":["MONDO:0002561","MONDO:0005066","MONDO:0002525"],"is_obsolete":false,"name":"triglyceride storage disease, type 2","secondary_identifiers":["MEDGEN:349896","MESH:C566030","OMIM:190430","UMLS:C1860820"],"synonyms":[{"name":"triglyceride storage disease, type II","type":"related"}],"termid":"MONDO:0008602","xrefs":{"Monarch":{"xref_id":"0008602"}}}


id: PBO:0086166
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein required for spore wall formation; subunit of leading edge protein (LEP) complex (Ssp1-Ady3-Don1-Irc10) that forms ring-like structure at leading edge of prospore membrane during meiosis II; mediates assembly of LEP complex, formation of ring-like structure via interaction with spindle pole body components, and prospore membrane maturation; potentially phosphorylated by Cdc28p; ADY3 has a paralog, CNM67, that arose from the whole genome duplication","termid":"PBO:0086166"}


id: PBO:0005770
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"twinfilin (predicted)","termid":"PBO:0005770"}


id: GO:0036279
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of directed movement of proteins from the nucleus into the cytoplasm in response to deprivation of glucose.","definition_xrefs":["GOC:al","PMID:3541942"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to glucose starvation","termid":"GO:0042149"},{"relation_name":"is_a","term_name":"positive regulation of protein export from nucleus","termid":"GO:0046827"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0006913"},{"rel_name":"regulates","termid":"GO:0006913"}],"interesting_parent_ids":["GO:0006913","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"positive regulation of protein export from nucleus in response to glucose starvation","termid":"GO:0036279"}


id: MONDO:0007000
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An disease caused by infection with Treponema.","definition_xrefs":["MONDO:patterns/specific_infectious_disease_by_agent"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bacterial sexually transmitted disease","termid":"MONDO:0005323"},{"relation_name":"is_a","term_name":"gram-negative bacterial infections","termid":"MONDO:0021678"},{"relation_name":"is_a","term_name":"spirochaetales infections","termid":"MONDO:0021839"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Treponema infectious disease","secondary_identifiers":["NCIT:C85197","EFO:1001217","MESH:D014211"],"synonyms":[{"name":"Bejels","type":"narrow"},{"name":"Treponema caused disease or disorder","type":"exact"},{"name":"Treponema disease or disorder","type":"exact"},{"name":"Treponemal infection","type":"related"},{"name":"bejel","type":"narrow"},{"name":"infection, Treponemal","type":"related"},{"name":"infections, Treponemal","type":"related"}],"termid":"MONDO:0007000","xrefs":{"Monarch":{"xref_id":"0007000"}}}


id: GO:0006688
data:
  {"annotated_genes":["SJAG_04878","SJAG_05311","SJAG_02168","SJAG_04913","SJAG_03953"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[91005,89946,94927,111671,94447],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051999"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of glycosphingolipid, a compound with residues of sphingoid and at least one monosaccharide.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycosphingolipid metabolic process","termid":"GO:0006687"},{"relation_name":"is_a","term_name":"glycolipid biosynthetic process","termid":"GO:0009247"},{"relation_name":"is_a","term_name":"sphingolipid biosynthetic process","termid":"GO:0030148"}],"gene_count":5,"genes_by_uniquename":{"SJAG_02168":null,"SJAG_03953":null,"SJAG_04878":null,"SJAG_04913":null,"SJAG_05311":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"glycosphingolipid biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"glycosphingolipid anabolism","type":"exact"},{"name":"glycosphingolipid biosynthesis","type":"exact"},{"name":"glycosphingolipid formation","type":"exact"},{"name":"glycosphingolipid synthesis","type":"exact"}],"termid":"GO:0006688","terms_by_termid":{"GO:0051999":null}}


id: PBO:0087368
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sporulation-specific protein with a leucine zipper motif; subunit of the MIS complex which controls mRNA methylation during during the induction of sporulation","termid":"PBO:0087368"}


id: GO:0016492
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with the tridecapeptide neurotensin to initiate a G-protein mediated change in cell activity. A G-protein is a signal transduction molecule that alternates between an inactive GDP-bound and an active GTP-bound state.","definition_xrefs":["PMID:10390649"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuropeptide receptor activity","termid":"GO:0008188"}],"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":"G protein-coupled neurotensin receptor activity","synonyms":[{"name":"G protein coupled neurotensin receptor activity","type":"exact"},{"name":"G-protein coupled neurotensin receptor activity","type":"exact"},{"name":"neurotensin receptor activity, G protein coupled","type":"exact"},{"name":"neurotensin receptor activity, G-protein coupled","type":"exact"}],"termid":"GO:0016492"}


id: GO:0016992
data:
  {"annotated_genes":["SJAG_03553"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[111824],"is_not":false,"summary":null,"term":"GO:0016992"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: protein N6-(octanoyl)lysine + 2 sulfur + 2 S-adenosyl-L-methionine = protein N6-(lipoyl)lysine + 2 L-methionine + 2 5'-deoxyadenosyl.","definition_xrefs":["EC:2.8.1.8","PMID:18307109"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfurtransferase activity","termid":"GO:0016783"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03553":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016782"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016740","GO:0016782","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"lipoate synthase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0017140","MetaCyc:RXN0-949","Reactome:R-HSA-6793591","RHEA:16585"],"synonyms":[{"name":"LS","type":"related"},{"name":"LipA","type":"related"},{"name":"lipoic acid synthase","type":"exact"},{"name":"lipoyl synthase activity","type":"related"},{"name":"protein 6-N-(octanoyl)lysine:sulfur sulfurtransferase activity","type":"related"},{"name":"protein N6-(octanoyl)lysine:sulfur sulfurtransferase activity","type":"related"}],"termid":"GO:0016992","terms_by_termid":{"GO:0016992":null}}


id: MONDO:0021013
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A subtype of trichothiodystrophy caused by mutation(s) in the MPLKIP gene, encoding M-phase-specific PLK1-interacting protein.","definition_xrefs":["NCIT:C146899"],"direct_ancestors":[{"relation_name":"is_a","term_name":"trichothiodystrophy","termid":"MONDO:0018053"}],"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":"trichothiodystrophy 4, nonphotosensitive","secondary_identifiers":["OMIM:234050","Orphanet:75790","GARD:5271","DOID:0050528","SCTID:403796005","UMLS:C1313961","ICD9:704.8","MEDGEN:272036","ICD9:783.43"],"synonyms":[{"name":"Amish brittle hair brain syndrome","type":"related"},{"name":"BIDS syndrome","type":"related"},{"name":"MPLKIP nonphotosensitive trichothiodystrophy","type":"exact"},{"name":"Pollitt syndrome","type":"exact"},{"name":"TTD4","type":"exact"},{"name":"hair-brain syndrome","type":"related"},{"name":"nonphotosensitive trichothiodystrophy","type":"related"},{"name":"nonphotosensitive trichothiodystrophy caused by mutation in MPLKIP","type":"exact"},{"name":"trichothiodystrophy 4, nonphotosensitive","type":"exact"},{"name":"trichothiodystrophy, nonphotosensitive 1","type":"related"},{"name":"trichothiodystrophy-neurocutaneous syndrome","type":"related"}],"termid":"MONDO:0021013","xrefs":{"Monarch":{"xref_id":"0021013"}}}


id: MONDO:1011346
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Post-Bacterial disorder that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"post-infectious disorder, non-human animal","termid":"MONDO:1011348"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"post-bacterial disorder, non-human animal","termid":"MONDO:1011346","xrefs":{"Monarch":{"xref_id":"1011346"}}}


id: FYPO:0003694
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 18S ribosomal RNA measured in a cell is lower than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased mature rRNA level","termid":"FYPO:0006470"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320","FYPO:0005447","FYPO:0006551"],"is_obsolete":false,"name":"decreased mature 18S rRNA level","synonyms":[{"name":"decreased 18S rRNA level","type":"broad"},{"name":"decreased mature 18S rRNA accumulation","type":"related"},{"name":"decreased mature 18S rRNA level during mitotic cell cycle","type":"related"},{"name":"decreased mature 18S rRNA level during vegetative growth","type":"exact"},{"name":"decreased mature 18S rRNA transcript level","type":"exact"},{"name":"reduced mature 18S rRNA level","type":"exact"}],"termid":"FYPO:0003694"}


id: PBO:0081308
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 90 pseudogene 3","termid":"PBO:0081308"}


id: MONDO:0015953
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete genetic central nervous system and retinal vascular disease (obsolete MONDO:0015953)","secondary_identifiers":["Orphanet:183503"],"termid":"MONDO:0015953","xrefs":{"Monarch":{"xref_id":"0015953"}}}


id: PBO:0047417
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box and WD repeat domain containing 8","termid":"PBO:0047417"}


id: PBO:0045761
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ethylmalonyl-CoA decarboxylase 1","termid":"PBO:0045761"}


id: PBO:0087458
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of a heterodimeric guanine nucleotide exchange factor (GEF); subunit of the Mon1-Ccz1 GEF complex, which stimulates nucleotide exchange and activation of Ypt7p, a Rab family GTPase involved in membrane tethering and fusion events at the late endosome and vacuole; GEF activity is stimulated by membrane association and anionic phospholipids; involved in localizing Ypt7p to the vacuolar membrane; required for macroautophagy, the CVT pathway and mitophagy","termid":"PBO:0087458"}


id: PBO:0087930
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Trans-golgi network aminophospholipid translocase (flippase); type 4 P-type ATPase; involved in phospholipid translocation, contributing to the maintenance of membrane lipid asymmetry in post-Golgi secretory vesicles; role in protein trafficking between the Golgi and endosomal system; localizes to the trans-Golgi network; localizes to the shmoo tip where it has a redundant role in the cellular response to mating pheromone","termid":"PBO:0087930"}


id: PBO:0065156
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein arginine methyltransferase 6","termid":"PBO:0065156"}


id: GO:1901781
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving p-cumate.","definition_xrefs":["GOC:TermGenie","GOC:yaf","PMID:8631713"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monocarboxylic acid metabolic process","termid":"GO:0032787"},{"relation_name":"is_a","term_name":"benzene-containing compound metabolic process","termid":"GO:0042537"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"p-cumate metabolic process","synonyms":[{"name":"p-cumate metabolism","type":"exact"}],"termid":"GO:1901781"}


id: MONDO:0005520
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Bone softening and weakening usually caused by deficiency or impaired metabolism of vitamin D. Deficiency of calcium, magnesium, or phosphorus may also cause rickets. It predominantly affects children who suffer from severe malnutrition. It manifests with bone pain, fractures, muscle weakness, and skeletal deformities.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bone remodeling disease","termid":"MONDO:0000833"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rickets","secondary_identifiers":["HP:0002748","EFO:0005583","MEDGEN:48470","MESH:D012279","ICD9:268.0","SCTID:41345002","GARD:5700","NCIT:C26878","DOID:10609","SCTID:68295002","UMLS:C0035579"],"synonyms":[{"name":"active rickets","type":"related"},{"name":"hypovitaminosis D","type":"related"},{"name":"nutritional rickets","type":"related"},{"name":"rachitis","type":"exact"},{"name":"rickets","type":"exact"},{"name":"rickets (disease)","type":"exact"},{"name":"vitamin D deficiency disease","type":"related"},{"name":"vitamin D hydroxylation-deficient rickets","type":"exact"},{"name":"vitamin-D deficiency rickets","type":"related"}],"termid":"MONDO:0005520","xrefs":{"Monarch":{"xref_id":"0005520"}}}


id: MOD:00624
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"Natural or modified residues with a mass of 113.0-113.1 Da.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"residues isobaric at a resolution below 0.1 Da","termid":"MOD:00616"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"residues isobaric at 113.0-113.1 Da","termid":"MOD:00624"}


id: GO:2000375
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of oxygen metabolic process.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of metabolic process","termid":"GO:0009892"},{"relation_name":"is_a","term_name":"regulation of oxygen metabolic process","termid":"GO:2000374"},{"relation_name":"negatively_regulates","term_name":"oxygen metabolic process","termid":"GO:0072592"}],"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 oxygen metabolic process","synonyms":[{"name":"negative regulation of diatomic oxygen metabolic process","type":"exact"},{"name":"negative regulation of oxygen metabolism","type":"exact"}],"termid":"GO:2000375"}


id: PBO:0052032
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"JRK like","termid":"PBO:0052032"}


id: MONDO:1012489
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hypotrichosis with short life expectancy, non-human animal","termid":"MONDO:1011759"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypotrichosis with short life expectancy, domestic cat","secondary_identifiers":["OMIA:001949-9685"],"termid":"MONDO:1012489","xrefs":{"Monarch":{"xref_id":"1012489"}}}


id: MONDO:0043172
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pfeiffer rockelein syndrome","secondary_identifiers":["MESH:C537890","UMLS:C2931656","MEDGEN:419465"],"synonyms":[{"name":"asymmetrical coronal synostosis, cutaneous syndactyly of fingers and toes, and jejunal atresia","type":"related"}],"termid":"MONDO:0043172","xrefs":{"Monarch":{"xref_id":"0043172"}}}


id: GO:0015189
data:
  {"annotated_genes":["SJAG_03400","SJAG_04637","SJAG_02029","SJAG_03256","SJAG_04725"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[96559,99549,101985,103020,109181],"is_not":false,"summary":null,"term":"GO:0015189"}]},"cv_name":"molecular_function","definition":"Enables the transfer of L-lysine from one side of a membrane to the other. L-lysine is 2,6-diaminohexanoic acid.","definition_xrefs":["GOC:ai","ISBN:0815340729","GOC:mtg_transport"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic cation transmembrane transporter activity","termid":"GO:0015101"},{"relation_name":"is_a","term_name":"basic amino acid transmembrane transporter activity","termid":"GO:0015174"},{"relation_name":"is_a","term_name":"L-amino acid transmembrane transporter activity","termid":"GO:0015179"}],"gene_count":5,"genes_by_uniquename":{"SJAG_02029":null,"SJAG_03256":null,"SJAG_03400":null,"SJAG_04637":null,"SJAG_04725":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"L-lysine transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0005293"],"synonyms":[{"name":"L-lysine permease","type":"related"},{"name":"histidine/arginine/lysine/ornithine porter activity","type":"narrow"},{"name":"lysine permease activity","type":"related"}],"termid":"GO:0015189","terms_by_termid":{"GO:0015189":null}}


id: GO:0045830
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of isotype switching.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of immunoglobulin production","termid":"GO:0002639"},{"relation_name":"is_a","term_name":"positive regulation of immunoglobulin mediated immune response","termid":"GO:0002891"},{"relation_name":"is_a","term_name":"regulation of isotype switching","termid":"GO:0045191"},{"relation_name":"is_a","term_name":"positive regulation of DNA recombination","termid":"GO:0045911"},{"relation_name":"is_a","term_name":"positive regulation of B cell activation","termid":"GO:0050871"},{"relation_name":"is_a","term_name":"positive regulation of developmental process","termid":"GO:0051094"},{"relation_name":"positively_regulates","term_name":"isotype switching","termid":"GO:0045190"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006310"},{"rel_name":"regulates","termid":"GO:0006310"},{"rel_name":"regulates","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"positively_regulates","termid":"GO:0010467"},{"rel_name":"positively_regulates","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0010467","GO:0006259","GO:0006310","GO:0008150"],"is_obsolete":false,"name":"positive regulation of isotype switching","synonyms":[{"name":"activation of isotype switching","type":"narrow"},{"name":"positive regulation of class switch recombination","type":"exact"},{"name":"positive regulation of class switching","type":"exact"},{"name":"positive regulation of isotype switch recombination","type":"exact"},{"name":"stimulation of isotype switching","type":"narrow"},{"name":"up regulation of isotype switching","type":"exact"},{"name":"up-regulation of isotype switching","type":"exact"},{"name":"upregulation of isotype switching","type":"exact"}],"termid":"GO:0045830"}


id: PBO:0076173
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sulfotransferase family 1C member 4","termid":"PBO:0076173"}


id: MONDO:0002696
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A sex cord-stromal tumor of the testis or the ovary. It is characterized by the presence of Sertoli cells forming tubules. Leydig cells are rare or absent. It may be associated with Peutz-Jeghers syndrome. In males, the presenting symptom is a slow growing testicular mass. Most cases follow a benign clinical course. In females it may present with estrogenic or androgenic manifestations. The vast majority of cases have a benign clinical course.","definition_xrefs":["NCIT:C39976"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sex cord-stromal tumor","termid":"MONDO:0006055"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sertoli cell tumor","secondary_identifiers":["MESH:D012707","UMLS:C0036769","MEDGEN:11387","DOID:3577","ICDO:8640/1","ICDO:8630/1"],"synonyms":[{"name":"Sertoli cell tumor","type":"exact"},{"name":"tubular androblastoma","type":"exact"},{"name":"tubular androblastoma NOS (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0002696","xrefs":{"Monarch":{"xref_id":"0002696"}}}


id: MONDO:0005584
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Serious heritable structural anomalies of the left side of the heart, including hypoplastic left heart syndrome, aortic valve stenosis, coarctation of the aorta, mitral valve anomalies and bicuspid aortic valve, that are present from birth.","definition_xrefs":["EFO:0005938"],"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 left-sided heart lesions","secondary_identifiers":["UMLS:C4022397","MEDGEN:868006"],"termid":"MONDO:0005584","xrefs":{"Monarch":{"xref_id":"0005584"}}}


id: GO:0033752
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: pentane-2,4-dione + O2 = acetate + 2-oxopropanal.","definition_xrefs":["EC:1.13.11.50"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen","termid":"GO:0016702"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"acetylacetone-cleaving enzyme activity","secondary_identifiers":["RHEA:12877"],"synonyms":[{"name":"Dke1","type":"related"},{"name":"acetylacetone dioxygenase activity","type":"related"},{"name":"acetylacetone-cleaving enzyme","type":"related"},{"name":"acetylacetone:oxygen oxidoreductase activity","type":"related"},{"name":"diketone cleaving dioxygenase activity","type":"related"},{"name":"diketone cleaving enzyme","type":"related"}],"termid":"GO:0033752"}


id: GO:0140028
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation of a transient pore in the plasma membrane and the attached contractile vacuolar membrane, to release water from the cell. This process does not involve fusion of the two membranes.","definition_xrefs":["Wikipedia:Exocytosis","PMID:22323285"],"direct_ancestors":[{"relation_name":"is_a","term_name":"exocytic process","termid":"GO:0140029"},{"relation_name":"part_of","term_name":"contractile vacuole discharge","termid":"GO:0070177"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0016192","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"pore formation during contractile vacuole discharge","termid":"GO:0140028"}


id: GO:0106383
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process which produces a dAMP from derivatives of it, without de novo synthesis.","definition_xrefs":["PMID:21829339","PMID:6605343"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dAMP biosynthetic process","termid":"GO:0006170"},{"relation_name":"is_a","term_name":"purine deoxyribonucleotide salvage","termid":"GO:0106381"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0055086","GO:0044281"],"is_obsolete":false,"name":"dAMP salvage","termid":"GO:0106383"}


id: PBO:0091643
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane fluoride export channel Fex2","termid":"PBO:0091643"}


id: GO:0005736
data:
  {"annotated_genes":["SJAG_01948","SJAG_01444","SJAG_03956","SJAG_04106","SJAG_01765","SJAG_01698","SJAG_01313","SJAG_02653","SJAG_03578","SJAG_02871","SJAG_02070","SJAG_03468","SJAG_01562","SJAG_04261","SJAG_03144","SJAG_02101","SJAG_00731","SJAG_01128"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[86889,86890,88761,89585,91226,93097,94936,101716,101863,102512,104043,104948,108931,109821,112271,112643,112644,112925,113346,114655],"is_not":false,"summary":null,"term":"GO:0005736"}]},"cv_name":"cellular_component","definition":"RNA polymerase I, one of three nuclear DNA-directed RNA polymerases found in all eukaryotes, is a multisubunit complex; typically it produces rRNAs. Two large subunits comprise the most conserved portion including the catalytic site and share similarity with other eukaryotic and bacterial multisubunit RNA polymerases. The remainder of the complex is composed of smaller subunits (generally ten or more), some of which are also found in RNA polymerase III and others of which are also found in RNA polymerases II and III. Although the core is competent to mediate ribonucleic acid synthesis, it requires additional factors to select the appropriate template.","definition_xrefs":["GOC:krc","GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear DNA-directed RNA polymerase complex","termid":"GO:0055029"},{"relation_name":"part_of","term_name":"nucleolus","termid":"GO:0005730"}],"gene_count":18,"genes_by_uniquename":{"SJAG_00731":null,"SJAG_01128":null,"SJAG_01313":null,"SJAG_01444":null,"SJAG_01562":null,"SJAG_01698":null,"SJAG_01765":null,"SJAG_01948":null,"SJAG_02070":null,"SJAG_02101":null,"SJAG_02653":null,"SJAG_02871":null,"SJAG_03144":null,"SJAG_03468":null,"SJAG_03578":null,"SJAG_03956":null,"SJAG_04106":null,"SJAG_04261":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005730"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0032991","GO:0005634","GO:0005575","GO:0005730"],"is_obsolete":false,"name":"RNA polymerase I complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"DNA-directed RNA polymerase I activity","type":"related"},{"name":"DNA-directed RNA polymerase I complex","type":"exact"}],"termid":"GO:0005736","terms_by_termid":{"GO:0005736":null}}


id: FYPO:0003593
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 occurrence of ubiquitin-dependent protein degradation with ubiquitin-protein ligation catalyzed by the anaphase-promoting complex, and mediated by the proteasome, is abolished.","definition_xrefs":["GO:0031145","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein modification during vegetative growth","termid":"FYPO:0000544"},{"relation_name":"is_a","term_name":"decreased anaphase-promoting complex-dependent protein catabolic process","termid":"FYPO:0003585"},{"relation_name":"is_a","term_name":"abolished proteolysis during vegetative growth","termid":"FYPO:0005377"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0002494","FYPO:0005447","FYPO:0002274","FYPO:0001320"],"is_obsolete":false,"name":"abolished anaphase-promoting complex-dependent protein catabolic process","synonyms":[{"name":"abolished anaphase-promoting complex-dependent proteasomal ubiquitin-dependent protein catabolic process","type":"exact"},{"name":"abolished anaphase-promoting complex-dependent protein catabolic process during mitotic cell cycle","type":"related"},{"name":"abolished anaphase-promoting complex-dependent protein catabolic process during vegetative growth","type":"exact"},{"name":"abolished anaphase-promoting complex-dependent protein degradation","type":"exact"},{"name":"anaphase-promoting complex-dependent protein catabolic process abolished","type":"exact"}],"termid":"FYPO:0003593"}


id: GO:0044678
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that in Methanobacterium thermoautotrophicum is composed of six subunits, and in Methanosarcina barkeri contains is composed of either two subunits or nine subunits. Catalyzes the conversion of coenzyme B, coenzyme M, and methanophenazine to form N-{7-[(2-sulfoethyl)dithio]heptanoyl}-3-O-phospho-L-threonine and dihydromethanophenazine.","definition_xrefs":["PMID:8119281","PMID:8174566","GOC:mengo_curators","PMID:9063468"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase complex","termid":"GO:1990204"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"CoB-CoM heterodisulfide reductase complex","synonyms":[{"name":"coenzyme M-7-mercaptoheptanoylthreonine-phosphate-heterodisulfide hydrogenase complex","type":"exact"},{"name":"hydrogen:coenzyme-M-7-mercaptoheptanoylthreonine-phosphate-heterodisulfide oxidoreductase complex","type":"exact"}],"termid":"GO:0044678"}


id: GO:1903440
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex which is capable of amylin receptor activity.","definition_xrefs":["GOC:TermGenie","PMID:10871296","GO_REF:0000088","PMID:18687416","GOC:bhm","PMID:12037140"],"direct_ancestors":[{"relation_name":"is_a","term_name":"calcitonin family receptor complex","termid":"GO:1903439"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005575","GO:0005886","GO:0032991"],"is_obsolete":false,"name":"amylin receptor complex","termid":"GO:1903440"}


id: MONDO:0021042
data:
  {"annotated_genes":["SJAG_04213","SJAG_01111"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86535,86536],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0024517"}]},"cv_name":"mondo","definition":"A benign or malignant brain and spinal cord tumor that arises from glial cells (astrocytes, oligodendrocytes, ependymal cells). Tumors that arise from astrocytes are called astrocytic tumors or astrocytomas. Tumors that arise from oligodendrocytes are called oligodendroglial tumors. Tumors that arise from ependymal cells are called ependymomas.","definition_xrefs":["NCIT:C3059"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuroepithelial neoplasm","termid":"MONDO:0021193"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01111":null,"SJAG_04213":null},"genotype_count":0,"is_obsolete":false,"name":"glioma","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["EFO:0005543","Orphanet:182067","MEDGEN:9030","GARD:6513","MESH:D005910","SCTID:393564001","UMLS:C0017638"],"synonyms":[{"name":"glial neoplasm","type":"exact"},{"name":"glial tumor","type":"exact"},{"name":"glial tumour","type":"exact"},{"name":"glioma","type":"exact"},{"name":"neoplasm of neuroglia","type":"exact"},{"name":"neoplasm of the neuroglia","type":"exact"},{"name":"neuroglial neoplasm","type":"exact"},{"name":"neuroglial tumor","type":"exact"},{"name":"neuroglial tumour","type":"exact"},{"name":"tumor of neuroglia","type":"exact"},{"name":"tumor of the neuroglia","type":"exact"},{"name":"tumour of neuroglia","type":"exact"},{"name":"tumour of the neuroglia","type":"exact"}],"termid":"MONDO:0021042","terms_by_termid":{"MONDO:0024517":null},"xrefs":{"Monarch":{"xref_id":"0021042"}}}


id: PBO:0003507
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DUF1769 family protein","termid":"PBO:0003507"}


id: PBO:0041215
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C1D nuclear receptor corepressor pseudogene 3","termid":"PBO:0041215"}


id: PBO:0069144
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 395, pseudogene","termid":"PBO:0069144"}


id: GO:0060686
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate, frequency, or extent of prostatic bud formation, the morphogenetic process in which a region of the fetal urogenital sinus epithelium is specified to become the prostate, resulting in prostate bud outgrowth.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of prostatic bud formation","termid":"GO:0060685"},{"relation_name":"is_a","term_name":"negative regulation of morphogenesis of an epithelium","termid":"GO:1905331"},{"relation_name":"is_a","term_name":"negative regulation of reproductive process","termid":"GO:2000242"},{"relation_name":"negatively_regulates","term_name":"prostatic bud formation","termid":"GO:0060513"}],"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 prostatic bud formation","termid":"GO:0060686"}


id: PBO:0079013
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-SeC (anticodon TCA) 1-1","termid":"PBO:0079013"}


id: MONDO:0859289
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"intestinal disorder","termid":"MONDO:0005020"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"intestinal dysmotility syndrome","secondary_identifiers":["MEDGEN:1823992","OMIM:620045","UMLS:C5774219"],"termid":"MONDO:0859289","xrefs":{"Monarch":{"xref_id":"0859289"}}}


id: MONDO:0015115
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare genetic metabolic liver disease (obsolete MONDO:0015115)","secondary_identifiers":["MedDRA:10019689","Orphanet:101940"],"termid":"MONDO:0015115","xrefs":{"Monarch":{"xref_id":"0015115"}}}


id: GO:1902902
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of autophagosome assembly.","definition_xrefs":["GOC:als","GOC:TermGenie","PMID:21975012","GO_REF:0000058","GOC:autophagy"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of macroautophagy","termid":"GO:0016242"},{"relation_name":"is_a","term_name":"negative regulation of organelle assembly","termid":"GO:1902116"},{"relation_name":"is_a","term_name":"regulation of autophagosome assembly","termid":"GO:2000785"},{"relation_name":"negatively_regulates","term_name":"autophagosome assembly","termid":"GO:0000045"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006914"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006914"}],"interesting_parent_ids":["GO:0006914","GO:0044085","GO:0008150"],"is_obsolete":false,"name":"negative regulation of autophagosome assembly","synonyms":[{"name":"down regulation of PAS formation","type":"narrow"},{"name":"down regulation of autophagic vacuole assembly","type":"exact"},{"name":"down regulation of autophagic vacuole formation","type":"related"},{"name":"down regulation of autophagosome biosynthesis","type":"exact"},{"name":"down regulation of autophagosome formation","type":"exact"},{"name":"down-regulation of PAS formation","type":"narrow"},{"name":"down-regulation of autophagic vacuole assembly","type":"exact"},{"name":"down-regulation of autophagic vacuole formation","type":"related"},{"name":"down-regulation of autophagosome biosynthesis","type":"exact"},{"name":"down-regulation of autophagosome formation","type":"exact"},{"name":"downregulation of PAS formation","type":"narrow"},{"name":"downregulation of autophagic vacuole assembly","type":"exact"},{"name":"downregulation of autophagic vacuole formation","type":"related"},{"name":"downregulation of autophagosome biosynthesis","type":"exact"},{"name":"downregulation of autophagosome formation","type":"exact"},{"name":"inhibition of PAS formation","type":"narrow"},{"name":"inhibition of autophagic vacuole assembly","type":"narrow"},{"name":"inhibition of autophagic vacuole formation","type":"related"},{"name":"inhibition of autophagosome biosynthesis","type":"narrow"},{"name":"inhibition of autophagosome formation","type":"narrow"},{"name":"negative regulation of PAS formation","type":"narrow"},{"name":"negative regulation of autophagic vacuole assembly","type":"exact"},{"name":"negative regulation of autophagic vacuole formation","type":"related"},{"name":"negative regulation of autophagosome biosynthesis","type":"exact"},{"name":"negative regulation of autophagosome formation","type":"exact"}],"termid":"GO:1902902"}


id: MONDO:0011999
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"otosclerosis","termid":"MONDO:0005349"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"otosclerosis 3","secondary_identifiers":["MESH:C564268","OMIM:608244","UMLS:C1842353","MEDGEN:334054","DOID:0060922"],"synonyms":[{"name":"OTSC3","type":"exact"},{"name":"otosclerosis 3","type":"exact"}],"termid":"MONDO:0011999","xrefs":{"Monarch":{"xref_id":"0011999"}}}


id: FYPO:0000938
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the cortical microtubule cytoskeleton during interphase of the mitotic cell cycle does not occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to cell cortex during vegetative growth","termid":"FYPO:0000930"},{"relation_name":"is_a","term_name":"abolished protein localization to microtubule cytoskeleton during vegetative growth","termid":"FYPO:0000934"},{"relation_name":"is_a","term_name":"abnormal protein localization to cortical microtubule cytoskeleton during vegetative growth","termid":"FYPO:0000935"},{"relation_name":"is_a","term_name":"abolished protein localization to cortical microtubule cytoskeleton","termid":"FYPO:0004266"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000138","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"abolished protein localization to cortical microtubule cytoskeleton during mitotic interphase","synonyms":[{"name":"abolished protein localisation to cortical microtubule cytoskeleton mitotic interphase during vegetative growth","type":"exact"},{"name":"abolished protein localization to cortical microtubule cytoskeleton during interphase of mitotic cell cycle","type":"exact"},{"name":"protein absent from cortical microtubule cytoskeleton during mitotic interphase","type":"related"},{"name":"protein localization to cortical microtubule cytoskeleton abolished during mitotic interphase","type":"exact"}],"termid":"FYPO:0000938"}


id: PBO:0084725
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial inner membrane protein; required for proteolytic processing of Cox2p and its assembly into cytochrome c oxidase","termid":"PBO:0084725"}


id: GO:0033784
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H+ + NADPH + O2 + senecionine = H2O + NADP+ + senecionine N-oxide.","definition_xrefs":["EC:1.14.13.101","RHEA:11420"],"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:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"senecionine N-oxygenase activity","secondary_identifiers":["MetaCyc:1.14.13.101-RXN","KEGG_REACTION:R07373"],"synonyms":[{"name":"SNO","type":"related"},{"name":"senecionine monooxygenase (N-oxide-forming) activity","type":"related"},{"name":"senecionine,NADPH:oxygen oxidoreductase (N-oxide-forming) activity","type":"related"}],"termid":"GO:0033784"}


id: GO:1905645
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of FACT complex assembly.","definition_xrefs":["PMID:20889714","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein-containing complex assembly","termid":"GO:0031333"},{"relation_name":"is_a","term_name":"regulation of FACT complex assembly","termid":"GO:1905644"},{"relation_name":"negatively_regulates","term_name":"FACT complex assembly","termid":"GO:1905635"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"negatively_regulates","termid":"GO:0065003"},{"rel_name":"regulates","termid":"GO:0065003"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044085","GO:0008150","GO:0065003"],"is_obsolete":false,"name":"negative regulation of FACT complex assembly","synonyms":[{"name":"down regulation of FACT complex assembly","type":"exact"},{"name":"down regulation of FACT complex formation","type":"exact"},{"name":"down regulation of Facilitates chromatin transcription complex assembly","type":"exact"},{"name":"down regulation of Facilitates chromatin transcription complex formation","type":"exact"},{"name":"down-regulation of FACT complex assembly","type":"exact"},{"name":"down-regulation of FACT complex formation","type":"exact"},{"name":"down-regulation of Facilitates chromatin transcription complex assembly","type":"exact"},{"name":"down-regulation of Facilitates chromatin transcription complex formation","type":"exact"},{"name":"downregulation of FACT complex assembly","type":"exact"},{"name":"downregulation of FACT complex formation","type":"exact"},{"name":"downregulation of Facilitates chromatin transcription complex assembly","type":"exact"},{"name":"downregulation of Facilitates chromatin transcription complex formation","type":"exact"},{"name":"inhibition of FACT complex assembly","type":"narrow"},{"name":"inhibition of FACT complex formation","type":"narrow"},{"name":"inhibition of Facilitates chromatin transcription complex assembly","type":"narrow"},{"name":"inhibition of Facilitates chromatin transcription complex formation","type":"narrow"},{"name":"negative regulation of FACT complex formation","type":"exact"},{"name":"negative regulation of Facilitates chromatin transcription complex assembly","type":"exact"},{"name":"negative regulation of Facilitates chromatin transcription complex formation","type":"exact"}],"termid":"GO:1905645"}


id: PATO:0000913
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000913 qualitative value (obsolete PATO:0000913)","termid":"PATO:0000913"}


id: PBO:0075981
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"signal transducer and activator of transcription 5B","termid":"PBO:0075981"}


id: PBO:0075831
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"structure specific recognition protein 1","termid":"PBO:0075831"}


id: FYPO:0005171
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the import of uracil into the cell occurs to a lower extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal uracil import","termid":"FYPO:0005170"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000138","FYPO:0005447","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"decreased uracil import","synonyms":[{"name":"decreased uracil import across plasma membrane","type":"exact"},{"name":"decreased uracil import during mitotic cell cycle","type":"related"},{"name":"decreased uracil import during vegetative growth","type":"exact"},{"name":"decreased uracil import into cell","type":"exact"},{"name":"decreased uracil uptake","type":"exact"},{"name":"reduced uracil import","type":"exact"}],"termid":"FYPO:0005171"}


id: GO:0000726
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A DNA repair process in which that does not require the exchange of genetic material between the broken DNA molecule and a homologous DNA region.","definition_xrefs":["GOC:elh"],"gene_count":0,"genotype_count":0,"name":"obsolete non-recombinational repair (obsolete GO:0000726)","termid":"GO:0000726"}


id: GO:1900026
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of substrate adhesion-dependent cell spreading.","definition_xrefs":["GOC:yaf","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell-substrate adhesion","termid":"GO:0010811"},{"relation_name":"is_a","term_name":"regulation of substrate adhesion-dependent cell spreading","termid":"GO:1900024"},{"relation_name":"positively_regulates","term_name":"substrate adhesion-dependent cell spreading","termid":"GO:0034446"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"positive regulation of substrate adhesion-dependent cell spreading","synonyms":[{"name":"positive regulation of cell spreading during cell substrate adhesion","type":"exact"},{"name":"positive regulation of substrate adhesion dependent cell spreading","type":"exact"},{"name":"up regulation of cell spreading during cell substrate adhesion","type":"exact"},{"name":"up regulation of substrate adhesion dependent cell spreading","type":"exact"},{"name":"up regulation of substrate adhesion-dependent cell spreading","type":"related"}],"termid":"GO:1900026"}


id: PBO:0110873
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat protein, DDB1 and CUL4-associated factor Dca7, implicated in gene expression","termid":"PBO:0110873"}


id: PBO:0051727
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inhibitory synaptic factor family member 2B","termid":"PBO:0051727"}


id: GO:2000518
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of T-helper 1 cell activation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of CD4-positive, alpha-beta T cell activation","termid":"GO:2000515"},{"relation_name":"is_a","term_name":"regulation of T-helper 1 cell activation","termid":"GO:2000517"},{"relation_name":"negatively_regulates","term_name":"T-helper 1 cell activation","termid":"GO:0035711"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007155"},{"rel_name":"negatively_regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"negative regulation of T-helper 1 cell activation","synonyms":[{"name":"negative regulation of Th1 cell activation","type":"exact"}],"termid":"GO:2000518"}


id: PBO:0078993
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Thr (anticodon AGT) 1-3","termid":"PBO:0078993"}


id: MONDO:0002462
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A renal disorder characterized by damage in the glomeruli. It may be acute or chronic, focal or diffuse, and it may lead to renal failure. Causes include autoimmune disorders, infections, diabetes, and malignancies.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nephritis","termid":"MONDO:0001166"},{"relation_name":"is_a","term_name":"glomerular disorder","termid":"MONDO:0019722"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"glomerulonephritis","secondary_identifiers":["MESH:D005921","ICD9:583.9","HP:0000099","NCIT:C26784","SCTID:36171008","DOID:2921","MEDGEN:6616","UMLS:C0017658","GARD:6516"],"synonyms":[{"name":"bright's disease","type":"related"},{"name":"glomerular nephritis","type":"exact"},{"name":"glomerulonephritis","type":"exact"},{"name":"glomerulonephritis (disease)","type":"exact"},{"name":"nephritis of renal glomerulus","type":"exact"},{"name":"renal glomerulus nephritis","type":"exact"}],"termid":"MONDO:0002462","xrefs":{"Monarch":{"xref_id":"0002462"}}}


id: PR:O14340
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC2F12.05c gene.","definition_xrefs":["UniProtKB:O14340","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":"oxysterol-binding protein homolog C2F12.05c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC2F12.05c","synonyms":[{"name":"Spom972h-SPBC2F12.05c","type":"exact"}],"termid":"PR:O14340"}


id: PBO:0038827
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADAM like decysin 1","termid":"PBO:0038827"}


id: PBO:0002448
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA-binding protein Rbp28","termid":"PBO:0002448"}


id: GO:0002557
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regulated release of histamine by a basophil or group of basophils.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histamine secretion involved in inflammatory response","termid":"GO:0002441"},{"relation_name":"is_a","term_name":"establishment of localization in cell","termid":"GO:0051649"},{"relation_name":"is_a","term_name":"exocytic process","termid":"GO:0140029"},{"relation_name":"part_of","term_name":"basophil degranulation","termid":"GO:0002561"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0016192"},{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0023052","GO:0008150","GO:0006810","GO:0051179","GO:0016192"],"is_obsolete":false,"name":"histamine secretion by basophil","termid":"GO:0002557"}


id: PBO:0029083
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_ubiquitination","termid":"PBO:0029083"}


id: PBO:0091504
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"centromeric lncRNA nam5","termid":"PBO:0091504"}


id: MONDO:0007876
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"laryngeal abductor paralysis-intellectual disability syndrome","termid":"MONDO:0010639"},{"relation_name":"is_a","term_name":"laryngeal disorder","termid":"MONDO:0004382"},{"relation_name":"is_a","term_name":"otorhinolaryngologic disease","termid":"MONDO:0024623"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"laryngeal abductor paralysis","secondary_identifiers":["SCTID:232442001","icd11.foundation:965049946","OMIM:150260","MEDGEN:96004","GARD:5509","Orphanet:2808","ICD9:748.3","UMLS:C0396059"],"synonyms":[{"name":"Gerhardt syndrome","type":"exact"},{"name":"Labd","type":"related"},{"name":"familial vocal cord dysfunction","type":"exact"},{"name":"laryngeal abductor paralysis","type":"exact"},{"name":"vocal cord dysfunction familial","type":"related"},{"name":"vocal cord dysfunction, familial","type":"related"}],"termid":"MONDO:0007876","xrefs":{"Monarch":{"xref_id":"0007876"}}}


id: FYECO:0000287
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which nigericin was added to the medium or assay buffer.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ nigericin","termid":"FYECO:0000287"}


id: GO:0060783
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals generated as a consequence of activation of the transmembrane Smoothened-type protein in the mesenchymal cells of the prostate that contribute to the progression of the prostate over time. This process contributes to lung development.","definition_xrefs":["PMID:12221011"],"direct_ancestors":[{"relation_name":"is_a","term_name":"smoothened signaling pathway","termid":"GO:0007224"},{"relation_name":"part_of","term_name":"epithelial-mesenchymal signaling involved in prostate gland development","termid":"GO:0060738"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"mesenchymal smoothened signaling pathway involved in prostate gland development","synonyms":[{"name":"mesenchymal hedgehog signaling pathway involved in prostate gland development","type":"exact"},{"name":"mesenchymal hh signaling pathway involved in prostate gland development","type":"exact"},{"name":"mesenchymal smoothened signalling pathway involved in prostate gland development","type":"exact"}],"termid":"GO:0060783"}


id: MONDO:0019727
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Type III mixed cryoglobulinemia, a relatively rare clinico-serological subtype of mixed cryoglobulinemia (MC), is an immune complex disorder characterized by purpura, weakness and arthralgia and defined immunochemically by cryoglobulins containing both polyclonal IgGs and polyclonal IgMs.","definition_xrefs":["Orphanet:93555"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Cryoglobulinemic vasculitis","termid":"MONDO:0007407"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mixed cryoglobulinemia type III","secondary_identifiers":["ICD10CM:D89.1","UMLS:C5680263","MEDGEN:1843066","GARD:19221"],"synonyms":[{"name":"MC type III","type":"exact"}],"termid":"MONDO:0019727","xrefs":{"Monarch":{"xref_id":"0019727"}}}


id: GO:2000822
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of behavioral fear response.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of defense response","termid":"GO:0031347"},{"relation_name":"is_a","term_name":"regulation of behavior","termid":"GO:0050795"},{"relation_name":"is_a","term_name":"regulation of fear response","termid":"GO:1903365"},{"relation_name":"regulates","term_name":"behavioral fear response","termid":"GO:0001662"}],"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 behavioral fear response","synonyms":[{"name":"regulation of behavioural fear response","type":"exact"}],"termid":"GO:2000822"}


id: PBO:0003003
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amidase (predicted)","termid":"PBO:0003003"}


id: MONDO:0009972
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":"respiratory underresponsiveness to hypoxia and hypercapnia","secondary_identifiers":["MEDGEN:341453","UMLS:C1849430","OMIM:267480","MESH:C564848"],"synonyms":[{"name":"respiratory underresponsiveness to hypoxia and hypercapnia","type":"exact"}],"termid":"MONDO:0009972","xrefs":{"Monarch":{"xref_id":"0009972"}}}


id: GO:1903842
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an arsenite ion stimulus.","definition_xrefs":["GO_REF:0000071","GOC:TermGenie","PMID:12106899","GOC:mr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to arsenic-containing substance","termid":"GO:0046685"},{"relation_name":"is_a","term_name":"response to oxygen-containing compound","termid":"GO:1901700"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to arsenite ion","termid":"GO:1903842"}


id: PBO:0074717
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, H/ACA box 77B","termid":"PBO:0074717"}


id: PBO:0075015
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 115-26","termid":"PBO:0075015"}


id: MOD:01353
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Chemical derivative -","definition_xrefs":["PubMed:15602776","PubMed:12643539","Unimod:141#K","PubMed:6273432"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amidination of lysines or N-terminal amines with methyl acetimidate","termid":"MOD:00509"},{"relation_name":"is_a","term_name":"modified L-lysine residue","termid":"MOD:00912"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amidination of lysines or N-terminal amines with methyl acetimidate - site K","synonyms":[{"name":"Amidine","type":"related"},{"name":"amidination of lysines or N-terminal amines with methyl acetimidate","type":"related"}],"termid":"MOD:01353"}


id: MONDO:0008653
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial vesicoureteral reflux","termid":"MONDO:0017329"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vesicoureteral reflux 1","secondary_identifiers":["GARD:18418","MEDGEN:1644868","OMIM:193000","UMLS:C4551858"],"synonyms":[{"name":"VUR","type":"related"},{"name":"VUR1","type":"exact"},{"name":"Vesicoureteral reflux","type":"exact"},{"name":"vesicoureteral reflux 1","type":"exact"}],"termid":"MONDO:0008653","xrefs":{"Monarch":{"xref_id":"0008653"}}}


id: RO:HOM0000073
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Synology that results from allopolyploidy.","direct_ancestors":[{"relation_name":"is_a","term_name":"in_ohnology_relationship_with","termid":"RO:HOM0000022"},{"relation_name":"is_a","term_name":"in_synology_relationship_with","termid":"RO:HOM0000053"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"in_homoeology_relationship_with","synonyms":[{"name":"homoeologous to","type":"exact"}],"termid":"RO:HOM0000073"}


id: PBO:0108909
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KIAA1191 pseudogene 3","termid":"PBO:0108909"}


id: PBO:0034055
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-determined_by","termid":"PBO:0034055"}


id: PBO:0044024
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"casein kinase 2 alpha 3","termid":"PBO:0044024"}


id: GO:0046779
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any viral process that discriminates against and subsequently inhibits host transcripts containing introns, thus allowing only intronless viral mRNA to be fully processed.","definition_xrefs":["PMID:11598019"],"gene_count":0,"genotype_count":0,"name":"obsolete suppression by virus of expression of host genes with introns (obsolete GO:0046779)","synonyms":[{"name":"negative regulation by virus of expression of host genes with introns","type":"exact"},{"name":"viral inhibition of expression of host genes with introns","type":"exact"}],"termid":"GO:0046779"}


id: PBO:0001960
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptionally regulates cfh4","termid":"PBO:0001960"}


id: GO:0044525
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The modification of a peptidyl-cystine residue in a protein by the addition of sulfur, to form peptidyl-cysteine persulfide.","definition_xrefs":["GOC:jl","GOC:jsg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein sulfhydration","termid":"GO:0044524"}],"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":"peptidyl-cystine sulfhydration","termid":"GO:0044525"}


id: GO:0038031
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 frizzled family receptor on the surface of the target cell, where the signal is passed on via the JNK cascade.","definition_xrefs":["GOC:BHF","PMID:20032469","PMID:19137009","GPC:rl"],"gene_count":0,"genotype_count":0,"name":"obsolete non-canonical Wnt signaling pathway via JNK cascade (obsolete GO:0038031)","synonyms":[{"name":"non-canonical Wnt receptor signaling pathway via JNK cascade","type":"exact"},{"name":"non-canonical Wnt receptor signalling pathway via JNK cascade","type":"exact"},{"name":"non-canonical Wnt-activated signaling pathway via JNK cascade","type":"exact"}],"termid":"GO:0038031"}


id: PBO:0068110
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 417","termid":"PBO:0068110"}


id: PBO:0044352
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CYCS pseudogene 39","termid":"PBO:0044352"}


id: PR:Q9UTM4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A T-complex protein 1 subunit epsilon that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00509","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":"T-complex protein 1 subunit epsilon (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1420.02c","secondary_identifiers":["UniProtKB:Q9UTM4"],"synonyms":[{"name":"CCT-epsilon (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-CCT5","type":"exact"},{"name":"TCP-1-epsilon (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9UTM4"}


id: MONDO:1011360
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Syndromic disease 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":"syndromic disease, non-human animal","termid":"MONDO:1011360","xrefs":{"Monarch":{"xref_id":"1011360"}}}


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


id: FYPO:0008030
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a blue light photoreceptor activity is abnormal.","definition_xrefs":["PMID:23873862"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal molecular function","termid":"FYPO:0000707"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000652","FYPO:0000707"],"is_obsolete":false,"name":"abnormal blue light photoreceptor activity","references_by_uniquename":{"PMID:23873862":null},"synonyms":[{"name":"defective blue light photoreceptor activity","type":"exact"}],"termid":"FYPO:0008030"}


id: GO:0106201
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the translocation of amino acids and peptides linked to the hydrolysis of a diphosphate.","definition_xrefs":["GOC:hjd"],"gene_count":0,"genotype_count":0,"name":"obsolete translocase activity acting on amino acids and peptides linked to the hydrolysis of a diphosphate (obsolete GO:0106201)","termid":"GO:0106201"}


id: _global:has_relative_magnitude
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_relative_magnitude","termid":"_global:has_relative_magnitude"}


id: PBO:0070860
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L13 pseudogene 13","termid":"PBO:0070860"}


id: MONDO:0014761
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hereditary pediatric Behçet-like disease (obsolete MONDO:0014761)","termid":"MONDO:0014761","xrefs":{"Monarch":{"xref_id":"0014761"}}}


id: GO:0102639
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 13-desoxypaxilline + NADPH + O2 + H+ = paspalicine + NADP + 2 H2O.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete paspalicine synthase activity (obsolete GO:0102639)","termid":"GO:0102639"}


id: GO:0070478
data:
  {"annotated_genes":["SJAG_04084","SJAG_03179","SJAG_03886","SJAG_01521","SJAG_04153","SJAG_00854","SJAG_04824","SJAG_04056","SJAG_04818","SJAG_00226","SJAG_04321","SJAG_04006","SJAG_05014","SJAG_03805","SJAG_04118","SJAG_01218","SJAG_01818"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[87966,89005,90727,92276,95114,96445,100423,101266,103580,104425,105628,106619,107976,115021,115284,116357,117427],"is_not":false,"summary":null,"term":"GO:0070478"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of the nuclear-transcribed mRNA transcript body of an mRNA in which an amino-acid codon has changed to a nonsense codon; occurs when the 3' end is not protected by a 3'-poly(A) tail; degradation proceeds in the 3' to 5' direction.","definition_xrefs":["PMID:12769863"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear-transcribed mRNA catabolic process, nonsense-mediated decay","termid":"GO:0000184"}],"gene_count":17,"genes_by_uniquename":{"SJAG_00226":null,"SJAG_00854":null,"SJAG_01218":null,"SJAG_01521":null,"SJAG_01818":null,"SJAG_03179":null,"SJAG_03805":null,"SJAG_03886":null,"SJAG_04006":null,"SJAG_04056":null,"SJAG_04084":null,"SJAG_04118":null,"SJAG_04153":null,"SJAG_04321":null,"SJAG_04818":null,"SJAG_04824":null,"SJAG_05014":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0016071"},{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0016071","GO:0008150"],"is_obsolete":false,"name":"nuclear-transcribed mRNA catabolic process, 3'-5' exonucleolytic nonsense-mediated decay","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"3'-5' NMD","type":"exact"},{"name":"3'-5' nonsense-mediated decay","type":"exact"},{"name":"3'-5' nonsense-mediated mRNA decay","type":"exact"},{"name":"nuclear-transcribed mRNA breakdown, 3'-5' exonucleolytic nonsense-mediated decay","type":"exact"},{"name":"nuclear-transcribed mRNA catabolism, 3'-5' exonucleolytic nonsense-mediated decay","type":"exact"},{"name":"nuclear-transcribed mRNA degradation, 3'-5' exonucleolytic nonsense-mediated decay","type":"exact"}],"termid":"GO:0070478","terms_by_termid":{"GO:0070478":null}}


id: PBO:0005610
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Swr1 complex bromodomain subunit Brf1","termid":"PBO:0005610"}


id: GO:0102535
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ladanein + S-adenosyl-L-methionine = H+ + S-adenosyl-L-homocysteine + salvigenin.","definition_xrefs":["RHEA:73247"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methyltransferase activity","termid":"GO:0008168"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016740","GO:0016741"],"is_obsolete":false,"name":"ladanein 6-O-methyltransferase activity","secondary_identifiers":["MetaCyc:RXN-14752"],"termid":"GO:0102535"}


id: GO:0048719
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the epistomal sclerite are generated and organized.","definition_xrefs":["GOC:rc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"post-embryonic animal morphogenesis","termid":"GO:0009886"},{"relation_name":"part_of","term_name":"clypeo-labral disc morphogenesis","termid":"GO:0007453"},{"relation_name":"part_of","term_name":"epistomal sclerite development","termid":"GO:0048724"}],"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":"epistomal sclerite morphogenesis","termid":"GO:0048719"}


id: PBO:0032716
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_error-free_translesion_synthesis","termid":"PBO:0032716"}


id: GO:0060938
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which an epicardial cell acquires the specialized structural and/or functional features of a cardiac fibroblast. A cardiac fibroblast is a connective tissue cell in the heart which secretes an extracellular matrix rich in collagen and other macromolecules.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiac fibroblast cell differentiation","termid":"GO:0060935"}],"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":"epicardium-derived cardiac fibroblast cell differentiation","termid":"GO:0060938"}


id: FYPO:0001003
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which a cell contains more, but smaller, vacuoles than normal when the cell is subject to nitrogen starvation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"lipid droplets present in spore cytoplasm in decreased numbers, mislocalized to ascus epiplasm","termid":"FYPO:0006053"},{"relation_name":"is_a","term_name":"small vacuoles present in increased numbers","termid":"FYPO:0002258"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"small vacuoles present in increased numbers during nitrogen starvation","synonyms":[{"name":"fragmented vacuoles during nitrogen starvation","type":"related"},{"name":"small vacuoles present in greater numbers during nitrogen starvation","type":"exact"},{"name":"small vacuoles present in increased numbers during nitrogen depletion","type":"exact"},{"name":"small vacuoles present in increased numbers during nitrogen deprivation","type":"exact"},{"name":"vacuole organization defects, fragmented vacuoles during nitrogen starvation","type":"related"},{"name":"vacuoles present in increased numbers, with decreased vacuole size, during nitrogen starvation","type":"exact"}],"termid":"FYPO:0001003"}


id: GO:0072366
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of a cellular ketone metabolic process by activating or increasing the frequency, rate or extent of transcription from an RNA polymerase II promoter.","definition_xrefs":["GOC:BHF","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of cellular ketone metabolic process by positive regulation of transcription from RNA polymerase II promoter (obsolete GO:0072366)","synonyms":[{"name":"regulation of cellular ketone metabolic process by positive regulation of transcription from an RNA polymerase II promoter","type":"exact"},{"name":"regulation of cellular ketone metabolism by positive regulation of transcription from an RNA polymerase II promoter","type":"exact"}],"termid":"GO:0072366"}


id: PBO:0018281
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mediator complex subunit Med17","termid":"PBO:0018281"}


id: PBO:0082368
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Basic helix-loop-helix (bHLH) protein; forms homodimer to bind E-box consensus sequence CACGTG present at MET gene promoters and centromere DNA element I (CDEI); affects nucleosome positioning at this motif; associates with other transcription factors such as Met4p and Isw1p to mediate transcriptional activation or repression; associates with kinetochore proteins, required for chromosome segregation; protein abundance increases in response to DNA replication stress","termid":"PBO:0082368"}


id: PBO:0056637
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mediator complex subunit 14","termid":"PBO:0056637"}


id: MONDO:0016028
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare neurovascular peripheral pain disorder due to the intermittent blockage of the blood vessels, usually in the lower extremities or hands. This causes hyperemia and inflammation at the origin of burning pain and skin redness. The attacks are periodic and are commonly triggered by heat, pressure, mild activity, exertion, insomnia or stress. Erythromelalgia may occur either as a primary or secondary disorder. Primary erythromelalgia is caused by gene mutations. Secondary erythromelalgia can result from small fiber peripheral neuropathy of any cause, essential thrombocytemia, hypercholesterolemia, mushroom or mercury poisoning, and some autoimmune disorders.","definition_xrefs":["Orphanet:1956"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"peripheral vascular disease","termid":"MONDO:0005294"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"erythromelalgia","secondary_identifiers":["ICD10CM:I73.81","MEDGEN:8687","ICD9:443.82","MESH:D004916","DOID:9240","NCIT:C34593","SCTID:37151006","MedDRA:10015284","icd11.foundation:838760425","UMLS:C0014804"],"termid":"MONDO:0016028","xrefs":{"Monarch":{"xref_id":"0016028"}}}


id: FYPO:0000249
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A vegetative cell population phenotype in which cell growth is decreased relative to normal in a medium containing ammonia as the nitrogen source.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased vegetative cell population growth","termid":"FYPO:0001355"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0002057","FYPO:0001985","FYPO:0000003","FYPO:0002060","FYPO:0005447","FYPO:0002058","FYPO:0000139"],"is_obsolete":false,"name":"decreased cell population growth on ammonia nitrogen source","secondary_identifiers":["FYPO:0000248"],"synonyms":[{"name":"decreased growth on ammonia nitrogen source","type":"broad"},{"name":"decreased vegetative cell growth on ammonia nitrogen source","type":"exact"},{"name":"growth defect, slow growth in minimal media","type":"related"},{"name":"growth defect, slow growth with ammonia nitrogen source","type":"narrow"},{"name":"reduced cell growth on ammonia nitrogen source","type":"exact"},{"name":"slow cell growth in minimal medium","type":"related"},{"name":"slow cell growth on ammonia nitrogen source","type":"narrow"}],"termid":"FYPO:0000249"}


id: MONDO:1011458
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Glaucoma, primary closed-angle that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glaucoma, non-human animal","termid":"MONDO:1011457"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glaucoma, primary closed-angle, non-human animal","secondary_identifiers":["OMIA:001871"],"termid":"MONDO:1011458","xrefs":{"Monarch":{"xref_id":"1011458"}}}


id: FYPO:0007856
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the duration of localization of a protein to the spindle is longer than normal during the first meiotic nuclear division.","definition_xrefs":["PMID:12606573","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to meiotic spindle","termid":"FYPO:0006454"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000138","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"increased duration of protein localization to spindle during meiosis I","synonyms":[{"name":"decreased protein phosphorylation during mitotic cell cycle spindle assembly checkpoint signaling","type":"exact"},{"name":"decreased protein phosphorylation during mitotic spindle assembly checkpoint signalling","type":"exact"},{"name":"decreased protein phosphorylation during mitotic spindle checkpoint","type":"related"},{"name":"decreased protein phosphorylation during signal transduction involved in mitotic spindle assembly checkpoint","type":"exact"},{"name":"decreased protein phosphorylation during spindle assembly checkpoint signaling during mitotic cell cycle","type":"exact"},{"name":"reduced protein phosphorylation during mitotic spindle assembly checkpoint signaling","type":"exact"}],"termid":"FYPO:0007856"}


id: PBO:0042305
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CD22 molecule","termid":"PBO:0042305"}


id: PBO:0004569
data:
  {"annotation_feature_type":"gene","cv_name":"genome_org","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alternative transcripts, alternative initiation site","termid":"PBO:0004569"}


id: PBO:0004387
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spermine family transmembrane transporter Caf5","termid":"PBO:0004387"}


id: GO:0141083
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont interferes with, inhibits or disrupts the host signal transduction pathways leading to the production of reactive oxygen species as part of the host innate immune response. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:31375544","PMID:27473656"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host cellular process","termid":"GO:0044068"},{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host defense response","termid":"GO:0052031"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated suppression of host reactive oxygen species generation","synonyms":[{"name":"inhibition by organism of defense-related host active oxygen species production","type":"exact"}],"termid":"GO:0141083"}


id: PBO:0110424
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TVP23B pseudogene 3","termid":"PBO:0110424"}


id: PBO:0014251
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Induced during Sporogenesis in Pombe","termid":"PBO:0014251"}


id: PBO:0004143
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1-phosphatidylinositol-3-phosphate 5-kinase Fab1","termid":"PBO:0004143"}


id: GO:0031064
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents, or reduces the frequency, rate or extent of the removal of acetyl groups from histones.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of histone deacetylation (obsolete GO:0031064)","synonyms":[{"name":"down regulation of histone deacetylation","type":"exact"},{"name":"down-regulation of histone deacetylation","type":"exact"},{"name":"downregulation of histone deacetylation","type":"exact"},{"name":"inhibition of histone deacetylation","type":"narrow"}],"termid":"GO:0031064"}


id: PBO:0006182
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inhibits_protease","termid":"PBO:0006182"}


id: GO:0004917
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with interleukin-7 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:jl"],"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:0003674","GO:0038023"],"is_obsolete":false,"name":"interleukin-7 receptor activity","synonyms":[{"name":"IL-7 receptor activity","type":"exact"},{"name":"IL-7R","type":"exact"}],"termid":"GO:0004917"}


id: PBO:0061314
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NPHS1 adhesion molecule, nephrin","termid":"PBO:0061314"}


id: MONDO:0017978
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete syndrome with disorder of sex development of gynecological interest (obsolete MONDO:0017978)","secondary_identifiers":["Orphanet:325638"],"synonyms":[{"name":"syndrome with DSD of gynecological interest","type":"exact"}],"termid":"MONDO:0017978","xrefs":{"Monarch":{"xref_id":"0017978"}}}


id: PBO:0053408
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 343","termid":"PBO:0053408"}


id: PBO:0083579
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; similar to YLR334C and YOL106W","termid":"PBO:0083579"}


id: MOD:01327
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-phenylalanine residue to 9x(13)C labeled L-phenylalanine.","definition_xrefs":["PubMed:12716131","Unimod:184#F"],"direct_ancestors":[{"relation_name":"is_a","term_name":"9x(13)C labeled residue","termid":"MOD:00540"},{"relation_name":"is_a","term_name":"modified L-phenylalanine residue","termid":"MOD:00914"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"9x(13)C labeled L-phenylalanine","synonyms":[{"name":"13C(9) Silac label","type":"related"},{"name":"Label:13C(9)","type":"related"}],"termid":"MOD:01327"}


id: GO:0000706
data:
  {"annotated_genes":["SJAG_01076","SJAG_05295","SJAG_01832"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89495,106909,115935],"is_not":false,"summary":null,"term":"GO:0000706"}]},"cv_name":"biological_process","definition":"The cell cycle process in which the 5' to 3' exonucleolytic resection of the DNA at the site of the break to form a 3' single-strand DNA overhang occurs. This takes place during meiosis.","definition_xrefs":["PMID:9334324","GOC:elh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA double-strand break processing","termid":"GO:0000729"},{"relation_name":"is_a","term_name":"meiotic cell cycle process","termid":"GO:1903046"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01076":null,"SJAG_01832":null,"SJAG_05295":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"part_of","termid":"GO:0006281"},{"rel_name":"part_of","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0006281","GO:0006259","GO:0007049"],"is_obsolete":false,"name":"meiotic DNA double-strand break processing","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0000706","terms_by_termid":{"GO:0000706":null}}


id: PBO:0081505
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 408","termid":"PBO:0081505"}


id: SO:1000102
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:1000102 sequence_variant_affecting_level_of_translational_product (obsolete SO:1000102)","synonyms":[{"name":"mutation affecting level of translational product","type":"related"},{"name":"sequence variant affecting level of translational product","type":"exact"}],"termid":"SO:1000102"}


id: PATO:0002065
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A shape quality inhering in a bearer by virtue of the bearer's being arranged like rays or radii; radiating from a common center.","definition_xrefs":["PATOC:me"],"direct_ancestors":[{"relation_name":"is_a","term_name":"shape","termid":"PATO:0000052"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"star shaped","synonyms":[{"name":"stellate","type":"exact"}],"termid":"PATO:0002065"}


id: PBO:0071186
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23a pseudogene 27","termid":"PBO:0071186"}


id: GO:0018838
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (S)-mandelate = (R)-mandelate.","definition_xrefs":["EC:5.1.2.2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"racemase and epimerase activity, acting on hydroxy acids and derivatives","termid":"GO:0016856"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016853"],"is_obsolete":false,"name":"mandelate racemase activity","secondary_identifiers":["RHEA:13945","MetaCyc:MANDELATE-RACEMASE-RXN","UM-BBD_reactionID:r0091"],"termid":"GO:0018838"}


id: PBO:0059467
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MSH5-SAPCD1 readthrough (NMD candidate)","termid":"PBO:0059467"}


id: GO:0010574
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of production of vascular endothelial growth factor.","definition_xrefs":["GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytokine production","termid":"GO:0001817"},{"relation_name":"regulates","term_name":"vascular endothelial growth factor production","termid":"GO:0010573"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"regulation of vascular endothelial growth factor production","termid":"GO:0010574"}


id: GO:0102416
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: quercetin-3-gentiotrioside + UDP-alpha-D-glucose = quercetin-3-gentiotetraside + UDP + H+.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete quercetin gentiotrioside 1,6-glucosyltransferase activity (obsolete GO:0102416)","termid":"GO:0102416"}


id: PBO:0085567
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein essential for meiotic DNA replication and sporulation; cytoplasmic protein; subunit of the MIS complex which controls mRNA methylation during during the induction of sporulation; also interacts with Orc2p, which is a component of the origin recognition complex","termid":"PBO:0085567"}


id: FYPO:0001549
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 protein measured in a cell differs from normal during a cellular response to hypoxia. Total protein or a specific protein may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"altered protein level during vegetative growth","termid":"FYPO:0001325"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0001320","FYPO:0006551"],"is_obsolete":false,"name":"altered protein level during cellular response to hypoxia","synonyms":[{"name":"abnormal protein level during cellular response to hypoxia","type":"exact"},{"name":"altered cellular protein level during cellular response to hypoxia during vegetative growth","type":"exact"},{"name":"altered protein level during cellular response to hypoxia during mitotic cell cycle","type":"related"}],"termid":"FYPO:0001549"}


id: GO:0060226
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the process in which a cell becomes committed to a retinal cone cell fate. Retinal cone cell fate commitment is the process in which the developmental fate of a cell becomes restricted such that it will develop into a retinal cone cell.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell fate commitment","termid":"GO:0010454"},{"relation_name":"is_a","term_name":"negative regulation of photoreceptor cell differentiation","termid":"GO:0046533"},{"relation_name":"is_a","term_name":"regulation of retinal cone cell fate commitment","termid":"GO:0060222"},{"relation_name":"negatively_regulates","term_name":"retinal cone cell fate commitment","termid":"GO:0046551"}],"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 retinal cone cell fate commitment","termid":"GO:0060226"}


id: MONDO:0003172
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hemangioma","termid":"MONDO:0006500"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glomeruloid hemangioma","secondary_identifiers":["SCTID:403976007","UMLS:C1304511","DOID:486","MEDGEN:224917","NCIT:C27505"],"termid":"MONDO:0003172","xrefs":{"Monarch":{"xref_id":"0003172"}}}


id: PBO:0051216
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable 5-78 (pseudogene)","termid":"PBO:0051216"}


id: PBO:0050713
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HSPA (Hsp70) binding protein 1","termid":"PBO:0050713"}


id: MONDO:0003757
data:
  {"annotated_genes":["SJAG_01159","SJAG_01530","SJAG_00773","SJAG_00199","SJAG_04292","SJAG_02322","SJAG_02306","SJAG_00660","SJAG_01537","SJAG_04913","SJAG_04506","SJAG_04110","SJAG_04757","SJAG_04145","SJAG_04325","SJAG_00564","SJAG_04566","SJAG_00308","SJAG_03320","SJAG_03895","SJAG_04628","SJAG_01848","SJAG_01857","SJAG_02615","SJAG_03866","SJAG_04537","SJAG_04123","SJAG_01854","SJAG_05289","SJAG_03457"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84244,84245],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014702"},{"annotations":[86215,86216],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014975"},{"annotations":[86482],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030669"},{"annotations":[84663],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014567"},{"annotations":[84878],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009748"},{"annotations":[84931],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011489"},{"annotations":[86284],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011532"},{"annotations":[84403],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010043"},{"annotations":[84407,84406,84408],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012256"},{"annotations":[84294],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012476"},{"annotations":[84413],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012453"},{"annotations":[86267],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012866"},{"annotations":[85537],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012787"},{"annotations":[85725,85726],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008438"},{"annotations":[85985],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012928"},{"annotations":[84511,84510,84509],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014018"},{"annotations":[84508],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014020"},{"annotations":[84870],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014305"},{"annotations":[84854],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014282"},{"annotations":[84341],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014644"},{"annotations":[85345],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014882"},{"annotations":[85716,85717],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011006"},{"annotations":[84325],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014679"},{"annotations":[85970],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012651"},{"annotations":[85756],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957221"},{"annotations":[85266],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957958"},{"annotations":[85924],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032906"},{"annotations":[85268],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030482"},{"annotations":[85312],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030512"},{"annotations":[86064,86063],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0031019"},{"annotations":[85561],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957308"},{"annotations":[85562],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957309"}]},"cv_name":"mondo","definition":"Complete paralysis of the lower half of the body including both legs, often caused by damage to the spinal cord.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"central nervous system 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lower","type":"exact"},{"name":"severe or complete loss of motor function in the lower extremities and lower portions of the trunk","type":"related"}],"termid":"MONDO:0003757","terms_by_termid":{"MONDO:0008438":null,"MONDO:0009748":null,"MONDO:0010043":null,"MONDO:0011006":null,"MONDO:0011489":null,"MONDO:0011532":null,"MONDO:0012256":null,"MONDO:0012453":null,"MONDO:0012476":null,"MONDO:0012651":null,"MONDO:0012787":null,"MONDO:0012866":null,"MONDO:0012928":null,"MONDO:0014018":null,"MONDO:0014020":null,"MONDO:0014282":null,"MONDO:0014305":null,"MONDO:0014567":null,"MONDO:0014644":null,"MONDO:0014679":null,"MONDO:0014702":null,"MONDO:0014882":null,"MONDO:0014975":null,"MONDO:0030482":null,"MONDO:0030512":null,"MONDO:0030669":null,"MONDO:0031019":null,"MONDO:0032906":null,"MONDO:0957221":null,"MONDO:0957308":null,"MONDO:0957309":null,"MONDO:0957958":null},"xrefs":{"Monarch":{"xref_id":"0003757"}}}


id: GO:0004964
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with luteinizing hormone (also called lutropin) to initiate a change in cell activity.","definition_xrefs":["ISBN:0198506732","PMID:1922095","PMID:18848524"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor activity","termid":"GO:0004930"},{"relation_name":"is_a","term_name":"protein-hormone receptor activity","termid":"GO:0016500"}],"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":"luteinizing hormone receptor activity","secondary_identifiers":["GO:0004976"],"synonyms":[{"name":"LH receptor","type":"exact"},{"name":"LHR","type":"exact"},{"name":"lutropin receptor","type":"exact"},{"name":"lutropin-choriogonadotropic hormone receptor","type":"related"}],"termid":"GO:0004964"}


id: MONDO:0007286
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cataract that has material basis in heterozygous mutation in the VIM gene on chromosome 10p13.","definition_xrefs":["PMID:19126778","DOID:0110248"],"direct_ancestors":[{"relation_name":"is_a","term_name":"early-onset partial cataract","termid":"MONDO:0020377"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"cataract 30","secondary_identifiers":["UMLS:C3805411","OMIM:116300","MEDGEN:811741","MESH:C566157"],"synonyms":[{"name":"CTRCT30","type":"exact"},{"name":"cataract 30","type":"exact"},{"name":"cataract 30 pulverulent","type":"exact"},{"name":"cataract 30, multiple types","type":"related"},{"name":"cataract 30, pulverulent","type":"related"},{"name":"cataract Coppock-like","type":"exact"},{"name":"cataract type 30","type":"exact"}],"termid":"MONDO:0007286","xrefs":{"Monarch":{"xref_id":"0007286"}}}


id: PBO:0028355
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_phosphatase_activity","termid":"PBO:0028355"}


id: PBO:0059928
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND2 pseudogene 14","termid":"PBO:0059928"}


id: GO:0055110
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The inturning of an epithelial sheet over the basal surface of an outer layer involved in deuterostomic gastrulation.","definition_xrefs":["ISBN:0878932437"],"direct_ancestors":[{"relation_name":"is_a","term_name":"embryonic morphogenesis","termid":"GO:0048598"},{"relation_name":"is_a","term_name":"morphogenesis of an epithelial fold","termid":"GO:0060571"},{"relation_name":"part_of","term_name":"gastrulation with mouth forming second","termid":"GO:0001702"}],"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":"involution involved in gastrulation with mouth forming second","termid":"GO:0055110"}


id: PBO:0075734
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SRP14 pseudogene 2","termid":"PBO:0075734"}


id: PBO:0018132
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial respiratory chain complex IV assembly protein Cox19 (predicted)","termid":"PBO:0018132"}


id: PBO:0061244
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NOP protein chaperone 1","termid":"PBO:0061244"}


id: PBO:0004613
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HDEL receptor (predicted)","termid":"PBO:0004613"}


id: PBO:0052155
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"potassium inwardly rectifying channel subfamily J member 4","termid":"PBO:0052155"}


id: GO:1903744
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of anterograde synaptic vesicle transport.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","GOC:kmv","PMID:25329901"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of vesicle transport along microtubule","termid":"GO:1901610"},{"relation_name":"is_a","term_name":"positive regulation of synaptic vesicle transport","termid":"GO:1902805"},{"relation_name":"is_a","term_name":"regulation of anterograde synaptic vesicle transport","termid":"GO:1903742"},{"relation_name":"positively_regulates","term_name":"anterograde synaptic vesicle transport","termid":"GO:0048490"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"positive regulation of anterograde synaptic vesicle transport","synonyms":[{"name":"activation of anterograde synaptic vesicle transport","type":"narrow"},{"name":"up regulation of anterograde synaptic vesicle transport","type":"exact"},{"name":"up-regulation of anterograde synaptic vesicle transport","type":"exact"},{"name":"upregulation of anterograde synaptic vesicle transport","type":"exact"}],"termid":"GO:1903744"}


id: PBO:0058459
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5188","termid":"PBO:0058459"}


id: PBO:0082196
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Allantoate permease; ureidosuccinate permease; also transports dipeptides, though with lower affinity than for allantoate and ureidosuccinate; expression is constitutive but sensitive to nitrogen catabolite repression","termid":"PBO:0082196"}


id: PBO:0054818
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 2231","termid":"PBO:0054818"}


id: GO:0120148
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A structure in a host cell comprised of a core structure (in most organisms, a pair of centrioles) and peripheral material from which a microtubule-based structure, such as a spindle apparatus, is organized. Centrosomes occur close to the nucleus during interphase in many eukaryotic cells, though in animal cells it changes continually during the cell-division cycle.","definition_xrefs":["ISBN:0198547684"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host cytoskeleton","termid":"GO:0044163"}],"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 centrosome","synonyms":[{"name":"host centrosome","type":"exact"}],"termid":"GO:0120148"}


id: PBO:0054277
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 1667","termid":"PBO:0054277"}


id: GO:0014844
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The multiplication or reproduction of myoblasts, resulting in the expansion of the cell population. This occurs as part of skeletal muscle regeneration. A myoblast is a mononucleate cell type that, by fusion with other myoblasts, gives rise to the myotubes that eventually develop into skeletal muscle fibers.","definition_xrefs":["GOC:ef","CL:0000056","GOC:mtg_muscle","PMID:16607119"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myoblast proliferation","termid":"GO:0051450"},{"relation_name":"part_of","term_name":"skeletal muscle tissue regeneration","termid":"GO:0043403"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"myoblast proliferation involved in skeletal muscle regeneration","termid":"GO:0014844"}


id: MONDO:0012563
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any holoprosencephaly in which the cause of the disease is a mutation in the GLI2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microform holoprosencephaly","termid":"MONDO:0017219"},{"relation_name":"is_a","term_name":"lobar holoprosencephaly","termid":"MONDO:0019756"},{"relation_name":"is_a","term_name":"alobar holoprosencephaly","termid":"MONDO:0019757"}],"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":"holoprosencephaly 9","secondary_identifiers":["UMLS:C1835819","MEDGEN:324369","DOID:0110873","OMIM:610829"],"synonyms":[{"name":"GLI2 holoprosencephaly","type":"exact"},{"name":"HPE9","type":"exact"},{"name":"holoprosencephaly 9","type":"exact"},{"name":"holoprosencephaly caused by mutation in GLI2","type":"exact"},{"name":"holoprosencephaly type 9","type":"exact"},{"name":"holoprosencephaly with microphthalmia and first branchial Arch anomalies","type":"related"},{"name":"holoprosencephaly with microphthalmia and first branchial arch anomalies","type":"exact"},{"name":"pituitary anomalies with holoprosencephaly-like features","type":"exact"}],"termid":"MONDO:0012563","xrefs":{"Monarch":{"xref_id":"0012563"}}}


id: GO:0002146
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of a steroid hormone receptor into the nucleus.","definition_xrefs":["GOC:hjd"],"gene_count":0,"genotype_count":0,"name":"obsolete steroid hormone receptor import into nucleus (obsolete GO:0002146)","synonyms":[{"name":"steroid hormone receptor nuclear translocation","type":"narrow"}],"termid":"GO:0002146"}


id: SO:0000740
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"DNA belonging to the genome of a plastid such as a chloroplast.","direct_ancestors":[{"relation_name":"is_a","term_name":"organelle_sequence","termid":"SO:0000736"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plastid_sequence","synonyms":[{"name":"plastid sequence","type":"exact"}],"termid":"SO:0000740"}


id: MONDO:1012193
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"thalamic-cerebellar neuropathy, non-human animal","termid":"MONDO:1011854"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thalamic-cerebellar neuropathy, sheep","secondary_identifiers":["OMIA:000723-9940"],"termid":"MONDO:1012193","xrefs":{"Monarch":{"xref_id":"1012193"}}}


id: GO:1903983
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that increases the length of a microvillus.","definition_xrefs":["GOC:als","PMID:22114352"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell projection organization","termid":"GO:0031346"},{"relation_name":"is_a","term_name":"regulation of microvillus length","termid":"GO:0032532"}],"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 microvillus length","synonyms":[{"name":"activation of regulation of microvillus length","type":"narrow"},{"name":"up regulation of regulation of microvillus length","type":"exact"},{"name":"up-regulation of regulation of microvillus length","type":"exact"},{"name":"upregulation of regulation of microvillus length","type":"exact"}],"termid":"GO:1903983"}


id: PBO:0031460
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-resistance_to_cadmium","termid":"PBO:0031460"}


id: GO:1901528
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any hydrogen peroxide mediated signaling pathway that is involved in stomatal movement.","definition_xrefs":["GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete hydrogen peroxide mediated signaling pathway involved in stomatal movement (obsolete GO:1901528)","synonyms":[{"name":"H2O2 mediated signaling pathway involved in stomatal movement","type":"exact"},{"name":"hydrogen peroxide mediated signalling pathway involved in stomatal movement","type":"exact"}],"termid":"GO:1901528"}


id: PBO:0085127
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nucleolar protein found in preribosomal complexes; contains an RNA recognition motif (RRM); relative distribution to the nucleolus increases upon DNA replication stress","termid":"PBO:0085127"}


id: PBO:0043546
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"COL1A2 antisense RNA 1","termid":"PBO:0043546"}


id: PBO:0043822
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ceruloplasmin pseudogene","termid":"PBO:0043822"}


id: MONDO:0001987
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"neurodegenerative disease","termid":"MONDO:0005559"}],"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":"senile degeneration of brain","secondary_identifiers":["ICD9:331.2","MEDGEN:509626","UMLS:C0154669","DOID:14524","SCTID:45864009"],"synonyms":[{"name":"Senile brain degen.","type":"exact"}],"termid":"MONDO:0001987","xrefs":{"Monarch":{"xref_id":"0001987"}}}


id: PBO:0076597
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TBC1 domain family member 19","termid":"PBO:0076597"}


id: PR:000046670
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe sre2 gene.","definition_xrefs":["PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor sre2 (Schizosaccharomyces pombe)","pombase_gene_id":"SPBC354.05c","synonyms":[{"name":"Spom-sre2","type":"exact"},{"name":"sterol regulatory element-binding protein 2 (Schizosaccharomyces pombe)","type":"exact"}],"termid":"PR:000046670"}


id: MONDO:0024630
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"phagocytic cell dysfunction","termid":"MONDO:0024627"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"defective phagocytic cell chemotaxis","secondary_identifiers":["MEDGEN:585047","UMLS:C0398735","SCTID:234580003","ICD9:279.8"],"synonyms":[{"name":"defective phagocytic cell chemotaxis","type":"exact"}],"termid":"MONDO:0024630","xrefs":{"Monarch":{"xref_id":"0024630"}}}


id: PBO:0048617
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GIMAP family P-loop NTPase domain containing 1","termid":"PBO:0048617"}


id: GO:1990391
data:
  {"annotated_genes":["SJAG_02527","SJAG_04199","SJAG_02237"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[113020,99126,115458],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032807"}]},"cv_name":"cellular_component","definition":"A protein complex involved in DNA repair processes including direct reversal, base excision repair, nucleotide excision repair, photoreactivation, bypass, double-strand break repair pathway, and mismatch repair pathway.","definition_xrefs":["GOC:bhm","PMID:20551348","PMID:17217467","PMID:24192350","PMID:22749910"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catalytic complex","termid":"GO:1902494"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02237":null,"SJAG_02527":null,"SJAG_04199":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"DNA repair complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"DNA damage repair complex","type":"exact"},{"name":"WHY1 complex","type":"narrow"}],"termid":"GO:1990391","terms_by_termid":{"GO:0032807":null}}


id: PBO:0062608
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 10 subfamily R member 3 pseudogene","termid":"PBO:0062608"}


id: PBO:0109261
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NELL2 interacting cell ontogeny regulator 1","termid":"PBO:0109261"}


id: PBO:0054615
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 2020","termid":"PBO:0054615"}


id: MONDO:0016306
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Niemann-Pick disease type C","termid":"MONDO:0018982"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002561"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0002525"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0002561","MONDO:0005066","MONDO:0006025","MONDO:0002525"],"is_obsolete":false,"name":"Niemann-Pick disease type C, severe perinatal form","secondary_identifiers":["UMLS:C5680866","Orphanet:216972","GARD:20504","MEDGEN:1842349"],"termid":"MONDO:0016306","xrefs":{"Monarch":{"xref_id":"0016306"}}}


id: GO:1905286
data:
  {"annotated_genes":["SJAG_03648","SJAG_02809","SJAG_03261","SJAG_01750","SJAG_03737","SJAG_02867"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[108344,107228],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042720"},{"annotations":[102992,111693,97613,86859],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005787"}]},"cv_name":"cellular_component","definition":"A protein complex which is capable of serine-type peptidase activity.","definition_xrefs":["GOC:bhm","GO_REF:0000088","GOC:TermGenie","PMID:18640965"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidase complex","termid":"GO:1905368"}],"gene_count":6,"genes_by_uniquename":{"SJAG_01750":null,"SJAG_02809":null,"SJAG_02867":null,"SJAG_03261":null,"SJAG_03648":null,"SJAG_03737":null},"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":"serine-type peptidase complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"Factor VII - TF complex","type":"narrow"}],"termid":"GO:1905286","terms_by_termid":{"GO:0005787":null,"GO:0042720":null}}


id: PBO:0066118
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAS like family 11 member B","termid":"PBO:0066118"}


id: MOD:00650
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a residue amino group with a myristoylamino group.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myristoylated residue","termid":"MOD:00438"},{"relation_name":"is_a","term_name":"N-acylated residue","termid":"MOD:00670"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01155"}],"interesting_parent_ids":["MOD:01155"],"is_obsolete":false,"name":"N-myristoylated residue","synonyms":[{"name":"NMyrRes","type":"exact"}],"termid":"MOD:00650"}


id: PBO:0031390
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-growth_auxotrophic_for_lysine","termid":"PBO:0031390"}


id: PBO:0058511
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5701-1","termid":"PBO:0058511"}


id: PBO:0031369
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-multinucleate_vegetative_cell","termid":"PBO:0031369"}


id: MOD:01232
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-lysine residue to 3x(12)C labeled N6-propanoyl-L-lysine.","definition_xrefs":["PubMed:12175151","PubMed:11857757","Unimod:58#K","PubMed:11999733"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N6-propanoyl-L-lysine","termid":"MOD:01398"}],"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:01155","MOD:01875"],"is_obsolete":false,"name":"3x(12)C labeled N6-propanoyl-L-lysine","synonyms":[{"name":"Propionate labeling reagent light form (N-term & K)","type":"related"},{"name":"Propionyl","type":"related"}],"termid":"MOD:01232"}


id: GO:0031129
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Signaling at short range between cells of different ancestry and developmental potential that results in one cell or group of cells effecting a developmental change in the other. This is often done by secretion of proteins by one cell which affects the neighboring cells and causes them to adopt a certain fate.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental induction","termid":"GO:0031128"}],"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":"inductive cell-cell signaling","synonyms":[{"name":"inductive cell-cell signalling","type":"exact"}],"termid":"GO:0031129"}


id: GO:1902047
data:
  {"annotated_genes":["SJAG_04469","SJAG_02344","SJAG_02060","SJAG_02059","SJAG_02125"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[105551],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1902267"},{"annotations":[116478,110074,57680,108591,108597,108603],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903711"},{"annotations":[109497,108598,68323,108592,110075,116479,108604],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903710"}]},"cv_name":"biological_process","definition":"The process in which a polyamine macromolecule is transported across a membrane.","definition_xrefs":["GOC:TermGenie","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyamine transport","termid":"GO:0015846"},{"relation_name":"is_a","term_name":"transmembrane transport","termid":"GO:0055085"}],"gene_count":5,"genes_by_uniquename":{"SJAG_02059":null,"SJAG_02060":null,"SJAG_02125":null,"SJAG_02344":null,"SJAG_04469":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0055085","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"polyamine transmembrane transport","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000108":null},"secondary_identifiers":["GO:1905122"],"synonyms":[{"name":"polyamine import","type":"related"},{"name":"polyamine uptake","type":"related"}],"termid":"GO:1902047","terms_by_termid":{"GO:1902267":null,"GO:1903710":null,"GO:1903711":null}}


id: PBO:0052465
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KLF11 divergent transcript","termid":"PBO:0052465"}


id: GO:1903421
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of synaptic vesicle recycling.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:22745285","GOC:pad","GOC:PARL"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transport","termid":"GO:0051049"},{"relation_name":"regulates","term_name":"synaptic vesicle recycling","termid":"GO:0036465"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"regulation of synaptic vesicle recycling","synonyms":[{"name":"regulation of kiss-and-run synaptic vesicle recycling","type":"narrow"},{"name":"regulation of kiss-and-stay synaptic vesicle recycling","type":"narrow"}],"termid":"GO:1903421"}


id: GO:0016593
data:
  {"annotated_genes":["SJAG_00139","SJAG_01151","SJAG_04933","SJAG_01610","SJAG_03118"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[94404,98342,102230,104526,110621],"is_not":false,"summary":null,"term":"GO:0016593"}]},"cv_name":"cellular_component","definition":"A multiprotein complex that associates with RNA polymerase II and general RNA polymerase II transcription factor complexes and may be involved in both transcriptional initiation and elongation. In Saccharomyces the complex contains Paf1p, Cdc73p, Ctr9p, Rtf1p, and Leo1p.","definition_xrefs":["PMID:11884586"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcription elongation factor complex","termid":"GO:0008023"},{"relation_name":"part_of","term_name":"RNA polymerase II, holoenzyme","termid":"GO:0016591"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00139":null,"SJAG_01151":null,"SJAG_01610":null,"SJAG_03118":null,"SJAG_04933":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"part_of","termid":"GO:0005654"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005654","GO:0005634"],"is_obsolete":false,"name":"Cdc73/Paf1 complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"Paf1 complex","type":"exact"},{"name":"Paf1p complex","type":"exact"}],"termid":"GO:0016593","terms_by_termid":{"GO:0016593":null}}


id: MONDO:0006474
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm arising from the transitional epithelium, usually affecting the urinary bladder, ureter, or renal pelvis. It may or may not have a papillary configuration. It is graded 1 to 3 or 4 according to the degree of cellular differentiation and architectural patterns. Grade 1 transitional cell carcinoma is histologically benign but it may recur. Transitional cell carcinomas may also affect the upper respiratory tract and the ovaries.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carcinoma","termid":"MONDO:0004993"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"transitional cell carcinoma","secondary_identifiers":["GARD:7794","NCIT:C2930","UMLS:C0007138","MEDGEN:2875","DOID:2671","MESH:D002295","ICDO:8120/3","NCIT:C6783","EFO:1000601"],"synonyms":[{"name":"carcinoma of transitional epithelial cell","type":"exact"},{"name":"carcinoma of urothelial cell","type":"exact"},{"name":"carcinoma, urothelial, malignant","type":"exact"},{"name":"transitional carcinoma","type":"exact"},{"name":"transitional cell carcinoma","type":"exact"},{"name":"transitional cell neoplasm","type":"broad"},{"name":"transitional cell tumor","type":"broad"},{"name":"transitional cell tumour","type":"broad"},{"name":"transitional epithelial cell carcinoma","type":"exact"},{"name":"urothelial cell carcinoma","type":"exact"}],"termid":"MONDO:0006474","xrefs":{"Monarch":{"xref_id":"0006474"}}}


id: MONDO:0015186
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Rare intestinal neoplasm.","definition_xrefs":["MONDO:patterns/rare"],"gene_count":0,"genotype_count":0,"name":"obsolete rare tumor of intestine (obsolete MONDO:0015186)","secondary_identifiers":["Orphanet:104011"],"synonyms":[{"name":"rare intestinal neoplasm","type":"exact"},{"name":"rare intestinal tumor","type":"exact"},{"name":"rare tumor of bowel","type":"exact"}],"termid":"MONDO:0015186","xrefs":{"Monarch":{"xref_id":"0015186"}}}


id: PBO:0042354
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CD96 molecule","termid":"PBO:0042354"}


id: PBO:0062717
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 51 subfamily N member 1 pseudogene","termid":"PBO:0062717"}


id: GO:2000368
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of acrosomal vesicle exocytosis.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of calcium ion-dependent exocytosis","termid":"GO:0045956"},{"relation_name":"is_a","term_name":"positive regulation of reproductive process","termid":"GO:2000243"},{"relation_name":"is_a","term_name":"regulation of acrosomal vesicle exocytosis","termid":"GO:2000367"},{"relation_name":"positively_regulates","term_name":"acrosomal vesicle exocytosis","termid":"GO:0060478"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0016192"],"is_obsolete":false,"name":"positive regulation of acrosomal vesicle exocytosis","synonyms":[{"name":"positive regulation of acrosomal granule exocytosis","type":"related"},{"name":"positive regulation of acrosome exocytosis","type":"exact"}],"termid":"GO:2000368"}


id: MONDO:0007482
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Dyschondrosteosis - nephritis is characterized by the association of short stature due to mesomelic shortening of the limbs and Madelung deformity, with hereditary nephritis.","definition_xrefs":["Orphanet:1765"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dyschondrosteosis-nephritis syndrome","secondary_identifiers":["GARD:1994","OMIM:127350","MEDGEN:342135","UMLS:C1851986","MESH:C565080"],"synonyms":[{"name":"dyschondrosteosis and nephritis","type":"related"},{"name":"dyschondrosteosis nephritis","type":"related"},{"name":"mesomelic shortening and hereditary nephritis","type":"related"}],"termid":"MONDO:0007482","xrefs":{"Monarch":{"xref_id":"0007482"}}}


id: GO:0071690
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of proteins to form the myosin-based thick filaments of myofibrils in cardiac muscle.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"striated muscle myosin thick filament assembly","termid":"GO:0071688"},{"relation_name":"part_of","term_name":"cardiac myofibril assembly","termid":"GO:0055003"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0030036"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0007010"},{"rel_name":"part_of","termid":"GO:0030036"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0007010"}],"interesting_parent_ids":["GO:0065003","GO:0030036","GO:0008150","GO:0007010","GO:0044085"],"is_obsolete":false,"name":"cardiac muscle myosin thick filament assembly","termid":"GO:0071690"}


id: PBO:0046749
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exocyst complex component 4","termid":"PBO:0046749"}


id: MONDO:0000748
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the mucosal lining of the mastoid antrum and mastoid air cell system of the mastoid process.","definition_xrefs":["NCIT:C128368"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bone inflammation disease","termid":"MONDO:0002614"},{"relation_name":"is_a","term_name":"inflammatory disease","termid":"MONDO:0021166"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mastoiditis","secondary_identifiers":["SCTID:52404001","UMLS:C0024904","DOID:0060322","HP:0000265","ICD9:383.9","MEDGEN:7480","MESH:D008417"],"synonyms":[{"name":"inflammation of mastoid process of temporal bone","type":"exact"},{"name":"mastoid process of temporal bone inflammation","type":"exact"},{"name":"mastoid process of temporal boneitis","type":"exact"},{"name":"mastoiditis","type":"exact"},{"name":"mastoiditis (disease)","type":"exact"}],"termid":"MONDO:0000748","xrefs":{"Monarch":{"xref_id":"0000748"}}}


id: PBO:0043678
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coronin 2B","termid":"PBO:0043678"}


id: PBO:0087741
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the SWI/SNF chromatin remodeling complex; involved in transcriptional regulation; functions interdependently in transcriptional activation with Snf2p and Snf5p; relocates to the cytosol under hypoxic conditions","termid":"PBO:0087741"}


id: GO:0060954
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process aimed at the progression of a neural crest-derived cardiac glial cell over time, from initial commitment of the cell to a specific fate, to the fully functional differentiated cell.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiac glial cell development","termid":"GO:0060952"},{"relation_name":"part_of","term_name":"neural crest-derived cardiac glial cell differentiation","termid":"GO:0060951"}],"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":"neural crest-derived cardiac glial cell development","termid":"GO:0060954"}


id: PBO:0080477
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vault RNA 1-3","termid":"PBO:0080477"}


id: GO:0010408
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving the cell wall arabinogalactan II glycoprotein variant which contains both an arabinogalactan protein (AGP) motif and a fasciclin domain.","definition_xrefs":["GOC:tair_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"arabinogalactan protein metabolic process","termid":"GO:0010405"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0071554"}],"interesting_parent_ids":["GO:0008150","GO:0071554"],"is_obsolete":false,"name":"fasciclin-like arabinogalactan protein metabolic process","synonyms":[{"name":"fasciclin-like arabinogalactan protein metabolism","type":"exact"}],"termid":"GO:0010408"}


id: PBO:0088256
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein phosphatase (Cdc14-related) Clp1/Flp1","termid":"PBO:0088256"}


id: GO:0090265
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency, or extent of the process of immune complex clearance by monocytes or macrophages.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of immune effector process","termid":"GO:0002699"},{"relation_name":"is_a","term_name":"regulation of immune complex clearance by monocytes and macrophages","termid":"GO:0090264"},{"relation_name":"positively_regulates","term_name":"immune complex clearance by monocytes and macrophages","termid":"GO:0002436"}],"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 immune complex clearance by monocytes and macrophages","termid":"GO:0090265"}


id: GO:0045292
data:
  {"annotated_genes":["SJAG_05212","SJAG_16453","SJAG_01064","SJAG_01200","SJAG_01504","SJAG_00998","SJAG_04230","SJAG_04898","SJAG_03214","SJAG_05211","SJAG_03954","SJAG_03894","SJAG_00818","SJAG_02396","SJAG_00531","SJAG_00577","SJAG_03983","SJAG_02879","SJAG_05208","SJAG_02227","SJAG_01015","SJAG_00859","SJAG_04783","SJAG_03427","SJAG_01433","SJAG_03210","SJAG_01547","SJAG_03469","SJAG_02843","SJAG_01557","SJAG_02005","SJAG_00414","SJAG_00363","SJAG_02686","SJAG_01654","SJAG_03430","SJAG_02455","SJAG_04318","SJAG_02905","SJAG_02295","SJAG_00888","SJAG_02304","SJAG_00446","SJAG_00094","SJAG_03369","SJAG_03245","SJAG_04079","SJAG_02687","SJAG_04497","SJAG_05235","SJAG_05224","SJAG_00643","SJAG_04117","SJAG_01810","SJAG_04163","SJAG_03601","SJAG_03687","SJAG_02688","SJAG_00911","SJAG_01144","SJAG_02772","SJAG_00989","SJAG_01958","SJAG_02018","SJAG_00322","SJAG_03995","SJAG_03291","SJAG_03498","SJAG_00571","SJAG_04589","SJAG_00147","SJAG_04071","SJAG_00498","SJAG_01040","SJAG_05009","SJAG_01452","SJAG_01152","SJAG_00639","SJAG_05240","SJAG_03070","SJAG_03279","SJAG_02317","SJAG_02279","SJAG_00504","SJAG_03410","SJAG_01408","SJAG_01214","SJAG_03937","SJAG_04293","SJAG_02558","SJAG_01440","SJAG_03301","SJAG_01870","SJAG_02469","SJAG_03711","SJAG_03993","SJAG_01819","SJAG_03966","SJAG_04214","SJAG_03849","SJAG_01327","SJAG_00539","SJAG_02844","SJAG_00083","SJAG_04782","SJAG_04025","SJAG_03547","SJAG_03890","SJAG_05025","SJAG_00809","SJAG_01634","SJAG_02722","SJAG_02185","SJAG_00076","SJAG_02083","SJAG_00313","SJAG_03112","SJAG_04949","SJAG_04222","SJAG_00225","SJAG_01629","SJAG_00058","SJAG_03238","SJAG_02078","SJAG_04405","SJAG_04863","SJAG_02862","SJAG_01308","SJAG_03460","SJAG_04694","SJAG_04914","SJAG_05349","SJAG_01008","SJAG_00597","SJAG_05926","SJAG_01852","SJAG_00249","SJAG_01511","SJAG_04433","SJAG_04529","SJAG_04911","SJAG_01301"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[86648,86988,87730,88200,88680,88743,89160,89438,89818,90627,90999,91303,91504,91567,91865,91886,91891,92089,92153,92250,92313,92515,92572,92784,93367,93928,94124,94196,94377,94532,94572,94588,94742,94801,94995,95023,95148,95175,95363,95407,95529,95638,96035,96598,96869,97208,97643,97987,98237,99818,99876,100434,100925,101370,101598,101660,101731,101829,101889,102166,102195,102200,102338,102368,102383,103692,103845,104021,104116,104651,104677,104793,104807,104996,105040,105507,105567,105599,105707,105921,106329,106803,107044,107392,107690,107828,107917,108019,108381,108382,108653,108703,108901,108938,109207,109219,109656,109772,110427,110673,110850,110885,110926,111584,111788,112021,112234,112301,112591,112974,112983,113487,113493,113993,114070,114117,114342,114381,115004,115098,115542,116013,116158,116350,117100,117535,117674,117843,118018,58945,78655,91354,94382],"is_not":false,"summary":null,"term":"GO:0045292"},{"annotations":[116957],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000354"},{"annotations":[90770,94800,97029,94376,101893,111503,109796,93198,105039,109785,112410,109771,94123,101730,109218,114380],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000395"},{"annotations":[117536],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1905746"},{"annotations":[97768],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1905744"}]},"cv_name":"biological_process","definition":"The joining together, after removal of an intervening sequence composed of one or more introns, of two segments of the same RNA molecule via spliceosomal catalysis to produce an mRNA composed only of exon sequences that all came from the same primary transcript.","definition_xrefs":["GOC:krc","ISBN:0879695897","PMID:18458335"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mRNA splicing, via 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cis splicing, via spliceosome","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"synonyms":[{"name":"nuclear mRNA cis splicing, via U2-type spliceosome","type":"narrow"},{"name":"nuclear mRNA cis splicing, via spliceosome","type":"exact"},{"name":"splicing","type":"broad"}],"termid":"GO:0045292","terms_by_termid":{"GO:0000354":null,"GO:0000395":null,"GO:0045292":null,"GO:1905744":null,"GO:1905746":null}}


id: PBO:0005434
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription elongation regulator (predicted)","termid":"PBO:0005434"}


id: PBO:0062685
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 51 subfamily A member 6 pseudogene","termid":"PBO:0062685"}


id: PBO:0053662
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 839","termid":"PBO:0053662"}


id: MONDO:0850115
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"early-onset obesity-hyperphagia-severe developmental delay syndrome","secondary_identifiers":["GARD:19685","Orphanet:99704"],"termid":"MONDO:0850115","xrefs":{"Monarch":{"xref_id":"0850115"}}}


id: PBO:0041334
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 3 common eliminated region 1","termid":"PBO:0041334"}


id: GO:0075271
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a fruiting body called zygosporangium is formed. A zygosporangium is a thick-walled structure in which spores are produced, and is characteristic of the Zygomycetes.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spore-bearing structure development","termid":"GO:0075259"}],"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":"zygosporangium development","termid":"GO:0075271"}


id: PR:Q9Y7L2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC2A9.10 gene.","definition_xrefs":["UniProtKB:Q9Y7L2","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":"RNA methyltransferase C2A9.10 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC2A9.10","synonyms":[{"name":"Spom972h-SPBC2A9.10","type":"exact"}],"termid":"PR:Q9Y7L2"}


id: MONDO:0859360
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive cerebellar ataxia","termid":"MONDO:0015244"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"spinocerebellar ataxia, autosomal recessive 33","secondary_identifiers":["DOID:0070414","MEDGEN:1824070","UMLS:C5774297","OMIM:620208"],"termid":"MONDO:0859360","xrefs":{"Monarch":{"xref_id":"0859360"}}}


id: PBO:0070086
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear variant sequence with SNRPE pseudogene sequence","termid":"PBO:0070086"}


id: PBO:0050708
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock protein family B (small) member 6","termid":"PBO:0050708"}


id: MONDO:0001769
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"nasolacrimal duct disorder","termid":"MONDO:0044984"}],"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":"acquired tear duct stenosis","secondary_identifiers":["DOID:13655","ICD9:375.56","MEDGEN:509872","UMLS:C0155248","SCTID:193995004"],"synonyms":[{"name":"acquired nasolacrimal duct stenosis","type":"exact"},{"name":"acquired stenosis of nasolacrimal duct","type":"exact"},{"name":"stenosis of nasolacrimal duct, acquired","type":"exact"},{"name":"tear duct - acquired stenosis","type":"exact"}],"termid":"MONDO:0001769","xrefs":{"Monarch":{"xref_id":"0001769"}}}


id: PBO:0081745
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 675","termid":"PBO:0081745"}


id: MONDO:0017200
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Polycystic ovaries-urethral sphincter dysfunction syndrome is characterized by urinary retention and incomplete emptying of the bladder associated with abnormal electromyographic activity. It has been described in 33 women, 14 of whom also had polycystic ovaries.","definition_xrefs":["Orphanet:2795"],"direct_ancestors":[{"relation_name":"is_a","term_name":"female reproductive system disorder","termid":"MONDO:0002263"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polycystic ovaries-urethral sphincter dysfunction syndrome","secondary_identifiers":["UMLS:C2931462","GARD:2365","MESH:C537271","MEDGEN:419813"],"synonyms":[{"name":"fowler Christmas Chapple syndrome","type":"related"},{"name":"fowler's syndrome","type":"related"},{"name":"fowler-Christmas-Chapple syndrome","type":"exact"},{"name":"polycystic ovaries urethral sphincter dysfunction","type":"related"},{"name":"voiding dysfunction and polycystic ovaries","type":"related"}],"termid":"MONDO:0017200","xrefs":{"Monarch":{"xref_id":"0017200"}}}


id: GO:0018756
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ammeline + H2O = ammelide + NH3.","definition_xrefs":["PMID:1991731"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amidines","termid":"GO:0016813"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016810","GO:0016787"],"is_obsolete":false,"name":"ammeline aminohydrolase activity","secondary_identifiers":["RHEA:26201","MetaCyc:RXN-8016"],"termid":"GO:0018756"}


id: MONDO:1012394
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"growth-hormone deficiency dwarfism,, non-human animal","termid":"MONDO:1011959"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"growth-hormone deficiency dwarfism, zebu cattle","secondary_identifiers":["OMIA:001473-9915"],"termid":"MONDO:1012394","xrefs":{"Monarch":{"xref_id":"1012394"}}}


id: GO:0047715
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + hypotaurocyamine = N(omega)-phosphohypotaurocyamine + ADP + 2 H+.","definition_xrefs":["RHEA:24008","EC:2.7.3.6"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinase activity","termid":"GO:0016301"},{"relation_name":"is_a","term_name":"phosphotransferase activity, nitrogenous group as acceptor","termid":"GO:0016775"}],"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:0003824"},{"rel_name":"is_a","termid":"GO:0016301"}],"interesting_parent_ids":["GO:0003674","GO:0016301","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"hypotaurocyamine kinase activity","secondary_identifiers":["MetaCyc:HYPOTAUROCYAMINE-KINASE-RXN","KEGG_REACTION:R03939"],"synonyms":[{"name":"ATP:hypotaurocyamine N-phosphotransferase activity","type":"related"}],"termid":"GO:0047715"}


