# terms

id: PR:O94601
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An ADP-ribosylation factor GTPase-activating protein 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["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 C622.14 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC622.14","secondary_identifiers":["UniProtKB:O94601"],"synonyms":[{"name":"Spom972h-ARFGAP1","type":"exact"}],"termid":"PR:O94601"}


id: MONDO:0017246
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital pulmonary sequestration","termid":"MONDO:0017843"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"extralobar congenital pulmonary sequestration","secondary_identifiers":["MEDGEN:1843113","Orphanet:280811","UMLS:C5679951","GARD:21091"],"synonyms":[{"name":"congenital extrapulmonary sequestration","type":"exact"},{"name":"extralobar congenital bronchopulmonary sequestration","type":"exact"}],"termid":"MONDO:0017246","xrefs":{"Monarch":{"xref_id":"0017246"}}}


id: GO:0001734
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: an adenosine in mRNA + S-adenosyl-L-methionine = an N(6)-methyladenosine in mRNA + H+ + S-adenosyl-L-homocysteine. This activity is the methylation of adenines in mRNA with the consensus sequence RRACH, where R is a purine, and H is C, A, or U.","definition_xrefs":["GOC:hjd","EC:2.1.1.348"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mRNA methyltransferase activity","termid":"GO:0008174"}],"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:0016740"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0016741"}],"interesting_parent_ids":["GO:0140098","GO:0016741","GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"mRNA m(6)A methyltransferase activity","secondary_identifiers":["Reactome:R-HSA-72095","RHEA:55584","MetaCyc:RXN-19346"],"synonyms":[{"name":"mRNA (N6-adenosine)-methyltransferase activity","type":"exact"}],"termid":"GO:0001734"}


id: PBO:0089336
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial carrier, pyruvate Mpc1","termid":"PBO:0089336"}


id: PBO:0046852
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fatty acid desaturase 1","termid":"PBO:0046852"}


id: SO:0001921
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A contig of mitochondria derived sequences.","definition_xrefs":["GMOD:ea"],"direct_ancestors":[{"relation_name":"has_origin","term_name":"mitochondrial_sequence","termid":"SO:0000737"},{"relation_name":"is_a","term_name":"contig","termid":"SO:0000149"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial_contig","synonyms":[{"name":"mitochondrial contig","type":"exact"}],"termid":"SO:0001921"}


id: GO:0009036
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the endonucleolytic cleavage of DNA to give specific double-stranded fragments with terminal 5'-phosphates and 3' hydroxyls. Cleavage is dependent on the presence in the DNA of a specific recognition site; cleavage occurs at or very near this recognition site.","definition_xrefs":["EC:3.1.21.4","PMID:12654995"],"direct_ancestors":[{"relation_name":"is_a","term_name":"restriction endodeoxyribonuclease activity","termid":"GO:0015666"},{"relation_name":"is_a","term_name":"DNA endonuclease activity, producing 5'-phosphomonoesters","termid":"GO:0016888"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0140097"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0140097","GO:0003674","GO:0003824","GO:0016788","GO:0016787"],"is_obsolete":false,"name":"type II site-specific deoxyribonuclease activity","secondary_identifiers":["MetaCyc:3.1.21.4-RXN"],"synonyms":[{"name":"type II restriction enzyme activity","type":"exact"}],"termid":"GO:0009036"}


id: PATO:0000015
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A chromatic scalar-circular quality inhering in an object that manifests in an observer by virtue of the dominant wavelength of the visible light; may be subject to fiat divisions, typically into 7 or 8 spectra.","definition_xrefs":["PATOC:cjm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromatic property","termid":"PATO:0001301"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"color hue","termid":"PATO:0000015"}


id: PR:000085728
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A histone H3.3, initiator methionine removed form (Schizosaccharomyces pombe) that has been methylated on Lys-9 and phosphorylated on Ser-10. UniProtKB:P10651, 2-136, Lys-10, MOD:00663|Ser-11, MOD:00046.","definition_xrefs":["PomBase:VW","PMID:19362535","PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fungal histone H3.3, initiator methionine removed form (Schizosaccharomyces pombe)","termid":"PR:000027598"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hht3/Me(K9),Phos(S10)","pombase_gene_id":"SPBC1105.11c","synonyms":[{"name":"PRO_0000221367, Lys-10, MOD:00663|Ser-11, MOD:00046","type":"exact"},{"name":"PomBase_original_PRO_term_name: histone H3.3, initiator methionine removed K9-methylated and phosphorylated 1 (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-hht3/InitMet-/K9MePhos:1","type":"exact"},{"name":"UniProtKB:P10651, 2-136, Lys-10, MOD:00663|Ser-11, MOD:00046","type":"exact"},{"name":"hht3/Me(K9),Phos(S10)","type":"exact"}],"termid":"PR:000085728"}


id: PBO:0061703
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NUS1 pseudogene 3","termid":"PBO:0061703"}


id: GO:0070219
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A homeostatic process involved in the maintenance of a steady state level of sulfide ions within a cell.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete intracellular sulfide ion homeostasis (obsolete GO:0070219)","synonyms":[{"name":"cellular sulfide homeostasis","type":"exact"},{"name":"cellular sulfide ion homeostasis","type":"exact"},{"name":"cellular sulphide homeostasis","type":"exact"},{"name":"cellular sulphide ion homeostasis","type":"exact"}],"termid":"GO:0070219"}


id: GO:2000396
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of ubiquitin-dependent endocytosis.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of endocytosis","termid":"GO:0045806"},{"relation_name":"is_a","term_name":"negative regulation of protein transport","termid":"GO:0051224"},{"relation_name":"is_a","term_name":"regulation of ubiquitin-dependent endocytosis","termid":"GO:2000395"},{"relation_name":"negatively_regulates","term_name":"ubiquitin-dependent endocytosis","termid":"GO:0070086"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0016192"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0006810","GO:0016192","GO:0008150"],"is_obsolete":false,"name":"negative regulation of ubiquitin-dependent endocytosis","synonyms":[{"name":"negative regulation of ubiquitin-mediated endocytosis","type":"exact"}],"termid":"GO:2000396"}


id: GO:0035498
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving the dipeptide beta-alanyl-L-histidine (carnosine).","definition_xrefs":["PMID:20097752"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid metabolic process","termid":"GO:0006520"},{"relation_name":"is_a","term_name":"carboxylic acid metabolic process","termid":"GO:0019752"},{"relation_name":"is_a","term_name":"amide metabolic process","termid":"GO:0043603"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006520","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"carnosine metabolic process","synonyms":[{"name":"carnosine metabolism","type":"exact"}],"termid":"GO:0035498"}


id: MOD:00451
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a residue alpha-amino- or alpha-imino-hydrogen with a propanoyl group.","definition_xrefs":["PubMed:11857757","Unimod:58#N-term","PubMed:11999733","PubMed:12175151"],"direct_ancestors":[{"relation_name":"is_a","term_name":"propanoylated residue","termid":"MOD:01894"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha-amino propanoylated residue","synonyms":[{"name":"Propionate labeling reagent light form (N-term & K)","type":"related"},{"name":"Propionyl","type":"related"}],"termid":"MOD:00451"}


id: MONDO:0004120
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare neuroendocrine carcinoma that arises from the Bartholin gland and is characterized by the presence of malignant small cells and high mitotic activity.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"small cell carcinoma","termid":"MONDO:0000402"},{"relation_name":"is_a","term_name":"bartholin gland carcinoma","termid":"MONDO:0002829"},{"relation_name":"is_a","term_name":"vulvar neuroendocrine carcinoma","termid":"MONDO:0056816"}],"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":"Bartholin gland small cell carcinoma","secondary_identifiers":["UMLS:C1511051","NCIT:C40298","DOID:7140","MEDGEN:267705"],"synonyms":[{"name":"Bartholin gland small cell carcinoma","type":"exact"},{"name":"Bartholin's gland small cell carcinoma","type":"exact"},{"name":"major vestibular gland small cell carcinoma","type":"exact"},{"name":"small cell carcinoma of major vestibular gland","type":"exact"}],"termid":"MONDO:0004120","xrefs":{"Monarch":{"xref_id":"0004120"}}}


id: MONDO:0013342
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal recessive spastic paraplegia type 48 (SPG48) is a form of hereditary spastic paraplegia usually characterized by a pure phenotype of a slowly progressive spastic paraplegia associated with urinary incontinence with an onset in mid- to late-adulthood. A complex phenotype, with the additional findings of cognitive impairment, sensorimotor polyneuropathy, ataxia and parkinsonism, as well as thin corpus callosum and white matter lesions (seen on magnetic resonance imaging), has also been reported.","definition_xrefs":["Orphanet:306511"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lysosomal storage disease","termid":"MONDO:0002561"},{"relation_name":"is_a","term_name":"hereditary spastic paraplegia","termid":"MONDO:0019064"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002561"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0002561","MONDO:0005559"],"is_obsolete":false,"name":"hereditary spastic paraplegia 48","secondary_identifiers":["DOID:0110800","GARD:17378","SCTID:763367009","UMLS:C3150901","MEDGEN:462251","OMIM:613647"],"synonyms":[{"name":"AP5Z1 hereditary spastic paraplegia","type":"exact"},{"name":"SPG48","type":"exact"},{"name":"autosomal recessive spastic paraplegia 48","type":"exact"},{"name":"autosomal recessive spastic paraplegia type 48","type":"exact"},{"name":"hereditary spastic paraplegia caused by mutation in AP5Z1","type":"exact"},{"name":"hereditary spastic paraplegia type 48","type":"exact"},{"name":"spastic paraplegia 48, autosomal recessive","type":"related"}],"termid":"MONDO:0013342","xrefs":{"Monarch":{"xref_id":"0013342"}}}


id: GO:1903207
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of hydrogen peroxide-induced neuron death.","definition_xrefs":["GOC:PARL","GO_REF:0000058","GOC:bf","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of hydrogen peroxide-induced neuron death (obsolete GO:1903207)","synonyms":[{"name":"regulation of neuron death in response to H2O2","type":"exact"},{"name":"regulation of neuron death in response to hydrogen peroxide","type":"exact"},{"name":"regulation of neuronal cell death in response to hydrogen peroxide","type":"exact"}],"termid":"GO:1903207"}


id: PR:Q9P7R0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- aro1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P7R0"],"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":"pentafunctional AROM polypeptide (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1834.02","synonyms":[{"name":"Spom972h-aro1","type":"exact"}],"termid":"PR:Q9P7R0"}


id: MONDO:0005204
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An antiphospholipid syndrome that occurs as an isolated disorder.","direct_ancestors":[{"relation_name":"is_a","term_name":"antiphospholipid syndrome","termid":"MONDO:8000010"}],"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":"primary antiphospholipid syndrome","secondary_identifiers":["UMLS:C0409980","icd11.foundation:85700944","MEDGEN:592740","NANDO:1200267","ICD9:795.79","SCTID:239892009"],"termid":"MONDO:0005204","xrefs":{"Monarch":{"xref_id":"0005204"}}}


id: PBO:0116395
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pseudogene, mug2/mug135/meu2 family","termid":"PBO:0116395"}


id: PBO:0049363
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 22","termid":"PBO:0049363"}


id: PBO:0108943
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPL7L1 pseudogene 22","termid":"PBO:0108943"}


id: GO:0030747
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: indole-3-pyruvate + S-adenosyl-L-methionine = (R)-3-(indol-3-yl)-2-oxobutanoate + H+ + S-adenosyl-L-homocysteine.","definition_xrefs":["EC:2.1.1.47"],"direct_ancestors":[{"relation_name":"is_a","term_name":"S-adenosylmethionine-dependent methyltransferase activity","termid":"GO:0008757"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016741","GO:0016740"],"is_obsolete":false,"name":"indolepyruvate C-methyltransferase activity","secondary_identifiers":["MetaCyc:RXN-17530","RHEA:12112"],"synonyms":[{"name":"S-adenosyl-L-methionine:(indol-3-yl)pyruvate C-methyltransferase activity","type":"related"},{"name":"S-adenosyl-L-methionine:indolepyruvate C-methyltransferase activity","type":"related"},{"name":"indolepyruvate 3-methyltransferase activity","type":"related"},{"name":"indolepyruvate methyltransferase activity","type":"related"},{"name":"indolepyruvic acid methyltransferase activity","type":"related"}],"termid":"GO:0030747"}


id: MOD:01374
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A modification that effectively oxygenates C5 of an L-leucine residue to form a (2S,4R)-5-oxoleucine.","definition_xrefs":["ChEBI:43739","PubMed:16858410","RESID:AA0444"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon oxygenated residue","termid":"MOD:00679"},{"relation_name":"is_a","term_name":"modified L-leucine residue","termid":"MOD:00911"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"(2S,4R)-5-oxoleucine","synonyms":[{"name":"(2S,4R)-2-amino-4-methyl-5-oxopentanoic acid","type":"exact"},{"name":"(2S,4R)-5-oxoleucine","type":"exact"},{"name":"(4R)-5-oxo-L-leucine","type":"exact"}],"termid":"MOD:01374"}


id: GO:0070478
data:
  {"annotated_genes":["SJAG_04153","SJAG_03805","SJAG_04006","SJAG_04118","SJAG_01521","SJAG_04824","SJAG_04818","SJAG_01218","SJAG_04056","SJAG_05014","SJAG_00226","SJAG_03886","SJAG_04321","SJAG_00854","SJAG_03179","SJAG_01818","SJAG_04084"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[77145,90567,91616,93338,94892,97734,99059,103056,103904,106226,107094,108303,109298,110671,117749,118010,120184],"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":"regulates","termid":"GO:0010467"},{"rel_name":"negatively_regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0016071","GO:0010467"],"is_obsolete":false,"name":"nuclear-transcribed mRNA catabolic process, 3'-5' exonucleolytic nonsense-mediated decay","references_by_uniquename":{"GO_REF:0000033":null,"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: MONDO:0021243
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplasm (disease) that involves the parotid gland.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"parotid disorder","termid":"MONDO:0005899"},{"relation_name":"is_a","term_name":"neoplasm of major salivary gland","termid":"MONDO:0021368"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"parotid gland neoplasm","secondary_identifiers":["EFO:0003873","NCIT:C3314","SCTID:126788000","MEDGEN:18313","UMLS:C0030581"],"synonyms":[{"name":"neoplasm of parotid","type":"exact"},{"name":"neoplasm of parotid gland","type":"exact"},{"name":"neoplasm of the parotid","type":"exact"},{"name":"neoplasm of the parotid gland","type":"exact"},{"name":"parotid gland neoplasm (disease)","type":"exact"},{"name":"parotid gland tumor","type":"exact"},{"name":"parotid gland tumour","type":"exact"},{"name":"parotid neoplasm","type":"exact"},{"name":"parotid tumor","type":"exact"},{"name":"parotid tumour","type":"exact"},{"name":"tumor of parotid","type":"exact"},{"name":"tumor of parotid gland","type":"exact"},{"name":"tumor of the parotid","type":"exact"},{"name":"tumor of the parotid gland","type":"exact"},{"name":"tumour of parotid","type":"exact"},{"name":"tumour of parotid gland","type":"exact"},{"name":"tumour of the parotid","type":"exact"},{"name":"tumour of the parotid gland","type":"exact"}],"termid":"MONDO:0021243","xrefs":{"Monarch":{"xref_id":"0021243"}}}


id: PBO:0028184
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_growth_on_copper","termid":"PBO:0028184"}


id: PBO:0027009
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_telomere_tethering_at_nuclear_periphery","termid":"PBO:0027009"}


id: PBO:0072036
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S10 pseudogene 6","termid":"PBO:0072036"}


id: PBO:0005835
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"human THADA ortholog","termid":"PBO:0005835"}


id: PBO:0055621
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 3060","termid":"PBO:0055621"}


id: PBO:0025446
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kinetochore protein, CENP-P ortholog Fta2","termid":"PBO:0025446"}


id: MOD:01476
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-phenylalanine residue to an 2'-fluoro-L-fluorophenylalanine.","definition_xrefs":["PubMed:18688235","PubMed:8172898"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monofluorinated L-phenylalanine","termid":"MOD:01227"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2'-fluoro-L-phenylalanine","synonyms":[{"name":"2-fluorophenylalanine","type":"exact"},{"name":"o-fluorophenylalanine","type":"exact"},{"name":"ortho-fluorophenylalanine","type":"exact"}],"termid":"MOD:01476"}


id: PBO:0004286
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glucan 1,3-beta-glucosidase Exg3","termid":"PBO:0004286"}


id: PBO:0046817
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fatty acid amide hydrolase 2","termid":"PBO:0046817"}


id: PBO:0002421
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rho family GTPase Rho1","termid":"PBO:0002421"}


id: MONDO:0002339
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hemangioma (obsolete MONDO:0002339)","termid":"MONDO:0002339","xrefs":{"Monarch":{"xref_id":"0002339"}}}


id: PBO:0067628
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 800, pseudogene","termid":"PBO:0067628"}


id: GO:1904758
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a protein is transported to, or maintained in, a location within a new growing cell tip.","definition_xrefs":["PMID:19431238","GO_REF:0000087","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization to growing cell tip","termid":"GO:1902486"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"protein localization to new growing cell tip","synonyms":[{"name":"protein localisation in new growing cell tip","type":"exact"},{"name":"protein localisation to new growing cell tip","type":"exact"},{"name":"protein localization in new growing cell tip","type":"exact"},{"name":"protein localization to new cell tip after activation of bipolar cell growth","type":"exact"},{"name":"protein localization to new growing cell end","type":"exact"},{"name":"protein localization to post-NETO new cell end","type":"exact"},{"name":"protein localization to post-NETO new cell tip","type":"exact"},{"name":"protein localization to post-new end take-off new cell tip","type":"exact"}],"termid":"GO:1904758"}


id: PBO:0068049
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 354","termid":"PBO:0068049"}


id: MONDO:0700199
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Adenocarcinoma arising from the lung of a sheep.","definition_xrefs":["NCIT:C147532"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sheep disease","termid":"MONDO:0024985"},{"relation_name":"is_a","term_name":"adenocarcinoma, non-human animal","termid":"MONDO:0700099"},{"relation_name":"is_a","term_name":"respiratory system disorder, non-human animal","termid":"MONDO:0700104"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sheep lung adenocarcinoma","termid":"MONDO:0700199","xrefs":{"Monarch":{"xref_id":"0700199"}}}


id: PBO:0068375
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring finger protein 168","termid":"PBO:0068375"}


id: PBO:0065940
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"receptor for activated C kinase 1","termid":"PBO:0065940"}


id: PBO:0003744
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase subunit VII Cox7 (predicted)","termid":"PBO:0003744"}


id: SO:0000975
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene found within a minicircle.","direct_ancestors":[{"relation_name":"is_a","term_name":"kinetoplast_gene","termid":"SO:0000089"},{"relation_name":"part_of","term_name":"minicircle","termid":"SO:0000980"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"minicircle_gene","synonyms":[{"name":"minicircle gene","type":"exact"}],"termid":"SO:0000975"}


id: PBO:0082606
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cochaperone protein; regulates activity of adenylyl cyclase Cyr1p; involved in kinetochore complex assembly; associates with the SCF (Skp1p/Cdc53p/F box protein) ubiquitin ligase complex; acts as a linker between Skp1p and HSP90 complexes; protein abundance increases in response to DNA replication stress","termid":"PBO:0082606"}


id: PBO:0086132
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein required for localizing proteasomes to the nucleus; involved in cotranslational protein degradation; mediates interaction between nuclear import factor Srp1p and the proteasome; Sts1p and Srp1p couple proteasomes to nascent polypeptides emerging from the ribosome for cotranslational degradation; involved in ubiquitin-mediated protein degradation","termid":"PBO:0086132"}


id: PBO:0002028
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"beta-fructofuranosidase (predicted)","termid":"PBO:0002028"}


id: PBO:0048230
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G antigen 2A","termid":"PBO:0048230"}


id: PBO:0087283
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Signal recognition particle (SRP) receptor beta subunit; involved in SRP-dependent protein targeting; anchors the alpha subunit, Srp101p to the ER membrane","termid":"PBO:0087283"}


id: PBO:0085373
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PIK-related protein kinase and rapamycin target; subunit of TORC1, a complex that controls growth in response to nutrients by regulating translation, transcription, ribosome biogenesis, nutrient transport and autophagy; involved in meiosis; indole-3-acetic acid, an ATP-competitive inhibitor of TORC1, accumulates upon entry into stationary phase; TOR1 has a paralog, TOR2, that arose from the whole genome duplication","termid":"PBO:0085373"}


id: PBO:0066582
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rhodopsin","termid":"PBO:0066582"}


id: PBO:0073331
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serpin family A member 7","termid":"PBO:0073331"}


id: PBO:0064435
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polyribonucleotide nucleotidyltransferase 1","termid":"PBO:0064435"}


id: FYPO:0008281
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 1,5-bisdiphospho-1D-myo-inositol 2,3,4,6-tetrakisphosphate (1,5-IP8) measured in a cell is lower than normal.","definition_xrefs":["PomBase:pc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased cellular myo-inositol level","termid":"FYPO:0008280"}],"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:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"decreased cellular 1,5-IP8 level","termid":"FYPO:0008281"}


id: PBO:0051414
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin lambda variable 1-62 (pseudogene)","termid":"PBO:0051414"}


id: PBO:0040398
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP6V1F neighbor","termid":"PBO:0040398"}


id: MONDO:0018500
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cutaneous larva migrans is a rare parasitic disease characterized by single or multiple, linear or serpinginous, erythematous, slightly elevated cutaneous tracks caused by the larval migration of various nematode species. Tracks are variable in length, generally a few millimeters wide and are frequently located on the feet (although any area of the body is possible). Patients typically present with severe, intractable pruritus, which, in some cases, may cause impaired concentration, loss of sleep, and mood disturbances.","definition_xrefs":["Orphanet:423717"],"direct_ancestors":[{"relation_name":"is_a","term_name":"parasitic infectious disease","termid":"MONDO:0005135"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cutaneous larva migrans","secondary_identifiers":["UMLS:C0546999","icd11.foundation:657025682","SCTID:19362000","GARD:1629","ICD9:126.9","MEDGEN:107487","MESH:D007815"],"synonyms":[{"name":"CLM","type":"related"},{"name":"creeping eruption","type":"related"},{"name":"dew itch","type":"related"},{"name":"ground itch","type":"related"}],"termid":"MONDO:0018500","xrefs":{"Monarch":{"xref_id":"0018500"}}}


id: PBO:0059446
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"membrane spanning 4-domains A19, pseudogene","termid":"PBO:0059446"}


id: PBO:0062691
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 B member 2","termid":"PBO:0062691"}


id: PBO:0076389
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tachykinin receptor 2","termid":"PBO:0076389"}


id: MONDO:0007004
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Group of diseases mediated by the deposition of large soluble complexes of antigen and antibody with resultant damage to tissue. Besides serum sickness and the arthus reaction, evidence supports a pathogenic role for immune complexes in many other immune system diseases including glomerulonephritis, systemic lupus erythematosus (lupus erythematosus, systemic) and polyarteritis nodosa.","definition_xrefs":["MESH:D007105"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypersensitivity reaction disease","termid":"MONDO:0000605"},{"relation_name":"is_a","term_name":"autoimmune disease","termid":"MONDO:0007179"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"type III hypersensitivity disease","secondary_identifiers":["UMLS:C0020951","DOID:1557","EFO:1001222","MedDRA:10045265","MEDGEN:7021","NCIT:C114346"],"synonyms":[{"name":"disorder of type III hypersensitivity","type":"exact"},{"name":"hypersensitivity reaction type III disease","type":"related"},{"name":"immune complex disease","type":"exact"},{"name":"type 3 hypersensitivity reaction","type":"exact"},{"name":"type III hypersensitivity","type":"exact"},{"name":"type III hypersensitivity reaction","type":"exact"}],"termid":"MONDO:0007004","xrefs":{"Monarch":{"xref_id":"0007004"}}}


id: PBO:0077337
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 74","termid":"PBO:0077337"}


id: PBO:0027807
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_growth_on_KT5823","termid":"PBO:0027807"}


id: FYPO:0000316
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A viability phenotype in which a spore germinates but fails to produce dividing cells that can survive under normal conditions.","definition_xrefs":["PomBase:jh","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable vegetative cell","termid":"FYPO:0001489"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0000004"],"is_obsolete":false,"name":"inviable after spore germination","synonyms":[{"name":"inviable germinated spore","type":"exact"},{"name":"inviable germinating spore","type":"related"},{"name":"lethal after spore germination","type":"exact"}],"termid":"FYPO:0000316"}


id: MONDO:0100075
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A traumatic or pathologic injury to the jaw in which the continuity of the bone is broken.","direct_ancestors":[{"relation_name":"is_a","term_name":"bone fracture","termid":"MONDO:0005315"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"jaw fracture","secondary_identifiers":["MESH:D007572","EFO:0009612"],"synonyms":[{"name":"lower jaw fracture","type":"narrow"},{"name":"upper jaw fracture","type":"narrow"}],"termid":"MONDO:0100075","xrefs":{"Monarch":{"xref_id":"0100075"}}}


id: PBO:0072157
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S15a pseudogene 34","termid":"PBO:0072157"}


id: PBO:0027693
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-viable_elongated_aseptate_vegetative_cell","termid":"PBO:0027693"}


id: GO:0051448
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to gonadotropin-releasing hormone (GnRH), a peptide hormone responsible for the release of follicle-stimulating hormone (FSH) and luteinizing hormone (LH) from the anterior pituitary. GnRH is synthesized and released by the hypothalamus.","definition_xrefs":["GOC:pr","PMID:1984190"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptide hormone binding","termid":"GO:0017046"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"gonadotropin-releasing hormone binding","synonyms":[{"name":"GnRH binding","type":"exact"},{"name":"gonadotrophin releasing hormone binding","type":"exact"}],"termid":"GO:0051448"}


id: GO:0098952
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the spine apparatus membrane consisting of the gene products and protein complexes having either part of their peptide sequence embedded in the hydrophobic region of the membrane or some other covalently attached group such as a GPI anchor that is similarly embedded in the membrane.","definition_xrefs":["GOC:dos","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete intrinsic component of spine apparatus membrane (obsolete GO:0098952)","synonyms":[{"name":"intrinsic to spine apparatus membrane","type":"exact"}],"termid":"GO:0098952"}


id: PBO:0005467
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteinase B inhibitor Pbi2 (predicted)","termid":"PBO:0005467"}


id: FYPO:0005544
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 plasma membrane surrounding the cell division site is abnormal.","definition_xrefs":["PomBase:mah","PMID:27082518"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to plasma membrane during vegetative growth","termid":"FYPO:0002125"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001320","FYPO:0000138","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"abnormal protein localization to plasma membrane at cell division site during vegetative growth","synonyms":[{"name":"abnormal protein localisation to plasma membrane at cell division site during vegetative growth","type":"exact"},{"name":"abnormal protein localization in plasma membrane at cell division site during vegetative growth","type":"exact"},{"name":"abnormal protein localization to cell division site plasma membrane during vegetative growth","type":"exact"},{"name":"abnormal protein localization to plasma membrane at cell division site during mitotic cell cycle","type":"related"},{"name":"abnormal protein localization to plasma membrane division site during vegetative growth","type":"exact"}],"termid":"FYPO:0005544"}


id: GO:0009922
data:
  {"annotated_genes":["SJAG_02885","SJAG_01356"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[67785,79478],"is_not":false,"summary":null,"term":"GO:0009922"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: a very-long-chain acyl-CoA + H+ + malonyl-CoA = a very-long-chain 3-oxoacyl-CoA + CO2 + CoA. This reaction is the first (condensation) step of the four-step fatty acid elongation cycle in the endoplasmic reticulum that extends fatty acids of C-16 or longer with an additional 2-C unit.","definition_xrefs":["PMID:16564093","RHEA:32727","PMID:19763486"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyltransferase activity, transferring groups other than amino-acyl groups","termid":"GO:0016747"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01356":null,"SJAG_02885":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016740","GO:0016746"],"is_obsolete":false,"name":"fatty acid elongase activity","references_by_uniquename":{"GO_REF:0000003":null,"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-2046094","Reactome:R-HSA-548814","Reactome:R-HSA-548830","Reactome:R-HSA-2046090","Reactome:R-HSA-2046095","MetaCyc:RXN-7697","Reactome:R-HSA-2046083","Reactome:R-HSA-548800","Reactome:R-HSA-2046100","Reactome:R-HSA-548815","EC:2.3.1.199","Reactome:R-HSA-2046088"],"synonyms":[{"name":"ELOVL","type":"exact"},{"name":"condensing enzyme","type":"broad"},{"name":"elongation of very long chain fatty acids activity","type":"exact"},{"name":"very-long-chain 3-ketoacyl-CoA synthase","type":"exact"},{"name":"very-long-chain 3-oxoacyl-CoA synthase","type":"exact"},{"name":"very-long-chain beta-ketoacyl-CoA synthase","type":"exact"}],"termid":"GO:0009922","terms_by_termid":{"GO:0009922":null}}


id: MONDO:0005894
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A systemic fungal infection caused by Paracoccidioides brasiliensis that is most often seen in immunocompromised patients. It affects the mucous membranes, lymph nodes, lungs and bones.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary systemic mycosis","termid":"MONDO:0000308"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paracoccidioidomycosis","secondary_identifiers":["EFO:0007417","ICD10CM:B41","GARD:7323","Orphanet:73260","UMLS:C0030409","MEDGEN:14601","ICD9:116.1","MedDRA:10061906","icd11.foundation:268777657","MESH:D010229","NCIT:C34891","NORD:1553","SCTID:36866003","DOID:12662"],"synonyms":[{"name":"Lutz-Splendore-Almeida disease","type":"related"},{"name":"PCM","type":"related"},{"name":"Paracoccidioidal granuloma","type":"related"},{"name":"South American blastomycosis","type":"related"},{"name":"lobo disease","type":"related"},{"name":"mucocutaneous-lymphangitic paracoccidioidomycosis","type":"exact"},{"name":"paracoccidioidal mycosis","type":"exact"}],"termid":"MONDO:0005894","xrefs":{"Monarch":{"xref_id":"0005894"}}}


id: MONDO:1011907
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"renal disease, non-human animal","termid":"MONDO:1011909"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nephropathy, non-human animal","secondary_identifiers":["OMIA:000710"],"termid":"MONDO:1011907","xrefs":{"Monarch":{"xref_id":"1011907"}}}


id: MONDO:0018511
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A epithelial neoplasm that involves the vermiform appendix.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"appendiceal neoplasm","termid":"MONDO:0001236"},{"relation_name":"is_a","term_name":"epithelial tumor of colon","termid":"MONDO:0024479"}],"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":"epithelial tumor of the appendix","secondary_identifiers":["MEDGEN:1842930","UMLS:C5680073","Orphanet:423982","GARD:21766"],"synonyms":[{"name":"appendiceal epithelial tumor","type":"exact"},{"name":"appendiceal epithelial tumour","type":"exact"},{"name":"vermiform appendix epithelial neoplasm","type":"exact"}],"termid":"MONDO:0018511","xrefs":{"Monarch":{"xref_id":"0018511"}}}


id: PBO:0111923
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kinesin Kip3 subfamily","termid":"PBO:0111923"}


id: MONDO:0003855
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete immature teratoma of ovary (obsolete MONDO:0003855)","termid":"MONDO:0003855","xrefs":{"Monarch":{"xref_id":"0003855"}}}


id: PBO:0087105
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribosomal protein of the small (40S) subunit; homologous to mammalian ribosomal protein S3A, no bacterial homolog; RPS1A has a paralog, RPS1B, that arose from the whole genome duplication","termid":"PBO:0087105"}


id: GO:0072639
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The appearance of interleukin-33 due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["PMID:29778524","GOC:BHF","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine production","termid":"GO:0001816"}],"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:0010467","GO:0008150"],"is_obsolete":false,"name":"interleukin-33 production","secondary_identifiers":["GO:0150126","GO:0072640"],"synonyms":[{"name":"C9orf26 production","type":"narrow"},{"name":"IL-33 production","type":"exact"},{"name":"IL1F11 production","type":"narrow"},{"name":"IL33 production","type":"exact"},{"name":"NF-HEV production","type":"exact"},{"name":"interleukin-33 biosynthetic process","type":"narrow"},{"name":"interleukin-33 secretion","type":"narrow"}],"termid":"GO:0072639"}


id: PBO:0017058
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sSchizosaccharomyces pombe specific protein, similar to a region of alpha-galactosidase","termid":"PBO:0017058"}


id: MONDO:0021357
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplasm (disease) that involves the saliva-secreting gland.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"salivary gland disorder","termid":"MONDO:0001142"},{"relation_name":"is_a","term_name":"head and neck neoplasm","termid":"MONDO:0005586"},{"relation_name":"is_a","term_name":"digestive system neoplasm","termid":"MONDO:0021223"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tumor of salivary gland","secondary_identifiers":["EFO:1000384","MEDGEN:20641","NCIT:C3361","UMLS:C0036095","SCTID:235132004"],"synonyms":[{"name":"neoplasm of saliva-secreting gland","type":"exact"},{"name":"neoplasm of salivary gland","type":"exact"},{"name":"neoplasm of the salivary gland","type":"exact"},{"name":"saliva-secreting gland neoplasm","type":"exact"},{"name":"saliva-secreting gland neoplasm (disease)","type":"exact"},{"name":"saliva-secreting gland tumor","type":"exact"},{"name":"saliva-secreting gland tumour","type":"exact"},{"name":"salivary gland neoplasm","type":"exact"},{"name":"salivary gland tumor","type":"exact"},{"name":"salivary gland tumour","type":"exact"},{"name":"tumor of saliva-secreting gland","type":"exact"},{"name":"tumor of the salivary gland","type":"exact"},{"name":"tumour of saliva-secreting gland","type":"exact"},{"name":"tumour of the salivary gland","type":"exact"}],"termid":"MONDO:0021357","xrefs":{"Monarch":{"xref_id":"0021357"}}}


id: MONDO:0019674
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"postaxial polydactyly of fingers","termid":"MONDO:0017426"},{"relation_name":"is_a","term_name":"postaxial polydactyly","termid":"MONDO:0020927"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"postaxial polydactyly type B","secondary_identifiers":["icd11.foundation:366939273","SCTID:715707008","MEDGEN:357425","UMLS:C1868120","Orphanet:93335","GARD:16818"],"synonyms":[{"name":"PAPB","type":"exact"}],"termid":"MONDO:0019674","xrefs":{"Monarch":{"xref_id":"0019674"}}}


id: GO:0102808
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: UDP-alpha-D-glucose + pelargonidin 3-O-beta-D-glucoside = H+ + pelargonidin 3-O-sophoroside + UDP.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete pelargonidin 3-O-glucoside 2''-O-glucosyltransferase activity (obsolete GO:0102808)","termid":"GO:0102808"}


id: MONDO:0044235
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hsr (obsolete MONDO:0044235)","secondary_identifiers":["OMIM:139900"],"synonyms":[{"name":"HSR","type":"related"},{"name":"Handedness","type":"exact"},{"name":"hand skill, relative","type":"related"},{"name":"handedness","type":"related"}],"termid":"MONDO:0044235","xrefs":{"Monarch":{"xref_id":"0044235"}}}


id: GO:0022014
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The division of a radial glial cell in the subpallium. A radial glial cell is a precursor cell that gives rise to neurons and astrocytes.","definition_xrefs":["GO_REF:0000021","GOC:cls","GOC:jid","GOC:dgh","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete radial glial cell division in subpallium (obsolete GO:0022014)","termid":"GO:0022014"}


id: FYPO:0000283
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A chromosome segregation phenotype in which chromosomes are broken during mitotic chromosome segregation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic sister chromatid segregation","termid":"FYPO:0000141"},{"relation_name":"is_a","term_name":"abnormal chromosome morphology during vegetative growth","termid":"FYPO:0000848"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000337","FYPO:0000631","FYPO:0000002","FYPO:0000707","FYPO:0000654","FYPO:0000661","FYPO:0001320","FYPO:0005447","FYPO:0001985","FYPO:0000652","FYPO:0000641"],"is_obsolete":false,"name":"mitotic chromosome fragmentation upon segregation","synonyms":[{"name":"chromosome fragmentation upon mitotic chromosome segregation","type":"exact"},{"name":"chromosome fragmentation upon segregation during mitosis","type":"exact"},{"name":"chromosome fragmentation upon segregation during mitotic cell cycle","type":"exact"},{"name":"chromosome fragmentation upon segregation during vegetative growth","type":"exact"},{"name":"chromosome segregation defects, chromosome fragmentation","type":"exact"},{"name":"fragmented mitotic chromosomes upon segregation","type":"exact"}],"termid":"FYPO:0000283"}


id: PBO:0006197
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-occurs_at","termid":"PBO:0006197"}


id: PBO:0075523
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"speedy/RINGO cell cycle regulator family member E3","termid":"PBO:0075523"}


id: GO:0072664
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in which a protein is maintained in a specific location in a peroxisome, and is prevented from moving elsewhere.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"maintenance of protein localization in organelle","termid":"GO:0072595"},{"relation_name":"part_of","term_name":"protein localization to peroxisome","termid":"GO:0072662"}],"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":"part_of","termid":"GO:0007031"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0007031"],"is_obsolete":false,"name":"maintenance of protein location in peroxisome","termid":"GO:0072664"}


id: PBO:0046590
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endogenous retrovirus group K member 32, envelope","termid":"PBO:0046590"}


id: PBO:0054415
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 1811","termid":"PBO:0054415"}


id: MONDO:0009495
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Keutel syndrome is characterized by diffuse cartilage calcification, brachytelephalangism, peripheral pulmonary artery stenoses and facial dysmorphism.","definition_xrefs":["Orphanet:85202"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"congenital limb malformation","termid":"MONDO:0019054"},{"relation_name":"is_a","term_name":"chondrodysplasia punctata","termid":"MONDO:0019701"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Keutel syndrome","secondary_identifiers":["MESH:C536167","GARD:8449","SCTID:724208006","UMLS:C1855607","icd11.foundation:1083151379","OMIM:245150","MEDGEN:383722"],"synonyms":[{"name":"KEUTEL syndrome","type":"related"},{"name":"KTLS","type":"related"},{"name":"Keutel syndrome","type":"exact"},{"name":"pulmonic stenosis brachytelephalangism and calcification of cartilages","type":"related"},{"name":"pulmonic stenosis, brachytelephalangism, and calcification of cartilages","type":"related"},{"name":"pulmonic stenosis-brachytelephalangism-calcification of cartilages syndrome","type":"exact"}],"termid":"MONDO:0009495","xrefs":{"Monarch":{"xref_id":"0009495"}}}


id: PBO:0074879
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 59A","termid":"PBO:0074879"}


id: PBO:0044817
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"defensin beta 108F (pseudogene)","termid":"PBO:0044817"}


id: PBO:0011071
data:
  {"annotation_feature_type":"gene","cv_name":"species_dist","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved in eukaryotes only","termid":"PBO:0011071"}


id: GO:0047271
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: glycosaminoglycan + UDP-galactose = D-galactosylglycosaminoglycan + UDP.","definition_xrefs":["MetaCyc:2.4.1.74-RXN","EC:2.4.1.74"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-galactosyltransferase activity","termid":"GO:0035250"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016757","GO:0003824","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"glycosaminoglycan galactosyltransferase activity","synonyms":[{"name":"UDP-galactose:glycosaminoglycan D-galactosyltransferase activity","type":"related"},{"name":"UDPgalactose:glycosaminoglycan D-galactosyltransferase activity","type":"related"},{"name":"uridine diphosphogalactose-mucopolysaccharide galactosyltransferase activity","type":"related"}],"termid":"GO:0047271"}


id: FYPO:0001978
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A spindle phenotype in which the mitotic spindle is not straight, but instead forms an angle where microtubules from opposite poles interdigitate.","definition_xrefs":["PMID:2145514","PMID:1538784","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal bipolar mitotic spindle","termid":"FYPO:0001574"},{"relation_name":"is_a","term_name":"abnormal spindle morphology","termid":"FYPO:0003607"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002399"},{"rel_name":"output_of","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000120"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000120","FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0002399","FYPO:0000054","FYPO:0001320"],"is_obsolete":false,"name":"bent mitotic spindle","synonyms":[{"name":"V-shaped bipolar mitotic spindle","type":"exact"},{"name":"bent bipolar mitotic spindle","type":"exact"},{"name":"bent mitotic spindle during vegetative growth","type":"exact"},{"name":"bent spindle during mitotic cell cycle","type":"related"}],"termid":"FYPO:0001978"}


id: MONDO:0800445
data:
  {"annotated_genes":["SJAG_02231"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88898],"is_not":false,"summary":null,"term":"MONDO:0800445"}]},"cv_name":"mondo","definition":"Any Birt-Hogg-Dube (BHD) syndrome in which the cause of the disease is a variation in the FLCN gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Birt-Hogg-Dube syndrome","termid":"MONDO:0800444"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02231":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"Birt-Hogg-Dube syndrome 1","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:110985001","Orphanet:122","GARD:2322","NCIT:C28244","DOID:0050676","MESH:D058249","OMIM:135150","ICD9:704.8","MedDRA:10067736"],"synonyms":[{"name":"Hornstein-Knickenberg syndrome","type":"exact"},{"name":"fibrofolliculomas with trichodiscomas and acrochordons","type":"exact"}],"termid":"MONDO:0800445","terms_by_termid":{"MONDO:0800445":null},"xrefs":{"Monarch":{"xref_id":"0800445"}}}


id: PBO:0112743
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"yeast hsp78 and hsp104 are related to human CLBP at the C-term but have different N-terminal domains possibly due to some rearrangement in the metazoan lineage","termid":"PBO:0112743"}


id: MONDO:0016805
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete isolated oxidative phosphorylation complex disorder (obsolete MONDO:0016805)","secondary_identifiers":["Orphanet:254846"],"synonyms":[{"name":"isolated respiratory chain complex disorder","type":"exact"}],"termid":"MONDO:0016805","xrefs":{"Monarch":{"xref_id":"0016805"}}}


id: MONDO:0012590
data:
  {"annotated_genes":["SJAG_02556"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88292],"is_not":false,"summary":null,"term":"MONDO:0012590"}]},"cv_name":"mondo","definition":"A syndrome characterized by aged bird-like facies, lack of subcutaneous fat, dwarfism, cachexia and microcephaly. Additional features include sun-sensitivity from birth, learning disabilities, hearing loss, and visual impairment. It has material basis in homozygous mutation in the ERCC4 gene on chromosome 16p13.","definition_xrefs":["DOID:0060590","PMID:17183314"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02556":null},"genotype_count":0,"is_obsolete":false,"name":"XFE progeroid syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:610965","UMLS:C1970416","NCIT:C173111","MEDGEN:410064","MESH:C567043"],"synonyms":[{"name":"XFE progeroid syndrome","type":"exact"},{"name":"XFEPS","type":"exact"},{"name":"XPF-ERCC1 progeroid syndrome","type":"exact"}],"termid":"MONDO:0012590","terms_by_termid":{"MONDO:0012590":null},"xrefs":{"Monarch":{"xref_id":"0012590"}}}


id: MONDO:0001335
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hypotrichosis that involves the eyelid.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"eyelid degenerative disorder","termid":"MONDO:0000941"},{"relation_name":"is_a","term_name":"hypotrichosis","termid":"MONDO:0003037"},{"relation_name":"is_a","term_name":"eyelid disorder","termid":"MONDO:0003382"}],"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":"hypotrichosis of eyelid","secondary_identifiers":["UMLS:C0155214","DOID:11671","MEDGEN:509854","SCTID:70738004","ICD9:374.55"],"synonyms":[{"name":"eyelid hypotrichosis","type":"exact"}],"termid":"MONDO:0001335","xrefs":{"Monarch":{"xref_id":"0001335"}}}


id: FYPO:0008143
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount heme A measured in a cell is too low to detect.","definition_xrefs":["PMID:11248251"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heme absent from cell","termid":"FYPO:0008142"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"heme A absent from cell","termid":"FYPO:0008143"}


id: PBO:0036195
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_localization_to_chromatin_during_mitotic_G1_phase","termid":"PBO:0036195"}


id: FYECO:0000248
data:
  {"alleles_by_uniquename":{"SJAG_02592:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02592","name":"sty1delta","uniquename":"SJAG_02592:allele-1"}},"annotation_feature_type":"gene","cv_annotations":{"fission_yeast_phenotype_condition":[{"annotations":[121116,121235],"is_not":false,"summary":null,"term":"FYECO:0000248"}]},"cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which latrunculin A 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":1,"genes_by_uniquename":{"SJAG_02592":null},"genotype_count":1,"genotypes_by_uniquename":{"sty1delta":{"display_name":"sty1delta","display_uniquename":"sty1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02592:allele-1","expression":"Null"}]}]}},"is_obsolete":false,"name":"+ latA","references_by_uniquename":{"PMID:32915139":null,"PMID:33791858":null},"single_locus_annotated_genes":["SJAG_02592"],"single_locus_genotype_uniquenames":["sty1delta"],"synonyms":[{"name":"+ latrunculin A","type":"related"}],"termid":"FYECO:0000248","terms_by_termid":{"FYECO:0000248":null,"FYPO_EXT:0000001":null}}


id: PBO:0072284
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S24 pseudogene 2","termid":"PBO:0072284"}


id: MONDO:0010799
data:
  {"annotated_genes":["SJAG_00358"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86796,89077],"is_not":false,"summary":null,"term":"MONDO:0010799"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"postlingual non-syndromic genetic hearing loss","termid":"MONDO:0016298"},{"relation_name":"is_a","term_name":"mitochondrial oxidative phosphorylation disorder","termid":"MONDO:0016387"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00358":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004069","MONDO:0019497"],"is_obsolete":false,"name":"deafness, aminoglycoside-induced","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:C564013","OMIM:580000","DOID:0111734","Orphanet:168609","UMLS:C1838854","MEDGEN:374074","GARD:18161"],"synonyms":[{"name":"aminoglycoside-induced deafness","type":"exact"},{"name":"aminoglycoside-induced hearing loss","type":"broad"},{"name":"deafness, aminoglycoside-induced","type":"exact"},{"name":"deafness, mitochondrial, modifier of, mitochondrial","type":"exact"},{"name":"deafness, streptomycin-induced","type":"exact"},{"name":"mitochondrial isolated neurosensory deafness with susceptibility to aminoglycoside exposure","type":"exact"},{"name":"mitochondrial isolated neurosensory hearing loss with susceptibility to aminoglycoside exposure","type":"broad"},{"name":"mitochondrial isolated sensorineural deafness with susceptibility to aminoglycoside exposure","type":"exact"},{"name":"mitochondrial isolated sensorineural hearing loss with susceptibility to aminoglycoside exposure","type":"broad"},{"name":"mitochondrial non-syndromic neurosensory deafness with susceptibility to aminoglycoside exposure","type":"exact"},{"name":"mitochondrial non-syndromic neurosensory hearing loss with susceptibility to aminoglycoside exposure","type":"broad"},{"name":"mitochondrial non-syndromic sensorineural deafness with susceptibility to aminoglycoside exposure","type":"exact"},{"name":"mitochondrial non-syndromic sensorineural hearing loss with susceptibility to aminoglycoside exposure","type":"broad"},{"name":"streptomycin ototoxicity","type":"exact"}],"termid":"MONDO:0010799","terms_by_termid":{"MONDO:0010799":null},"xrefs":{"Monarch":{"xref_id":"0010799"}}}


id: GO:0033992
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 1,5-anhydro-D-fructose = 1,5-anhydro-4-deoxy-D-glycero-hex-3-en-2-ulose + H2O.","definition_xrefs":["EC:4.2.1.111"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydro-lyase activity","termid":"GO:0016836"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0016829","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"1,5-anhydro-D-fructose dehydratase activity","secondary_identifiers":["MetaCyc:4.2.1.111-RXN","RHEA:15725"],"synonyms":[{"name":"1,5-anhydro-D-arabino-hex-2-ulose dehydratase activity","type":"related"},{"name":"1,5-anhydro-D-fructose 4-dehydratase activity","type":"related"},{"name":"1,5-anhydro-D-fructose hydro-lyase (ascopyrone-M-forming) activity","type":"related"},{"name":"1,5-anhydro-D-fructose hydro-lyase activity","type":"related"},{"name":"1,5-anhydro-D-fructose hydrolyase activity","type":"related"},{"name":"AF dehydratase activity","type":"related"},{"name":"AFDH","type":"related"}],"termid":"GO:0033992"}


id: PBO:0031031
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_plasma_membrane_organization","termid":"PBO:0031031"}


id: GO:1900897
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of heptadecane biosynthetic process.","definition_xrefs":["GOC:TermGenie","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of heptadecane biosynthetic process","termid":"GO:1900896"},{"relation_name":"is_a","term_name":"negative regulation of heptadecane metabolic process","termid":"GO:1900900"},{"relation_name":"is_a","term_name":"negative regulation of alkane biosynthetic process","termid":"GO:1901578"},{"relation_name":"negatively_regulates","term_name":"heptadecane biosynthetic process","termid":"GO:1900636"}],"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 heptadecane biosynthetic process","synonyms":[{"name":"down regulation of heptadecane anabolism","type":"related"},{"name":"down regulation of heptadecane biosynthesis","type":"related"},{"name":"down regulation of heptadecane biosynthetic process","type":"exact"},{"name":"down regulation of heptadecane formation","type":"related"},{"name":"down regulation of heptadecane synthesis","type":"related"},{"name":"down-regulation of heptadecane anabolism","type":"related"},{"name":"down-regulation of heptadecane biosynthesis","type":"related"},{"name":"down-regulation of heptadecane biosynthetic process","type":"exact"},{"name":"down-regulation of heptadecane formation","type":"related"},{"name":"down-regulation of heptadecane synthesis","type":"related"},{"name":"downregulation of heptadecane anabolism","type":"related"},{"name":"downregulation of heptadecane biosynthesis","type":"related"},{"name":"downregulation of heptadecane biosynthetic process","type":"exact"},{"name":"downregulation of heptadecane formation","type":"related"},{"name":"downregulation of heptadecane synthesis","type":"related"},{"name":"inhibition of heptadecane anabolism","type":"narrow"},{"name":"inhibition of heptadecane biosynthesis","type":"narrow"},{"name":"inhibition of heptadecane biosynthetic process","type":"narrow"},{"name":"inhibition of heptadecane formation","type":"narrow"},{"name":"inhibition of heptadecane synthesis","type":"narrow"},{"name":"negative regulation of heptadecane anabolism","type":"related"},{"name":"negative regulation of heptadecane biosynthesis","type":"related"},{"name":"negative regulation of heptadecane formation","type":"related"},{"name":"negative regulation of heptadecane synthesis","type":"related"}],"termid":"GO:1900897"}


id: PBO:0045132
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynein axonemal assembly factor 2","termid":"PBO:0045132"}


id: PBO:0090742
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CCR4/nocturin family endoribonuclease","termid":"PBO:0090742"}


id: PBO:0080004
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"USP12 antisense RNA 1","termid":"PBO:0080004"}


id: MOD:01961
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"OBSOLETE because redundant and identical to MOD:01785. Remap to MOD:01785.","definition_xrefs":["PubMed:16618936","RESID:AA0536#THR","PubMed:18555071","PubMed:17051152","PubMed:17687277"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE MOD:01961 O-(L-isoglutamyl)-L-threonine (THR) (obsolete MOD:01961)","synonyms":[{"name":"(2S)-2-amino-5-([(1S,2R)-1-amino-1-carboxypropan-2-yl]oxy)-5-oxopentanoic acid","type":"exact"},{"name":"(2S,3R)-2-amino-3-([(4S)-4-amino-4-carboxybutanoyl]oxy)-propanoic acid","type":"exact"},{"name":"5-(threon-O3-yl)glutamate","type":"exact"},{"name":"O(beta)-(gamma-glutamyl)threonine","type":"exact"},{"name":"O-(L-isoglutamyl)-L-threonine","type":"exact"},{"name":"O3-(isoglutamyl)threonine","type":"exact"}],"termid":"MOD:01961"}


id: GO:0001514
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The incorporation of selenocysteine into a peptide; uses a special tRNA that recognizes the UGA codon as selenocysteine, rather than as a termination codon. Selenocysteine is synthesized from serine before its incorporation; it is not a posttranslational modification of peptidyl-cysteine.","definition_xrefs":["RESID:AA0022"],"direct_ancestors":[{"relation_name":"is_a","term_name":"translational readthrough","termid":"GO:0006451"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"selenocysteine incorporation","termid":"GO:0001514"}


id: PBO:0048653
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gap junction protein delta 3","termid":"PBO:0048653"}


id: PBO:0047731
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"formin binding protein 1 like","termid":"PBO:0047731"}


id: MONDO:0016221
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete temporomandibular joint anomaly (obsolete MONDO:0016221)","secondary_identifiers":["Orphanet:210581"],"termid":"MONDO:0016221","xrefs":{"Monarch":{"xref_id":"0016221"}}}


id: PBO:0047170
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 197 Y-linked member 3","termid":"PBO:0047170"}


id: MONDO:0019887
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Distal trisomy 16q is a rare chromosomal anomaly syndrome, resulting from the partial trisomy of the long arm of chromosome 16, with variable phenotype principally characterized by developmental delay, severe intellectual disability, hypotonia, facial dysmorphism (incl. high, prominent forehead, epicanthic folds, dysplastic ears, broad/depressed nasal bridge, malar hypoplasia, narrow and arched palate, thin upper lip vermilion, micrognathia) and hand/feet anomalies (e.g. arachnodactyly, talipes equinovarus). Cardiac defects, genitourinary malformations and vertebral anomalies are also associated. Thrombocytopenia and recurrent infections have also been reported.","definition_xrefs":["Orphanet:96106"],"direct_ancestors":[{"relation_name":"is_a","term_name":"partial trisomy of the long arm of chromosome 16","termid":"MONDO:0016966"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"distal trisomy 16q","secondary_identifiers":["MEDGEN:1633675","GARD:19320","UMLS:C4706934","SCTID:764459008"],"synonyms":[{"name":"distal duplication 16q","type":"exact"},{"name":"distal trisomy type 16q","type":"exact"},{"name":"telomeric duplication 16q","type":"exact"},{"name":"trisomy 16qter","type":"exact"}],"termid":"MONDO:0019887","xrefs":{"Monarch":{"xref_id":"0019887"}}}


id: PBO:0044348
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CYCS pseudogene 33","termid":"PBO:0044348"}


id: PBO:0039505
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin repeat domain 26 pseudogene 3","termid":"PBO:0039505"}


id: PBO:0058480
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5587","termid":"PBO:0058480"}


id: PATO:0000631
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A positional quality inhering in a bearer by virtue of the bearer's being stretched out and lying at full length along the ground.","definition_xrefs":["thefreedictionary.com:thefreedictionary.com"],"direct_ancestors":[{"relation_name":"is_a","term_name":"position","termid":"PATO:0000140"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prostrate","termid":"PATO:0000631"}


id: MONDO:0019474
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An extranodal, mature T-cell non-Hodgkin lymphoma that originates from cytotoxic T-cells, usually of gamma/delta T-cell type. It is characterized by the presence of medium-size neoplastic lymphocytes infiltrating the hepatic sinusoids. A similar infiltrating pattern is also present in the spleen and bone marrow that are usually involved at the time of the diagnosis.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"T-cell non-Hodgkin lymphoma","termid":"MONDO:0015760"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"hepatosplenic T-cell lymphoma","secondary_identifiers":["GARD:19077","UMLS:C1333984","Orphanet:86882","ICDO:9716/3","DOID:0081049","icd11.foundation:1301206942","MedDRA:10066957","ICD9:202.80","MEDGEN:272711","NCIT:C8459","ONCOTREE:HSTCL","ICD10CM:C86.1","SCTID:445406001"],"synonyms":[{"name":"HSTCL","type":"related"},{"name":"Hepatosplenic gamma/Delta T-cell lymphoma","type":"exact"}],"termid":"MONDO:0019474","xrefs":{"Monarch":{"xref_id":"0019474"}}}


id: PR:O42657
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC27D7.02c gene.","definition_xrefs":["PRO:DNx","UniProtKB:O42657"],"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":"GRIP and coiled-coil domain-containing protein C27D7.02c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC27D7.02c","synonyms":[{"name":"Spom972h-SPAC27D7.02c","type":"exact"}],"termid":"PR:O42657"}


id: PBO:0042881
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cilia and flagella associated protein 221","termid":"PBO:0042881"}


id: MONDO:1012756
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A developmental disorder of the biliary system caused by a congenital defect in the remodeling of the ductal plate at the level of the interlobular ducts, resulting in persistence of excessive abnormal embryonic bile duct structures, irregular portal veins, and progressive fibrosis of the portal tracts that occurs in horses due to a mutation in the PKHD1 gene.","definition_xrefs":["PMID:29402207"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"liver disorder, non-human animal","termid":"MONDO:1012967"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital liver fibrosis, PKHD1-related, horse","secondary_identifiers":["OMIA:001938-9796"],"synonyms":[{"name":"congenital hepatic fibrosis, horse","type":"related"},{"name":"congenital liver fibrosis, horse","type":"related"}],"termid":"MONDO:1012756","xrefs":{"Monarch":{"xref_id":"1012756"}}}


id: GO:0061565
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of introducing a phosphate group into dAMP, deoxyadenosine monophosphate, to produce dADP. Addition of two phosphate groups produces dATP.","definition_xrefs":["PMID:23416111","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside monophosphate phosphorylation","termid":"GO:0046940"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0055086"],"is_obsolete":false,"name":"dAMP phosphorylation","termid":"GO:0061565"}


id: GO:0043910
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + factor gamma-F420-2 + H+ = coenzyme F390-A + diphosphate.","definition_xrefs":["MetaCyc:RXN-9385","PMID:7957247","GOC:jl","PMID:8550473"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenylyltransferase activity","termid":"GO:0070566"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016779"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016740","GO:0016779"],"is_obsolete":false,"name":"ATP:coenzyme F420 adenylyltransferase activity","synonyms":[{"name":"ATP:coenzyme F420 adenyltransferase activity","type":"exact"},{"name":"coenzyme F390-A synthetase activity","type":"exact"}],"termid":"GO:0043910"}


id: PBO:0069471
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 738, pseudogene","termid":"PBO:0069471"}


id: PBO:0062535
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 9 subfamily A member 4","termid":"PBO:0062535"}


id: PBO:0047370
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box protein 2","termid":"PBO:0047370"}


id: PBO:0087220
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Scaffold protein involved in the formation of early endocytic sites; putative regulator of cytokinesis; homo-oligomerization is required for localization to and organization of endocytic sites; functions in autophagy of aberrant clathrin-mediated endocytosis (CME) protein condensates; binds membranes in a ubiquitin-dependent manner; interacts with Cmk2 and functions upstream of CMK2 in regulating non-apoptotic cell death; homolog of mammalian Eps15","termid":"PBO:0087220"}


id: PBO:0111810
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rho family","termid":"PBO:0111810"}


id: PBO:0083685
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Enolase, a phosphopyruvate hydratase; catalyzes the conversion of 2-phosphoglycerate to phosphoenolpyruvate; complements the growth defect of an ENO1 ENO2 double mutant","termid":"PBO:0083685"}


id: GO:0110053
data:
  {"annotated_genes":["SJAG_01993","SJAG_00279","SJAG_00521","SJAG_03086","SJAG_04479","SJAG_02700","SJAG_01894","SJAG_02566","SJAG_04522","SJAG_04100","SJAG_03455"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[77285,94138,80885,81936],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051016"},{"annotations":[76246],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034316"},{"annotations":[109450],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032231"},{"annotations":[68641,69537,78478,79119,81183],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030833"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of actin filament organization.","definition_xrefs":["GOC:kmv"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of actin cytoskeleton organization","termid":"GO:0032956"},{"relation_name":"is_a","term_name":"regulation of supramolecular fiber organization","termid":"GO:1902903"},{"relation_name":"regulates","term_name":"actin filament organization","termid":"GO:0007015"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00279":null,"SJAG_00521":null,"SJAG_01894":null,"SJAG_01993":null,"SJAG_02566":null,"SJAG_02700":null,"SJAG_03086":null,"SJAG_03455":null,"SJAG_04100":null,"SJAG_04479":null,"SJAG_04522":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007010"},{"rel_name":"regulates","termid":"GO:0030036"}],"interesting_parent_ids":["GO:0030036","GO:0007010","GO:0008150"],"is_obsolete":false,"name":"regulation of actin filament organization","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0110053","terms_by_termid":{"GO:0030833":null,"GO:0032231":null,"GO:0034316":null,"GO:0051016":null}}


id: GO:1903965
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of monounsaturated fatty acid.","definition_xrefs":["PMID:16443825","GOC:hjd","GOC:TermGenie","GO_REF:0000068"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fatty acid catabolic process","termid":"GO:0009062"},{"relation_name":"is_a","term_name":"monounsaturated fatty acid metabolic process","termid":"GO:1903964"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0044281","GO:0006629","GO:0008150"],"is_obsolete":false,"name":"monounsaturated fatty acid catabolic process","synonyms":[{"name":"monounsaturated fatty acid breakdown","type":"exact"},{"name":"monounsaturated fatty acid catabolism","type":"exact"},{"name":"monounsaturated fatty acid degradation","type":"exact"}],"termid":"GO:1903965"}


id: GO:0043528
data:
  {"annotated_genes":["SJAG_04181","SJAG_04890"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[77141,105957],"is_not":false,"summary":null,"term":"GO:0043528"}]},"cv_name":"cellular_component","definition":"A protein complex required for the methylation of the guanosine nucleotide at position 10 (m2G10) in tRNA. In S. cerevisiae, this complex consists of at least two subunits, Trm11p and Trm112p.","definition_xrefs":["PMID:15899842"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA methyltransferase complex","termid":"GO:0043527"}],"gene_count":2,"genes_by_uniquename":{"SJAG_04181":null,"SJAG_04890":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":"tRNA (m2G10) methyltransferase complex","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0043528","terms_by_termid":{"GO:0043528":null}}


id: GO:0019213
data:
  {"annotated_genes":["SJAG_03013","SJAG_00581","SJAG_04039","SJAG_03844","SJAG_04186","SJAG_03627","SJAG_01416","SJAG_01075"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[93590],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004099"},{"annotations":[64795,111319],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031078"},{"annotations":[91868,79088],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032041"},{"annotations":[106018],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0141222"},{"annotations":[91869],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140765"},{"annotations":[111320],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032129"},{"annotations":[79089,116286],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046969"},{"annotations":[111321],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140937"},{"annotations":[111322,99029],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034739"},{"annotations":[79090],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046970"},{"annotations":[111323],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0180032"},{"annotations":[111324],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0180033"},{"annotations":[72389],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000225"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of an acetyl group from a substrate molecule.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"deacylase activity","termid":"GO:0160215"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00581":null,"SJAG_01075":null,"SJAG_01416":null,"SJAG_03013":null,"SJAG_03627":null,"SJAG_03844":null,"SJAG_04039":null,"SJAG_04186":null},"genotype_count":0,"in_subsets":["mf_goslim_japonicus"],"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674"],"is_obsolete":false,"name":"deacetylase activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-5689000"],"termid":"GO:0019213","terms_by_termid":{"GO:0000225":null,"GO:0004099":null,"GO:0031078":null,"GO:0032041":null,"GO:0032129":null,"GO:0034739":null,"GO:0046969":null,"GO:0046970":null,"GO:0140765":null,"GO:0140937":null,"GO:0141222":null,"GO:0180032":null,"GO:0180033":null}}


id: GO:0003401
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The developmental growth that results in the elongation of a line that defines polarity or symmetry in an anatomical structure.","definition_xrefs":["GOC:dph","GOC:tb","GOC:ascb_2009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental growth involved in morphogenesis","termid":"GO:0060560"}],"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":"axis elongation","synonyms":[{"name":"elongation of an axis","type":"related"}],"termid":"GO:0003401"}


id: PBO:0081447
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 311","termid":"PBO:0081447"}


id: PBO:0051959
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ITPR interacting domain containing 2","termid":"PBO:0051959"}


id: GO:0072712
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a thiabendazole stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"}],"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 thiabendazole","synonyms":[{"name":"response to TBZ","type":"exact"}],"termid":"GO:0072712"}


id: GO:0047287
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: beta-D-galactoside + CMP-N-acetyl-beta-neuraminate = an N-acetyl-alpha-neuraminyl-(2->6)-beta-D-galactosyl derivative + CMP + H+.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete lactosylceramide alpha-2,6-N-sialyltransferase activity (obsolete GO:0047287)","termid":"GO:0047287"}


id: MONDO:0003575
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A high grade carcinoma characterized by the presence of comedo-type of tumor cell necrosis in which the necrotic areas are surrounded by a solid proliferation of malignant pleomorphic cells.","definition_xrefs":["NCIT:C4188"],"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":"comedocarcinoma","secondary_identifiers":["MEDGEN:90773","ICDO:8501/3","UMLS:C0334370","DOID:5670"],"synonyms":[{"name":"Comedocarcinoma","type":"exact"},{"name":"comedo carcinoma","type":"exact"}],"termid":"MONDO:0003575","xrefs":{"Monarch":{"xref_id":"0003575"}}}


id: PBO:0028982
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_rate_of_mitotic_spindle_elongation","termid":"PBO:0028982"}


id: GO:0006924
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A T cell apoptotic process that occurs towards the end of the expansion phase following the initial activation of mature T cells by antigen and is triggered by T cell receptor stimulation and signals transmitted via various surface-expressed members of the TNF receptor family such as Fas ligand, Fas, and TNF and the p55 and p75 TNF receptors.","definition_xrefs":["ISBN:0781765196","PMID:12752672","GOC:add","GOC:mtg_apoptosis","PMID:12414721"],"direct_ancestors":[{"relation_name":"is_a","term_name":"T cell apoptotic process","termid":"GO:0070231"},{"relation_name":"part_of","term_name":"T cell homeostasis","termid":"GO:0043029"}],"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":"activation-induced cell death of T cells","synonyms":[{"name":"AICD","type":"broad"},{"name":"activated T cell apoptosis","type":"broad"},{"name":"activation-induced cell death of T lymphocytes","type":"exact"},{"name":"activation-induced cell death of T-cells","type":"exact"},{"name":"activation-induced cell death of T-lymphocytes","type":"exact"},{"name":"antigen-driven apoptosis","type":"broad"}],"termid":"GO:0006924"}


id: MONDO:0021199
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A disease that disrupts the functioning of an organ system.","gene_count":0,"genotype_count":0,"name":"obsolete disease by anatomical system (obsolete MONDO:0021199)","secondary_identifiers":["ICD9:796.4","DOID:7","SCTID:362965005"],"synonyms":[{"name":"anatomical system disease","type":"exact"},{"name":"disease of anatomical entity","type":"related"},{"name":"disease of anatomical system","type":"exact"},{"name":"disorder of anatomical system","type":"related"}],"termid":"MONDO:0021199","xrefs":{"Monarch":{"xref_id":"0021199"}}}


id: PBO:0057930
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3657","termid":"PBO:0057930"}


id: MONDO:1010713
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pyruvate dehydrogenase deficiency that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyruvate dehydrogenase deficiency, non-human animal","termid":"MONDO:1010105"},{"relation_name":"is_a","term_name":"peripheral neuropathy, dog","termid":"MONDO:1011007"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyruvate dehydrogenase deficiency, dog","secondary_identifiers":["OMIA:001406-9615"],"termid":"MONDO:1010713","xrefs":{"Monarch":{"xref_id":"1010713"}}}


id: PBO:0043536
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"component of oligomeric golgi complex 4","termid":"PBO:0043536"}


id: PBO:0077179
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"toll like receptor 3","termid":"PBO:0077179"}


id: MONDO:0022775
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":"cleft lip and palate malrotation cardiopathy","termid":"MONDO:0022775","xrefs":{"Monarch":{"xref_id":"0022775"}}}


id: MONDO:0015116
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Rare biliary tract disease.","gene_count":0,"genotype_count":0,"name":"obsolete rare biliary tract disease (obsolete MONDO:0015116)","secondary_identifiers":["Orphanet:101941"],"synonyms":[{"name":"rare biliary tract disease","type":"exact"}],"termid":"MONDO:0015116","xrefs":{"Monarch":{"xref_id":"0015116"}}}


id: MONDO:0019579
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Discrete papular lichen myxedematosus is a rare chronic, slowly progressive form of localized lichen myxedematosus characterized by the development of a few to multiple small symmetrical skin-coloured mucinous papules on the limbs and trunk.","definition_xrefs":["Orphanet:90394"],"direct_ancestors":[{"relation_name":"is_a","term_name":"localized lichen myxedematosus","termid":"MONDO:0019446"}],"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":"discrete papular lichen myxedematosus","secondary_identifiers":["MEDGEN:898313","SCTID:717258005","UMLS:C4273967","GARD:19138"],"termid":"MONDO:0019579","xrefs":{"Monarch":{"xref_id":"0019579"}}}


id: PBO:0075663
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spectrin beta, non-erythrocytic 4","termid":"PBO:0075663"}


id: GO:0150111
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of transepithelial transport.","definition_xrefs":["GOC:aruk","PMID:27593915"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transport","termid":"GO:0051049"},{"relation_name":"regulates","term_name":"transepithelial transport","termid":"GO:0070633"}],"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 transepithelial transport","termid":"GO:0150111"}


id: GO:0060456
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the frequency, rate or extent of a digestive system process, a physical, chemical, or biochemical process carried out by living organisms to break down ingested nutrients into components that may be easily absorbed and directed into metabolism.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of digestive system process","termid":"GO:0044058"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"positively_regulates","term_name":"digestive system process","termid":"GO:0022600"}],"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 digestive system process","termid":"GO:0060456"}


id: PBO:0090518
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-directed RNA polymerase complex I TFIIS subunit Rpa12","termid":"PBO:0090518"}


id: MONDO:0100084
data:
  {"annotated_genes":["SJAG_03145"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87072],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008070"},{"annotations":[87580],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014800"}]},"cv_name":"mondo","definition":"A musculoskeletal system disorder that covers a wide spectrum of phenotypes and is caused by pathogenic variants in the skeletal muscle α-actin gene (ACTA1). These variants lead to a variety of overlapping adult onset and congenital myopathies characterized by muscle weakness, hypotonia, myopathic face, respiratory dysfunction, and rarely cardiac involvement. Specific skeletal muscle structural lesions visible on muscle biopsy include actin accumulations, nemaline and intranuclear bodies, fiber-type disproportion, cores, caps, dystrophic features and zebra bodies. Disorders associated with ACTA1 pathogenic variants can have autosomal dominant (90%) or recessive (10%) inheritance.","definition_xrefs":["PMID:22825594"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"qualitative or quantitative protein defects in neuromuscular diseases","termid":"MONDO:0016139"},{"relation_name":"is_a","term_name":"congenital myopathy","termid":"MONDO:0019952"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03145":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:0005336","MONDO:0002320"],"is_obsolete":false,"name":"alpha-actinopathy","references_by_uniquename":{"PB_REF:0000006":null},"synonyms":[{"name":"ACTA1 disease","type":"exact"},{"name":"actin myopathy","type":"broad"},{"name":"actinopathy","type":"broad"},{"name":"alpha actinopathy","type":"exact"},{"name":"alpha-actinopathy","type":"exact"}],"termid":"MONDO:0100084","terms_by_termid":{"MONDO:0008070":null,"MONDO:0014800":null},"xrefs":{"Monarch":{"xref_id":"0100084"}}}


id: MONDO:0011339
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the WASHC5 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pure hereditary spastic paraplegia","termid":"MONDO:0015149"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"hereditary spastic paraplegia 8","secondary_identifiers":["GARD:9591","Orphanet:100989","MEDGEN:400359","MESH:C580458","OMIM:603563","UMLS:C1863704","DOID:0110823"],"synonyms":[{"name":"SPG8","type":"exact"},{"name":"WASHC5 hereditary spastic paraplegia","type":"exact"},{"name":"autosomal dominant spastic paraplegia 8","type":"exact"},{"name":"autosomal dominant spastic paraplegia type 8","type":"exact"},{"name":"hereditary spastic paraplegia caused by mutation in WASHC5","type":"exact"},{"name":"hereditary spastic paraplegia type 8","type":"exact"},{"name":"spastic paraplegia 8","type":"related"},{"name":"spastic paraplegia 8, autosomal dominant","type":"related"}],"termid":"MONDO:0011339","xrefs":{"Monarch":{"xref_id":"0011339"}}}


id: PBO:0043311
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chloride intracellular channel 4","termid":"PBO:0043311"}


id: GO:0097224
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The segment of the sperm flagellum that attaches to the implantation fossa of the nucleus in the sperm head; from the remnant of the centriole at this point, the axoneme extends throughout the length of the flagellum.","definition_xrefs":["MP:0009830","GOC:cjm"],"gene_count":0,"genotype_count":0,"name":"obsolete sperm connecting piece (obsolete GO:0097224)","termid":"GO:0097224"}


id: MOD:01475
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-serine residue to O-[S-(carboxamidomethyl)phosphopantetheine]-L-serine.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"derives_from","term_name":"O-phosphopantetheine-L-serine","termid":"MOD:00159"},{"relation_name":"is_a","term_name":"iodoacetamide derivatized residue","termid":"MOD:00397"},{"relation_name":"is_a","term_name":"phosphorus containing modified residue","termid":"MOD:00861"},{"relation_name":"is_a","term_name":"modified L-serine residue","termid":"MOD:00916"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"O-[S-(carboxamidomethyl)phosphopantetheine]-L-serine","termid":"MOD:01475"}


id: GO:0120520
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a 1,2-saturated fatty acid + 2 Fe(II)-[cytochrome b5] + 2 H+ + O2 = a (R)-2-hydroxy fatty acid + 2 Fe(III)-[cytochrome b5] + H2O. Note that the substrate is a free fatty acid, not a fatty acyl chain within a sphingolipid.","definition_xrefs":["GOC:sjm","RHEA:38855"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fatty acid 2-hydroxylase activity","termid":"GO:0080132"}],"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":"free fatty acid 2-hydroxylase activity","termid":"GO:0120520"}


id: PBO:0067072
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 101, pseudogene","termid":"PBO:0067072"}


id: GO:0018464
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 3-hydroxypimelyl-CoA + NAD+ = 3-oxopimelyl-CoA + H+ + NADH.","definition_xrefs":["EC:1.1.1.259","RHEA:11168"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"3-hydroxypimeloyl-CoA dehydrogenase activity","secondary_identifiers":["KEGG_REACTION:R05305","UM-BBD_reactionID:r0196","MetaCyc:1.1.1.259-RXN"],"synonyms":[{"name":"3-hydroxypimeloyl-CoA:NAD+ oxidoreductase activity","type":"related"}],"termid":"GO:0018464"}


id: PBO:0089961
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BTB/POZ domain","termid":"PBO:0089961"}


id: GO:0075214
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The physiological, developmental and morphological changes that occur in a symbiont spore during the process of its encystment. Encystment means to enter a state of essentially suspended animation in which the spore is protected by an outer coating and remains immobile and inactive until favorable conditions for growth occur again. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators","GOC:kmv"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dormancy process","termid":"GO:0022611"},{"relation_name":"is_a","term_name":"cell development","termid":"GO:0048468"}],"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":"spore encystment","synonyms":[{"name":"spore encystment on host","type":"related"}],"termid":"GO:0075214"}


id: FYPO:0004435
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to tingenone. Cells stop growing (and may die) at a concentration of tingenone that allows wild type cells to grow.","definition_xrefs":["PMID:18204818","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0002683","FYPO:0001985","FYPO:0005447","FYPO:0000003"],"is_obsolete":false,"name":"sensitive to tingenone","synonyms":[{"name":"hypersensitive to tingenone","type":"exact"},{"name":"sensitive to tingenone during mitotic cell cycle","type":"related"},{"name":"sensitive to tingenone during vegetative growth","type":"exact"}],"termid":"FYPO:0004435"}


id: PBO:0067746
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 45","termid":"PBO:0067746"}


id: FYPO:0000014
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype in which the cell tapers at one end to a diameter smaller than the other. The cell diameter at the narrow end is smaller than that of a wild-type cell.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell shape","termid":"FYPO:0001126"}],"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:0000005"}],"interesting_parent_ids":["FYPO:0000005","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"tapered cell","synonyms":[{"name":"bottle-shaped cell","type":"exact"},{"name":"cell morphology, bottle/skittle","type":"exact"},{"name":"skittle-shaped cell","type":"exact"}],"termid":"FYPO:0000014"}


id: PBO:0051486
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IGSF3 pseudogene 1","termid":"PBO:0051486"}


id: GO:0010929
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency or extent of auxin mediated signaling pathway. Auxin mediated signaling pathway is the series of molecular signals generated in response to detection of auxin.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of signal transduction","termid":"GO:0009967"},{"relation_name":"is_a","term_name":"regulation of auxin mediated signaling pathway","termid":"GO:0010928"},{"relation_name":"positively_regulates","term_name":"auxin-activated signaling pathway","termid":"GO:0009734"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of auxin mediated signaling pathway","synonyms":[{"name":"positive regulation of auxin mediated signalling pathway","type":"exact"}],"termid":"GO:0010929"}


id: GO:0034697
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a prostagladin I stimulus.","definition_xrefs":["GOC:vk","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to prostaglandin","termid":"GO:0034694"},{"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 prostaglandin I","synonyms":[{"name":"response to prostaglandin I stimulus","type":"exact"}],"termid":"GO:0034697"}


id: GO:0044472
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which an organism alters or subverts the activity of a calcium channel in another organism via the action of a venom.","definition_xrefs":["GOC:fj","GOC:jl","PMID:20920515"],"direct_ancestors":[{"relation_name":"is_a","term_name":"venom-mediated perturbation of ion channel activity","termid":"GO:0044560"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"venom-mediated perturbation of calcium channel activity","synonyms":[{"name":"envenomation resulting in modulation of calcium channel activity in another organism","type":"exact"},{"name":"envenomation resulting in modulation of calcium channel activity in other organism","type":"exact"}],"termid":"GO:0044472"}


id: PBO:0046154
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ELAV like RNA binding protein 2","termid":"PBO:0046154"}


id: PBO:0031551
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_peptidase_activity","termid":"PBO:0031551"}


id: PATO:0000371
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000371 distance value (obsolete PATO:0000371)","termid":"PATO:0000371"}


id: GO:2000815
data:
  {"annotated_genes":["SJAG_03886","SJAG_05014","SJAG_02573"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[91618,92008,93340],"is_not":false,"summary":null,"term":"GO:2000815"}]},"cv_name":"biological_process","definition":"A process of regulation of mRNA stability that is involved in a response to oxidative stress.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mRNA stability involved in response to stress","termid":"GO:0010610"},{"relation_name":"part_of","term_name":"response to oxidative stress","termid":"GO:0006979"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02573":null,"SJAG_03886":null,"SJAG_05014":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0016071"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0016071","GO:0010467","GO:0008150"],"is_obsolete":false,"name":"regulation of mRNA stability involved in response to oxidative stress","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:2000815","terms_by_termid":{"GO:2000815":null}}


id: GO:1904886
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The disaggregation of a beta-catenin destruction complex into its constituent components.","definition_xrefs":["GOC:TermGenie","PMID:23169527","GOC:PARL","GO_REF:0000079","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex disassembly","termid":"GO:0032984"},{"relation_name":"part_of","term_name":"canonical Wnt signaling pathway","termid":"GO:0060070"}],"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":"beta-catenin destruction complex disassembly","synonyms":[{"name":"23S APC complex disassembly","type":"narrow"},{"name":"APC-Axin-1-beta-catenin complex disassembly","type":"exact"},{"name":"Axin-APC-beta-catenin-GSK3B complex disassembly","type":"exact"},{"name":"BDC disassembly","type":"exact"},{"name":"beta-catenin degradation complex disassembly","type":"exact"},{"name":"dissociation of beta-catenin degradation complex","type":"exact"}],"termid":"GO:1904886"}


id: GO:0033302
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving O-glucosylated derivatives of quercetin.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycoside metabolic process","termid":"GO:0016137"},{"relation_name":"is_a","term_name":"flavone metabolic process","termid":"GO:0051552"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"quercetin O-glucoside metabolic process","synonyms":[{"name":"quercetin O-glucoside metabolism","type":"exact"}],"termid":"GO:0033302"}


id: PBO:0036013
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_acetylation_during_vegetative_growth","termid":"PBO:0036013"}


id: GO:0071739
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex composed of two identical immunoglobulin heavy chains of the IgD isotype and two identical immunoglobulin light chains, held together by disulfide bonds, and present in the extracellular space, in mucosal areas or other tissues, or circulating in the blood or lymph.","definition_xrefs":["GOC:add","ISBN:0781765196","PMID:11282392"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immunoglobulin complex, circulating","termid":"GO:0042571"},{"relation_name":"is_a","term_name":"IgD immunoglobulin complex","termid":"GO:0071738"}],"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:0005576"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005576"],"is_obsolete":false,"name":"IgD immunoglobulin complex, circulating","synonyms":[{"name":"IgD antibody","type":"exact"}],"termid":"GO:0071739"}


id: MONDO:0001994
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm involving the sphenoidal sinus.","direct_ancestors":[{"relation_name":"is_a","term_name":"paranasal sinus carcinoma","termid":"MONDO:0000380"},{"relation_name":"is_a","term_name":"sphenoidal sinus neoplasm","termid":"MONDO:0004047"}],"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":"sphenoidal sinus cancer","secondary_identifiers":["SCTID:363428005","ICD9:160.5","UMLS:C0153479","ICD10CM:C31.3","MEDGEN:102273","NCIT:C3543","DOID:14546"],"synonyms":[{"name":"cancer of sphenoidal sinus","type":"exact"},{"name":"malignant neoplasm of sphenoid sinus","type":"exact"},{"name":"malignant neoplasm of sphenoidal sinus","type":"exact"},{"name":"malignant neoplasm of the sphenoid sinus","type":"exact"},{"name":"malignant neoplasm of the sphenoidal sinus","type":"exact"},{"name":"malignant sphenoid sinus neoplasm","type":"exact"},{"name":"malignant sphenoid sinus tumor","type":"exact"},{"name":"malignant sphenoid sinus tumour","type":"exact"},{"name":"malignant sphenoidal sinus neoplasm","type":"exact"},{"name":"malignant sphenoidal sinus tumor","type":"exact"},{"name":"malignant sphenoidal sinus tumour","type":"exact"},{"name":"malignant tumor of sphenoid sinus","type":"exact"},{"name":"malignant tumor of sphenoidal sinus","type":"exact"},{"name":"malignant tumor of the sphenoid sinus","type":"exact"},{"name":"malignant tumor of the sphenoidal sinus","type":"exact"},{"name":"malignant tumour of sphenoid sinus","type":"exact"},{"name":"malignant tumour of sphenoidal sinus","type":"exact"},{"name":"malignant tumour of the sphenoid sinus","type":"exact"},{"name":"malignant tumour of the sphenoidal sinus","type":"exact"},{"name":"sphenoidal sinus cancer","type":"exact"}],"termid":"MONDO:0001994","xrefs":{"Monarch":{"xref_id":"0001994"}}}


id: PBO:0071829
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S2 pseudogene 24","termid":"PBO:0071829"}


id: PR:O42832
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An rRNA methyltransferase 3 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO00360"],"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":"AdoMet-dependent rRNA methyltransferase spb1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1687.11","secondary_identifiers":["UniProtKB:O42832"],"synonyms":[{"name":"2'-O-ribose RNA methyltransferase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"S-adenosyl-L-methionine-dependent methyltransferase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-FTSJ3","type":"exact"}],"termid":"PR:O42832"}


id: MONDO:0011746
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":"symphalangism, distal, with microdontia, dental pulp stones, and narrowed zygomatic arch","secondary_identifiers":["UMLS:C1847185","MESH:C538148","MEDGEN:376067","OMIM:606895"],"synonyms":[{"name":"distal symphalangism, hypoplastic carpal bones, microdontia, dental pulp stones, and narrowing of the zygomatic arch","type":"related"},{"name":"symphalangism, distal, with microdontia, dental pulp stones, and narrowed zygomatic arch","type":"exact"}],"termid":"MONDO:0011746","xrefs":{"Monarch":{"xref_id":"0011746"}}}


id: GO:0006042
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of glucosamine (2-amino-2-deoxyglucopyranose), an aminodeoxysugar that occurs in combined form in chitin.","definition_xrefs":["GOC:jl","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glucosamine metabolic process","termid":"GO:0006041"},{"relation_name":"is_a","term_name":"glucosamine-containing compound biosynthetic process","termid":"GO:1901073"}],"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":"glucosamine biosynthetic process","synonyms":[{"name":"chitosamine biosynthesis","type":"exact"},{"name":"chitosamine biosynthetic process","type":"exact"},{"name":"glucosamine anabolism","type":"exact"},{"name":"glucosamine biosynthesis","type":"exact"},{"name":"glucosamine formation","type":"exact"},{"name":"glucosamine synthesis","type":"exact"}],"termid":"GO:0006042"}


id: PBO:0072851
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"secretion associated Ras related GTPase 1A pseudogene 1","termid":"PBO:0072851"}


id: GO:1902195
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving isovaleryl-CoA(4-).","definition_xrefs":["PMID:11231285","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fatty-acyl-CoA metabolic process","termid":"GO:0035337"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006790"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0006629","GO:0055086","GO:0006790"],"is_obsolete":false,"name":"isovaleryl-CoA(4-) metabolic process","synonyms":[{"name":"isovaleryl-CoA(4-) metabolism","type":"exact"}],"termid":"GO:1902195"}


id: GO:0010556
data:
  {"annotated_genes":["SJAG_01441","SJAG_00184","SJAG_00037","SJAG_00746","SJAG_04880","SJAG_03366","SJAG_04061","SJAG_03319","SJAG_04186","SJAG_00686","SJAG_00600","SJAG_04097","SJAG_04586","SJAG_00297","SJAG_03916","SJAG_00792","SJAG_00909","SJAG_00424","SJAG_04206","SJAG_01873","SJAG_00926","SJAG_03036","SJAG_00758","SJAG_01867","SJAG_03752","SJAG_02474","SJAG_02275","SJAG_05288","SJAG_03918","SJAG_02808","SJAG_07011","SJAG_03448","SJAG_01040","SJAG_02203","SJAG_01787","SJAG_00391","SJAG_01725","SJAG_01532","SJAG_01046","SJAG_05234","SJAG_02810","SJAG_01818","SJAG_01622","SJAG_01193","SJAG_02549","SJAG_00425","SJAG_00802","SJAG_00934","SJAG_01919","SJAG_03680","SJAG_01720","SJAG_02104","SJAG_03884","SJAG_04213","SJAG_00854","SJAG_02036","SJAG_03214","SJAG_02048","SJAG_02409","SJAG_00766","SJAG_02213","SJAG_03883","SJAG_02540","SJAG_03421","SJAG_04085","SJAG_00251","SJAG_02382","SJAG_02278","SJAG_02698","SJAG_03033","SJAG_03735","SJAG_02381","SJAG_01952","SJAG_01252","SJAG_00456","SJAG_03279","SJAG_04879","SJAG_00343","SJAG_00868","SJAG_05006","SJAG_00693","SJAG_00713","SJAG_00210","SJAG_05153","SJAG_04813","SJAG_03126","SJAG_00156","SJAG_03230","SJAG_01938","SJAG_03473","SJAG_00987","SJAG_04462","SJAG_01658","SJAG_02447","SJAG_04396","SJAG_01764","SJAG_01513","SJAG_04056","SJAG_00573","SJAG_04758","SJAG_02906","SJAG_02817","SJAG_02406","SJAG_03061","SJAG_00743","SJAG_03628","SJAG_05161","SJAG_04668","SJAG_03981","SJAG_01653","SJAG_03356","SJAG_02138","SJAG_04712","SJAG_01403","SJAG_00169","SJAG_00769","SJAG_00756","SJAG_05010","SJAG_03067","SJAG_02165","SJAG_01778","SJAG_04009","SJAG_04756","SJAG_00067","SJAG_02956","SJAG_01325","SJAG_02569","SJAG_03383","SJAG_03157","SJAG_04407","SJAG_01830","SJAG_01529","SJAG_02629","SJAG_06576","SJAG_04682","SJAG_00786","SJAG_00610","SJAG_02303","SJAG_02394","SJAG_01601","SJAG_01230","SJAG_03624","SJAG_00163","SJAG_02720","SJAG_01675","SJAG_01694","SJAG_03787","SJAG_02149","SJAG_03886","SJAG_02872","SJAG_05020","SJAG_04942","SJAG_04825","SJAG_04006","SJAG_01218","SJAG_00414","SJAG_02057","SJAG_01799","SJAG_03590","SJAG_04619","SJAG_02043","SJAG_06599","SJAG_02391","SJAG_04509","SJAG_01151","SJAG_04527","SJAG_04005","SJAG_02018","SJAG_05242","SJAG_04253","SJAG_04274","SJAG_04666","SJAG_04921","SJAG_01610","SJAG_01311","SJAG_00797","SJAG_02254","SJAG_01255","SJAG_02285","SJAG_03945","SJAG_02374","SJAG_03952","SJAG_04335","SJAG_04039","SJAG_02589","SJAG_03869","SJAG_02768","SJAG_00342","SJAG_05343","SJAG_00701","SJAG_02383","SJAG_02981","SJAG_01611","SJAG_01465","SJAG_00058","SJAG_04601","SJAG_04659","SJAG_01343","SJAG_02846","SJAG_04369","SJAG_03967","SJAG_02189","SJAG_04576","SJAG_00676","SJAG_04099","SJAG_04026","SJAG_04038","SJAG_02621","SJAG_03501","SJAG_03234","SJAG_03792","SJAG_04749","SJAG_00690","SJAG_02439","SJAG_05203","SJAG_04374","SJAG_01149","SJAG_06641","SJAG_04824","SJAG_04283","SJAG_03113","SJAG_04268","SJAG_01016","SJAG_02119","SJAG_01412","SJAG_03183","SJAG_03694","SJAG_00452","SJAG_01511","SJAG_02551","SJAG_01204","SJAG_04427","SJAG_00979","SJAG_03484","SJAG_00873","SJAG_02601","SJAG_01254","SJAG_03179","SJAG_00160","SJAG_05014","SJAG_03118","SJAG_03283","SJAG_02526","SJAG_03867","SJAG_02691","SJAG_04768","SJAG_04793","SJAG_01176","SJAG_01047","SJAG_03454","SJAG_06638","SJAG_02849","SJAG_04839","SJAG_00892","SJAG_02329","SJAG_00302","SJAG_00440","SJAG_04205","SJAG_00266","SJAG_03876","SJAG_00698","SJAG_03042","SJAG_01075","SJAG_02058","SJAG_01436","SJAG_01843","SJAG_01249","SJAG_01944","SJAG_01804","SJAG_02066","SJAG_00822","SJAG_04771","SJAG_03745","SJAG_03388","SJAG_01150","SJAG_02898","SJAG_03550","SJAG_03023","SJAG_01926","SJAG_03689","SJAG_04820","SJAG_00293","SJAG_04890","SJAG_01711","SJAG_00142","SJAG_01113","SJAG_02314","SJAG_04421","SJAG_04989","SJAG_04584","SJAG_03599","SJAG_01331","SJAG_00423","SJAG_03106","SJAG_01916","SJAG_01579","SJAG_03193","SJAG_03805","SJAG_04388","SJAG_02401","SJAG_00045","SJAG_02938","SJAG_01111","SJAG_03668","SJAG_03143","SJAG_03897","SJAG_04863","SJAG_00470","SJAG_02752","SJAG_05247","SJAG_00584","SJAG_04596","SJAG_04321","SJAG_03997","SJAG_04198","SJAG_03394","SJAG_00861","SJAG_01000","SJAG_05243","SJAG_03466","SJAG_01625","SJAG_03346","SJAG_03498","SJAG_03145","SJAG_02415","SJAG_04539","SJAG_02709","SJAG_03573","SJAG_02869","SJAG_03081","SJAG_04118","SJAG_00996","SJAG_02458","SJAG_03431","SJAG_04153","SJAG_01745","SJAG_00904","SJAG_02319","SJAG_00441","SJAG_01376","SJAG_04551","SJAG_01836","SJAG_02725","SJAG_00304","SJAG_02370","SJAG_04435","SJAG_02052","SJAG_00641","SJAG_03441","SJAG_02798","SJAG_00507","SJAG_03255","SJAG_05337","SJAG_02773","SJAG_04383","SJAG_05000","SJAG_02239","SJAG_01475","SJAG_04500","SJAG_03844","SJAG_00735","SJAG_00664","SJAG_03931","SJAG_02218","SJAG_02467","SJAG_04312","SJAG_00124","SJAG_02500","SJAG_00739","SJAG_03241","SJAG_03132","SJAG_00226","SJAG_04452","SJAG_01286","SJAG_02756","SJAG_02541","SJAG_02730","SJAG_01008","SJAG_02472","SJAG_00335","SJAG_00087","SJAG_04755","SJAG_00963","SJAG_04025","SJAG_02812","SJAG_03576","SJAG_03006","SJAG_00164","SJAG_00969","SJAG_02342","SJAG_02671","SJAG_02879","SJAG_05313","SJAG_04249","SJAG_01910","SJAG_05265","SJAG_04782","SJAG_01553","SJAG_03635","SJAG_02255","SJAG_02072","SJAG_04574","SJAG_01878","SJAG_01823","SJAG_05322","SJAG_03984","SJAG_01062","SJAG_00285","SJAG_06608","SJAG_03627","SJAG_16454","SJAG_00670","SJAG_00410","SJAG_05192","SJAG_03622","SJAG_02608","SJAG_02326","SJAG_02444","SJAG_01599","SJAG_04855","SJAG_04705","SJAG_03879","SJAG_04949","SJAG_02466","SJAG_05694","SJAG_02196","SJAG_03223","SJAG_05187","SJAG_01058","SJAG_00961","SJAG_03041","SJAG_01157","SJAG_03911","SJAG_02908","SJAG_02576","SJAG_04389","SJAG_04092","SJAG_05276","SJAG_00269","SJAG_01583","SJAG_02592","SJAG_04613","SJAG_04036","SJAG_01521","SJAG_00613","SJAG_03705","SJAG_05341","SJAG_03548","SJAG_01822","SJAG_02389","SJAG_16457","SJAG_03289","SJAG_00386","SJAG_02594","SJAG_02571","SJAG_04544","SJAG_03776","SJAG_02311","SJAG_00320","SJAG_02723","SJAG_04159","SJAG_02873","SJAG_03519","SJAG_00973","SJAG_04141","SJAG_02785","SJAG_02778","SJAG_02416","SJAG_03543","SJAG_00341","SJAG_04611","SJAG_03982","SJAG_03942","SJAG_00150","SJAG_02385","SJAG_04130","SJAG_00349","SJAG_03538","SJAG_02494","SJAG_00642","SJAG_03597","SJAG_02194","SJAG_03839","SJAG_03664","SJAG_01540","SJAG_04360","SJAG_03677","SJAG_03128","SJAG_01307","SJAG_03286","SJAG_01053","SJAG_03070","SJAG_02990","SJAG_04355","SJAG_00290","SJAG_02701","SJAG_02005","SJAG_02927","SJAG_02573","SJAG_02638","SJAG_02858","SJAG_04084","SJAG_00966","SJAG_02252","SJAG_01079","SJAG_04818","SJAG_00759","SJAG_00073","SJAG_04381","SJAG_02026","SJAG_02170","SJAG_04607","SJAG_03758","SJAG_00579","SJAG_04350","SJAG_00596","SJAG_01213","SJAG_02922","SJAG_04647","SJAG_03845","SJAG_03706","SJAG_01728","SJAG_03579","SJAG_04873","SJAG_01740","SJAG_04030","SJAG_04194","SJAG_01517","SJAG_03944","SJAG_01110","SJAG_01805","SJAG_01191","SJAG_01696","SJAG_01680","SJAG_00896","SJAG_01243","SJAG_03618","SJAG_04614","SJAG_01771","SJAG_04291","SJAG_04191","SJAG_00581","SJAG_01707","SJAG_01930","SJAG_01199","SJAG_00545","SJAG_01431","SJAG_04640","SJAG_04946","SJAG_02622","SJAG_01942","SJAG_03047","SJAG_01936","SJAG_03696","SJAG_04373","SJAG_05240","SJAG_01169","SJAG_04512","SJAG_03276"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[120194],"is_not":false,"rel_names":["is_a","regulates","positively_regulates"],"summary":null,"term":"GO:0061158"},{"annotations":[80501,101917,80461,92005],"is_not":false,"rel_names":["negatively_regulates","is_a","regulates"],"summary":null,"term":"GO:0070935"},{"annotations":[100932,119961,112334,117843,101378],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033562"},{"annotations":[115463],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140719"},{"annotations":[79312,77542,58876,81364,113858,76150],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0000290"},{"annotations":[77775,80537],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031087"},{"annotations":[95202,69829,93052,118071,120726,60263,66587],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0040029"},{"annotations":[95890,61315],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140718"},{"annotations":[100935,114472,119617,114473,100961,95891,104879,92566,97978,64636,100720,114911,61309,118990,117114,89970],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0033696"},{"annotations":[74630,121112,72116,74941,75525,78427,81701,72079,117268,121113,76529,73999],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031507"},{"annotations":[72363],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071044"},{"annotations":[115743],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000958"},{"annotations":[78022,116712],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006402"},{"annotations":[119981],"is_not":false,"rel_names":["regulates","positively_regulates","is_a"],"summary":null,"term":"GO:0061157"},{"annotations":[91302,72370],"is_not":false,"rel_names":["regulates","negatively_regulates","is_a"],"summary":null,"term":"GO:0048255"},{"annotations":[109810],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0060195"},{"annotations":[116713,97407,101255,120099],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000766"},{"annotations":[114010,93122],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904689"},{"annotations":[117480,96179,71679,76982,101149,111520],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990625"},{"annotations":[102893],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045892"},{"annotations":[113614],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904332"},{"annotations":[102729,90624],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010629"},{"annotations":[104942,99140,95015,95054,99027,116006],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045814"},{"annotations":[80766,78840],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045719"},{"annotations":[63927,70034],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010558"},{"annotations":[91603],"is_not":false,"rel_names":["regulates","negatively_regulates","is_a"],"summary":null,"term":"GO:0120271"},{"annotations":[93489],"is_not":false,"rel_names":["regulates","is_a","negatively_regulates"],"summary":null,"term":"GO:0060212"},{"annotations":[79086,108487],"is_not":false,"rel_names":["regulates","negatively_regulates","is_a"],"summary":null,"term":"GO:0061188"},{"annotations":[110330],"is_not":false,"rel_names":["negatively_regulates","regulates","is_a"],"summary":null,"term":"GO:0060906"},{"annotations":[76042,93069,71838,61783,72272,89407,103670,75543,105376,96455,116125,107737,96539,74156,95553,110413,92997,93973,108083,81336,105777,100702,107641,108332,110073,110858,73622,58371,95206,108584,112574,113000,114832,115690,119236,106082,78497,95107,95696,96040,108564,109812,75769,78880,102819,98104,113947,75413,77083,82204,74964,93951],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000122"},{"annotations":[75528],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016480"},{"annotations":[119798],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034244"},{"annotations":[77097],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001125"},{"annotations":[117307,73357,76065,102858,94889,90897,96777,74182,73062,91261,98348,117746,64176,74948],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071028"},{"annotations":[119983,98543,89302,94057,106124,109293,100906,93682,113155,111104,92680,92605,111085],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033621"},{"annotations":[99055,95256,72011,76330,119984],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071031"},{"annotations":[118190],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071032"},{"annotations":[108140,111105,92606,89303,111634,119985,117413,90652,94179,96818],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071030"},{"annotations":[106224,109295,94890,99056,103902,107092,117747,120182,94060,97732,108301,117308],"is_not":false,"rel_names":["regulates","is_a","positively_regulates"],"summary":null,"term":"GO:0071042"},{"annotations":[67869,69448,79646,117188,103987,81625,113106,74811,59612],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000956"},{"annotations":[117749,103904,91616,108303,120184,103056,106226,107094,93338,109298,90567,97734,99059,118010,110671,94892,77145],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070478"},{"annotations":[99955,72338,101751,99868,78358,117007,60449,81389],"is_not":false,"rel_names":["positively_regulates","is_a","regulates"],"summary":null,"term":"GO:0000288"},{"annotations":[76287,109011,115967],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070966"},{"annotations":[120185,107095,117750,110672,99060,118011,119095,108304,63407,106227,103057,94893,103905,97735,109299],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070481"},{"annotations":[71645,107721,115440,75055,91719,106587,117237],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000184"},{"annotations":[106603,75337],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000294"},{"annotations":[94412,77224,117523,118467,81491,71983,80543,79454,92596,94315,96145,75423,97325,91604],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0000289"},{"annotations":[64639,114482,93890,95257,61313,115152,94639,113126,106013,105912,74154,115847,116284,92026,114481,109999,96160,113963,100067,104604,95893],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031508"},{"annotations":[93160],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140462"},{"annotations":[73409],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034587"},{"annotations":[93490],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0036450"},{"annotations":[67872,92597,119096],"is_not":false,"rel_names":["is_a","regulates","positively_regulates"],"summary":null,"term":"GO:1990074"},{"annotations":[71520,108489,118996],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000767"},{"annotations":[72000,81561],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032786"},{"annotations":[91337],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010628"},{"annotations":[100779],"is_not":false,"rel_names":["is_a","regulates","positively_regulates"],"summary":null,"term":"GO:0031453"},{"annotations":[100520,114532],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070131"},{"annotations":[102281],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070134"},{"annotations":[120293,91291],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905746"},{"annotations":[75764,93974,112779,77066],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048026"},{"annotations":[108491],"is_not":false,"rel_names":["is_a","positively_regulates","regulates"],"summary":null,"term":"GO:0120272"},{"annotations":[74475,106748,91515],"is_not":false,"rel_names":["regulates","positively_regulates","is_a"],"summary":null,"term":"GO:0060213"},{"annotations":[92998],"is_not":false,"rel_names":["regulates","positively_regulates","is_a"],"summary":null,"term":"GO:0090053"},{"annotations":[89326,94234],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140748"},{"annotations":[95305,91278,89774,108493],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0060963"},{"annotations":[91526,81314],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045899"},{"annotations":[77140,79778],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000234"},{"annotations":[96186,112193,92999],"is_not":false,"rel_names":["is_a","regulates","positively_regulates"],"summary":null,"term":"GO:0090055"},{"annotations":[113819],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904595"},{"annotations":[74917,78089,81224,80287,79779],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045943"},{"annotations":[109813,99337,65037,63013,77371,78495,71113,75108,75617,73265,80344,89224,99339,80868,73619,79146,81333,81403,104047,109252,70854,110302,81564,96187,111537,118139,63786,69063,62015,100391,110888,77661,110650,102319,95524,79788,94565,70132,74228,74633,120102,99338,103967,104520,97506,99336,120980,73424,70336,116691,99105,75540,81704,64143,96898,72519,100231,62917,98740,78126,66488,68626,114152,99335,109412,79188,110475,102308,118329,76557,74002,104094,76788,119238,67628,97346,72510,60736,95622,75127,72003,101317,113605,77551,106266,118853,72082,113733,120979,101109,104991],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045944"},{"annotations":[73241,81297,118862,65744,72831,79938],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032968"},{"annotations":[89261,105494,65407,97198,110565,110592,108204,97680,92492,100840,100489,108067,116592,107523,105235,120814,96149,107878,92181,103776,96264],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0060261"},{"annotations":[67841,70301],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045901"},{"annotations":[74472],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045948"},{"annotations":[70302,67842,78279],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045905"},{"annotations":[121110,121111],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016441"},{"annotations":[90191,72988,119963,119846],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990431"},{"annotations":[93891,72692,105913,110000,113964,115153,74157],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000183"},{"annotations":[114926,107317,94705,66172,113386],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000381"},{"annotations":[89710],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032951"},{"annotations":[119771,69409,92583,94218,107174,107745,119904],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090334"},{"annotations":[119320,102537,102093,104401,107080,92081,111556,113018,114251,118684,97897,98041],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000765"},{"annotations":[112001,97281,115830,111336],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140018"},{"annotations":[105783,105151,97042],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990611"},{"annotations":[77241,80439,77569,73387,60714,57324,69948,78249,71864,57892,74592,76693,70652,77634,73733,80436,61218,77886,72686,77844,80721,62236,80818,81888,73509,82011],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006355"},{"annotations":[96756,91254,94240,104671],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070610"},{"annotations":[72163,63926,75470,70033],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010468"},{"annotations":[100381,92624],"is_not":false,"rel_names":["regulates","is_a"],"summary":null,"term":"GO:0031445"},{"annotations":[118489],"is_not":false,"rel_names":["regulates","is_a"],"summary":null,"term":"GO:0061013"},{"annotations":[100382],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905744"},{"annotations":[95556],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048024"},{"annotations":[90222],"is_not":false,"rel_names":["is_a","regulates"],"summary":null,"term":"GO:0043488"},{"annotations":[93340,91618,92008],"is_not":false,"rel_names":["regulates","is_a"],"summary":null,"term":"GO:2000815"},{"annotations":[100325],"is_not":false,"rel_names":["regulates","is_a"],"summary":null,"term":"GO:0060211"},{"annotations":[102123,98999],"is_not":false,"rel_names":["is_a","regulates"],"summary":null,"term":"GO:0090052"},{"annotations":[119618],"is_not":false,"rel_names":["regulates","is_a"],"summary":null,"term":"GO:0010964"},{"annotations":[119988,99000,119619,93683,102124],"is_not":false,"rel_names":["is_a","regulates"],"summary":null,"term":"GO:1902801"},{"annotations":[78795],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032210"},{"annotations":[110247],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006356"},{"annotations":[119479,67796,81768,76128,72681,59519,92401,74718,105187,100315,75706,78337,98391,99633,58481,63792,80862,79603,91153,114987,91030,109280,79153,61328,78261,70023,61081,94316,57633,94109,96020,99183,71101,78308,97709,79815,74416,74458,74077,81896,98871,78034,70717,75251,90307,60444,89473,81393,78094,80888,61472,103867,73309,90924,73462,60027,105858,107598,71641,74667,93423,74429,68139,79389,112324,73614,95945,109762,80134,68683,107220],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006357"},{"annotations":[77765,79857],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006359"},{"annotations":[104922],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990983"},{"annotations":[75762],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006449"},{"annotations":[93684,94640,119989],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0043628"},{"annotations":[94065,117524,89304,91605],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031047"},{"annotations":[110961,105914,109190,109619,114913,113711],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031048"},{"annotations":[101263],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0141014"},{"annotations":[109816,110001,94568,113127,106014,115531,117286,98545,97338,95894,100942,96162,105915,112336,119563,119848,119965,93086,113063,115849,101381,114067,61312,73401,113965,115154,117846,120698],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030466"},{"annotations":[119966,72989],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990432"},{"annotations":[117847,73412,73660],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030422"},{"annotations":[113966,92608,89305,118399,106015,112337],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902794"},{"annotations":[108141],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902795"},{"annotations":[115850],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0141194"},{"annotations":[116429,115532,119564,100943,98546,93087,90590,101383,119849,117287,114068,112338,113064,119967,116169,97156,95906,120699,112505,108385,117848,90647],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140727"},{"annotations":[93088,95895,119565,60484,74155,79091,113967,119968,110002,92027,61314,113128,114069,105916,120700,100944,115155,96163,112339,100068,98547,93893,115533,115851],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031509"},{"annotations":[92449],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090669"},{"annotations":[112325,116085,91098,107452,109166,111317,89474,116872,118208,119316,119409,119137,89618,111194,95822,106858,118768,97266,119431,98268,99635,108585,117116,94607,118400,119829,95946,67725,92508,109518,110910,108737,117248,114988,97703,109281,100482,89973,114410,117569,96118,105188,89796,112461,116096,103383,95932,64517,91880,116170,90308,100956,116261,109718,115177,61575,93225,116578,97710,98466,115008,117262,102798,90688,95593,95993,96456,106394,92522,59099,90157,98900,110303,97291,104943,95324,105668,107599,100316,119480,94110,100050,114834,101206,113607,66117,67672,91613,111425,95965],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045815"},{"annotations":[118401],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0141005"}]},"cv_name":"biological_process","definition":"Any process that modulates the rate, frequency or extent of the chemical reactions and pathways resulting in the formation of a macromolecule, any molecule of high relative molecular mass, the structure of which essentially comprises the multiple repetition of units derived, actually or conceptually, from molecules of low relative molecular mass.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of biosynthetic process","termid":"GO:0009889"},{"relation_name":"is_a","term_name":"regulation of macromolecule metabolic process","termid":"GO:0060255"},{"relation_name":"regulates","term_name":"macromolecule biosynthetic process","termid":"GO:0009059"}],"gene_count":559,"genes_by_uniquename":{"SJAG_00037":null,"SJAG_00045":null,"SJAG_00058":null,"SJAG_00067":null,"SJAG_00073":null,"SJAG_00087":null,"SJAG_00124":null,"SJAG_00142":null,"SJAG_00150":null,"SJAG_00156":null,"SJAG_00160":null,"SJAG_00163":null,"SJAG_00164":null,"SJAG_00169":null,"SJAG_00184":null,"SJAG_00210":null,"SJAG_00226":null,"SJAG_00251":null,"SJAG_00266":null,"SJAG_00269":null,"SJAG_00285":null,"SJAG_00290":null,"SJAG_00293":null,"SJAG_00297":null,"SJAG_00302":null,"SJAG_00304":null,"SJAG_00320":null,"SJAG_00335":null,"SJAG_00341":null,"SJAG_00342":null,"SJAG_00343":null,"SJAG_00349":null,"SJAG_00386":null,"SJAG_00391":null,"SJAG_00410":null,"SJAG_00414":null,"SJAG_00423":null,"SJAG_00424":null,"SJAG_00425":null,"SJAG_00440":null,"SJAG_00441":null,"SJAG_00452":null,"SJAG_00456":null,"SJAG_00470":null,"SJAG_00507":null,"SJAG_00545":null,"SJAG_00573":null,"SJAG_00579":null,"SJAG_00581":null,"SJAG_00584":null,"SJAG_00596":null,"SJAG_00600":null,"SJAG_00610":null,"SJAG_00613":null,"SJAG_00641":null,"SJAG_00642":null,"SJAG_00664":null,"SJAG_00670":null,"SJAG_00676":null,"SJAG_00686":null,"SJAG_00690":null,"SJAG_00693":null,"SJAG_00698":null,"SJAG_00701":null,"SJAG_00713":null,"SJAG_00735":null,"SJAG_00739":null,"SJAG_00743":null,"SJAG_00746":null,"SJAG_00756":null,"SJAG_00758":null,"SJAG_00759":null,"SJAG_00766":null,"SJAG_00769":null,"SJAG_00786":null,"SJAG_00792":null,"SJAG_00797":null,"SJAG_00802":null,"SJAG_00822":null,"SJAG_00854":null,"SJAG_00861":null,"SJAG_00868":null,"SJAG_00873":null,"SJAG_00892":null,"SJAG_00896":null,"SJAG_00904":null,"SJAG_00909":null,"SJAG_00926":null,"SJAG_00934":null,"SJAG_00961":null,"SJAG_00963":null,"SJAG_00966":null,"SJAG_00969":null,"SJAG_00973":null,"SJAG_00979":null,"SJAG_00987":null,"SJAG_00996":null,"SJAG_01000":null,"SJAG_01008":null,"SJAG_01016":null,"SJAG_01040":null,"SJAG_01046":null,"SJAG_01047":null,"SJAG_01053":null,"SJAG_01058":null,"SJAG_01062":null,"SJAG_01075":null,"SJAG_01079":null,"SJAG_01110":null,"SJAG_01111":null,"SJAG_01113":null,"SJAG_01149":null,"SJAG_01150":null,"SJAG_01151":null,"SJAG_01157":null,"SJAG_01169":null,"SJAG_01176":null,"SJAG_01191":null,"SJAG_01193":null,"SJAG_01199":null,"SJAG_01204":null,"SJAG_01213":null,"SJAG_01218":null,"SJAG_01230":null,"SJAG_01243":null,"SJAG_01249":null,"SJAG_01252":null,"SJAG_01254":null,"SJAG_01255":null,"SJAG_01286":null,"SJAG_01307":null,"SJAG_01311":null,"SJAG_01325":null,"SJAG_01331":null,"SJAG_01343":null,"SJAG_01376":null,"SJAG_01403":null,"SJAG_01412":null,"SJAG_01431":null,"SJAG_01436":null,"SJAG_01441":null,"SJAG_01465":null,"SJAG_01475":null,"SJAG_01511":null,"SJAG_01513":null,"SJAG_01517":null,"SJAG_01521":null,"SJAG_01529":null,"SJAG_01532":null,"SJAG_01540":null,"SJAG_01553":null,"SJAG_01579":null,"SJAG_01583":null,"SJAG_01599":null,"SJAG_01601":null,"SJAG_01610":null,"SJAG_01611":null,"SJAG_01622":null,"SJAG_01625":null,"SJAG_01653":null,"SJAG_01658":null,"SJAG_01675":null,"SJAG_01680":null,"SJAG_01694":null,"SJAG_01696":null,"SJAG_01707":null,"SJAG_01711":null,"SJAG_01720":null,"SJAG_01725":null,"SJAG_01728":null,"SJAG_01740":null,"SJAG_01745":null,"SJAG_01764":null,"SJAG_01771":null,"SJAG_01778":null,"SJAG_01787":null,"SJAG_01799":null,"SJAG_01804":null,"SJAG_01805":null,"SJAG_01818":null,"SJAG_01822":null,"SJAG_01823":null,"SJAG_01830":null,"SJAG_01836":null,"SJAG_01843":null,"SJAG_01867":null,"SJAG_01873":null,"SJAG_01878":null,"SJAG_01910":null,"SJAG_01916":null,"SJAG_01919":null,"SJAG_01926":null,"SJAG_01930":null,"SJAG_01936":null,"SJAG_01938":null,"SJAG_01942":null,"SJAG_01944":null,"SJAG_01952":null,"SJAG_02005":null,"SJAG_02018":null,"SJAG_02026":null,"SJAG_02036":null,"SJAG_02043":null,"SJAG_02048":null,"SJAG_02052":null,"SJAG_02057":null,"SJAG_02058":null,"SJAG_02066":null,"SJAG_02072":null,"SJAG_02104":null,"SJAG_02119":null,"SJAG_02138":null,"SJAG_02149":null,"SJAG_02165":null,"SJAG_02170":null,"SJAG_02189":null,"SJAG_02194":null,"SJAG_02196":null,"SJAG_02203":null,"SJAG_02213":null,"SJAG_02218":null,"SJAG_02239":null,"SJAG_02252":null,"SJAG_02254":null,"SJAG_02255":null,"SJAG_02275":null,"SJAG_02278":null,"SJAG_02285":null,"SJAG_02303":null,"SJAG_02311":null,"SJAG_02314":null,"SJAG_02319":null,"SJAG_02326":null,"SJAG_02329":null,"SJAG_02342":null,"SJAG_02370":null,"SJAG_02374":null,"SJAG_02381":null,"SJAG_02382":null,"SJAG_02383":null,"SJAG_02385":null,"SJAG_02389":null,"SJAG_02391":null,"SJAG_02394":null,"SJAG_02401":null,"SJAG_02406":null,"SJAG_02409":null,"SJAG_02415":null,"SJAG_02416":null,"SJAG_02439":null,"SJAG_02444":null,"SJAG_02447":null,"SJAG_02458":null,"SJAG_02466":null,"SJAG_02467":null,"SJAG_02472":null,"SJAG_02474":null,"SJAG_02494":null,"SJAG_02500":null,"SJAG_02526":null,"SJAG_02540":null,"SJAG_02541":null,"SJAG_02549":null,"SJAG_02551":null,"SJAG_02569":null,"SJAG_02571":null,"SJAG_02573":null,"SJAG_02576":null,"SJAG_02589":null,"SJAG_02592":null,"SJAG_02594":null,"SJAG_02601":null,"SJAG_02608":null,"SJAG_02621":null,"SJAG_02622":null,"SJAG_02629":null,"SJAG_02638":null,"SJAG_02671":null,"SJAG_02691":null,"SJAG_02698":null,"SJAG_02701":null,"SJAG_02709":null,"SJAG_02720":null,"SJAG_02723":null,"SJAG_02725":null,"SJAG_02730":null,"SJAG_02752":null,"SJAG_02756":null,"SJAG_02768":null,"SJAG_02773":null,"SJAG_02778":null,"SJAG_02785":null,"SJAG_02798":null,"SJAG_02808":null,"SJAG_02810":null,"SJAG_02812":null,"SJAG_02817":null,"SJAG_02846":null,"SJAG_02849":null,"SJAG_02858":null,"SJAG_02869":null,"SJAG_02872":null,"SJAG_02873":null,"SJAG_02879":null,"SJAG_02898":null,"SJAG_02906":null,"SJAG_02908":null,"SJAG_02922":null,"SJAG_02927":null,"SJAG_02938":null,"SJAG_02956":null,"SJAG_02981":null,"SJAG_02990":null,"SJAG_03006":null,"SJAG_03023":null,"SJAG_03033":null,"SJAG_03036":null,"SJAG_03041":null,"SJAG_03042":null,"SJAG_03047":null,"SJAG_03061":null,"SJAG_03067":null,"SJAG_03070":null,"SJAG_03081":null,"SJAG_03106":null,"SJAG_03113":null,"SJAG_03118":null,"SJAG_03126":null,"SJAG_03128":null,"SJAG_03132":null,"SJAG_03143":null,"SJAG_03145":null,"SJAG_03157":null,"SJAG_03179":null,"SJAG_03183":null,"SJAG_03193":null,"SJAG_03214":null,"SJAG_03223":null,"SJAG_03230":null,"SJAG_03234":null,"SJAG_03241":null,"SJAG_03255":null,"SJAG_03276":null,"SJAG_03279":null,"SJAG_03283":null,"SJAG_03286":null,"SJAG_03289":null,"SJAG_03319":null,"SJAG_03346":null,"SJAG_03356":null,"SJAG_03366":null,"SJAG_03383":null,"SJAG_03388":null,"SJAG_03394":null,"SJAG_03421":null,"SJAG_03431":null,"SJAG_03441":null,"SJAG_03448":null,"SJAG_03454":null,"SJAG_03466":null,"SJAG_03473":null,"SJAG_03484":null,"SJAG_03498":null,"SJAG_03501":null,"SJAG_03519":null,"SJAG_03538":null,"SJAG_03543":null,"SJAG_03548":null,"SJAG_03550":null,"SJAG_03573":null,"SJAG_03576":null,"SJAG_03579":null,"SJAG_03590":null,"SJAG_03597":null,"SJAG_03599":null,"SJAG_03618":null,"SJAG_03622":null,"SJAG_03624":null,"SJAG_03627":null,"SJAG_03628":null,"SJAG_03635":null,"SJAG_03664":null,"SJAG_03668":null,"SJAG_03677":null,"SJAG_03680":null,"SJAG_03689":null,"SJAG_03694":null,"SJAG_03696":null,"SJAG_03705":null,"SJAG_03706":null,"SJAG_03735":null,"SJAG_03745":null,"SJAG_03752":null,"SJAG_03758":null,"SJAG_03776":null,"SJAG_03787":null,"SJAG_03792":null,"SJAG_03805":null,"SJAG_03839":null,"SJAG_03844":null,"SJAG_03845":null,"SJAG_03867":null,"SJAG_03869":null,"SJAG_03876":null,"SJAG_03879":null,"SJAG_03883":null,"SJAG_03884":null,"SJAG_03886":null,"SJAG_03897":null,"SJAG_03911":null,"SJAG_03916":null,"SJAG_03918":null,"SJAG_03931":null,"SJAG_03942":null,"SJAG_03944":null,"SJAG_03945":null,"SJAG_03952":null,"SJAG_03967":null,"SJAG_03981":null,"SJAG_03982":null,"SJAG_03984":null,"SJAG_03997":null,"SJAG_04005":null,"SJAG_04006":null,"SJAG_04009":null,"SJAG_04025":null,"SJAG_04026":null,"SJAG_04030":null,"SJAG_04036":null,"SJAG_04038":null,"SJAG_04039":null,"SJAG_04056":null,"SJAG_04061":null,"SJAG_04084":null,"SJAG_04085":null,"SJAG_04092":null,"SJAG_04097":null,"SJAG_04099":null,"SJAG_04118":null,"SJAG_04130":null,"SJAG_04141":null,"SJAG_04153":null,"SJAG_04159":null,"SJAG_04186":null,"SJAG_04191":null,"SJAG_04194":null,"SJAG_04198":null,"SJAG_04205":null,"SJAG_04206":null,"SJAG_04213":null,"SJAG_04249":null,"SJAG_04253":null,"SJAG_04268":null,"SJAG_04274":null,"SJAG_04283":null,"SJAG_04291":null,"SJAG_04312":null,"SJAG_04321":null,"SJAG_04335":null,"SJAG_04350":null,"SJAG_04355":null,"SJAG_04360":null,"SJAG_04369":null,"SJAG_04373":null,"SJAG_04374":null,"SJAG_04381":null,"SJAG_04383":null,"SJAG_04388":null,"SJAG_04389":null,"SJAG_04396":null,"SJAG_04407":null,"SJAG_04421":null,"SJAG_04427":null,"SJAG_04435":null,"SJAG_04452":null,"SJAG_04462":null,"SJAG_04500":null,"SJAG_04509":null,"SJAG_04512":null,"SJAG_04527":null,"SJAG_04539":null,"SJAG_04544":null,"SJAG_04551":null,"SJAG_04574":null,"SJAG_04576":null,"SJAG_04584":null,"SJAG_04586":null,"SJAG_04596":null,"SJAG_04601":null,"SJAG_04607":null,"SJAG_04611":null,"SJAG_04613":null,"SJAG_04614":null,"SJAG_04619":null,"SJAG_04640":null,"SJAG_04647":null,"SJAG_04659":null,"SJAG_04666":null,"SJAG_04668":null,"SJAG_04682":null,"SJAG_04705":null,"SJAG_04712":null,"SJAG_04749":null,"SJAG_04755":null,"SJAG_04756":null,"SJAG_04758":null,"SJAG_04768":null,"SJAG_04771":null,"SJAG_04782":null,"SJAG_04793":null,"SJAG_04813":null,"SJAG_04818":null,"SJAG_04820":null,"SJAG_04824":null,"SJAG_04825":null,"SJAG_04839":null,"SJAG_04855":null,"SJAG_04863":null,"SJAG_04873":null,"SJAG_04879":null,"SJAG_04880":null,"SJAG_04890":null,"SJAG_04921":null,"SJAG_04942":null,"SJAG_04946":null,"SJAG_04949":null,"SJAG_04989":null,"SJAG_05000":null,"SJAG_05006":null,"SJAG_05010":null,"SJAG_05014":null,"SJAG_05020":null,"SJAG_05153":null,"SJAG_05161":null,"SJAG_05187":null,"SJAG_05192":null,"SJAG_05203":null,"SJAG_05234":null,"SJAG_05240":null,"SJAG_05242":null,"SJAG_05243":null,"SJAG_05247":null,"SJAG_05265":null,"SJAG_05276":null,"SJAG_05288":null,"SJAG_05313":null,"SJAG_05322":null,"SJAG_05337":null,"SJAG_05341":null,"SJAG_05343":null,"SJAG_05694":null,"SJAG_06576":null,"SJAG_06599":null,"SJAG_06608":null,"SJAG_06638":null,"SJAG_06641":null,"SJAG_07011":null,"SJAG_16454":null,"SJAG_16457":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of macromolecule biosynthetic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000024":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000108":null,"GO_REF:0000117":null,"PMID:35226668":null},"termid":"GO:0010556","terms_by_termid":{"GO:0000122":null,"GO:0000183":null,"GO:0000184":null,"GO:0000288":null,"GO:0000289":null,"GO:0000290":null,"GO:0000294":null,"GO:0000381":null,"GO:0000956":null,"GO:0000958":null,"GO:0006355":null,"GO:0006356":null,"GO:0006357":null,"GO:0006359":null,"GO:0006402":null,"GO:0006449":null,"GO:0010468":null,"GO:0010558":null,"GO:0010628":null,"GO:0010629":null,"GO:0010964":null,"GO:0016441":null,"GO:0016480":null,"GO:0030422":null,"GO:0030466":null,"GO:0031047":null,"GO:0031048":null,"GO:0031087":null,"GO:0031445":null,"GO:0031453":null,"GO:0031507":null,"GO:0031508":null,"GO:0031509":null,"GO:0032210":null,"GO:0032786":null,"GO:0032951":null,"GO:0032968":null,"GO:0033562":null,"GO:0033621":null,"GO:0033696":null,"GO:0034244":null,"GO:0034587":null,"GO:0036450":null,"GO:0040029":null,"GO:0043488":null,"GO:0043628":null,"GO:0045719":null,"GO:0045814":null,"GO:0045815":null,"GO:0045892":null,"GO:0045899":null,"GO:0045901":null,"GO:0045905":null,"GO:0045943":null,"GO:0045944":null,"GO:0045948":null,"GO:0048024":null,"GO:0048026":null,"GO:0048255":null,"GO:0060195":null,"GO:0060211":null,"GO:0060212":null,"GO:0060213":null,"GO:0060261":null,"GO:0060906":null,"GO:0060963":null,"GO:0061013":null,"GO:0061157":null,"GO:0061158":null,"GO:0061188":null,"GO:0070131":null,"GO:0070134":null,"GO:0070478":null,"GO:0070481":null,"GO:0070610":null,"GO:0070935":null,"GO:0070966":null,"GO:0071028":null,"GO:0071030":null,"GO:0071031":null,"GO:0071032":null,"GO:0071042":null,"GO:0071044":null,"GO:0090052":null,"GO:0090053":null,"GO:0090055":null,"GO:0090334":null,"GO:0090669":null,"GO:0120271":null,"GO:0120272":null,"GO:0140018":null,"GO:0140462":null,"GO:0140718":null,"GO:0140719":null,"GO:0140727":null,"GO:0140748":null,"GO:0141005":null,"GO:0141014":null,"GO:0141194":null,"GO:1902794":null,"GO:1902795":null,"GO:1902801":null,"GO:1904332":null,"GO:1904595":null,"GO:1904689":null,"GO:1905744":null,"GO:1905746":null,"GO:1990074":null,"GO:1990431":null,"GO:1990432":null,"GO:1990611":null,"GO:1990625":null,"GO:1990983":null,"GO:2000234":null,"GO:2000765":null,"GO:2000766":null,"GO:2000767":null,"GO:2000815":null,"GO:2001125":null}}


id: PBO:0056978
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 29b-2","termid":"PBO:0056978"}


id: GO:0043703
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a cell becomes capable of differentiating autonomously into a photoreceptor cell regardless of its environment; upon determination, the cell fate cannot be reversed.","definition_xrefs":["GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuron fate determination","termid":"GO:0048664"},{"relation_name":"part_of","term_name":"photoreceptor cell fate commitment","termid":"GO:0046552"}],"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":"photoreceptor cell fate determination","termid":"GO:0043703"}


id: GO:0033695
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of an oxidation-reduction (redox) reaction in which a CH2 group acts as a hydrogen or electron donor and reduces a quinone or similar acceptor molecule.","definition_xrefs":["GOC:mah","EC:1.17.5.-"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on CH or CH2 groups","termid":"GO:0016725"}],"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:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"oxidoreductase activity, acting on CH or CH2 groups, quinone or similar compound as acceptor","termid":"GO:0033695"}


id: PBO:0068959
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 203, pseudogene","termid":"PBO:0068959"}


id: PBO:0001170
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase regulatory subunit Glc9 (predicted)","termid":"PBO:0001170"}


id: PBO:0064725
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl isomerase A pseudogene 61","termid":"PBO:0064725"}


id: PBO:0028965
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_alpha,alpha-trehalase_activity_during_cellular_response_to_nutrient","termid":"PBO:0028965"}


id: PBO:0087379
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sterol-binding protein; has a probable role in retrograde transport of sterols from the plasma membrane to the ER; contains two StART-like domains that bind sterols and a GRAM domain; co-localizes to puncta in the cortical ER with Sip3p; one of six StART-like domain-containing proteins in yeast that may be involved in sterol transfer between intracellular membranes; conserved across eukaryotes","termid":"PBO:0087379"}


id: GO:0035708
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The switching of activated B cells from IgM biosynthesis to IgE biosynthesis, accomplished through a recombination process involving an intrachromosomal deletion between switch regions that reside 5' of the IgM and IgE constant region gene segments in the immunoglobulin heavy chain locus, that is dependent on the activity of interleukin 4 (IL-4).","definition_xrefs":["PMID:12496423","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isotype switching to IgE isotypes","termid":"GO:0048289"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0006310"}],"interesting_parent_ids":["GO:0010467","GO:0006310","GO:0006259","GO:0008150"],"is_obsolete":false,"name":"interleukin-4-dependent isotype switching to IgE isotypes","synonyms":[{"name":"IL-4-dependent isotype switching to IgE isotypes","type":"exact"}],"termid":"GO:0035708"}


id: MONDO:0020089
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An instance of lipodystrophy (disease) that is acquired during the lifetime of the individual.","definition_xrefs":["MONDO:patterns/acquired"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acquired metabolic disease","termid":"MONDO:0006504"},{"relation_name":"is_a","term_name":"lipodystrophy","termid":"MONDO:0006573"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005093"],"is_obsolete":false,"name":"acquired lipodystrophy","secondary_identifiers":["UMLS:C0877192","MedDRA:10049287","MEDGEN:798705","Orphanet:98307","GARD:12602"],"synonyms":[{"name":"acquired lipodystrophy (disease)","type":"exact"}],"termid":"MONDO:0020089","xrefs":{"Monarch":{"xref_id":"0020089"}}}


id: PBO:0001146
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial heat shock protein Hsp70","termid":"PBO:0001146"}


id: PBO:0070288
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, variant U1 small nuclear 29","termid":"PBO:0070288"}


id: PBO:0050654
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock protein 90 alpha family class B member 4, pseudogene","termid":"PBO:0050654"}


id: PBO:0085432
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Polyamine transporter of the major facilitator superfamily; member of the 12-spanner drug:H(+) antiporter DHA1 family; recognizes spermine, putrescine, and spermidine; localizes to the plasma membrane","termid":"PBO:0085432"}


id: PBO:0001047
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosome biogenesis protein Tsr1 (predicted)","termid":"PBO:0001047"}


id: MONDO:0008529
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":"T-cell Subgroups, non-HLA-linked","secondary_identifiers":["OMIM:186950","MEDGEN:348312","UMLS:C1861277"],"synonyms":[{"name":"T-cell Subgroups, non-HLA-linked","type":"exact"}],"termid":"MONDO:0008529","xrefs":{"Monarch":{"xref_id":"0008529"}}}


id: GO:0008002
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The electron-lucent layer of the basal lamina adjacent to the basal plasma membrane of the cells that rest on the lamina.","definition_xrefs":["ISBN:0815316194"],"gene_count":0,"genotype_count":0,"name":"obsolete lamina lucida (obsolete GO:0008002)","secondary_identifiers":["Wikipedia:Lamina_lucida"],"termid":"GO:0008002"}


id: MONDO:0024522
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any primary cutaneous amyloidosis in which the cause of the disease is a mutation in the OSMR gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial primary localized cutaneous amyloidosis","termid":"MONDO:0007101"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0021179"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005066","MONDO:0021179"],"is_obsolete":false,"name":"amyloidosis, primary localized cutaneous, 1","secondary_identifiers":["UMLS:C4551501","OMIM:105250","DOID:0080930","GARD:18637","MEDGEN:1639046"],"synonyms":[{"name":"OSMR primary cutaneous amyloidosis","type":"exact"},{"name":"PCA","type":"related"},{"name":"PLCA1","type":"exact"},{"name":"amyloidosis 9","type":"exact"},{"name":"amyloidosis, familial cutaneous lichen","type":"related"},{"name":"amyloidosis, primary cutaneous, 1","type":"exact"},{"name":"amyloidosis, primary localised cutaneous, type 1","type":"exact"},{"name":"amyloidosis, primary localized cutaneous, 1","type":"exact"},{"name":"amyloidosis, primary localized cutaneous, type 1","type":"exact"},{"name":"lichen amyloidosis, familial","type":"related"},{"name":"primary cutaneous amyloidosis caused by mutation in OSMR","type":"exact"}],"termid":"MONDO:0024522","xrefs":{"Monarch":{"xref_id":"0024522"}}}


id: PBO:0030545
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_cellular_cAMP_level","termid":"PBO:0030545"}


id: GO:1905817
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of dorsal/ventral axon guidance.","definition_xrefs":["GO_REF:0000058","PMID:18434533","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of axon guidance","termid":"GO:1902669"},{"relation_name":"is_a","term_name":"regulation of dorsal/ventral axon guidance","termid":"GO:1905815"},{"relation_name":"positively_regulates","term_name":"dorsal/ventral axon guidance","termid":"GO:0033563"}],"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 dorsal/ventral axon guidance","synonyms":[{"name":"activation of dorsal-ventral axon guidance","type":"narrow"},{"name":"activation of dorsal/ventral axon guidance","type":"narrow"},{"name":"activation of dorsal/ventral axon pathfinding","type":"narrow"},{"name":"activation of dorsoventral axon guidance","type":"narrow"},{"name":"positive regulation of dorsal-ventral axon guidance","type":"exact"},{"name":"positive regulation of dorsal/ventral axon pathfinding","type":"exact"},{"name":"positive regulation of dorsoventral axon guidance","type":"exact"},{"name":"up regulation of dorsal-ventral axon guidance","type":"exact"},{"name":"up regulation of dorsal/ventral axon guidance","type":"exact"},{"name":"up regulation of dorsal/ventral axon pathfinding","type":"exact"},{"name":"up regulation of dorsoventral axon guidance","type":"exact"},{"name":"up-regulation of dorsal-ventral axon guidance","type":"exact"},{"name":"up-regulation of dorsal/ventral axon guidance","type":"exact"},{"name":"up-regulation of dorsal/ventral axon pathfinding","type":"exact"},{"name":"up-regulation of dorsoventral axon guidance","type":"exact"},{"name":"upregulation of dorsal-ventral axon guidance","type":"exact"},{"name":"upregulation of dorsal/ventral axon guidance","type":"exact"},{"name":"upregulation of dorsal/ventral axon pathfinding","type":"exact"},{"name":"upregulation of dorsoventral axon guidance","type":"exact"}],"termid":"GO:1905817"}


id: PBO:0058002
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3926-1","termid":"PBO:0058002"}


id: MONDO:0019790
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Neuroleptic malignant syndrome (NMS) is an idiosyncratic condition associated with administration of antipsychotic and other central dopaminergic blockers, and characterized by hyperthermia, muscular rigidity, autonomic dysfunction and altered consciousness.","definition_xrefs":["Orphanet:94093"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"nervous system disorder","termid":"MONDO:0005071"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuroleptic malignant syndrome","secondary_identifiers":["SCTID:15244003","MESH:D009459","ICD9:333.92","DOID:14464","NORD:1504","ICD10CM:G21.0","GARD:7195","MedDRA:10029282","UMLS:C0027849","MEDGEN:10320","NCIT:C94829","EFO:1001379","icd11.foundation:498240876"],"synonyms":[{"name":"NMS","type":"exact"}],"termid":"MONDO:0019790","xrefs":{"Monarch":{"xref_id":"0019790"}}}


id: MONDO:0015616
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare genetic intestinal disease (obsolete MONDO:0015616)","secondary_identifiers":["Orphanet:165655"],"synonyms":[{"name":"genetic intestinal disease","type":"exact"}],"termid":"MONDO:0015616","xrefs":{"Monarch":{"xref_id":"0015616"}}}


id: GO:1902487
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a protein is transported to, or maintained in, a location within a non-growing cell tip.","definition_xrefs":["PMID:21652630","GOC:TermGenie","PMID:23041194"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization to cell tip","termid":"GO:1990151"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"protein localization to non-growing cell tip","synonyms":[{"name":"protein localisation in non-growing cell tip","type":"exact"},{"name":"protein localisation to non-growing cell tip","type":"exact"},{"name":"protein localization in non-growing cell tip","type":"exact"}],"termid":"GO:1902487"}


id: GO:1901523
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of icosanoid.","definition_xrefs":["GOC:TermGenie","GOC:pr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fatty acid derivative catabolic process","termid":"GO:1901569"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"icosanoid catabolic process","synonyms":[{"name":"icosanoid breakdown","type":"exact"},{"name":"icosanoid catabolism","type":"exact"},{"name":"icosanoid degradation","type":"exact"}],"termid":"GO:1901523"}


id: SO:0000966
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Structural unit composed of a self-replicating, single-stranded, circular DNA molecule.","definition_xrefs":["SO:ma"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"circular","termid":"SO:0000988"},{"relation_name":"is_a","term_name":"single_stranded_RNA_chromosome","termid":"SO:0000962"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"circular_single_stranded_RNA_chromosome","synonyms":[{"name":"circular single stranded RNA chromosome","type":"exact"}],"termid":"SO:0000966"}


id: GO:0015686
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of ferric triacetylfusarinine C into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"siderophore-iron import into cell","termid":"GO:0033214"},{"relation_name":"is_a","term_name":"nitrogen compound transport","termid":"GO:0071705"}],"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:0098771"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810","GO:0098771"],"is_obsolete":false,"name":"ferric triacetylfusarinine C import into cell","synonyms":[{"name":"ferric triacetylfusarinine C transport","type":"broad"}],"termid":"GO:0015686"}


id: PBO:0001095
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UBX domain protein Ubx3, Cdc48 cofactor","termid":"PBO:0001095"}


id: GO:0001001
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a single subunit mitochondrial RNA polymerase enzyme, which is composed of a single catalytic subunit similar to the RNA polymerase enzymes from phages T3, T7, and SP6.","definition_xrefs":["GOC:txnOH","PMID:20701995","PMID:2088182"],"direct_ancestors":[{"relation_name":"is_a","term_name":"single-subunit type RNA polymerase binding","termid":"GO:0001050"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005515","GO:0005488"],"is_obsolete":false,"name":"mitochondrial single-subunit type RNA polymerase binding","termid":"GO:0001001"}


id: FYPO:0004927
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which prospore formation assembly is normal (i.e. indistinguishable from wild type). In prospore formation, the nascent membrane forms at the meiotic outer plaque and grows until closure occurs and forespores, or prospores, are formed.","definition_xrefs":["GO:0032120","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular component organization","termid":"FYPO:0006003"},{"relation_name":"is_a","term_name":"normal meiotic cell cycle process","termid":"FYPO:0007078"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal prospore membrane formation","synonyms":[{"name":"normal ascospore-type prospore membrane assembly","type":"exact"},{"name":"normal forespore membrane formation","type":"exact"}],"termid":"FYPO:0004927"}


id: PBO:0002169
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TLDc domain protein 1","termid":"PBO:0002169"}


id: GO:0046520
data:
  {"annotated_genes":["SJAG_00880","SJAG_02429","SJAG_02706","SJAG_04178","SJAG_02305","SJAG_01057"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[75439,107821,111563,78597,80661,98715],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046512"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of sphingoids, any of a class of compounds comprising sphinganine and its homologues and stereoisomers, and derivatives of these compounds.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sphingolipid biosynthetic process","termid":"GO:0030148"},{"relation_name":"is_a","term_name":"sphingoid metabolic process","termid":"GO:0046519"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00880":null,"SJAG_01057":null,"SJAG_02305":null,"SJAG_02429":null,"SJAG_02706":null,"SJAG_04178":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"sphingoid biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"sphingoid anabolism","type":"exact"},{"name":"sphingoid biosynthesis","type":"exact"},{"name":"sphingoid formation","type":"exact"},{"name":"sphingoid synthesis","type":"exact"}],"termid":"GO:0046520","terms_by_termid":{"GO:0046512":null}}


id: GO:0045612
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of hemocyte differentiation.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of immune system process","termid":"GO:0002684"},{"relation_name":"is_a","term_name":"positive regulation of cell differentiation","termid":"GO:0045597"},{"relation_name":"is_a","term_name":"regulation of hemocyte differentiation","termid":"GO:0045610"},{"relation_name":"positively_regulates","term_name":"hemocyte differentiation","termid":"GO:0042386"}],"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 hemocyte differentiation","synonyms":[{"name":"activation of hemocyte differentiation","type":"narrow"},{"name":"positive regulation of arthropod blood cell differentiation","type":"exact"},{"name":"stimulation of hemocyte differentiation","type":"narrow"},{"name":"up regulation of hemocyte differentiation","type":"exact"},{"name":"up-regulation of hemocyte differentiation","type":"exact"},{"name":"upregulation of hemocyte differentiation","type":"exact"}],"termid":"GO:0045612"}


id: PBO:0068086
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 392","termid":"PBO:0068086"}


id: MONDO:0013929
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the TSPEAR gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0019497"}],"interesting_parent_ids":["MONDO:0019497","MONDO:0006025"],"is_obsolete":false,"name":"autosomal recessive nonsyndromic hearing loss 98","secondary_identifiers":["OMIM:614861","DOID:0110540","GARD:22644","UMLS:C3553932","MEDGEN:766846"],"synonyms":[{"name":"DFNB98","type":"narrow"},{"name":"TSPEAR autosomal recessive nonsyndromic deafness","type":"narrow"},{"name":"autosomal recessive deafness 98","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 98","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness caused by mutation in TSPEAR","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 98","type":"narrow"},{"name":"autosomal recessive nonsyndromic hearing loss 98","type":"exact"},{"name":"deafness, autosomal recessive 98","type":"narrow"},{"name":"deafness, autosomal recessive type 98","type":"narrow"}],"termid":"MONDO:0013929","xrefs":{"Monarch":{"xref_id":"0013929"}}}


id: GO:0072573
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Tolerance induction directed at lipopolysaccharide antigens.","definition_xrefs":["GOC:mah","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tolerance induction","termid":"GO:0002507"},{"relation_name":"is_a","term_name":"negative regulation of lipopolysaccharide-mediated signaling pathway","termid":"GO:0031665"},{"relation_name":"part_of","term_name":"cellular response to lipopolysaccharide","termid":"GO:0071222"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"tolerance induction to lipopolysaccharide","synonyms":[{"name":"tolerance induction to LPS","type":"exact"},{"name":"tolerance induction to endotoxin","type":"broad"}],"termid":"GO:0072573"}


id: PBO:0072261
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S21","termid":"PBO:0072261"}


id: PR:O74869
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- nic1 gene.","definition_xrefs":["UniProtKB:O74869","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":"high-affinity nickel transport protein nic1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1884.02","synonyms":[{"name":"Spom972h-nic1","type":"exact"}],"termid":"PR:O74869"}


id: GO:1902815
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of N,N'-diacetylchitobiose into a cell or organelle.","definition_xrefs":["GOC:am","PMID:9405618","GOC:TermGenie","GO_REF:0000073"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbohydrate derivative transport","termid":"GO:1901264"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"N,N'-diacetylchitobiose import","termid":"GO:1902815"}


id: PBO:0077953
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Ala (anticodon AGC) 11-1","termid":"PBO:0077953"}


id: GO:0052903
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + N(1)-acetylspermine + O2 = 3-acetamidopropanal + H2O2 + spermidine. Also converts N(1)-acetylspermidine to putrescine.","definition_xrefs":["EC:1.5.3.13"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyamine oxidase activity","termid":"GO:0046592"}],"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":"N(1)-acetylpolyamine oxidase (3-acetamidopropanal-forming) activity","secondary_identifiers":["KEGG_REACTION:R03899","MetaCyc:RXN-12090"],"synonyms":[{"name":"N(1)-acetylpolyamine oxidase activity","type":"broad"},{"name":"N1-acetylspermidine:oxygen oxidoreductase (3-acetamidopropanal-forming) activity","type":"narrow"},{"name":"N1-acetylspermine:oxygen oxidoreductase (3-acetamidopropanal-forming) activity","type":"narrow"}],"termid":"GO:0052903"}


id: PBO:0066391
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"receptor accessory protein 1","termid":"PBO:0066391"}


id: MONDO:0005348
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An irregularly shaped, elevated mark on the skin caused by deposits of excessive amounts of collagen during wound healing. It extends beyond the original boundaries of the wound and may enlarge progressively.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reactive cutaneous fibrous lesion","termid":"MONDO:0006603"}],"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":"keloid","secondary_identifiers":["icd11.foundation:2057714006","MESH:D007627","UMLS:C0022548","MEDGEN:7197","NCIT:C3145","SCTID:33659008","EFO:0004212","ICD9:701.4"],"termid":"MONDO:0005348","xrefs":{"Monarch":{"xref_id":"0005348"}}}


id: MONDO:0001891
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete malignant anus melanoma (obsolete MONDO:0001891)","termid":"MONDO:0001891","xrefs":{"Monarch":{"xref_id":"0001891"}}}


id: PBO:0045949
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EGF like and EMI domain containing 1, pseudogene","termid":"PBO:0045949"}


id: GO:0008507
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: iodide(out) + Na+(out) = iodide(in) + Na+(in).","definition_xrefs":["TC:2.A.21.5.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iodide transmembrane transporter activity","termid":"GO:0015111"},{"relation_name":"is_a","term_name":"monoatomic anion:sodium symporter activity","termid":"GO:0015373"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"sodium:iodide symporter activity","secondary_identifiers":["Reactome:R-HSA-5658195","Reactome:R-HSA-429591"],"synonyms":[{"name":"sodium/iodide symporter activity","type":"exact"}],"termid":"GO:0008507"}


id: PBO:0051737
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"integrator complex subunit 6 like","termid":"PBO:0051737"}


id: PR:Q9UTS0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- psp3 gene.","definition_xrefs":["UniProtKB:Q9UTS0","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":"subtilase-type proteinase psp3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1006.01","synonyms":[{"name":"Spom972h-psp3","type":"exact"}],"termid":"PR:Q9UTS0"}


id: PBO:0059848
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase pseudogene 1","termid":"PBO:0059848"}


id: MONDO:0002995
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A well differentiated, low or intermediate grade tumor with neuroendocrine differentiation that arises from the small intestine.","definition_xrefs":["NCIT:C96061"],"direct_ancestors":[{"relation_name":"is_a","term_name":"digestive system neuroendocrine tumor, grade 1/2","termid":"MONDO:0000386"},{"relation_name":"is_a","term_name":"small intestine neuroendocrine neoplasm","termid":"MONDO:0018510"}],"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":"small intestine neuroendocrine tumor, well differentiated, low or intermediate grade","secondary_identifiers":["UMLS:C3272528","MEDGEN:474161"],"synonyms":[{"name":"carcinoid tumor of small intestine","type":"related"},{"name":"carcinoid tumour of small intestine","type":"related"},{"name":"small intestinal NET","type":"broad"},{"name":"small intestinal neuroendocrine tumor","type":"broad"},{"name":"small intestinal neuroendocrine tumour","type":"broad"},{"name":"small intestinal well differentiated endocrine tumor","type":"broad"},{"name":"small intestinal well differentiated endocrine tumor/carcinoma","type":"narrow"},{"name":"small intestinal well differentiated endocrine tumour","type":"broad"},{"name":"small intestine neuroendocrine tumor","type":"broad"},{"name":"small intestine neuroendocrine tumour","type":"broad"}],"termid":"MONDO:0002995","xrefs":{"Monarch":{"xref_id":"0002995"}}}


id: FYPO:0004684
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which a cell is inviable, is elongated, and has two nuclei but no septum.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable elongated multinucleate aseptate vegetative cell","termid":"FYPO:0002024"},{"relation_name":"is_a","term_name":"binucleate aseptate vegetative cell","termid":"FYPO:0004562"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0000005","FYPO:0000004","FYPO:0005447","FYPO:0000631","FYPO:0000032","FYPO:0001320"],"is_obsolete":false,"name":"inviable elongated binucleate aseptate cell","synonyms":[{"name":"inviable elongated binucleate aseptate cell during mitotic cell cycle","type":"related"},{"name":"inviable elongated binucleate aseptate cell during vegetative growth","type":"exact"},{"name":"inviable elongated binucleate aseptate vegetative cell","type":"exact"},{"name":"lethal; elongated binucleate aseptate cell","type":"exact"}],"termid":"FYPO:0004684"}


id: PR:O74779
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mmb1 gene.","definition_xrefs":["UniProtKB:O74779","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":"microtubule-associated protein mug164 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC25B2.07c","synonyms":[{"name":"Spom972h-mmb1","type":"exact"},{"name":"meiotically up-regulated gene 164 protein (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74779"}


id: PR:O14047
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A serine/threonine-protein kinase 26 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO01777","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":"serine/threonine-protein kinase ppk11 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC2C4.14c","secondary_identifiers":["UniProtKB:O14047"],"synonyms":[{"name":"Spom972h-STK26","type":"exact"}],"termid":"PR:O14047"}


id: GO:0044361
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which an organism stops, prevents or reduces the frequency, rate or extent of the activity of a voltage-gated potassium channel in another organism.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of voltage-gated potassium channel activity in another organism (obsolete GO:0044361)","synonyms":[{"name":"negative regulation of voltage-gated potassium channel activity in other organism","type":"exact"}],"termid":"GO:0044361"}


id: PBO:0069522
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 791, pseudogene","termid":"PBO:0069522"}


id: PBO:0072229
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S20 pseudogene 4","termid":"PBO:0072229"}


id: GO:0086010
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which membrane potential changes in the depolarizing direction from the negative resting potential towards the positive membrane potential that will be the peak of the action potential.","definition_xrefs":["GOC:BHF","GOC:mtg_cardiac_conduct_nov11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane depolarization","termid":"GO:0051899"},{"relation_name":"part_of","term_name":"action potential","termid":"GO:0001508"}],"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":"membrane depolarization during action potential","termid":"GO:0086010"}


id: PBO:0060159
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-RNR2 like 7 (pseudogene)","termid":"PBO:0060159"}


id: PR:Q9HGK2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A homologous-pairing protein 2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00387","PRO:DNx","PANTHER:PTHR15938:SF0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homologous-pairing protein 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC222.15","secondary_identifiers":["UniProtKB:Q9HGK2"],"synonyms":[{"name":"Spom972h-PSMC3IP","type":"exact"},{"name":"meiotic expression up-regulated protein 13 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9HGK2"}


id: PBO:0046912
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 27 member E4","termid":"PBO:0046912"}


id: MONDO:0002027
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder characterized by an enduring pattern of avoidance of social situations and interpersonal contact due to overwhelming feelings of social inadequacy and a hypersensitivity to negative evaluation or rejection.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"personality disorder","termid":"MONDO:0002028"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"avoidant personality disorder","secondary_identifiers":["ICD10CM:F60.6","MEDGEN:13985","icd11.foundation:429615620","UMLS:C0004444","ICD9:301.82","NCIT:C92636","DOID:1509","SCTID:231528008"],"synonyms":[{"name":"anxious personality disorder","type":"exact"}],"termid":"MONDO:0002027","xrefs":{"Monarch":{"xref_id":"0002027"}}}


id: PBO:0091701
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"is not complemented by human ATR","termid":"PBO:0091701"}


id: PBO:0005807
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin-protein ligase E3 Brl1","termid":"PBO:0005807"}


id: PBO:0000282
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sad1 interacting factor 3 (predicted)","termid":"PBO:0000282"}


id: PBO:0064416
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PNMA family member 8C","termid":"PBO:0064416"}


id: PBO:0084439
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Maltase (alpha-D-glucosidase); encoded within the complex locus MAL4","termid":"PBO:0084439"}


id: PBO:0000067
data:
  {"annotation_feature_type":"gene","cv_name":"species_dist","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"identified in S. pombe only","termid":"PBO:0000067"}


id: GO:0047983
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: beta-alanine + L-gamma-glutamyl-L-cysteine + ATP = gamma-L-glutamyl-L-cysteinyl-beta-alanine + ADP + 2 H+ + phosphate.","definition_xrefs":["EC:6.3.2.23","RHEA:17993"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acid-amino acid ligase activity","termid":"GO:0016881"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016874","GO:0003674"],"is_obsolete":false,"name":"homoglutathione synthase activity","secondary_identifiers":["MetaCyc:HOMOGLUTATHIONE-SYNTHASE-RXN","KEGG_REACTION:R02741"],"synonyms":[{"name":"beta-alanine specific hGSH synthetase activity","type":"related"},{"name":"gamma-L-glutamyl-L-cysteine:beta-alanine ligase (ADP-forming)","type":"related"},{"name":"homoglutathione synthetase activity","type":"related"}],"termid":"GO:0047983"}


id: PR:Q9USW1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A basic salivary proline-rich protein 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02949","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 C21B10.03c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC21B10.03c","secondary_identifiers":["UniProtKB:Q9USW1"],"synonyms":[{"name":"Spom972h-PRB1","type":"exact"}],"termid":"PR:Q9USW1"}


id: GO:0097640
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of L-ornithine from outside of a cell, across the plasma membrane and into the cytosol.","definition_xrefs":["GOC:krc","PMID:8195186"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid import across plasma membrane","termid":"GO:0089718"},{"relation_name":"is_a","term_name":"L-ornithine transmembrane transport","termid":"GO:1903352"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0055085","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"L-ornithine import across plasma membrane","secondary_identifiers":["GO:1903411"],"synonyms":[{"name":"L-ornithine import into cell","type":"exact"}],"termid":"GO:0097640"}


id: GO:1903111
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of single-strand break repair via homologous recombination.","definition_xrefs":["GO_REF:0000058","PMID:24339919","GOC:bhm","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of DNA recombination","termid":"GO:0045910"},{"relation_name":"is_a","term_name":"regulation of single-strand break repair via homologous recombination","termid":"GO:1903110"},{"relation_name":"is_a","term_name":"negative regulation of single strand break repair","termid":"GO:1903517"},{"relation_name":"negatively_regulates","term_name":"single-strand break repair via homologous recombination","termid":"GO:1990396"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006259"},{"rel_name":"regulates","termid":"GO:0006310"},{"rel_name":"negatively_regulates","termid":"GO:0006259"},{"rel_name":"negatively_regulates","termid":"GO:0006281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006281"},{"rel_name":"negatively_regulates","termid":"GO:0006310"}],"interesting_parent_ids":["GO:0006281","GO:0008150","GO:0006259","GO:0006310"],"is_obsolete":false,"name":"negative regulation of single-strand break repair via homologous recombination","synonyms":[{"name":"down regulation of single-strand break repair via homologous recombination","type":"exact"},{"name":"down-regulation of single-strand break repair via homologous recombination","type":"exact"},{"name":"downregulation of single-strand break repair via homologous recombination","type":"exact"},{"name":"inhibition of single-strand break repair via homologous recombination","type":"narrow"}],"termid":"GO:1903111"}


id: PBO:0027853
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_protein_localization_to_vacuolar_membrane","termid":"PBO:0027853"}


id: PBO:0030446
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_protein_phosphatase_activity","termid":"PBO:0030446"}


id: GO:0102210
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + a rhamnogalacturonan type I = [rhamnogalacturonan I oligosaccharide]-alpha-L-rhamnose + 4-deoxy-4,5-unsaturated D-galactopyranosyluronate-[rhamnogalacturonan I oligosaccharide].","definition_xrefs":["GOC:pz","EC:4.2.2.23"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-oxygen lyase activity, acting on polysaccharides","termid":"GO:0016837"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016829","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"rhamnogalacturonan endolyase activity","secondary_identifiers":["MetaCyc:RXN-12173"],"termid":"GO:0102210"}


id: GO:0102201
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-cis,6-trans-farnesyl diphosphate = (+)-2-epi-prezizaene + diphosphoric acid.","definition_xrefs":["GOC:pz","PMID:20201526","PMID:20175559"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-oxygen lyase activity, acting on phosphates","termid":"GO:0016838"}],"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:0016829"}],"interesting_parent_ids":["GO:0003674","GO:0016829","GO:0003824"],"is_obsolete":false,"name":"(+)-2-epi-prezizaene synthase activity","secondary_identifiers":["MetaCyc:RXN-12117"],"termid":"GO:0102201"}


id: MONDO:0013901
data:
  {"annotated_genes":["SJAG_00663"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89026],"is_not":false,"summary":null,"term":"MONDO:0013901"}]},"cv_name":"mondo","definition":"Any azoospermia in which the cause of the disease is a mutation in the SEPT12 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spermatogenic failure","termid":"MONDO:0004983"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00663":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"spermatogenic failure 10","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:614822","DOID:0070178","GARD:18401","MEDGEN:766707","UMLS:C3553793"],"synonyms":[{"name":"SEPT12 azoospermia","type":"exact"},{"name":"SPGF10","type":"related"},{"name":"azoospermia caused by mutation in SEPT12","type":"exact"},{"name":"spermatogenic failure 10","type":"exact"},{"name":"spermatogenic failure type 10","type":"exact"},{"name":"spermatogenic failure with defective sperm annulus","type":"related"}],"termid":"MONDO:0013901","terms_by_termid":{"MONDO:0013901":null},"xrefs":{"Monarch":{"xref_id":"0013901"}}}


id: GO:0036390
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form the bacterial pre-replicative complex, a protein-DNA complex that forms at the bacterial oriC during the initial step of DNA replication and allows the origin to become competent, or 'licensed', for replication.","definition_xrefs":["GOC:bhm","GOC:jh2","PMID:19833870","GOC:bf","PMID:21035377","PMID:21895796"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pre-replicative complex assembly involved in cell cycle DNA replication","termid":"GO:1902299"},{"relation_name":"part_of","term_name":"bacterial-type DNA replication","termid":"GO:0044787"}],"gene_count":0,"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:0006260"},{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0044085","GO:0007049","GO:0006259","GO:0065003","GO:0006260","GO:0008150"],"is_obsolete":false,"name":"pre-replicative complex assembly involved in bacterial-type DNA replication","synonyms":[{"name":"bacterial pre-RC assembly","type":"exact"},{"name":"bacterial pre-replicative complex assembly","type":"exact"}],"termid":"GO:0036390"}


id: PBO:0070591
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7a pseudogene 57","termid":"PBO:0070591"}


id: MONDO:0007982
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Jansen's metaphyseal chondrodysplasia (JMC) is a very rare autosomal dominant skeletal dysplasia characterized by short-limbed short stature (due to severe metaphyseal changes that are often discovered in childhood by imaging), waddling gait, bowed legs, contracture deformities of the joints, short hands with clubbed fingers, clinodactyly, prominent upper face and small mandible, as well as chronic parathyroid hormone-independent hypercalcemia, hypercalciuria, and mild hypophosphatemia.","definition_xrefs":["Orphanet:33067"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"Pyle disease","termid":"MONDO:0009943"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"osteochondrodysplasia","termid":"MONDO:0005516"}],"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":"metaphyseal chondrodysplasia, Jansen type","secondary_identifiers":["MESH:C537564","OMIM:156400","SCTID:24629003","NCIT:C131868","GARD:79","NORD:1307","UMLS:C0265295","DOID:0080020","icd11.foundation:1652660420","MEDGEN:120529"],"synonyms":[{"name":"Jansen Type Metaphyseal Chondrodysplasia","type":"exact"},{"name":"Jansen disease","type":"exact"},{"name":"Jansen metaphyseal chondrodysplasia","type":"exact"},{"name":"Jansen metaphyseal dysostosis","type":"exact"},{"name":"Jansen type metaphyseal chondrodysplasia","type":"exact"},{"name":"Jansen's metaphyseal chondrodysplasia","type":"exact"},{"name":"metaphyseal chondrodysplasia murk Jansen type","type":"exact"},{"name":"metaphyseal chondrodysplasia, Jansen type","type":"exact"},{"name":"metaphyseal chondrodysplasia, murk Jansen type","type":"exact"},{"name":"murk Jansen type metaphyseal chondrodysplasia","type":"exact"}],"termid":"MONDO:0007982","xrefs":{"Monarch":{"xref_id":"0007982"}}}


id: FYPO:0002227
data:
  {"alleles_by_uniquename":{"SJAG_00426:allele-1":{"allele_type":"amino_acid_mutation","description":"P363S","gene_uniquename":"SJAG_00426","name":"bbl1-P363S","uniquename":"SJAG_00426:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[121083],"is_not":false,"summary":null,"term":"FYPO:0002227"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of one or more triglycerides measured in a cell is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased level of substance in cell during vegetative growth","termid":"FYPO:0001330"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00426":null},"genotype_count":1,"genotypes_by_uniquename":{"bbl1-P363S-P363S-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"bbl1-P363S(aa)","display_uniquename":"bbl1-P363S-P363S-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00426:allele-1","expression":"Not assayed or wild type"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"increased cellular triglyceride level during vegetative growth","references_by_uniquename":{"PMID:25318672":null},"single_locus_annotated_genes":["SJAG_00426"],"single_locus_genotype_uniquenames":["bbl1-P363S-P363S-amino_acid_mutation-expression-not_assayed_or_wild_type"],"synonyms":[{"name":"increased cellular TAG level during vegetative growth","type":"exact"},{"name":"increased cellular triacylglycerol level during vegetative growth","type":"exact"},{"name":"increased cellular triglyceride level during mitotic cell cycle","type":"related"},{"name":"increased triglyceride accumulation during vegetative growth","type":"related"}],"termid":"FYPO:0002227","terms_by_termid":{"FYECO:0000004":null,"FYECO:0000006":null,"FYECO:0000162":null,"FYPO:0002227":null}}


id: GO:0035364
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of thymine, 5-methyluracil, into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GO:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine nucleobase transport","termid":"GO:0015855"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"thymine transport","synonyms":[{"name":"5-methyluracil transport","type":"exact"},{"name":"thymine transmembrane transport","type":"exact"}],"termid":"GO:0035364"}


id: GO:0007169
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by an extracellular ligand binding to a receptor on the surface of the target cell where the receptor possesses tyrosine kinase activity, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["GOC:signaling","GOC:ceb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme-linked receptor protein signaling pathway","termid":"GO:0007167"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"cell surface receptor protein tyrosine kinase signaling pathway","secondary_identifiers":["Reactome:R-HSA-187015"],"synonyms":[{"name":"transmembrane receptor protein serine/threonine kinase signaling pathway","type":"broad"},{"name":"transmembrane receptor protein tyrosine kinase signalling pathway","type":"exact"}],"termid":"GO:0007169"}


id: GO:1903168
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of pyrroline-5-carboxylate reductase activity.","definition_xrefs":["GOC:PARL","GOC:bf","PMID:23743200","GO_REF:0000059","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of pyrroline-5-carboxylate reductase activity (obsolete GO:1903168)","synonyms":[{"name":"activation of 1-pyrroline-5-carboxylate reductase activity","type":"narrow"},{"name":"activation of L-proline oxidase activity","type":"narrow"},{"name":"activation of L-proline-NAD(P)+ 5-oxidoreductase activity","type":"narrow"},{"name":"activation of L-proline:NAD(P)+ 5-oxidoreductase activity","type":"narrow"},{"name":"activation of NADPH-L-delta1-pyrroline carboxylic acid reductase activity","type":"narrow"},{"name":"activation of P5CR activity","type":"narrow"},{"name":"activation of pyrroline-5-carboxylate reductase activity","type":"narrow"},{"name":"positive regulation of 1-pyrroline-5-carboxylate reductase activity","type":"exact"},{"name":"positive regulation of L-proline oxidase activity","type":"exact"},{"name":"positive regulation of L-proline-NAD(P)+ 5-oxidoreductase activity","type":"exact"},{"name":"positive regulation of L-proline:NAD(P)+ 5-oxidoreductase activity","type":"exact"},{"name":"positive regulation of NADPH-L-delta1-pyrroline carboxylic acid reductase activity","type":"exact"},{"name":"positive regulation of P5CR activity","type":"exact"},{"name":"up regulation of 1-pyrroline-5-carboxylate reductase activity","type":"exact"},{"name":"up regulation of L-proline oxidase activity","type":"exact"},{"name":"up regulation of L-proline-NAD(P)+ 5-oxidoreductase activity","type":"exact"},{"name":"up regulation of L-proline:NAD(P)+ 5-oxidoreductase activity","type":"exact"},{"name":"up regulation of NADPH-L-delta1-pyrroline carboxylic acid reductase activity","type":"exact"},{"name":"up regulation of P5CR activity","type":"exact"},{"name":"up regulation of pyrroline-5-carboxylate reductase activity","type":"exact"},{"name":"up-regulation of 1-pyrroline-5-carboxylate reductase activity","type":"exact"},{"name":"up-regulation of L-proline oxidase activity","type":"exact"},{"name":"up-regulation of L-proline-NAD(P)+ 5-oxidoreductase activity","type":"exact"},{"name":"up-regulation of L-proline:NAD(P)+ 5-oxidoreductase activity","type":"exact"},{"name":"up-regulation of NADPH-L-delta1-pyrroline carboxylic acid reductase activity","type":"exact"},{"name":"up-regulation of P5CR activity","type":"exact"},{"name":"up-regulation of pyrroline-5-carboxylate reductase activity","type":"exact"},{"name":"upregulation of 1-pyrroline-5-carboxylate reductase activity","type":"exact"},{"name":"upregulation of L-proline oxidase activity","type":"exact"},{"name":"upregulation of L-proline-NAD(P)+ 5-oxidoreductase activity","type":"exact"},{"name":"upregulation of L-proline:NAD(P)+ 5-oxidoreductase activity","type":"exact"},{"name":"upregulation of NADPH-L-delta1-pyrroline carboxylic acid reductase activity","type":"exact"},{"name":"upregulation of P5CR activity","type":"exact"},{"name":"upregulation of pyrroline-5-carboxylate reductase activity","type":"exact"}],"termid":"GO:1903168"}


id: FYPO:0006203
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 dATP measured in the cell is lower than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased cellular dNTP level","termid":"FYPO:0006401"},{"relation_name":"is_a","term_name":"decreased cellular pentose phosphate level","termid":"FYPO:0006705"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"decreased cellular dATP level","synonyms":[{"name":"decreased cellular dATP level during mitotic cell cycle","type":"related"},{"name":"decreased cellular dATP level during vegetative growth","type":"exact"},{"name":"reduced cellular dATP level","type":"exact"}],"termid":"FYPO:0006203"}


id: PBO:0074857
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 45A","termid":"PBO:0074857"}


id: PBO:0082613
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cohesion maintenance factor; involved in sister chromatid condensation and cohesion; colocalizes with cohesin on chromosomes; performs its cohesin maintenance function in pre-anaphase cells by protecting the integrity of the cohesion complex; also required during meiosis; relocalizes to the cytosol in response to hypoxia","termid":"PBO:0082613"}


id: GO:1905217
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 astaxanthin stimulus.","definition_xrefs":["GOC:TermGenie","PMID:22309505","GO_REF:0000071"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to lipid","termid":"GO:0033993"}],"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 astaxanthin","synonyms":[{"name":"response to (3S,3'S)-3,3'-dihydroxy-beta,beta-carotene-4,4'-dione","type":"exact"}],"termid":"GO:1905217"}


id: MONDO:0014836
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Charcot-Marie-Tooth disease in which the cause of the disease is a mutation in the NEFH gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Charcot-Marie-Tooth disease type 2","termid":"MONDO:0018993"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"Charcot-Marie-Tooth disease axonal type 2CC","secondary_identifiers":["MEDGEN:934757","OMIM:616924","DOID:0110180","UMLS:C4310790"],"synonyms":[{"name":"CMT2CC","type":"exact"},{"name":"Charcot-Marie-Tooth disease axonal type 2CC","type":"exact"},{"name":"Charcot-Marie-Tooth disease caused by mutation in NEFH","type":"exact"},{"name":"Charcot-Marie-Tooth disease, axonal, type 2CC","type":"related"},{"name":"Charcot-Marie-Tooth disease, axonal, type 2cc","type":"exact"},{"name":"Charcot-Marie-Tooth neuropathy type 2CC","type":"exact"},{"name":"Charcot-Marie-Tooth neuropathy, type 2Cc","type":"related"},{"name":"NEFH Charcot-Marie-Tooth disease","type":"exact"}],"termid":"MONDO:0014836","xrefs":{"Monarch":{"xref_id":"0014836"}}}


id: GO:0090114
data:
  {"annotated_genes":["SJAG_00072","SJAG_03558","SJAG_03907","SJAG_02539","SJAG_05345","SJAG_05344","SJAG_02349","SJAG_03153"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[74752],"is_not":false,"summary":null,"term":"GO:0090114"},{"annotations":[80201,78269,76580,78844,77379,73086,76934],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0090110"}]},"cv_name":"biological_process","definition":"The evagination of an endoplasmic reticulum membrane, resulting in formation of a COPII-coated vesicle.","definition_xrefs":["GOC:dph","GOC:tb","GOC:ascb_2009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle budding from membrane","termid":"GO:0006900"},{"relation_name":"part_of","term_name":"endoplasmic reticulum to Golgi vesicle-mediated transport","termid":"GO:0006888"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00072":null,"SJAG_02349":null,"SJAG_02539":null,"SJAG_03153":null,"SJAG_03558":null,"SJAG_03907":null,"SJAG_05344":null,"SJAG_05345":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"part_of","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0016192","GO:0006810","GO:0061024","GO:0008150"],"is_obsolete":false,"name":"COPII-coated vesicle budding","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"COPII vesicle budding","type":"related"},{"name":"ER exit","type":"narrow"},{"name":"ER vesicle budding","type":"broad"}],"termid":"GO:0090114","terms_by_termid":{"GO:0090110":null,"GO:0090114":null}}


id: MONDO:0016748
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hemangioblastoma is a rare, benign, highly vascularized tumor of the central nervous system, most often located in the cerebellum or spinal cord, presenting in adulthood and manifesting with dizziness, nausea, malaise, headache, bladder or bowel dysfunction, numbness, weakness and pain in the upper or lower extremities, and often associated with von Hippel-Lindau disease (VHL). Exceptional cases of hemangioblastoma arising outside of the central nervous system have been reported.","definition_xrefs":["Orphanet:252054"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system benign neoplasm","termid":"MONDO:0000648"},{"relation_name":"is_a","term_name":"capillary hemangioma","termid":"MONDO:0002407"},{"relation_name":"is_a","term_name":"neurovascular disorder","termid":"MONDO:0043218"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hemangioblastoma","secondary_identifiers":["NCIT:C3801","ICDO:9161/1","MESH:D018325","GARD:8232","ONCOTREE:HMBL","UMLS:C0206734","MedDRA:10018813","DOID:5241","MEDGEN:104929","ICD10CM:D33.4"],"synonyms":[{"name":"HMBL","type":"related"},{"name":"angioblastoma","type":"exact"},{"name":"capillary hemangioblastoma","type":"exact"},{"name":"hemangioblastoma","type":"exact"}],"termid":"MONDO:0016748","xrefs":{"Monarch":{"xref_id":"0016748"}}}


id: MONDO:0004745
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Persistent and usually painful erection that lasts for at least four hours in the absence of physical or psychological stimulation, which can be caused by hematologic disorders, including sickle cell disease and leukemia, spinal cord injuries, and medications.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peripheral vascular disease","termid":"MONDO:0005294"},{"relation_name":"is_a","term_name":"erectile dysfunction","termid":"MONDO:0005362"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"priapism","secondary_identifiers":["DOID:9286","MEDGEN:19462","GARD:19933","UMLS:C0033117","SCTID:6273006","ICD10CM:N48.3","ICD9:607.3","icd11.foundation:1983776037","MESH:D011317","Orphanet:140949"],"synonyms":[{"name":"low-flow priapism","type":"narrow"},{"name":"mentulagra","type":"exact"}],"termid":"MONDO:0004745","xrefs":{"Monarch":{"xref_id":"0004745"}}}


id: PBO:0064570
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"popeye domain containing 2","termid":"PBO:0064570"}


id: PBO:0079354
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tubulin alpha 1b","termid":"PBO:0079354"}


id: PBO:0004322
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3.1.3.41","termid":"PBO:0004322"}


id: PBO:0005779
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U6 snRNP-associated protein core protein (predicted)","termid":"PBO:0005779"}


id: MONDO:0010283
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Distal Xq duplications refer to chromosomal disorders resulting from involvement of the long arm of the X chromosome (Xq). Clinical manifestations vary widely depending on the gender of the patient and on the gene content of the duplicated segment. The prevalence of Xq duplications remains unknown.","definition_xrefs":["Orphanet:1762"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"partial duplication of the long arm of chromosome X","termid":"MONDO:0017010"},{"relation_name":"is_a","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"}],"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":"syndromic X-linked intellectual disability Lubs type","secondary_identifiers":["DECIPHER:45","ICD9:758.89","NCIT:C126747","MEDGEN:337496","NANDO:2200984","GARD:9781","SCTID:702816000","UMLS:C1846058","DOID:0060799","OMIM:300260","MESH:C537723"],"synonyms":[{"name":"Lubs X-linked intellectual disability syndrome","type":"exact"},{"name":"Lubs X-linked intellectual disability syndrome (formerly)","type":"related"},{"name":"Lubs X-linked mental retardation syndrome","type":"exact"},{"name":"Lubs X-linked mental retardation syndrome (formerly)","type":"related"},{"name":"MECP2 Duplication syndrome","type":"related"},{"name":"MECP2 duplication syndrome","type":"exact"},{"name":"MRXSL","type":"exact"},{"name":"X-linked intellectual disability-hypotonia-recurrent infections syndrome","type":"exact"},{"name":"XLMR syndrome, Lubs type","type":"related"},{"name":"Xq28 (MECP2) duplication","type":"exact"},{"name":"distal duplication Xq","type":"exact"},{"name":"intellectual developmental disorder, X-linked syndromic, Lubs type, X-linked recessive","type":"exact"},{"name":"intellectual disability, X-linked, Lubs type (formerly)","type":"related"},{"name":"intellectual disability, X-linked, syndromic, Lubs type","type":"exact"},{"name":"intellectual disability, X-linked, with recurrent respiratory infections","type":"exact"},{"name":"mental retardation, X-linked, Lubs type (formerly)","type":"related"},{"name":"mental retardation, X-linked, syndromic, Lubs type","type":"exact"},{"name":"mental retardation, X-linked, with recurrent respiratory infections","type":"exact"},{"name":"syndromic X-linked intellectual disability Lubs type","type":"exact"},{"name":"telomeric duplication Xq","type":"exact"},{"name":"trisomy Xq28","type":"related"}],"termid":"MONDO:0010283","xrefs":{"Monarch":{"xref_id":"0010283"}}}


id: PBO:0084384
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Low-affinity glucose transporter of the major facilitator superfamily; expression is induced by Hxk2p in the presence of glucose and repressed by Rgt1p when glucose is limiting; HXT1 has a paralog, HXT6, what arose from the whole genome duplication","termid":"PBO:0084384"}


id: FYPO:0004762
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the kinetochore is abnormal during one or both meiotic nuclear divisions.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization during meiosis","termid":"FYPO:0003549"},{"relation_name":"is_a","term_name":"abnormal protein localization to kinetochore","termid":"FYPO:0005209"},{"relation_name":"is_a","term_name":"abnormal protein localization to centromere during meiotic cell cycle","termid":"FYPO:0006529"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0000138","FYPO:0001985"],"is_obsolete":false,"name":"abnormal protein localization to kinetochore during meiosis","synonyms":[{"name":"abnormal protein localisation to kinetochore during meiosis","type":"exact"},{"name":"abnormal protein localization to kinetochore during meiotic nuclear division","type":"exact"},{"name":"abnormal protein localization to meiotic kinetochore","type":"exact"}],"termid":"FYPO:0004762"}


id: GO:1901976
data:
  {"annotated_genes":["SJAG_02169","SJAG_01679","SJAG_03353","SJAG_00883","SJAG_04259","SJAG_03681","SJAG_01297","SJAG_02451","SJAG_03327","SJAG_01837","SJAG_02336","SJAG_03126"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[92535,101405,109066,116131,105713,115643,117762,110094,113815],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902426"},{"annotations":[96010],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140499"},{"annotations":[115648],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905326"},{"annotations":[118538],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090267"},{"annotations":[103160],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905325"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cell cycle checkpoint.","definition_xrefs":["GOC:TermGenie","PMID:23028116","GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell cycle phase transition","termid":"GO:1901987"},{"relation_name":"is_a","term_name":"regulation of intracellular signal transduction","termid":"GO:1902531"},{"relation_name":"regulates","term_name":"cell cycle checkpoint signaling","termid":"GO:0000075"}],"gene_count":12,"genes_by_uniquename":{"SJAG_00883":null,"SJAG_01297":null,"SJAG_01679":null,"SJAG_01837":null,"SJAG_02169":null,"SJAG_02336":null,"SJAG_02451":null,"SJAG_03126":null,"SJAG_03327":null,"SJAG_03353":null,"SJAG_03681":null,"SJAG_04259":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0007049","GO:0023052"],"is_obsolete":false,"name":"regulation of cell cycle checkpoint","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:2001047"],"synonyms":[{"name":"regulation of G1/S checkpoint","type":"related"},{"name":"regulation of G1/S transition checkpoint","type":"related"}],"termid":"GO:1901976","terms_by_termid":{"GO:0090267":null,"GO:0140499":null,"GO:1902426":null,"GO:1905325":null,"GO:1905326":null}}


id: MONDO:0800421
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cardiomyopathy, familial hypertrophic, 4, susceptibility to","secondary_identifiers":["UMLS:C2751427","MEDGEN:414013"],"termid":"MONDO:0800421","xrefs":{"Monarch":{"xref_id":"0800421"}}}


id: GO:0045485
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the introduction of an omega-6 double bond into the fatty acid hydrocarbon chain.","definition_xrefs":["PMID:7846158"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen","termid":"GO:0016705"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"omega-6 fatty acid desaturase activity","secondary_identifiers":["Reactome:R-HSA-2046089","Reactome:R-HSA-2046092"],"termid":"GO:0045485"}


id: GO:0006732
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways involving coenzymes, any of various nonprotein organic cofactors that are required, in addition to an enzyme and a substrate, for an enzymatic reaction to proceed.","definition_xrefs":["ISBN:0198506732"],"gene_count":0,"genotype_count":0,"name":"obsolete coenzyme metabolic process (obsolete GO:0006732)","synonyms":[{"name":"coenzyme and prosthetic group metabolic process","type":"broad"},{"name":"coenzyme and prosthetic group metabolism","type":"broad"},{"name":"coenzyme metabolism","type":"exact"},{"name":"group transfer coenzyme metabolic process","type":"narrow"},{"name":"group transfer coenzyme metabolism","type":"narrow"}],"termid":"GO:0006732"}


id: FYPO:0007192
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 rapid, back-and-forth movement of the mitotic spindle pole body (SPB), and associated chromosome movement, do not occur. Normally, SPB oscillation occurs during mitotic interphase (as well as prophase) but is restricted to a small space.","definition_xrefs":["PMID:31483748","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal spindle pole body-led chromosome movement during mitotic interphase","termid":"FYPO:0005348"},{"relation_name":"is_a","term_name":"abolished cellular process","termid":"FYPO:0005449"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"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:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000138","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"abolished spindle pole body-led chromosome movement during mitotic interphase","synonyms":[{"name":"abolished mitotic SPB oscillation during mitotic interphase","type":"exact"},{"name":"abolished mitotic spindle pole body movement during mitotic interphase","type":"exact"},{"name":"abolished mitotic spindle pole body oscillation during mitotic interphase","type":"exact"},{"name":"abolished spindle pole body-led chromosome movement during interphase of mitotic cell cycle","type":"related"},{"name":"abolished spindle pole body-led chromosome movement during mitotic interphase during vegetative growth","type":"exact"},{"name":"mitotic spindle pole body oscillation abolished during mitotic interphase","type":"exact"}],"termid":"FYPO:0007192"}


id: PBO:0083421
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 uncharacterized gene YOR012W; null mutant displays increased levels of spontaneous Rad52 foci","termid":"PBO:0083421"}


id: FYPO:0001991
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a spore germinates to produce a cell that dies without completing cell division.","definition_xrefs":["PomBase:al","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable after spore germination","termid":"FYPO:0000316"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000004"}],"interesting_parent_ids":["FYPO:0000004","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"inviable after spore germination, without cell division","synonyms":[{"name":"inviable after spore germination, no cell division","type":"exact"},{"name":"inviable following spore germination, without cell division","type":"exact"},{"name":"inviable germinated spore, without cell division","type":"exact"},{"name":"lethal after spore germination, without cell division","type":"exact"}],"termid":"FYPO:0001991"}


id: GO:0006034
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways involving cuticle chitin, a linear polysaccharide consisting of beta-(1->4)-linked N-acetyl-D-glucosamine residues, found in cuticles.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete cuticle chitin metabolic process (obsolete GO:0006034)","synonyms":[{"name":"cuticle chitin metabolism","type":"exact"}],"termid":"GO:0006034"}


id: GO:0016785
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of a selenium-containing group from one compound (donor) to another (acceptor).","definition_xrefs":["GOC:jl","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity","termid":"GO:0016740"}],"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"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"selenotransferase activity","secondary_identifiers":["EC:2.9.1.-","GO:0016786"],"synonyms":[{"name":"transferase activity, transferring selenium-containing groups","type":"exact"}],"termid":"GO:0016785"}


id: MONDO:1012423
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"vitamin D-deficiency rickets, non-type I, non-type II, non-human animal","termid":"MONDO:1011962"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vitamin D-deficiency rickets, non-type I, non-type II, domestic cat","secondary_identifiers":["OMIA:001614-9685"],"termid":"MONDO:1012423","xrefs":{"Monarch":{"xref_id":"1012423"}}}


id: PBO:0077111
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translocase of inner mitochondrial membrane 17B pseudogene 1","termid":"PBO:0077111"}


id: GO:0016274
data:
  {"annotated_genes":["SJAG_00596","SJAG_02271","SJAG_03548","SJAG_02756"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[77238],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008469"},{"annotations":[81984],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019702"},{"annotations":[114524,102241],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035242"},{"annotations":[114525,102242],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035241"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + (protein)-arginine = S-adenosyl-L-homocysteine + (protein)-N-methyl-arginine.","definition_xrefs":["PMID:12351636","PMID:31284549","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein methyltransferase activity","termid":"GO:0008276"},{"relation_name":"is_a","term_name":"arginine N-methyltransferase activity","termid":"GO:0016273"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00596":null,"SJAG_02271":null,"SJAG_02756":null,"SJAG_03548":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0008276"},{"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:0016741"}],"interesting_parent_ids":["GO:0016741","GO:0140096","GO:0016740","GO:0008276","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"protein-arginine N-methyltransferase activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-5229010","Reactome:R-HSA-8879123","Reactome:R-HSA-5205798","Reactome:R-HSA-5661126","Reactome:R-HSA-191790","Reactome:R-HSA-5205824","Reactome:R-HSA-5205820","Reactome:R-HSA-5218952","Reactome:R-HSA-8934735","Reactome:R-HSA-5229203","Reactome:R-HSA-5205867","Reactome:R-HSA-5205822"],"synonyms":[{"name":"PRMT activity","type":"exact"}],"termid":"GO:0016274","terms_by_termid":{"GO:0008469":null,"GO:0019702":null,"GO:0035241":null,"GO:0035242":null}}


id: MONDO:1012577
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any neurocristopathy in cattle in which the cause of the disease is a mutation in the CHD7 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"neurocristopathy, non-human animal","termid":"MONDO:1011337"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neurocristopathy, CHD7-related, cattle","secondary_identifiers":["OMIA:002125-9913"],"termid":"MONDO:1012577","xrefs":{"Monarch":{"xref_id":"1012577"}}}


id: MONDO:0010971
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infundibulopelvic stenosis-multicystic kidney syndrome is a rare, genetic renal malformation syndrome characterized by variable degrees of malformation in the pelvicalyceal system (including unilateral or bilateral calyceal dilatation, infundibular stenosis, hypoplasia or stenosis of the renal pelvis) which lead to multicystic kidney. Clinically it exhibits abdominal, lumbar or flank pain, recurrent urinary tract infections, hypertension, proteinuria and often progresses to renal insufficiency. Calyceal dilatation and hydronephrosis are frequently seen on imaging.","definition_xrefs":["Orphanet:1849"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"infundibulopelvic stenosis-multicystic kidney syndrome","secondary_identifiers":["OMIM:600989","UMLS:C1832949","MEDGEN:318751","SCTID:725905005","MESH:C535528"],"synonyms":[{"name":"infundibulopelvic dysgenesis","type":"related"}],"termid":"MONDO:0010971","xrefs":{"Monarch":{"xref_id":"0010971"}}}


id: MONDO:0008687
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":"Woronets trait","secondary_identifiers":["OMIM:194320","MEDGEN:348570","UMLS:C1860237"],"synonyms":[{"name":"Woronets trait","type":"exact"}],"termid":"MONDO:0008687","xrefs":{"Monarch":{"xref_id":"0008687"}}}


id: MONDO:0100002
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign inflammatory colitis caused by a non-IgE-mediated immune reaction to ingested food proteins.","definition_xrefs":["PMID:17584315"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gastrointestinal allergy","termid":"MONDO:0000777"},{"relation_name":"is_a","term_name":"proctocolitis","termid":"MONDO:0024278"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0005046"],"is_obsolete":false,"name":"food protein-induced allergic proctocolitis","secondary_identifiers":["UMLS:C4750318","MEDGEN:1663071"],"synonyms":[{"name":"FPIPC","type":"exact"},{"name":"allergic proctocolitis","type":"broad"},{"name":"milk protein proctocololitis","type":"narrow"}],"termid":"MONDO:0100002","xrefs":{"Monarch":{"xref_id":"0100002"}}}


id: PATO:0000276
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A reproductive quality inhering in the young of an animal by virtue of their number.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brood quality","termid":"PATO:0001496"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"brood size","synonyms":[{"name":"litter size","type":"related"}],"termid":"PATO:0000276"}


id: GO:1903553
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of extracellular vesicular exosome assembly.","definition_xrefs":["GOC:TermGenie","PMID:24105262","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of organelle assembly","termid":"GO:1902117"},{"relation_name":"is_a","term_name":"regulation of extracellular exosome assembly","termid":"GO:1903551"},{"relation_name":"positively_regulates","term_name":"extracellular exosome assembly","termid":"GO:0071971"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"positive regulation of extracellular exosome assembly","synonyms":[{"name":"activation of extracellular vesicular exosome assembly","type":"narrow"},{"name":"positive regulation of extracellular vesicular exosome assembly","type":"related"},{"name":"up regulation of extracellular vesicular exosome assembly","type":"exact"},{"name":"up-regulation of extracellular vesicular exosome assembly","type":"exact"},{"name":"upregulation of extracellular vesicular exosome assembly","type":"exact"}],"termid":"GO:1903553"}


id: FYPO:0001443
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which transcription does not occur. All genes, or a specific subset of genes, may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased transcription during vegetative growth","termid":"FYPO:0000781"},{"relation_name":"is_a","term_name":"abolished transcription","termid":"FYPO:0002877"}],"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:0000294"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000294","FYPO:0005447","FYPO:0006551","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"abolished transcription during vegetative growth","synonyms":[{"name":"abolished transcription during mitotic cell cycle","type":"related"},{"name":"transcription abolished during vegetative growth","type":"exact"}],"termid":"FYPO:0001443"}


id: PBO:0026804
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_meiotic_recombination_double-strand_break_repair","termid":"PBO:0026804"}


id: GO:0047140
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: oxidized glutathione + CoA = reduced glutathione + CoA-glutathione.","definition_xrefs":["MetaCyc:1.8.4.3-RXN","EC:1.8.4.3"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on a sulfur group of donors, disulfide as acceptor","termid":"GO:0016671"}],"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":"glutathione-CoA-glutathione transhydrogenase activity","secondary_identifiers":["RHEA:13125"],"synonyms":[{"name":"CoA:glutathione-disulfide oxidoreductase activity","type":"related"},{"name":"coenzyme A:glutathione-disulfide oxidoreductase activity","type":"related"},{"name":"coenzyme A:oxidized-glutathione oxidoreductase activity","type":"related"},{"name":"glutathione coenzyme A-glutathione transhydrogenase activity","type":"related"},{"name":"glutathione-coenzyme A glutathione disulfide transhydrogenase activity","type":"related"},{"name":"glutathione:coenzyme A-glutathione transhydrogenase activity","type":"related"}],"termid":"GO:0047140"}


id: MONDO:0007136
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"anorectal malformation","termid":"MONDO:0019938"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hereditary anorectal anomalies","secondary_identifiers":["MEDGEN:501217","MESH:C567938","OMIM:107100","UMLS:C3495676"],"synonyms":[{"name":"anorectal anomalies","type":"related"},{"name":"genetic anorectal anomalies","type":"exact"}],"termid":"MONDO:0007136","xrefs":{"Monarch":{"xref_id":"0007136"}}}


id: PBO:0050125
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group box 1 pseudogene 35","termid":"PBO:0050125"}


id: PBO:0091006
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DUF4449 family conserved fungal protein, involved in cell-cell communication in N. crassa","termid":"PBO:0091006"}


id: GO:2000086
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of mesenchymal to epithelial transition involved in mesonephros morphogenesis.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mesenchymal to epithelial transition involved in mesonephros morphogenesis","termid":"GO:2000084"},{"relation_name":"is_a","term_name":"positive regulation of epithelial cell differentiation involved in kidney development","termid":"GO:2000698"},{"relation_name":"positively_regulates","term_name":"mesenchymal to epithelial transition involved in mesonephros morphogenesis","termid":"GO:0061261"}],"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 mesenchymal to epithelial transition involved in mesonephros morphogenesis","synonyms":[{"name":"positive regulation of mesonephric mesenchyme to epithelial transition","type":"related"}],"termid":"GO:2000086"}


id: SO:0000934
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A miRNA target site is a binding site where the molecule is a micro RNA.","definition_xrefs":["FB:cds"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide_binding_site","termid":"SO:0001655"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"miRNA_target_site","synonyms":[{"name":"miRNA target site","type":"exact"}],"termid":"SO:0000934"}


id: PBO:0067538
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 683, pseudogene","termid":"PBO:0067538"}


id: FYPO:0003485
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 biosynthesis of DNA does not occur.","definition_xrefs":["GO:0071897","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA metabolism phenotype during vegetative growth","termid":"FYPO:0001346"},{"relation_name":"is_a","term_name":"abolished cellular process","termid":"FYPO:0005449"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0001320","FYPO:0000293","FYPO:0005447"],"is_obsolete":false,"name":"abolished DNA synthesis","synonyms":[{"name":"abolished DNA biosynthesis","type":"exact"},{"name":"abolished DNA biosynthetic process","type":"exact"},{"name":"abolished DNA synthesis during mitotic cell cycle","type":"related"},{"name":"abolished DNA synthesis during vegetative growth","type":"exact"}],"termid":"FYPO:0003485"}


id: GO:0071344
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving diphosphate, the anion or salt of diphosphoric acid.","definition_xrefs":["GOC:pde"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphorus metabolic process","termid":"GO:0006793"},{"relation_name":"is_a","term_name":"oxoacid metabolic process","termid":"GO:0043436"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"diphosphate metabolic process","secondary_identifiers":["Reactome:R-HSA-71737"],"synonyms":[{"name":"pyrophosphate metabolism","type":"exact"}],"termid":"GO:0071344"}


id: PBO:0060404
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-alpha-acetyltransferase 15, NatA auxiliary subunit","termid":"PBO:0060404"}


id: GO:0103060
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: kaempferol-3-rhamnoside + UDP-L-rhamnose = kaempferol-3-rhamnoside-7-rhamnoside + UDP.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete kaempferol 3-rhamnoside 7-O-rhamnosyltransferase activity (obsolete GO:0103060)","termid":"GO:0103060"}


id: PBO:0079540
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin like modifier activating enzyme 1","termid":"PBO:0079540"}


id: MONDO:0013742
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete familial mesial temporal lobe epilepsy with febrile seizures (obsolete MONDO:0013742)","secondary_identifiers":["Orphanet:165805"],"synonyms":[{"name":"FEB11","type":"related"},{"name":"febrile seizures, familial, 11","type":"related"},{"name":"febrile seizures, familial, type 11","type":"exact"}],"termid":"MONDO:0013742","xrefs":{"Monarch":{"xref_id":"0013742"}}}


id: PBO:0081806
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 735","termid":"PBO:0081806"}


id: PBO:0046267
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER membrane protein complex subunit 6","termid":"PBO:0046267"}


id: MOD:00534
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Post-translational","definition_xrefs":["PubMed:9448752","Unimod:176"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reagent derivatized residue","termid":"MOD:00848"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Michael addition of BHT quinone methide to cysteine and lysine","synonyms":[{"name":"BHT","type":"related"},{"name":"Michael addition of BHT quinone methide to Cysteine and Lysine","type":"related"}],"termid":"MOD:00534"}


id: PBO:0074802
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 13G","termid":"PBO:0074802"}


id: PR:O13713
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- nab2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O13713"],"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":"nuclear polyadenylated RNA-binding protein nab2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC14C4.06c","synonyms":[{"name":"Spom972h-nab2","type":"exact"}],"termid":"PR:O13713"}


id: PBO:0028398
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_35S_rRNA_precursor_level","termid":"PBO:0028398"}


id: MONDO:0800064
data:
  {"annotated_genes":["SJAG_00120","SJAG_00288","SJAG_02349","SJAG_00516","SJAG_04956","SJAG_01005","SJAG_04934","SJAG_02413"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88891],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0018163"},{"annotations":[86946],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013051"},{"annotations":[88497],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007204"},{"annotations":[87225],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014573"},{"annotations":[88293],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012592"},{"annotations":[88055],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009805"},{"annotations":[87925],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013889"},{"annotations":[87952],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009910"},{"annotations":[87386],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010208"}]},"cv_name":"mondo","definition":"A skeletal dysplasia characterized by osteogenesis imperfecta and decreased bone density.","definition_xrefs":["PMID:31633310","HP:0004349"],"direct_ancestors":[{"relation_name":"is_a","term_name":"osteogenesis imperfecta","termid":"MONDO:0019019"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00120":null,"SJAG_00288":null,"SJAG_00516":null,"SJAG_01005":null,"SJAG_02349":null,"SJAG_02413":null,"SJAG_04934":null,"SJAG_04956":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"osteogenesis imperfecta and a reduction of bone mineral density.","references_by_uniquename":{"PB_REF:0000006":null},"termid":"MONDO:0800064","terms_by_termid":{"MONDO:0007204":null,"MONDO:0009805":null,"MONDO:0009910":null,"MONDO:0010208":null,"MONDO:0012592":null,"MONDO:0013051":null,"MONDO:0013889":null,"MONDO:0014573":null,"MONDO:0018163":null},"xrefs":{"Monarch":{"xref_id":"0800064"}}}


id: PBO:0018108
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Golgi to ER protein (predicted)","termid":"PBO:0018108"}


id: PBO:0069589
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 863, pseudogene","termid":"PBO:0069589"}


id: PR:O94639
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- zrt1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94639"],"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":"zinc-regulated transporter 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC16D10.06","synonyms":[{"name":"Spom972h-zrt1","type":"exact"},{"name":"high-affinity zinc transport protein zrt1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94639"}


id: GO:0016560
data:
  {"annotated_genes":["SJAG_00891","SJAG_02693","SJAG_00702"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[63446,72420,75452],"is_not":false,"summary":null,"term":"GO:0016560"}]},"cv_name":"biological_process","definition":"The process in which a complex formed of a peroxisome targeting sequence (PTS) receptor bound to a PTS-bearing protein docks with translocation machinery in the peroxisomal membrane.","definition_xrefs":["PMID:14754507","PMID:11687502","PMID:11988772"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular protein localization","termid":"GO:0008104"},{"relation_name":"part_of","term_name":"protein import into peroxisome matrix","termid":"GO:0016558"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00702":null,"SJAG_00891":null,"SJAG_02693":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0055085"},{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007031"}],"interesting_parent_ids":["GO:0055085","GO:0006810","GO:0007031","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"protein import into peroxisome matrix, docking","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null},"synonyms":[{"name":"peroxisome matrix protein import, docking","type":"exact"},{"name":"peroxisome receptor docking","type":"related"},{"name":"protein docking during peroxisome matrix protein import","type":"exact"},{"name":"protein docking during protein import into peroxisome matrix","type":"exact"},{"name":"protein docking during protein transport into peroxisome matrix","type":"exact"},{"name":"protein transport into peroxisome matrix, docking","type":"exact"}],"termid":"GO:0016560","terms_by_termid":{"GO:0016560":null}}


id: GO:0032263
data:
  {"annotated_genes":["SJAG_04634","SJAG_06634"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[77381,103014],"is_not":false,"summary":null,"term":"GO:0032263"}]},"cv_name":"biological_process","definition":"Any process which produces guanosine monophosphate from derivatives of it, without de novo synthesis.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"GMP biosynthetic process","termid":"GO:0006177"},{"relation_name":"is_a","term_name":"purine ribonucleotide salvage","termid":"GO:0106380"}],"gene_count":2,"genes_by_uniquename":{"SJAG_04634":null,"SJAG_06634":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"GMP salvage","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0032263","terms_by_termid":{"GO:0032263":null}}


id: SO:0002208
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An RNA that is transcribed from a long terminal repeat.","definition_xrefs":["PMID:24256266","PomBase:mh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcript","termid":"SO:0000673"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long_terminal_repeat_transcript","synonyms":[{"name":"LTR transcript","type":"exact"},{"name":"long terminal repeat transcript","type":"exact"}],"termid":"SO:0002208"}


id: PBO:0002504
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER to Golgi tethering factor Uso1 (predicted)","termid":"PBO:0002504"}


id: MONDO:0002968
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cystic lesion containing lymph. It usually results from injury, gynecologic surgery, or urologic surgery.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymphatic system disorder","termid":"MONDO:0005833"}],"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":"lymphocele","secondary_identifiers":["DOID:4347","ICD9:457.8","MEDGEN:7414","MESH:D008210","icd11.foundation:1806199285","SCTID:234110002","UMLS:C0024248"],"synonyms":[{"name":"lymph cyst","type":"exact"}],"termid":"MONDO:0002968","xrefs":{"Monarch":{"xref_id":"0002968"}}}


id: GO:0050714
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the controlled release of a protein from a cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein secretion","termid":"GO:0050708"},{"relation_name":"is_a","term_name":"positive regulation of protein transport","termid":"GO:0051222"},{"relation_name":"is_a","term_name":"positive regulation of secretion by cell","termid":"GO:1903532"},{"relation_name":"positively_regulates","term_name":"protein secretion","termid":"GO:0009306"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"positive regulation of protein secretion","synonyms":[{"name":"activation of protein secretion","type":"narrow"},{"name":"stimulation of protein secretion","type":"narrow"},{"name":"up regulation of protein secretion","type":"exact"},{"name":"up-regulation of protein secretion","type":"exact"},{"name":"upregulation of protein secretion","type":"exact"}],"termid":"GO:0050714"}


id: MONDO:0022697
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A subtype of cerebral palsy characterized by involuntary, purposeless writhing movements which affect the hands, feet, arms, and legs; the face and tongue may be affected as well, leading to involuntary grimacing, drooling, dysarthria and difficulty eating.","definition_xrefs":["NCIT:C97169"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerebral palsy","termid":"MONDO:0006497"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"athetoid cerebral palsy","secondary_identifiers":["MEDGEN:82853","SCTID:75019001","UMLS:C0270742","DOID:0050672","SCTID:230780007","ICD10CM:G80.3"],"synonyms":[{"name":"ADCP","type":"related"},{"name":"athetoid cerebral palsy","type":"exact"},{"name":"athetoid dyskinetic cerebral palsy","type":"exact"},{"name":"cerebral palsy dyskinetic","type":"related"},{"name":"dyskinetic cerebral palsy","type":"exact"}],"termid":"MONDO:0022697","xrefs":{"Monarch":{"xref_id":"0022697"}}}


id: PBO:0108672
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MARK/PAR-1 kinase Kin1","termid":"PBO:0108672"}


id: SO:0000502
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region of sequence that is transcribed. This region may cover the transcript of a gene, it may emcompas the sequence covered by all of the transcripts of a alternately spliced gene, or it may cover the region transcribed by a polycistronic transcript. A gene may have 1 or more transcribed regions and a transcribed_region may belong to one or more genes.","definition_xrefs":["SO:ke"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:0000502 transcribed_region (obsolete SO:0000502)","termid":"SO:0000502"}


id: PR:O74907
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A BRCA2 and CDKN1A-interacting protein that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO04180","PANTHER:PTHR13261:SF0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein bcp1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC613.08","secondary_identifiers":["UniProtKB:O74907"],"synonyms":[{"name":"Spom972h-BCCIP","type":"exact"}],"termid":"PR:O74907"}


id: MONDO:0044219
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. The Duffy blood group system, which consists of 4 alleles, 5 phenotypes, and 5 antigens, is important in clinical medicine because of transfusion incompatibilities and hemolytic disease of the newborn. Duffy antigens are located on ACKR1 (OMIM:613665), or DARC, an acidic glycoprotein found on erythrocytes and other cells throughout the body. The 2 principal antigens, Fy(a) and Fy(b), are produced by the FYA and FYB codominant alleles (see {613665.0001}). Four phenotypes are defined by the corresponding antibodies, anti-Fy(a) and anti-Fy(b): Fy(a+b-), Fy(a-b+), Fy(a+b+), and Fy(a-b-). Fy(a-b-), or Duffy null, is the major phenotype in African and American blacks and is characterized by the presence of Fy(b) on nonerythroid cells, but an absence of Fy(b) on erythrocytes. The Fy(a-b-) phenotype is associated with complete resistance to infection by the malarial parasite Plasmodium vivax (see OMIM:611162). Individuals with the Fy(a-b-) phenotype have the FYB-erythroid silent (FYB-ES) allele with a mutation in the DARC promoter ({613665.0002}). A fifth phenotype, Fy(bwk), or Fy(x), is characterized by weak Fy(b) expression on erythrocytes due to a reduced amount of protein. Individuals with the Fy(bwk) phenotype have the FYB-weak (FYB-WK) allele, also called the FYX allele, with a missense mutation in DARC ({613665.0003}). Other Duffy antigens include Fy3, Fy4, Fy5, and Fy6 (reviews by {21:Pogo and Chaudhuri (2000)}, {10:Langhi and Bordin (2006)}, and {14:Meny (2010)}).","definition_xrefs":["OMIM:110700"],"gene_count":0,"genotype_count":0,"name":"obsolete blood group, duffy system (obsolete MONDO:0044219)","synonyms":[{"name":"Duffy blood Group system","type":"related"},{"name":"FY","type":"related"},{"name":"Plasmodium vivax, resistance to","type":"related"},{"name":"blood group, DUFFY system","type":"related"},{"name":"blood group, Duffy system","type":"exact"}],"termid":"MONDO:0044219","xrefs":{"Monarch":{"xref_id":"0044219"}}}


id: FYPO:0001823
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to chlorpromazine. Cells stop growing (and may die) at a concentration of chlorpromazine that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000003","FYPO:0002683","FYPO:0000139"],"is_obsolete":false,"name":"sensitive to chlorpromazine","synonyms":[{"name":"hypersensitive to chlorpromazine","type":"exact"},{"name":"sensitive to chlorpromazine during mitotic cell cycle","type":"related"},{"name":"sensitive to chlorpromazine during vegetative growth","type":"exact"}],"termid":"FYPO:0001823"}


id: PBO:0052384
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kinesin family member 25","termid":"PBO:0052384"}


id: PBO:0059657
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO1 pseudogene 23","termid":"PBO:0059657"}


id: MOD:02023
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a residue amino group with a cervonoylamino group.","direct_ancestors":[{"relation_name":"is_a","term_name":"N-acylated residue","termid":"MOD:00670"},{"relation_name":"is_a","term_name":"cervonoylated residue","termid":"MOD:02024"}],"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-cervonoylated residue","termid":"MOD:02023"}


id: GO:0003036
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which information about the levels of hydrogen ions are received and are converted to a molecular signal by chemoreceptors in an aortic body.","definition_xrefs":["GOC:mtg_cardio"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detection of pH by chemoreceptor signaling","termid":"GO:0003022"},{"relation_name":"part_of","term_name":"detection of hypoxic conditions in blood by aortic body chemoreceptor signaling","termid":"GO:0003033"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"detection of pH by aortic body chemoreceptor signaling","synonyms":[{"name":"detection of pH by aortic body chemoreceptor signalling","type":"exact"}],"termid":"GO:0003036"}


id: PBO:0045640
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"double homeobox 4 like 52 (pseudogene)","termid":"PBO:0045640"}


id: MONDO:0005012
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A primary melanoma arising from atypical melanocytes in the skin. Precursor lesions include acquired and congenital melanocytic nevi, and dysplastic nevi. Several histologic variants have been recognized, including superficial spreading melanoma, acral lentiginous melanoma, nodular melanoma, and lentigo maligna melanoma.","definition_xrefs":["NCIT:C3510"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skin cancer","termid":"MONDO:0002898"},{"relation_name":"is_a","term_name":"melanoma","termid":"MONDO:0005105"},{"relation_name":"is_a","term_name":"melanocytic skin neoplasm","termid":"MONDO:0021583"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0004992"],"is_obsolete":false,"name":"cutaneous melanoma","secondary_identifiers":["UMLS:C0151779","ICD9:172.0","ICD10CM:C43","MEDGEN:57486","ICD9:172","EFO:0000389","ICD9:172.4","ICD9:172.5","ICD9:172.2","ICD9:172.3","ICD9:172.8","DOID:8923","ONCOTREE:SKCM","SCTID:93655004","HP:0012056","ICD9:172.9"],"synonyms":[{"name":"cutaneous (skin) melanoma","type":"exact"},{"name":"cutaneous melanoma","type":"exact"},{"name":"cutaneous melanoma (disease)","type":"exact"},{"name":"malignant cutaneous melanoma","type":"exact"},{"name":"malignant ear melanoma","type":"exact"},{"name":"malignant lip melanoma","type":"exact"},{"name":"malignant lower limb melanoma","type":"exact"},{"name":"malignant melanoma (of skin), stage unspecified","type":"exact"},{"name":"malignant melanoma of ear and/or external auricular canal","type":"exact"},{"name":"malignant melanoma of skin","type":"exact"},{"name":"malignant melanoma of skin of lower limb","type":"exact"},{"name":"malignant melanoma of skin of trunk except scrotum","type":"exact"},{"name":"malignant melanoma of skin of upper limb","type":"exact"},{"name":"malignant melanoma of skin stage unspecified","type":"exact"},{"name":"malignant neck melanoma","type":"exact"},{"name":"malignant scalp melanoma","type":"exact"},{"name":"malignant trunk melanoma","type":"exact"},{"name":"malignant upper limb melanoma","type":"exact"},{"name":"melanoma (disease) of zone of skin","type":"exact"},{"name":"melanoma of skin","type":"exact"},{"name":"melanoma of the skin","type":"exact"},{"name":"skin melanoma","type":"exact"},{"name":"skin, melanoma","type":"exact"},{"name":"zone of skin melanoma","type":"exact"},{"name":"zone of skin melanoma (disease)","type":"exact"}],"termid":"MONDO:0005012","xrefs":{"Monarch":{"xref_id":"0005012"}}}


id: PBO:0073853
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 9 member 3 pseudogene 3","termid":"PBO:0073853"}


id: MOD:01416
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-isoleucine residue to a dihydroxylated isoleucine.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dihydroxylated residue","termid":"MOD:00428"},{"relation_name":"is_a","term_name":"hydroxylated isoleucine","termid":"MOD:01414"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dihydroxylated isoleucine","synonyms":[{"name":"Hy2Ile","type":"exact"}],"termid":"MOD:01416"}


id: PBO:0040999
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bolA family member 3 pseudogene 4","termid":"PBO:0040999"}


id: PATO:0001493
data:
  {"annotation_feature_type":"gene","cv_name":"quality","direct_ancestors":[{"relation_name":"is_a","term_name":"growth rate","termid":"PATO:0001492"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypertrophic growth","termid":"PATO:0001493"}


id: PR:O94488
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mto1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94488"],"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":"microtubule organizer protein 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC417.07c","synonyms":[{"name":"Spom972h-mto1","type":"exact"},{"name":"morphology defective protein 20 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94488"}


id: FYPO:0000695
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of DNA-1,N6-ethenoadenine N-glycosylase activity is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal DNA-1,N6-ethenoadenine N-glycosylase activity","termid":"FYPO:0000692"},{"relation_name":"is_a","term_name":"increased DNA N-glycosylase activity","termid":"FYPO:0008217"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000654","FYPO:0000661","FYPO:0000707","FYPO:0000652","FYPO:0001985"],"is_obsolete":false,"name":"increased DNA-1,N6-ethenoadenine N-glycosylase activity","termid":"FYPO:0000695"}


id: FYPO:0003342
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which a cell contains more than one nucleus, is longer than normal, and has a greater length:diameter ratio than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multinucleate","termid":"FYPO:0003341"},{"relation_name":"is_a","term_name":"increased cell length","termid":"FYPO:0006633"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0000005"],"is_obsolete":false,"name":"elongated multinucleate cell","synonyms":[{"name":"long multinucleate cell","type":"exact"}],"termid":"FYPO:0003342"}


id: MONDO:0003455
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-invasive, papillary epithelial neoplasm that arises from the epithelium of the intrahepatic or extrahepatic bile ducts.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign digestive system neoplasm","termid":"MONDO:0000385"},{"relation_name":"is_a","term_name":"benign endocrine neoplasm","termid":"MONDO:0000627"},{"relation_name":"is_a","term_name":"intraductal papilloma","termid":"MONDO:0002060"},{"relation_name":"is_a","term_name":"bile duct neoplasm","termid":"MONDO:0021662"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0002515"],"is_obsolete":false,"name":"bile duct papillary neoplasm","secondary_identifiers":["DOID:5468","MEDGEN:360303","UMLS:C1879344","NCIT:C6881","ICDO:8503/0"],"synonyms":[{"name":"IPN","type":"exact"},{"name":"bile duct papillary epithelial neoplasm","type":"exact"},{"name":"bile duct papillary neoplasm","type":"exact"},{"name":"bile duct papillomatosis","type":"exact"},{"name":"biliary papillomatosis","type":"exact"},{"name":"intraductal papillary neoplasm","type":"exact"}],"termid":"MONDO:0003455","xrefs":{"Monarch":{"xref_id":"0003455"}}}


id: MOD:01649
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively removes or replaces an L-tyrosine.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-tyrosine residue","termid":"MOD:00919"},{"relation_name":"is_a","term_name":"natural, standard, encoded residue removal","termid":"MOD:01651"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-tyrosine removal","termid":"MOD:01649"}


id: GO:0033311
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways leading to the formation of chlorophyll a, via the intermediate phytyl diphosphate.","definition_xrefs":["MetaCyc:PWY-5086","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chlorophyll a biosynthetic process","termid":"GO:0033305"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0033013"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0033013","GO:0008150"],"is_obsolete":false,"name":"chlorophyll a biosynthetic process via phytyl diphosphate","synonyms":[{"name":"chlorophyll a anabolism via phytyl diphosphate","type":"exact"},{"name":"chlorophyll a biosynthesis via phytyl diphosphate","type":"exact"},{"name":"chlorophyll a biosynthetic process via phytyl-PP","type":"exact"},{"name":"chlorophyll a formation via phytyl chlorophyll a formation via phytyl-PP","type":"exact"},{"name":"chlorophyll a synthesis via phytyl diphosphate","type":"exact"}],"termid":"GO:0033311"}


id: PATO:0001782
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An intensity which is relatively high.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"increased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"intensity","termid":"PATO:0000049"},{"relation_name":"is_a","term_name":"increased quality","termid":"PATO:0002300"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased intensity","synonyms":[{"name":"high intensity","type":"exact"}],"termid":"PATO:0001782"}


id: MOD:02067
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that contains an L-cysteine residue coordinated to one or more metal atoms or metal clusters.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"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":"metal or metal cluster coordinated L-cysteine residue","termid":"MOD:02067"}


id: PBO:0059797
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CYB pseudogene 23","termid":"PBO:0059797"}


id: MONDO:1010508
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cerebral amyloid angiopathy that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerebral amyloid angiopathy, non-human animal","termid":"MONDO:1010028"},{"relation_name":"is_a","term_name":"amyloidosis, dog","termid":"MONDO:1011467"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cerebral amyloid angiopathy, dog","secondary_identifiers":["OMIA:002138-9615"],"termid":"MONDO:1010508","xrefs":{"Monarch":{"xref_id":"1010508"}}}


id: MONDO:0008329
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Renal pseudohypoaldosteronism type 1 (renal PHA1) is a mild form of primary mineralocorticoid resistance restricted to the kidney.","definition_xrefs":["Orphanet:171871"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pseudohypoaldosteronism type 1","termid":"MONDO:0019161"}],"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":"autosomal dominant pseudohypoaldosteronism type 1","secondary_identifiers":["MEDGEN:260623","DOID:0060855","NCIT:C126810","OMIM:177735","GARD:9145","UMLS:C1449842"],"synonyms":[{"name":"PHA I, autosomal dominant","type":"related"},{"name":"PHA1A","type":"exact"},{"name":"autosomal dominant PHA 1","type":"exact"},{"name":"autosomal dominant pseudohypoaldosteronism type 1","type":"exact"},{"name":"pseudohypoaldosteronism type 1 autosomal dominant","type":"related"},{"name":"pseudohypoaldosteronism type 1, dominant","type":"related"},{"name":"pseudohypoaldosteronism type i, autosomal dominant","type":"exact"},{"name":"pseudohypoaldosteronism, type I, autosomal dominant","type":"related"},{"name":"renal PHA1","type":"related"},{"name":"renal pseudohypoaldosteronism type 1","type":"related"}],"termid":"MONDO:0008329","xrefs":{"Monarch":{"xref_id":"0008329"}}}


id: GO:0010476
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals generated as a consequence of gibberellin stimulus.","definition_xrefs":["PMID:17521411"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hormone-mediated signaling pathway","termid":"GO:0009755"},{"relation_name":"part_of","term_name":"cellular response to gibberellin stimulus","termid":"GO:0071370"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"gibberellin mediated signaling pathway","synonyms":[{"name":"gibberellin-mediated signalling","type":"exact"}],"termid":"GO:0010476"}


id: GO:0071052
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of an alpha9-beta1 integrin complex bound to the transmembrane metallopeptidase ADAM1.","definition_xrefs":["PMID:11882657"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0032991","GO:0005886","GO:0005575"],"is_obsolete":false,"name":"alpha9-beta1 integrin-ADAM1 complex","synonyms":[{"name":"ITGA9-ITGB1-ADAM1 complex","type":"narrow"}],"termid":"GO:0071052"}


id: MONDO:0008672
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Watson syndrome is believed to be a variant of neurofibromatosis type 1. The symptoms of this condition are pulmonary valvular stenosis, cafe-au-lait spots and short stature. IQTest scores for individuals with Watson syndromecan rangebetween 60-100.Many people with this condition also have a larger than average head size (macrocephaly) and Lisch nodules. While mutations in the NF1 gene have been found in families with Watson syndrome, the exactcause of this condition is unknown. The conditionis inherited in an autosomal dominant pattern. Treatment aims at managing the specific symptoms of an individual.","direct_ancestors":[{"relation_name":"is_a","term_name":"neurofibromatosis-Noonan syndrome","termid":"MONDO:0011035"}],"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":"Watson syndrome","secondary_identifiers":["icd11.foundation:1674178232","OMIM:193520","DOID:0070483","ICD9:709.8","Orphanet:3444","UMLS:C0553586","GARD:5540","MEDGEN:107817","SCTID:403820003"],"synonyms":[{"name":"WTSN","type":"related"},{"name":"Watson syndrome","type":"exact"},{"name":"cafe-Au-lait Spots with pulmonic stenosis","type":"related"},{"name":"pulmonic stenosis with cafe-Au-lait Spots","type":"related"}],"termid":"MONDO:0008672","xrefs":{"Monarch":{"xref_id":"0008672"}}}


id: PBO:0044233
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cullin 2","termid":"PBO:0044233"}


id: GO:0061158
data:
  {"annotated_genes":["SJAG_04825"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[120194],"is_not":false,"summary":null,"term":"GO:0061158"}]},"cv_name":"biological_process","definition":"An mRNA destabilization process in which one or more RNA-binding proteins associate with the 3'-untranslated region (UTR) of an mRNA.","definition_xrefs":["GOC:jh","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mRNA destabilization","termid":"GO:0061157"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04825":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0016071"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0016071"},{"rel_name":"negatively_regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0016071","GO:0010467"],"is_obsolete":false,"name":"3'-UTR-mediated mRNA destabilization","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0061158","terms_by_termid":{"GO:0061158":null}}


id: PBO:0089215
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription elongation regulator, PHD finger Bye1","termid":"PBO:0089215"}


id: GO:0045138
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structure of the adult male tail tip is generated and organized. In some species of rhabitid nematodes, the male tail tip undergoes a morphological change such that the most posterior hypodermal cells in the tail (hyp8-11 in C. elegans) fuse and retract anteriorly, changing the shape of the tail from a pointed, tapered cone, or spike, to a rounded, blunt dome.","definition_xrefs":["PMID:21408209","PMID:16806150","PMID:7409314","GOC:kmv","PMID:18050419"],"direct_ancestors":[{"relation_name":"is_a","term_name":"male anatomical structure morphogenesis","termid":"GO:0090598"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"nematode male tail tip morphogenesis","synonyms":[{"name":"male tail morphogenesis","type":"broad"},{"name":"male tail tip morphogenesis","type":"related"},{"name":"tail tip morphogenesis","type":"related"}],"termid":"GO:0045138"}


id: GO:0043388
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the frequency, rate or extent of DNA binding. DNA binding is any process in which a gene product interacts selectively with DNA (deoxyribonucleic acid).","definition_xrefs":["GOC:dph","GOC:tb","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of binding","termid":"GO:0051099"},{"relation_name":"is_a","term_name":"regulation of DNA binding","termid":"GO:0051101"}],"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 DNA binding","synonyms":[{"name":"activation of DNA binding","type":"narrow"},{"name":"stimulation of DNA binding","type":"narrow"},{"name":"up regulation of DNA binding","type":"exact"},{"name":"up-regulation of DNA binding","type":"exact"},{"name":"upregulation of DNA binding","type":"exact"}],"termid":"GO:0043388"}


id: PBO:0091128
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schizosaccharomyces specific microprotein Smp3","termid":"PBO:0091128"}


id: GO:0048082
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of establishment of the adult pattern of pigmentation in the cuticle of an organism.","definition_xrefs":["GOC:jid","GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cuticle pigmentation","termid":"GO:0048079"},{"relation_name":"regulates","term_name":"adult chitin-containing cuticle pigmentation","termid":"GO:0048085"}],"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 adult chitin-containing cuticle pigmentation","termid":"GO:0048082"}


id: PBO:0048496
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"guanine deaminase","termid":"PBO:0048496"}


id: PBO:0049973
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HIG1 hypoxia inducible domain family member 1B","termid":"PBO:0049973"}


id: GO:0044219
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A fine cytoplasmic channel, found in all higher plants, that connects the cytoplasm of one host cell to that of an adjacent host cell.","definition_xrefs":["GOC:rph","PMID:16903353"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host cell junction","termid":"GO:0044156"}],"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 plasmodesma","termid":"GO:0044219"}


id: PBO:0069403
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 663, pseudogene","termid":"PBO:0069403"}


id: PBO:0053430
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 375","termid":"PBO:0053430"}


id: PBO:0048921
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"golgin A8 family member R","termid":"PBO:0048921"}


id: PBO:0073582
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SH3KBP1 binding protein 1","termid":"PBO:0073582"}


id: GO:2000312
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of kainate selective glutamate receptor activity.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of neurotransmitter receptor activity","termid":"GO:0099601"},{"relation_name":"is_a","term_name":"regulation of potassium ion transmembrane transporter activity","termid":"GO:1901016"},{"relation_name":"is_a","term_name":"regulation of sodium ion transmembrane transporter activity","termid":"GO:2000649"},{"relation_name":"is_a","term_name":"regulation of cation channel activity","termid":"GO:2001257"}],"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"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0006810","GO:0055085","GO:0023052","GO:0008150"],"is_obsolete":false,"name":"regulation of kainate selective glutamate receptor activity","termid":"GO:2000312"}


id: PBO:0061655
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear FMR1 interacting protein 2","termid":"PBO:0061655"}


id: GO:0140484
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of 5-aminolevulinic acid from outside of a cell, across the plasma membrane and into the cytosol.","definition_xrefs":["PMID:31989647"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic cation transport","termid":"GO:0015695"},{"relation_name":"is_a","term_name":"monocarboxylic acid transport","termid":"GO:0015718"},{"relation_name":"is_a","term_name":"nitrogen compound transport","termid":"GO:0071705"},{"relation_name":"is_a","term_name":"amino acid import across plasma membrane","termid":"GO:0089718"},{"relation_name":"is_a","term_name":"carboxylic acid transmembrane transport","termid":"GO:1905039"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055085"},{"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:0055085","GO:0008150","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"5-aminolevulinic acid import across plasma membrane","termid":"GO:0140484"}


id: PATO:0000886
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000886 absolute litter size value (obsolete PATO:0000886)","termid":"PATO:0000886"}


id: MONDO:0012297
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, complex type of hereditary spastic paraplegia characterized by early-onset progressive spastic paraplegia presenting in infancy, associated with optic atrophy, fixation nystagmus, polyneuropathy occurring in late childhood/early adolescence leading to severe motor disability and progressive joint contractures and scoliosis. SPOAN syndrome is caused by mutations in the KLC2 gene (11q13.1), encoding kinesin light chain 2.","definition_xrefs":["Orphanet:320406"],"direct_ancestors":[{"relation_name":"is_a","term_name":"complex hereditary spastic paraplegia","termid":"MONDO:0015150"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"spastic paraplegia, optic atropy, and neuropathy","secondary_identifiers":["MEDGEN:324411","MESH:C563702","GARD:17479","OMIM:609541","UMLS:C1836010","DOID:0060491"],"synonyms":[{"name":"SPOAN","type":"exact"},{"name":"SPOAN syndrome","type":"exact"},{"name":"spastic paraplegia, optic atropy, and neuropathy syndrome","type":"exact"},{"name":"spastic paraplegia-optic atrophy-neuropathy syndrome","type":"exact"}],"termid":"MONDO:0012297","xrefs":{"Monarch":{"xref_id":"0012297"}}}


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:0001985"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0000652","FYPO:0001985","FYPO:0000707","FYPO:0000654"],"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:1902546
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of DNA N-glycosylase activity.","definition_xrefs":["GOC:TermGenie","GOC:rph","PMID:15518571"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of DNA N-glycosylase activity (obsolete GO:1902546)","synonyms":[{"name":"activation of DNA N-glycosylase activity","type":"narrow"},{"name":"activation of DNA glycosylase activity","type":"narrow"},{"name":"activation of endonuclease VIII activity","type":"related"},{"name":"positive regulation of DNA glycosylase activity","type":"exact"},{"name":"positive regulation of endonuclease VIII activity","type":"related"},{"name":"up regulation of DNA N-glycosylase activity","type":"exact"},{"name":"up regulation of DNA glycosylase activity","type":"exact"},{"name":"up regulation of endonuclease VIII activity","type":"related"},{"name":"up-regulation of DNA N-glycosylase activity","type":"exact"},{"name":"up-regulation of DNA glycosylase activity","type":"exact"},{"name":"up-regulation of endonuclease VIII activity","type":"related"},{"name":"upregulation of DNA N-glycosylase activity","type":"exact"},{"name":"upregulation of DNA glycosylase activity","type":"exact"},{"name":"upregulation of endonuclease VIII activity","type":"related"}],"termid":"GO:1902546"}


id: GO:0000025
data:
  {"annotated_genes":["SJAG_03824","SJAG_02131"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[103418,103419],"is_not":false,"summary":null,"term":"GO:0000025"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of the disaccharide maltose (4-O-alpha-D-glucopyranosyl-D-glucopyranose).","definition_xrefs":["ISBN:0198506732","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"maltose metabolic process","termid":"GO:0000023"},{"relation_name":"is_a","term_name":"disaccharide catabolic process","termid":"GO:0046352"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02131":null,"SJAG_03824":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"maltose catabolic process","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:MALTOSECAT-PWY"],"synonyms":[{"name":"malt sugar catabolic process","type":"exact"},{"name":"malt sugar catabolism","type":"exact"},{"name":"maltose breakdown","type":"exact"},{"name":"maltose degradation","type":"exact"},{"name":"maltose hydrolysis","type":"narrow"}],"termid":"GO:0000025","terms_by_termid":{"GO:0000025":null}}


id: PBO:0080195
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VENT homeobox pseudogene 3","termid":"PBO:0080195"}


id: PBO:0074711
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 74C-1","termid":"PBO:0074711"}


id: FYPO:0003331
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of a protein kinase activity is decreased during interphase of the mitotic cell cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein kinase activity","termid":"FYPO:0001382"}],"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"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000661"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0000654","FYPO:0000661","FYPO:0000652","FYPO:0001985"],"is_obsolete":false,"name":"decreased protein kinase activity during mitotic interphase","synonyms":[{"name":"reduced protein kinase activity during mitotic interphase","type":"exact"}],"termid":"FYPO:0003331"}


id: GO:0102413
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 6-O-methyl-N-deacetylisoipecoside + H2O = 6-O-methyl-N-deacetylisoipecoside aglycon + D-glucose.","definition_xrefs":["RHEA:78891"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, hydrolyzing O-glycosyl compounds","termid":"GO:0004553"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016798","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"6-O-methyl-deacetylisoipecoside beta-glucosidase activity","secondary_identifiers":["MetaCyc:RXN-13791"],"termid":"GO:0102413"}


id: PBO:0090672
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA specific adenosine-37 deaminase Tad1","termid":"PBO:0090672"}


id: PBO:0049589
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H3 clustered histone 7","termid":"PBO:0049589"}


id: PBO:0046394
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"erythrocyte membrane protein band 4.1 like 1","termid":"PBO:0046394"}


id: PBO:0077222
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane BAX inhibitor motif containing 6","termid":"PBO:0077222"}


id: PBO:0062394
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 7 subfamily E member 15 pseudogene","termid":"PBO:0062394"}


id: PBO:0087969
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transverse filament protein of the synaptonemal complex; required for normal levels of meiotic recombination and pairing between homologous chromosome during meiosis; required for meiotic recombination between non-allelc sites; potential Cdc28p substrate","termid":"PBO:0087969"}


id: PBO:0119645
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribonuclease MRP subunit p64","termid":"PBO:0119645"}


id: _global:has_part_structure_that_is_capable_of
data:
  {"annotation_feature_type":"gene","cv_name":"external","definition":"s 'has part structure that is capable of' p if and only if there exists some part x such that s 'has part' x and x 'capable of' p","direct_ancestors":[{"relation_name":"is_a","term_name":"causal_relation_between_material_entity_and_a_process","termid":"_global:causal_relation_between_material_entity_and_a_process"},{"relation_name":"is_a","term_name":"functionally_related_to","termid":"_global:functionally_related_to"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_part_structure_that_is_capable_of","secondary_identifiers":["RO:0002584"],"termid":"_global:has_part_structure_that_is_capable_of"}


id: PBO:0054747
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 2156","termid":"PBO:0054747"}


id: GO:0030616
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. A TGF-beta cytoplasmic mediator that forms a complex with a phosphorylated pathway-specific mediator. The heterocomplex translocates to the nucleus to regulate transcription.","definition_xrefs":["GOC:hjd"],"gene_count":0,"genotype_count":0,"name":"obsolete transforming growth factor beta receptor, common-partner cytoplasmic mediator activity (obsolete GO:0030616)","synonyms":[{"name":"TGF-beta receptor, common-partner cytoplasmic mediator activity","type":"exact"},{"name":"TGFbeta receptor, common-partner cytoplasmic mediator activity","type":"exact"},{"name":"co-SMAD protein","type":"related"},{"name":"common mediator SMAD protein","type":"related"},{"name":"common partner SMAD protein","type":"related"},{"name":"common-mediator SMAD protein","type":"related"},{"name":"common-partner SMAD protein","type":"related"}],"termid":"GO:0030616"}


id: MONDO:0009340
data:
  {"annotated_genes":["SJAG_04495","SJAG_04334"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88254,88255],"is_not":false,"summary":null,"term":"MONDO:0009340"}]},"cv_name":"mondo","definition":"Nonspherocytic hemolytic anemia due to hexokinase deficiency (NSHA due to HK1 deficiency) is a very rare conditionmainly characterized by severe, chronic hemolysis, beginning in infancy. Approximately 20 cases of this condition have been described to date. Signs and symptoms of hexokinase deficiency are very similar to those of pyruvate kinase deficiency but anemia is generally more severe. Some affected individuals reportedly have had various abnormalities in addition to NSHA including multiple malformations, panmyelopathy, and latent diabetes.Itcan be caused by mutations in the HK1 gene and is inherited in an autosomal recessive manner. Treatment may include red cell transfusions for those with severe anemia.","definition_xrefs":["GARD:0003672"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nonspherocytic hemolytic anemia","termid":"MONDO:0006506"},{"relation_name":"is_a","term_name":"disorder of glycolysis","termid":"MONDO:0017688"},{"relation_name":"is_a","term_name":"anemia due to erythrocyte enzyme disorder","termid":"MONDO:0020585"}],"gene_count":2,"genes_by_uniquename":{"SJAG_04334":null,"SJAG_04495":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0019254"},{"rel_name":"is_a","termid":"MONDO:0002280"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0002280","MONDO:0019254","MONDO:0005066","MONDO:0037792"],"is_obsolete":false,"name":"non-spherocytic hemolytic anemia due to hexokinase deficiency","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:3672","UMLS:C3150343","MEDGEN:461693","MESH:C562995","Orphanet:90031","OMIM:235700"],"synonyms":[{"name":"anemia, congenital, nonspherocytic hemolytic, 5, hexokinase deficient","type":"exact"},{"name":"hemolytic anaemia due to hexokinase deficiency","type":"exact"},{"name":"hemolytic anemia due to hexokinase deficiency","type":"exact"},{"name":"hemolytic anemia, nonspherocytic, due to hexokinase deficiency","type":"exact"},{"name":"hexokinase deficiency hemolytic anaemia","type":"related"},{"name":"hexokinase deficiency hemolytic anemia","type":"related"},{"name":"nonspherocytic hemolytic anaemia due to hexokinase deficiency","type":"exact"},{"name":"nonspherocytic hemolytic anemia due to hexokinase deficiency","type":"exact"}],"termid":"MONDO:0009340","terms_by_termid":{"MONDO:0009340":null},"xrefs":{"Monarch":{"xref_id":"0009340"}}}


id: GO:0019333
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The reduction of nitrate to dinitrogen by four reduction reactions: nitrate reduced to nitrite, then to nitric oxide, then to nitrous oxide, and finally to dinitrogen.","definition_xrefs":["MetaCyc:DENITRIFICATION-PWY"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nitrogen cycle metabolic process","termid":"GO:0071941"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0071941"}],"interesting_parent_ids":["GO:0071941","GO:0008150"],"is_obsolete":false,"name":"denitrification pathway","secondary_identifiers":["kegg.module:M00529"],"termid":"GO:0019333"}


id: PBO:0071737
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L39 pseudogene 35","termid":"PBO:0071737"}


id: SOFP:ontology_term
data:
  {"annotation_feature_type":"gene","cv_name":"feature_property","definition":"A term from some ontology classifying the feature","direct_ancestors":[{"relation_name":"is_a","term_name":"feature_property","termid":"SOFP:feature_property"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ontology_term","termid":"SOFP:ontology_term"}


id: FYPO:0000831
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An increased chemical resistance phenotype observed in the vegetative growth phase of the life cycle in which cells grow in the presence of a higher concentration of actinomycin D than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002682"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000003","FYPO:0000139","FYPO:0002682","FYPO:0005447"],"is_obsolete":false,"name":"resistance to actinomycin D","synonyms":[{"name":"resistance to actinomycin D during mitotic cell cycle","type":"related"},{"name":"resistance to actinomycin D during vegetative growth","type":"exact"},{"name":"resistant to actinomycin D","type":"exact"}],"termid":"FYPO:0000831"}


id: GO:1905163
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of phagosome maturation.","definition_xrefs":["GOC:bf","GO_REF:0000058","GOC:PARL","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of organelle organization","termid":"GO:0010639"},{"relation_name":"is_a","term_name":"regulation of phagosome maturation","termid":"GO:1905162"},{"relation_name":"negatively_regulates","term_name":"phagosome maturation","termid":"GO:0090382"}],"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 phagosome maturation","synonyms":[{"name":"down regulation of phagosome maturation","type":"exact"},{"name":"down-regulation of phagosome maturation","type":"exact"},{"name":"downregulation of phagosome maturation","type":"exact"},{"name":"inhibition of phagosome maturation","type":"narrow"}],"termid":"GO:1905163"}


id: PR:Q9P7I6
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC24B10.20 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P7I6"],"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 oxidoreductase C24B10.20 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC24B10.20","synonyms":[{"name":"Spom972h-SPCC24B10.20","type":"exact"}],"termid":"PR:Q9P7I6"}


id: GO:2000141
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of octopamine signaling pathway involved in response to food.","definition_xrefs":["GOC:mah","PMID:19609300"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of response to food","termid":"GO:0032097"},{"relation_name":"is_a","term_name":"positive regulation of octopamine signaling pathway","termid":"GO:2000130"},{"relation_name":"is_a","term_name":"regulation of octopamine signaling pathway involved in response to food","termid":"GO:2000139"},{"relation_name":"positively_regulates","term_name":"octopamine signaling pathway involved in response to food","termid":"GO:0071935"}],"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 octopamine signaling pathway involved in response to food","synonyms":[{"name":"positive regulation of octopamine signalling pathway involved in response to food","type":"exact"}],"termid":"GO:2000141"}


id: PBO:0059625
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial carrier 1","termid":"PBO:0059625"}


id: PBO:0004101
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CAF1 family ribonuclease (predicted)","termid":"PBO:0004101"}


id: GO:0050573
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: dTDP-D-fucose + NADP+ = dTDP-4-dehydro-6-deoxy-alpha-D-glucose + H+ + NADPH.","definition_xrefs":["RHEA:36583","EC:1.1.1.266"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"dTDP-4-dehydro-6-deoxyglucose reductase activity","secondary_identifiers":["MetaCyc:1.1.1.266-RXN","KEGG_REACTION:R05687"],"synonyms":[{"name":"dTDP-4-keto-6-deoxyglucose reductase activity","type":"related"},{"name":"dTDP-D-fucose:NADP+ oxidoreductase activity","type":"related"}],"termid":"GO:0050573"}


id: MONDO:0012716
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Spondyloepiphyseal dysplasia, Cantu type is an extremely rare type of spondyloepiphyseal dysplasia described in about 5 patients to date and characterized by clinical signs including short stature, peculiar facies with blepharophimosis, upward slanted eyes, abundant eyebrows and eyelashes, coarse voice, and short hands and feet (brachymetacarpalia, brachymetatarsalia and brachyphalangia).","definition_xrefs":["Orphanet:163654"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spondyloepiphyseal dysplasia","termid":"MONDO:0016761"}],"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":"spondyloepiphyseal dysplasia, Cantu type","secondary_identifiers":["MEDGEN:435975","OMIM:611717","UMLS:C2673649","icd11.foundation:897226700","DOID:0112287","GARD:10629","SCTID:718765003","MESH:C567128"],"synonyms":[{"name":"SED-BDS","type":"exact"},{"name":"Sed-BDS","type":"related"},{"name":"Tatoo dysplasia","type":"related"},{"name":"fantasy Island syndrome","type":"related"},{"name":"spondyloepiphyseal dysplasia-brachydactyly and distinctive speech","type":"related"},{"name":"spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome","type":"exact"},{"name":"tattoo dysplasia","type":"exact"}],"termid":"MONDO:0012716","xrefs":{"Monarch":{"xref_id":"0012716"}}}


id: MONDO:0012518
data:
  {"annotated_genes":["SJAG_04728"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87759],"is_not":false,"summary":null,"term":"MONDO:0012518"}]},"cv_name":"mondo","definition":"Any congenital myasthenic syndromes with glycosylation defect in which the cause of the disease is a mutation in the GFPT1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital myasthenic syndrome with tubular aggregates","termid":"MONDO:0000182"},{"relation_name":"is_a","term_name":"congenital disorder of glycosylation","termid":"MONDO:0015286"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04728":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0024322","MONDO:0005066"],"is_obsolete":false,"name":"congenital myasthenic syndrome 12","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:610542","GARD:18451","NCIT:C168997","MEDGEN:765249","DOID:0110660","UMLS:C3552335"],"synonyms":[{"name":"CMS12","type":"exact"},{"name":"GFPT1 congenital myasthenic syndromes with glycosylation defect","type":"exact"},{"name":"congenital myasthenia 12 with tubular aggregates","type":"exact"},{"name":"congenital myasthenic syndrome type 12","type":"exact"},{"name":"congenital myasthenic syndromes with glycosylation defect caused by mutation in GFPT1","type":"exact"},{"name":"myasthenia, congenital, 12, with tubular aggregates","type":"exact"},{"name":"myasthenic syndrome, congenital, 12","type":"related"},{"name":"myasthenic syndrome, congenital, type 12","type":"exact"},{"name":"myasthenic syndrome, congenital, with tubular aggregates 1","type":"related"}],"termid":"MONDO:0012518","terms_by_termid":{"MONDO:0012518":null},"xrefs":{"Monarch":{"xref_id":"0012518"}}}


id: PBO:0043149
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"capicua transcriptional repressor pseudogene 17","termid":"PBO:0043149"}


id: FYPO:0002195
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cell population phenotype in which all cells in the population are viable and have normal morphology (i.e. size, shape, and structure) in the vegetative growth phase of the life cycle.","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete normal morphology viable vegetative cell population (obsolete FYPO:0002195)","synonyms":[{"name":"viable vegetative cell population with normal cell morphology","type":"exact"},{"name":"viable vegetative cell population with normal cell shape and size","type":"exact"}],"termid":"FYPO:0002195"}


id: GO:0005815
data:
  {"annotated_genes":["SJAG_04901","SJAG_00082","SJAG_01422","SJAG_01483","SJAG_03062","SJAG_04461","SJAG_04280","SJAG_01775","SJAG_05205","SJAG_02045","SJAG_03615","SJAG_02332","SJAG_01785","SJAG_04609","SJAG_04980","SJAG_02098","SJAG_00910","SJAG_04931","SJAG_03891","SJAG_02299","SJAG_04551","SJAG_04140","SJAG_03092","SJAG_02737","SJAG_00430","SJAG_02561","SJAG_05185","SJAG_04468","SJAG_02246","SJAG_02186","SJAG_00317","SJAG_03810","SJAG_00104","SJAG_00666","SJAG_03915","SJAG_03052","SJAG_03048","SJAG_00724","SJAG_01799","SJAG_00472","SJAG_02616","SJAG_02556","SJAG_03843","SJAG_00142","SJAG_05309","SJAG_01188","SJAG_01232","SJAG_00100","SJAG_00140","SJAG_05266","SJAG_03287","SJAG_03936","SJAG_03026","SJAG_03376","SJAG_00800","SJAG_03525","SJAG_00907","SJAG_03699","SJAG_00856","SJAG_00113","SJAG_03612","SJAG_04595","SJAG_01790","SJAG_04884","SJAG_04653","SJAG_00526","SJAG_04457","SJAG_00229","SJAG_03501","SJAG_03681","SJAG_02529","SJAG_00356","SJAG_03835","SJAG_01563","SJAG_02431","SJAG_05207","SJAG_04745","SJAG_01215","SJAG_00405","SJAG_01745","SJAG_01082","SJAG_02368","SJAG_01146","SJAG_03264","SJAG_03342","SJAG_03216","SJAG_04498","SJAG_02104","SJAG_03708","SJAG_03351","SJAG_02550","SJAG_01546","SJAG_07018","SJAG_05264","SJAG_03073","SJAG_02336","SJAG_04597","SJAG_01613","SJAG_04010","SJAG_03508","SJAG_01777","SJAG_02609","SJAG_02286","SJAG_06270","SJAG_02624","SJAG_01386","SJAG_01050","SJAG_02058","SJAG_04558","SJAG_03259","SJAG_04239","SJAG_00982","SJAG_01464","SJAG_02169","SJAG_03892","SJAG_02514","SJAG_05196","SJAG_04841","SJAG_01297","SJAG_02724","SJAG_02923","SJAG_00719","SJAG_01242","SJAG_03116","SJAG_02795","SJAG_03592","SJAG_04455","SJAG_00646","SJAG_01401","SJAG_00918","SJAG_02921","SJAG_04143","SJAG_01538","SJAG_02542","SJAG_03544","SJAG_04943","SJAG_01370","SJAG_02248","SJAG_02736","SJAG_01756","SJAG_01330","SJAG_03491","SJAG_05290","SJAG_01662","SJAG_05978","SJAG_03200","SJAG_02444","SJAG_00807","SJAG_01760","SJAG_03695","SJAG_02886","SJAG_00794","SJAG_01371","SJAG_02761","SJAG_01805","SJAG_03602","SJAG_00773","SJAG_02266","SJAG_05315","SJAG_00333","SJAG_01224","SJAG_05260","SJAG_03540","SJAG_02232","SJAG_01620"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[80025,101026,106148],"is_not":false,"summary":null,"term":"GO:0005815"},{"annotations":[61137,80672],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990334"},{"annotations":[100084,101669,98673],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061493"},{"annotations":[91459],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005814"},{"annotations":[111443,110683,114620,118799,119052,108276,102186,103246,112425,102801,101902,104140],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000923"},{"annotations":[112426,119053,80770,101903,99458,102802,111444,108277],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000931"},{"annotations":[110685,102803,112427,111445],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0008275"},{"annotations":[114494,110686,112428,114696,116981,111446,118800],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061496"},{"annotations":[110687,113283,102804,111447,112429,104629],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061497"},{"annotations":[114621,98525,104141,118801,102805,111448,110688,104630],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031021"},{"annotations":[104170,113256,93100,104633,102543,113076,116982,89206,101644,111449,108215,98678,117331,91575,101671,102665,105948,95601,106931,110197,113284,94103,92800,89567,91054,99389,95674,98577,102761,104739,115787,97021,120005,96216,112369,118786,108930,101741,92530,94651,97123,101480,114495,101643],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035974"},{"annotations":[105534,93569,107008,108146,108678,103438,95070,110867,112904,92993,98209,103959,105637,110581,102192,111400,114328,104870,116775,96036,112016,121448,91559,98090,92801,108278,111807,112774,76417,98199,98527,72283,95604,96211,116545,91055,116812,117863,119160,113352,120094,91804,94337,96585,91939,96063,99615,108187,115523,119054,92532,94104,118570,99264,107308,94738,95269,121446,110090,109339,66727,102022,92791,96219,95688,110177,121458,100430,98142,110596,113534,89207,95749,70174,101417,111749,103087,114860,119140,72483,99087,101957,101904,93193,106401,116659,118881,105709,117760,93147,117152,100239,114623,90767,91461,112024,99841,118373,102417,108463,120638,119066,102339,91427,98580,102355,95546,98287,104142],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044732"},{"annotations":[101673,104635,102763,104174,108217,107183,92949,113044,108976,112371],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071958"},{"annotations":[108218,110693,104177,112373,94653,104638,109376,113050,114700,116355,112432,111452,97453,101483,106872],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071957"},{"annotations":[110694,118805,108932],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061499"},{"annotations":[117334,94654],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0160065"},{"annotations":[121273,121278,121296,121445],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005816"}]},"cv_name":"cellular_component","definition":"An intracellular structure that can catalyze gamma-tubulin-dependent microtubule nucleation and that can anchor microtubules by interacting with their minus ends, plus ends or sides.","definition_xrefs":["PMID:17072892","Wikipedia:Microtubule_organizing_center","PMID:17245416","ISBN:0815316194","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"microtubule cytoskeleton","termid":"GO:0015630"}],"gene_count":165,"genes_by_uniquename":{"SJAG_00082":null,"SJAG_00100":null,"SJAG_00104":null,"SJAG_00113":null,"SJAG_00140":null,"SJAG_00142":null,"SJAG_00229":null,"SJAG_00317":null,"SJAG_00333":null,"SJAG_00356":null,"SJAG_00405":null,"SJAG_00430":null,"SJAG_00472":null,"SJAG_00526":null,"SJAG_00646":null,"SJAG_00666":null,"SJAG_00719":null,"SJAG_00724":null,"SJAG_00773":null,"SJAG_00794":null,"SJAG_00800":null,"SJAG_00807":null,"SJAG_00856":null,"SJAG_00907":null,"SJAG_00910":null,"SJAG_00918":null,"SJAG_00982":null,"SJAG_01050":null,"SJAG_01082":null,"SJAG_01146":null,"SJAG_01188":null,"SJAG_01215":null,"SJAG_01224":null,"SJAG_01232":null,"SJAG_01242":null,"SJAG_01297":null,"SJAG_01330":null,"SJAG_01370":null,"SJAG_01371":null,"SJAG_01386":null,"SJAG_01401":null,"SJAG_01422":null,"SJAG_01464":null,"SJAG_01483":null,"SJAG_01538":null,"SJAG_01546":null,"SJAG_01563":null,"SJAG_01613":null,"SJAG_01620":null,"SJAG_01662":null,"SJAG_01745":null,"SJAG_01756":null,"SJAG_01760":null,"SJAG_01775":null,"SJAG_01777":null,"SJAG_01785":null,"SJAG_01790":null,"SJAG_01799":null,"SJAG_01805":null,"SJAG_02045":null,"SJAG_02058":null,"SJAG_02098":null,"SJAG_02104":null,"SJAG_02169":null,"SJAG_02186":null,"SJAG_02232":null,"SJAG_02246":null,"SJAG_02248":null,"SJAG_02266":null,"SJAG_02286":null,"SJAG_02299":null,"SJAG_02332":null,"SJAG_02336":null,"SJAG_02368":null,"SJAG_02431":null,"SJAG_02444":null,"SJAG_02514":null,"SJAG_02529":null,"SJAG_02542":null,"SJAG_02550":null,"SJAG_02556":null,"SJAG_02561":null,"SJAG_02609":null,"SJAG_02616":null,"SJAG_02624":null,"SJAG_02724":null,"SJAG_02736":null,"SJAG_02737":null,"SJAG_02761":null,"SJAG_02795":null,"SJAG_02886":null,"SJAG_02921":null,"SJAG_02923":null,"SJAG_03026":null,"SJAG_03048":null,"SJAG_03052":null,"SJAG_03062":null,"SJAG_03073":null,"SJAG_03092":null,"SJAG_03116":null,"SJAG_03200":null,"SJAG_03216":null,"SJAG_03259":null,"SJAG_03264":null,"SJAG_03287":null,"SJAG_03342":null,"SJAG_03351":null,"SJAG_03376":null,"SJAG_03491":null,"SJAG_03501":null,"SJAG_03508":null,"SJAG_03525":null,"SJAG_03540":null,"SJAG_03544":null,"SJAG_03592":null,"SJAG_03602":null,"SJAG_03612":null,"SJAG_03615":null,"SJAG_03681":null,"SJAG_03695":null,"SJAG_03699":null,"SJAG_03708":null,"SJAG_03810":null,"SJAG_03835":null,"SJAG_03843":null,"SJAG_03891":null,"SJAG_03892":null,"SJAG_03915":null,"SJAG_03936":null,"SJAG_04010":null,"SJAG_04140":null,"SJAG_04143":null,"SJAG_04239":null,"SJAG_04280":null,"SJAG_04455":null,"SJAG_04457":null,"SJAG_04461":null,"SJAG_04468":null,"SJAG_04498":null,"SJAG_04551":null,"SJAG_04558":null,"SJAG_04595":null,"SJAG_04597":null,"SJAG_04609":null,"SJAG_04653":null,"SJAG_04745":null,"SJAG_04841":null,"SJAG_04884":null,"SJAG_04901":null,"SJAG_04931":null,"SJAG_04943":null,"SJAG_04980":null,"SJAG_05185":null,"SJAG_05196":null,"SJAG_05205":null,"SJAG_05207":null,"SJAG_05260":null,"SJAG_05264":null,"SJAG_05266":null,"SJAG_05290":null,"SJAG_05309":null,"SJAG_05315":null,"SJAG_05978":null,"SJAG_06270":null,"SJAG_07018":null},"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":"microtubule organizing center","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null,"PMID:21733045":null,"PMID:32109380":null,"PMID:32243490":null},"synonyms":[{"name":"MTOC","type":"exact"},{"name":"microtubule organising centre","type":"exact"}],"termid":"GO:0005815","terms_by_termid":{"GO:0000093":null,"GO:0000923":null,"GO:0000931":null,"GO:0005814":null,"GO:0005815":null,"GO:0005816":null,"GO:0008275":null,"GO:0031021":null,"GO:0035974":null,"GO:0044732":null,"GO:0061493":null,"GO:0061496":null,"GO:0061497":null,"GO:0061499":null,"GO:0071957":null,"GO:0071958":null,"GO:0160065":null,"GO:1990334":null}}


id: GO:0061450
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Trophoblast cell migration that is accomplished by extension and retraction of a pseudopodium. Trophoblast cells line the outside of the blastocyst.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ameboidal-type cell migration","termid":"GO:0001667"},{"relation_name":"part_of","term_name":"embryo implantation","termid":"GO:0007566"}],"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":"trophoblast cell migration","termid":"GO:0061450"}


id: GO:0035307
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of removal of phosphate groups from a protein.","definition_xrefs":["GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of protein dephosphorylation (obsolete GO:0035307)","synonyms":[{"name":"activation of protein amino acid dephosphorylation","type":"narrow"},{"name":"positive regulation of protein amino acid dephosphorylation","type":"exact"},{"name":"stimulation of protein amino acid dephosphorylation","type":"narrow"},{"name":"up regulation of protein amino acid dephosphorylation","type":"exact"},{"name":"up-regulation of protein amino acid dephosphorylation","type":"exact"},{"name":"upregulation of protein amino acid dephosphorylation","type":"exact"}],"termid":"GO:0035307"}


id: PBO:0052049
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KAT8 regulatory NSL complex subunit 1","termid":"PBO:0052049"}


id: PBO:0001179
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ubp5 interacting protein Ftp105","termid":"PBO:0001179"}


id: PBO:0081894
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 845","termid":"PBO:0081894"}


id: MONDO:0016684
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Anaplastic astrocytoma is a rare, high-grade, malignant glial tumor, histologically characterized by abundance of pleomorphic astrocytes and multiple mitotic figures, often associated with diffuse infiltration of the surrounding tissue, considerable edema and mass effect and involvement of the contralateral brain. Depending on the primary localization of the tumor, patients can present with signs of raised intracranial pressure (headache, vomiting, papilledema), seizures, progressive neurological deficits, and/or behavioral changes. The tumor is most commonly localized in the frontal and temporal lobes, brain stem and spinal cord.","definition_xrefs":["Orphanet:251589"],"direct_ancestors":[{"relation_name":"is_a","term_name":"high grade astrocytic tumor","termid":"MONDO:0016680"},{"relation_name":"is_a","term_name":"astrocytoma (excluding glioblastoma)","termid":"MONDO:0019781"},{"relation_name":"is_a","term_name":"anaplastic cancer","termid":"MONDO:0020633"}],"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":"anaplastic astrocytoma","secondary_identifiers":["MEDGEN:137784","ONCOTREE:AASTR","UMLS:C0334579","EFO:0002499","ICDO:9401/3","MedDRA:10060971","NANDO:2200086","MedDRA:10002224","GARD:5860","NORD:769","NCIT:C9477","DOID:3078"],"synonyms":[{"name":"anaplastic astrocytoma","type":"exact"},{"name":"astrocytoma, anaplastic, malignant","type":"exact"},{"name":"grade III astrocytic neoplasm","type":"exact"},{"name":"grade III astrocytic tumor","type":"exact"},{"name":"grade III astrocytic tumour","type":"exact"},{"name":"grade III astrocytoma","type":"exact"},{"name":"malignant astrocytoma","type":"exact"}],"termid":"MONDO:0016684","xrefs":{"Monarch":{"xref_id":"0016684"}}}


id: PBO:0111899
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GRIP domain","termid":"PBO:0111899"}


id: PBO:0075053
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 116-16","termid":"PBO:0075053"}


id: PR:O74839
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- msy1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74839"],"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 MscS family protein C1183.11 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1183.11","synonyms":[{"name":"Spom972h-msy1","type":"exact"}],"termid":"PR:O74839"}


id: PBO:0002166
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BolA domain protein","termid":"PBO:0002166"}


id: GO:0038054
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with estrogen and transmitting the signal across the membrane by activating an associated G-protein; promotes the exchange of GDP for GTP on the alpha subunit of a heterotrimeric G-protein complex.","definition_xrefs":["PMID:20960099","GOC:signaling","PMID:17379646"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor activity","termid":"GO:0004930"}],"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":"G protein-coupled estrogen receptor activity","synonyms":[{"name":"G-protein coupled estrogen receptor activity","type":"exact"},{"name":"estrogen receptor activity","type":"broad"}],"termid":"GO:0038054"}


id: GO:0005724
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. Heterochromatic regions of the chromosome found at the telomeres of a chromosome in the nucleus.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete nuclear telomeric heterochromatin (obsolete GO:0005724)","termid":"GO:0005724"}


id: MONDO:0002797
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A medulloblastoma occurring in children.","definition_xrefs":["NCIT:C3997"],"direct_ancestors":[{"relation_name":"is_a","term_name":"childhood cerebellar neoplasm","termid":"MONDO:0003263"},{"relation_name":"is_a","term_name":"medulloblastoma","termid":"MONDO:0007959"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"childhood medulloblastoma","secondary_identifiers":["DOID:3869","GARD:9350","NANDO:2200090","MEDGEN:75829","UMLS:C0278510"],"synonyms":[{"name":"childhood medulloblastoma","type":"exact"},{"name":"medulloblastoma","type":"broad"},{"name":"medulloblastoma of childhood","type":"exact"},{"name":"medulloblastoma, childhood","type":"related"},{"name":"paediatric medulloblastoma","type":"exact"},{"name":"pediatric medulloblastoma","type":"exact"}],"termid":"MONDO:0002797","xrefs":{"Monarch":{"xref_id":"0002797"}}}


id: GO:0009984
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: substrate + ATP = substrate-AMP + diphosphate.","definition_xrefs":["PMID:12084835"],"gene_count":0,"genotype_count":0,"name":"obsolete adenylate forming enzyme activity (obsolete GO:0009984)","synonyms":[{"name":"adenylate forming enzyme activity","type":"exact"}],"termid":"GO:0009984"}


id: MOD:01106
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-tryptophan residue to N-formyl-L-tryptophan.","definition_xrefs":["DeltaMass:0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-formylated residue","termid":"MOD:00409"},{"relation_name":"is_a","term_name":"modified L-tryptophan residue","termid":"MOD:00918"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-formyl-L-tryptophan","synonyms":[{"name":"formyl tryptophanyl","type":"exact"}],"termid":"MOD:01106"}


id: FYPO:0003958
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of diacylglycerol O-acyltransferase activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal catalytic activity","termid":"FYPO:0000661"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0000707","FYPO:0000652","FYPO:0001985","FYPO:0000654"],"is_obsolete":false,"name":"abnormal diacylglycerol O-acyltransferase activity","synonyms":[{"name":"abnormal DGAT activity","type":"exact"},{"name":"abnormal diacylglycerol acyltransferase activity","type":"broad"}],"termid":"FYPO:0003958"}


id: GO:1901103
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of gramicidin S.","definition_xrefs":["GOC:yaf","PMID:7534306","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amide biosynthetic process","termid":"GO:0043604"}],"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":"gramicidin S biosynthetic process","synonyms":[{"name":"gramicidin S anabolism","type":"exact"},{"name":"gramicidin S biosynthesis","type":"exact"},{"name":"gramicidin S formation","type":"exact"},{"name":"gramicidin S synthesis","type":"exact"}],"termid":"GO:1901103"}


id: MONDO:1012739
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any xanthinuria that occurs in dogs due to a mutation in the MOCOS gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"xanthinuria, dog","termid":"MONDO:1011623"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"xanthinuria, type II, dog","secondary_identifiers":["OMIA:001819-9615"],"synonyms":[{"name":"xanthinuria, type II, dog","type":"exact"}],"termid":"MONDO:1012739","xrefs":{"Monarch":{"xref_id":"1012739"}}}


id: GO:0010356
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (2E,6E,10E)-geranylgeranyl diphosphate + H+ + homogentisate = 6-geranylgeranyl-2-methylbenzene-1,4-diol + CO2 + diphosphate.","definition_xrefs":["EC:2.5.1.116","PMID:16989822","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"homogentisate prenyltransferase activity","termid":"GO:0010354"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016765"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016740","GO:0003824","GO:0016765","GO:0003674"],"is_obsolete":false,"name":"homogentisate geranylgeranyltransferase activity","secondary_identifiers":["RHEA:38003","MetaCyc:RXN-14929"],"synonyms":[{"name":"HGGT activity","type":"exact"},{"name":"homogentisate geranylgeranyl transferase activity","type":"exact"}],"termid":"GO:0010356"}


id: PBO:0065654
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein tyrosine phosphatase receptor type E","termid":"PBO:0065654"}


id: GO:0045184
data:
  {"annotated_genes":["SJAG_00586","SJAG_01981","SJAG_01456","SJAG_01223","SJAG_05950","SJAG_04148","SJAG_00899","SJAG_01114","SJAG_00850","SJAG_01025","SJAG_04509","SJAG_04837","SJAG_04275","SJAG_04391","SJAG_00171","SJAG_04402","SJAG_01013","SJAG_02210","SJAG_01809","SJAG_05302","SJAG_04552","SJAG_03411","SJAG_04129","SJAG_02117","SJAG_02453","SJAG_03536","SJAG_04763","SJAG_00143","SJAG_00284","SJAG_01328","SJAG_01917","SJAG_02998","SJAG_00900","SJAG_04023","SJAG_00072","SJAG_04609","SJAG_02211","SJAG_03246","SJAG_01633","SJAG_03593","SJAG_03470","SJAG_01211","SJAG_02456","SJAG_01586","SJAG_00416","SJAG_01281","SJAG_05414","SJAG_01840","SJAG_03662","SJAG_03860","SJAG_04600","SJAG_00192","SJAG_03737","SJAG_02731","SJAG_00332","SJAG_00804","SJAG_02241","SJAG_01805","SJAG_01027","SJAG_04411","SJAG_05344","SJAG_01282","SJAG_03693","SJAG_00093","SJAG_01224","SJAG_01409","SJAG_04740","SJAG_02264","SJAG_03499","SJAG_03633","SJAG_04112","SJAG_02839","SJAG_02371","SJAG_04598","SJAG_02640","SJAG_02809","SJAG_00375","SJAG_01242","SJAG_01088","SJAG_01496","SJAG_03907","SJAG_01039","SJAG_03838","SJAG_01584","SJAG_04641","SJAG_01909","SJAG_04451","SJAG_05315","SJAG_03643","SJAG_05300","SJAG_00687","SJAG_01405","SJAG_02355","SJAG_00326","SJAG_01527","SJAG_00314","SJAG_03781","SJAG_03440","SJAG_04474","SJAG_04051","SJAG_04645","SJAG_02204","SJAG_02361","SJAG_00906","SJAG_01655","SJAG_00895","SJAG_01135","SJAG_02482","SJAG_02422","SJAG_01560","SJAG_03986","SJAG_01240","SJAG_05220","SJAG_02539","SJAG_03153","SJAG_04569","SJAG_03955","SJAG_00357","SJAG_01065","SJAG_00277","SJAG_03385","SJAG_02867","SJAG_00569","SJAG_01789","SJAG_02282","SJAG_04966","SJAG_04294","SJAG_01598","SJAG_04956","SJAG_03048","SJAG_05319","SJAG_01925","SJAG_03415","SJAG_01449","SJAG_01229","SJAG_03358","SJAG_02586","SJAG_01879","SJAG_00820","SJAG_03930","SJAG_04400","SJAG_00054","SJAG_01120","SJAG_03892","SJAG_03345","SJAG_01167","SJAG_04349","SJAG_04565","SJAG_00379","SJAG_00603","SJAG_07010","SJAG_00204","SJAG_00702","SJAG_00851","SJAG_01311","SJAG_00919","SJAG_02588","SJAG_03299","SJAG_05030","SJAG_02520","SJAG_03467","SJAG_02997","SJAG_05266","SJAG_03137","SJAG_02750","SJAG_01647","SJAG_04960","SJAG_04909","SJAG_04643","SJAG_00840","SJAG_04996","SJAG_03244","SJAG_04432","SJAG_00907","SJAG_02425","SJAG_01748","SJAG_02584","SJAG_03270","SJAG_04070","SJAG_03540","SJAG_00065","SJAG_03347","SJAG_04312","SJAG_03396","SJAG_02208","SJAG_02437","SJAG_01782","SJAG_01004","SJAG_02336","SJAG_01508","SJAG_02592","SJAG_00564","SJAG_01245","SJAG_02525","SJAG_01488","SJAG_03783","SJAG_00530","SJAG_01626","SJAG_03684","SJAG_01030","SJAG_05194","SJAG_04196","SJAG_01178","SJAG_04466","SJAG_02315","SJAG_01684","SJAG_04886","SJAG_01834","SJAG_01382","SJAG_01772","SJAG_01759","SJAG_02349","SJAG_02511","SJAG_02034","SJAG_03029","SJAG_01642","SJAG_02320","SJAG_00373","SJAG_03915","SJAG_00104","SJAG_00578","SJAG_00959","SJAG_04044","SJAG_05207","SJAG_05210","SJAG_03072","SJAG_05013","SJAG_01371","SJAG_02789","SJAG_00144","SJAG_01185","SJAG_03315","SJAG_02824","SJAG_00858","SJAG_01299","SJAG_00360","SJAG_02805","SJAG_04366","SJAG_01940","SJAG_04024","SJAG_01750","SJAG_00430","SJAG_03959","SJAG_01367","SJAG_02004","SJAG_01165","SJAG_01999","SJAG_00916","SJAG_01415","SJAG_00208","SJAG_02368","SJAG_04517","SJAG_03963","SJAG_00471","SJAG_01374","SJAG_04489","SJAG_03889","SJAG_03054","SJAG_02103","SJAG_02277","SJAG_03250","SJAG_01358","SJAG_04592","SJAG_00826","SJAG_01534","SJAG_04021","SJAG_01379","SJAG_04513","SJAG_03836","SJAG_01951","SJAG_01641","SJAG_01775","SJAG_00380","SJAG_03504","SJAG_02234","SJAG_02397","SJAG_05345","SJAG_01733","SJAG_03437","SJAG_00196","SJAG_04902","SJAG_03756","SJAG_02077","SJAG_04358","SJAG_04931","SJAG_01546","SJAG_03865","SJAG_00181","SJAG_02797","SJAG_01558","SJAG_03502","SJAG_01597","SJAG_00557","SJAG_03560","SJAG_03416","SJAG_01615","SJAG_03648","SJAG_00108","SJAG_03324","SJAG_01949","SJAG_16459","SJAG_01297","SJAG_05184","SJAG_00383","SJAG_04857","SJAG_00404","SJAG_04208","SJAG_04072","SJAG_01071","SJAG_03300","SJAG_00918","SJAG_00216","SJAG_00137","SJAG_02065","SJAG_01349","SJAG_02274","SJAG_01442","SJAG_02914","SJAG_03011","SJAG_01516","SJAG_04002","SJAG_02757","SJAG_02811","SJAG_01127","SJAG_00803","SJAG_00175","SJAG_01360","SJAG_02912","SJAG_03515","SJAG_04014","SJAG_01621","SJAG_00891","SJAG_02693","SJAG_03552","SJAG_00800","SJAG_03848","SJAG_01697","SJAG_04203","SJAG_02330","SJAG_00330","SJAG_04978","SJAG_00938","SJAG_03729","SJAG_03158","SJAG_00032","SJAG_04336","SJAG_01435","SJAG_01083","SJAG_01640","SJAG_01780","SJAG_01112","SJAG_00968","SJAG_02655","SJAG_02761","SJAG_04936","SJAG_03002","SJAG_04343","SJAG_04912","SJAG_00490","SJAG_02619","SJAG_02418","SJAG_04472","SJAG_00064","SJAG_03970","SJAG_05259","SJAG_00821","SJAG_04428","SJAG_04218","SJAG_04656","SJAG_00971","SJAG_00753","SJAG_01459","SJAG_03933","SJAG_04629","SJAG_03005","SJAG_02354","SJAG_03453","SJAG_04739","SJAG_00632","SJAG_01686","SJAG_01324","SJAG_03404","SJAG_03726","SJAG_04684","SJAG_02524","SJAG_00645","SJAG_05303","SJAG_03976","SJAG_02160","SJAG_04464","SJAG_03864","SJAG_03044"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[99726,109137],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006613"},{"annotations":[64512,69296,70912,89824,89937,65861,93455,107585,64926,116310,93316,115166],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120113"},{"annotations":[61966,67803,93105,114862,96714,120767,114645,102949],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0099638"},{"annotations":[97532],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061951"},{"annotations":[102836],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140569"},{"annotations":[76427],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140570"},{"annotations":[96967,108877,110639,71926,108248,79334,114864,111428],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043001"},{"annotations":[68574,104354,113869,101725,79262,114047,118834,58665,89870,58649,96089,70765,70607,114314,81691,104131,92962,118235,97333,93290,103741,72240,116991,118696,79765,110263,90967,81759,101533,63832,96763,115329,95677,95449,109393,118760,112599,69927,68671,64216,64331,102671,73701,99560,99121,115489,106731,68346,77535,78220,97598,96968,100269,107983,100920,69773,111501,98122,120720,59327,70544,118286,98693,96812,104516,90438,58253,97909,79589,107858,73712,95708,97432,99579,109331,93447,64486,91535,78687,66927,99910,109867,96618,107018,92983,109225,111345,114023,69919,114544,116017,100728,108963,111429,64952,111675,117089,120900,72607,101581,71525,58900,106799,105548,65606,67326,59113,71017,73693,95857,80743,101330,75379,80555,93347,81422,105558,95045,59070,69524,109143,116738,119416,64554,96202,102902,95311,100860,97872,66137,72190,106435,90479,116230,80280,77054,63301,92383,68873,101842,77911,111025,98697,74009,104962,94959,76239,61008],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006886"},{"annotations":[98946,100304],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0160203"},{"annotations":[89903],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0042997"},{"annotations":[107640],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0042308"},{"annotations":[76727,75404,102972,74923,78693,77809],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006607"},{"annotations":[95620,103672,112867,102260],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0046827"},{"annotations":[92661,96185,104207],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0042307"},{"annotations":[97551,111185,81253,111474],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006620"},{"annotations":[81991,99147,74905,99863,110152],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0031204"},{"annotations":[74750],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032527"},{"annotations":[111436,65612,119890,119540,73315,119256,94982,102973,65972],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006611"},{"annotations":[79441,78819],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045041"},{"annotations":[90145,109425,92707,101057,102139,117090,113653,119115,101357,107019,105105,104517,109348,101241,109402,96332,91356,108005,111725,98698],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030150"},{"annotations":[72740,77326,75466,108169,82164,73256,75746,76881,74539,75493,77415,80236,97942,81828,74351,77422,71744,73044,72141,76202,96096,75964,60872,67503,81427,81940,95801,117664,74598,78068,99642,90725,79660,73314,106892,74751],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006606"},{"annotations":[72395,98290,81410,75060,73790,71882,104082,113246],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016558"},{"annotations":[63446,72420,75452],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0016560"},{"annotations":[100386,119174,65297,117161],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0016562"},{"annotations":[113247,92239,97245],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045046"},{"annotations":[100175,114110,111186,106306,108000,106614,96650,99864,93486,110240,115699,103012,69308,110153,100407,112251,105332,116253],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045048"},{"annotations":[79524,75175,109426,77448,90470,58495,75719,104747,118128],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045039"},{"annotations":[58620,80289,80350,76218,80031],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032979"},{"annotations":[109403,71687,78347,100045,112248,113647,111895,59123,100396],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045040"},{"annotations":[78575,71579,79933,81710,82095],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006627"},{"annotations":[69772],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006605"},{"annotations":[70792,114418,71360,89462,100176,100226],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045047"},{"annotations":[60746,76776,74676,72791,76611,97716],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006612"},{"annotations":[100206,68637,104281],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006626"},{"annotations":[92248,97246,92240,98771,104918],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006625"},{"annotations":[92816],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044395"},{"annotations":[82126,98366,79033,79909,72974,75731,77476,79457,78932,74485],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006623"},{"annotations":[57233,67851,61838],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071806"},{"annotations":[66166,77544,81840,74856,61828],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015031"},{"annotations":[105568],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0099117"},{"annotations":[120548,102206,105724,110107],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140210"},{"annotations":[102343,109343,92794,111740,91564,98589,118780,100440,115957,110730,90957],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990976"},{"annotations":[118042,109976],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904601"},{"annotations":[89771,102712,75242,73901,79483,111222,72664,73865,93458,72834,99773,80216,79945,97781,75263,89940,93319,116569,108397],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043328"},{"annotations":[89716,93837],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0033157"},{"annotations":[77353,80851],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030970"},{"annotations":[70543,74709,111475,67598,96090],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006614"},{"annotations":[93448,116231,116992],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006617"},{"annotations":[75366,110154,104406,99865,74957,77296],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0006616"},{"annotations":[74549,89738,115989,76806,116956],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071816"},{"annotations":[80974,112882,107548,94021,120749,80265,80934,74774],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070086"}]},"cv_name":"biological_process","definition":"The directed movement of a protein to a specific location.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment of localization","termid":"GO:0051234"}],"gene_count":392,"genes_by_uniquename":{"SJAG_00032":null,"SJAG_00054":null,"SJAG_00064":null,"SJAG_00065":null,"SJAG_00072":null,"SJAG_00093":null,"SJAG_00104":null,"SJAG_00108":null,"SJAG_00137":null,"SJAG_00143":null,"SJAG_00144":null,"SJAG_00171":null,"SJAG_00175":null,"SJAG_00181":null,"SJAG_00192":null,"SJAG_00196":null,"SJAG_00204":null,"SJAG_00208":null,"SJAG_00216":null,"SJAG_00277":null,"SJAG_00284":null,"SJAG_00314":null,"SJAG_00326":null,"SJAG_00330":null,"SJAG_00332":null,"SJAG_00357":null,"SJAG_00360":null,"SJAG_00373":null,"SJAG_00375":null,"SJAG_00379":null,"SJAG_00380":null,"SJAG_00383":null,"SJAG_00404":null,"SJAG_00416":null,"SJAG_00430":null,"SJAG_00471":null,"SJAG_00490":null,"SJAG_00530":null,"SJAG_00557":null,"SJAG_00564":null,"SJAG_00569":null,"SJAG_00578":null,"SJAG_00586":null,"SJAG_00603":null,"SJAG_00632":null,"SJAG_00645":null,"SJAG_00687":null,"SJAG_00702":null,"SJAG_00753":null,"SJAG_00800":null,"SJAG_00803":null,"SJAG_00804":null,"SJAG_00820":null,"SJAG_00821":null,"SJAG_00826":null,"SJAG_00840":null,"SJAG_00850":null,"SJAG_00851":null,"SJAG_00858":null,"SJAG_00891":null,"SJAG_00895":null,"SJAG_00899":null,"SJAG_00900":null,"SJAG_00906":null,"SJAG_00907":null,"SJAG_00916":null,"SJAG_00918":null,"SJAG_00919":null,"SJAG_00938":null,"SJAG_00959":null,"SJAG_00968":null,"SJAG_00971":null,"SJAG_01004":null,"SJAG_01013":null,"SJAG_01025":null,"SJAG_01027":null,"SJAG_01030":null,"SJAG_01039":null,"SJAG_01065":null,"SJAG_01071":null,"SJAG_01083":null,"SJAG_01088":null,"SJAG_01112":null,"SJAG_01114":null,"SJAG_01120":null,"SJAG_01127":null,"SJAG_01135":null,"SJAG_01165":null,"SJAG_01167":null,"SJAG_01178":null,"SJAG_01185":null,"SJAG_01211":null,"SJAG_01223":null,"SJAG_01224":null,"SJAG_01229":null,"SJAG_01240":null,"SJAG_01242":null,"SJAG_01245":null,"SJAG_01281":null,"SJAG_01282":null,"SJAG_01297":null,"SJAG_01299":null,"SJAG_01311":null,"SJAG_01324":null,"SJAG_01328":null,"SJAG_01349":null,"SJAG_01358":null,"SJAG_01360":null,"SJAG_01367":null,"SJAG_01371":null,"SJAG_01374":null,"SJAG_01379":null,"SJAG_01382":null,"SJAG_01405":null,"SJAG_01409":null,"SJAG_01415":null,"SJAG_01435":null,"SJAG_01442":null,"SJAG_01449":null,"SJAG_01456":null,"SJAG_01459":null,"SJAG_01488":null,"SJAG_01496":null,"SJAG_01508":null,"SJAG_01516":null,"SJAG_01527":null,"SJAG_01534":null,"SJAG_01546":null,"SJAG_01558":null,"SJAG_01560":null,"SJAG_01584":null,"SJAG_01586":null,"SJAG_01597":null,"SJAG_01598":null,"SJAG_01615":null,"SJAG_01621":null,"SJAG_01626":null,"SJAG_01633":null,"SJAG_01640":null,"SJAG_01641":null,"SJAG_01642":null,"SJAG_01647":null,"SJAG_01655":null,"SJAG_01684":null,"SJAG_01686":null,"SJAG_01697":null,"SJAG_01733":null,"SJAG_01748":null,"SJAG_01750":null,"SJAG_01759":null,"SJAG_01772":null,"SJAG_01775":null,"SJAG_01780":null,"SJAG_01782":null,"SJAG_01789":null,"SJAG_01805":null,"SJAG_01809":null,"SJAG_01834":null,"SJAG_01840":null,"SJAG_01879":null,"SJAG_01909":null,"SJAG_01917":null,"SJAG_01925":null,"SJAG_01940":null,"SJAG_01949":null,"SJAG_01951":null,"SJAG_01981":null,"SJAG_01999":null,"SJAG_02004":null,"SJAG_02034":null,"SJAG_02065":null,"SJAG_02077":null,"SJAG_02103":null,"SJAG_02117":null,"SJAG_02160":null,"SJAG_02204":null,"SJAG_02208":null,"SJAG_02210":null,"SJAG_02211":null,"SJAG_02234":null,"SJAG_02241":null,"SJAG_02264":null,"SJAG_02274":null,"SJAG_02277":null,"SJAG_02282":null,"SJAG_02315":null,"SJAG_02320":null,"SJAG_02330":null,"SJAG_02336":null,"SJAG_02349":null,"SJAG_02354":null,"SJAG_02355":null,"SJAG_02361":null,"SJAG_02368":null,"SJAG_02371":null,"SJAG_02397":null,"SJAG_02418":null,"SJAG_02422":null,"SJAG_02425":null,"SJAG_02437":null,"SJAG_02453":null,"SJAG_02456":null,"SJAG_02482":null,"SJAG_02511":null,"SJAG_02520":null,"SJAG_02524":null,"SJAG_02525":null,"SJAG_02539":null,"SJAG_02584":null,"SJAG_02586":null,"SJAG_02588":null,"SJAG_02592":null,"SJAG_02619":null,"SJAG_02640":null,"SJAG_02655":null,"SJAG_02693":null,"SJAG_02731":null,"SJAG_02750":null,"SJAG_02757":null,"SJAG_02761":null,"SJAG_02789":null,"SJAG_02797":null,"SJAG_02805":null,"SJAG_02809":null,"SJAG_02811":null,"SJAG_02824":null,"SJAG_02839":null,"SJAG_02867":null,"SJAG_02912":null,"SJAG_02914":null,"SJAG_02997":null,"SJAG_02998":null,"SJAG_03002":null,"SJAG_03005":null,"SJAG_03011":null,"SJAG_03029":null,"SJAG_03044":null,"SJAG_03048":null,"SJAG_03054":null,"SJAG_03072":null,"SJAG_03137":null,"SJAG_03153":null,"SJAG_03158":null,"SJAG_03244":null,"SJAG_03246":null,"SJAG_03250":null,"SJAG_03270":null,"SJAG_03299":null,"SJAG_03300":null,"SJAG_03315":null,"SJAG_03324":null,"SJAG_03345":null,"SJAG_03347":null,"SJAG_03358":null,"SJAG_03385":null,"SJAG_03396":null,"SJAG_03404":null,"SJAG_03411":null,"SJAG_03415":null,"SJAG_03416":null,"SJAG_03437":null,"SJAG_03440":null,"SJAG_03453":null,"SJAG_03467":null,"SJAG_03470":null,"SJAG_03499":null,"SJAG_03502":null,"SJAG_03504":null,"SJAG_03515":null,"SJAG_03536":null,"SJAG_03540":null,"SJAG_03552":null,"SJAG_03560":null,"SJAG_03593":null,"SJAG_03633":null,"SJAG_03643":null,"SJAG_03648":null,"SJAG_03662":null,"SJAG_03684":null,"SJAG_03693":null,"SJAG_03726":null,"SJAG_03729":null,"SJAG_03737":null,"SJAG_03756":null,"SJAG_03781":null,"SJAG_03783":null,"SJAG_03836":null,"SJAG_03838":null,"SJAG_03848":null,"SJAG_03860":null,"SJAG_03864":null,"SJAG_03865":null,"SJAG_03889":null,"SJAG_03892":null,"SJAG_03907":null,"SJAG_03915":null,"SJAG_03930":null,"SJAG_03933":null,"SJAG_03955":null,"SJAG_03959":null,"SJAG_03963":null,"SJAG_03970":null,"SJAG_03976":null,"SJAG_03986":null,"SJAG_04002":null,"SJAG_04014":null,"SJAG_04021":null,"SJAG_04023":null,"SJAG_04024":null,"SJAG_04044":null,"SJAG_04051":null,"SJAG_04070":null,"SJAG_04072":null,"SJAG_04112":null,"SJAG_04129":null,"SJAG_04148":null,"SJAG_04196":null,"SJAG_04203":null,"SJAG_04208":null,"SJAG_04218":null,"SJAG_04275":null,"SJAG_04294":null,"SJAG_04312":null,"SJAG_04336":null,"SJAG_04343":null,"SJAG_04349":null,"SJAG_04358":null,"SJAG_04366":null,"SJAG_04391":null,"SJAG_04400":null,"SJAG_04402":null,"SJAG_04411":null,"SJAG_04428":null,"SJAG_04432":null,"SJAG_04451":null,"SJAG_04464":null,"SJAG_04466":null,"SJAG_04472":null,"SJAG_04474":null,"SJAG_04489":null,"SJAG_04509":null,"SJAG_04513":null,"SJAG_04517":null,"SJAG_04552":null,"SJAG_04565":null,"SJAG_04569":null,"SJAG_04592":null,"SJAG_04598":null,"SJAG_04600":null,"SJAG_04609":null,"SJAG_04629":null,"SJAG_04641":null,"SJAG_04643":null,"SJAG_04645":null,"SJAG_04656":null,"SJAG_04684":null,"SJAG_04739":null,"SJAG_04740":null,"SJAG_04763":null,"SJAG_04837":null,"SJAG_04857":null,"SJAG_04886":null,"SJAG_04902":null,"SJAG_04909":null,"SJAG_04912":null,"SJAG_04931":null,"SJAG_04936":null,"SJAG_04956":null,"SJAG_04960":null,"SJAG_04966":null,"SJAG_04978":null,"SJAG_04996":null,"SJAG_05013":null,"SJAG_05030":null,"SJAG_05184":null,"SJAG_05194":null,"SJAG_05207":null,"SJAG_05210":null,"SJAG_05220":null,"SJAG_05259":null,"SJAG_05266":null,"SJAG_05300":null,"SJAG_05302":null,"SJAG_05303":null,"SJAG_05315":null,"SJAG_05319":null,"SJAG_05344":null,"SJAG_05345":null,"SJAG_05414":null,"SJAG_05950":null,"SJAG_07010":null,"SJAG_16459":null},"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":"establishment of protein localization","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000108":null,"GO_REF:0000117":null},"synonyms":[{"name":"establishment of protein localisation","type":"exact"},{"name":"protein positioning","type":"exact"},{"name":"protein recruitment","type":"exact"}],"termid":"GO:0045184","terms_by_termid":{"GO:0006605":null,"GO:0006606":null,"GO:0006607":null,"GO:0006611":null,"GO:0006612":null,"GO:0006613":null,"GO:0006614":null,"GO:0006616":null,"GO:0006617":null,"GO:0006620":null,"GO:0006623":null,"GO:0006625":null,"GO:0006626":null,"GO:0006627":null,"GO:0006886":null,"GO:0015031":null,"GO:0016558":null,"GO:0016560":null,"GO:0016562":null,"GO:0030150":null,"GO:0030970":null,"GO:0031204":null,"GO:0032527":null,"GO:0032979":null,"GO:0033157":null,"GO:0042307":null,"GO:0042308":null,"GO:0042997":null,"GO:0043001":null,"GO:0043328":null,"GO:0044395":null,"GO:0045039":null,"GO:0045040":null,"GO:0045041":null,"GO:0045046":null,"GO:0045047":null,"GO:0045048":null,"GO:0046827":null,"GO:0061951":null,"GO:0070086":null,"GO:0071806":null,"GO:0071816":null,"GO:0099117":null,"GO:0099638":null,"GO:0120113":null,"GO:0140210":null,"GO:0140569":null,"GO:0140570":null,"GO:0160203":null,"GO:1904601":null,"GO:1990976":null}}


id: GO:0015836
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of lipid-linked peptidoglycans into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidoglycan transport","termid":"GO:0015835"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"lipid-linked peptidoglycan transport","synonyms":[{"name":"lipid-linked murein transport","type":"exact"}],"termid":"GO:0015836"}


id: PBO:0004784
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycerol-3-phosphate dehydrogenase Gpd1","termid":"PBO:0004784"}


id: PBO:0074713
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 74D","termid":"PBO:0074713"}


id: PBO:0042709
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cadherin EGF LAG seven-pass G-type receptor 1","termid":"PBO:0042709"}


id: SO:0002079
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant that intersects the splice region of an incompletely annotated transcript.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"incomplete_transcript_variant","termid":"SO:0002075"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"incomplete_transcript_splice_region_variant","synonyms":[{"name":"incomplete transcript splice region variant","type":"exact"}],"termid":"SO:0002079"}


id: FYPO:0009085
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An increased chemical resistance phenotype observed in the vegetative growth phase of the life cycle in which cells grow in the presence of higher concentrations of lithium chloride and sodium dodecyl sulfate than normal.","definition_xrefs":["PomBase:mlr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002682"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0002682","FYPO:0000139","FYPO:0000003","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"resistance to lithium chloride and sodium dodecyl sulfate","synonyms":[{"name":"resistance to lithium chloride and SDS","type":"exact"},{"name":"resistance to lithium chloride and SDS during vegetative growth","type":"exact"},{"name":"resistance to lithium chloride and SDS in combination","type":"exact"},{"name":"resistance to lithium chloride and sodium dodecyl sulfate during mitotic cell cycle","type":"related"},{"name":"resistance to lithium chloride and sodium dodecyl sulfate during vegetative growth","type":"exact"},{"name":"resistance to lithium chloride and sodium dodecyl sulfate in combination","type":"exact"},{"name":"resistant to lithium chloride and SDS","type":"exact"},{"name":"resistant to lithium chloride and sodium dodecyl sulfate","type":"exact"}],"termid":"FYPO:0009085"}


id: GO:0046587
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of calcium-dependent cell-cell adhesion.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell-cell adhesion","termid":"GO:0022409"},{"relation_name":"is_a","term_name":"regulation of calcium-dependent cell-cell adhesion","termid":"GO:0046586"},{"relation_name":"positively_regulates","term_name":"calcium-dependent cell-cell adhesion via plasma membrane cell adhesion molecules","termid":"GO:0016339"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"positive regulation of calcium-dependent cell-cell adhesion","synonyms":[{"name":"activation of calcium-dependent cell-cell adhesion","type":"narrow"},{"name":"stimulation of calcium-dependent cell-cell adhesion","type":"narrow"},{"name":"up regulation of calcium-dependent cell-cell adhesion","type":"exact"},{"name":"up-regulation of calcium-dependent cell-cell adhesion","type":"exact"},{"name":"upregulation of calcium-dependent cell-cell adhesion","type":"exact"}],"termid":"GO:0046587"}


id: PBO:0087849
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Trans-aconitate methyltransferase; cytosolic enzyme that catalyzes the methyl esterification of 3-isopropylmalate, an intermediate of the leucine biosynthetic pathway, and trans-aconitate, which inhibits the citric acid cycle","termid":"PBO:0087849"}


id: PR:O94701
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- fic1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94701"],"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":"ingression protein fic1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC83.18c","synonyms":[{"name":"Spom972h-fic1","type":"exact"},{"name":"cdc15-interacting C2 domain-containing protein 1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94701"}


id: GO:1904995
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of leukocyte adhesion to vascular endothelial cell.","definition_xrefs":["GOC:BHF_miRNA","PMID:23897866","GOC:BHF","GO_REF:0000058","GOC:bc","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of leukocyte cell-cell adhesion","termid":"GO:1903038"},{"relation_name":"is_a","term_name":"regulation of leukocyte adhesion to vascular endothelial cell","termid":"GO:1904994"},{"relation_name":"negatively_regulates","term_name":"leukocyte adhesion to vascular endothelial cell","termid":"GO:0061756"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007155"},{"rel_name":"negatively_regulates","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"negative regulation of leukocyte adhesion to vascular endothelial cell","synonyms":[{"name":"down regulation of leukocyte adhesion to vascular endothelial cell","type":"exact"},{"name":"down-regulation of leukocyte adhesion to vascular endothelial cell","type":"exact"},{"name":"downregulation of leukocyte adhesion to vascular endothelial cell","type":"exact"},{"name":"inhibition of leukocyte adhesion to vascular endothelial cell","type":"narrow"}],"termid":"GO:1904995"}


id: PBO:0078254
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor beta variable 29-1","termid":"PBO:0078254"}


id: PBO:0060139
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial tRNA translation optimization 1","termid":"PBO:0060139"}


id: PBO:0058594
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6726","termid":"PBO:0058594"}


id: MONDO:0032697
data:
  {"annotated_genes":["SJAG_00600"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87873],"is_not":false,"summary":null,"term":"MONDO:0032697"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"},{"relation_name":"is_a","term_name":"Houge-Janssens syndrome","termid":"MONDO:0957553"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00600":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"Houge-Janssens syndrome 3","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1677130","OMIM:618354","UMLS:C5193048"],"synonyms":[{"name":"NEDLBA","type":"exact"},{"name":"neurodevelopmental disorder and language delay with or without structural brain abnormalities","type":"exact"}],"termid":"MONDO:0032697","terms_by_termid":{"MONDO:0032697":null},"xrefs":{"Monarch":{"xref_id":"0032697"}}}


id: GO:0014811
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of skeletal muscle contraction via the regulation of the release of sequestered calcium ion by sarcoplasmic reticulum into cytosol. The sarcoplasmic reticulum is the endoplasmic reticulum of striated muscle, specialised for the sequestration of calcium ions that are released upon receipt of a signal relayed by the T tubules from the neuromuscular junction.","definition_xrefs":["GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of skeletal muscle contraction by regulation of release of sequestered calcium ion","termid":"GO:0014809"},{"relation_name":"is_a","term_name":"negative regulation of striated muscle contraction","termid":"GO:0045988"}],"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"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0055085","GO:0023052"],"is_obsolete":false,"name":"negative regulation of skeletal muscle contraction by regulation of release of sequestered calcium ion","termid":"GO:0014811"}


id: PBO:0077750
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"target of myb1 membrane trafficking protein","termid":"PBO:0077750"}


id: PBO:0073856
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 9 member A5","termid":"PBO:0073856"}


id: SO:0000844
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region of sequence which is a promoter for RNA polymerase II.","definition_xrefs":["SO:ke"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:0000844 RNApol_II_promoter_region (obsolete SO:0000844)","termid":"SO:0000844"}


id: PBO:0029204
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_interkinetochore_distance_before_mitotic_anaphase","termid":"PBO:0029204"}


id: FYPO:0002647
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the phosphorylation of threonine residues in one or more specific proteins, or of specific protein sites, occurs to a lower extent than normal during mitosis.","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete decreased protein threonine phosphorylation during mitosis (obsolete FYPO:0002647)","synonyms":[{"name":"decreased peptidyl-threonine phosphorylation during mitosis","type":"exact"},{"name":"decreased protein threonine phosphorylation during mitosis during vegetative growth","type":"exact"},{"name":"decreased protein threonine phosphorylation during mitotic M phase","type":"related"},{"name":"decreased protein threonine phosphorylation during mitotic M phase during mitotic cell cycle","type":"related"},{"name":"decreased threonine phosphorylation during mitosis","type":"exact"},{"name":"reduced protein threonine phosphorylation during mitosis","type":"exact"}],"termid":"FYPO:0002647"}


id: MONDO:1011483
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Beta-mannosidosis that occurs in goat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"beta-mannosidosis, non-human animal","termid":"MONDO:1011432"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"beta-mannosidosis, goat","secondary_identifiers":["OMIA:000626-9925"],"termid":"MONDO:1011483","xrefs":{"Monarch":{"xref_id":"1011483"}}}


id: PBO:0049885
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HERC2 pseudogene 4","termid":"PBO:0049885"}


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:0015318
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Pierre Robin syndrome associated with collagen disease (obsolete MONDO:0015318)","termid":"MONDO:0015318","xrefs":{"Monarch":{"xref_id":"0015318"}}}


id: PBO:0065673
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PTPRT antisense RNA 1","termid":"PBO:0065673"}


id: MONDO:1012893
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ichthyosis that occurs in dogs due to a mutation in the KRT1 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"ichthyosis, dog","termid":"MONDO:1012978"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ichthyosis, KRT1-related, dog","secondary_identifiers":["OMIA:002425-9615"],"synonyms":[{"name":"non-epidermolytic ichthyosis, dog","type":"related"}],"termid":"MONDO:1012893","xrefs":{"Monarch":{"xref_id":"1012893"}}}


id: MONDO:0032790
data:
  {"annotated_genes":["SJAG_00861"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88755],"is_not":false,"summary":null,"term":"MONDO:0032790"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00861":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5193134","DOID:0081443","OMIM:618505","MEDGEN:1682403"],"synonyms":[{"name":"NEDCFSA","type":"related"},{"name":"NEURODEVELOPMENTAL DISORDER WITH COARSE FACIES AND MILD DISTAL SKELETAL ABNORMALITIES","type":"related"}],"termid":"MONDO:0032790","terms_by_termid":{"MONDO:0032790":null},"xrefs":{"Monarch":{"xref_id":"0032790"}}}


id: MONDO:0006173
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A low-grade squamous cell carcinoma that arises from the conjunctiva. It is the most common primary malignant tumor that arises from the conjunctiva. It usually affects older white males. Excessive exposure to sunlight is a risk factor. Patients may present with a mass, red eye, or pain.","definition_xrefs":["NCIT:C4549"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eye carcinoma","termid":"MONDO:0002466"},{"relation_name":"is_a","term_name":"conjunctival cancer","termid":"MONDO:0003454"},{"relation_name":"is_a","term_name":"head and neck squamous cell carcinoma","termid":"MONDO:0010150"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005328"],"is_obsolete":false,"name":"conjunctival squamous cell carcinoma","secondary_identifiers":["MEDGEN:87558","DOID:1748","SCTID:255003007","UMLS:C0346359","EFO:1000206"],"synonyms":[{"name":"conjunctiva epidermoid carcinoma","type":"exact"},{"name":"conjunctiva squamous cell carcinoma","type":"exact"},{"name":"conjunctival epidermoid carcinoma","type":"exact"},{"name":"conjunctival squamous cell cancer","type":"exact"},{"name":"conjunctival squamous cell carcinoma","type":"exact"},{"name":"epidermoid carcinoma of conjunctiva","type":"exact"},{"name":"epidermoid carcinoma of the conjunctiva","type":"exact"},{"name":"invasive squamous cell carcinoma of the conjunctiva","type":"exact"},{"name":"ocular surface squamous neoplasia","type":"broad"},{"name":"squamous cell carcinoma of conjunctiva","type":"exact"},{"name":"squamous cell carcinoma of the conjunctiva","type":"exact"}],"termid":"MONDO:0006173","xrefs":{"Monarch":{"xref_id":"0006173"}}}


id: GO:0000076
data:
  {"annotated_genes":["SJAG_04287","SJAG_03026","SJAG_01605","SJAG_03927","SJAG_03695","SJAG_04671","SJAG_00364","SJAG_02074","SJAG_01205","SJAG_01010","SJAG_02098","SJAG_02266","SJAG_01076","SJAG_01044","SJAG_03160","SJAG_02771","SJAG_02563"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[108449,93243,117919],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033315"},{"annotations":[101005,80677,119142,81268,111162,108452,72857,95776,113890,102358,93244,74071,76642,101172,118665,118970,117921],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033314"}]},"cv_name":"biological_process","definition":"A signal transduction process that contributes to a DNA replication checkpoint, that prevents the initiation of nuclear division until DNA replication is complete, thereby ensuring that progeny inherit a full complement of the genome.","definition_xrefs":["PMID:12537518","GOC:curators","PMID:11728327","GOC:rn"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA integrity checkpoint signaling","termid":"GO:0031570"}],"gene_count":17,"genes_by_uniquename":{"SJAG_00364":null,"SJAG_01010":null,"SJAG_01044":null,"SJAG_01076":null,"SJAG_01205":null,"SJAG_01605":null,"SJAG_02074":null,"SJAG_02098":null,"SJAG_02266":null,"SJAG_02563":null,"SJAG_02771":null,"SJAG_03026":null,"SJAG_03160":null,"SJAG_03695":null,"SJAG_03927":null,"SJAG_04287":null,"SJAG_04671":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"negatively_regulates","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052","GO:0007049"],"is_obsolete":false,"name":"DNA replication checkpoint signaling","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0072437"],"synonyms":[{"name":"DNA replication checkpoint","type":"exact"},{"name":"signal transduction involved in DNA replication checkpoint","type":"exact"}],"termid":"GO:0000076","terms_by_termid":{"GO:0033314":null,"GO:0033315":null}}


