# terms

id: PR:O94353
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- apq12 gene.","definition_xrefs":["UniProtKB:O94353","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":"nuclear membrane organization protein apq12 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC428.04","synonyms":[{"name":"Spom972h-apq12","type":"exact"}],"termid":"PR:O94353"}


id: PBO:0004472
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L5","termid":"PBO:0004472"}


id: PBO:0004728
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dolichol-phosphate mannosyltransferase subunit 3","termid":"PBO:0004728"}


id: PBO:0074881
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 60","termid":"PBO:0074881"}


id: MONDO:0971034
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A thyroid gland carcinoma that is characterized by the presence of cribriform, trabecular, follicular, papillary, and solid growth patterns and squamoid morulae formation.","definition_xrefs":["DOID:0081458"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thyroid gland carcinoma","termid":"MONDO:0015075"}],"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":"thyroid gland cribriform morular carcinoma","secondary_identifiers":["UMLS:C4289734","MEDGEN:927266"],"termid":"MONDO:0971034","xrefs":{"Monarch":{"xref_id":"0971034"}}}


id: PBO:0081913
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 880","termid":"PBO:0081913"}


id: PBO:0002333
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3.5.1.41","termid":"PBO:0002333"}


id: PBO:0031197
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-resistance_to_canavanine","termid":"PBO:0031197"}


id: SO:1000040
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A tandem duplication where the individual regions are not in the same orientation.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tandem_duplication","termid":"SO:1000173"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inverted_tandem_duplication","synonyms":[{"name":"inverted tandem duplication","type":"exact"},{"name":"mirror duplication","type":"related"}],"termid":"SO:1000040"}


id: GO:0034087
data:
  {"annotated_genes":["SJAG_00796"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[74751],"is_not":false,"summary":null,"term":"GO:0034087"}]},"cv_name":"biological_process","definition":"The process in which the sister chromatids of a replicated chromosome become joined along the entire length of the chromosome during S phase during a mitotic cell cycle.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment of sister chromatid cohesion","termid":"GO:0034085"},{"relation_name":"is_a","term_name":"mitotic cell cycle process","termid":"GO:1903047"},{"relation_name":"part_of","term_name":"mitotic sister chromatid cohesion","termid":"GO:0007064"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00796":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"establishment of mitotic sister chromatid cohesion","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0034087","terms_by_termid":{"GO:0034087":null}}


id: PBO:0060833
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NEDD4 E3 ubiquitin protein ligase","termid":"PBO:0060833"}


id: MONDO:0006779
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A localized bulging or dilatation in the muscle wall of a heart (myocardium), usually in the left ventricle. Blood-filled aneurysms are dangerous because they may burst. Fibrous aneurysms interfere with the heart function through the loss of contractility. True aneurysm is bound by the vessel wall or cardiac wall. False aneurysms are hematoma caused by myocardial rupture.","definition_xrefs":["MESH:D006322"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heart disorder","termid":"MONDO:0005267"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"heart aneurysm","secondary_identifiers":["ICD10CM:I25.3","ICD9:414.19","MedDRA:10002350","DOID:9768","ICD9:414.10","SCTID:65340007","EFO:1000959","UMLS:C0018789","MEDGEN:42360","NANDO:2200234"],"synonyms":[{"name":"cardiac aneurysm","type":"exact"}],"termid":"MONDO:0006779","xrefs":{"Monarch":{"xref_id":"0006779"}}}


id: PBO:0090668
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TPR domain protein, DNAJC7 family","termid":"PBO:0090668"}


id: MONDO:0034204
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"congenital sodium diarrhea","termid":"MONDO:0015170"}],"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":"syndromic congenital sodium diarrhea","secondary_identifiers":["Orphanet:563708","MEDGEN:1805017","UMLS:C5680120","GARD:22262"],"termid":"MONDO:0034204","xrefs":{"Monarch":{"xref_id":"0034204"}}}


id: GO:0070873
data:
  {"annotated_genes":["SJAG_00963","SJAG_01376"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[78630,76913],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045719"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways involving glycogen.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of polysaccharide metabolic process","termid":"GO:0032881"},{"relation_name":"is_a","term_name":"regulation of generation of precursor metabolites and energy","termid":"GO:0043467"},{"relation_name":"regulates","term_name":"glycogen metabolic process","termid":"GO:0005977"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00963":null,"SJAG_01376":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006091"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0008150","GO:0006091","GO:0005975"],"is_obsolete":false,"name":"regulation of glycogen metabolic process","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"regulation of glycogen metabolism","type":"exact"}],"termid":"GO:0070873","terms_by_termid":{"GO:0045719":null}}


id: GO:0071107
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 parathyroid hormone stimulus.","definition_xrefs":["GOC:yaf","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to hormone","termid":"GO:0009725"}],"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 parathyroid hormone","synonyms":[{"name":"response to parathyroid hormone stimulus","type":"exact"}],"termid":"GO:0071107"}


id: PBO:0073520
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SH3 domain binding protein 2","termid":"PBO:0073520"}


id: GO:0014814
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regrowth of axons following their loss or damage at the neuromuscular junction. Motor axons regenerate after injury and they form neuro-muscular junctions with skeletal myofibers similar to normal ones.","definition_xrefs":["GOC:mtg_muscle","GOC:ef"],"direct_ancestors":[{"relation_name":"is_a","term_name":"axon regeneration","termid":"GO:0031103"}],"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":"axon regeneration at neuromuscular junction","termid":"GO:0014814"}


id: PBO:0078727
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Met (anticodon CAT) 3-1","termid":"PBO:0078727"}


id: MONDO:0009693
data:
  {"annotated_genes":["SJAG_02527"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87081],"is_not":false,"summary":null,"term":"MONDO:0009693"}]},"cv_name":"mondo","definition":"A bone marrow-based plasma cell neoplasm characterized by a serum monoclonal protein and skeletal destruction with osteolytic lesions, pathological fractures, bone pain, hypercalcemia, and anemia. Clinical variants include non-secretory myeloma, smoldering myeloma, indolent myeloma, and plasma cell leukemia. (WHO, 2001)","definition_xrefs":["NCIT:C3242"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune system cancer","termid":"MONDO:0000621"},{"relation_name":"is_a","term_name":"plasma cell neoplasm","termid":"MONDO:0004959"},{"relation_name":"is_a","term_name":"myeloid neoplasm","termid":"MONDO:0005170"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02527":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0004992","MONDO:0005570"],"is_obsolete":false,"name":"plasma cell myeloma","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:9538","NORD:1469","MEDGEN:10122","EFO:0001378","ICD9:203.0","UMLS:C0026764","ICD10CM:C90.0","ONCOTREE:PCM","GARD:7108","MedDRA:10028228","icd11.foundation:1582389689","ICDO:9732/3","MESH:D009101","OMIM:254500","Orphanet:29073","icd11.foundation:526287100"],"synonyms":[{"name":"Al amyloidosis","type":"related"},{"name":"Kahler disease","type":"exact"},{"name":"Kahler's disease","type":"exact"},{"name":"Multiple Myeloma","type":"exact"},{"name":"amyloidosis, systemic","type":"related"},{"name":"medullary plasmacytoma","type":"exact"},{"name":"multiple myeloma","type":"exact"},{"name":"multiple myeloma, resistance to, Somatic mutation","type":"exact"},{"name":"multiple myeloma, susceptibility to, Somatic mutation","type":"exact"},{"name":"multiple myeloma/plasma cell myeloma","type":"exact"},{"name":"myeloid neoplasm of plasma cell","type":"exact"},{"name":"myeloma","type":"exact"},{"name":"myeloma - multiple","type":"related"},{"name":"myeloma, multiple","type":"exact"},{"name":"myeloma, plasma cell, malignant","type":"exact"},{"name":"myelomatosis","type":"exact"},{"name":"plasma cell myeloid neoplasm","type":"exact"},{"name":"plasma cell myeloma","type":"exact"}],"termid":"MONDO:0009693","terms_by_termid":{"MONDO:0009693":null},"xrefs":{"Monarch":{"xref_id":"0009693"}}}


id: PBO:0063393
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PDCD6IP divergent transcript","termid":"PBO:0063393"}


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: MONDO:0025425
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A contagious disease caused by canine adenovirus (adenoviruses, canine) infecting the liver, the eye, the kidney, and other organs in dogs, other canids, and bears. Symptoms include fever; edema; vomiting; and diarrhea.","definition_xrefs":["MESH:D006522"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dog disease","termid":"MONDO:0024919"},{"relation_name":"is_a","term_name":"hepatitis, viral, animal","termid":"MONDO:0025085"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hepatitis, infectious canine","synonyms":[{"name":"Hepatitides, canine infectious","type":"related"},{"name":"Hepatitides, infectious canine","type":"related"},{"name":"Hepatitis, canine infectious","type":"related"},{"name":"canine Hepatitides, infectious","type":"related"},{"name":"canine Hepatitis, infectious","type":"related"},{"name":"canine infectious Hepatitides","type":"related"},{"name":"canine infectious Hepatitis","type":"related"},{"name":"infectious Hepatitides, canine","type":"related"},{"name":"infectious Hepatitis, canine","type":"related"},{"name":"infectious canine Hepatitides","type":"related"},{"name":"infectious canine Hepatitis","type":"related"}],"termid":"MONDO:0025425","xrefs":{"Monarch":{"xref_id":"0025425"}}}


id: MONDO:0020401
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital unguarded mitral orifice is a rare, congenital, mitral valve malformation characterized by complete absence of mitral valve leaflets and tensor apparatus at the mitral annulus, which can present clinically with cyanosis, heart murmur, electrocardiogram abnormalities, mild cardiomegaly, or congestive heart failure. Association with heterotaxy, discordant atrioventricular connections, double-outlet right ventricle, pulmonary atresia or stenosis, thin left ventricular wall, and hypoplastic left heart syndrome has been reported.","definition_xrefs":["Orphanet:99060"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital mitral valve insufficiency and/or stenosis","termid":"MONDO:0019817"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital unguarded mitral orifice","secondary_identifiers":["GARD:19627","MEDGEN:576490","icd11.foundation:1824064279","UMLS:C0344769"],"termid":"MONDO:0020401","xrefs":{"Monarch":{"xref_id":"0020401"}}}


id: GO:0034051
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the hypersensitive response in a plant.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of plant-type hypersensitive response","termid":"GO:0010363"},{"relation_name":"is_a","term_name":"negative regulation of programmed cell death","termid":"GO:0043069"},{"relation_name":"is_a","term_name":"negative regulation of innate immune response","termid":"GO:0045824"},{"relation_name":"negatively_regulates","term_name":"plant-type hypersensitive response","termid":"GO:0009626"}],"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 plant-type hypersensitive response","synonyms":[{"name":"down regulation of plant-type hypersensitive response","type":"exact"},{"name":"down-regulation of plant-type hypersensitive response","type":"exact"},{"name":"downregulation of plant-type hypersensitive response","type":"exact"},{"name":"inhibition of plant-type hypersensitive response","type":"narrow"},{"name":"negative regulation of HR","type":"exact"},{"name":"negative regulation of HR-PCD","type":"exact"},{"name":"negative regulation of plant hypersensitive response","type":"exact"}],"termid":"GO:0034051"}


id: GO:0042863
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving the siderochrome pyochelin (2-(2-o-hydroxyphenyl-2-thiazolin-4-yl)-3-methylthiazolidine-4-carboxylic acid).","definition_xrefs":["GOC:jl","PMID:6794030"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfur compound metabolic process","termid":"GO:0006790"},{"relation_name":"is_a","term_name":"siderophore metabolic process","termid":"GO:0009237"},{"relation_name":"is_a","term_name":"phenol-containing compound metabolic process","termid":"GO:0018958"},{"relation_name":"is_a","term_name":"carboxylic acid metabolic process","termid":"GO:0019752"}],"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:0006790"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0019748","GO:0006790"],"is_obsolete":false,"name":"pyochelin metabolic process","synonyms":[{"name":"pyochelin metabolism","type":"exact"}],"termid":"GO:0042863"}


id: PBO:0048046
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"follistatin like 4","termid":"PBO:0048046"}


id: PBO:0050542
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypoxanthine phosphoribosyltransferase 1 pseudogene 3","termid":"PBO:0050542"}


id: PBO:0052283
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lysine demethylase 8","termid":"PBO:0052283"}


id: PBO:0051035
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IGF like family member 3","termid":"PBO:0051035"}


id: GO:0018278
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The deamination of N-terminal peptidyl-threonine to form peptidyl-2-oxobutanoic acid.","definition_xrefs":["RESID:AA0129"],"gene_count":0,"genotype_count":0,"name":"obsolete N-terminal peptidyl-threonine deamination (obsolete GO:0018278)","termid":"GO:0018278"}


id: GO:1990624
data:
  {"annotated_genes":["SJAG_03629","SJAG_02786"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[91959,97004],"is_not":false,"summary":null,"term":"GO:1990624"}]},"cv_name":"molecular_function","definition":"Binds to and stops, prevents or reduces the activity of a guanyl nucleotide exchange factor.","definition_xrefs":["GOC:vw","PMID:25635048"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme inhibitor activity","termid":"GO:0004857"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02786":null,"SJAG_03629":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0004857"},{"rel_name":"is_a","termid":"GO:0140678"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0030234"}],"interesting_parent_ids":["GO:0098772","GO:0030234","GO:0004857","GO:0140678","GO:0003674"],"is_obsolete":false,"name":"guanyl nucleotide exchange factor inhibitor activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1990624","terms_by_termid":{"GO:1990624":null}}


id: PBO:0085175
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Omega-class glutathione transferase; induced under oxidative stress; putative peroxisomal localization","termid":"PBO:0085175"}


id: MONDO:0022948
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Fanconi renotubular syndrome","termid":"MONDO:0001083"}],"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":"Deal Barratt Dillon syndrome","secondary_identifiers":["GARD:1717","MEDGEN:444139","UMLS:C2931773","MESH:C538206"],"synonyms":[{"name":"Fanconi syndrome, ichthyosis, dysmorphism, jaundice and diarrhea","type":"related"},{"name":"Fanconi syndrome, ichthyosis, dysmorphism, jaundice and diarrhoea","type":"related"}],"termid":"MONDO:0022948","xrefs":{"Monarch":{"xref_id":"0022948"}}}


id: GO:0009780
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An NADPH regeneration process that contributes to the light reactions of photosynthesis. The light reactions of photosynthesis use energy from photons to generate high-energy electrons. These electrons are used directly to reduce NADP+ to NADPH. NADPH is a relatively stable molecule and can pass on its hydrogen atom to other molecules in chemical reactions.","definition_xrefs":["ISBN:0816017360","GOC:jid","ISBN:0716746840"],"direct_ancestors":[{"relation_name":"is_a","term_name":"NADPH regeneration","termid":"GO:0006740"},{"relation_name":"part_of","term_name":"photosynthesis, light reaction","termid":"GO:0019684"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0006091"},{"rel_name":"part_of","termid":"GO:0006091"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006091","GO:0044281","GO:0055086","GO:0008150"],"is_obsolete":false,"name":"photosynthetic NADP+ reduction","termid":"GO:0009780"}


id: PBO:0066447
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"required for excision 1-B domain containing","termid":"PBO:0066447"}


id: PR:Q9USN5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- gdh2 gene.","definition_xrefs":["UniProtKB:Q9USN5","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":"NAD-specific glutamate dehydrogenase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC132.04c","synonyms":[{"name":"NAD-GDH (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-gdh2","type":"exact"}],"termid":"PR:Q9USN5"}


id: MONDO:1011152
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Anodontia that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anodontia, non-human animal","termid":"MONDO:1010293"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anodontia, domestic cat","secondary_identifiers":["OMIA:000048-9685"],"termid":"MONDO:1011152","xrefs":{"Monarch":{"xref_id":"1011152"}}}


id: GO:0001666
data:
  {"annotated_genes":["SJAG_01150","SJAG_03345","SJAG_04018","SJAG_00221","SJAG_00642","SJAG_01585"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[111509,109651,101008,116793],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071456"},{"annotations":[89009,116201],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1900039"}]},"cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a stimulus indicating lowered oxygen tension. Hypoxia, defined as a decline in O2 levels below normoxic levels of 20.8 - 20.95%, results in metabolic adaptation at both the cellular and organismal level.","definition_xrefs":["GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to stress","termid":"GO:0006950"},{"relation_name":"is_a","term_name":"response to decreased oxygen levels","termid":"GO:0036293"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00221":null,"SJAG_00642":null,"SJAG_01150":null,"SJAG_01585":null,"SJAG_03345":null,"SJAG_04018":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to hypoxia","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"response to hypoxic stress","type":"exact"},{"name":"response to intermittent hypoxia","type":"narrow"},{"name":"response to lowered oxygen tension","type":"exact"},{"name":"response to sustained hypoxia","type":"narrow"}],"termid":"GO:0001666","terms_by_termid":{"GO:0071456":null,"GO:1900039":null}}


id: PBO:0025471
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kinetochore protein, CENP-L ortholog Fta1","termid":"PBO:0025471"}


id: RO:0002476
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"c is a child nucleus of d if and only if c and d are both nuclei and parts of cells c' and d', where c' is derived from d' by mitosis and the genetic material in c is a copy of the generic material in d","direct_ancestors":[{"relation_name":"is_a","term_name":"developmentally_preceded_by","termid":"RO:0002258"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"child_nucleus_of","termid":"RO:0002476"}


id: PBO:0047247
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 238 member A","termid":"PBO:0047247"}


id: MONDO:0026170
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete genetic central nervous system malformation (obsolete MONDO:0026170)","secondary_identifiers":["Orphanet:183506"],"termid":"MONDO:0026170","xrefs":{"Monarch":{"xref_id":"0026170"}}}


id: PBO:0040515
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acyl-CoA wax alcohol acyltransferase 2","termid":"PBO:0040515"}


id: PBO:0077583
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tropomodulin 2","termid":"PBO:0077583"}


id: PBO:0114488
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial aldehyde dehydrogenase; required for growth on ethanol and conversion of acetaldehyde to acetate; phosphorylated; activity is K+ dependent; utilizes NADP+ or NAD+ equally as coenzymes; expression is glucose repressed; can substitute for cytosolic NADP-dependent aldehyde dehydrogenase when directed to the cytosol; polymerizes into filaments in meiotic cells; human homolog ALDH2 can complement yeast ald4 mutant","termid":"PBO:0114488"}


id: PBO:0047992
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FSHD region gene 2 family member I, pseudogene","termid":"PBO:0047992"}


id: PBO:0034428
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_level_of_iron_ion_starvation-induced_proteins_during_glutathione_starvation","termid":"PBO:0034428"}


id: GO:0036499
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals mediated by the endoplasmic reticulum membrane stress sensor PERK (PKR-like ER kinase). Begins with activation of PERK in response to endoplasmic reticulum (ER) stress and ends with regulation of a downstream cellular process, e.g. transcription. The main substrate of PERK is the translation initiation factor eIF2alpha. Serine-phosphorylation of eIF2alpha by PERK inactivates eIF2alpha and inhibits general protein translation. In addition, eIF2alpha phosphorylation preferentially increases the translation of selective mRNAs such as ATF4 (activating transcription factor 4), which up regulates a subset of UPR genes required to restore folding capacity.","definition_xrefs":["GOC:PARL","PMID:22013210","PMID:27629041","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ER-nucleus signaling pathway","termid":"GO:0006984"},{"relation_name":"is_a","term_name":"endoplasmic reticulum unfolded protein response","termid":"GO:0030968"},{"relation_name":"is_a","term_name":"integrated stress response signaling","termid":"GO:0140467"}],"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":"PERK-mediated unfolded protein response","secondary_identifiers":["Reactome:R-HSA-381042"],"synonyms":[{"name":"EIF2AK3-mediated unfolded protein response","type":"related"},{"name":"PERK branch of UPR","type":"exact"},{"name":"PERK signal transduction pathway","type":"broad"},{"name":"PERK signaling in response to endoplasmic reticulum stress","type":"related"},{"name":"PKR-like ER kinase signal transduction","type":"exact"},{"name":"UPR signaling by PERK stress sensor","type":"exact"},{"name":"endoplasmic reticulum unfolded protein response; PERK signaling","type":"exact"},{"name":"eukaryotic translation initiation factor 2-alpha kinase 3-mediated unfolded protein response","type":"related"}],"termid":"GO:0036499"}


id: MONDO:0000734
data:
  {"annotated_genes":["SJAG_02165","SJAG_00156"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86677],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010477"},{"annotations":[86289],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011365"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"blepharophimosis - intellectual disability syndrome","termid":"MONDO:0017393"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00156":null,"SJAG_02165":null},"genotype_count":0,"is_obsolete":false,"name":"Ohdo syndrome and variants","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0060289"],"synonyms":[{"name":"Ohdo blepharophimosis syndrome","type":"narrow"},{"name":"Ohdo syndrome","type":"related"}],"termid":"MONDO:0000734","terms_by_termid":{"MONDO:0010477":null,"MONDO:0011365":null},"xrefs":{"Monarch":{"xref_id":"0000734"}}}


id: MONDO:0018306
data:
  {"annotated_genes":["SJAG_03011","SJAG_00938"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86780,86781],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008962"}]},"cv_name":"mondo","definition":"Griscelli syndrome (GS) is characterized by silvery gray sheen of the hair and hypopigmentation of the skin which can be associated to neurological impairment (type 1), immunodeficiency (type 2) or be isolated (type 3).","definition_xrefs":["Orphanet:381"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic oculocutaneous albinism","termid":"MONDO:0017305"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00938":null,"SJAG_03011":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005093"],"is_obsolete":false,"name":"Griscelli syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:585090","NANDO:1200640","GARD:10913","UMLS:C0398794","OMIMPS:214450","SCTID:37548006","ICD10CM:E70.3","DOID:0060831","ICD9:270.2"],"synonyms":[{"name":"ChC)diak-Higashi-like syndrome","type":"exact"},{"name":"Chédiak-Higashi-like syndrome","type":"exact"},{"name":"Ch��diak-Higashi-like syndrome","type":"exact"},{"name":"Griscelli disease","type":"related"},{"name":"Griscelli-PruniC)ras syndrome","type":"exact"},{"name":"Griscelli-Pruniéras syndrome","type":"exact"},{"name":"Griscelli-Pruni��ras syndrome","type":"exact"},{"name":"partial albinism-immunodeficiency syndrome","type":"exact"}],"termid":"MONDO:0018306","terms_by_termid":{"MONDO:0008962":null},"xrefs":{"Monarch":{"xref_id":"0018306"}}}


id: PBO:0080382
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VPS13A antisense RNA 1","termid":"PBO:0080382"}


id: GO:0018020
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The addition of a methyl group to a glutamic acid residue in a protein.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-glutamic acid methylation (obsolete GO:0018020)","termid":"GO:0018020"}


id: MONDO:0009800
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Blount disease","termid":"MONDO:0017194"}],"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":"Blount disease, adolescent","secondary_identifiers":["GARD:15217","UMLS:C3151572","OMIM:259200","MEDGEN:462922"],"synonyms":[{"name":"Blount disease, adolescent","type":"exact"},{"name":"Osteochondrosis deformans tibiae, adolescent","type":"related"},{"name":"tibia vara, adolescent","type":"related"}],"termid":"MONDO:0009800","xrefs":{"Monarch":{"xref_id":"0009800"}}}


id: GO:0016328
data:
  {"annotated_genes":["SJAG_00053","SJAG_01564","SJAG_04522","SJAG_04413","SJAG_03247","SJAG_02613"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[90158,91238,97231,107407,117343,118486],"is_not":false,"summary":null,"term":"GO:0016328"}]},"cv_name":"cellular_component","definition":"The portion of the plasma membrane at the lateral side of the cell. In epithelial cells, lateral plasma membranes are on the sides of cells which lie at the interface of adjacent cells.","definition_xrefs":["GOC:pr","GOC:hb","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"plasma membrane","termid":"GO:0005886"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00053":null,"SJAG_01564":null,"SJAG_02613":null,"SJAG_03247":null,"SJAG_04413":null,"SJAG_04522":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005886","GO:0005575"],"is_obsolete":false,"name":"lateral plasma membrane","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0016328","terms_by_termid":{"GO:0016328":null}}


id: GO:1901580
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of telomeric RNA transcription from RNA pol II promoter.","definition_xrefs":["GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of telomeric RNA transcription from RNA pol II promoter (obsolete GO:1901580)","synonyms":[{"name":"regulation of telomeric RNA transcription from Pol II promoter","type":"exact"}],"termid":"GO:1901580"}


id: PBO:0002502
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box protein Pof11","termid":"PBO:0002502"}


id: PBO:0046893
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 13 member C","termid":"PBO:0046893"}


id: PBO:0042949
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 3","termid":"PBO:0042949"}


id: PBO:0004880
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA-binding protein Cip1","termid":"PBO:0004880"}


id: PBO:0039533
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ANKRD34C antisense RNA 1","termid":"PBO:0039533"}


id: PBO:0060638
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear receptor coactivator 1","termid":"PBO:0060638"}


id: GO:0051961
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of nervous system development, the origin and formation of nervous tissue.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of developmental process","termid":"GO:0051093"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"is_a","term_name":"regulation of nervous system development","termid":"GO:0051960"},{"relation_name":"negatively_regulates","term_name":"nervous system development","termid":"GO:0007399"}],"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 nervous system development","synonyms":[{"name":"down regulation of nervous system development","type":"exact"},{"name":"down-regulation of nervous system development","type":"exact"},{"name":"downregulation of nervous system development","type":"exact"},{"name":"inhibition of nervous system development","type":"narrow"}],"termid":"GO:0051961"}


id: GO:0106016
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the inflammatory response to wounding.","definition_xrefs":["GOC:BHF_miRNA","GOC:BHF","GOC:rph","PMID:26022821"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of inflammatory response","termid":"GO:0050729"},{"relation_name":"is_a","term_name":"regulation of inflammatory response to wounding","termid":"GO:0106014"},{"relation_name":"is_a","term_name":"positive regulation of response to wounding","termid":"GO:1903036"},{"relation_name":"positively_regulates","term_name":"inflammatory response to wounding","termid":"GO:0090594"}],"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 inflammatory response to wounding","termid":"GO:0106016"}


id: PBO:0005848
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aspartate semialdehyde dehydrogenase (predicted)","termid":"PBO:0005848"}


id: GO:0070269
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A gasdermin-dependent inflammatory response that is associated with the generation of pyrogenic mediators such as IL-1beta and IL-18. Gasdermins are activated by caspase-1 or caspase-4/11, or by certain granzymes. In some, but not all cells, it can lead to pyroptotic programmed cell death.","definition_xrefs":["PMID:18846107","PMID:21760595","PMID:33883744"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inflammatory response","termid":"GO:0006954"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"pyroptotic inflammatory response","secondary_identifiers":["Reactome:R-HSA-5620971"],"synonyms":[{"name":"pyroptosis","type":"broad"}],"termid":"GO:0070269"}


id: MONDO:0007470
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"This syndrome is characterized by multiple doughnut-shaped hyperostotic or osteosclerotic lesions of the calvaria.","definition_xrefs":["Orphanet:85192"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with decreased bone density (obsolete MONDO:0019704)","termid":"MONDO:0019704"},{"relation_name":"is_a","term_name":"osteogenesis imperfecta and a reduction of bone mineral density.","termid":"MONDO:0800064"}],"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":"calvarial doughnut lesions-bone fragility syndrome","secondary_identifiers":["DOID:0080721","MESH:C565089","GARD:16739","UMLS:C1852022","MEDGEN:377572","SCTID:720598005","OMIM:126550"],"synonyms":[{"name":"calvarial doughnut lesions with bone fragility with or without spondylometaphyseal dysplasia","type":"exact"},{"name":"doughnut lesions of skull, familial","type":"related"},{"name":"familial doughnut lesions of skull","type":"exact"}],"termid":"MONDO:0007470","xrefs":{"Monarch":{"xref_id":"0007470"}}}


id: PBO:0081782
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 709","termid":"PBO:0081782"}


id: PBO:0084496
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Meiosis-specific protein involved in synaptonemal complex assembly; implicated in regulation of crossover formation; required for sporulation","termid":"PBO:0084496"}


id: PBO:0073326
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serpin family A member 2 (gene/pseudogene)","termid":"PBO:0073326"}


id: MONDO:0004699
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-Hodgkin or Hodgkin lymphoma that arises from any part of the digestive system, with the bulk of the disease localized to that site.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"digestive system cancer","termid":"MONDO:0002516"},{"relation_name":"is_a","term_name":"lymphoma","termid":"MONDO:0005062"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0005570","MONDO:0004992"],"is_obsolete":false,"name":"gastrointestinal lymphoma","secondary_identifiers":["SCTID:449072004","DOID:903","NCIT:C38162","MEDGEN:148147","ICD9:202.80","UMLS:C0740372"],"synonyms":[{"name":"digestive system lymphoma","type":"exact"},{"name":"gastrointestinal lymphoma","type":"exact"},{"name":"lymphoma of digestive system","type":"exact"},{"name":"primary digestive system lymphoma","type":"exact"},{"name":"primary gastrointestinal lymphoma","type":"exact"}],"termid":"MONDO:0004699","xrefs":{"Monarch":{"xref_id":"0004699"}}}


id: PBO:0018066
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"threonine ammonia-lyase Tda1","termid":"PBO:0018066"}


id: PR:O42914
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- oga1 gene.","definition_xrefs":["UniProtKB:O42914","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 C16A3.08c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC16A3.08c","synonyms":[{"name":"Spom972h-oga1","type":"exact"}],"termid":"PR:O42914"}


id: MONDO:0008097
data:
  {"annotated_genes":["SJAG_03453"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85639],"is_not":false,"summary":null,"term":"MONDO:0008097"}]},"cv_name":"mondo","definition":"Linear nevus sebaceous syndrome (LNSS) is characterized by the association of a large sebaceous nevus, usually appearing on the face or on the scalp, with a broad spectrum of abnormalities that may affect every organ system, including the central nervous system (brain neoplasms, hemimegalencephaly and lateral ventricle enlargement).","definition_xrefs":["Orphanet:2612"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hamartoma","termid":"MONDO:0006499"},{"relation_name":"is_a","term_name":"developmental defect during embryogenesis","termid":"MONDO:0019755"},{"relation_name":"is_a","term_name":"palpebral nevus","termid":"MONDO:0020179"},{"relation_name":"is_a","term_name":"hereditary skin disorder","termid":"MONDO:0100118"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03453":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005328"],"is_obsolete":false,"name":"linear nevus sebaceous syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1646345","DOID:0111530","NCIT:C4678","OMIM:163200","GARD:10291","NORD:1692","UMLS:C4552097"],"synonyms":[{"name":"Epidermal Nevus syndrome, formerly","type":"related"},{"name":"JNP","type":"related"},{"name":"Jadassohn Nevus phakomatosis","type":"related"},{"name":"Jadassohn nevus phakomatosis","type":"related"},{"name":"Nevus Sebaceus Syndrome","type":"exact"},{"name":"Nevus sebaceous of Jadassohn","type":"exact"},{"name":"Nevus sebaceus of Jadassohn","type":"exact"},{"name":"Nevus sebaceus syndrome","type":"exact"},{"name":"SCHIMMELPENNING-FEUERSTEIN-MIMS syndrome","type":"related"},{"name":"SFM","type":"related"},{"name":"SFM syndrome","type":"related"},{"name":"Schimmelpenning Feuerstein Mims syndrome","type":"related"},{"name":"Schimmelpenning syndrome","type":"exact"},{"name":"Schimmelpenning-Feuerstein-Mims syndrome, somatic mosaic","type":"exact"},{"name":"Sfm syndrome","type":"related"},{"name":"Solomon syndrome","type":"exact"},{"name":"epidermal nevus syndrome","type":"related"},{"name":"linear sebaceous Nevus","type":"exact"},{"name":"linear sebaceous Nevus syndrome","type":"related"},{"name":"organoid Nevus","type":"exact"},{"name":"organoid Nevus phakomatosis","type":"related"},{"name":"organoid nevus phakomatosis","type":"related"},{"name":"organoid nevus syndrome","type":"exact"},{"name":"sebaceous Nevus syndrome, linear","type":"related"},{"name":"sebaceous nevus syndrome linear","type":"related"}],"termid":"MONDO:0008097","terms_by_termid":{"MONDO:0008097":null},"xrefs":{"Monarch":{"xref_id":"0008097"}}}


id: PBO:0046737
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exonuclease 3'-5' domain containing 3","termid":"PBO:0046737"}


id: GO:0044511
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that begins with venom being forced into an organism by the bite or sting of another organism, and ends with the resultant modulation of receptor activity in of the bitten organism.","definition_xrefs":["GOC:fj","GOC:jl","PMID:8405712"],"direct_ancestors":[{"relation_name":"is_a","term_name":"envenomation resulting in modulation of process in another organism","termid":"GO:0035738"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"envenomation resulting in modulation of receptor activity in another organism","synonyms":[{"name":"envenomation resulting in modulation of receptor activity in other organism","type":"exact"}],"termid":"GO:0044511"}


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


id: PR:Q06182
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- swi10 gene.","definition_xrefs":["UniProtKB:Q06182","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":"mating-type switching protein swi10 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC4F6.15c","synonyms":[{"name":"Spom972h-swi10","type":"exact"}],"termid":"PR:Q06182"}


id: PR:000027845
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- dma1 gene or a 1:1 ortholog thereof.","definition_xrefs":["PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein","termid":"PR:000000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"E3 ubiquitin-protein ligase dma1","synonyms":[{"name":"dma1","type":"exact"}],"termid":"PR:000027845"}


id: MONDO:0700263
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any type 1 interferonopathies in which the cause of the disease is a variation in the RNU7-1 gene. Individuals with variants in RNUF7-1 can present with a variety of phenotypes, including Aicardi-Goutieres syndrome.","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disorder of connective tissue","termid":"MONDO:0023603"},{"relation_name":"is_a","term_name":"type 1 interferonopathy","termid":"MONDO:0700264"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNU7-1-related type 1 interferonopathy","termid":"MONDO:0700263","xrefs":{"Monarch":{"xref_id":"0700263"}}}


id: PBO:0087745
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the SWI/SNF chromatin remodeling complex; SWI/SNF regulates transcription by remodeling chromosomes; contains SANT domain that is required for SWI/SNF assembly; is essential for displacement of histone H2A-H2B dimers during ATP-dependent remodeling; required for transcription of many genes, including ADH1, ADH2, GAL1, HO, INO1 and SUC2; relocates to the cytosol under hypoxic conditions","termid":"PBO:0087745"}


id: PBO:0071713
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L39 pseudogene 11","termid":"PBO:0071713"}


id: GO:0043734
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the oxidative demethylation of N1-methyladenine and N3-methylcytosine in DNA, with concomitant decarboxylation of 2-oxoglutarate and releases oxidized methyl group on N1-methyladenine and N3-methylcytosine as formaldehyde.","definition_xrefs":["PMID:19786499"],"gene_count":0,"genotype_count":0,"name":"obsolete DNA-N1-methyladenine dioxygenase activity (obsolete GO:0043734)","synonyms":[{"name":"AlkB","type":"narrow"},{"name":"alpha-ketoglutarate-dependent dioxygenase","type":"narrow"}],"termid":"GO:0043734"}


id: MONDO:0018343
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial periodic paralysis","termid":"MONDO:0000995"},{"relation_name":"is_a","term_name":"mitochondrial oxidative phosphorylation disorder","termid":"MONDO:0016387"},{"relation_name":"is_a","term_name":"hereditary neuromuscular disease","termid":"MONDO:0100546"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005066"],"is_obsolete":false,"name":"periodic paralysis with later-onset distal motor neuropathy","secondary_identifiers":["Orphanet:397750","UMLS:C4751573","MEDGEN:1670241","GARD:21634"],"termid":"MONDO:0018343","xrefs":{"Monarch":{"xref_id":"0018343"}}}


id: GO:0065010
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Organized structure of distinctive morphology and function, bounded by a lipid bilayer membrane and occurring outside the cell.","definition_xrefs":["GOC:isa_complete"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane-bounded organelle","termid":"GO:0043227"},{"relation_name":"is_a","term_name":"extracellular organelle","termid":"GO:0043230"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005576"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005576"],"is_obsolete":false,"name":"extracellular membrane-bounded organelle","synonyms":[{"name":"extracellular membrane-enclosed organelle","type":"exact"}],"termid":"GO:0065010"}


id: GO:0034969
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of a histone by addition of a methyl group to an arginine residue.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete histone arginine methylation (obsolete GO:0034969)","termid":"GO:0034969"}


id: PBO:0084571
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Membrane protein involved in zinc ion homeostasis; member of the four-protein IZH family; transcription is regulated directly by Zap1p, expression induced by zinc deficiency and fatty acids; deletion increases sensitivity to elevated zinc; IZH1 has a paralog, IZH4, that arose from the whole genome duplication","termid":"PBO:0084571"}


id: GO:0047243
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a flavanone + UDP-D-glucose = a flavanone 7-O-beta-D-glucoside + UDP.","definition_xrefs":["MetaCyc:2.4.1.185-RXN","EC:2.4.1.185"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glucosyltransferase activity","termid":"GO:0035251"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016740","GO:0003674","GO:0016757"],"is_obsolete":false,"name":"flavanone 7-O-beta-glucosyltransferase activity","synonyms":[{"name":"UDP-glucose:flavanone 7-O-beta-D-glucosyltransferase activity","type":"related"},{"name":"UDPglucose:flavanone 7-O-beta-D-glucosyltransferase activity","type":"related"},{"name":"hesperetin 7-O-glucosyl-transferase activity","type":"related"},{"name":"naringenin 7-O-glucosyltransferase activity","type":"related"},{"name":"uridine diphosphoglucose-flavanone 7-O-glucosyltransferase activity","type":"related"}],"termid":"GO:0047243"}


id: FYPO:0006902
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell population phenotype in which a smaller than normal proportion of cells in the population remains viable after exposure to 4-nitroquinoline N-oxide.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal phenotype","termid":"FYPO:0001985"},{"relation_name":"is_a","term_name":"cell population viability","termid":"FYPO:0002057"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002057"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0002057","FYPO:0001985"],"is_obsolete":false,"name":"loss of viability following cellular response to 4-nitroquinoline N-oxide","synonyms":[{"name":"decreased viability following cellular response to 4-nitroquinoline N-oxide","type":"exact"},{"name":"loss of cell population viability following cellular response to 4-nitroquinoline N-oxide","type":"exact"},{"name":"loss of viability following 4-NQO exposure","type":"exact"},{"name":"loss of viability following cellular response to 4-NQO","type":"exact"},{"name":"reduced viability following cellular response to 4-nitroquinoline N-oxide","type":"related"}],"termid":"FYPO:0006902"}


id: PBO:0031513
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_molecular_function","termid":"PBO:0031513"}


id: PBO:0080495
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"von Willebrand factor C and EGF domains","termid":"PBO:0080495"}


id: PR:Q10156
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- lkh1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q10156"],"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":"dual specificity protein kinase lkh1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1D4.11c","synonyms":[{"name":"Spom972h-lkh1","type":"exact"}],"termid":"PR:Q10156"}


id: MONDO:0019464
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Heavy-chain diseases (HCDs) are rare monoclonal lymphoplasma-cell proliferative disorders involving B cells and are characterized by the synthesis of truncated heavy chains without associated light chains.","definition_xrefs":["Orphanet:86864"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"type IV hypersensitivity disease","termid":"MONDO:0002459"},{"relation_name":"is_a","term_name":"plasma cell neoplasm","termid":"MONDO:0004959"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"heavy chain disease","secondary_identifiers":["ICD10CM:C88.3","EFO:1001341","DOID:0060125","ICD9:273.2","ICDO:9762/3","MedDRA:10019350","UMLS:C0018852","MESH:D006362","SCTID:68979007","MEDGEN:5469","NCIT:C3082","ICD10CM:C88.2","GARD:19074"],"synonyms":[{"name":"HCD","type":"exact"},{"name":"heavy chain disease","type":"exact"}],"termid":"MONDO:0019464","xrefs":{"Monarch":{"xref_id":"0019464"}}}


id: PBO:0116274
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cytosolic gamma-glutamyl kinase; catalyzes the first step in proline biosynthesis; required for nitrogen starvation-induced ribophagy but not for nonselective autophagy; PRO1 has a paralog, YHR033W, that arose from the whole genome duplication","termid":"PBO:0116274"}


id: GO:0001079
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A transcription regulation process in which the presence of one nitrogen source leads to the modulation of the frequency, rate, or extent of transcription, from an RNA polymerase II promoter, of specific genes involved in the metabolism of other nitrogen sources.","definition_xrefs":["PMID:19104072","GOC:mah","GOC:txnOH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transcription by RNA polymerase II","termid":"GO:0006357"},{"relation_name":"is_a","term_name":"nitrogen catabolite regulation of transcription","termid":"GO:0090293"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006355"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006351"}],"interesting_parent_ids":["GO:0006351","GO:0010467","GO:0008150","GO:0006355"],"is_obsolete":false,"name":"nitrogen catabolite regulation of transcription from RNA polymerase II promoter","synonyms":[{"name":"regulation of transcription from RNA polymerase II promoter by nitrogen catabolites","type":"exact"}],"termid":"GO:0001079"}


id: GO:1905914
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of calcium ion export across the plasma membrane.","definition_xrefs":["GOC:BHF","PMID:22362515","GOC:rph","GOC:TermGenie","GO_REF:0000058","GOC:BHF_miRNA"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of calcium ion transmembrane transport","termid":"GO:1904427"},{"relation_name":"is_a","term_name":"regulation of calcium ion export across plasma membrane","termid":"GO:1905912"},{"relation_name":"positively_regulates","term_name":"calcium ion export across plasma membrane","termid":"GO:1990034"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0055085"},{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0055085","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"positive regulation of calcium ion export across plasma membrane","synonyms":[{"name":"activation of calcium ion efflux from cell","type":"narrow"},{"name":"activation of calcium ion export from cell","type":"narrow"},{"name":"positive regulation of calcium ion efflux from cell","type":"exact"},{"name":"positive regulation of calcium ion export from cell","type":"exact"},{"name":"up regulation of calcium ion efflux from cell","type":"exact"},{"name":"up regulation of calcium ion export from cell","type":"exact"},{"name":"up-regulation of calcium ion efflux from cell","type":"exact"},{"name":"up-regulation of calcium ion export from cell","type":"exact"},{"name":"upregulation of calcium ion efflux from cell","type":"exact"},{"name":"upregulation of calcium ion export from cell","type":"exact"}],"termid":"GO:1905914"}


id: MONDO:0010421
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"X-linked agammaglobulinemia (XLA) is a clinically variable form of isolated agammaglobulinemia, an inherited immunodeficiency disorder, and is characterized in affected males by recurrent bacterial infections during infancy.","definition_xrefs":["Orphanet:47"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isolated agammaglobulinemia","termid":"MONDO:0016462"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"Bruton-type agammaglobulinemia","secondary_identifiers":["SCTID:65880007","UMLS:C0221026","GARD:1033","OMIM:300755","NANDO:1200343","DOID:14179","MedDRA:10060360","MESH:C537409","MEDGEN:65123","NANDO:2200716","NCIT:C3822"],"synonyms":[{"name":"BTK deficiency","type":"exact"},{"name":"BTK-deficiency","type":"exact"},{"name":"Bruton agammaglobulinemia tyrosine kinase deficiency","type":"exact"},{"name":"Bruton type agammaglobulinemia","type":"exact"},{"name":"Bruton's Sex-linked agammaglobulinemia","type":"exact"},{"name":"Bruton's X-linked agammaglobulinemia","type":"exact"},{"name":"Bruton's agammaglobulinaemia","type":"exact"},{"name":"Bruton's agammaglobulinemia","type":"related"},{"name":"Bruton's type agammaglobulinemia","type":"exact"},{"name":"Bruton-type agammaglobulinemia","type":"exact"},{"name":"X-linked agammaglobulinemia","type":"exact"},{"name":"XLA","type":"related"},{"name":"agammaglobulinemia, BTK","type":"related"},{"name":"agammaglobulinemia, Bruton tyrosine kinase","type":"related"},{"name":"agammaglobulinemia, X-linked","type":"related"},{"name":"agammaglobulinemia, X-linked 1, X-linked recessive","type":"exact"},{"name":"agammaglobulinemia, X-linked, type 1","type":"related"},{"name":"hypogammaglobulinemia, X-linked","type":"related"},{"name":"immunodeficiency 1","type":"related"}],"termid":"MONDO:0010421","xrefs":{"Monarch":{"xref_id":"0010421"}}}


id: PATO:0000424
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000424 occurence value (obsolete PATO:0000424)","termid":"PATO:0000424"}


id: MONDO:0011243
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Grange syndrome is characterized by stenosis or occlusion of multiple arteries (including the renal, cerebral and abdominal vessels), hypertension, brachysyndactyly, syndactyly, increased bone fragility, and learning difficulties or borderline intellectual deficit. Congenital heart defects were also reported in some cases.","definition_xrefs":["Orphanet:79094"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"grange syndrome","secondary_identifiers":["OMIM:602531","GARD:16697","MESH:C566529","UMLS:C1865267","MEDGEN:355427","SCTID:717824007","icd11.foundation:729368905"],"synonyms":[{"name":"GRNG","type":"related"},{"name":"arterial occlusive disease, progressive, with hypertension, heart defects, bone fragility, and brachysyndactyly","type":"related"},{"name":"grange occlusive arterial syndrome","type":"exact"},{"name":"grange syndrome","type":"exact"},{"name":"progressive arterial occlusive disease-hypertension-heart defects-bone fragility-brachysyndactyly syndrome","type":"exact"}],"termid":"MONDO:0011243","xrefs":{"Monarch":{"xref_id":"0011243"}}}


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


id: GO:0032379
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the directed movement of lipids within cells.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of lipid transport","termid":"GO:0032370"},{"relation_name":"is_a","term_name":"regulation of intracellular lipid transport","termid":"GO:0032377"},{"relation_name":"is_a","term_name":"positive regulation of intracellular transport","termid":"GO:0032388"},{"relation_name":"positively_regulates","term_name":"intracellular lipid transport","termid":"GO:0032365"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"positive regulation of intracellular lipid transport","synonyms":[{"name":"activation of intracellular lipid transport","type":"narrow"},{"name":"stimulation of intracellular lipid transport","type":"narrow"},{"name":"up regulation of intracellular lipid transport","type":"exact"},{"name":"up-regulation of intracellular lipid transport","type":"exact"},{"name":"upregulation of intracellular lipid transport","type":"exact"}],"termid":"GO:0032379"}


id: GO:0061527
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regulated release of dopamine by a cell in which the dopamine acts as a neurotransmitter.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"axonal dopamine secretion","termid":"GO:0099124"},{"relation_name":"is_a","term_name":"catecholamine secretion, neurotransmission","termid":"GO:0160043"},{"relation_name":"part_of","term_name":"synaptic transmission, dopaminergic","termid":"GO:0001963"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"dopamine secretion, neurotransmission","termid":"GO:0061527"}


id: GO:0044856
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in which plasma membrane rafts are transported to, or maintained in, a specific location.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane organization","termid":"GO:0007009"},{"relation_name":"is_a","term_name":"membrane raft localization","termid":"GO:0051665"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0061024","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"plasma membrane raft localization","termid":"GO:0044856"}


id: GO:0043063
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of the intracellular bridge. An intracellular bridge is a direct link between the cytoplasms of sister cells that allows cells to communicate with one another.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extracellular structure organization","termid":"GO:0043062"}],"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":"intercellular bridge organization","synonyms":[{"name":"intercellular bridge organisation","type":"exact"},{"name":"intercellular bridge organization and biogenesis","type":"related"}],"termid":"GO:0043063"}


id: GO:0014876
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 injury. This process occurs as part of the regulation of muscle adaptation.","definition_xrefs":["GOC:mtg_muscle","GOC:ef"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to wounding","termid":"GO:0009611"},{"relation_name":"is_a","term_name":"response to stimulus involved in regulation of muscle adaptation","termid":"GO:0014874"}],"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 injury involved in regulation of muscle adaptation","synonyms":[{"name":"response to injury involved in regulation of muscle plasticity","type":"related"}],"termid":"GO:0014876"}


id: GO:0039022
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the pronephric duct over time, from its formation to the mature structure. The pronephric duct collects the filtrate from the pronephric tubules and opens to the exterior of the pronephric kidney.","definition_xrefs":["PMID:15647339","ZFA:0000150","XAO:0000063","GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nephric duct development","termid":"GO:0072176"},{"relation_name":"part_of","term_name":"pronephros development","termid":"GO:0048793"}],"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":"pronephric duct development","termid":"GO:0039022"}


id: GO:0061471
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process where the nuclear membrane engulfs condensed chromosomes to form karyomeres during M phase of the mitotic cell cycle.","definition_xrefs":["GOC:dph","PMID:9732278"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organelle assembly","termid":"GO:0070925"},{"relation_name":"is_a","term_name":"mitotic cell cycle process","termid":"GO:1903047"},{"relation_name":"part_of","term_name":"mitotic nuclear membrane reassembly","termid":"GO:0007084"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0061024"}],"interesting_parent_ids":["GO:0008150","GO:0044085","GO:0061024","GO:0007049"],"is_obsolete":false,"name":"karyomere assembly","termid":"GO:0061471"}


id: MONDO:0056822
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":"amyotonia congenita","secondary_identifiers":["OMIM:205000","UMLS:C0002735","MEDGEN:8042"],"synonyms":[{"name":"Oppenheim disease","type":"related"},{"name":"amyotonia congenita","type":"exact"}],"termid":"MONDO:0056822","xrefs":{"Monarch":{"xref_id":"0056822"}}}


id: PBO:0091042
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ESCRT III complex subunit Cmp7","termid":"PBO:0091042"}


id: GO:0070902
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The intramolecular conversion of uridine to pseudouridine in a mitochondrial tRNA molecule.","definition_xrefs":["GOC:mcc","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA pseudouridine synthesis","termid":"GO:0031119"},{"relation_name":"is_a","term_name":"mitochondrial tRNA modification","termid":"GO:0070900"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006399"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0140053"},{"rel_name":"is_a","termid":"GO:0010467"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0140053","GO:0010467","GO:0006399"],"is_obsolete":false,"name":"mitochondrial tRNA pseudouridine synthesis","termid":"GO:0070902"}


id: PBO:0084212
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Homocitrate synthase isozyme and functions in DNA repair; catalyzes the condensation of acetyl-CoA and alpha-ketoglutarate to form homocitrate, which is the first step in the lysine biosynthesis pathway; LYS20 has a paralog, LYS21, that arose from the whole genome duplication","termid":"PBO:0084212"}


id: PBO:0058061
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4281","termid":"PBO:0058061"}


id: PBO:0029205
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_activation_of_mitotic_cell_cycle_spindle_assembly_checkpoint","termid":"PBO:0029205"}


id: GO:0102132
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: NADP + a 3R-hydroxypimeloyl-[acp] methyl ester = NADPH + H+ + a 3-oxo-pimeloyl-[acp] methyl ester.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 3-oxo-pimeloyl-[acp] methyl ester reductase activity (obsolete GO:0102132)","termid":"GO:0102132"}


id: MONDO:0022770
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":"circumscribed cutaneous aplasia of the vertex","termid":"MONDO:0022770","xrefs":{"Monarch":{"xref_id":"0022770"}}}


id: FYECO:0000261
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which calcium chloride was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ CaCl2","synonyms":[{"name":"+ calcium chloride","type":"exact"}],"termid":"FYECO:0000261"}


id: MONDO:0013946
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the HS6ST1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Kallmann syndrome","termid":"MONDO:0018800"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypogonadotropic hypogonadism 15 with or without anosmia","secondary_identifiers":["UMLS:C3553977","DOID:0090075","MEDGEN:766891","GARD:15872","OMIM:614880"],"synonyms":[{"name":"HH15","type":"related"},{"name":"HS6ST1 hypogonadotropic hypogonadism","type":"exact"},{"name":"hypogonadotropic hypogonadism 15 with or without anosmia","type":"exact"},{"name":"hypogonadotropic hypogonadism caused by mutation in HS6ST1","type":"exact"}],"termid":"MONDO:0013946","xrefs":{"Monarch":{"xref_id":"0013946"}}}


id: GO:0070137
data:
  {"annotated_genes":["SJAG_02214","SJAG_16454"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[105933,74631],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070139"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of peptide bonds between an alpha-carboxyl group and an alpha-amino group within a small protein such as ubiquitin or a ubiquitin-like protein (e.g. APG8, ISG15, NEDD8, SUMO).","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cysteine-type endopeptidase activity","termid":"GO:0004197"},{"relation_name":"is_a","term_name":"ubiquitin-like protein peptidase activity","termid":"GO:0019783"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02214":null,"SJAG_16454":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008233"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016787","GO:0140096","GO:0003824","GO:0003674","GO:0008233"],"is_obsolete":false,"name":"ubiquitin-like protein-specific endopeptidase activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"small conjugating protein-specific endopeptidase activity","type":"exact"}],"termid":"GO:0070137","terms_by_termid":{"GO:0070139":null}}


id: PBO:0038884
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adenylate cyclase 10","termid":"PBO:0038884"}


id: GO:0005664
data:
  {"annotated_genes":["SJAG_05301","SJAG_03451","SJAG_03927","SJAG_02800","SJAG_01267","SJAG_02394"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[61107,69651,73482,74712,78411,79172],"is_not":false,"summary":null,"term":"GO:0005664"}]},"cv_name":"cellular_component","definition":"A multisubunit complex that is located at the replication origins of a chromosome in the nucleus.","definition_xrefs":["GOC:elh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"origin recognition complex","termid":"GO:0000808"},{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"},{"relation_name":"part_of","term_name":"nuclear chromosome","termid":"GO:0000228"}],"gene_count":6,"genes_by_uniquename":{"SJAG_01267":null,"SJAG_02394":null,"SJAG_02800":null,"SJAG_03451":null,"SJAG_03927":null,"SJAG_05301":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005634","GO:0005694","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"nuclear origin of replication recognition complex","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null},"synonyms":[{"name":"eukaryotic ORC","type":"exact"},{"name":"nuclear ORC","type":"exact"}],"termid":"GO:0005664","terms_by_termid":{"GO:0005664":null}}


id: PBO:0070432
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosome production factor 2 homolog pseudogene 2","termid":"PBO:0070432"}


id: MONDO:0006969
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Sialadenitis is an infection of the salivary glands. It is usually caused by a virus or bacteria. The parotid (in front ofthe ear) and submandibular (under the chin) glands are most commonly affected. Sialadenitis may be associated with pain, tenderness, redness, and gradual, localized swelling of the affected area. Sialadenitis most commonly affects the elderly and chronically ill especially those with dry mouth or who are dehydrated, but can also affected people of any age including newborn babies. Diagnosis is usually made by clinical exam but a CT scan, MRI scan or ultrasound may be done if the doctor suspects an abscess or to look for stones. Treatment may include an antibiotic (if bacterial), warm compresses, increasing fluid intake and good oral hygiene. Most salivary gland infections go away on their own or are cured with treatment. Complications are not common.","direct_ancestors":[{"relation_name":"is_a","term_name":"salivary gland disorder","termid":"MONDO:0001142"},{"relation_name":"is_a","term_name":"lymphadenitis","termid":"MONDO:0002052"}],"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":"sialadenitis","secondary_identifiers":["DOID:10303","ICD9:527.2","NCIT:C115165","MESH:D012793","UMLS:C0037023","EFO:1001179","NCIT:C26882","SCTID:42982001","MedDRA:10040627","MEDGEN:48657"],"synonyms":[{"name":"adenitis, salivary gland","type":"related"},{"name":"lymphadenitis (disease) of saliva-secreting gland","type":"exact"},{"name":"saliva-secreting gland lymphadenitis (disease)","type":"exact"},{"name":"salivary gland inflammation","type":"related"},{"name":"sialitis","type":"exact"},{"name":"sialoadenitis","type":"exact"}],"termid":"MONDO:0006969","xrefs":{"Monarch":{"xref_id":"0006969"}}}


id: PBO:0000462
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PX domain protein","termid":"PBO:0000462"}


id: PBO:0061509
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neurexin 3","termid":"PBO:0061509"}


id: GO:0032929
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of enzymatic generation of superoxide by a cell.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of superoxide anion generation","termid":"GO:0032928"},{"relation_name":"is_a","term_name":"negative regulation of reactive oxygen species metabolic process","termid":"GO:2000378"},{"relation_name":"negatively_regulates","term_name":"superoxide anion generation","termid":"GO:0042554"}],"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 superoxide anion generation","synonyms":[{"name":"down regulation of superoxide release","type":"exact"},{"name":"down-regulation of superoxide release","type":"exact"},{"name":"downregulation of superoxide release","type":"exact"},{"name":"inhibition of superoxide release","type":"narrow"},{"name":"negative regulation of superoxide release","type":"exact"}],"termid":"GO:0032929"}


id: GO:0050458
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-oxoglutarate + H2O + lauroyl-CoA = (3S,4S)-3-hydroxytetradecane-1,3,4-tricarboxylate + CoA + H+.","definition_xrefs":["RHEA:10364"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyltransferase activity, acyl groups converted into alkyl on transfer","termid":"GO:0046912"}],"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:0003674"},{"rel_name":"is_a","termid":"GO:0016746"}],"interesting_parent_ids":["GO:0003674","GO:0016746","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"decylhomocitrate synthase activity","secondary_identifiers":["KEGG_REACTION:R03859","MetaCyc:DECYLHOMOCITRATE-SYNTHASE-RXN","EC:2.3.3.4"],"synonyms":[{"name":"2-decylhomocitrate synthase activity","type":"related"},{"name":"3-hydroxytetradecane-1,3,4-tricarboxylate 2-oxoglutarate-lyase (CoA- acylating) activity","type":"related"},{"name":"3-hydroxytetradecane-1,3,4-tricarboxylate 2-oxoglutarate-lyase (CoA-acylating)","type":"related"},{"name":"dodecanoyl-CoA:2-oxoglutarate C-dodecanoyltransferase (thioester-hydrolysing, 1-carboxyundecyl-forming)","type":"related"}],"termid":"GO:0050458"}


id: GO:0047389
data:
  {"annotated_genes":["SJAG_00622"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[71231],"is_not":false,"summary":null,"term":"GO:0047389"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + L-1-glycero-3-phosphocholine = glycerol-3-phosphate + choline.","definition_xrefs":["EC:3.1.4.2","MetaCyc:3.1.4.2-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphoric diester hydrolase activity","termid":"GO:0008081"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00622":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016788"}],"interesting_parent_ids":["GO:0016788","GO:0003824","GO:0016787","GO:0003674"],"is_obsolete":false,"name":"glycerophosphocholine phosphodiesterase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-6814132","RHEA:16061"],"synonyms":[{"name":"glycerolphosphorylcholine phosphodiesterase activity","type":"related"},{"name":"glycerophosphinicocholine diesterase activity","type":"related"},{"name":"glycerophosphohydrolase activity","type":"related"},{"name":"glycerylphosphorylcholinediesterase activity","type":"related"},{"name":"sn-glycero-3-phosphocholine glycerophosphohydrolase activity","type":"related"},{"name":"sn-glycero-3-phosphorylcholine diesterase activity","type":"related"}],"termid":"GO:0047389","terms_by_termid":{"GO:0047389":null}}


id: PBO:0079212
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis specific serine kinase 4","termid":"PBO:0079212"}


id: GO:0032124
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of the macronucleus.","definition_xrefs":["GOC:dph","GOC:mah","PMID:10503190","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleus organization","termid":"GO:0006997"}],"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":"macronucleus organization","synonyms":[{"name":"macronuclear organization","type":"exact"},{"name":"macronuclear organization and biogenesis","type":"related"},{"name":"macronucleus organisation","type":"exact"}],"termid":"GO:0032124"}


id: MOD:00054
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-glutamine residue to N-acetyl-L-glutamine.","definition_xrefs":["RESID:AA0045"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-glutamine residue","termid":"MOD:00907"},{"relation_name":"is_a","term_name":"alpha-amino acetylated residue","termid":"MOD:01458"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00408"}],"interesting_parent_ids":["MOD:00408"],"is_obsolete":false,"name":"N-acetyl-L-glutamine","synonyms":[{"name":"(2S)-2-acetamido-5-pentanediamic acid","type":"exact"},{"name":"2-acetylamino-5-amino-5-oxopentanoic acid","type":"exact"},{"name":"2-acetylamino-5-pentanediamic acid","type":"exact"},{"name":"2-acetylazanyl-5-azanyl-5-oxopentanoic acid","type":"exact"},{"name":"AcGln","type":"exact"},{"name":"N-acetyl-L-glutamine","type":"exact"},{"name":"N-acetylated L-glutamine","type":"exact"},{"name":"acetylglutamine","type":"exact"}],"termid":"MOD:00054"}


id: MONDO:0054844
data:
  {"annotated_genes":["SJAG_04824"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86149],"is_not":false,"summary":null,"term":"MONDO:0054844"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"pontocerebellar hypoplasia","termid":"MONDO:0020135"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04824":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0020022"}],"interesting_parent_ids":["MONDO:0020022"],"is_obsolete":false,"name":"pontocerebellar hypoplasia, type 1D","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1648387","OMIM:618065","DOID:0112323","UMLS:C4748058","GARD:16289"],"synonyms":[{"name":"PCH1D","type":"related"},{"name":"pontocerebellar hypoplasia, type 1D","type":"exact"}],"termid":"MONDO:0054844","terms_by_termid":{"MONDO:0054844":null},"xrefs":{"Monarch":{"xref_id":"0054844"}}}


id: PBO:0031836
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_RNA_localization_during_vegetative_growth","termid":"PBO:0031836"}


id: MONDO:0017417
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, genetic, developmental defect during embryogenesis syndrome characterized by the triad of pancreatic fibrosis (and cysts, with a reduction of parenchymal tissue), renal dysplasia (with peripheral cortical cysts, primitive collecting ducts, glomerular cysts and metaplastic cartilage) and hepatic dysgenesis (enlarged portal areas containing numerous elongated binary profiles with a tendency to perilobular fibrosis). Situs abnormalities, skeletal anomalies and anencephaly have also been associated. Patients that survive the neonatal period present renal insufficiency, chronic jaundice and insulin-dependant diabetes.","definition_xrefs":["Orphanet:294415"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete syndromic visceral malformation (obsolete MONDO:0015214)","termid":"MONDO:0015214"},{"relation_name":"excluded_subClassOf","term_name":"familial cystic renal disease","termid":"MONDO:0019741"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"renal-hepatic-pancreatic dysplasia","secondary_identifiers":["SCTID:763891005","UMLS:C2673883","MEDGEN:382215","GARD:17356","OMIMPS:208540","DOID:0060259"],"synonyms":[{"name":"Ivemark II syndrome","type":"exact"},{"name":"Ivemark's syndrome","type":"exact"},{"name":"Renohepaticopancreatic dysplasia","type":"exact"}],"termid":"MONDO:0017417","xrefs":{"Monarch":{"xref_id":"0017417"}}}


id: MONDO:0000188
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An epileptic encephalopathy resulting from impaired glucose transport into the brain.","definition_xrefs":["PMID:17718830"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inborn carbohydrate metabolic disorder","termid":"MONDO:0019214"},{"relation_name":"is_a","term_name":"carbohydrate transport disease","termid":"MONDO:0045015"},{"relation_name":"is_a","term_name":"metabolic epilepsy","termid":"MONDO:0100033"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0037792","MONDO:0005066","MONDO:0005027"],"is_obsolete":false,"name":"GLUT1 deficiency syndrome","secondary_identifiers":["MEDGEN:337833","DOID:0070560","NANDO:1200799","UMLS:C1847501","OMIMPS:606777"],"synonyms":[{"name":"GLUT1 deficiency syndrome","type":"exact"},{"name":"GLUT1DS","type":"exact"}],"termid":"MONDO:0000188","xrefs":{"Monarch":{"xref_id":"0000188"}}}


id: GO:0044373
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a cytokinin, any of a class of adenine-derived compounds that can function in plants as growth regulators.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hormone binding","termid":"GO:0042562"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"cytokinin binding","termid":"GO:0044373"}


id: MONDO:0021150
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete genetic characteristic (obsolete MONDO:0021150)","termid":"MONDO:0021150","xrefs":{"Monarch":{"xref_id":"0021150"}}}


id: FYPO:0007805
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the ATP hydrolysis-dependent activity that loads H3-H4 histone dimers onto DNA is absent.","definition_xrefs":["PomBase:mah","PMID:31848341"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished catalytic activity","termid":"FYPO:0000664"},{"relation_name":"is_a","term_name":"abnormal H3-H4 dimer loading onto DNA","termid":"FYPO:0007804"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0000661","FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0000641","FYPO:0000652","FYPO:0000654"],"is_obsolete":false,"name":"abolished H3-H4 dimer loading onto DNA","synonyms":[{"name":"abolished H3-H4 dimer loading activity","type":"exact"},{"name":"abolished histone H3-H4 dimer loading activity","type":"exact"}],"termid":"FYPO:0007805"}


id: PBO:0003174
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"20S proteasome component alpha 4 Pre6","termid":"PBO:0003174"}


id: PBO:0031616
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_rate_of_transposition","termid":"PBO:0031616"}


id: PBO:0058636
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6768","termid":"PBO:0058636"}


id: FYPO:0006511
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which cells form telomeres that are shorter than normal during G0 phase. Normally, telomere length is stable in G0, whereas telomere sequences can be lost in mutants.","definition_xrefs":["PMID:29167439","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal telomere length","termid":"FYPO:0006509"},{"relation_name":"is_a","term_name":"abnormal telomere morphology during G0","termid":"FYPO:0007413"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"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:0000293"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0000293","FYPO:0005447","FYPO:0000641"],"is_obsolete":false,"name":"shortened telomeres during G0","synonyms":[{"name":"decreased telomere length during G0","type":"related"},{"name":"loss of telomeric sequence during G0","type":"exact"},{"name":"loss of telomeric sequence during quiescence","type":"exact"},{"name":"reduced telomere length during G0","type":"exact"},{"name":"short telomeres during G0","type":"exact"},{"name":"shortened telomeres during cell quiescence","type":"exact"},{"name":"shortened telomeres during quiescence","type":"exact"}],"termid":"FYPO:0006511"}


id: FYPO:0000541
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the occurrence of protein transport is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein transport during vegetative growth","termid":"FYPO:0000540"}],"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:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000138","FYPO:0005447","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"decreased protein transport during vegetative growth","synonyms":[{"name":"decreased protein transport during mitotic cell cycle","type":"related"},{"name":"protein transport: decreased","type":"related"},{"name":"reduced protein transport during vegetative growth","type":"exact"}],"termid":"FYPO:0000541"}


id: GO:0035207
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the rate or extent of hemocyte proliferation. Hemocytes are blood cells associated with a hemocoel (the cavity containing most of the major organs of the arthropod body) which are involved in defense and clotting of hemolymph, but not involved in transport of oxygen. An example of this is found in Drosophila melanogaster.","definition_xrefs":["GOC:bf","GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of immune system process","termid":"GO:0002683"},{"relation_name":"is_a","term_name":"negative regulation of cell population proliferation","termid":"GO:0008285"},{"relation_name":"is_a","term_name":"regulation of hemocyte proliferation","termid":"GO:0035206"},{"relation_name":"negatively_regulates","term_name":"hemocyte proliferation","termid":"GO:0035172"}],"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 hemocyte proliferation","synonyms":[{"name":"down regulation of hemocyte proliferation","type":"exact"},{"name":"down-regulation of hemocyte proliferation","type":"exact"},{"name":"downregulation of hemocyte proliferation","type":"exact"},{"name":"inhibition of hemocyte proliferation","type":"narrow"},{"name":"negative regulation of arthropod blood cell proliferation","type":"exact"}],"termid":"GO:0035207"}


id: GO:0071251
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a silicon dioxide stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to silicon dioxide","termid":"GO:0034021"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to silicon dioxide","synonyms":[{"name":"cellular response to silica","type":"exact"},{"name":"cellular response to silox","type":"exact"}],"termid":"GO:0071251"}


id: GO:1902057
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving (25S)-Delta(4)-dafachronate.","definition_xrefs":["PMID:20178781","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"steroid metabolic process","termid":"GO:0008202"},{"relation_name":"is_a","term_name":"carboxylic acid metabolic process","termid":"GO:0019752"},{"relation_name":"is_a","term_name":"ketone metabolic process","termid":"GO:0042180"},{"relation_name":"is_a","term_name":"olefinic compound metabolic process","termid":"GO:0120254"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0006629","GO:0044281"],"is_obsolete":false,"name":"(25S)-Delta(4)-dafachronate metabolic process","synonyms":[{"name":"(25S)-Delta(4)-dafachronate metabolism","type":"exact"}],"termid":"GO:1902057"}


id: PBO:0071273
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPL24 pseudogene 7","termid":"PBO:0071273"}


id: GO:0120133
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the assembly of actin cortical patches.","definition_xrefs":["PMID:19962315"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of actin cytoskeleton organization","termid":"GO:0032956"},{"relation_name":"is_a","term_name":"regulation of cellular component biogenesis","termid":"GO:0044087"},{"relation_name":"is_a","term_name":"negative regulation of cytoskeleton organization","termid":"GO:0051494"},{"relation_name":"negatively_regulates","term_name":"actin cortical patch assembly","termid":"GO:0000147"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"negatively_regulates","termid":"GO:0030036"},{"rel_name":"regulates","termid":"GO:0030036"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007010"},{"rel_name":"negatively_regulates","termid":"GO:0007010"}],"interesting_parent_ids":["GO:0030036","GO:0007010","GO:0008150","GO:0044085"],"is_obsolete":false,"name":"negative regulation of actin cortical patch assembly","synonyms":[{"name":"down regulation of actin cortical patch assembly","type":"exact"},{"name":"down-regulation of actin cortical patch assembly","type":"exact"},{"name":"downregulation of actin cortical patch assembly","type":"exact"},{"name":"inhibition of actin cortical patch assembly","type":"narrow"}],"termid":"GO:0120133"}


id: PBO:0036531
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytoplasmic translation release factor class II eRF3","termid":"PBO:0036531"}


id: GO:0003148
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the outflow tract septum are generated and organized. The outflow tract septum is a partition in the outflow tract.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiac septum morphogenesis","termid":"GO:0060411"},{"relation_name":"part_of","term_name":"outflow tract morphogenesis","termid":"GO:0003151"}],"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":"outflow tract septum morphogenesis","termid":"GO:0003148"}


id: PBO:0064712
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl isomerase A pseudogene 48","termid":"PBO:0064712"}


id: GO:0102347
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: icosanoyl-CoA(4-) + NADP(3-) = trans-2-icosenoyl-CoA(4-) + NADPH(4-) + H+.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete trans-arachidon-2-enoyl-CoA reductase activity (obsolete GO:0102347)","termid":"GO:0102347"}


id: PBO:0061609
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear distribution C, dynein complex regulator","termid":"PBO:0061609"}


id: FYPO:0004019
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the occurrence of mitochondrial electron transport from succinate to ubiquinone is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular respiration","termid":"FYPO:0000566"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0000002","FYPO:0000257","FYPO:0001320"],"is_obsolete":false,"name":"normal mitochondrial electron transport, succinate to ubiquinone","synonyms":[{"name":"normal mitochondrial electron transport, succinate to ubiquinone, during mitotic cell cycle","type":"related"},{"name":"normal mitochondrial electron transport, succinate to ubiquinone, during vegetative growth","type":"exact"},{"name":"normal succinate cytochrome c oxidoreductase","type":"related"},{"name":"normal succinate dehydrogenase (ubiquinone) activity and ubiquinol-cytochrome-c reductase activity","type":"related"}],"termid":"FYPO:0004019"}


id: PR:O59666
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A copper-exporting P-type ATPase A that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO03101"],"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":"copper-transporting ATPase ccc2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC29A3.01","secondary_identifiers":["UniProtKB:O59666"],"synonyms":[{"name":"Cu(2+)-ATPase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-copA","type":"exact"}],"termid":"PR:O59666"}


id: PR:O74372
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- duo1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74372"],"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":"DASH complex subunit duo1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC32F12.08c","synonyms":[{"name":"Spom972h-duo1","type":"exact"},{"name":"outer kinetochore protein duo1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74372"}


id: MONDO:1011321
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hereditary disease that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-human animal disease","termid":"MONDO:0005583"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hereditary disease, non-human animal","termid":"MONDO:1011321","xrefs":{"Monarch":{"xref_id":"1011321"}}}


id: PBO:0000193
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alkali-sensitive linkage","termid":"PBO:0000193"}


id: GO:1900824
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of ergot alkaloid biosynthetic process.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of secondary metabolite biosynthetic process","termid":"GO:1900378"},{"relation_name":"is_a","term_name":"regulation of ergot alkaloid biosynthetic process","termid":"GO:1900822"},{"relation_name":"positively_regulates","term_name":"ergot alkaloid biosynthetic process","termid":"GO:0035837"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0008150","GO:0019748"],"is_obsolete":false,"name":"positive regulation of ergot alkaloid biosynthetic process","synonyms":[{"name":"activation of ergot alkaloid anabolism","type":"exact"},{"name":"activation of ergot alkaloid biosynthesis","type":"exact"},{"name":"activation of ergot alkaloid biosynthetic process","type":"narrow"},{"name":"activation of ergot alkaloid formation","type":"exact"},{"name":"activation of ergot alkaloid synthesis","type":"exact"},{"name":"positive regulation of ergot alkaloid anabolism","type":"exact"},{"name":"positive regulation of ergot alkaloid biosynthesis","type":"exact"},{"name":"positive regulation of ergot alkaloid formation","type":"exact"},{"name":"positive regulation of ergot alkaloid synthesis","type":"exact"},{"name":"up regulation of ergot alkaloid anabolism","type":"exact"},{"name":"up regulation of ergot alkaloid biosynthesis","type":"exact"},{"name":"up regulation of ergot alkaloid biosynthetic process","type":"exact"},{"name":"up regulation of ergot alkaloid formation","type":"exact"},{"name":"up regulation of ergot alkaloid synthesis","type":"exact"},{"name":"up-regulation of ergot alkaloid anabolism","type":"exact"},{"name":"up-regulation of ergot alkaloid biosynthesis","type":"exact"},{"name":"up-regulation of ergot alkaloid biosynthetic process","type":"exact"},{"name":"up-regulation of ergot alkaloid formation","type":"exact"},{"name":"up-regulation of ergot alkaloid synthesis","type":"exact"},{"name":"upregulation of ergot alkaloid anabolism","type":"exact"},{"name":"upregulation of ergot alkaloid biosynthesis","type":"exact"},{"name":"upregulation of ergot alkaloid biosynthetic process","type":"exact"},{"name":"upregulation of ergot alkaloid formation","type":"exact"},{"name":"upregulation of ergot alkaloid synthesis","type":"exact"}],"termid":"GO:1900824"}


id: GO:0044389
data:
  {"annotated_genes":["SJAG_01540","SJAG_02591","SJAG_02253","SJAG_00032","SJAG_03643","SJAG_03575","SJAG_03843","SJAG_00615","SJAG_01686","SJAG_00803","SJAG_00452","SJAG_04335","SJAG_01134","SJAG_01226","SJAG_01365"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[75141],"is_not":false,"summary":null,"term":"GO:0044389"},{"annotations":[70033,72459,74518,66830,75421,71533,78801,72631,78914,78967,76611,80147,79430,78254],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031625"}]},"cv_name":"molecular_function","definition":"Binding to a ubiquitin-like protein ligase, such as ubiquitin-ligase.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme binding","termid":"GO:0019899"}],"gene_count":15,"genes_by_uniquename":{"SJAG_00032":null,"SJAG_00452":null,"SJAG_00615":null,"SJAG_00803":null,"SJAG_01134":null,"SJAG_01226":null,"SJAG_01365":null,"SJAG_01540":null,"SJAG_01686":null,"SJAG_02253":null,"SJAG_02591":null,"SJAG_03575":null,"SJAG_03643":null,"SJAG_03843":null,"SJAG_04335":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"ubiquitin-like protein ligase binding","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null},"synonyms":[{"name":"E3 protein ligase binding","type":"exact"},{"name":"small conjugating protein ligase binding","type":"exact"}],"termid":"GO:0044389","terms_by_termid":{"GO:0031625":null,"GO:0044389":null}}


id: FYPO:0003491
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 cells show increased sensitivity to ultraviolet light during G1 phase of the mitotic cell cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sensitive to UV during vegetative growth","termid":"FYPO:0000268"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000139","FYPO:0000003","FYPO:0005447"],"is_obsolete":false,"name":"sensitive to UV during mitotic G1 phase","synonyms":[{"name":"decreased growth during cellular response to UV during mitotic G1 phase","type":"exact"},{"name":"decreased vegetative cell population growth during cellular response to UV during mitotic G1 phase","type":"exact"},{"name":"hypersensitive to UV during mitotic G1 phase","type":"exact"},{"name":"increased sensitivity to UV irradiation during mitotic G1 phase","type":"exact"},{"name":"sensitive to UV during G1 phase during vegetative growth","type":"exact"},{"name":"sensitive to UV during G1 phase of mitotic cell cycle","type":"exact"},{"name":"sensitive to ultraviolet light during mitotic G1 phase","type":"exact"}],"termid":"FYPO:0003491"}


id: GO:0039018
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the nephrostome over time, from its formation to the mature structure. The nephrostome is the opening of the pronephros into the body cavity.","definition_xrefs":["GOC:mtg_kidney_jan10","PMID:14686690","XAO:0000062","PMID:15647339"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"pronephros development","termid":"GO:0048793"}],"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":"nephrostome development","termid":"GO:0039018"}


id: GO:0009246
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of the enterobacterial common antigen, an acidic polysaccharide containing N-acetyl-D-glucosamine, N-acetyl-D-mannosaminouronic acid, and 4-acetamido-4,6-dideoxy-D-galactose. A major component of the cell wall outer membrane of Gram-negative bacteria.","definition_xrefs":["GOC:ma"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polysaccharide biosynthetic process","termid":"GO:0000271"},{"relation_name":"is_a","term_name":"enterobacterial common antigen metabolic process","termid":"GO:0046378"},{"relation_name":"is_a","term_name":"carbohydrate derivative biosynthetic process","termid":"GO:1901137"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"enterobacterial common antigen biosynthetic process","secondary_identifiers":["MetaCyc:ECASYN-PWY"],"synonyms":[{"name":"enterobacterial common antigen anabolism","type":"exact"},{"name":"enterobacterial common antigen biosynthesis","type":"exact"},{"name":"enterobacterial common antigen formation","type":"exact"},{"name":"enterobacterial common antigen synthesis","type":"exact"}],"termid":"GO:0009246"}


id: MONDO:0015530
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A headache disorder characterized by episodes of unilateral, short lasting pain and associated ipsilateral cranial autonomic symptoms.","definition_xrefs":["NCIT:C117074"],"direct_ancestors":[{"relation_name":"is_a","term_name":"trigeminal nerve disorder","termid":"MONDO:0003543"},{"relation_name":"is_a","term_name":"hypnic headache","termid":"MONDO:0017181"},{"relation_name":"is_a","term_name":"neurovascular disorder","termid":"MONDO:0043218"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trigeminal autonomic cephalalgia","secondary_identifiers":["icd11.foundation:607078588","GARD:20017","ICD9:339.09","MEDGEN:327950","MESH:D051303","SCTID:449814007","Orphanet:157843","UMLS:C1565172"],"termid":"MONDO:0015530","xrefs":{"Monarch":{"xref_id":"0015530"}}}


id: GO:0031361
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the thylakoid membrane consisting of the gene products having at least some part of their peptide sequence embedded in the hydrophobic region of the membrane.","definition_xrefs":["GOC:mah","GOC:dos"],"gene_count":0,"genotype_count":0,"name":"obsolete integral component of thylakoid membrane (obsolete GO:0031361)","synonyms":[{"name":"integral to thylakoid membrane","type":"narrow"}],"termid":"GO:0031361"}


id: GO:0044687
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (2E,6E,10E)-geranylgeranyl diphosphate + isopentenyl diphosphate = (2E,6E,10E,14E)-geranylfarnesyl diphosphate + diphosphate.","definition_xrefs":["RHEA:25694","PMID:20097171"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prenyl diphosphate synthase activity","termid":"GO:0120531"}],"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:0016765"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0016765","GO:0003824"],"is_obsolete":false,"name":"geranylfarnesyl diphosphate synthase activity","secondary_identifiers":["EC:2.5.1.81","MetaCyc:RXN-8813"],"synonyms":[{"name":"FGPP synthase activity","type":"exact"}],"termid":"GO:0044687"}


id: PBO:0047367
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box and leucine rich repeat protein 20","termid":"PBO:0047367"}


id: MONDO:0006015
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A serious disorder characterized by massive adrenal gland hemorrhage secondary to a bacterial infection, most often Neisseria meningitidis infection. It is manifested with decreased blood pressure, shock, disseminated intravascular coagulation, and adrenocortical insufficiency.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"acute adrenal insufficiency","termid":"MONDO:0019801"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Waterhouse-Friderichsen syndrome","secondary_identifiers":["MEDGEN:234675","UMLS:C1403891","EFO:0007544","ICD10CM:A39.1","MESH:D014884","Orphanet:100067","DOID:9931","icd11.foundation:2072098125","ICD10EXP:A39.1+","GARD:9449","ICD9:036.3","MedDRA:10047847","ICD10EXP:E35.1*","NCIT:C85225","SCTID:36102002"],"synonyms":[{"name":"WFS","type":"exact"},{"name":"Waterhouse–Friderichsen syndrome","type":"related"},{"name":"fatal pneumococcal Waterhouse-Friderichsen syndrome","type":"related"},{"name":"meningococcal hemorrhagic adrenalitis","type":"exact"}],"termid":"MONDO:0006015","xrefs":{"Monarch":{"xref_id":"0006015"}}}


id: PBO:0079000
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Thr (AGT) 7-1","termid":"PBO:0079000"}


id: PBO:0028090
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_centromeric_chromatin","termid":"PBO:0028090"}


id: GO:0005992
data:
  {"annotated_genes":["SJAG_01427","SJAG_01862","SJAG_00182","SJAG_01646","SJAG_01531","SJAG_00129","SJAG_01209"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[61518,62206,64082,67704,68164,68775,108703],"is_not":false,"summary":null,"term":"GO:0005992"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of trehalose, a disaccharide that consists of two molecules of glucose and is isomeric with sucrose.","definition_xrefs":["GOC:jl","ISBN:0028623819"],"direct_ancestors":[{"relation_name":"is_a","term_name":"trehalose metabolic process","termid":"GO:0005991"},{"relation_name":"is_a","term_name":"disaccharide biosynthetic process","termid":"GO:0046351"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00129":null,"SJAG_00182":null,"SJAG_01209":null,"SJAG_01427":null,"SJAG_01531":null,"SJAG_01646":null,"SJAG_01862":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"trehalose biosynthetic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000107":null},"synonyms":[{"name":"mycose biosynthesis","type":"exact"},{"name":"mycose biosynthetic process","type":"exact"},{"name":"mykose biosynthesis","type":"exact"},{"name":"mykose biosynthetic process","type":"exact"},{"name":"trehalose anabolism","type":"exact"},{"name":"trehalose biosynthesis","type":"exact"},{"name":"trehalose formation","type":"exact"},{"name":"trehalose synthesis","type":"exact"}],"termid":"GO:0005992","terms_by_termid":{"GO:0005992":null}}


id: PBO:0041763
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calpain 2","termid":"PBO:0041763"}


id: PBO:0049554
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H2B clustered histone 16, pseudogene","termid":"PBO:0049554"}


id: MONDO:0014551
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":"short stature with nonspecific skeletal abnormalities","secondary_identifiers":["OMIM:616255","UMLS:C4225399","MEDGEN:906874"],"synonyms":[{"name":"SNSK","type":"related"},{"name":"short stature with nonspecific skeletal abnormalities","type":"exact"}],"termid":"MONDO:0014551","xrefs":{"Monarch":{"xref_id":"0014551"}}}


id: MONDO:0014880
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Duane syndrome type 3 is a disorder of eye movement.The affected eye, or eyes, has limited ability to move both inward toward the nose and outward toward the ears. The eye opening narrows and the eyeball pulls in when looking inward toward the nose. About 15 percent of all cases of Duane syndrome are type 3. Most cases occur without other signs and symptoms.In most people with Duane syndrome type 3, the cause is unknown; but it can sometimes be caused by mutations in the CHN1 gene and inherited in an autosomal dominant fashion.","definition_xrefs":["GARD:0010691"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Duane retraction syndrome","termid":"MONDO:0007473"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Duane retraction syndrome 3 with or without deafness","secondary_identifiers":["MEDGEN:934719","OMIM:617041","UMLS:C4310752","GARD:10691"],"synonyms":[{"name":"DURS3","type":"exact"},{"name":"Duane retraction syndrome 3","type":"related"},{"name":"Duane retraction syndrome 3 with or without deafness","type":"exact"},{"name":"Duane retraction syndrome caused by mutation in MAFB","type":"exact"},{"name":"Duane syndrome type 3","type":"related"},{"name":"MAFB Duane retraction syndrome","type":"exact"}],"termid":"MONDO:0014880","xrefs":{"Monarch":{"xref_id":"0014880"}}}


id: PBO:0061422
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuropeptide Y receptor Y6 (pseudogene)","termid":"PBO:0061422"}


id: PBO:0064968
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRAME family member 22","termid":"PBO:0064968"}


id: PBO:0001014
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"auxin family transmembrane transporter (predicted)","termid":"PBO:0001014"}


id: PBO:0077548
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 256 pseudogene 1","termid":"PBO:0077548"}


id: MONDO:0016109
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Autosomal recessive form of distal myopathy.","definition_xrefs":["MONDO:patterns/autosomal_recessive"],"gene_count":0,"genotype_count":0,"name":"obsolete autosomal recessive distal myopathy (obsolete MONDO:0016109)","secondary_identifiers":["Orphanet:206653"],"synonyms":[{"name":"distal myopathy, autosomal recessive","type":"exact"}],"termid":"MONDO:0016109","xrefs":{"Monarch":{"xref_id":"0016109"}}}


id: GO:0010483
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An interaction between the pollen tube, part of the male gametophyte, and the female gametophyte (typically the synergid cells), that results in the arrest of pollen tube growth, rupture of the pollen tube and the release of the sperm cells.","definition_xrefs":["PMID:37640641"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biological process involved in intraspecies interaction between organisms","termid":"GO:0051703"},{"relation_name":"part_of","term_name":"pollination","termid":"GO:0009856"}],"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":"pollen tube reception","termid":"GO:0010483"}


id: MONDO:0011357
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":"eccrine syringofibroadenomatosis with eyelid abnormalities","secondary_identifiers":["OMIM:603669","MEDGEN:355022","MESH:C566347","UMLS:C1863618"],"synonyms":[{"name":"eccrine syringofibroadenomatosis with eyelid abnormalities","type":"exact"}],"termid":"MONDO:0011357","xrefs":{"Monarch":{"xref_id":"0011357"}}}


id: PBO:0116283
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Splicing factor, structural and functional homolog of human FAM192A; plays structural role in intermediate spliceosomal C* complex, which executes exon ligation; required for survival upon exposure to K1 killer toxin; proposed to regulate double-strand break repair via non-homologous end-joining","termid":"PBO:0116283"}


id: PBO:0082808
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of yeast cortical actin cytoskeleton; binds and cross links actin filaments; originally identified by its homology to calponin (contains a calponin-like repeat) but the Scp1p domain structure is more similar to transgelin","termid":"PBO:0082808"}


id: PBO:0063327
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 1 pseudogene 3","termid":"PBO:0063327"}


id: RO:0002360
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","direct_ancestors":[{"relation_name":"is_a","term_name":"overlaps","termid":"RO:0002131"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_dendrite_location","termid":"RO:0002360"}


id: PBO:0071232
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23a pseudogene 73","termid":"PBO:0071232"}


id: PBO:0000774
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Lsd1/2 complex PHD finger containing protein Phf2","termid":"PBO:0000774"}


id: PBO:0003173
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5.3.3.2","termid":"PBO:0003173"}


id: PBO:0085137
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nucleolar protein required for maturation of 18S rRNA; member of the eIF4A subfamily of DEAD-box ATP-dependent RNA helicases; 18S rRNA biogenesis defect of the null mutant is functionally complemented by human EIF4A3","termid":"PBO:0085137"}


id: GO:0090361
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency, or extent of the appearance of any platelet-derived growth factor due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytokine production","termid":"GO:0001817"},{"relation_name":"regulates","term_name":"platelet-derived growth factor production","termid":"GO:0090360"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"regulation of platelet-derived growth factor production","termid":"GO:0090361"}


id: GO:0018600
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: alpha-pinene + O2 + 2 H+ + 2 e- = H2O + myrtenol.","definition_xrefs":["UM-BBD_reactionID:r0709"],"gene_count":0,"genotype_count":0,"name":"obsolete alpha-pinene dehydrogenase activity (obsolete GO:0018600)","termid":"GO:0018600"}


id: PBO:0016895
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by S. cerevisiae KNS1","termid":"PBO:0016895"}


id: FYPO:0005820
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the occurrence of neddylation of one or more specific proteins, or of specific protein sites, is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein neddylation during vegetative growth","termid":"FYPO:0005819"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002274"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0002274","FYPO:0001320","FYPO:0005447","FYPO:0002494"],"is_obsolete":false,"name":"increased protein neddylation during vegetative growth","synonyms":[{"name":"increased protein neddylation during mitotic cell cycle","type":"related"}],"termid":"FYPO:0005820"}


id: GO:0002059
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to thymine.","definition_xrefs":["GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine nucleobase binding","termid":"GO:0002061"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"thymine binding","termid":"GO:0002059"}


id: PBO:0039377
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"angiomotin like 2","termid":"PBO:0039377"}


id: GO:1990604
data:
  {"annotated_genes":["SJAG_04435"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[77625],"is_not":false,"summary":null,"term":"GO:1990604"}]},"cv_name":"cellular_component","definition":"A protein complex of the endoplasmic reticulum membrane that consists of IRE1 (Inositol-requiring enzyme-1), TRAF2 (TNF receptor-associated factor 2) and ASK1 (Apoptosis signal-regulating kinase 1, a MAP3K).","definition_xrefs":["PMID:23000344","GOC:bf","PMID:12050113","GOC:PARL"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane protein complex","termid":"GO:0098796"},{"relation_name":"is_a","term_name":"endoplasmic reticulum protein-containing complex","termid":"GO:0140534"},{"relation_name":"part_of","term_name":"endoplasmic reticulum membrane","termid":"GO:0005789"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04435":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005783"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005789"}],"interesting_parent_ids":["GO:0032991","GO:0005737","GO:0005575","GO:0005789","GO:0005783"],"is_obsolete":false,"name":"IRE1-TRAF2-ASK1 complex","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"ERN1-TRAF2-ASK1 complex","type":"related"}],"termid":"GO:1990604","terms_by_termid":{"GO:1990604":null}}


id: PBO:0076752
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"teratocarcinoma-derived growth factor 1 pseudogene 2","termid":"PBO:0076752"}


id: GO:0038082
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: a phosphorylated MAP kinase + H2O = a MAP kinase + phosphate, where the MAP kinase (MAPK) is part of a MAPK signaling cascade that passes on a signal within an osmosensory signaling pathway.","definition_xrefs":["GOC:signaling"],"gene_count":0,"genotype_count":0,"name":"obsolete MAP kinase phosphatase activity involved in regulation of osmosensory signaling pathway (obsolete GO:0038082)","synonyms":[{"name":"Hog1 phosphatase activity","type":"narrow"},{"name":"MAP kinase phosphatase activity involved in regulation of osmosensory signalling pathway","type":"exact"},{"name":"MAPK phosphatase activity involved in regulation of osmosensory signaling pathway","type":"exact"}],"termid":"GO:0038082"}


id: MONDO:0015810
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"indolent primary cutaneous T-cell lymphoma","termid":"MONDO:0015816"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005093","MONDO:0004992"],"is_obsolete":false,"name":"primary cutaneous CD4+ small/medium-sized pleomorphic T-cell lymphoma","secondary_identifiers":["MEDGEN:1842165","UMLS:C5680503","ICD10CM:C84.4","GARD:20156","Orphanet:178522"],"termid":"MONDO:0015810","xrefs":{"Monarch":{"xref_id":"0015810"}}}


id: GO:0141027
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which an organism effects a change that impairs the structure or function of the host actin cytoskeleton. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:20688909"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host cytoskeleton","termid":"GO:0052039"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated perturbation of host actin cytoskeleton","synonyms":[{"name":"disruption by symbiont of actin cytoskeleton","type":"related"},{"name":"modification by symbiont of host actin cytoskeleton","type":"related"},{"name":"perturbation by symbiont of host actin cytoskeleton","type":"exact"}],"termid":"GO:0141027"}


id: PBO:0042681
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CEBPB antisense RNA 1","termid":"PBO:0042681"}


id: PBO:0078785
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Asn (anticodon GTT) 9-2","termid":"PBO:0078785"}


id: MONDO:0017451
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-syndromic brachydactyly that involves the manus.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-syndromic brachydactyly","termid":"MONDO:0017424"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-syndromic brachydactyly of fingers","secondary_identifiers":["Orphanet:294996"],"synonyms":[{"name":"manus non-syndromic brachydactyly","type":"exact"},{"name":"non-syndromic brachydactyly of manus","type":"exact"},{"name":"short fingers","type":"exact"}],"termid":"MONDO:0017451","xrefs":{"Monarch":{"xref_id":"0017451"}}}


id: MONDO:0016609
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammatory myopathy with abundant macrophages is a rare inflammatory myopathy characterized by diffuse destructive infiltration of CD68+ macrophages into the fascia rather than muscle fibers in muscle biopsies, proximal muscle weakness and myalgia with or without scaly dermatomyositis-like or atypical non-dermatomyositis-like skin lesions, elevation of creatine kinase levels and thickening of muscle fascia in muscle MRI.","definition_xrefs":["Orphanet:247718"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acquired idiopathic inflammatory myopathy","termid":"MONDO:0020122"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"inflammatory myopathy with abundant macrophages","secondary_identifiers":["MEDGEN:1638939","SCTID:766706007","GARD:20663","UMLS:C4707791"],"synonyms":[{"name":"IMAM","type":"exact"},{"name":"imam","type":"exact"}],"termid":"MONDO:0016609","xrefs":{"Monarch":{"xref_id":"0016609"}}}


id: GO:0007119
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Unlocalized bud growth such that the entire surface of the bud expands evenly, in a cell that reproduces by budding.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"budding cell bud growth","termid":"GO:0007117"}],"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":"budding cell isotropic bud growth","synonyms":[{"name":"isotropic bud growth","type":"broad"}],"termid":"GO:0007119"}


id: PBO:0088326
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-binding transcription factor, MADS-box Map1","termid":"PBO:0088326"}


id: MONDO:0100271
data:
  {"annotated_genes":["SJAG_05950"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86981],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013938"},{"annotations":[86979],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013939"}]},"cv_name":"mondo","definition":"Any Zellweger spectrum disorder in which the cause of the disease is a mutation in the PEX26 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Zellweger spectrum disorders","termid":"MONDO:0019609"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05950":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0019053"},{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244","MONDO:0019053","MONDO:0005559","MONDO:0005066","MONDO:0006025"],"is_obsolete":false,"name":"peroxisome biogenesis disorder due to PEX26 defect","references_by_uniquename":{"PB_REF:0000006":null},"synonyms":[{"name":"PEX26 related Zellweger spectrum disorder","type":"exact"},{"name":"peroxisome biogenesis disorder due to PEX26 defect","type":"exact"}],"termid":"MONDO:0100271","terms_by_termid":{"MONDO:0013938":null,"MONDO:0013939":null},"xrefs":{"Monarch":{"xref_id":"0100271"}}}


id: PBO:0046728
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"envoplakin","termid":"PBO:0046728"}


id: GO:0052571
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. 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 detecting the immune response of the symbiont organism. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo"],"gene_count":0,"genotype_count":0,"name":"obsolete response to symbiont immune response (obsolete GO:0052571)","synonyms":[{"name":"response to symbiont immune response","type":"exact"}],"termid":"GO:0052571"}


id: GO:0102643
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: scalarane-17alpha-19-diol = all-trans-geranylfarnesol + H2O.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete scalarane-17alpha-19-diol synthase activity (obsolete GO:0102643)","termid":"GO:0102643"}


id: PBO:0077765
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TOMM22 pseudogene 1","termid":"PBO:0077765"}


id: PBO:0072168
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S15 pseudogene 5","termid":"PBO:0072168"}


id: PBO:0086722
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; non-essential gene identified in a screen for mutants with increased levels of rDNA transcription; weak similarity with uridine kinases and with phosphoribokinases","termid":"PBO:0086722"}


id: PBO:0089877
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SSU-rRNA maturation protein Tsr4 homolog 1 Tsr401","termid":"PBO:0089877"}


id: GO:1990189
data:
  {"annotated_genes":["SJAG_03537","SJAG_04631"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[73805,77093],"is_not":false,"summary":null,"term":"GO:1990189"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: acetyl-CoA + N-terminal L-seryl-[protein] = CoA + H+ + N-terminal Nalpha-acetyl-L-seryl-[protein].","definition_xrefs":["RHEA:50504","PMID:23912279"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-N-terminal amino-acid acetyltransferase activity","termid":"GO:0004596"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03537":null,"SJAG_04631":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0034212"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0034212","GO:0016746","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"protein N-terminal-serine acetyltransferase activity","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"peptide-serine-alpha-N-acetyltransferase activity","type":"exact"}],"termid":"GO:1990189","terms_by_termid":{"GO:1990189":null}}


id: GO:0102953
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: glutathionate + hypoglycin A = L-cysteinylglycine + hypoglycin B.","definition_xrefs":["GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aminoacyltransferase activity","termid":"GO:0016755"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016746","GO:0016740","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"hypoglycin A gamma-glutamyl transpeptidase activity","secondary_identifiers":["MetaCyc:RXN-9157"],"termid":"GO:0102953"}


id: PATO:0001938
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A spheroid quality inhering in a bearer by virtue of the bearer's being oval and a little angular in the middle.","definition_xrefs":["ISBN:0881923214"],"direct_ancestors":[{"relation_name":"is_a","term_name":"parallelogram","termid":"PATO:0002317"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rhomboid","termid":"PATO:0001938"}


id: GO:0051179
data:
  {"annotated_genes":["SJAG_02399","SJAG_02619","SJAG_04111","SJAG_05736","SJAG_03721","SJAG_01096","SJAG_02147","SJAG_04338","SJAG_00632","SJAG_04469","SJAG_04701","SJAG_02074","SJAG_03432","SJAG_03608","SJAG_07002","SJAG_00850","SJAG_02453","SJAG_01011","SJAG_03048","SJAG_00542","SJAG_02209","SJAG_02234","SJAG_03683","SJAG_02735","SJAG_03345","SJAG_02062","SJAG_04724","SJAG_01837","SJAG_04508","SJAG_01135","SJAG_02316","SJAG_01125","SJAG_00864","SJAG_02437","SJAG_00525","SJAG_02504","SJAG_02587","SJAG_00516","SJAG_04402","SJAG_03710","SJAG_01027","SJAG_05268","SJAG_04666","SJAG_04515","SJAG_00287","SJAG_04379","SJAG_03358","SJAG_04295","SJAG_02045","SJAG_03416","SJAG_04644","SJAG_04734","SJAG_01505","SJAG_02077","SJAG_04400","SJAG_02917","SJAG_04703","SJAG_04947","SJAG_00922","SJAG_00906","SJAG_00645","SJAG_02750","SJAG_02716","SJAG_05414","SJAG_05012","SJAG_05178","SJAG_04884","SJAG_00521","SJAG_04472","SJAG_02564","SJAG_04275","SJAG_02805","SJAG_01025","SJAG_03209","SJAG_04428","SJAG_01641","SJAG_00149","SJAG_03895","SJAG_00330","SJAG_00402","SJAG_02537","SJAG_02511","SJAG_03088","SJAG_01789","SJAG_00093","SJAG_04051","SJAG_04366","SJAG_02789","SJAG_02661","SJAG_02354","SJAG_04912","SJAG_01669","SJAG_00229","SJAG_03774","SJAG_01777","SJAG_01030","SJAG_02833","SJAG_04413","SJAG_02346","SJAG_03848","SJAG_03508","SJAG_02451","SJAG_02645","SJAG_02117","SJAG_00405","SJAG_01534","SJAG_00397","SJAG_02139","SJAG_00053","SJAG_03741","SJAG_01546","SJAG_03092","SJAG_01655","SJAG_04148","SJAG_03577","SJAG_00702","SJAG_05220","SJAG_04466","SJAG_01278","SJAG_01449","SJAG_00840","SJAG_02208","SJAG_00976","SJAG_01636","SJAG_07003","SJAG_03085","SJAG_04185","SJAG_04202","SJAG_01305","SJAG_01335","SJAG_02371","SJAG_01597","SJAG_01790","SJAG_03593","SJAG_01994","SJAG_06270","SJAG_05196","SJAG_04328","SJAG_03989","SJAG_02704","SJAG_00015","SJAG_01660","SJAG_02520","SJAG_03470","SJAG_01677","SJAG_03842","SJAG_02624","SJAG_02011","SJAG_01095","SJAG_01640","SJAG_00373","SJAG_00080","SJAG_00553","SJAG_01649","SJAG_03864","SJAG_01082","SJAG_05346","SJAG_01863","SJAG_01998","SJAG_04070","SJAG_06440","SJAG_04923","SJAG_01803","SJAG_03054","SJAG_00192","SJAG_02344","SJAG_00152","SJAG_00144","SJAG_02602","SJAG_04134","SJAG_00335","SJAG_01621","SJAG_03447","SJAG_01941","SJAG_00612","SJAG_04996","SJAG_04857","SJAG_03403","SJAG_04112","SJAG_02419","SJAG_04731","SJAG_00204","SJAG_03754","SJAG_02445","SJAG_01127","SJAG_02525","SJAG_04960","SJAG_04828","SJAG_02968","SJAG_01924","SJAG_01349","SJAG_01437","SJAG_04218","SJAG_02140","SJAG_02114","SJAG_03239","SJAG_02509","SJAG_04021","SJAG_00915","SJAG_03976","SJAG_01090","SJAG_00586","SJAG_00357","SJAG_04050","SJAG_04325","SJAG_01379","SJAG_00578","SJAG_02581","SJAG_05950","SJAG_04905","SJAG_02315","SJAG_04822","SJAG_02063","SJAG_00065","SJAG_04554","SJAG_03029","SJAG_01007","SJAG_01951","SJAG_02814","SJAG_03891","SJAG_03644","SJAG_01563","SJAG_02484","SJAG_02397","SJAG_01370","SJAG_04592","SJAG_00484","SJAG_04417","SJAG_01299","SJAG_04451","SJAG_03401","SJAG_04745","SJAG_04598","SJAG_02753","SJAG_04370","SJAG_01405","SJAG_00031","SJAG_01445","SJAG_03670","SJAG_00646","SJAG_04284","SJAG_02957","SJAG_01329","SJAG_02322","SJAG_01872","SJAG_03726","SJAG_03347","SJAG_03719","SJAG_04358","SJAG_01338","SJAG_01410","SJAG_03847","SJAG_01001","SJAG_01344","SJAG_00971","SJAG_01190","SJAG_02586","SJAG_05182","SJAG_00900","SJAG_MIT09","SJAG_00655","SJAG_05175","SJAG_00649","SJAG_00700","SJAG_00284","SJAG_04002","SJAG_02193","SJAG_04480","SJAG_00877","SJAG_00671","SJAG_04718","SJAG_02529","SJAG_04558","SJAG_04003","SJAG_04565","SJAG_04552","SJAG_00938","SJAG_00899","SJAG_00277","SJAG_00154","SJAG_03400","SJAG_01991","SJAG_03050","SJAG_01129","SJAG_01834","SJAG_02992","SJAG_04629","SJAG_01541","SJAG_04068","SJAG_02332","SJAG_02361","SJAG_02210","SJAG_MIT37","SJAG_03442","SJAG_01071","SJAG_00279","SJAG_00019","SJAG_01116","SJAG_04645","SJAG_02023","SJAG_01168","SJAG_02211","SJAG_03693","SJAG_00530","SJAG_01183","SJAG_04551","SJAG_04221","SJAG_04387","SJAG_04787","SJAG_01775","SJAG_02534","SJAG_01373","SJAG_00800","SJAG_05315","SJAG_04643","SJAG_03156","SJAG_00328","SJAG_04706","SJAG_04903","SJAG_02646","SJAG_04115","SJAG_03012","SJAG_03079","SJAG_04465","SJAG_02103","SJAG_01733","SJAG_04136","SJAG_02715","SJAG_03250","SJAG_00777","SJAG_04455","SJAG_03338","SJAG_01084","SJAG_03783","SJAG_01560","SJAG_03986","SJAG_01374","SJAG_02592","SJAG_01167","SJAG_00991","SJAG_01225","SJAG_03315","SJAG_03231","SJAG_01467","SJAG_02231","SJAG_01917","SJAG_01940","SJAG_04517","SJAG_00360","SJAG_03907","SJAG_00339","SJAG_04978","SJAG_01415","SJAG_04902","SJAG_01913","SJAG_01281","SJAG_01382","SJAG_07010","SJAG_02867","SJAG_03882","SJAG_01360","SJAG_01048","SJAG_01642","SJAG_03334","SJAG_00208","SJAG_03114","SJAG_03829","SJAG_03697","SJAG_00835","SJAG_01309","SJAG_01279","SJAG_02651","SJAG_01328","SJAG_02883","SJAG_03385","SJAG_00930","SJAG_00082","SJAG_03817","SJAG_04714","SJAG_01039","SJAG_02473","SJAG_05229","SJAG_02698","SJAG_04830","SJAG_01514","SJAG_05326","SJAG_03300","SJAG_03449","SJAG_00018","SJAG_02986","SJAG_04966","SJAG_00594","SJAG_02022","SJAG_00434","SJAG_04623","SJAG_05030","SJAG_04308","SJAG_01268","SJAG_00171","SJAG_00687","SJAG_04901","SJAG_02166","SJAG_01033","SJAG_02059","SJAG_00803","SJAG_00767","SJAG_02848","SJAG_03777","SJAG_05303","SJAG_02282","SJAG_02240","SJAG_01809","SJAG_03005","SJAG_03365","SJAG_02941","SJAG_02118","SJAG_02250","SJAG_03836","SJAG_03490","SJAG_01067","SJAG_01590","SJAG_00275","SJAG_03915","SJAG_00727","SJAG_01741","SJAG_03960","SJAG_04167","SJAG_03756","SJAG_03725","SJAG_01133","SJAG_04246","SJAG_00113","SJAG_03808","SJAG_00804","SJAG_01772","SJAG_01013","SJAG_02897","SJAG_00587","SJAG_01770","SJAG_03970","SJAG_01004","SJAG_02274","SJAG_01899","SJAG_02133","SJAG_02516","SJAG_04721","SJAG_01336","SJAG_03820","SJAG_04955","SJAG_05344","SJAG_04015","SJAG_04143","SJAG_03781","SJAG_02736","SJAG_02012","SJAG_04616","SJAG_01448","SJAG_03497","SJAG_00851","SJAG_01240","SJAG_04296","SJAG_04072","SJAG_04047","SJAG_02598","SJAG_02398","SJAG_00596","SJAG_00467","SJAG_01065","SJAG_01378","SJAG_04990","SJAG_04434","SJAG_05245","SJAG_05185","SJAG_03440","SJAG_01647","SJAG_02824","SJAG_03581","SJAG_00051","SJAG_04457","SJAG_04359","SJAG_02375","SJAG_02797","SJAG_00891","SJAG_02431","SJAG_01890","SJAG_02584","SJAG_00826","SJAG_01258","SJAG_02852","SJAG_04867","SJAG_04615","SJAG_01738","SJAG_01080","SJAG_03268","SJAG_03763","SJAG_04024","SJAG_01529","SJAG_03955","SJAG_01684","SJAG_02782","SJAG_00576","SJAG_02050","SJAG_03217","SJAG_02699","SJAG_00104","SJAG_05345","SJAG_01088","SJAG_02779","SJAG_03963","SJAG_00919","SJAG_01422","SJAG_04162","SJAG_03324","SJAG_02943","SJAG_03810","SJAG_01263","SJAG_04698","SJAG_03690","SJAG_02425","SJAG_00547","SJAG_03516","SJAG_00543","SJAG_02277","SJAG_04336","SJAG_02113","SJAG_00669","SJAG_00379","SJAG_00970","SJAG_04219","SJAG_01589","SJAG_00962","SJAG_02761","SJAG_03596","SJAG_04461","SJAG_05319","SJAG_03685","SJAG_03452","SJAG_04589","SJAG_03182","SJAG_00072","SJAG_02463","SJAG_04122","SJAG_04533","SJAG_03453","SJAG_02155","SJAG_05296","SJAG_04737","SJAG_01196","SJAG_03415","SJAG_02443","SJAG_00032","SJAG_05300","SJAG_01397","SJAG_00601","SJAG_04196","SJAG_01508","SJAG_02060","SJAG_00418","SJAG_03851","SJAG_04548","SJAG_00380","SJAG_01282","SJAG_05328","SJAG_01927","SJAG_03411","SJAG_03502","SJAG_00029","SJAG_04100","SJAG_03357","SJAG_07004","SJAG_03073","SJAG_01381","SJAG_00858","SJAG_01493","SJAG_02572","SJAG_02349","SJAG_03662","SJAG_02684","SJAG_03843","SJAG_02079","SJAG_00514","SJAG_03899","SJAG_03299","SJAG_01409","SJAG_01400","SJAG_00383","SJAG_03543","SJAG_02857","SJAG_01876","SJAG_04142","SJAG_03528","SJAG_02946","SJAG_04725","SJAG_03172","SJAG_04140","SJAG_01981","SJAG_03138","SJAG_02532","SJAG_01447","SJAG_04717","SJAG_00589","SJAG_03511","SJAG_01615","SJAG_04715","SJAG_02912","SJAG_02823","SJAG_00207","SJAG_03072","SJAG_04697","SJAG_03540","SJAG_00546","SJAG_03785","SJAG_00756","SJAG_02104","SJAG_00137","SJAG_00768","SJAG_01353","SJAG_00140","SJAG_05204","SJAG_00569","SJAG_03044","SJAG_05325","SJAG_00048","SJAG_00211","SJAG_04411","SJAG_06598","SJAG_01224","SJAG_00404","SJAG_00760","SJAG_05372","SJAG_01384","SJAG_02392","SJAG_00314","SJAG_00333","SJAG_03850","SJAG_04312","SJAG_02457","SJAG_02997","SJAG_02809","SJAG_00820","SJAG_04757","SJAG_00299","SJAG_05260","SJAG_00054","SJAG_02707","SJAG_04126","SJAG_01613","SJAG_00355","SJAG_01242","SJAG_01999","SJAG_01078","SJAG_01339","SJAG_01145","SJAG_02693","SJAG_01840","SJAG_04740","SJAG_05011","SJAG_02955","SJAG_01371","SJAG_02366","SJAG_01598","SJAG_01909","SJAG_04471","SJAG_03746","SJAG_01558","SJAG_04203","SJAG_01686","SJAG_03503","SJAG_01003","SJAG_03680","SJAG_03406","SJAG_00332","SJAG_01731","SJAG_03488","SJAG_04957","SJAG_03737","SJAG_00794","SJAG_01945","SJAG_02125","SJAG_03327","SJAG_05259","SJAG_01923","SJAG_03499","SJAG_00959","SJAG_01879","SJAG_03865","SJAG_02640","SJAG_05294","SJAG_02065","SJAG_04052","SJAG_01745","SJAG_02336","SJAG_02655","SJAG_02588","SJAG_04343","SJAG_01715","SJAG_01488","SJAG_03010","SJAG_04930","SJAG_02368","SJAG_16459","SJAG_00301","SJAG_05223","SJAG_03264","SJAG_01177","SJAG_04076","SJAG_00064","SJAG_03602","SJAG_00821","SJAG_04622","SJAG_02440","SJAG_03146","SJAG_04931","SJAG_03504","SJAG_01178","SJAG_03404","SJAG_00678","SJAG_01470","SJAG_03170","SJAG_03011","SJAG_00968","SJAG_04474","SJAG_04014","SJAG_04412","SJAG_02384","SJAG_05019","SJAG_02264","SJAG_01960","SJAG_03860","SJAG_04983","SJAG_02120","SJAG_03247","SJAG_03560","SJAG_02049","SJAG_02320","SJAG_01459","SJAG_01456","SJAG_00178","SJAG_02605","SJAG_02514","SJAG_03838","SJAG_00557","SJAG_00916","SJAG_01324","SJAG_03938","SJAG_04675","SJAG_03827","SJAG_04637","SJAG_04593","SJAG_04280","SJAG_00261","SJAG_04597","SJAG_00985","SJAG_03951","SJAG_01697","SJAG_01059","SJAG_01652","SJAG_01185","SJAG_00564","SJAG_01527","SJAG_05210","SJAG_01077","SJAG_06588","SJAG_03283","SJAG_03287","SJAG_04763","SJAG_04277","SJAG_02245","SJAG_05198","SJAG_02839","SJAG_04956","SJAG_01759","SJAG_05013","SJAG_03673","SJAG_00212","SJAG_04739","SJAG_01817","SJAG_02518","SJAG_00230","SJAG_04673","SJAG_00232","SJAG_05342","SJAG_00895","SJAG_03729","SJAG_01973","SJAG_00785","SJAG_04892","SJAG_00368","SJAG_02418","SJAG_02029","SJAG_01645","SJAG_04391","SJAG_02583","SJAG_04909","SJAG_00222","SJAG_02355","SJAG_03437","SJAG_03889","SJAG_03200","SJAG_03595","SJAG_02144","SJAG_05302","SJAG_01083","SJAG_02858","SJAG_00114","SJAG_02241","SJAG_00136","SJAG_01538","SJAG_01293","SJAG_03667","SJAG_01929","SJAG_01311","SJAG_00092","SJAG_02731","SJAG_01722","SJAG_02075","SJAG_02626","SJAG_02780","SJAG_04513","SJAG_03467","SJAG_04129","SJAG_02323","SJAG_01732","SJAG_04716","SJAG_02561","SJAG_04419","SJAG_03158","SJAG_02150","SJAG_01564","SJAG_04208","SJAG_01211","SJAG_03652","SJAG_02737","SJAG_03558","SJAG_03126","SJAG_01584","SJAG_02160","SJAG_04058","SJAG_00175","SJAG_MIT15","SJAG_04360","SJAG_01780","SJAG_02727","SJAG_03987","SJAG_03835","SJAG_03633","SJAG_03892","SJAG_01990","SJAG_04347","SJAG_04886","SJAG_03962","SJAG_03363","SJAG_01119","SJAG_04001","SJAG_05266","SJAG_00233","SJAG_00298","SJAG_00041","SJAG_03039","SJAG_04569","SJAG_02330","SJAG_02877","SJAG_03643","SJAG_04846","SJAG_01114","SJAG_03399","SJAG_00471","SJAG_01120","SJAG_01471","SJAG_03002","SJAG_04509","SJAG_02539","SJAG_00416","SJAG_01229","SJAG_02958","SJAG_04609","SJAG_03698","SJAG_04733","SJAG_03137","SJAG_03270","SJAG_01586","SJAG_04489","SJAG_00133","SJAG_01516","SJAG_03515","SJAG_02947","SJAG_04920","SJAG_04083","SJAG_04464","SJAG_01496","SJAG_03086","SJAG_04258","SJAG_03606","SJAG_02456","SJAG_04600","SJAG_03631","SJAG_02034","SJAG_01367","SJAG_02482","SJAG_03220","SJAG_00641","SJAG_02524","SJAG_00030","SJAG_03925","SJAG_00522","SJAG_04432","SJAG_01748","SJAG_02751","SJAG_04940","SJAG_04479","SJAG_00752","SJAG_04618","SJAG_01435","SJAG_03933","SJAG_01319","SJAG_00430","SJAG_02016","SJAG_01949","SJAG_01964","SJAG_01782","SJAG_03281","SJAG_00302","SJAG_04259","SJAG_02578","SJAG_00102","SJAG_04938","SJAG_02811","SJAG_02177","SJAG_03663","SJAG_01639","SJAG_03396","SJAG_04984","SJAG_04023","SJAG_05194","SJAG_00883","SJAG_03244","SJAG_04528","SJAG_00626","SJAG_03650","SJAG_04506","SJAG_03368","SJAG_04536","SJAG_02019","SJAG_01925","SJAG_02422","SJAG_04158","SJAG_04668","SJAG_00375","SJAG_04656","SJAG_01223","SJAG_01076","SJAG_03959","SJAG_01017","SJAG_01756","SJAG_01626","SJAG_04340","SJAG_03153","SJAG_04684","SJAG_03718","SJAG_04936","SJAG_01572","SJAG_02228","SJAG_01166","SJAG_03021","SJAG_01442","SJAG_01662","SJAG_03591","SJAG_00276","SJAG_00196","SJAG_00185","SJAG_04017","SJAG_02286","SJAG_01750","SJAG_00057","SJAG_04260","SJAG_01358","SJAG_01406","SJAG_04677","SJAG_01112","SJAG_01460","SJAG_00603","SJAG_01601","SJAG_01633","SJAG_04349","SJAG_03873","SJAG_05226","SJAG_02834","SJAG_02299","SJAG_01297","SJAG_05184","SJAG_03465","SJAG_03648","SJAG_02837","SJAG_03119","SJAG_05213","SJAG_05209","SJAG_02105","SJAG_02004","SJAG_00445","SJAG_00296","SJAG_04013","SJAG_04837","SJAG_04040","SJAG_00176","SJAG_00181","SJAG_02914","SJAG_03696","SJAG_00845","SJAG_04044","SJAG_00268","SJAG_04641","SJAG_00438","SJAG_01206","SJAG_02152","SJAG_00992","SJAG_01165","SJAG_00753","SJAG_00918","SJAG_02204","SJAG_02695","SJAG_03256","SJAG_00661","SJAG_02132","SJAG_03246","SJAG_01245","SJAG_05207","SJAG_04028","SJAG_02998","SJAG_01407","SJAG_02962","SJAG_02757","SJAG_00280","SJAG_04743","SJAG_03145","SJAG_04406","SJAG_03536","SJAG_05295","SJAG_04588","SJAG_00836","SJAG_01983","SJAG_01391","SJAG_01355","SJAG_00490","SJAG_01842","SJAG_00907","SJAG_03926","SJAG_04829","SJAG_01600","SJAG_04310","SJAG_02831","SJAG_04096","SJAG_00326","SJAG_07012","SJAG_00143","SJAG_03866","SJAG_05290","SJAG_03684","SJAG_01805","SJAG_03930","SJAG_04294","SJAG_03552","SJAG_04241","SJAG_00763","SJAG_00108","SJAG_04135","SJAG_00216","SJAG_03142"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[59390],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035348"},{"annotations":[104941,73643,75776,78960,74939,112100,79316,71737],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051666"},{"annotations":[112342],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098702"},{"annotations":[74300],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015866"},{"annotations":[71329],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015742"},{"annotations":[76810],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032974"},{"annotations":[75263,118066,89452,118069,95460,79695,78333,77471,118064,118070,118065,72875,75076,75959,118068,99812,77447,76403,80098,103315,76563,79831,118063,118067],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003333"},{"annotations":[68302],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0140331"},{"annotations":[74374],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0015917"},{"annotations":[75133,69464],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072488"},{"annotations":[102587,109823],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990591"},{"annotations":[95399,74344,107340,109966,101060,104836],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061509"},{"annotations":[93588,87614],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051456"},{"annotations":[110112,72550,71592,118469,117954,116334,87500,87749,105275,91140,95319,100166,90748,75532,111481,110157,89788,97681],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051315"},{"annotations":[91096,94363,88821],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140698"},{"annotations":[94386],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016240"},{"annotations":[90147],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034488"},{"annotations":[94352],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034490"},{"annotations":[103813,103810,103811,103812,97114],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990822"},{"annotations":[71490,79033],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905135"},{"annotations":[110758],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140159"},{"annotations":[118012],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036249"},{"annotations":[63622],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070574"},{"annotations":[97125,95392],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036444"},{"annotations":[66567,74120,92158,114242],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098703"},{"annotations":[115370],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140146"},{"annotations":[65523,94577,69136,95213,73062,78181,72066,109173],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070588"},{"annotations":[58245,60654,64400,60603],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034219"},{"annotations":[58234,68764,87205,68677],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905039"},{"annotations":[111755],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098653"},{"annotations":[89339,116750,91097,102605],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072766"},{"annotations":[73176,70050,76817],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902476"},{"annotations":[79417],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0072318"},{"annotations":[99493],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0035652"},{"annotations":[102529,110484,91965,112712,96054,74075,91300,58189,111474,117335,79418,107858,108137,105519,73372,94653,112108,92345,77845,118684],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072583"},{"annotations":[117555,70971],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0048205"},{"annotations":[72753],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0090114"},{"annotations":[76249,75278,74508,71092,76790,78137,74863],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0090110"},{"annotations":[107652],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0060003"},{"annotations":[78437],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015677"},{"annotations":[87686,114395],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098705"},{"annotations":[101272],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097430"},{"annotations":[61744,103574,104413],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035434"},{"annotations":[104504],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006825"},{"annotations":[97689],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006613"},{"annotations":[63246],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903712"},{"annotations":[105557,91393,90823,87756,114254,87869,87834,91258,113113],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0120113"},{"annotations":[110442,113978],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046323"},{"annotations":[117020],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098708"},{"annotations":[91818],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905136"},{"annotations":[71585],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140206"},{"annotations":[118156,118155],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035442"},{"annotations":[75660,79133,96485],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990683"},{"annotations":[87502,111200,90749,100514,102753,110846,113749,91141,97352,116751,94966,103046,91600],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0030989"},{"annotations":[115031,71080],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0034498"},{"annotations":[74423],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0045022"},{"annotations":[79228,72722,74388,115453,115532,80062,72770,79239,79712],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0032456"},{"annotations":[108778,73498,71154,93779,103104,110062,115999,73058,77211,99500,74937,74989,107933,99472,102853,104408,106653,79817,99260,78959,93804,79662,97696,79509,89574,98624,102302,99653,108867,71757,90430,71020,73640,87376,87898,77413,71734,101236,104946,104963,118645,87870,69420,105718,101909,71099,75688,69940,72160,79314,71466,98695,99747,90500,115987,78311,101506],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006897"},{"annotations":[87737],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0120207"},{"annotations":[71906,74786,78556,79302,90922,110543,69502,118745,74615,91866,70504,87978,95814,63654,73552,74136,73237,73468,70076,92902,109297,98238,92988,74402,114804,59022,100537,75975,118614,93652,91287,79634,75298,66264,70640,72453,101970,94786,100867,73994,112224,76809,106925,112482,78116,104397,97537,116325,74957,78524,100124,77394,77779,78477,95374,116182,71848,78611,71031,57829,76702,110636,106210,106627,97685,79048],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0006888"},{"annotations":[111461,71550,61758,60048,61255,91239,117970,97232,90161],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061817"},{"annotations":[102303,67951,70809,101759,71754,71463,79659],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0016197"},{"annotations":[76922,79482,74291,99299,99501,70885],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034058"},{"annotations":[91047,118695,100917,112806,112585,94654],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0099638"},{"annotations":[117337],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0032509"},{"annotations":[109421,73056,72716,73348,73833,117326],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0035621"},{"annotations":[69611,106386],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051654"},{"annotations":[102551],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034643"},{"annotations":[116752,76122,104332,96747,104663],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0000132"},{"annotations":[95478],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061951"},{"annotations":[70951,71019,70429,71712,70719,77752,90903,94753,97228,92029,69939,87738,91776,102453,88143,88509,91232,112713,94787,104868,93621,73057,116946],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006887"},{"annotations":[68514,118558,117280,57272,61330],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140115"},{"annotations":[100802],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140569"},{"annotations":[74432],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140570"},{"annotations":[113545],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140116"},{"annotations":[61496],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015884"},{"annotations":[110443],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140425"},{"annotations":[116998],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990735"},{"annotations":[93098],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036085"},{"annotations":[71440],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990570"},{"annotations":[92246],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140270"},{"annotations":[63102],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006868"},{"annotations":[95284],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098709"},{"annotations":[112938],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0160007"},{"annotations":[95832,118014,96823],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071996"},{"annotations":[102381,102382,102380],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001407"},{"annotations":[69583,98008],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904983"},{"annotations":[76667,94182],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0034203"},{"annotations":[90955],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061856"},{"annotations":[118240,76636,77404,99699,88897,73024,77362,100039,100097,79508,100906,112807,116775,61234],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0006895"},{"annotations":[106843,106949,109382,69717,94907,106211,108599,77187,112808],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043001"},{"annotations":[70430,71623,92030,75653,57276,72306,107186,77124,99549,106093,100637],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006893"},{"annotations":[99701,93947,117363,95894,77524,77804,75890,75726,111297,101237,79226,77363,110063,77405,69487,96648,90330,73025,108600,99300,96918],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0006896"},{"annotations":[77192],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0048194"},{"annotations":[70077],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0048211"},{"annotations":[95708],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0048210"},{"annotations":[57935],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048193"},{"annotations":[112343],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098710"},{"annotations":[63497],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903790"},{"annotations":[102770],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008645"},{"annotations":[90036,87557,101121,93552,115344,116869,107621,113585,98405],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0031619"},{"annotations":[101219,106387,111023],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032118"},{"annotations":[64302],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0051170"},{"annotations":[76496],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0170036"},{"annotations":[89244],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098661"},{"annotations":[97874],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048219"},{"annotations":[109165,102400,108004,57264,111125,94005,116028],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0120009"},{"annotations":[90657,98415,88975,103831,108453,109327,100312,106538,107447,101071,116051,105647,97266,97327,107321],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0120010"},{"annotations":[106127],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0120011"},{"annotations":[116476],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0120110"},{"annotations":[96062,100125,69720,70546,77781,103163,109364,74963,77085,57261,79635,88411,97082,69950,97519,78557,71081,69177,78117,98239,73239,99550,102319,75725,104693,106926,109627],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006891"},{"annotations":[76140,107013,107225],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048312"},{"annotations":[117095],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008298"},{"annotations":[107293,90904,97875,101710,68574,66991,90324,118825,67952,62122,116183,74956,63186,95815,91288,70075,114681,71847,102320,108981,67008,73236,88369,68754,93622,65316,116706,88898,67853,94908,111989,112483,102483,94149,95853,96063,67943,76162,100868,77778,103526,109628,94754,78699,70544,97520,107107,78270,109299,64654,93259,76701,92903,58433,71681,91385,98240,107187,98833,96653,105950,107826,116776,93805,110544,113960,100638,95545,117364,79651,65712,63538,106927,112254,70158,113272,77141,57980,115037,69070,62809,66615,104398,74135,108227,113433,89465,93400,104984,99808,105824,77482,97083,66522,103516,97538,114168,101238,63199,95276,71711,99301,79257,98893,99551,58619,95375,109455,94038,69391,99691,116236,63050,88412,58191,71515,64089,99502,75889,92989,109383,111811,58685,118648,91233,102098,104762,98696,116642,94705,68558,111966,102927,75525,104694,96649,114938,90925,87802,78476,67699,94559,110064,58352,93653,107358,60070,79736],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0006886"},{"annotations":[76890,71673,61984],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0032366"},{"annotations":[63299,68759,63502,74638],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0046907"},{"annotations":[113594,69812,97857],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048250"},{"annotations":[75329,77636,113017,61156,112594],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034755"},{"annotations":[89021],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140466"},{"annotations":[109824,102588],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903714"},{"annotations":[100028],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0170046"},{"annotations":[95786],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902475"},{"annotations":[100146],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097638"},{"annotations":[97129],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990818"},{"annotations":[103618],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090518"},{"annotations":[98608,63103],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903826"},{"annotations":[96325],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070778"},{"annotations":[98009],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110141"},{"annotations":[103619],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901481"},{"annotations":[103620],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090515"},{"annotations":[96326],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015813"},{"annotations":[97130],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0089708"},{"annotations":[103621],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090513"},{"annotations":[100147],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097639"},{"annotations":[102589,103622],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901482"},{"annotations":[97131],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0089707"},{"annotations":[109825],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090517"},{"annotations":[103624],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090516"},{"annotations":[65084],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015825"},{"annotations":[103625],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090514"},{"annotations":[80060],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0034499"},{"annotations":[100099,75338,89929,101771,105514,108793,107427,116707,110686,118242,76381,73743,109608,76965,100041,100907],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0045324"},{"annotations":[98472,74950,75704,98651,70450,103911,102933,106928,110007,79056],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0032511"},{"annotations":[108055],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0099607"},{"annotations":[102708,116737],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140043"},{"annotations":[75223],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990616"},{"annotations":[56718,57259,116781,62220],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903830"},{"annotations":[90162,104164],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0051685"},{"annotations":[66546],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0032065"},{"annotations":[110659,93781,99962,104445],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0097248"},{"annotations":[101443],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098714"},{"annotations":[67124],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071423"},{"annotations":[63522],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015743"},{"annotations":[101444],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098715"},{"annotations":[64253],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901553"},{"annotations":[95528],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106081"},{"annotations":[61157,63621,108469,70308],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071421"},{"annotations":[64213,89510],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0070197"},{"annotations":[87145,89511,102606,99710,104901],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032121"},{"annotations":[102224,117957,118472,115733,93555,100168,95071,108943,99009],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990571"},{"annotations":[117372,115753,117509,96486],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0045141"},{"annotations":[113791],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0044821"},{"annotations":[58699],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030001"},{"annotations":[99040],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072489"},{"annotations":[94531,109707],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0099606"},{"annotations":[96328],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990551"},{"annotations":[101144],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990554"},{"annotations":[101145],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990553"},{"annotations":[58733],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140021"},{"annotations":[96329],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990550"},{"annotations":[58732,102643],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990544"},{"annotations":[71331,72198],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006843"},{"annotations":[70153],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990559"},{"annotations":[96907,94810,98275],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0160203"},{"annotations":[107362],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990548"},{"annotations":[114958],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140140"},{"annotations":[88157],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990556"},{"annotations":[107707],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990575"},{"annotations":[77062],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045016"},{"annotations":[92661],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990549"},{"annotations":[88158],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990555"},{"annotations":[67449],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990547"},{"annotations":[93980],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140141"},{"annotations":[62713,76687],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006850"},{"annotations":[88012,102395],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990543"},{"annotations":[88159],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990557"},{"annotations":[103424],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990545"},{"annotations":[100879,89245,96889],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990542"},{"annotations":[111927],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048311"},{"annotations":[102553],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000001"},{"annotations":[72190],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051646"},{"annotations":[116422,69608,74378,69523,79878],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990456"},{"annotations":[108058,100170,103683],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007079"},{"annotations":[98407,108059,99016,103684,93957],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:1990942"},{"annotations":[93590,112419,113900,103333,114304,118501,113034,103685,88888,107304,93958,100307,108687,77670,98911,112417,109693,116724,98409,102225,89493,89108,90736,108060,112418],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990758"},{"annotations":[100388,103248,89880,112644,111232,102607],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140480"},{"annotations":[75829,98913,116677,104902,89512],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0044820"},{"annotations":[58978],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098656"},{"annotations":[88160,57205,104415,112526],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006820"},{"annotations":[61253,58183,68938,68685],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098655"},{"annotations":[65085],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034220"},{"annotations":[62130,79989,73698,117072,72551,100939,77283,72308,76411,89232,60881],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0006406"},{"annotations":[72857],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0031990"},{"annotations":[59602,58015,64233],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0051028"},{"annotations":[71791,72618],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904679"},{"annotations":[102150],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1902424"},{"annotations":[113165,90973],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1905949"},{"annotations":[94339],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0045806"},{"annotations":[87835],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0042997"},{"annotations":[87836],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1905533"},{"annotations":[102159],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1904537"},{"annotations":[105613],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0042308"},{"annotations":[90718,95614],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1903067"},{"annotations":[94168],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0140325"},{"annotations":[107033],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1902543"},{"annotations":[114276],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1900181"},{"annotations":[95615],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1903077"},{"annotations":[100785],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010621"},{"annotations":[87837],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1905530"},{"annotations":[79719],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098716"},{"annotations":[76780,72854,73310,74483,100940,75840],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0006607"},{"annotations":[104665,112568,104334],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0007097"},{"annotations":[101230,109411,107229,70333,113751,74665,116755],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0098863"},{"annotations":[99021,97427],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0090561"},{"annotations":[76124,91143,87506,97354,99022],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0000743"},{"annotations":[77825],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015851"},{"annotations":[87119,117100,67383,64349,97718,104587,115850],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0006913"},{"annotations":[108065],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051647"},{"annotations":[80138],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071562"},{"annotations":[75272],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090374"},{"annotations":[72144],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098717"},{"annotations":[106987],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090539"},{"annotations":[115599],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0180029"},{"annotations":[109501,112527,116315],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035435"},{"annotations":[76331,93099],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990536"},{"annotations":[90273,90277,109313,99261,90275,101073,90270,62403,72606,71650,72577,74202,90272,90271,90274,90276,90278,59704,74383,102005],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0045332"},{"annotations":[95833,96824,118015],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036246"},{"annotations":[98484],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006847"},{"annotations":[72858],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0017121"},{"annotations":[74454,73970,71130,101180,80116,107434,77046,115610,73625,110916,73287,116122,109660,110225,74087,96299,96718,101652,103731,117833,118736,91952,72852,102440,72732,115864,69433,75489,111547,114264],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0016973"},{"annotations":[106475,88851,114320],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0180042"},{"annotations":[111758,104977,115818],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1902425"},{"annotations":[101934],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1905665"},{"annotations":[103486],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0045807"},{"annotations":[99964],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0045921"},{"annotations":[89675],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0035432"},{"annotations":[91499,98663,110336,93090],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1905589"},{"annotations":[93091,98664,91500],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1905534"},{"annotations":[93092],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1905626"},{"annotations":[110999,102170,93564,89748,116487],"is_not":false,"rel_names":["part_of","regulates"],"summary":null,"term":"GO:0140429"},{"annotations":[94173],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1902854"},{"annotations":[101640,110807,100227,93565],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0046827"},{"annotations":[90604,94131,102173],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0042307"},{"annotations":[98215],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0120047"},{"annotations":[73126,74386,93995,79237,110470],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006892"},{"annotations":[95496,79156,69556],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006620"},{"annotations":[72912,80123,72869,73225,97109,97827,108110],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0031204"},{"annotations":[112143],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097623"},{"annotations":[72020,70222],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990573"},{"annotations":[67059,79855,61027,57296],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071805"},{"annotations":[100140,101002],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905647"},{"annotations":[72752],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0032527"},{"annotations":[100941,117201,109389,71242,92926,64301,117488,64465],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0006611"},{"annotations":[77342,76874],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0045041"},{"annotations":[99328,96654,102484,105974,88076,107310,99214,107367,117058,99030,94277,109679,104985,107389,90650,103071,100104,111596,89287,115038,116589],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0030150"},{"annotations":[73783,88659,97604,74816,74088,78225,94045,95886,73288,93746,65938,75449,79800,73432,75200,71086,115611,75490,80117,59993,79990,70530,71241,72350,69707,70025,71027,72552,79436,106134,72428,73798,104856,76082,77619,72748],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0006606"},{"annotations":[102052,79437,73078,111189,70404,71740,69680,96235],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0016558"},{"annotations":[73512,62321,70235],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0016560"},{"annotations":[117118,115109,98357,63911],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0016562"},{"annotations":[111190,90180,95186],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0045046"},{"annotations":[108202,100979,113640,110199,114191,70965,97828,67689,91423,98149,94590,104270,112050,104578,105968,103301,108111,98378,109138],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0045048"},{"annotations":[90143,75336,73192,107390,77558,113001,116076,88403,102711,107368,73682],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0045039"},{"annotations":[78428,57974,78003,74148,78353],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0032979"},{"annotations":[98367,107369,111590,69607,76289,58691,110197,109845,98016],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0045040"},{"annotations":[106964],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044379"},{"annotations":[91051,113850,115989],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990896"},{"annotations":[95421],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072741"},{"annotations":[99508],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070198"},{"annotations":[96749],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904518"},{"annotations":[77816,70505],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070973"},{"annotations":[98504],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034067"},{"annotations":[74998,77669,59182],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034501"},{"annotations":[104321,99877],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903360"},{"annotations":[90894,105156],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071574"},{"annotations":[113735,91052,96642],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902441"},{"annotations":[71661,77230,77878],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072657"},{"annotations":[70262],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035372"},{"annotations":[92085,110597,118451],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904498"},{"annotations":[89751],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902440"},{"annotations":[74814,76779],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036228"},{"annotations":[90305,90605,114760,65269,89277,67981,101186],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072659"},{"annotations":[79720,101997,69476,76583,79995,77811],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006627"},{"annotations":[91888],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0006621"},{"annotations":[69185,112357,87390,68814,98150,98199],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045047"},{"annotations":[72545,95660,70756,59990,74660,74732,75812],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006612"},{"annotations":[102248,98180],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006626"},{"annotations":[95187,102882,96728,90181,90189],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006625"},{"annotations":[90759],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0044395"},{"annotations":[80027,73744,72485,77361,75339,77803,96316,76923,70886,76967],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0006623"},{"annotations":[66237,56931,61045],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071806"},{"annotations":[72765,75442,79707,64581,60738],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015031"},{"annotations":[103536],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0099117"},{"annotations":[103691,118476,108067,100174],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0140210"},{"annotations":[109694,113901,98411,116725,108688,88889,107305,89494,90737,100308,96546],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:1990976"},{"annotations":[107935,115990],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904601"},{"annotations":[73022,97737,87872,91396,106360,114515,70609,109177,77402,73048,95726,91261,70626,71774,87703,71780,77969,78185,100678],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0043328"},{"annotations":[57699,60687,66306,66636],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120029"},{"annotations":[66962,62366,65130,61068,60334,67396,61525,68048,61982,108592,64339,90957,60652,59085,60941,60604,57100,57295,64678,92332,103469,63606,59446,68563,60432,118869,63140,59649,58330,59120,66134,64015,118875,64398,63718,67470,78144,107703,63620,60992,58008,66540,95529,61624,57767,62481,61278,72638,60377,67159,63577,60005,58243,118880,69058,94603,67974],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902600"},{"annotations":[70268],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015847"},{"annotations":[89889,89888,117281,118559],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903090"},{"annotations":[89890,118560,117282,89891],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903091"},{"annotations":[117283,89892,118561,89893],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903092"},{"annotations":[88180],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904082"},{"annotations":[78974],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990519"},{"annotations":[72721],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031623"},{"annotations":[77260,92208,112595],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0033215"},{"annotations":[111466,118667,110816],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:2000369"},{"annotations":[87644],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:2001135"},{"annotations":[113040,77299,90719,78026,113168,92467,102721,89619,92183],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0030100"},{"annotations":[76347],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0060628"},{"annotations":[93605,98183,87647],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0017157"},{"annotations":[91777,87648],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0033157"},{"annotations":[99182],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:2000185"},{"annotations":[106189],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1902267"},{"annotations":[107755],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1905391"},{"annotations":[103113],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1905634"},{"annotations":[113426],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:2000156"},{"annotations":[116490],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1904967"},{"annotations":[108470],"is_not":false,"rel_names":["regulates","negatively_regulates","is_a"],"summary":null,"term":"GO:0061454"},{"annotations":[75240,78791],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0030970"},{"annotations":[112809,118309,112586,70157,97522,92045,79225,94706,62266,98473,75687,71680,63653,77140,105330,71245,75724,77058,78341,70732,100918,118697,76961,69486,79650,101922,102455,96919,71284,75524],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0042147"},{"annotations":[116643,90905,88710,109300],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000301"},{"annotations":[73238,77780,97523,75299,63930,74958,70545,77570,99262,98241,70641,72450,90325,92990,68584,70940,92654,65307,66669,76345,77190,113434,73553,71939,98332],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006890"},{"annotations":[117489,105549,116036,76715,75922,76357,79991,99426],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0000055"},{"annotations":[69506,79992,75923,69989],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0000056"},{"annotations":[91479,94739,95887,105960,93747,100200,101181,111241,88755,71087,110228,79086,105185,76143,103732],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0000054"},{"annotations":[76090,93748,95888,74815,104858,79799,75199],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0006405"},{"annotations":[102345],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0006404"},{"annotations":[90371],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140300"},{"annotations":[61660,61769,68829],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044718"},{"annotations":[112596],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015891"},{"annotations":[61661,61770,68830],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0033214"},{"annotations":[108945],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031134"},{"annotations":[75212],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0035493"},{"annotations":[57110,76161],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0035494"},{"annotations":[79503,97724],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048254"},{"annotations":[66634],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036376"},{"annotations":[60991,89063,67058],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035725"},{"annotations":[57717,110728,117159],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903711"},{"annotations":[117160,68512,110729],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903710"},{"annotations":[101125,107306,108689,110158,100309,109695,113902,115735,95072,113035,102226,90738,105278,110115,107625,88890,95320,108946,97682,116726,89495,93569,98413],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051455"},{"annotations":[116756],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0140405"},{"annotations":[66011,94039,68557,72657,69555],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006614"},{"annotations":[114169,114939,91386],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006617"},{"annotations":[108112,102372,72910,73223,97829,75151],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0006616"},{"annotations":[115323,114088,88917,91294,98851,89345,98735,116614,109763,109359,95942,96456],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120290"},{"annotations":[109167,116031,94008,102402,108007,111127],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0015918"},{"annotations":[91103],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140464"},{"annotations":[101445],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098720"},{"annotations":[95530],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106082"},{"annotations":[109918],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902434"},{"annotations":[61491],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902358"},{"annotations":[74756,113932,72374],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0071816"},{"annotations":[75198,72853],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034398"},{"annotations":[107784],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901583"},{"annotations":[100464],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140125"},{"annotations":[89895,89894],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071934"},{"annotations":[75985,66601,67255,69686,70561,63057,77007,62874,58622,58616,57677,65762,59604,74166,65245,68912,58091,69219,72559,79214,69398,116397,65631],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0055085"},{"annotations":[90906],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0010970"},{"annotations":[112056,92867],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035436"},{"annotations":[102800],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140207"},{"annotations":[78299,71684,105550,105075],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0006409"},{"annotations":[78872],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0016031"},{"annotations":[79372],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0071528"},{"annotations":[63101],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015828"},{"annotations":[72632,118677,110822,78915,105520,91966,78255,78968],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070086"},{"annotations":[74597,88113],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097624"},{"annotations":[75640],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072334"},{"annotations":[74864],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015786"},{"annotations":[112171],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0120112"},{"annotations":[77381],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990569"},{"annotations":[66030],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015790"},{"annotations":[95297],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098721"},{"annotations":[57716],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071918"},{"annotations":[73174],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034486"},{"annotations":[71660,88852,95594,77229,70526,114321],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0007034"},{"annotations":[106826,115012],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:1990854"},{"annotations":[94081],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140057"},{"annotations":[70448,69673,76098,73371,79055],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006900"},{"annotations":[95278],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006901"},{"annotations":[109456,71715,100101,99303,109611,112484,117366,75893,77485,100911],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0048278"},{"annotations":[79864,59985,69392,90331,79556,118026,74668,92090],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0006904"},{"annotations":[77483,109457,76277,97876,100869,117322,75891,117367,77753,90332,100639,71713,112485],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006906"},{"annotations":[77395,73555,57526,75728],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0048280"},{"annotations":[118246],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0099022"},{"annotations":[65713,117540,90502,113961,88370,59987,101711,99337],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0090522"},{"annotations":[115992],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0030050"},{"annotations":[104335,104668],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0047496"},{"annotations":[60181,106274,105211,107294,79057,104466,105420,78266,110734,95719,104968,75939,94040,60740,98628,116309,99308,93730,114051,98600,104604,107756,71513,66759,97834,87805,110644,76595,117812],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016192"},{"annotations":[79723],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042906"},{"annotations":[63380,117765,58290],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990961"},{"annotations":[57271,117284,118562,68513,61329],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042908"},{"annotations":[114143],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140147"},{"annotations":[113018,103963],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071578"},{"annotations":[93529,93530],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0140209"},{"annotations":[104102,74320],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904257"},{"annotations":[78035],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071577"}]},"cv_name":"biological_process","definition":"Any process in which a cell, a substance, or a cellular entity, such as a protein complex or organelle, is transported, tethered to or otherwise maintained in a specific location. In the case of substances, localization may also be achieved via selective degradation.","definition_xrefs":["GOC:dos","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biological_process","termid":"GO:0008150"}],"gene_count":1067,"genes_by_uniquename":{"SJAG_00015":null,"SJAG_00018":null,"SJAG_00019":null,"SJAG_00029":null,"SJAG_00030":null,"SJAG_00031":null,"SJAG_00032":null,"SJAG_00041":null,"SJAG_00048":null,"SJAG_00051":null,"SJAG_00053":null,"SJAG_00054":null,"SJAG_00057":null,"SJAG_00064":null,"SJAG_00065":null,"SJAG_00072":null,"SJAG_00080":null,"SJAG_00082":null,"SJAG_00092":null,"SJAG_00093":null,"SJAG_00102":null,"SJAG_00104":null,"SJAG_00108":null,"SJAG_00113":null,"SJAG_00114":null,"SJAG_00133":null,"SJAG_00136":null,"SJAG_00137":null,"SJAG_00140":null,"SJAG_00143":null,"SJAG_00144":null,"SJAG_00149":null,"SJAG_00152":null,"SJAG_00154":null,"SJAG_00171":null,"SJAG_00175":null,"SJAG_00176":null,"SJAG_00178":null,"SJAG_00181":null,"SJAG_00185":null,"SJAG_00192":null,"SJAG_00196":null,"SJAG_00204":null,"SJAG_00207":null,"SJAG_00208":null,"SJAG_00211":null,"SJAG_00212":null,"SJAG_00216":null,"SJAG_00222":null,"SJAG_00229":null,"SJAG_00230":null,"SJAG_00232":null,"SJAG_00233":null,"SJAG_00261":null,"SJAG_00268":null,"SJAG_00275":null,"SJAG_00276":null,"SJAG_00277":null,"SJAG_00279":null,"SJAG_00280":null,"SJAG_00284":null,"SJAG_00287":null,"SJAG_00296":null,"SJAG_00298":null,"SJAG_00299":null,"SJAG_00301":null,"SJAG_00302":null,"SJAG_00314":null,"SJAG_00326":null,"SJAG_00328":null,"SJAG_00330":null,"SJAG_00332":null,"SJAG_00333":null,"SJAG_00335":null,"SJAG_00339":null,"SJAG_00355":null,"SJAG_00357":null,"SJAG_00360":null,"SJAG_00368":null,"SJAG_00373":null,"SJAG_00375":null,"SJAG_00379":null,"SJAG_00380":null,"SJAG_00383":null,"SJAG_00397":null,"SJAG_00402":null,"SJAG_00404":null,"SJAG_00405":null,"SJAG_00416":null,"SJAG_00418":null,"SJAG_00430":null,"SJAG_00434":null,"SJAG_00438":null,"SJAG_00445":null,"SJAG_00467":null,"SJAG_00471":null,"SJAG_00484":null,"SJAG_00490":null,"SJAG_00514":null,"SJAG_00516":null,"SJAG_00521":null,"SJAG_00522":null,"SJAG_00525":null,"SJAG_00530":null,"SJAG_00542":null,"SJAG_00543":null,"SJAG_00546":null,"SJAG_00547":null,"SJAG_00553":null,"SJAG_00557":null,"SJAG_00564":null,"SJAG_00569":null,"SJAG_00576":null,"SJAG_00578":null,"SJAG_00586":null,"SJAG_00587":null,"SJAG_00589":null,"SJAG_00594":null,"SJAG_00596":null,"SJAG_00601":null,"SJAG_00603":null,"SJAG_00612":null,"SJAG_00626":null,"SJAG_00632":null,"SJAG_00641":null,"SJAG_00645":null,"SJAG_00646":null,"SJAG_00649":null,"SJAG_00655":null,"SJAG_00661":null,"SJAG_00669":null,"SJAG_00671":null,"SJAG_00678":null,"SJAG_00687":null,"SJAG_00700":null,"SJAG_00702":null,"SJAG_00727":null,"SJAG_00752":null,"SJAG_00753":null,"SJAG_00756":null,"SJAG_00760":null,"SJAG_00763":null,"SJAG_00767":null,"SJAG_00768":null,"SJAG_00777":null,"SJAG_00785":null,"SJAG_00794":null,"SJAG_00800":null,"SJAG_00803":null,"SJAG_00804":null,"SJAG_00820":null,"SJAG_00821":null,"SJAG_00826":null,"SJAG_00835":null,"SJAG_00836":null,"SJAG_00840":null,"SJAG_00845":null,"SJAG_00850":null,"SJAG_00851":null,"SJAG_00858":null,"SJAG_00864":null,"SJAG_00877":null,"SJAG_00883":null,"SJAG_00891":null,"SJAG_00895":null,"SJAG_00899":null,"SJAG_00900":null,"SJAG_00906":null,"SJAG_00907":null,"SJAG_00915":null,"SJAG_00916":null,"SJAG_00918":null,"SJAG_00919":null,"SJAG_00922":null,"SJAG_00930":null,"SJAG_00938":null,"SJAG_00959":null,"SJAG_00962":null,"SJAG_00968":null,"SJAG_00970":null,"SJAG_00971":null,"SJAG_00976":null,"SJAG_00985":null,"SJAG_00991":null,"SJAG_00992":null,"SJAG_01001":null,"SJAG_01003":null,"SJAG_01004":null,"SJAG_01007":null,"SJAG_01011":null,"SJAG_01013":null,"SJAG_01017":null,"SJAG_01025":null,"SJAG_01027":null,"SJAG_01030":null,"SJAG_01033":null,"SJAG_01039":null,"SJAG_01048":null,"SJAG_01059":null,"SJAG_01065":null,"SJAG_01067":null,"SJAG_01071":null,"SJAG_01076":null,"SJAG_01077":null,"SJAG_01078":null,"SJAG_01080":null,"SJAG_01082":null,"SJAG_01083":null,"SJAG_01084":null,"SJAG_01088":null,"SJAG_01090":null,"SJAG_01095":null,"SJAG_01096":null,"SJAG_01112":null,"SJAG_01114":null,"SJAG_01116":null,"SJAG_01119":null,"SJAG_01120":null,"SJAG_01125":null,"SJAG_01127":null,"SJAG_01129":null,"SJAG_01133":null,"SJAG_01135":null,"SJAG_01145":null,"SJAG_01165":null,"SJAG_01166":null,"SJAG_01167":null,"SJAG_01168":null,"SJAG_01177":null,"SJAG_01178":null,"SJAG_01183":null,"SJAG_01185":null,"SJAG_01190":null,"SJAG_01196":null,"SJAG_01206":null,"SJAG_01211":null,"SJAG_01223":null,"SJAG_01224":null,"SJAG_01225":null,"SJAG_01229":null,"SJAG_01240":null,"SJAG_01242":null,"SJAG_01245":null,"SJAG_01258":null,"SJAG_01263":null,"SJAG_01268":null,"SJAG_01278":null,"SJAG_01279":null,"SJAG_01281":null,"SJAG_01282":null,"SJAG_01293":null,"SJAG_01297":null,"SJAG_01299":null,"SJAG_01305":null,"SJAG_01309":null,"SJAG_01311":null,"SJAG_01319":null,"SJAG_01324":null,"SJAG_01328":null,"SJAG_01329":null,"SJAG_01335":null,"SJAG_01336":null,"SJAG_01338":null,"SJAG_01339":null,"SJAG_01344":null,"SJAG_01349":null,"SJAG_01353":null,"SJAG_01355":null,"SJAG_01358":null,"SJAG_01360":null,"SJAG_01367":null,"SJAG_01370":null,"SJAG_01371":null,"SJAG_01373":null,"SJAG_01374":null,"SJAG_01378":null,"SJAG_01379":null,"SJAG_01381":null,"SJAG_01382":null,"SJAG_01384":null,"SJAG_01391":null,"SJAG_01397":null,"SJAG_01400":null,"SJAG_01405":null,"SJAG_01406":null,"SJAG_01407":null,"SJAG_01409":null,"SJAG_01410":null,"SJAG_01415":null,"SJAG_01422":null,"SJAG_01435":null,"SJAG_01437":null,"SJAG_01442":null,"SJAG_01445":null,"SJAG_01447":null,"SJAG_01448":null,"SJAG_01449":null,"SJAG_01456":null,"SJAG_01459":null,"SJAG_01460":null,"SJAG_01467":null,"SJAG_01470":null,"SJAG_01471":null,"SJAG_01488":null,"SJAG_01493":null,"SJAG_01496":null,"SJAG_01505":null,"SJAG_01508":null,"SJAG_01514":null,"SJAG_01516":null,"SJAG_01527":null,"SJAG_01529":null,"SJAG_01534":null,"SJAG_01538":null,"SJAG_01541":null,"SJAG_01546":null,"SJAG_01558":null,"SJAG_01560":null,"SJAG_01563":null,"SJAG_01564":null,"SJAG_01572":null,"SJAG_01584":null,"SJAG_01586":null,"SJAG_01589":null,"SJAG_01590":null,"SJAG_01597":null,"SJAG_01598":null,"SJAG_01600":null,"SJAG_01601":null,"SJAG_01613":null,"SJAG_01615":null,"SJAG_01621":null,"SJAG_01626":null,"SJAG_01633":null,"SJAG_01636":null,"SJAG_01639":null,"SJAG_01640":null,"SJAG_01641":null,"SJAG_01642":null,"SJAG_01645":null,"SJAG_01647":null,"SJAG_01649":null,"SJAG_01652":null,"SJAG_01655":null,"SJAG_01660":null,"SJAG_01662":null,"SJAG_01669":null,"SJAG_01677":null,"SJAG_01684":null,"SJAG_01686":null,"SJAG_01697":null,"SJAG_01715":null,"SJAG_01722":null,"SJAG_01731":null,"SJAG_01732":null,"SJAG_01733":null,"SJAG_01738":null,"SJAG_01741":null,"SJAG_01745":null,"SJAG_01748":null,"SJAG_01750":null,"SJAG_01756":null,"SJAG_01759":null,"SJAG_01770":null,"SJAG_01772":null,"SJAG_01775":null,"SJAG_01777":null,"SJAG_01780":null,"SJAG_01782":null,"SJAG_01789":null,"SJAG_01790":null,"SJAG_01803":null,"SJAG_01805":null,"SJAG_01809":null,"SJAG_01817":null,"SJAG_01834":null,"SJAG_01837":null,"SJAG_01840":null,"SJAG_01842":null,"SJAG_01863":null,"SJAG_01872":null,"SJAG_01876":null,"SJAG_01879":null,"SJAG_01890":null,"SJAG_01899":null,"SJAG_01909":null,"SJAG_01913":null,"SJAG_01917":null,"SJAG_01923":null,"SJAG_01924":null,"SJAG_01925":null,"SJAG_01927":null,"SJAG_01929":null,"SJAG_01940":null,"SJAG_01941":null,"SJAG_01945":null,"SJAG_01949":null,"SJAG_01951":null,"SJAG_01960":null,"SJAG_01964":null,"SJAG_01973":null,"SJAG_01981":null,"SJAG_01983":null,"SJAG_01990":null,"SJAG_01991":null,"SJAG_01994":null,"SJAG_01998":null,"SJAG_01999":null,"SJAG_02004":null,"SJAG_02011":null,"SJAG_02012":null,"SJAG_02016":null,"SJAG_02019":null,"SJAG_02022":null,"SJAG_02023":null,"SJAG_02029":null,"SJAG_02034":null,"SJAG_02045":null,"SJAG_02049":null,"SJAG_02050":null,"SJAG_02059":null,"SJAG_02060":null,"SJAG_02062":null,"SJAG_02063":null,"SJAG_02065":null,"SJAG_02074":null,"SJAG_02075":null,"SJAG_02077":null,"SJAG_02079":null,"SJAG_02103":null,"SJAG_02104":null,"SJAG_02105":null,"SJAG_02113":null,"SJAG_02114":null,"SJAG_02117":null,"SJAG_02118":null,"SJAG_02120":null,"SJAG_02125":null,"SJAG_02132":null,"SJAG_02133":null,"SJAG_02139":null,"SJAG_02140":null,"SJAG_02144":null,"SJAG_02147":null,"SJAG_02150":null,"SJAG_02152":null,"SJAG_02155":null,"SJAG_02160":null,"SJAG_02166":null,"SJAG_02177":null,"SJAG_02193":null,"SJAG_02204":null,"SJAG_02208":null,"SJAG_02209":null,"SJAG_02210":null,"SJAG_02211":null,"SJAG_02228":null,"SJAG_02231":null,"SJAG_02234":null,"SJAG_02240":null,"SJAG_02241":null,"SJAG_02245":null,"SJAG_02250":null,"SJAG_02264":null,"SJAG_02274":null,"SJAG_02277":null,"SJAG_02282":null,"SJAG_02286":null,"SJAG_02299":null,"SJAG_02315":null,"SJAG_02316":null,"SJAG_02320":null,"SJAG_02322":null,"SJAG_02323":null,"SJAG_02330":null,"SJAG_02332":null,"SJAG_02336":null,"SJAG_02344":null,"SJAG_02346":null,"SJAG_02349":null,"SJAG_02354":null,"SJAG_02355":null,"SJAG_02361":null,"SJAG_02366":null,"SJAG_02368":null,"SJAG_02371":null,"SJAG_02375":null,"SJAG_02384":null,"SJAG_02392":null,"SJAG_02397":null,"SJAG_02398":null,"SJAG_02399":null,"SJAG_02418":null,"SJAG_02419":null,"SJAG_02422":null,"SJAG_02425":null,"SJAG_02431":null,"SJAG_02437":null,"SJAG_02440":null,"SJAG_02443":null,"SJAG_02445":null,"SJAG_02451":null,"SJAG_02453":null,"SJAG_02456":null,"SJAG_02457":null,"SJAG_02463":null,"SJAG_02473":null,"SJAG_02482":null,"SJAG_02484":null,"SJAG_02504":null,"SJAG_02509":null,"SJAG_02511":null,"SJAG_02514":null,"SJAG_02516":null,"SJAG_02518":null,"SJAG_02520":null,"SJAG_02524":null,"SJAG_02525":null,"SJAG_02529":null,"SJAG_02532":null,"SJAG_02534":null,"SJAG_02537":null,"SJAG_02539":null,"SJAG_02561":null,"SJAG_02564":null,"SJAG_02572":null,"SJAG_02578":null,"SJAG_02581":null,"SJAG_02583":null,"SJAG_02584":null,"SJAG_02586":null,"SJAG_02587":null,"SJAG_02588":null,"SJAG_02592":null,"SJAG_02598":null,"SJAG_02602":null,"SJAG_02605":null,"SJAG_02619":null,"SJAG_02624":null,"SJAG_02626":null,"SJAG_02640":null,"SJAG_02645":null,"SJAG_02646":null,"SJAG_02651":null,"SJAG_02655":null,"SJAG_02661":null,"SJAG_02684":null,"SJAG_02693":null,"SJAG_02695":null,"SJAG_02698":null,"SJAG_02699":null,"SJAG_02704":null,"SJAG_02707":null,"SJAG_02715":null,"SJAG_02716":null,"SJAG_02727":null,"SJAG_02731":null,"SJAG_02735":null,"SJAG_02736":null,"SJAG_02737":null,"SJAG_02750":null,"SJAG_02751":null,"SJAG_02753":null,"SJAG_02757":null,"SJAG_02761":null,"SJAG_02779":null,"SJAG_02780":null,"SJAG_02782":null,"SJAG_02789":null,"SJAG_02797":null,"SJAG_02805":null,"SJAG_02809":null,"SJAG_02811":null,"SJAG_02814":null,"SJAG_02823":null,"SJAG_02824":null,"SJAG_02831":null,"SJAG_02833":null,"SJAG_02834":null,"SJAG_02837":null,"SJAG_02839":null,"SJAG_02848":null,"SJAG_02852":null,"SJAG_02857":null,"SJAG_02858":null,"SJAG_02867":null,"SJAG_02877":null,"SJAG_02883":null,"SJAG_02897":null,"SJAG_02912":null,"SJAG_02914":null,"SJAG_02917":null,"SJAG_02941":null,"SJAG_02943":null,"SJAG_02946":null,"SJAG_02947":null,"SJAG_02955":null,"SJAG_02957":null,"SJAG_02958":null,"SJAG_02962":null,"SJAG_02968":null,"SJAG_02986":null,"SJAG_02992":null,"SJAG_02997":null,"SJAG_02998":null,"SJAG_03002":null,"SJAG_03005":null,"SJAG_03010":null,"SJAG_03011":null,"SJAG_03012":null,"SJAG_03021":null,"SJAG_03029":null,"SJAG_03039":null,"SJAG_03044":null,"SJAG_03048":null,"SJAG_03050":null,"SJAG_03054":null,"SJAG_03072":null,"SJAG_03073":null,"SJAG_03079":null,"SJAG_03085":null,"SJAG_03086":null,"SJAG_03088":null,"SJAG_03092":null,"SJAG_03114":null,"SJAG_03119":null,"SJAG_03126":null,"SJAG_03137":null,"SJAG_03138":null,"SJAG_03142":null,"SJAG_03145":null,"SJAG_03146":null,"SJAG_03153":null,"SJAG_03156":null,"SJAG_03158":null,"SJAG_03170":null,"SJAG_03172":null,"SJAG_03182":null,"SJAG_03200":null,"SJAG_03209":null,"SJAG_03217":null,"SJAG_03220":null,"SJAG_03231":null,"SJAG_03239":null,"SJAG_03244":null,"SJAG_03246":null,"SJAG_03247":null,"SJAG_03250":null,"SJAG_03256":null,"SJAG_03264":null,"SJAG_03268":null,"SJAG_03270":null,"SJAG_03281":null,"SJAG_03283":null,"SJAG_03287":null,"SJAG_03299":null,"SJAG_03300":null,"SJAG_03315":null,"SJAG_03324":null,"SJAG_03327":null,"SJAG_03334":null,"SJAG_03338":null,"SJAG_03345":null,"SJAG_03347":null,"SJAG_03357":null,"SJAG_03358":null,"SJAG_03363":null,"SJAG_03365":null,"SJAG_03368":null,"SJAG_03385":null,"SJAG_03396":null,"SJAG_03399":null,"SJAG_03400":null,"SJAG_03401":null,"SJAG_03403":null,"SJAG_03404":null,"SJAG_03406":null,"SJAG_03411":null,"SJAG_03415":null,"SJAG_03416":null,"SJAG_03432":null,"SJAG_03437":null,"SJAG_03440":null,"SJAG_03442":null,"SJAG_03447":null,"SJAG_03449":null,"SJAG_03452":null,"SJAG_03453":null,"SJAG_03465":null,"SJAG_03467":null,"SJAG_03470":null,"SJAG_03488":null,"SJAG_03490":null,"SJAG_03497":null,"SJAG_03499":null,"SJAG_03502":null,"SJAG_03503":null,"SJAG_03504":null,"SJAG_03508":null,"SJAG_03511":null,"SJAG_03515":null,"SJAG_03516":null,"SJAG_03528":null,"SJAG_03536":null,"SJAG_03540":null,"SJAG_03543":null,"SJAG_03552":null,"SJAG_03558":null,"SJAG_03560":null,"SJAG_03577":null,"SJAG_03581":null,"SJAG_03591":null,"SJAG_03593":null,"SJAG_03595":null,"SJAG_03596":null,"SJAG_03602":null,"SJAG_03606":null,"SJAG_03608":null,"SJAG_03631":null,"SJAG_03633":null,"SJAG_03643":null,"SJAG_03644":null,"SJAG_03648":null,"SJAG_03650":null,"SJAG_03652":null,"SJAG_03662":null,"SJAG_03663":null,"SJAG_03667":null,"SJAG_03670":null,"SJAG_03673":null,"SJAG_03680":null,"SJAG_03683":null,"SJAG_03684":null,"SJAG_03685":null,"SJAG_03690":null,"SJAG_03693":null,"SJAG_03696":null,"SJAG_03697":null,"SJAG_03698":null,"SJAG_03710":null,"SJAG_03718":null,"SJAG_03719":null,"SJAG_03721":null,"SJAG_03725":null,"SJAG_03726":null,"SJAG_03729":null,"SJAG_03737":null,"SJAG_03741":null,"SJAG_03746":null,"SJAG_03754":null,"SJAG_03756":null,"SJAG_03763":null,"SJAG_03774":null,"SJAG_03777":null,"SJAG_03781":null,"SJAG_03783":null,"SJAG_03785":null,"SJAG_03808":null,"SJAG_03810":null,"SJAG_03817":null,"SJAG_03820":null,"SJAG_03827":null,"SJAG_03829":null,"SJAG_03835":null,"SJAG_03836":null,"SJAG_03838":null,"SJAG_03842":null,"SJAG_03843":null,"SJAG_03847":null,"SJAG_03848":null,"SJAG_03850":null,"SJAG_03851":null,"SJAG_03860":null,"SJAG_03864":null,"SJAG_03865":null,"SJAG_03866":null,"SJAG_03873":null,"SJAG_03882":null,"SJAG_03889":null,"SJAG_03891":null,"SJAG_03892":null,"SJAG_03895":null,"SJAG_03899":null,"SJAG_03907":null,"SJAG_03915":null,"SJAG_03925":null,"SJAG_03926":null,"SJAG_03930":null,"SJAG_03933":null,"SJAG_03938":null,"SJAG_03951":null,"SJAG_03955":null,"SJAG_03959":null,"SJAG_03960":null,"SJAG_03962":null,"SJAG_03963":null,"SJAG_03970":null,"SJAG_03976":null,"SJAG_03986":null,"SJAG_03987":null,"SJAG_03989":null,"SJAG_04001":null,"SJAG_04002":null,"SJAG_04003":null,"SJAG_04013":null,"SJAG_04014":null,"SJAG_04015":null,"SJAG_04017":null,"SJAG_04021":null,"SJAG_04023":null,"SJAG_04024":null,"SJAG_04028":null,"SJAG_04040":null,"SJAG_04044":null,"SJAG_04047":null,"SJAG_04050":null,"SJAG_04051":null,"SJAG_04052":null,"SJAG_04058":null,"SJAG_04068":null,"SJAG_04070":null,"SJAG_04072":null,"SJAG_04076":null,"SJAG_04083":null,"SJAG_04096":null,"SJAG_04100":null,"SJAG_04111":null,"SJAG_04112":null,"SJAG_04115":null,"SJAG_04122":null,"SJAG_04126":null,"SJAG_04129":null,"SJAG_04134":null,"SJAG_04135":null,"SJAG_04136":null,"SJAG_04140":null,"SJAG_04142":null,"SJAG_04143":null,"SJAG_04148":null,"SJAG_04158":null,"SJAG_04162":null,"SJAG_04167":null,"SJAG_04185":null,"SJAG_04196":null,"SJAG_04202":null,"SJAG_04203":null,"SJAG_04208":null,"SJAG_04218":null,"SJAG_04219":null,"SJAG_04221":null,"SJAG_04241":null,"SJAG_04246":null,"SJAG_04258":null,"SJAG_04259":null,"SJAG_04260":null,"SJAG_04275":null,"SJAG_04277":null,"SJAG_04280":null,"SJAG_04284":null,"SJAG_04294":null,"SJAG_04295":null,"SJAG_04296":null,"SJAG_04308":null,"SJAG_04310":null,"SJAG_04312":null,"SJAG_04325":null,"SJAG_04328":null,"SJAG_04336":null,"SJAG_04338":null,"SJAG_04340":null,"SJAG_04343":null,"SJAG_04347":null,"SJAG_04349":null,"SJAG_04358":null,"SJAG_04359":null,"SJAG_04360":null,"SJAG_04366":null,"SJAG_04370":null,"SJAG_04379":null,"SJAG_04387":null,"SJAG_04391":null,"SJAG_04400":null,"SJAG_04402":null,"SJAG_04406":null,"SJAG_04411":null,"SJAG_04412":null,"SJAG_04413":null,"SJAG_04417":null,"SJAG_04419":null,"SJAG_04428":null,"SJAG_04432":null,"SJAG_04434":null,"SJAG_04451":null,"SJAG_04455":null,"SJAG_04457":null,"SJAG_04461":null,"SJAG_04464":null,"SJAG_04465":null,"SJAG_04466":null,"SJAG_04469":null,"SJAG_04471":null,"SJAG_04472":null,"SJAG_04474":null,"SJAG_04479":null,"SJAG_04480":null,"SJAG_04489":null,"SJAG_04506":null,"SJAG_04508":null,"SJAG_04509":null,"SJAG_04513":null,"SJAG_04515":null,"SJAG_04517":null,"SJAG_04528":null,"SJAG_04533":null,"SJAG_04536":null,"SJAG_04548":null,"SJAG_04551":null,"SJAG_04552":null,"SJAG_04554":null,"SJAG_04558":null,"SJAG_04565":null,"SJAG_04569":null,"SJAG_04588":null,"SJAG_04589":null,"SJAG_04592":null,"SJAG_04593":null,"SJAG_04597":null,"SJAG_04598":null,"SJAG_04600":null,"SJAG_04609":null,"SJAG_04615":null,"SJAG_04616":null,"SJAG_04618":null,"SJAG_04622":null,"SJAG_04623":null,"SJAG_04629":null,"SJAG_04637":null,"SJAG_04641":null,"SJAG_04643":null,"SJAG_04644":null,"SJAG_04645":null,"SJAG_04656":null,"SJAG_04666":null,"SJAG_04668":null,"SJAG_04673":null,"SJAG_04675":null,"SJAG_04677":null,"SJAG_04684":null,"SJAG_04697":null,"SJAG_04698":null,"SJAG_04701":null,"SJAG_04703":null,"SJAG_04706":null,"SJAG_04714":null,"SJAG_04715":null,"SJAG_04716":null,"SJAG_04717":null,"SJAG_04718":null,"SJAG_04721":null,"SJAG_04724":null,"SJAG_04725":null,"SJAG_04731":null,"SJAG_04733":null,"SJAG_04734":null,"SJAG_04737":null,"SJAG_04739":null,"SJAG_04740":null,"SJAG_04743":null,"SJAG_04745":null,"SJAG_04757":null,"SJAG_04763":null,"SJAG_04787":null,"SJAG_04822":null,"SJAG_04828":null,"SJAG_04829":null,"SJAG_04830":null,"SJAG_04837":null,"SJAG_04846":null,"SJAG_04857":null,"SJAG_04867":null,"SJAG_04884":null,"SJAG_04886":null,"SJAG_04892":null,"SJAG_04901":null,"SJAG_04902":null,"SJAG_04903":null,"SJAG_04905":null,"SJAG_04909":null,"SJAG_04912":null,"SJAG_04920":null,"SJAG_04923":null,"SJAG_04930":null,"SJAG_04931":null,"SJAG_04936":null,"SJAG_04938":null,"SJAG_04940":null,"SJAG_04947":null,"SJAG_04955":null,"SJAG_04956":null,"SJAG_04957":null,"SJAG_04960":null,"SJAG_04966":null,"SJAG_04978":null,"SJAG_04983":null,"SJAG_04984":null,"SJAG_04990":null,"SJAG_04996":null,"SJAG_05011":null,"SJAG_05012":null,"SJAG_05013":null,"SJAG_05019":null,"SJAG_05030":null,"SJAG_05175":null,"SJAG_05178":null,"SJAG_05182":null,"SJAG_05184":null,"SJAG_05185":null,"SJAG_05194":null,"SJAG_05196":null,"SJAG_05198":null,"SJAG_05204":null,"SJAG_05207":null,"SJAG_05209":null,"SJAG_05210":null,"SJAG_05213":null,"SJAG_05220":null,"SJAG_05223":null,"SJAG_05226":null,"SJAG_05229":null,"SJAG_05245":null,"SJAG_05259":null,"SJAG_05260":null,"SJAG_05266":null,"SJAG_05268":null,"SJAG_05290":null,"SJAG_05294":null,"SJAG_05295":null,"SJAG_05296":null,"SJAG_05300":null,"SJAG_05302":null,"SJAG_05303":null,"SJAG_05315":null,"SJAG_05319":null,"SJAG_05325":null,"SJAG_05326":null,"SJAG_05328":null,"SJAG_05342":null,"SJAG_05344":null,"SJAG_05345":null,"SJAG_05346":null,"SJAG_05372":null,"SJAG_05414":null,"SJAG_05736":null,"SJAG_05950":null,"SJAG_06270":null,"SJAG_06440":null,"SJAG_06588":null,"SJAG_06598":null,"SJAG_07002":null,"SJAG_07003":null,"SJAG_07004":null,"SJAG_07010":null,"SJAG_07012":null,"SJAG_16459":null,"SJAG_MIT09":null,"SJAG_MIT15":null,"SJAG_MIT37":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"localization","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000043":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000108":null,"GO_REF:0000117":null},"secondary_identifiers":["GO:1902578"],"synonyms":[{"name":"establishment and maintenance of cellular component location","type":"narrow"},{"name":"establishment and maintenance of localization","type":"exact"},{"name":"establishment and maintenance of position","type":"exact"},{"name":"establishment and maintenance of substance location","type":"narrow"},{"name":"establishment and maintenance of substrate location","type":"narrow"},{"name":"localisation","type":"exact"},{"name":"single organism localization","type":"related"},{"name":"single-organism localization","type":"related"}],"termid":"GO:0051179","terms_by_termid":{"GO:0000001":null,"GO:0000054":null,"GO:0000055":null,"GO:0000056":null,"GO:0000132":null,"GO:0000301":null,"GO:0000743":null,"GO:0001407":null,"GO:0003333":null,"GO:0006404":null,"GO:0006405":null,"GO:0006406":null,"GO:0006409":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:0006621":null,"GO:0006623":null,"GO:0006625":null,"GO:0006626":null,"GO:0006627":null,"GO:0006820":null,"GO:0006825":null,"GO:0006843":null,"GO:0006847":null,"GO:0006850":null,"GO:0006868":null,"GO:0006886":null,"GO:0006887":null,"GO:0006888":null,"GO:0006890":null,"GO:0006891":null,"GO:0006892":null,"GO:0006893":null,"GO:0006895":null,"GO:0006896":null,"GO:0006897":null,"GO:0006900":null,"GO:0006901":null,"GO:0006904":null,"GO:0006906":null,"GO:0006913":null,"GO:0007034":null,"GO:0007079":null,"GO:0007097":null,"GO:0008298":null,"GO:0008645":null,"GO:0010621":null,"GO:0010970":null,"GO:0015031":null,"GO:0015677":null,"GO:0015742":null,"GO:0015743":null,"GO:0015786":null,"GO:0015790":null,"GO:0015813":null,"GO:0015825":null,"GO:0015828":null,"GO:0015847":null,"GO:0015851":null,"GO:0015866":null,"GO:0015884":null,"GO:0015891":null,"GO:0015917":null,"GO:0015918":null,"GO:0016031":null,"GO:0016192":null,"GO:0016197":null,"GO:0016240":null,"GO:0016558":null,"GO:0016560":null,"GO:0016562":null,"GO:0016973":null,"GO:0017121":null,"GO:0017157":null,"GO:0030001":null,"GO:0030050":null,"GO:0030100":null,"GO:0030150":null,"GO:0030970":null,"GO:0030989":null,"GO:0031134":null,"GO:0031204":null,"GO:0031619":null,"GO:0031623":null,"GO:0031990":null,"GO:0032065":null,"GO:0032118":null,"GO:0032121":null,"GO:0032366":null,"GO:0032456":null,"GO:0032509":null,"GO:0032511":null,"GO:0032527":null,"GO:0032974":null,"GO:0032979":null,"GO:0033157":null,"GO:0033214":null,"GO:0033215":null,"GO:0034058":null,"GO:0034067":null,"GO:0034203":null,"GO:0034219":null,"GO:0034220":null,"GO:0034398":null,"GO:0034486":null,"GO:0034488":null,"GO:0034490":null,"GO:0034498":null,"GO:0034499":null,"GO:0034501":null,"GO:0034643":null,"GO:0034755":null,"GO:0035348":null,"GO:0035372":null,"GO:0035432":null,"GO:0035434":null,"GO:0035435":null,"GO:0035436":null,"GO:0035442":null,"GO:0035493":null,"GO:0035494":null,"GO:0035621":null,"GO:0035652":null,"GO:0035725":null,"GO:0036085":null,"GO:0036228":null,"GO:0036246":null,"GO:0036249":null,"GO:0036376":null,"GO:0036444":null,"GO:0042147":null,"GO:0042307":null,"GO:0042308":null,"GO:0042906":null,"GO:0042908":null,"GO:0042997":null,"GO:0043001":null,"GO:0043328":null,"GO:0044379":null,"GO:0044395":null,"GO:0044718":null,"GO:0044820":null,"GO:0044821":null,"GO:0045016":null,"GO:0045022":null,"GO:0045039":null,"GO:0045040":null,"GO:0045041":null,"GO:0045046":null,"GO:0045047":null,"GO:0045048":null,"GO:0045141":null,"GO:0045324":null,"GO:0045332":null,"GO:0045806":null,"GO:0045807":null,"GO:0045921":null,"GO:0046323":null,"GO:0046827":null,"GO:0046907":null,"GO:0047496":null,"GO:0048193":null,"GO:0048194":null,"GO:0048205":null,"GO:0048210":null,"GO:0048211":null,"GO:0048219":null,"GO:0048250":null,"GO:0048254":null,"GO:0048278":null,"GO:0048280":null,"GO:0048311":null,"GO:0048312":null,"GO:0051028":null,"GO:0051170":null,"GO:0051315":null,"GO:0051455":null,"GO:0051456":null,"GO:0051646":null,"GO:0051647":null,"GO:0051654":null,"GO:0051666":null,"GO:0051685":null,"GO:0055085":null,"GO:0060003":null,"GO:0060628":null,"GO:0061454":null,"GO:0061509":null,"GO:0061817":null,"GO:0061856":null,"GO:0061951":null,"GO:0070086":null,"GO:0070197":null,"GO:0070198":null,"GO:0070574":null,"GO:0070588":null,"GO:0070778":null,"GO:0070973":null,"GO:0071421":null,"GO:0071423":null,"GO:0071528":null,"GO:0071562":null,"GO:0071574":null,"GO:0071577":null,"GO:0071578":null,"GO:0071805":null,"GO:0071806":null,"GO:0071816":null,"GO:0071918":null,"GO:0071934":null,"GO:0071996":null,"GO:0072318":null,"GO:0072334":null,"GO:0072488":null,"GO:0072489":null,"GO:0072583":null,"GO:0072657":null,"GO:0072659":null,"GO:0072741":null,"GO:0072766":null,"GO:0089707":null,"GO:0089708":null,"GO:0090110":null,"GO:0090114":null,"GO:0090374":null,"GO:0090513":null,"GO:0090514":null,"GO:0090515":null,"GO:0090516":null,"GO:0090517":null,"GO:0090518":null,"GO:0090522":null,"GO:0090539":null,"GO:0090561":null,"GO:0097248":null,"GO:0097430":null,"GO:0097623":null,"GO:0097624":null,"GO:0097638":null,"GO:0097639":null,"GO:0098653":null,"GO:0098655":null,"GO:0098656":null,"GO:0098661":null,"GO:0098702":null,"GO:0098703":null,"GO:0098705":null,"GO:0098708":null,"GO:0098709":null,"GO:0098710":null,"GO:0098714":null,"GO:0098715":null,"GO:0098716":null,"GO:0098717":null,"GO:0098720":null,"GO:0098721":null,"GO:0098863":null,"GO:0099022":null,"GO:0099117":null,"GO:0099606":null,"GO:0099607":null,"GO:0099638":null,"GO:0106081":null,"GO:0106082":null,"GO:0110141":null,"GO:0120009":null,"GO:0120010":null,"GO:0120011":null,"GO:0120029":null,"GO:0120047":null,"GO:0120110":null,"GO:0120112":null,"GO:0120113":null,"GO:0120207":null,"GO:0120290":null,"GO:0140021":null,"GO:0140043":null,"GO:0140057":null,"GO:0140115":null,"GO:0140116":null,"GO:0140125":null,"GO:0140140":null,"GO:0140141":null,"GO:0140146":null,"GO:0140147":null,"GO:0140159":null,"GO:0140206":null,"GO:0140207":null,"GO:0140209":null,"GO:0140210":null,"GO:0140270":null,"GO:0140300":null,"GO:0140325":null,"GO:0140331":null,"GO:0140405":null,"GO:0140425":null,"GO:0140429":null,"GO:0140464":null,"GO:0140466":null,"GO:0140480":null,"GO:0140569":null,"GO:0140570":null,"GO:0140698":null,"GO:0160007":null,"GO:0160203":null,"GO:0170036":null,"GO:0170046":null,"GO:0180029":null,"GO:0180042":null,"GO:1900181":null,"GO:1901481":null,"GO:1901482":null,"GO:1901553":null,"GO:1901583":null,"GO:1902267":null,"GO:1902358":null,"GO:1902424":null,"GO:1902425":null,"GO:1902434":null,"GO:1902440":null,"GO:1902441":null,"GO:1902475":null,"GO:1902476":null,"GO:1902543":null,"GO:1902600":null,"GO:1902854":null,"GO:1903067":null,"GO:1903077":null,"GO:1903090":null,"GO:1903091":null,"GO:1903092":null,"GO:1903360":null,"GO:1903710":null,"GO:1903711":null,"GO:1903712":null,"GO:1903714":null,"GO:1903790":null,"GO:1903826":null,"GO:1903830":null,"GO:1904082":null,"GO:1904257":null,"GO:1904498":null,"GO:1904518":null,"GO:1904537":null,"GO:1904601":null,"GO:1904679":null,"GO:1904967":null,"GO:1904983":null,"GO:1905039":null,"GO:1905135":null,"GO:1905136":null,"GO:1905391":null,"GO:1905530":null,"GO:1905533":null,"GO:1905534":null,"GO:1905589":null,"GO:1905626":null,"GO:1905634":null,"GO:1905647":null,"GO:1905665":null,"GO:1905949":null,"GO:1990456":null,"GO:1990519":null,"GO:1990536":null,"GO:1990542":null,"GO:1990543":null,"GO:1990544":null,"GO:1990545":null,"GO:1990547":null,"GO:1990548":null,"GO:1990549":null,"GO:1990550":null,"GO:1990551":null,"GO:1990553":null,"GO:1990554":null,"GO:1990555":null,"GO:1990556":null,"GO:1990557":null,"GO:1990559":null,"GO:1990569":null,"GO:1990570":null,"GO:1990571":null,"GO:1990573":null,"GO:1990575":null,"GO:1990591":null,"GO:1990616":null,"GO:1990683":null,"GO:1990735":null,"GO:1990758":null,"GO:1990818":null,"GO:1990822":null,"GO:1990854":null,"GO:1990896":null,"GO:1990942":null,"GO:1990961":null,"GO:1990976":null,"GO:2000156":null,"GO:2000185":null,"GO:2000369":null,"GO:2001135":null}}


id: GO:1905676
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of adaptive immune memory response.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:26831526"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of adaptive immune response","termid":"GO:0002821"},{"relation_name":"is_a","term_name":"regulation of adaptive immune memory response","termid":"GO:1905674"},{"relation_name":"positively_regulates","term_name":"adaptive immune memory response","termid":"GO:0090716"}],"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 adaptive immune memory response","synonyms":[{"name":"activation of adaptive immune memory response","type":"narrow"},{"name":"up regulation of adaptive immune memory response","type":"exact"},{"name":"up-regulation of adaptive immune memory response","type":"exact"},{"name":"upregulation of adaptive immune memory response","type":"exact"}],"termid":"GO:1905676"}


id: GO:0042082
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of a glycosylsphingolipidinositol (GSI) anchor that attaches some membrane proteins to the lipid bilayer of the cell membrane. The sphingolipid group is linked, via the C-6 hydroxyl residue of inositol to a carbohydrate chain which is itself linked to the protein via a ethanolamine phosphate group, its amino group forming an amide linkage with the C-terminal carboxyl of the protein. Some GSI anchors have variants on this canonical linkage.","definition_xrefs":["GOC:jsg","GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete GSI anchor biosynthetic process (obsolete GO:0042082)","synonyms":[{"name":"GPI/GSI anchor biosynthesis","type":"broad"},{"name":"GPI/GSI anchor biosynthetic process","type":"broad"},{"name":"GSI anchor anabolism","type":"exact"},{"name":"GSI anchor biosynthesis","type":"exact"},{"name":"GSI anchor formation","type":"exact"},{"name":"GSI anchor synthesis","type":"exact"}],"termid":"GO:0042082"}


id: PBO:0058108
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4323","termid":"PBO:0058108"}


id: PBO:0086526
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; conserved across S. cerevisiae strains; YCR025C is not an essential gene","termid":"PBO:0086526"}


id: GO:0061328
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the posterior Malpighian tubule over time, from its formation to the mature structure. The pair of posterior tubules arise from a ventrolateral region of the embryonic hindgut and project backwards through the body cavity. A Malpighian tubule is a fine, thin-walled excretory tubule in insects which connects with the posterior part of the gut.","definition_xrefs":["GOC:dph","GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Malpighian tubule development","termid":"GO:0072002"}],"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":"posterior Malpighian tubule development","termid":"GO:0061328"}


id: PBO:0054457
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 1854","termid":"PBO:0054457"}


id: MONDO:0031040
data:
  {"annotated_genes":["SJAG_05194"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85632],"is_not":false,"summary":null,"term":"MONDO:0031040"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"progressive familial intrahepatic cholestasis","termid":"MONDO:0015762"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05194":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0002515","MONDO:0005066","MONDO:0004335"],"is_obsolete":false,"name":"cholestasis, progressive familial intrahepatic, 12","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5774311","MEDGEN:1824084","OMIM:620010"],"synonyms":[{"name":"PFIC12","type":"exact"},{"name":"cholestasis, isolated low-ggt","type":"exact"},{"name":"cholestasis, progressive familial intrahepatic, 12","type":"exact"}],"termid":"MONDO:0031040","terms_by_termid":{"MONDO:0031040":null},"xrefs":{"Monarch":{"xref_id":"0031040"}}}


id: PBO:0005881
data:
  {"annotation_feature_type":"gene","cv_name":"genome_org","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein in cox1 intron-2","termid":"PBO:0005881"}


id: GO:1903393
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of adherens junction organization.","definition_xrefs":["GO_REF:0000058","PMID:21724833","GOC:als","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cellular component organization","termid":"GO:0051130"},{"relation_name":"is_a","term_name":"regulation of adherens junction organization","termid":"GO:1903391"},{"relation_name":"positively_regulates","term_name":"adherens junction organization","termid":"GO:0034332"}],"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 adherens junction organization","synonyms":[{"name":"activation of adherens junction assembly and maintenance","type":"narrow"},{"name":"activation of adherens junction organisation","type":"narrow"},{"name":"activation of adherens junction organization","type":"narrow"},{"name":"positive regulation of adherens junction assembly and maintenance","type":"exact"},{"name":"positive regulation of adherens junction organisation","type":"exact"},{"name":"up regulation of adherens junction assembly and maintenance","type":"exact"},{"name":"up regulation of adherens junction organisation","type":"exact"},{"name":"up regulation of adherens junction organization","type":"exact"},{"name":"up-regulation of adherens junction assembly and maintenance","type":"exact"},{"name":"up-regulation of adherens junction organisation","type":"exact"},{"name":"up-regulation of adherens junction organization","type":"exact"},{"name":"upregulation of adherens junction assembly and maintenance","type":"exact"},{"name":"upregulation of adherens junction organisation","type":"exact"},{"name":"upregulation of adherens junction organization","type":"exact"}],"termid":"GO:1903393"}


id: PBO:0036182
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_histone_H3-K9_dimethylation_at_centromere_inner_repeat_during_vegetative_growth","termid":"PBO:0036182"}


id: MONDO:0003348
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An uncommon, aggressive malignant smooth muscle neoplasm. It is characterized by the presence of atypical large spindle or round cells, nuclear palisading, tumor cell necrosis, mitotic figures and may be associated with vascular invasion.","definition_xrefs":["NCIT:C9428"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leiomyosarcoma","termid":"MONDO:0005058"}],"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":"conventional leiomyosarcoma","secondary_identifiers":["MEDGEN:232394","UMLS:C1333157","DOID:5253"],"synonyms":[{"name":"classic leiomyosarcoma","type":"exact"},{"name":"conventional leiomyosarcoma","type":"exact"}],"termid":"MONDO:0003348","xrefs":{"Monarch":{"xref_id":"0003348"}}}


id: PBO:0089758
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U3 snoRNP-associated protein Utp5","termid":"PBO:0089758"}


id: GO:0015833
data:
  {"annotated_genes":["SJAG_01983","SJAG_00922","SJAG_03577","SJAG_02139","SJAG_05182","SJAG_05213","SJAG_03497","SJAG_02602","SJAG_01660","SJAG_01344"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[71585],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140206"},{"annotations":[118156,118155],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035442"},{"annotations":[95284],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098709"},{"annotations":[112938],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0160007"},{"annotations":[95832,118014,96823],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071996"},{"annotations":[75272],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090374"},{"annotations":[118015,96824,95833],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036246"},{"annotations":[107784],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901583"},{"annotations":[102800],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140207"}]},"cv_name":"biological_process","definition":"The directed movement of peptides, compounds of two or more amino acids where the alpha carboxyl group of one is bound to the alpha amino group of another, 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":"amide transport","termid":"GO:0042886"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00922":null,"SJAG_01344":null,"SJAG_01660":null,"SJAG_01983":null,"SJAG_02139":null,"SJAG_02602":null,"SJAG_03497":null,"SJAG_03577":null,"SJAG_05182":null,"SJAG_05213":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"peptide transport","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0015833","terms_by_termid":{"GO:0035442":null,"GO:0036246":null,"GO:0071996":null,"GO:0090374":null,"GO:0098709":null,"GO:0140206":null,"GO:0140207":null,"GO:0160007":null,"GO:1901583":null}}


id: PBO:0054791
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 2204","termid":"PBO:0054791"}


id: PBO:0039902
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARHGEF4 antisense RNA 1","termid":"PBO:0039902"}


id: GO:1901620
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of smoothened signaling pathway involved in dorsal/ventral neural tube patterning.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of smoothened signaling pathway","termid":"GO:0008589"},{"relation_name":"regulates","term_name":"smoothened signaling pathway involved in dorsal/ventral neural tube patterning","termid":"GO:0060831"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"regulation of smoothened signaling pathway involved in dorsal/ventral neural tube patterning","synonyms":[{"name":"regulation of hedgehog signaling pathway involved in dorsal/ventral neural tube patterning","type":"exact"},{"name":"regulation of hh signaling pathway involved in dorsal/ventral neural tube patterning","type":"exact"},{"name":"regulation of smoothened signalling pathway involved in dorsal/ventral neural tube patterning","type":"exact"}],"termid":"GO:1901620"}


id: MONDO:0010979
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Timothy syndrome is a multi-system disorder characterized by cardiac, hand, facial and neurodevelopmental features that include QT prolongation, webbed fingers and toes, flattened nasal bridge, low-set ears, small upper jaw, thin upper lip, and characteristic features of autism or autistic spectrum disorders.","definition_xrefs":["Orphanet:65283"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"familial long QT syndrome","termid":"MONDO:0019171"},{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"familial long QT syndrome","termid":"MONDO:0019171"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0005267","MONDO:0000426"],"is_obsolete":false,"name":"Timothy syndrome","secondary_identifiers":["UMLS:C1832916","MEDGEN:331395","DOID:0060173","NORD:1772","OMIM:601005","NCIT:C142894","MESH:C536962","GARD:9294"],"synonyms":[{"name":"LQT8","type":"related"},{"name":"TIMOTHY syndrome","type":"exact"},{"name":"TS","type":"exact"},{"name":"Timothy syndrome","type":"exact"},{"name":"long QT syndrome 8","type":"related"},{"name":"long QT syndrome type 8","type":"related"},{"name":"long QT syndrome with syndactyly","type":"related"},{"name":"long QT syndrome-syndactyly syndrome","type":"exact"}],"termid":"MONDO:0010979","xrefs":{"Monarch":{"xref_id":"0010979"}}}


id: PBO:0056826
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAX dimerization protein MGA","termid":"PBO:0056826"}


id: MONDO:0019467
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An aggressive immature hematologic neoplasm formerly known as blastic NK cell lymphoma, composed of cells with a lymphoblast-like morphology. Recent evidence suggests derivation from a plasmacytoid monocyte. Patients present with cutaneous tumors and bone marrow involvement.","definition_xrefs":["NCIT:C7203"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skin cancer","termid":"MONDO:0002898"},{"relation_name":"is_a","term_name":"myeloid neoplasm","termid":"MONDO:0005170"},{"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"},{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005570","MONDO:0005093"],"is_obsolete":false,"name":"CD4+/CD56+ hematodermic neoplasm","secondary_identifiers":["ONCOTREE:BPDCN","ICD9:202.80","SCTID:445105005","DOID:0081076","EFO:0010580","GARD:10556","ICDO:9727/3","icd11.foundation:783045723","UMLS:C1301363","MEDGEN:220972","Orphanet:86870"],"synonyms":[{"name":"BPDCN","type":"exact"},{"name":"CD4+/CD56+ hematodermic neoplasm","type":"exact"},{"name":"agranular CD4+ CD56+ hematodermic neoplasm/tumor","type":"exact"},{"name":"agranular CD4+ natural Killer cell leukaemia","type":"exact"},{"name":"agranular CD4+ natural Killer cell leukemia","type":"exact"},{"name":"blastic NK-cell lymphoma","type":"exact"},{"name":"blastic natural Killer leukemia/lymphoma","type":"exact"},{"name":"blastic plasmacytoid Dendritic cell neoplasm","type":"exact"},{"name":"blastic plasmacytoid dendritic cell","type":"related"},{"name":"blastic plasmacytoid dendritic cell neoplasm","type":"exact"},{"name":"early plasmacytoid Dendritic cell leukemia/lymphoma","type":"exact"},{"name":"lymphoblastoid variant of NK-cell lymphoma","type":"exact"},{"name":"monomorphic NK-cell lymphoma","type":"exact"},{"name":"primary cutaneous CD4+/CD56+ hematolymphoid neoplasm","type":"exact"}],"termid":"MONDO:0019467","xrefs":{"Monarch":{"xref_id":"0019467"}}}


id: GO:0003347
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A transition where an epicardial cell loses apical/basolateral polarity, severs intercellular adhesive junctions, degrades basement membrane components and becomes a migratory mesenchymal cell. The epicardium is a part of the pericardium.","definition_xrefs":["PMID:18722343","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial to mesenchymal transition","termid":"GO:0001837"}],"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":"epicardial cell to mesenchymal cell transition","termid":"GO:0003347"}


id: GO:0102468
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-alpha-D-glucuronate + wogonin = UDP + wogonin 7-O-beta-D-glucuronate + H+.","definition_xrefs":["RHEA:28322"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hexosyltransferase activity","termid":"GO:0016758"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016740","GO:0016757"],"is_obsolete":false,"name":"wogonin 7-O-glucuronosyltransferase activity","secondary_identifiers":["MetaCyc:RXN-14060"],"termid":"GO:0102468"}


id: GO:0018616
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2,3,5-trihydroxytoluene + O2 = 2,4,6-trioxoheptanoate.","definition_xrefs":["UM-BBD_reactionID:r0093","PMID:1254564"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of two atoms of oxygen into one donor","termid":"GO:0016708"}],"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":"trihydroxytoluene dioxygenase activity","secondary_identifiers":["MetaCyc:R305-RXN"],"termid":"GO:0018616"}


id: MONDO:1011236
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Microphthalmia that occurs in water buffalo.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microphthalmia, non-human animal","termid":"MONDO:1010324"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microphthalmia, water buffalo","secondary_identifiers":["OMIA:000649-89462"],"termid":"MONDO:1011236","xrefs":{"Monarch":{"xref_id":"1011236"}}}


id: PBO:0071016
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 18","termid":"PBO:0071016"}


id: MONDO:0014895
data:
  {"annotated_genes":["SJAG_04351"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85887],"is_not":false,"summary":null,"term":"MONDO:0014895"}]},"cv_name":"mondo","definition":"Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the GUF1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"West syndrome","termid":"MONDO:0018097"},{"relation_name":"is_a","term_name":"developmental and epileptic encephalopathy","termid":"MONDO:0100062"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04351":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"},{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0005027","MONDO:0700092"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy, 40","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:934704","DOID:0080427","GARD:16182","OMIM:617065","UMLS:C4310737"],"synonyms":[{"name":"DEE40","type":"exact"},{"name":"EIEE40","type":"exact"},{"name":"GUF1 early infantile epileptic encephalopathy","type":"exact"},{"name":"developmental and epileptic encephalopathy 40","type":"exact"},{"name":"early infantile epileptic encephalopathy caused by mutation in GUF1","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 40","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 40; EIEE40","type":"exact"},{"name":"epileptic encephalopathy, early infantile, type 40","type":"exact"}],"termid":"MONDO:0014895","terms_by_termid":{"MONDO:0014895":null},"xrefs":{"Monarch":{"xref_id":"0014895"}}}


id: MONDO:0021067
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A germ cell tumor that arises from the mediastinum. Representative examples include seminoma, embryonal carcinoma, yolk sac tumor, teratoma, and mixed germ cell tumor.","definition_xrefs":["NCIT:C6437"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extragonadal germ cell tumor","termid":"MONDO:0018201"},{"relation_name":"is_a","term_name":"neoplasm of mediastinum","termid":"MONDO:0021386"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mediastinal germ cell tumor","secondary_identifiers":["UMLS:C1334655","MEDGEN:233678"],"synonyms":[{"name":"germ cell neoplasm of mediastinum","type":"exact"},{"name":"germ cell neoplasm of the mediastinum","type":"exact"},{"name":"germ cell tumor of mediastinum","type":"exact"},{"name":"germ cell tumor of the mediastinum","type":"exact"},{"name":"germ cell tumour of mediastinum","type":"exact"},{"name":"germ cell tumour of the mediastinum","type":"exact"},{"name":"mediastinal germ cell neoplasm","type":"exact"},{"name":"mediastinal germ cell tumor","type":"exact"},{"name":"mediastinum germ cell tumor","type":"exact"},{"name":"mediastinum germ cell tumour","type":"exact"},{"name":"thymic germ cell tumor","type":"exact"},{"name":"thymic germ cell tumour","type":"exact"}],"termid":"MONDO:0021067","xrefs":{"Monarch":{"xref_id":"0021067"}}}


id: PBO:0003091
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mRNA cleavage factor complex subunit (predicted)","termid":"PBO:0003091"}


id: PBO:0067353
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 451, pseudogene","termid":"PBO:0067353"}


id: GO:0060803
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of molecular signals initiated by the binding of a member of the BMP (bone morphogenetic protein) family to its receptor on the surface of a target cell, which contributes to a cell becoming specified to adopt a mesodermal fate.","definition_xrefs":["GOC:dph","GOC:sdb_2009","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete BMP signaling pathway involved in mesodermal cell fate specification (obsolete GO:0060803)","synonyms":[{"name":"BMP signalling pathway involved in mesodermal cell fate specification","type":"exact"}],"termid":"GO:0060803"}


id: PBO:0110474
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynein regulatory complex subunit 12 homolog","termid":"PBO:0110474"}


id: GO:0061249
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that gives rise to a mesonephric glomerular capillary. This process pertains to the initial formation of a structure from unspecified parts.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glomerular capillary formation","termid":"GO:0072104"},{"relation_name":"part_of","term_name":"mesonephric glomerulus vasculature morphogenesis","termid":"GO:0061248"}],"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":"mesonephric glomerular capillary formation","termid":"GO:0061249"}


id: PBO:0000982
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA snR96","termid":"PBO:0000982"}


id: GO:0002259
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A change in the morphology or behavior of an endothelial cell within a high endothelial venule resulting from exposure to an activating factor such as a cellular or soluble ligand, leading to the initiation or perpetuation of an immune response.","definition_xrefs":["ISBN:0781735149","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endothelial cell activation involved in immune response","termid":"GO:0002264"}],"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":"endothelial cell activation within high endothelial venule involved in immune response","synonyms":[{"name":"endothelial cell activation within high endothelial venule during immune response","type":"related"}],"termid":"GO:0002259"}


id: MONDO:1011614
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Von Willebrand disease that occurs in horse.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Von Willebrand disease, non-human animal","termid":"MONDO:1011411"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Von Willebrand disease, horse","secondary_identifiers":["OMIA:001056-9796"],"termid":"MONDO:1011614","xrefs":{"Monarch":{"xref_id":"1011614"}}}


id: GO:0051590
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the directed movement of a neurotransmitter 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":"positive regulation of transport","termid":"GO:0051050"},{"relation_name":"is_a","term_name":"regulation of neurotransmitter transport","termid":"GO:0051588"},{"relation_name":"positively_regulates","term_name":"neurotransmitter transport","termid":"GO:0006836"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"positive regulation of neurotransmitter transport","synonyms":[{"name":"activation of neurotransmitter transport","type":"narrow"},{"name":"stimulation of neurotransmitter transport","type":"narrow"},{"name":"up regulation of neurotransmitter transport","type":"exact"},{"name":"up-regulation of neurotransmitter transport","type":"exact"},{"name":"upregulation of neurotransmitter transport","type":"exact"}],"termid":"GO:0051590"}


id: PBO:0085176
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"O-methyltransferase; catalyzes two different O-methylation steps in ubiquinone (Coenzyme Q) biosynthesis; component of a mitochondrial ubiquinone-synthesizing complex; phosphoprotein","termid":"PBO:0085176"}


id: GO:0035200
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The establishment, maintenance and elaboration of the anterior/posterior axis of the leg imaginal disc.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anterior/posterior pattern specification, imaginal disc","termid":"GO:0007448"},{"relation_name":"is_a","term_name":"leg disc pattern formation","termid":"GO:0035223"}],"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":"leg disc anterior/posterior pattern formation","termid":"GO:0035200"}


id: GO:0009076
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of amino acids of the histidine family.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete histidine family amino acid biosynthetic process (obsolete GO:0009076)","synonyms":[{"name":"histidine family amino acid anabolism","type":"exact"},{"name":"histidine family amino acid biosynthesis","type":"exact"},{"name":"histidine family amino acid biosynthetic process","type":"exact"},{"name":"histidine family amino acid formation","type":"exact"},{"name":"histidine family amino acid synthesis","type":"exact"}],"termid":"GO:0009076"}


id: PBO:0060588
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NBR1 autophagy cargo receptor","termid":"PBO:0060588"}


id: FYPO:0000470
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the occurrence of mating type switching is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mating type switching","termid":"FYPO:0000468"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000293","FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"decreased mating type switching","synonyms":[{"name":"decreased mating type switching during mitotic cell cycle","type":"related"},{"name":"decreased mating type switching during vegetative growth","type":"exact"},{"name":"mating type switching: decreased","type":"related"},{"name":"reduced mating type switching","type":"exact"}],"termid":"FYPO:0000470"}


id: MONDO:0000720
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete basal ganglia calcification (obsolete MONDO:0000720)","termid":"MONDO:0000720","xrefs":{"Monarch":{"xref_id":"0000720"}}}


id: GO:0140479
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A biosynthetic process that results in the formation of ergothioneine from histidine via a set of steps including the hercynylcysteine sulfoxide synthase reaction, which converts N-alpha,N-alpha,N-alpha-trimethyl-L-histidine directly to hercynylcysteine sulfoxide.","definition_xrefs":["PMID:22209968","PMID:24828577"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ergothioneine biosynthetic process","termid":"GO:0052699"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0006790","GO:0044281"],"is_obsolete":false,"name":"ergothioneine biosynthesis from histidine via hercynylcysteine sulfoxide synthase","termid":"GO:0140479"}


id: MONDO:0003089
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A mucoepidermoid carcinoma that arises from the extrahepatic bile ducts.","definition_xrefs":["NCIT:C5862"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extrahepatic bile duct mucinous adenocarcinoma","termid":"MONDO:0002739"},{"relation_name":"is_a","term_name":"mucoepidermoid carcinoma","termid":"MONDO:0003036"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0002515"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0002515","MONDO:0004335"],"is_obsolete":false,"name":"extrahepatic bile duct mucoepidermoid carcinoma","secondary_identifiers":["MEDGEN:272368","UMLS:C1332552","DOID:4681"],"synonyms":[{"name":"bile duct mucoepidermoid carcinoma","type":"exact"},{"name":"extrahepatic bile duct mucoepidermoid carcinoma","type":"exact"},{"name":"mucoepidermoid carcinoma of bile duct","type":"exact"},{"name":"mucoepidermoid carcinoma of the bile duct","type":"exact"}],"termid":"MONDO:0003089","xrefs":{"Monarch":{"xref_id":"0003089"}}}


id: PBO:0054628
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 2033","termid":"PBO:0054628"}


id: PBO:0042485
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cadherin 10","termid":"PBO:0042485"}


id: PBO:0049766
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HLA complex group 4 pseudogene 3","termid":"PBO:0049766"}


id: GO:0047228
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a 1,2-diacyl-sn-glycerol + UDP-alpha-D-glucose = a 1,2-diacyl-3-O-(alpha-D-glucopyranosyl)-sn-glycerol + H+ + UDP.","definition_xrefs":["RHEA:47612"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glucosyltransferase activity","termid":"GO:0035251"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO: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:0003824","GO:0016757","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"1,2-diacylglycerol 3-glucosyltransferase activity","secondary_identifiers":["EC:2.4.1.337","MetaCyc:2.4.1.157-RXN"],"synonyms":[{"name":"UDP-glucose-diacylglycerol glucosyltransferase activity","type":"related"},{"name":"UDP-glucose:1,2-diacylglycerol 3-D-glucosyltransferase activity","type":"related"},{"name":"UDP-glucose:1,2-diacylglycerol glucosyltransferase activity","type":"related"},{"name":"UDPglucose:1,2-diacylglycerol 3-D-glucosyltransferase activity","type":"related"},{"name":"UDPglucose:diacylglycerol glucosyltransferase activity","type":"related"},{"name":"uridine diphosphoglucose-diacylglycerol glucosyltransferase activity","type":"related"}],"termid":"GO:0047228"}


id: GO:0045112
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of integrins, a large family of transmembrane proteins that act as receptors for cell-adhesion molecules.","definition_xrefs":["GOC:go_curators","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"macromolecule biosynthetic process","termid":"GO:0009059"},{"relation_name":"part_of","term_name":"plasma membrane organization","termid":"GO:0007009"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0061024","GO:0008150"],"is_obsolete":false,"name":"integrin biosynthetic process","synonyms":[{"name":"integrin anabolism","type":"exact"},{"name":"integrin biosynthesis","type":"exact"},{"name":"integrin formation","type":"exact"},{"name":"integrin synthesis","type":"exact"}],"termid":"GO:0045112"}


id: MONDO:0010296
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"agammaglobulinemia","termid":"MONDO:0015977"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"immunodeficiency 61","secondary_identifiers":["OMIM:300310","GARD:10007","DOID:0111999","MESH:C538057","MEDGEN:337462","UMLS:C1845903"],"synonyms":[{"name":"AGMX2","type":"exact"},{"name":"XLA2","type":"related"},{"name":"agammaglobulinemia X-linked type 2","type":"related"},{"name":"agammaglobulinemia, X-linked, type 2","type":"related"},{"name":"immunodeficiency 61, X-linked recessive","type":"exact"}],"termid":"MONDO:0010296","xrefs":{"Monarch":{"xref_id":"0010296"}}}


id: PBO:0061201
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NOC2 like nucleolar associated transcriptional repressor pseudogene 1","termid":"PBO:0061201"}


id: FYPO:0004781
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 mitotic G2 DNA damage checkpoint begins later than normal under conditions that normally trigger the checkpoint signaling and response. Normally, the mitotic G2 DNA damage checkpoint negatively regulates progression through the G2/M transition of the cell cycle in response to DNA damage.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic G2 DNA damage checkpoint","termid":"FYPO:0004373"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001320","FYPO:0001985","FYPO:0000631","FYPO:0000298"],"is_obsolete":false,"name":"delayed onset of mitotic G2 DNA damage checkpoint","synonyms":[{"name":"delayed mitotic G2 DNA damage checkpoint","type":"exact"},{"name":"delayed onset of G2 DNA damage checkpoint during mitotic cell cycle","type":"exact"},{"name":"delayed onset of mitotic G2 DNA damage checkpoint during vegetative growth","type":"exact"}],"termid":"FYPO:0004781"}


id: GO:0098891
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The component of the presynaptic active zone membrane consisting of gene products and protein complexes that are loosely bound to one of its surfaces, but not integrated into the hydrophobic region.","definition_xrefs":["GOC:mf","GOC:autophagy"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extrinsic component of presynaptic membrane","termid":"GO:0098888"},{"relation_name":"part_of","term_name":"presynaptic active zone membrane","termid":"GO:0048787"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005886","GO:0005575"],"is_obsolete":false,"name":"extrinsic component of presynaptic active zone membrane","termid":"GO:0098891"}


id: MONDO:0044646
data:
  {"annotated_genes":["SJAG_04074"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86946],"is_not":false,"summary":null,"term":"MONDO:0044646"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"excluded_subClassOf","term_name":"neurodegenerative disease","termid":"MONDO:0005559"},{"relation_name":"excluded_subClassOf","term_name":"monogenic epilepsy","termid":"MONDO:0015653"},{"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":"inherited neurodegenerative disorder","termid":"MONDO:0024237"},{"relation_name":"is_a","term_name":"Mendelian encephalopathy","termid":"MONDO:0100198"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04074":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0002320"],"is_obsolete":false,"name":"early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0070423","OMIM:617193","MEDGEN:1798877","Orphanet:496641","UMLS:C5567454","GARD:17911"],"synonyms":[{"name":"PEBAT","type":"exact"},{"name":"encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum","type":"exact"},{"name":"encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum; PEBAT","type":"exact"}],"termid":"MONDO:0044646","terms_by_termid":{"MONDO:0044646":null},"xrefs":{"Monarch":{"xref_id":"0044646"}}}


id: PR:Q9P378
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- gas1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P378"],"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":"1,3-beta-glucanosyltransferase gas1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC19B12.02c","synonyms":[{"name":"Spom972h-gas1","type":"exact"}],"termid":"PR:Q9P378"}


id: PBO:0053451
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 399","termid":"PBO:0053451"}


id: MONDO:0021027
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. An instance of hair anomaly that is caused by a modification of the individual's genome.","definition_xrefs":["MONDO:patterns/genetic"],"gene_count":0,"genotype_count":0,"name":"obsolete genetic hair anomaly (obsolete MONDO:0021027)","secondary_identifiers":["Orphanet:183450"],"synonyms":[{"name":"genetic hair anomaly","type":"exact"}],"termid":"MONDO:0021027","xrefs":{"Monarch":{"xref_id":"0021027"}}}


id: GO:0047198
data:
  {"annotated_genes":["SJAG_01899"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[87979],"is_not":false,"summary":null,"term":"GO:0047198"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: S-substituted L-cysteine + acetyl-CoA = S-substituted N-acetyl-L-cysteine + CoA + H+.","definition_xrefs":["RHEA:19213","EC:2.3.1.80"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-amino-acid N-acetyltransferase activity","termid":"GO:0140085"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01899":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:0003674","GO:0003824","GO:0016746","GO:0016740"],"is_obsolete":false,"name":"L-cysteine-S-conjugate N-acetyltransferase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:2.3.1.80-RXN","Reactome:R-HSA-5433066","KEGG_REACTION:R04950"],"synonyms":[{"name":"acetyl-CoA:S-substituted L-cysteine N-acetyltransferase activity","type":"related"},{"name":"cysteine-S-conjugate N-acetyltransferase activity","type":"exact"}],"termid":"GO:0047198","terms_by_termid":{"GO:0047198":null}}


id: PBO:0052650
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 8 pseudogene 18","termid":"PBO:0052650"}


id: FYECO:0000326
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which 4-nitroquinoline N-oxide was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ 4-NQO","synonyms":[{"name":"+ 4-nitroquinoline N-oxide","type":"exact"},{"name":"+ 4NQO","type":"exact"}],"termid":"FYECO:0000326"}


id: PBO:0034081
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-child_nucleus_of_in_hermaphrodite","termid":"PBO:0034081"}


id: PBO:0046423
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EPH receptor A7","termid":"PBO:0046423"}


id: MONDO:0004641
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A in situ carcinoma that involves the zone of skin.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skin carcinoma","termid":"MONDO:0002656"},{"relation_name":"is_a","term_name":"in situ carcinoma","termid":"MONDO:0004647"}],"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":"skin carcinoma in situ","secondary_identifiers":["ICD9:232.3","ICD9:232.0","MEDGEN:102308","ICD9:232","ICD9:232.5","ICD9:232.6","ICD10CM:D04","UMLS:C0154073","ICD9:232.2","DOID:8687","NCIT:C3640","ICD9:232.8","ICD9:232.7","ICD9:232.9","ICD9:232.4","SCTID:92749008"],"synonyms":[{"name":"carcinoma in situ of skin","type":"exact"},{"name":"carcinoma in situ of the skin","type":"exact"},{"name":"carcinoma in situ of zone of skin","type":"exact"},{"name":"carcinoma of skin stage 0","type":"exact"},{"name":"carcinoma of the skin stage 0","type":"exact"},{"name":"cutaneous carcinoma in situ","type":"exact"},{"name":"nonmelanoma carcinoma in situ","type":"exact"},{"name":"skin cancer stage 0","type":"exact"},{"name":"skin carcinoma in situ","type":"exact"},{"name":"skin carcinoma stage 0","type":"exact"},{"name":"stage 0 nonmelanoma skin carcinoma in situ","type":"exact"},{"name":"stage 0 skin cancer","type":"exact"},{"name":"stage 0 skin cancer aJCC v6","type":"exact"},{"name":"stage 0 skin cancer aJCC v7","type":"exact"},{"name":"stage 0 skin carcinoma","type":"exact"},{"name":"stage 0 zone of skin carcinoma","type":"exact"},{"name":"zone of skin carcinoma in situ","type":"exact"},{"name":"zone of skin in situ carcinoma","type":"exact"}],"termid":"MONDO:0004641","xrefs":{"Monarch":{"xref_id":"0004641"}}}


id: PBO:0047469
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Fc receptor like B","termid":"PBO:0047469"}


id: PBO:0065743
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2-phosphoxylose phosphatase 1","termid":"PBO:0065743"}


id: PBO:0011418
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_penetrance","termid":"PBO:0011418"}


id: GO:0097266
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: phenylacetyl-CoA + H+ + NADPH + O2 = 2-(1,2-epoxy-1,2-dihydrophenyl)acetyl-CoA + H2O + NADP+.","definition_xrefs":["EC:1.14.13.149","PMID:20660314","GOC:gk","PMID:21247899","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen","termid":"GO:0016709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"phenylacetyl-CoA 1,2-epoxidase activity","secondary_identifiers":["KEGG_REACTION:R09838","RHEA:32171"],"synonyms":[{"name":"phenylacetyl-CoA epoxidase activity","type":"exact"},{"name":"phenylacetyl-CoA monooxygenase activity","type":"related"},{"name":"ring 1,2-phenylacetyl-CoA epoxidase activity","type":"related"}],"termid":"GO:0097266"}


id: MONDO:0005277
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A common, severe type of vascular headache often associated with increased sympathetic activity, resulting in nausea, vomiting, and light sensitivity.","definition_xrefs":["NCIT:C89715"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brain disorder","termid":"MONDO:0005560"},{"relation_name":"is_a","term_name":"hypnic headache","termid":"MONDO:0017181"},{"relation_name":"is_a","term_name":"neurovascular disorder","termid":"MONDO:0043218"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"migraine disorder","secondary_identifiers":["MEDGEN:57451","ICD9:346","MESH:D008881","UMLS:C0149931","ICD9:346.9","DOID:6364"],"synonyms":[{"name":"migraine","type":"exact"},{"name":"migraine disorder","type":"exact"},{"name":"migraine headache","type":"exact"},{"name":"migraine variant","type":"exact"},{"name":"migraine with or without aura","type":"exact"}],"termid":"MONDO:0005277","xrefs":{"Monarch":{"xref_id":"0005277"}}}


id: PBO:0045237
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 5","termid":"PBO:0045237"}


id: MONDO:0012695
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Meckel syndrome in which the cause of the disease is a mutation in the RPGRIP1L gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Meckel syndrome","termid":"MONDO:0018921"},{"relation_name":"is_a","term_name":"polydactyly-syndactyly-triphalangism","termid":"MONDO:0800066"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Meckel syndrome, type 5","secondary_identifiers":["OMIM:611561","DOID:0070119","MESH:C566915","UMLS:C1969052","GARD:15520","MEDGEN:409740"],"synonyms":[{"name":"MKS5","type":"exact"},{"name":"Meckel syndrome 5","type":"related"},{"name":"Meckel syndrome caused by mutation in RPGRIP1L","type":"exact"},{"name":"Meckel syndrome, type 5","type":"exact"},{"name":"Meckel-Gruber syndrome, type 5","type":"exact"},{"name":"RPGRIP1L Meckel syndrome","type":"exact"}],"termid":"MONDO:0012695","xrefs":{"Monarch":{"xref_id":"0012695"}}}


id: MONDO:0012999
data:
  {"annotated_genes":["SJAG_02271"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85215],"is_not":false,"summary":null,"term":"MONDO:0012999"}]},"cv_name":"mondo","definition":"A creatine deficiency syndrome characterized by global developmental delay/intellectual disability (DD/ID), prominent speech delay, autistic/hyperactive behavioral disorders, seizures, and various types of pyramidal and/or extra-pyramidal manifestations.","definition_xrefs":["Orphanet:382"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerebral creatine deficiency syndrome","termid":"MONDO:0000456"},{"relation_name":"is_a","term_name":"creatine biosynthetic process disease","termid":"MONDO:0045018"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02271":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004736"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004736"],"is_obsolete":false,"name":"guanidinoacetate methyltransferase deficiency","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:124239003","DOID:0050799","UMLS:C0574080","MESH:C537622","NANDO:1201034","GARD:2578","NANDO:2201300","MEDGEN:154356","NORD:1967","icd11.foundation:1811642217","ICD9:277.6","OMIM:612736"],"synonyms":[{"name":"CCDS2","type":"related"},{"name":"GAMT deficiency","type":"exact"},{"name":"cerebral creatine deficiency syndrome 2","type":"exact"},{"name":"cerebral creatine deficiency syndrome type 2","type":"exact"},{"name":"creatine deficiency syndrome due to GAMT deficiency","type":"related"},{"name":"disorder of guanidinoacetate N-methyltransferase activity","type":"exact"},{"name":"guanidinoacetate N-methyltransferase activity disease","type":"exact"},{"name":"guanidinoacetate methyltransferase deficiency","type":"exact"}],"termid":"MONDO:0012999","terms_by_termid":{"MONDO:0012999":null},"xrefs":{"Monarch":{"xref_id":"0012999"}}}


id: PBO:0089272
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Lsm2-8 complex subunit Lsm8","termid":"PBO:0089272"}


id: GO:0070319
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A transport vesicle that mediates transport from the Golgi to the plasma membrane, and fuses with the plasma membrane to release various cargo molecules, such as proteins or hormones, by exocytosis.","definition_xrefs":["GOC:mah","GOC:kad"],"direct_ancestors":[{"relation_name":"is_a","term_name":"exocytic vesicle","termid":"GO:0070382"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0031410"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0031410","GO:0005737"],"is_obsolete":false,"name":"Golgi to plasma membrane transport vesicle","synonyms":[{"name":"Golgi to plasma membrane constitutive secretory pathway transport vesicle","type":"exact"},{"name":"Golgi-plasma membrane transport vesicle","type":"exact"}],"termid":"GO:0070319"}


id: MONDO:0005802
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A parasitic infection caused by tapeworms. Most infected individuals do not have symptoms. When symptoms appear, they include diarrhea, abdominal pain, restlessness, and irritability.","definition_xrefs":["NCIT:C84768"],"direct_ancestors":[{"relation_name":"is_a","term_name":"helminthiasis","termid":"MONDO:0004664"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hymenolepiasis","secondary_identifiers":["icd11.foundation:2028864113","MESH:D006925","Orphanet:401","EFO:0007317","GARD:2787","ICD10CM:B71.0","SCTID:44917000","UMLS:C0020413","ICD9:123.6","MedDRA:10020546","MEDGEN:43772","DOID:10074"],"synonyms":[{"name":"Hymenolepis infectious disease","type":"exact"},{"name":"Hymenolepsis infection","type":"related"},{"name":"dwarf tapeworm infection","type":"exact"},{"name":"hymenolepiasis","type":"exact"}],"termid":"MONDO:0005802","xrefs":{"Monarch":{"xref_id":"0005802"}}}


id: PBO:0090485
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thioredoxin family protein Mpd1","termid":"PBO:0090485"}


id: MONDO:0011516
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":"early response to neural induction gene","secondary_identifiers":["MEDGEN:344332","OMIM:605105","UMLS:C1854633"],"synonyms":[{"name":"Erni","type":"related"},{"name":"early response to neural induction gene","type":"exact"}],"termid":"MONDO:0011516","xrefs":{"Monarch":{"xref_id":"0011516"}}}


id: GO:0046239
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of phthalate, the anion of phthalic acid.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phthalate metabolic process","termid":"GO:0018963"},{"relation_name":"is_a","term_name":"xenobiotic catabolic process","termid":"GO:0042178"},{"relation_name":"is_a","term_name":"carboxylic acid catabolic process","termid":"GO:0046395"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044248"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0044248","GO:0008150"],"is_obsolete":false,"name":"phthalate catabolic process","synonyms":[{"name":"phthalate breakdown","type":"exact"},{"name":"phthalate catabolism","type":"exact"},{"name":"phthalate degradation","type":"exact"}],"termid":"GO:0046239"}


id: MONDO:0020750
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"polycystic lipomembranous osteodysplasia with sclerosing leukoencephaly","termid":"MONDO:0009092"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005559"],"is_obsolete":false,"name":"polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2","secondary_identifiers":["OMIM:618193","UMLS:C4748657","MEDGEN:1648374"],"termid":"MONDO:0020750","xrefs":{"Monarch":{"xref_id":"0020750"}}}


id: GO:0006400
data:
  {"annotated_genes":["SJAG_04700","SJAG_01638","SJAG_02042","SJAG_00235","SJAG_00352","SJAG_01575","SJAG_00499","SJAG_02863","SJAG_05023","SJAG_02637","SJAG_06284","SJAG_00325","SJAG_05334","SJAG_00683","SJAG_01172","SJAG_01375","SJAG_01269","SJAG_00319","SJAG_04735","SJAG_03367","SJAG_04181","SJAG_04649","SJAG_05249","SJAG_04680","SJAG_00186","SJAG_02179","SJAG_04756","SJAG_04993","SJAG_02099","SJAG_02386","SJAG_00579","SJAG_00088","SJAG_04233","SJAG_04265","SJAG_03240","SJAG_05228","SJAG_00865","SJAG_01302","SJAG_01877","SJAG_03236","SJAG_04113","SJAG_04848","SJAG_04175","SJAG_01024","SJAG_04704","SJAG_04367","SJAG_00886","SJAG_04736","SJAG_04189","SJAG_03896","SJAG_01418","SJAG_00174","SJAG_01041","SJAG_03616","SJAG_03677","SJAG_01781","SJAG_02084","SJAG_02352","SJAG_02978","SJAG_01314","SJAG_04380","SJAG_04453","SJAG_04452","SJAG_03572","SJAG_06560","SJAG_01261","SJAG_00358","SJAG_00378","SJAG_04201","SJAG_04890","SJAG_04182","SJAG_00255","SJAG_00892","SJAG_03932","SJAG_02302","SJAG_04065"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[60896,70573],"is_not":false,"summary":null,"term":"GO:0006400"},{"annotations":[70963],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019988"},{"annotations":[80041],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061504"},{"annotations":[77850],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070901"},{"annotations":[118427,75274],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072670"},{"annotations":[94025,116767],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990799"},{"annotations":[76058,92554],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070899"},{"annotations":[102886],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990983"},{"annotations":[67260,58824],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106004"},{"annotations":[107122,71890],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051391"},{"annotations":[109954,106567],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106217"},{"annotations":[90210,105583],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002946"},{"annotations":[74185,65596,60382,64572],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002943"},{"annotations":[75643,94460,97852,74991,95985,76056,71932,72347,73762,72071,73510,62787],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030488"},{"annotations":[77849,70796],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002939"},{"annotations":[103924,73027],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002940"},{"annotations":[114630],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002128"},{"annotations":[90964,102281,106029,75470,78208,72576],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031119"},{"annotations":[58711,78553,99246,100924,98067],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002949"},{"annotations":[100898,73419,58784],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002100"},{"annotations":[113776,71983,100361,79487,109951,118587],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002926"},{"annotations":[88008,93685],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002127"},{"annotations":[71887],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002101"},{"annotations":[77154,106680,73866,117007,73855],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002143"},{"annotations":[105355,95819,118455,87536],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002098"},{"annotations":[61368,73654,72345,65986],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0101030"},{"annotations":[97625,102678],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002130"},{"annotations":[71933,94461,73511,74734],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031591"}]},"cv_name":"biological_process","definition":"The covalent alteration of one or more nucleotides within a tRNA molecule to produce a tRNA molecule with a sequence that differs from that coded genetically.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA processing","termid":"GO:0008033"},{"relation_name":"is_a","term_name":"RNA modification","termid":"GO:0009451"}],"gene_count":76,"genes_by_uniquename":{"SJAG_00088":null,"SJAG_00174":null,"SJAG_00186":null,"SJAG_00235":null,"SJAG_00255":null,"SJAG_00319":null,"SJAG_00325":null,"SJAG_00352":null,"SJAG_00358":null,"SJAG_00378":null,"SJAG_00499":null,"SJAG_00579":null,"SJAG_00683":null,"SJAG_00865":null,"SJAG_00886":null,"SJAG_00892":null,"SJAG_01024":null,"SJAG_01041":null,"SJAG_01172":null,"SJAG_01261":null,"SJAG_01269":null,"SJAG_01302":null,"SJAG_01314":null,"SJAG_01375":null,"SJAG_01418":null,"SJAG_01575":null,"SJAG_01638":null,"SJAG_01781":null,"SJAG_01877":null,"SJAG_02042":null,"SJAG_02084":null,"SJAG_02099":null,"SJAG_02179":null,"SJAG_02302":null,"SJAG_02352":null,"SJAG_02386":null,"SJAG_02637":null,"SJAG_02863":null,"SJAG_02978":null,"SJAG_03236":null,"SJAG_03240":null,"SJAG_03367":null,"SJAG_03572":null,"SJAG_03616":null,"SJAG_03677":null,"SJAG_03896":null,"SJAG_03932":null,"SJAG_04065":null,"SJAG_04113":null,"SJAG_04175":null,"SJAG_04181":null,"SJAG_04182":null,"SJAG_04189":null,"SJAG_04201":null,"SJAG_04233":null,"SJAG_04265":null,"SJAG_04367":null,"SJAG_04380":null,"SJAG_04452":null,"SJAG_04453":null,"SJAG_04649":null,"SJAG_04680":null,"SJAG_04700":null,"SJAG_04704":null,"SJAG_04735":null,"SJAG_04736":null,"SJAG_04756":null,"SJAG_04848":null,"SJAG_04890":null,"SJAG_04993":null,"SJAG_05023":null,"SJAG_05228":null,"SJAG_05249":null,"SJAG_05334":null,"SJAG_06284":null,"SJAG_06560":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0006399"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0006399","GO:0008150"],"is_obsolete":false,"name":"tRNA modification","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},"secondary_identifiers":["GO:0016549","Reactome:R-HSA-6782315"],"synonyms":[{"name":"tRNA editing","type":"narrow"}],"termid":"GO:0006400","terms_by_termid":{"GO:0002098":null,"GO:0002100":null,"GO:0002101":null,"GO:0002127":null,"GO:0002128":null,"GO:0002130":null,"GO:0002143":null,"GO:0002926":null,"GO:0002939":null,"GO:0002940":null,"GO:0002943":null,"GO:0002946":null,"GO:0002949":null,"GO:0006400":null,"GO:0019988":null,"GO:0030488":null,"GO:0031119":null,"GO:0031591":null,"GO:0051391":null,"GO:0061504":null,"GO:0070899":null,"GO:0070901":null,"GO:0072670":null,"GO:0101030":null,"GO:0106004":null,"GO:0106217":null,"GO:1990799":null,"GO:1990983":null}}


id: GO:0043178
data:
  {"annotated_genes":["SJAG_03362","SJAG_02591","SJAG_03325","SJAG_00233","SJAG_04131","SJAG_03847"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[71821,90358,103369,74457,101104],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000822"},{"annotations":[66800],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030975"}]},"cv_name":"molecular_function","definition":"Binding to an alcohol, any of a class of alkyl compounds containing a hydroxyl group.","definition_xrefs":["ISBN:0198506732","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"small molecule binding","termid":"GO:0036094"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00233":null,"SJAG_02591":null,"SJAG_03325":null,"SJAG_03362":null,"SJAG_03847":null,"SJAG_04131":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"alcohol binding","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0043178","terms_by_termid":{"GO:0000822":null,"GO:0030975":null}}


id: MONDO:0016314
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Rare pancreatic carcinoma.","gene_count":0,"genotype_count":0,"name":"obsolete rare carcinoma of pancreas (obsolete MONDO:0016314)","secondary_identifiers":["MedDRA:10033604","Orphanet:217074","MedDRA:10033609"],"synonyms":[{"name":"rare exocrine pancreatic carcinoma","type":"exact"},{"name":"rare pancreatic carcinoma","type":"exact"}],"termid":"MONDO:0016314","xrefs":{"Monarch":{"xref_id":"0016314"}}}


id: FYPO:0006304
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which F-actin forms a large spot in the medial region of the cell, instead of assembling into a contractile ring.","definition_xrefs":["PMID:19713940","PMID:9635188","PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"actomyosin contractile ring absent","termid":"FYPO:0001008"},{"relation_name":"is_a","term_name":"actomyosin contractile ring absent","termid":"FYPO:0001008"},{"relation_name":"is_a","term_name":"abnormal actin cytoskeleton during vegetative growth","termid":"FYPO:0002398"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0004803"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0004803","FYPO:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"medial F-actin spot present","synonyms":[{"name":"actomyosin contractile ring absent, with medial F-actin spot present","type":"exact"},{"name":"medial F-actin spot present during mitotic cell cycle","type":"related"},{"name":"medial F-actin spot present during vegetative growth","type":"exact"}],"termid":"FYPO:0006304"}


id: MONDO:0024339
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplasm involving a lymph node.","definition_xrefs":["MONDO:patterns/neoplasm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hematopoietic and lymphoid system neoplasm","termid":"MONDO:0002334"},{"relation_name":"is_a","term_name":"lymph node disorder","termid":"MONDO:0004928"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"lymph node neoplasm","secondary_identifiers":["UMLS:C0596869","MEDGEN:108920","GARD:6932","NCIT:C35497"],"synonyms":[{"name":"lymph node neoplasm","type":"exact"},{"name":"lymph node neoplasm (disease)","type":"exact"},{"name":"lymph node tumor","type":"exact"},{"name":"lymph node tumour","type":"exact"},{"name":"neoplasm of lymph node","type":"exact"},{"name":"tumor of lymph node","type":"exact"},{"name":"tumour of lymph node","type":"exact"}],"termid":"MONDO:0024339","xrefs":{"Monarch":{"xref_id":"0024339"}}}


id: GO:1903694
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of mitotic G1 cell cycle arrest in response to nitrogen starvation.","definition_xrefs":["PMID:15713656","GO_REF:0000058","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of mitotic G1 cell cycle arrest in response to nitrogen starvation (obsolete GO:1903694)","synonyms":[{"name":"activation of G1 mitotic cell cycle arrest in response to nitrogen starvation","type":"narrow"},{"name":"activation of mitotic G1 cell cycle arrest in response to nitrogen starvation","type":"narrow"},{"name":"positive regulation of G1 mitotic cell cycle arrest in response to nitrogen starvation","type":"exact"},{"name":"up regulation of G1 mitotic cell cycle arrest in response to nitrogen starvation","type":"exact"},{"name":"up regulation of mitotic G1 cell cycle arrest in response to nitrogen starvation","type":"exact"},{"name":"up-regulation of G1 mitotic cell cycle arrest in response to nitrogen starvation","type":"exact"},{"name":"up-regulation of mitotic G1 cell cycle arrest in response to nitrogen starvation","type":"exact"},{"name":"upregulation of G1 mitotic cell cycle arrest in response to nitrogen starvation","type":"exact"},{"name":"upregulation of mitotic G1 cell cycle arrest in response to nitrogen starvation","type":"exact"}],"termid":"GO:1903694"}


id: PBO:0079314
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis-specific transcript, Y-linked 7","termid":"PBO:0079314"}


id: PBO:0083006
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Daughter cell-specific protein, may help establish daughter fate; relocalizes from bud neck to cytoplasm upon DNA replication stress; interacts with Csm1p","termid":"PBO:0083006"}


id: PBO:0003416
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SHREC complex subunit Mit1","termid":"PBO:0003416"}


id: PBO:0051623
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"integrin linked kinase","termid":"PBO:0051623"}


id: PBO:0055018
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 2433","termid":"PBO:0055018"}


id: GO:0050653
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The elongation of chondroitin sulfate proteoglycan chains by alternate addition of N-acetylhexosamine and GlcUA residues to the GAG-protein linkage region tetrasaccharide of chondroitin sulfate.","definition_xrefs":["GOC:ai","PMID:11788602"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polysaccharide biosynthetic process","termid":"GO:0000271"},{"relation_name":"part_of","term_name":"chondroitin sulfate proteoglycan biosynthetic process","termid":"GO:0050650"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006790"}],"interesting_parent_ids":["GO:0008150","GO:0006790","GO:0005975"],"is_obsolete":false,"name":"chondroitin sulfate proteoglycan biosynthetic process, chain elongation","synonyms":[{"name":"chondroitin sulfate proteoglycan anabolism, polysaccharide chain anabolism","type":"exact"},{"name":"chondroitin sulfate proteoglycan biosynthetic process, polysaccharide chain biosynthetic process","type":"exact"},{"name":"chondroitin sulfate proteoglycan chain elongation","type":"exact"},{"name":"chondroitin sulfate proteoglycan formation, polysaccharide chain biosynthesis","type":"exact"},{"name":"chondroitin sulfate proteoglycan formation, polysaccharide chain formation","type":"exact"},{"name":"chondroitin sulfate proteoglycan synthesis, polysaccharide chain synthesis","type":"exact"},{"name":"chondroitin sulphate proteoglycan biosynthesis, polysaccharide chain biosynthesis","type":"exact"},{"name":"chondroitin sulphate proteoglycan biosynthesis, polysaccharide chain biosynthetic process","type":"exact"}],"termid":"GO:0050653"}


id: PBO:0073547
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SH3 and multiple ankyrin repeat domains 1","termid":"PBO:0073547"}


id: PBO:0083499
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the verified gene YMC1/YPR058W","termid":"PBO:0083499"}


id: MONDO:0011093
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal recessive lysosomal storage disease caused by mutation(s) in the HYAL1 gene, encoding hyaluronidase-1. It is characterized by short stature and hyaluronidase deficiency.","definition_xrefs":["NCIT:C129073"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bone disorder","termid":"MONDO:0005381"},{"relation_name":"is_a","term_name":"mucopolysaccharidosis","termid":"MONDO:0019249"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0002561"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0002561","MONDO:0005066","MONDO:0037792"],"is_obsolete":false,"name":"mucopolysaccharidosis type 9","secondary_identifiers":["DOID:0050809","MEDGEN:226942","GARD:16675","MESH:C563209","Orphanet:67041","SCTID:124473006","OMIM:601492","UMLS:C1291490","icd11.foundation:952591271","ICD9:277.6","NANDO:1200115"],"synonyms":[{"name":"MPS 9","type":"related"},{"name":"MPS9","type":"exact"},{"name":"MPSIX","type":"exact"},{"name":"hyaluronidase deficiency","type":"related"},{"name":"mucopolysaccharidosis IX","type":"related"},{"name":"mucopolysaccharidosis type 9","type":"exact"},{"name":"mucopolysaccharidosis type IX","type":"exact"},{"name":"mucopolysaccharidosis, type 9","type":"related"},{"name":"mucopolysaccharidosis, type IX","type":"related"}],"termid":"MONDO:0011093","xrefs":{"Monarch":{"xref_id":"0011093"}}}


id: PBO:0065608
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PTP4A1 pseudogene 2","termid":"PBO:0065608"}


id: PBO:0112846
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"asynchronous replication autosomal RNA 6-2","termid":"PBO:0112846"}


id: MONDO:0020433
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ectasia of the left atrial appendage is a rare cardiac malformation characterized by the enlargement of the left auricle without any other associated cardiac lesions. It can be asymptomatic (discovered fortuitously during routine chest imaging as an unusual cardiac shadow) or present clinically with supraventricular tachyarrhythmia, paroxysmal tachycardia, embolic events, respiratory distress, chest pain, angina pectoris or heart failure.","definition_xrefs":["Orphanet:99102"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital heart malformation","termid":"MONDO:0019512"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ectasia of the left appendage","secondary_identifiers":["UMLS:C4749282","GARD:19650","MEDGEN:1656788"],"synonyms":[{"name":"dilatation of the left appendage","type":"exact"},{"name":"dilatation of the left atrial appendage","type":"exact"},{"name":"dilatation of the left auricle","type":"exact"},{"name":"ectasia of the left atrial appendage","type":"related"},{"name":"ectasia of the left auricle","type":"exact"}],"termid":"MONDO:0020433","xrefs":{"Monarch":{"xref_id":"0020433"}}}


id: MONDO:0018417
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","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":"autosomal recessive spastic paraplegia type 60","secondary_identifiers":["GARD:21696","Orphanet:401800","UMLS:C5190589","MEDGEN:1683240"],"synonyms":[{"name":"SPG60","type":"exact"}],"termid":"MONDO:0018417","xrefs":{"Monarch":{"xref_id":"0018417"}}}


id: GO:0038067
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: protein + ATP = protein phosphate + ADP by a mitogen-activated protein kinase, as part of a MAPK signaling cascade that contributes to cell wall organization or biogenesis.","definition_xrefs":["GOC:signaling"],"gene_count":0,"genotype_count":0,"name":"obsolete MAP kinase activity involved in cell wall organization or biogenesis (obsolete GO:0038067)","synonyms":[{"name":"MAP kinase activity involved in cell wall biogenesis","type":"narrow"},{"name":"MAP kinase activity involved in cell wall integrity","type":"related"},{"name":"MAPK activity involved in cell wall biogenesis","type":"narrow"}],"termid":"GO:0038067"}


id: PBO:0039927
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARHGEF28 pseudogene 1","termid":"PBO:0039927"}


id: PBO:0028512
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_histone_H3-K9_methylation","termid":"PBO:0028512"}


id: MONDO:0007760
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":"hyperlipoproteinemia, type II, and deafness","secondary_identifiers":["MESH:C564170","UMLS:C1840425","MEDGEN:326732","OMIM:144300"],"synonyms":[{"name":"hyperlipoproteinemia, type II, and deafness","type":"exact"}],"termid":"MONDO:0007760","xrefs":{"Monarch":{"xref_id":"0007760"}}}


id: MONDO:0008928
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cataract-ataxia-deafness syndrome is characterized by mild intellectual deficit, congenital cataract, progressive sensorineural deafness and ataxia. It has been described in two sisters. The inheritance is likely to be autosomal recessive.","definition_xrefs":["Orphanet:1368"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary ataxia","termid":"MONDO:0100309"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cataract-ataxia-deafness syndrome","secondary_identifiers":["MEDGEN:163216","UMLS:C0796123","GARD:1141","MESH:C538283","OMIM:212710"],"synonyms":[{"name":"Begeer syndrome","type":"related"},{"name":"cataract ataxia deafness","type":"related"},{"name":"cataract ataxia deafness syndrome","type":"related"},{"name":"cataract-ataxia-deafness-retardation syndrome","type":"related"},{"name":"polyneuropathy, cataract, deafness syndrome","type":"related"},{"name":"polyneuropathy-cataract-deafness syndrome","type":"related"}],"termid":"MONDO:0008928","xrefs":{"Monarch":{"xref_id":"0008928"}}}


id: PBO:0067016
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 26, pseudogene","termid":"PBO:0067016"}


id: MOD:01220
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Chemical derivative -","definition_xrefs":["Unimod:286#E","PubMed:15121203","PubMed:9254591"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Sulfanilic Acid (SA), heavy C13","termid":"MOD:00606"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sulfanilic Acid (SA), heavy C13 - site E","synonyms":[{"name":"Heavy Sulfanilic Acid (SA) C13","type":"related"},{"name":"SulfanilicAcid:13C(6)","type":"related"}],"termid":"MOD:01220"}


id: GO:0140359
data:
  {"annotated_genes":["SJAG_05213","SJAG_04277","SJAG_03497","SJAG_03363","SJAG_03785","SJAG_02602","SJAG_02457","SJAG_01344","SJAG_03850"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[57676,58053],"is_not":false,"summary":null,"term":"GO:0140359"},{"annotations":[89022],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140481"},{"annotations":[108471],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015410"},{"annotations":[75270],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015421"},{"annotations":[118017,96825],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044604"},{"annotations":[117766,95834],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008559"}]},"cv_name":"molecular_function","definition":"Primary active transporter characterized by two nucleotide-binding domains and two transmembrane domains. Uses the energy generated from ATP hydrolysis to drive the transport of a substance across a membrane.","definition_xrefs":["PMID:26517899"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ATPase-coupled transmembrane transporter activity","termid":"GO:0042626"}],"gene_count":9,"genes_by_uniquename":{"SJAG_01344":null,"SJAG_02457":null,"SJAG_02602":null,"SJAG_03363":null,"SJAG_03497":null,"SJAG_03785":null,"SJAG_03850":null,"SJAG_04277":null,"SJAG_05213":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"ABC-type transporter activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-429157","Wikipedia:ATP-binding_cassette_transporter","Reactome:R-HSA-5387389","Reactome:R-HSA-9661405","TC:3.A.1","Reactome:R-HSA-266070","Reactome:R-HSA-9750656","Reactome:R-HSA-5362459"],"synonyms":[{"name":"ABC transporter","type":"exact"},{"name":"ABC-type efflux permease activity","type":"exact"},{"name":"ABC-type efflux porter activity","type":"exact"},{"name":"ABC-type transmembrane transporter activity","type":"exact"},{"name":"ABC-type uptake permease activity","type":"exact"},{"name":"ATP binding cassette transporter","type":"exact"},{"name":"ATP-binding cassette (ABC) transporter activity","type":"exact"},{"name":"ATP-binding cassette transporter","type":"exact"}],"termid":"GO:0140359","terms_by_termid":{"GO:0008559":null,"GO:0015410":null,"GO:0015421":null,"GO:0044604":null,"GO:0140359":null,"GO:0140481":null}}


id: FYPO:0003446
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the occurrence of SRP-dependent cotranslational protein targeting to the ER membrane is decreased.","definition_xrefs":["GO:0006614","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal intracellular protein transport during vegetative growth","termid":"FYPO:0000215"},{"relation_name":"is_a","term_name":"abnormal protein secretion during vegetative growth","termid":"FYPO:0000536"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000138","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"decreased SRP-dependent cotranslational protein targeting to membrane during vegetative growth","synonyms":[{"name":"decreased SRP-dependent cotranslational protein targeting to membrane during mitotic cell cycle","type":"related"},{"name":"reduced SRP-dependent cotranslational protein targeting to membrane during vegetative growth","type":"exact"}],"termid":"FYPO:0003446"}


id: PBO:0070424
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribulose-5-phosphate-3-epimerase pseudogene 2","termid":"PBO:0070424"}


id: PBO:0109383
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis expressed transcript, Y-linked 14","termid":"PBO:0109383"}


id: PBO:0000463
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"regulated by oleic acid","termid":"PBO:0000463"}


id: GO:1990901
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The cell pole distal from the most recent cell division.","definition_xrefs":["GOC:jh2","PMID:8226658","PMID:10231492"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell pole","termid":"GO:0060187"}],"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":"old cell pole","termid":"GO:1990901"}


id: FYPO:0007399
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the kinetochore of a chromosome is normal (i.e. indistinguishable from wild type) during interphase of the mitotic cell cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to kinetochore during vegetative growth","termid":"FYPO:0002901"}],"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:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257","FYPO:0001320","FYPO:0000138","FYPO:0001312"],"is_obsolete":false,"name":"normal protein localization to kinetochore during mitotic interphase","synonyms":[{"name":"normal protein localisation to kinetochore during interphase during vegetative growth","type":"exact"},{"name":"normal protein localization to kinetochore during interphase of mitotic cell cycle","type":"related"}],"termid":"FYPO:0007399"}


id: PBO:0070739
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L10a pseudogene 9","termid":"PBO:0070739"}


id: MONDO:0007582
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Cockayne syndrome B (obsolete MONDO:0007582)","termid":"MONDO:0007582","xrefs":{"Monarch":{"xref_id":"0007582"}}}


id: MONDO:0001222
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A broad classification of inherited disorders presenting at birth that affect the cell-mediated aspect of the immune response. Circulating numbers of T lymphocytes are decreased or ineffective.","definition_xrefs":["NCIT:C27872"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"inborn error of immunity","termid":"MONDO:0003778"},{"relation_name":"is_a","term_name":"T-cell immunodeficiency","termid":"MONDO:0003780"}],"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":"congenital T-cell immunodeficiency","secondary_identifiers":["UMLS:C1333147","MEDGEN:232099","DOID:11200"],"synonyms":[{"name":"T cell deficiency","type":"related"},{"name":"congenital T-cell immunodeficiency","type":"exact"}],"termid":"MONDO:0001222","xrefs":{"Monarch":{"xref_id":"0001222"}}}


id: GO:0140981
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: an omega-methyl-medium-chain fatty acid + O2 + reduced [NADPH--hemoprotein reductase] = an omega-hydroxy-medium-chain fatty acid + H+ + H2O + oxidized [NADPH--hemoprotein reductase]. A medium-chain fatty acid has an aliphatic tail containing 6 to 12 carbons.","definition_xrefs":["RHEA:75279"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fatty acid omega-hydroxylase activity","termid":"GO:0120250"}],"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":"medium-chain fatty acid omega-hydroxylase activity","secondary_identifiers":["MetaCyc:RXN-19719"],"termid":"GO:0140981"}


id: GO:0022850
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transmembrane transfer of a cation by a channel that opens when serotonin has been bound by the channel complex or one of its constituent parts.","definition_xrefs":["GOC:mtg_transport","PMID:12867984"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmitter-gated monoatomic ion channel activity","termid":"GO:0022824"},{"relation_name":"is_a","term_name":"ligand-gated monoatomic cation channel activity","termid":"GO:0099094"},{"relation_name":"is_a","term_name":"serotonin receptor activity","termid":"GO:0099589"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0038023","GO:0003674"],"is_obsolete":false,"name":"serotonin-gated monoatomic cation channel activity","secondary_identifiers":["Reactome:R-HSA-975311","Reactome:R-HSA-9648983","GO:0005232"],"synonyms":[{"name":"5-hydroxytryptamine-gated receptor-channel","type":"narrow"},{"name":"serotonin-activated cation-selective channel activity","type":"exact"},{"name":"serotonin-gated cation channel activity","type":"narrow"},{"name":"serotonin-gated cation-selective channel activity","type":"broad"},{"name":"serotonin-gated monoatomic cation-selective channel activity","type":"exact"}],"termid":"GO:0022850"}


id: GO:0043632
data:
  {"annotated_genes":["SJAG_02299","SJAG_04661","SJAG_03561","SJAG_02502","SJAG_01281","SJAG_02992","SJAG_03218","SJAG_01956","SJAG_04888","SJAG_00766","SJAG_03831","SJAG_01472","SJAG_00910","SJAG_02197","SJAG_00452","SJAG_04335","SJAG_01134","SJAG_00312","SJAG_00300","SJAG_00778","SJAG_00808","SJAG_01544","SJAG_00644","SJAG_16455","SJAG_00416","SJAG_03984","SJAG_00651","SJAG_02822","SJAG_01617","SJAG_01467","SJAG_03970","SJAG_01497","SJAG_05264","SJAG_01527","SJAG_04619","SJAG_01392","SJAG_01528","SJAG_01981","SJAG_04541","SJAG_03783","SJAG_00615","SJAG_01679","SJAG_03876","SJAG_02723","SJAG_04384","SJAG_01253","SJAG_02912","SJAG_03350","SJAG_01176","SJAG_00795","SJAG_03523","SJAG_00475","SJAG_01533","SJAG_04357","SJAG_01360","SJAG_05329","SJAG_00146","SJAG_01242","SJAG_03345","SJAG_02186","SJAG_03892","SJAG_04349","SJAG_00188","SJAG_00054","SJAG_02651","SJAG_00738","SJAG_01586","SJAG_04540","SJAG_03860","SJAG_01886","SJAG_01540","SJAG_05340","SJAG_02900","SJAG_01431","SJAG_03219","SJAG_01203","SJAG_00712","SJAG_03151","SJAG_02162","SJAG_01572","SJAG_05012","SJAG_05236","SJAG_02341","SJAG_04912","SJAG_01068","SJAG_01507","SJAG_01074","SJAG_04655","SJAG_02253","SJAG_02383","SJAG_04151","SJAG_02685","SJAG_04572","SJAG_02117","SJAG_03809","SJAG_03968","SJAG_00855","SJAG_00293","SJAG_05303","SJAG_03575","SJAG_04853","SJAG_02244","SJAG_01678","SJAG_04969","SJAG_03651","SJAG_04573","SJAG_01900","SJAG_02371","SJAG_04520","SJAG_01637","SJAG_00071","SJAG_03699","SJAG_00128","SJAG_01593","SJAG_04144","SJAG_04612","SJAG_03763","SJAG_03408","SJAG_04088","SJAG_04539","SJAG_01226","SJAG_00052","SJAG_00435","SJAG_00552","SJAG_05022","SJAG_00173","SJAG_05316","SJAG_01131","SJAG_02041","SJAG_03321","SJAG_03351","SJAG_03048","SJAG_01210","SJAG_03615","SJAG_01014","SJAG_04489","SJAG_03756","SJAG_03858","SJAG_02370","SJAG_01585","SJAG_02584","SJAG_00821","SJAG_03250","SJAG_00192","SJAG_02021","SJAG_02591","SJAG_03037","SJAG_00762","SJAG_04024","SJAG_00490","SJAG_04505","SJAG_04600","SJAG_03175","SJAG_02562","SJAG_04309","SJAG_07000","SJAG_03417","SJAG_04948","SJAG_02668","SJAG_00900","SJAG_02705","SJAG_01022","SJAG_01535","SJAG_02419","SJAG_05274","SJAG_04211","SJAG_01365","SJAG_04936","SJAG_04429","SJAG_02116","SJAG_00853","SJAG_02044","SJAG_00941","SJAG_03385","SJAG_04477","SJAG_00341","SJAG_03211","SJAG_04118","SJAG_03680","SJAG_04306","SJAG_03971","SJAG_04915","SJAG_01737","SJAG_00984","SJAG_01556","SJAG_04484","SJAG_01760","SJAG_03638","SJAG_01489","SJAG_02891","SJAG_03657","SJAG_04229","SJAG_02485","SJAG_00666","SJAG_04633","SJAG_00642","SJAG_03454"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[69829,79934,112015,104661,70392,77527,78670,79743,107399,94925,114071,76268,57808,60586,73593,78831,72687],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031145"},{"annotations":[114211],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0140708"},{"annotations":[109544,110131,109440,113425,107803],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071629"},{"annotations":[103197,89007,112786,87540],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0180027"},{"annotations":[90790,79426,75417,90789,72454,80143],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019941"},{"annotations":[102149],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1905785"},{"annotations":[106749,76984],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0032435"},{"annotations":[76184,110651],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071630"},{"annotations":[66784],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070407"},{"annotations":[75963,99401,113072],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043634"},{"annotations":[100825],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043633"},{"annotations":[91427],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0036450"},{"annotations":[66180,90538,117039],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990074"},{"annotations":[88692],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1905786"},{"annotations":[102171,111511,116881,108696,106456],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0032436"},{"annotations":[72633,101441,88039,75096,98591,76832,93111,104147,94281,99421,79400,69694,78540,66582,73920,79208,77677,71612,71953,78463,71351,78921,93918,76065,97481,109110,114934,70591,69423,77769,77871,98182,74821,77037,117012,79598,65963,72787,73867,117825,77104,63250,78777,75322,71051,101893,110514,66000,94746,114056,77642,79103,95995,112929,106252,73357,116202,70784,80026,115073,78139,72191,79760,95572,88328,100975,112617,109041,110941,71799,78022,111498,110951,93755],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043161"},{"annotations":[106360,91396,97737,77402,109177,87872,77969,78185,71780,87703,70626,114515,73048,95726,71774,73022,100678,91261,70609],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0043328"},{"annotations":[114435],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0032434"},{"annotations":[103760,76292,96471,104612,89011,69410],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990116"},{"annotations":[104383,107027,104666,98242,79919,97548,74018,95301,94110,116658,101898,108886,71535],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031146"},{"annotations":[106591,87915,62684,78435,75086,99756,78851,109184,92645,96555,113200,76214,65143,109764,75869,110827,64402,75111,76204,75266,79639,77242,73587,106082,96457,88311,91295,71108,71520,98321],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006511"},{"annotations":[112619,96305,102936],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043162"},{"annotations":[73992,64107,96714],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071596"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of a macromolecule, initiated by covalent modification of the target molecule.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"macromolecule catabolic process","termid":"GO:0009057"}],"gene_count":197,"genes_by_uniquename":{"SJAG_00052":null,"SJAG_00054":null,"SJAG_00071":null,"SJAG_00128":null,"SJAG_00146":null,"SJAG_00173":null,"SJAG_00188":null,"SJAG_00192":null,"SJAG_00293":null,"SJAG_00300":null,"SJAG_00312":null,"SJAG_00341":null,"SJAG_00416":null,"SJAG_00435":null,"SJAG_00452":null,"SJAG_00475":null,"SJAG_00490":null,"SJAG_00552":null,"SJAG_00615":null,"SJAG_00642":null,"SJAG_00644":null,"SJAG_00651":null,"SJAG_00666":null,"SJAG_00712":null,"SJAG_00738":null,"SJAG_00762":null,"SJAG_00766":null,"SJAG_00778":null,"SJAG_00795":null,"SJAG_00808":null,"SJAG_00821":null,"SJAG_00853":null,"SJAG_00855":null,"SJAG_00900":null,"SJAG_00910":null,"SJAG_00941":null,"SJAG_00984":null,"SJAG_01014":null,"SJAG_01022":null,"SJAG_01068":null,"SJAG_01074":null,"SJAG_01131":null,"SJAG_01134":null,"SJAG_01176":null,"SJAG_01203":null,"SJAG_01210":null,"SJAG_01226":null,"SJAG_01242":null,"SJAG_01253":null,"SJAG_01281":null,"SJAG_01360":null,"SJAG_01365":null,"SJAG_01392":null,"SJAG_01431":null,"SJAG_01467":null,"SJAG_01472":null,"SJAG_01489":null,"SJAG_01497":null,"SJAG_01507":null,"SJAG_01527":null,"SJAG_01528":null,"SJAG_01533":null,"SJAG_01535":null,"SJAG_01540":null,"SJAG_01544":null,"SJAG_01556":null,"SJAG_01572":null,"SJAG_01585":null,"SJAG_01586":null,"SJAG_01593":null,"SJAG_01617":null,"SJAG_01637":null,"SJAG_01678":null,"SJAG_01679":null,"SJAG_01737":null,"SJAG_01760":null,"SJAG_01886":null,"SJAG_01900":null,"SJAG_01956":null,"SJAG_01981":null,"SJAG_02021":null,"SJAG_02041":null,"SJAG_02044":null,"SJAG_02116":null,"SJAG_02117":null,"SJAG_02162":null,"SJAG_02186":null,"SJAG_02197":null,"SJAG_02244":null,"SJAG_02253":null,"SJAG_02299":null,"SJAG_02341":null,"SJAG_02370":null,"SJAG_02371":null,"SJAG_02383":null,"SJAG_02419":null,"SJAG_02485":null,"SJAG_02502":null,"SJAG_02562":null,"SJAG_02584":null,"SJAG_02591":null,"SJAG_02651":null,"SJAG_02668":null,"SJAG_02685":null,"SJAG_02705":null,"SJAG_02723":null,"SJAG_02822":null,"SJAG_02891":null,"SJAG_02900":null,"SJAG_02912":null,"SJAG_02992":null,"SJAG_03037":null,"SJAG_03048":null,"SJAG_03151":null,"SJAG_03175":null,"SJAG_03211":null,"SJAG_03218":null,"SJAG_03219":null,"SJAG_03250":null,"SJAG_03321":null,"SJAG_03345":null,"SJAG_03350":null,"SJAG_03351":null,"SJAG_03385":null,"SJAG_03408":null,"SJAG_03417":null,"SJAG_03454":null,"SJAG_03523":null,"SJAG_03561":null,"SJAG_03575":null,"SJAG_03615":null,"SJAG_03638":null,"SJAG_03651":null,"SJAG_03657":null,"SJAG_03680":null,"SJAG_03699":null,"SJAG_03756":null,"SJAG_03763":null,"SJAG_03783":null,"SJAG_03809":null,"SJAG_03831":null,"SJAG_03858":null,"SJAG_03860":null,"SJAG_03876":null,"SJAG_03892":null,"SJAG_03968":null,"SJAG_03970":null,"SJAG_03971":null,"SJAG_03984":null,"SJAG_04024":null,"SJAG_04088":null,"SJAG_04118":null,"SJAG_04144":null,"SJAG_04151":null,"SJAG_04211":null,"SJAG_04229":null,"SJAG_04306":null,"SJAG_04309":null,"SJAG_04335":null,"SJAG_04349":null,"SJAG_04357":null,"SJAG_04384":null,"SJAG_04429":null,"SJAG_04477":null,"SJAG_04484":null,"SJAG_04489":null,"SJAG_04505":null,"SJAG_04520":null,"SJAG_04539":null,"SJAG_04540":null,"SJAG_04541":null,"SJAG_04572":null,"SJAG_04573":null,"SJAG_04600":null,"SJAG_04612":null,"SJAG_04619":null,"SJAG_04633":null,"SJAG_04655":null,"SJAG_04661":null,"SJAG_04853":null,"SJAG_04888":null,"SJAG_04912":null,"SJAG_04915":null,"SJAG_04936":null,"SJAG_04948":null,"SJAG_04969":null,"SJAG_05012":null,"SJAG_05022":null,"SJAG_05236":null,"SJAG_05264":null,"SJAG_05274":null,"SJAG_05303":null,"SJAG_05316":null,"SJAG_05329":null,"SJAG_05340":null,"SJAG_07000":null,"SJAG_16455":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"modification-dependent macromolecule catabolic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"termid":"GO:0043632","terms_by_termid":{"GO:0006511":null,"GO:0019941":null,"GO:0031145":null,"GO:0031146":null,"GO:0032434":null,"GO:0032435":null,"GO:0032436":null,"GO:0036450":null,"GO:0043161":null,"GO:0043162":null,"GO:0043328":null,"GO:0043633":null,"GO:0043634":null,"GO:0070407":null,"GO:0071596":null,"GO:0071629":null,"GO:0071630":null,"GO:0140708":null,"GO:0180027":null,"GO:1905785":null,"GO:1905786":null,"GO:1990074":null,"GO:1990116":null}}


id: PBO:0071260
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23 pseudogene 5","termid":"PBO:0071260"}


id: PBO:0026846
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_after_spore_germination,_multiple_cell_divisions,_binucleate_septated_cell","termid":"PBO:0026846"}


id: PBO:0049580
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H3.4 histone, cluster member","termid":"PBO:0049580"}


id: PBO:0116196
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"yippee-like protein, Moh1","termid":"PBO:0116196"}


id: PBO:0005374
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase subunit VIIa (predicted)","termid":"PBO:0005374"}


id: PBO:0078538
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripartite motif containing 31","termid":"PBO:0078538"}


id: MONDO:0030859
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"COACH syndrome","termid":"MONDO:0100349"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"COACH syndrome 2","secondary_identifiers":["GARD:16422","MEDGEN:1752166","UMLS:C5436837","OMIM:619111"],"synonyms":[{"name":"COACH2","type":"exact"}],"termid":"MONDO:0030859","xrefs":{"Monarch":{"xref_id":"0030859"}}}


id: GO:1902651
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of histone H2A-H2B dimer displacement.","definition_xrefs":["GOC:TermGenie","PMID:22199252","GOC:di","GO_REF:0000058"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of histone H2A-H2B dimer displacement (obsolete GO:1902651)","synonyms":[{"name":"activation of histone H2A-H2B dimer displacement","type":"narrow"},{"name":"up regulation of histone H2A-H2B dimer displacement","type":"exact"},{"name":"up-regulation of histone H2A-H2B dimer displacement","type":"exact"},{"name":"upregulation of histone H2A-H2B dimer displacement","type":"exact"}],"termid":"GO:1902651"}


id: GO:0097079
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: selenite(out) + H+(out) = selenite(in) + H+(in).","definition_xrefs":["GOC:mcc","PMID:20861301"],"direct_ancestors":[{"relation_name":"is_a","term_name":"solute:proton symporter activity","termid":"GO:0015295"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"selenite:proton symporter activity","synonyms":[{"name":"selenite:H+ symporter activity","type":"exact"},{"name":"selenite:hydrogen symporter activity","type":"exact"}],"termid":"GO:0097079"}


id: GO:0002394
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Tolerance induction taking place in the gut-associated lymphoid tissue (GALT).","definition_xrefs":["ISBN:0781735149","GOC:jal"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune response in gut-associated lymphoid tissue","termid":"GO:0002387"},{"relation_name":"is_a","term_name":"tolerance induction in mucosal-associated lymphoid tissue","termid":"GO:0002401"}],"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":"tolerance induction in gut-associated lymphoid tissue","synonyms":[{"name":"oral tolerance","type":"related"},{"name":"tolerance induction in GALT","type":"exact"}],"termid":"GO:0002394"}


id: GO:1903650
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of cytoplasmic transport.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:25049409"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of cytoplasmic transport (obsolete GO:1903650)","synonyms":[{"name":"down regulation of cytoplasmic streaming","type":"narrow"},{"name":"down regulation of cytoplasmic transport","type":"exact"},{"name":"down-regulation of cytoplasmic streaming","type":"narrow"},{"name":"down-regulation of cytoplasmic transport","type":"exact"},{"name":"downregulation of cytoplasmic streaming","type":"narrow"},{"name":"downregulation of cytoplasmic transport","type":"exact"},{"name":"inhibition of cytoplasmic streaming","type":"narrow"},{"name":"inhibition of cytoplasmic transport","type":"narrow"},{"name":"negative regulation of cytoplasmic streaming","type":"narrow"}],"termid":"GO:1903650"}


id: MONDO:0018399
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare disorder with female infertility due to a congenital hypogonadotropic hypogonadism (obsolete MONDO:0018399)","termid":"MONDO:0018399","xrefs":{"Monarch":{"xref_id":"0018399"}}}


id: PBO:0046920
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 32 member D, pseudogene","termid":"PBO:0046920"}


id: MONDO:1010693
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"AA amyloidosis that occurs in sheep.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"AA amyloidosis, non-human animal","termid":"MONDO:1010092"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AA amyloidosis, sheep","secondary_identifiers":["OMIA:000038-9940"],"termid":"MONDO:1010693","xrefs":{"Monarch":{"xref_id":"1010693"}}}


id: PBO:0067282
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 363, pseudogene","termid":"PBO:0067282"}


id: PBO:0091238
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane transporter Mfs2","termid":"PBO:0091238"}


id: MONDO:1012093
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"glomerulonephropathy, non-human animal","termid":"MONDO:1011905"},{"relation_name":"is_a","term_name":"renal disease, dog","termid":"MONDO:1012235"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glomerulonephropathy, dog","secondary_identifiers":["OMIA:000414-9615"],"termid":"MONDO:1012093","xrefs":{"Monarch":{"xref_id":"1012093"}}}


id: SO:1000081
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A mutation that alters the rate a which transcription of the sequence occurs.","definition_xrefs":["SO:ke"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:1000081 sequence_variant_affecting_rate_of_transcription (obsolete SO:1000081)","synonyms":[{"name":"mutation affecting rate of transcription","type":"related"},{"name":"sequence variant affecting rate of transcription","type":"exact"}],"termid":"SO:1000081"}


id: PBO:0050862
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inhibitor of DNA binding 1","termid":"PBO:0050862"}


id: MONDO:0008559
data:
  {"annotated_genes":["SJAG_01466","SJAG_03712"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87031,87032],"is_not":false,"summary":null,"term":"MONDO:0008559"}]},"cv_name":"mondo","definition":"The formation of a blood clot (thrombus) in the lumen of a vein.","definition_xrefs":["NCIT:C99107"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited thrombophilia","termid":"MONDO:0100240"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01466":null,"SJAG_03712":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"thrombophilia due to thrombin defect","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD9:453.9","UMLS:C3160733","MEDGEN:463623","DOID:0080701","GARD:10815","OMIM:188050","DOID:0111907","SCTID:111293003"],"synonyms":[{"name":"THPH1","type":"related"},{"name":"Venous thromboembolism","type":"broad"},{"name":"factor II-related thrombophilia","type":"related"},{"name":"hyperprothrombinemia","type":"related"},{"name":"prothrombin 20210G>A thrombophilia","type":"related"},{"name":"prothrombin G20210A thrombophilia","type":"related"},{"name":"prothrombin thrombophilia","type":"exact"},{"name":"prothrombin-related thrombophilia","type":"exact"},{"name":"thromboembolism, susceptibility to","type":"related"},{"name":"thrombophilia 1 due to thrombin defect","type":"exact"},{"name":"thrombophilia due to factor 2 defect","type":"related"},{"name":"thrombophilia due to thrombin defect","type":"exact"},{"name":"thrombosis, protection against","type":"related"},{"name":"venous thromboembolism, susceptibility to","type":"exact"},{"name":"venous thrombosis","type":"related"},{"name":"venous thrombosis, protection against","type":"exact"}],"termid":"MONDO:0008559","terms_by_termid":{"MONDO:0008559":null},"xrefs":{"Monarch":{"xref_id":"0008559"}}}


id: PR:Q9Y7X8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An actin-related protein 5 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03309","PRO:DNx","PANTHER:PTHR11937:SF16"],"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":"actin-like protein arp5 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC365.10","secondary_identifiers":["UniProtKB:Q9Y7X8"],"synonyms":[{"name":"Spom972h-ACTR5","type":"exact"}],"termid":"PR:Q9Y7X8"}


id: GO:0043387
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of a mycotoxin, any poisonous substance produced by a fungus.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"toxin catabolic process","termid":"GO:0009407"},{"relation_name":"is_a","term_name":"mycotoxin metabolic process","termid":"GO:0043385"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044248"},{"rel_name":"is_a","termid":"GO:0098754"}],"interesting_parent_ids":["GO:0044248","GO:0008150","GO:0019748","GO:0098754"],"is_obsolete":false,"name":"mycotoxin catabolic process","synonyms":[{"name":"mycotoxin breakdown","type":"exact"},{"name":"mycotoxin catabolism","type":"exact"},{"name":"mycotoxin degradation","type":"exact"}],"termid":"GO:0043387"}


id: PBO:0071371
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L29 pseudogene 30","termid":"PBO:0071371"}


id: GO:0006463
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a steroid hormone receptor complex, an intracellular receptor that binds steroid hormones. The complex is often a dimer, and forms after the steroid has bound the receptor.","definition_xrefs":["Wikipedia:Steroid_hormone_receptor","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex assembly","termid":"GO:0065003"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0065003","GO:0008150","GO:0044085"],"is_obsolete":false,"name":"steroid hormone receptor complex assembly","termid":"GO:0006463"}


id: GO:0010105
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops or prevents ethylene (ethene) signal transduction.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of ethylene-activated signaling pathway","termid":"GO:0010104"},{"relation_name":"is_a","term_name":"negative regulation of phosphorelay signal transduction system","termid":"GO:0070298"},{"relation_name":"negatively_regulates","term_name":"ethylene-activated signaling pathway","termid":"GO:0009873"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"negative regulation of ethylene-activated signaling pathway","synonyms":[{"name":"down regulation of ethylene mediated signaling pathway","type":"exact"},{"name":"down-regulation of ethylene mediated signaling pathway","type":"exact"},{"name":"downregulation of ethylene mediated signaling pathway","type":"exact"},{"name":"inhibition of ethylene mediated signaling pathway","type":"narrow"},{"name":"negative regulation of ethene mediated signaling pathway","type":"exact"},{"name":"negative regulation of ethene mediated signalling pathway","type":"exact"},{"name":"negative regulation of ethylene mediated signaling pathway","type":"related"},{"name":"negative regulation of ethylene mediated signalling pathway","type":"exact"}],"termid":"GO:0010105"}


id: PBO:0079806
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UDP glucuronosyltransferase family 2 member B27, pseudogene","termid":"PBO:0079806"}


id: PBO:0061502
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neurensin 1","termid":"PBO:0061502"}


id: GO:0047528
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2,3-dihydroxyindole + O2 = anthranilate + CO2 + H+.","definition_xrefs":["RHEA:19445","EC:1.13.11.23"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen","termid":"GO:0016702"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"2,3-dihydroxyindole 2,3-dioxygenase activity","secondary_identifiers":["KEGG_REACTION:R00983","MetaCyc:23-DIHYDROXYINDOLE-23-DIOXYGENASE-RXN"],"synonyms":[{"name":"2,3-dihydroxyindole:oxygen 2,3-oxidoreductase (decyclizing) activity","type":"related"}],"termid":"GO:0047528"}


id: PBO:0071211
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23a pseudogene 52","termid":"PBO:0071211"}


id: PBO:0034245
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-results_in_assembly_of","termid":"PBO:0034245"}


id: GO:0000097
data:
  {"annotated_genes":["SJAG_03614","SJAG_00395","SJAG_03881","SJAG_03712","SJAG_02689","SJAG_04459","SJAG_04425","SJAG_01466","SJAG_00832","SJAG_02293","SJAG_00881","SJAG_04953","SJAG_03856","SJAG_00365","SJAG_02972","SJAG_04305","SJAG_00582","SJAG_03671","SJAG_01404","SJAG_00309","SJAG_00234","SJAG_03152","SJAG_00419","SJAG_01880","SJAG_04042","SJAG_02290"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[105790,68123,65055,110885],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071266"},{"annotations":[75871,72383,77121],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006535"},{"annotations":[110303],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019343"},{"annotations":[111334,103412],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052699"},{"annotations":[100457],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019280"},{"annotations":[99790,106403,95324],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990355"},{"annotations":[78107,79014,80069,58503,76695,77564],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019509"},{"annotations":[70468,78812,115593,74240,76005,111767,71538],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009086"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of amino acids containing sulfur, comprising cysteine, methionine and selenocysteine.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfur amino acid metabolic process","termid":"GO:0000096"},{"relation_name":"is_a","term_name":"sulfur compound biosynthetic process","termid":"GO:0044272"},{"relation_name":"is_a","term_name":"carboxylic acid biosynthetic process","termid":"GO:0046394"}],"gene_count":26,"genes_by_uniquename":{"SJAG_00234":null,"SJAG_00309":null,"SJAG_00365":null,"SJAG_00395":null,"SJAG_00419":null,"SJAG_00582":null,"SJAG_00832":null,"SJAG_00881":null,"SJAG_01404":null,"SJAG_01466":null,"SJAG_01880":null,"SJAG_02290":null,"SJAG_02293":null,"SJAG_02689":null,"SJAG_02972":null,"SJAG_03152":null,"SJAG_03614":null,"SJAG_03671":null,"SJAG_03712":null,"SJAG_03856":null,"SJAG_03881":null,"SJAG_04042":null,"SJAG_04305":null,"SJAG_04425":null,"SJAG_04459":null,"SJAG_04953":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0006790","GO:0008150"],"is_obsolete":false,"name":"sulfur amino acid biosynthetic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000107":null,"GO_REF:0000108":null},"synonyms":[{"name":"sulfur amino acid anabolism","type":"exact"},{"name":"sulfur amino acid biosynthesis","type":"exact"},{"name":"sulfur amino acid formation","type":"exact"},{"name":"sulfur amino acid synthesis","type":"exact"},{"name":"sulphur amino acid biosynthesis","type":"exact"},{"name":"sulphur amino acid biosynthetic process","type":"exact"}],"termid":"GO:0000097","terms_by_termid":{"GO:0006535":null,"GO:0009086":null,"GO:0019280":null,"GO:0019343":null,"GO:0019509":null,"GO:0052699":null,"GO:0071266":null,"GO:1990355":null}}


id: PBO:0056854
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIA SH3 domain containing","termid":"PBO:0056854"}


id: GO:1905430
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a glycine stimulus.","definition_xrefs":["PMID:18984164","GOC:TermGenie","GO_REF:0000071"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to amino acid stimulus","termid":"GO:0071230"},{"relation_name":"is_a","term_name":"cellular response to nitrogen compound","termid":"GO:1901699"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"},{"relation_name":"is_a","term_name":"response to glycine","termid":"GO:1905429"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to glycine","synonyms":[{"name":"cellular response to Gly","type":"exact"},{"name":"cellular response to aminoacetic acid","type":"exact"},{"name":"cellular response to aminoethanoic acid","type":"exact"},{"name":"cellular response to glycin","type":"exact"}],"termid":"GO:1905430"}


id: PBO:0077191
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell leukemia homeobox 2","termid":"PBO:0077191"}


id: PBO:0076603
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TBC1 domain family member 22B","termid":"PBO:0076603"}


id: GO:2000040
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of planar cell polarity pathway involved in axis elongation.","definition_xrefs":["GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of planar cell polarity pathway involved in axis elongation (obsolete GO:2000040)","termid":"GO:2000040"}


id: GO:0031786
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a type 1B melatonin receptor.","definition_xrefs":["GOC:nln","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"melatonin receptor binding","termid":"GO:0031784"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"type 1B melatonin receptor binding","synonyms":[{"name":"type 1B melatonin receptor ligand","type":"narrow"}],"termid":"GO:0031786"}


id: MONDO:1012471
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"pentalogy of Fallot, non-human animal","termid":"MONDO:1011650"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pentalogy of Fallot, sheep","secondary_identifiers":["OMIA:001857-9940"],"termid":"MONDO:1012471","xrefs":{"Monarch":{"xref_id":"1012471"}}}


id: PBO:0074358
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"structural maintenance of chromosomes 4 pseudogene 1","termid":"PBO:0074358"}


id: PBO:0055340
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 2768","termid":"PBO:0055340"}


id: MONDO:0020202
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete conjunctival lymphangiectasia (obsolete MONDO:0020202)","secondary_identifiers":["SCTID:231871007","Orphanet:98614","ICD9:372.89"],"termid":"MONDO:0020202","xrefs":{"Monarch":{"xref_id":"0020202"}}}


id: FYPO:0007170
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype an ascus contains four nuclei, as in wild type.","definition_xrefs":["PomBase:mah","PMID:20826461"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal phenotype","termid":"FYPO:0000257"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000257"],"is_obsolete":false,"name":"normal number of nuclei in ascus","termid":"FYPO:0007170"}


id: PBO:0047453
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FCHO2 divergent transcript","termid":"PBO:0047453"}


id: PBO:0038473
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP binding cassette subfamily A member 11, pseudogene","termid":"PBO:0038473"}


id: MONDO:1011650
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cardiovascular disorder, non-human animal","termid":"MONDO:1011306"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pentalogy of Fallot, non-human animal","secondary_identifiers":["OMIA:001857"],"termid":"MONDO:1011650","xrefs":{"Monarch":{"xref_id":"1011650"}}}


id: PBO:0038844
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADAM metallopeptidase with thrombospondin type 1 motif 13","termid":"PBO:0038844"}


id: PBO:0069269
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 525, pseudogene","termid":"PBO:0069269"}


id: PBO:0036012
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_histone_H3_acetylation_at_centromere_outer_repeat_during_vegetative_growth","termid":"PBO:0036012"}


id: PBO:0086567
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; conserved among S. cerevisiae strains; YOR015W is not an essential gene","termid":"PBO:0086567"}


id: PBO:0060986
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NGRN pseudogene 2","termid":"PBO:0060986"}


id: PBO:0055391
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 2821","termid":"PBO:0055391"}


id: MONDO:0054833
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"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:0000426"},{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244","MONDO:0000426"],"is_obsolete":false,"name":"charcot-marie-tooth disease, axonal, type 2DD","secondary_identifiers":["GARD:17959","MEDGEN:1648475","OMIM:618036","UMLS:C4747974","Orphanet:521414","DOID:0111558"],"synonyms":[{"name":"CMT2DD","type":"related"},{"name":"Charcot-Marie-Tooth neuropathy, type 2Dd","type":"related"},{"name":"Charcot-Marie-tooth disease, axonal, type 2DD","type":"related"}],"termid":"MONDO:0054833","xrefs":{"Monarch":{"xref_id":"0054833"}}}


id: PBO:0046791
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EZR antisense RNA 1","termid":"PBO:0046791"}


id: GO:0099631
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The cytoplasmic component of the postsynaptic endocytic zone.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell cortex region","termid":"GO:0099738"},{"relation_name":"part_of","term_name":"postsynaptic endocytic zone","termid":"GO:0098843"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0005938"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0005938"],"is_obsolete":false,"name":"postsynaptic endocytic zone cytoplasmic component","termid":"GO:0099631"}


id: PBO:0075754
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sushi repeat containing protein X-linked","termid":"PBO:0075754"}


id: PR:000050481
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A G2-specific protein kinase fin1 (Schizosaccharomyces pombe) that has been phosphorylated at the positions equivalent to Ser-377, Ser-526, and Ser-698 of the amino acid sequence represented by UniProtKB:O13839. Example: UniProtKB:O13839, Ser-377/Ser-526/Ser-698, MOD:00046.","definition_xrefs":["PRO:DAN","PMID:22684255","PomBase:VW"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G2-specific protein kinase fin1 (Schizosaccharomyces pombe)","termid":"PR:000050480"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fin1/Phos(S377,S526,S698)","pombase_gene_id":"SPAC19E9.02","synonyms":[{"name":"PomBase_original_PRO_term_name: G2-specific protein kinase fin1 phosphorylated 1 (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-fin1/Phos:1","type":"exact"},{"name":"UniProtKB:O13839, Ser-377/Ser-526/Ser-698, MOD:00046","type":"narrow"},{"name":"fin1/Phos(S377,S526,S698)","type":"exact"}],"termid":"PR:000050481"}


id: GO:0044642
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A process that begins with venom being forced into an organism by the bite or sting of another organism, and ends with the resultant modulation of complement activation via the alternative pathway in the bitten/stung organism.","definition_xrefs":["PMID:20837040","GOC:fj","GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete envenomation resulting in modulation of complement activation, alternative pathway in another organism (obsolete GO:0044642)","synonyms":[{"name":"envenomation resulting in modulation of complement activation, alternative pathway in other organism","type":"exact"},{"name":"envenomation resulting in regulation of complement activation, alternative pathway in other organism","type":"exact"}],"termid":"GO:0044642"}


id: PBO:0078040
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor alpha joining 30","termid":"PBO:0078040"}


id: PBO:0052832
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin associated protein 1-1","termid":"PBO:0052832"}


id: PBO:0084484
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Meiosis specific DNA helicase; involved in the conversion of double-stranded breaks to later recombination intermediates and in crossover control; catalyzes the unwinding of Holliday junctions; has ssDNA and dsDNA stimulated ATPase activity","termid":"PBO:0084484"}


id: PBO:0085552
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein component of the synaptonemal complex axial elements; involved in chromosome segregation during the first meiotic division; critical for coupling checkpoint signaling to SC formation; promotes interhomolog recombination by phosphorylating Hop1p; also interacts with Mec3p and Ddc1p","termid":"PBO:0085552"}


id: GO:0010650
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the frequency, rate or extent of cell communication via electrical coupling. Cell communication via electrical coupling is the process that mediates signaling interactions between one cell and another cell by transfer of current between their adjacent cytoplasms via intercellular protein channels.","definition_xrefs":["GOC:kmv","GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell communication","termid":"GO:0010647"},{"relation_name":"is_a","term_name":"regulation of cell communication by electrical coupling","termid":"GO:0010649"},{"relation_name":"positively_regulates","term_name":"cell communication by electrical coupling","termid":"GO:0010644"}],"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 cell communication by electrical coupling","termid":"GO:0010650"}


id: GO:0022877
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the PEP-dependent, phosphoryl transfer-driven transport of substances across a membrane. The transport happens by catalysis of the reaction: protein N-phosphohistidine + fructose(out) = protein histidine + fructose phosphate(in). This differs from primary and secondary active transport in that the solute is modified during transport.","definition_xrefs":["ISBN:0815340729","GOC:mtg_transport"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fructose transmembrane transporter activity","termid":"GO:0005353"},{"relation_name":"is_a","term_name":"protein-N(PI)-phosphohistidine-sugar phosphotransferase activity","termid":"GO:0008982"}],"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:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0005215","GO:0016740","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"protein-N(PI)-phosphohistidine-fructose phosphotransferase system transporter activity","synonyms":[{"name":"fructose PTS transporter activity","type":"exact"}],"termid":"GO:0022877"}


id: MONDO:0008085
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete neuropathy, hereditary sensorimotor, with upper motor neuron, visual pathway and autonomic disturbance (obsolete MONDO:0008085)","secondary_identifiers":["MESH:C563517","OMIM:162380"],"synonyms":[{"name":"neuropathy, hereditary sensorimotor, with upper motor neuron, visual pathway and autonomic disturbance","type":"exact"}],"termid":"MONDO:0008085","xrefs":{"Monarch":{"xref_id":"0008085"}}}


id: PBO:0060510
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NSF attachment protein beta","termid":"PBO:0060510"}


id: PBO:0038825
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADAM metallopeptidase domain 32","termid":"PBO:0038825"}


id: PBO:0111765
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HEAT repeat","termid":"PBO:0111765"}


id: PBO:0084322
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Karyopherin beta; mediates nuclear import of ribosomal proteins prior to assembly into ribosomes and import of histones H3 and H4; localizes to the nuclear pore, nucleus, and cytoplasm; exhibits genetic interactions with RAI1","termid":"PBO:0084322"}


id: PBO:0056880
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MICOS10-NBL1 readthrough","termid":"PBO:0056880"}


id: PBO:0039963
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADP ribosylation factor like GTPase 2 binding protein pseudogene 6","termid":"PBO:0039963"}


id: GO:0140793
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: histone H2AX tyrosine phosphate (position 142) + H2O = histone H2AX tyrosine (position 142) + phosphate.","definition_xrefs":["PMID:19351884","PMID:19234442"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone phosphatase activity","termid":"GO:0140789"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0004721"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016788","GO:0016787","GO:0140096","GO:0004721","GO:0003824"],"is_obsolete":false,"name":"histone H2AXY142 phosphatase activity","synonyms":[{"name":"histone H2-Y142 phosphatase activity","type":"exact"},{"name":"histone H2Y142 phosphatase activity","type":"related"},{"name":"histone tyrosine phosphatase activity (H2-Y142 specific)","type":"exact"}],"termid":"GO:0140793"}


id: GO:0120078
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The attachment of a cell, either to another cell or to an underlying substrate such as the extracellular matrix, via cell adhesion molecules that contributes to the formation of a blood vessel network.","definition_xrefs":["GOC:cvs","PMID:28264837"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell adhesion","termid":"GO:0007155"},{"relation_name":"part_of","term_name":"angiogenic sprout fusion","termid":"GO:0120077"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"cell adhesion involved in sprouting angiogenesis","synonyms":[{"name":"cell adhesion involved in blood vessel anastomosis","type":"exact"},{"name":"cell adhesion involved in vascular anastomosis","type":"related"}],"termid":"GO:0120078"}


id: PBO:0029687
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_level_of_iron_ion_starvation-repressed_proteins","termid":"PBO:0029687"}


id: PBO:0013230
data:
  {"annotation_feature_type":"gene","cv_name":"feature_cvtermprop_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"curator_name","termid":"PBO:0013230"}


id: PBO:0090494
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rix1 complex WD repeat subunit Crb3","termid":"PBO:0090494"}


id: PBO:0064181
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phospholipase A2 group XH, pseudogene","termid":"PBO:0064181"}


id: RO:0002430
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","direct_ancestors":[{"relation_name":"is_a","term_name":"involved_in_regulation_of","termid":"RO:0002428"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"involved_in_negative_regulation_of","termid":"RO:0002430"}


id: GO:0061544
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The controlled release of a peptide from a cell in which the peptide acts as a neurotransmitter.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptide secretion","termid":"GO:0002790"},{"relation_name":"is_a","term_name":"neurotransmitter secretion","termid":"GO:0007269"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0023052","GO:0008150"],"is_obsolete":false,"name":"peptide secretion, neurotransmission","termid":"GO:0061544"}


id: GO:0035501
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a MH1 (MAD homology 1) protein domain. The MH1 domain is found at the amino terminus of MAD related proteins such as Smads and can mediate DNA binding in some proteins. Smads also use the MH1 domain to interact with some transcription factors.","definition_xrefs":["Pfam:PF03165"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein domain specific binding","termid":"GO:0019904"}],"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:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"MH1 domain binding","synonyms":[{"name":"MAD homology 1 domain binding","type":"exact"}],"termid":"GO:0035501"}


id: FYPO:0002176
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype observed in the vegetative growth phase of the life cycle in which a cell has normal volume and dimensions and is viable.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"normal vegetative cell size","termid":"FYPO:0001124"},{"relation_name":"is_a","term_name":"viable cell","termid":"FYPO:0000124"},{"relation_name":"is_a","term_name":"normal vegetative cell size","termid":"FYPO:0001124"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"has_part","termid":"FYPO:0000257"},{"rel_name":"has_part","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0000257","FYPO:0000004","FYPO:0001312"],"is_obsolete":false,"name":"viable vegetative cell with normal cell size","synonyms":[{"name":"viable cell with normal cell size during vegetative growth","type":"exact"},{"name":"viable vegetative cell with normal cell length","type":"narrow"},{"name":"viable vegetative cell with normal cell size during mitotic cell cycle","type":"related"}],"termid":"FYPO:0002176"}


id: PBO:0058293
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4667","termid":"PBO:0058293"}


id: MONDO:0009140
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Dyssegmental dysplasia, Silverman-Handmaker type is a rare, genetic, primary bone dysplasia, and lethal form of neonatal short-limbed dwarfism, characterized by anisospondyly, severe short stature and limb shortening, metaphyseal flaring and distinct dysmorphic features (i.e. flat facial appearance, abnormal ears, short neck, narrow thorax). Additional features may include other skeletal findings (e.g. joint contractures, bowed limbs, talipes equinovarus) and urogenital and cardiovascular abnormalities.","definition_xrefs":["Orphanet:1865"],"direct_ancestors":[{"relation_name":"is_a","term_name":"qualitative or quantitative defects of perlecan","termid":"MONDO:0016151"},{"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":"Silverman-Handmaker type dyssegmental dysplasia","secondary_identifiers":["SCTID:93132001","MESH:C537998","DOID:0090032","OMIM:224410","MEDGEN:347372","UMLS:C1857100","ICD9:759.89","GARD:2026"],"synonyms":[{"name":"Anisospondylic Camptomicromelic dwarfism, Silverman-Handmaker type","type":"related"},{"name":"Anisospondylic camptomicromelic dwarfism Silverman-Handmaker type","type":"related"},{"name":"DDSH","type":"related"},{"name":"dyssegmental dwarfism Silverman-Handmaker type","type":"related"},{"name":"dyssegmental dwarfism, Silverman-Handmaker type","type":"related"},{"name":"dyssegmental dysplasia Silverman-Handmaker type","type":"related"},{"name":"dyssegmental dysplasia, Silverman-Handmaker type","type":"related"}],"termid":"MONDO:0009140","xrefs":{"Monarch":{"xref_id":"0009140"}}}


id: MONDO:0016623
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Any of the forms of deficiency anemia that have a rare incidence.","definition_xrefs":["MONDO:patterns/rare"],"gene_count":0,"genotype_count":0,"name":"obsolete rare deficiency anemia (obsolete MONDO:0016623)","secondary_identifiers":["Orphanet:248293"],"synonyms":[{"name":"rare deficiency anemia","type":"exact"}],"termid":"MONDO:0016623","xrefs":{"Monarch":{"xref_id":"0016623"}}}


id: PBO:0079116
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA splicing endonuclease subunit 34","termid":"PBO:0079116"}


id: GO:0061501
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + GTP = 2 diphosphate + cyclic G-P(2'-5')A-P(3'-5') (cyclic 2',3' GAMP).","definition_xrefs":["GOC:dph","PMID:23258413","RHEA:42064"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cyclic GMP-AMP synthase activity","termid":"GO:0140699"}],"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:0016740"},{"rel_name":"is_a","termid":"GO:0016779"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016740","GO:0016779"],"is_obsolete":false,"name":"2',3'-cyclic GMP-AMP synthase activity","secondary_identifiers":["EC:2.7.7.86","Reactome:R-HSA-3244614"],"synonyms":[{"name":"2',3' cyclic GMP-AMP synthase activity","type":"exact"},{"name":"2',3' cyclic-GMP-AMP synthase activity","type":"exact"},{"name":"cyclic 2',3' GAMP synthase activity","type":"exact"},{"name":"cyclic-GMP-AMP synthase activity","type":"broad"}],"termid":"GO:0061501"}


id: GO:0042064
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete cell adhesion receptor regulator activity (obsolete GO:0042064)","synonyms":[{"name":"cell adhesion receptor regulator activity","type":"exact"}],"termid":"GO:0042064"}


id: PBO:0028809
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_autophosphorylation_during_cellular_response_to_DNA_damage","termid":"PBO:0028809"}


id: PBO:0059495
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myostatin","termid":"PBO:0059495"}


id: PBO:0040489
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ataxin 7 like 3B","termid":"PBO:0040489"}


id: PBO:0116704
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 2 subfamily T member 7 (gene/pseudogene)","termid":"PBO:0116704"}


id: PBO:0116790
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cholesin","termid":"PBO:0116790"}


id: PBO:0047266
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 246 member A","termid":"PBO:0047266"}


id: MONDO:0015208
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A esophageal malformation that is part of a larger syndrome.","definition_xrefs":["MONDO:patterns/syndromic"],"gene_count":0,"genotype_count":0,"name":"obsolete syndromic esophageal malformation (obsolete MONDO:0015208)","secondary_identifiers":["Orphanet:108961"],"synonyms":[{"name":"syndrome associated with esophageal malformation","type":"exact"},{"name":"syndromic esophageal malformation","type":"exact"}],"termid":"MONDO:0015208","xrefs":{"Monarch":{"xref_id":"0015208"}}}


id: MONDO:0958181
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial trifunctional protein deficiency","termid":"MONDO:0012172"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0002525","MONDO:0005066","MONDO:0004069"],"is_obsolete":false,"name":"mitochondrial trifunctional protein deficiency 1","secondary_identifiers":["OMIM:609015"],"termid":"MONDO:0958181","xrefs":{"Monarch":{"xref_id":"0958181"}}}


id: PBO:0057293
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 511","termid":"PBO:0057293"}


id: GO:0098002
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The processes by which a bacteriophage initially commits to infection by binding the host receptor irreversibly. Disruption of the phage:cell complex at this step results in the loss of infective phage virions since the process is characterized by conformational changes of bacteriophage head and tail proteins and injection of bacteriophage proteins into the infected cell.","definition_xrefs":["GOC:bm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"entry receptor-mediated virion attachment to host cell","termid":"GO:0098670"}],"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":"receptor-mediated bacteriophage irreversible attachment to host cell","synonyms":[{"name":"irreversible bacteriophage attachment, binding of host cell surface receptor","type":"exact"},{"name":"phage irreversible adsorption","type":"related"}],"termid":"GO:0098002"}


id: PBO:0048879
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"golgin A6 family member E, pseudogene","termid":"PBO:0048879"}


