# terms

id: GO:0004023
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: an alcohol + NAD+ = an aldehyde or ketone + NADH + H+; can proceed in the absence of a metal ion.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete alcohol dehydrogenase (NAD+) activity, metal ion-independent (obsolete GO:0004023)","synonyms":[{"name":"alcohol dehydrogenase activity, metal ion-independent","type":"broad"}],"termid":"GO:0004023"}


id: PBO:0090492
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane anchored protein, claudin family, predicted membrane sensor Mac1","termid":"PBO:0090492"}


id: PBO:0028063
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_transposon_gene_mRNA_level","termid":"PBO:0028063"}


id: MOD:00614
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a hydrogen atom of an amino acid residue or of a modifying group with a fucose (6-deoxy-D-galactose) group through a glycosidic bond.","definition_xrefs":["PubMed:11344537","PubMed:15189151","Unimod:295"],"direct_ancestors":[{"relation_name":"is_a","term_name":"deoxyhexosylated","termid":"MOD:00736"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00764"}],"interesting_parent_ids":["MOD:00764"],"is_obsolete":false,"name":"fucosylated","synonyms":[{"name":"Fuc","type":"exact"},{"name":"Fucose","type":"related"},{"name":"dHex","type":"related"}],"termid":"MOD:00614"}


id: GO:0032601
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The appearance of connective tissue growth factor due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine production","termid":"GO:0001816"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"connective tissue growth factor production","synonyms":[{"name":"CCN2 production","type":"exact"},{"name":"CTGF production","type":"exact"},{"name":"Fisp12 production","type":"exact"},{"name":"Hcs24 production","type":"exact"},{"name":"IGFBP8 production","type":"exact"},{"name":"hypertrophic chondrocyte-specific gene product 24 production","type":"exact"}],"termid":"GO:0032601"}


id: PBO:0047636
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FKBP prolyl isomerase 1A","termid":"PBO:0047636"}


id: PBO:0081644
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 570","termid":"PBO:0081644"}


id: GO:0036509
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The removal of an alpha-1,2-linked mannose from the B-chain of a glycoprotein oligosaccharide in the endoplasmic reticulum.","definition_xrefs":["PMID:22160784","GOC:PARL","GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete trimming of terminal mannose on B branch (obsolete GO:0036509)","synonyms":[{"name":"conversion of (Man)9(GlcNAc)2 to (Man)8B(GlcNAc)2","type":"related"},{"name":"conversion of M9 to M8B","type":"related"},{"name":"glycoprotein mannose trimming on B branch","type":"exact"}],"termid":"GO:0036509"}


id: GO:0015072
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: ATP + 1-phosphatidyl-1D-myo-inositol = ADP + 1-phosphatidyl-1D-myo-inositol 3-phosphate.","definition_xrefs":["EC:2.7.1.137"],"gene_count":0,"genotype_count":0,"name":"obsolete phosphatidylinositol 3-kinase, class I, catalyst activity (obsolete GO:0015072)","synonyms":[{"name":"phosphatidylinositol 3-kinase, class I, catalyst activity","type":"exact"}],"termid":"GO:0015072"}


id: PBO:0067607
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 775, pseudogene","termid":"PBO:0067607"}


id: GO:0044753
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Intermediate organelles formed during macroautophagy through the fusion between autophagosomes and endosomes.","definition_xrefs":["GOC:sart","PMID:19008921","GOC:autophagy","PMID:9705327"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autophagosome","termid":"GO:0005776"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005773"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005773","GO:0005737","GO:0005575"],"is_obsolete":false,"name":"amphisome","termid":"GO:0044753"}


id: GO:0090336
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency, or extent of brown fat cell differentiation. Brown fat cell differentiation is the process in which a relatively unspecialized cell acquires specialized features of a brown adipocyte, an animal connective tissue cell involved in adaptive thermogenesis. Brown adipocytes contain multiple small droplets of triglycerides and a high number of mitochondria.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of fat cell differentiation","termid":"GO:0045600"},{"relation_name":"is_a","term_name":"regulation of brown fat cell differentiation","termid":"GO:0090335"},{"relation_name":"positively_regulates","term_name":"brown fat cell differentiation","termid":"GO:0050873"}],"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 brown fat cell differentiation","termid":"GO:0090336"}


id: GO:0018131
data:
  {"annotated_genes":["SJAG_00827"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[75420],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052837"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of oxazole or thiazole, five-membered heterocyclic ring structures containing an oxygen and a sulfur, respectively, in the 1-position and a nitrogen in the 3-position.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxazole or thiazole metabolic process","termid":"GO:0046484"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00827":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"oxazole or thiazole biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"oxazole or thiazole anabolism","type":"exact"},{"name":"oxazole or thiazole biosynthesis","type":"exact"},{"name":"oxazole or thiazole formation","type":"exact"},{"name":"oxazole or thiazole synthesis","type":"exact"}],"termid":"GO:0018131","terms_by_termid":{"GO:0052837":null}}


id: PBO:0084455
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mannosyltransferase; involved in adding the 4th and 5th mannose residues of O-linked glycans","termid":"PBO:0084455"}


id: MOD:01335
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Chemical derivative -","definition_xrefs":["Unimod:464#K","PubMed:11467524","PubMed:16526082"],"direct_ancestors":[{"relation_name":"is_a","term_name":"6x(13)C labeled 4-sulfophenyl isothiocyanate derivatized residue","termid":"MOD:00880"},{"relation_name":"is_a","term_name":"modified L-lysine residue","termid":"MOD:00912"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"6x(13)C labeled 4-sulfophenyl isothiocyanate derivatized lysine","synonyms":[{"name":"4-sulfophenyl isothiocyanate (Heavy C13)","type":"related"},{"name":"SPITC:13C(6)","type":"related"}],"termid":"MOD:01335"}


id: SO:0001892
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A feature amplification of a region containing a transcription factor binding site.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulatory_region_amplification","termid":"SO:0001891"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TFBS_amplification","secondary_identifiers":["http:www.ensembl.org/info/genome/variation/predicted_data.html#consequences"],"synonyms":[{"name":"TFBS amplification ","type":"exact"},{"name":"VEP:TFBS_amplification","type":"exact"},{"name":"transcription factor binding site amplification","type":"exact"}],"termid":"SO:0001892"}


id: MONDO:0011139
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"diabetic embryopathy","termid":"MONDO:0016018"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"preaxial hallucal polydactyly","secondary_identifiers":["MEDGEN:356507","MESH:C566632","OMIM:601759","UMLS:C1866339"],"synonyms":[{"name":"preaxial hallucal polydactyly","type":"exact"}],"termid":"MONDO:0011139","xrefs":{"Monarch":{"xref_id":"0011139"}}}


id: MONDO:0015184
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare disease involving intestinal motility (obsolete MONDO:0015184)","secondary_identifiers":["Orphanet:104009"],"synonyms":[{"name":"rare genetic intestinal motility disease","type":"exact"}],"termid":"MONDO:0015184","xrefs":{"Monarch":{"xref_id":"0015184"}}}


id: PBO:0014262
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"not functionally complemented by S. cerevisiae RAD17","termid":"PBO:0014262"}


id: GO:0052761
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: [beta-(1->4)-D-glucosamine]n-[N-acetyl-D-glucosamine]m = D-glucosamine + [beta-(1->4)-D-glucosamine](n-1)-[N-acetyl-D-glucosamine]m. This reaction is the hydrolysis of chitosan or chitosan oligosaccharides to remove a D-glucosamine residue from the non-reducing termini; chitosan is a linear polysaccharide composed of randomly distributed beta-(1->4)-linked D-glucosamine and N-acetyl-D-glucosamine units.","definition_xrefs":["GOC:mengo_curators","EC:3.2.1.165","MetaCyc:3.2.1.165-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, hydrolyzing O-glycosyl compounds","termid":"GO:0004553"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016798","GO:0016787"],"is_obsolete":false,"name":"exo-1,4-beta-D-glucosaminidase activity","secondary_identifiers":["KEGG_REACTION:R08715"],"synonyms":[{"name":"chitosan exo-1,4-beta-D-glucosaminidase activity","type":"exact"},{"name":"chitosan glucosaminohydrolase activity","type":"exact"},{"name":"exo-beta-D-glucosaminidase activity","type":"related"},{"name":"exochitosanase activity","type":"related"}],"termid":"GO:0052761"}


id: PBO:0031393
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-growth_auxotrophic_for_asparagine","termid":"PBO:0031393"}


id: PBO:0110428
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"USP10 pseudogene 3","termid":"PBO:0110428"}


id: GO:0052714
data:
  {"annotated_genes":["SJAG_01219"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[110666],"is_not":false,"summary":null,"term":"GO:0052714"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: mannosyl-inositol phosphorylceramide + H2O = C26-phytoceramide + mannosylphosphorylinositol.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inositol phosphorylceramide phospholipase activity","termid":"GO:0052713"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01219":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016788","GO:0016787","GO:0003674"],"is_obsolete":false,"name":"mannosyl-inositol phosphorylceramide phospholipase activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0052714","terms_by_termid":{"GO:0052714":null}}


id: PBO:0065138
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRKX pseudogene 1","termid":"PBO:0065138"}


id: GO:0031142
data:
  {"annotated_genes":["SJAG_00781"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[117450],"is_not":false,"summary":null,"term":"GO:0031142"}]},"cv_name":"biological_process","definition":"The process in which a cell initiates conjugation with cellular fusion upon nitrogen starvation.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to nitrogen starvation","termid":"GO:0006995"},{"relation_name":"is_a","term_name":"induction of conjugation upon nutrient starvation","termid":"GO:0031140"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00781":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0000747"},{"rel_name":"regulates","termid":"GO:0000747"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0000747","GO:0008150"],"is_obsolete":false,"name":"induction of conjugation upon nitrogen starvation","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0031142","terms_by_termid":{"GO:0031142":null}}


id: GO:0035675
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a neuromast hair cell over time, from its formation to the mature structure. A neuromast hair cell is a hair cell that acts as a sensory receptor of the neuromast; it is morphologically polarized as a result of the relative position of the single kinocilium and the clusters of stereocilia on its apical surface. Cell development does not include the steps involved in committing a cell to a specific fate.","definition_xrefs":["CL:0000856"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuron development","termid":"GO:0048666"},{"relation_name":"part_of","term_name":"neuromast hair cell differentiation","termid":"GO:0048886"}],"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":"neuromast hair cell development","termid":"GO:0035675"}


id: PBO:0073315
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"secretion regulating guanine nucleotide exchange factor","termid":"PBO:0073315"}


id: GO:0110054
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of actin filament annealing, i.e. the end-to-end joining of existing actin filaments.","definition_xrefs":["PMID:10585915","PMID:15743909","PMID:19244341","PMID:11575927","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of actin filament organization","termid":"GO:0110053"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007010"},{"rel_name":"regulates","termid":"GO:0030036"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007010","GO:0030036","GO:0008150"],"is_obsolete":false,"name":"regulation of actin filament annealing","termid":"GO:0110054"}


id: PBO:0048679
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gliomedin","termid":"PBO:0048679"}


id: PBO:0042383
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CD274 molecule","termid":"PBO:0042383"}


id: PATO:0000452
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000452 relative pilosity value (obsolete PATO:0000452)","termid":"PATO:0000452"}


id: MONDO:0004007
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A group of non-invasive epithelial proliferations that occur in the ductal system of the breast. The vast majority of cases arise in the terminal ductal lobular units. This category includes atypical ductal hyperplasia, usual ductal hyperplasia, flat epithelial atypia, and ductal carcinoma in situ. There is an increased risk for subsequent development of invasive breast carcinoma.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intraductal breast neoplasm","termid":"MONDO:0002488"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"breast intraductal proliferative lesion","secondary_identifiers":["NCIT:C27942","UMLS:C1334631","MEDGEN:277343","DOID:6839"],"synonyms":[{"name":"DIN","type":"exact"},{"name":"ductal intraepithelial neoplasia","type":"exact"},{"name":"intraductal proliferative lesion","type":"exact"},{"name":"intraductal proliferative lesion of the breast","type":"exact"},{"name":"mammary intraepithelial neoplasia, ductal type","type":"exact"}],"termid":"MONDO:0004007","xrefs":{"Monarch":{"xref_id":"0004007"}}}


id: MONDO:1012712
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ichthyosis that occurs in dogs due to a mutation in the PNPLA1 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"ichthyosis, dog","termid":"MONDO:1012978"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ichthyosis, PNPLA1-related, dog","secondary_identifiers":["OMIA:001588-9615"],"termid":"MONDO:1012712","xrefs":{"Monarch":{"xref_id":"1012712"}}}


id: PBO:0044241
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cutA divalent cation tolerance homolog","termid":"PBO:0044241"}


id: GO:1901154
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of paromomycin.","definition_xrefs":["UniPathway:UPA00970","GOC:TermGenie","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aminoglycoside antibiotic catabolic process","termid":"GO:0030649"},{"relation_name":"is_a","term_name":"polyol catabolic process","termid":"GO:0046174"},{"relation_name":"is_a","term_name":"paromomycin metabolic process","termid":"GO:1901153"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"paromomycin catabolic process","synonyms":[{"name":"paromomycin breakdown","type":"exact"},{"name":"paromomycin catabolism","type":"exact"},{"name":"paromomycin degradation","type":"exact"}],"termid":"GO:1901154"}


id: MONDO:0014670
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any lethal congenital contracture syndrome in which the cause of the disease is a mutation in the ADGRG6 gene.","definition_xrefs":["MONDO:design_pattern"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lethal congenital contracture syndrome","termid":"MONDO:0017436"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lethal congenital contracture syndrome 9","secondary_identifiers":["MEDGEN:903881","OMIM:616503","UMLS:C4225303"],"synonyms":[{"name":"ADGRG6 lethal congenital contracture syndrome","type":"exact"},{"name":"LCCS9","type":"related"},{"name":"lethal congenital contracture syndrome 9","type":"exact"},{"name":"lethal congenital contracture syndrome caused by mutation in ADGRG6","type":"exact"},{"name":"lethal congenital contracture syndrome type 9","type":"exact"}],"termid":"MONDO:0014670","xrefs":{"Monarch":{"xref_id":"0014670"}}}


id: GO:0005958
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A large protein complex which is involved in the repair of DNA double-strand breaks and, in mammals, V(D)J recombination events. It consists of the DNA-dependent protein kinase catalytic subunit (DNA-PKcs), the DNA end-binding heterodimer Ku, the nuclear phosphoprotein XRCC4 or a homolog thereof, and DNA ligase IV.","definition_xrefs":["PMID:10854421","PMID:12235392","GOC:mah","PMID:17072889","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nonhomologous end joining complex","termid":"GO:0070419"},{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005634","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"DNA-dependent protein kinase-DNA ligase 4 complex","secondary_identifiers":["GO:0005959"],"termid":"GO:0005958"}


id: PATO:0001537
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A solubility quality inhering in a substance by virtue of the bearer's disposition to dissolve in a liquid.","definition_xrefs":["edp:edp"],"direct_ancestors":[{"relation_name":"is_a","term_name":"solubility","termid":"PATO:0001536"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"soluble in","synonyms":[{"name":"soluble","type":"exact"}],"termid":"PATO:0001537"}


id: PBO:0053779
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 1029","termid":"PBO:0053779"}


id: PBO:0059045
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MMS22 like, DNA repair protein","termid":"PBO:0059045"}


id: PBO:0049694
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"huntingtin associated protein 1","termid":"PBO:0049694"}


id: GO:2000063
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of ureter smooth muscle cell differentiation.","definition_xrefs":["GOC:obol","GOC:yaf","GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of smooth muscle cell differentiation","termid":"GO:0051152"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"is_a","term_name":"regulation of ureter smooth muscle cell differentiation","termid":"GO:2000061"},{"relation_name":"positively_regulates","term_name":"ureter smooth muscle cell differentiation","termid":"GO:0072193"}],"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 ureter smooth muscle cell differentiation","termid":"GO:2000063"}


id: FYPO:0007080
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the initial release of duplicated spindle pole bodies that begins with the nucleation of microtubules from each SPB within the nucleus, and occurs as part of the first meiotic nuclear division, is abnormal.","definition_xrefs":["PomBase:mah","PMID:31532702"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal spindle pole body organization","termid":"FYPO:0003560"},{"relation_name":"is_a","term_name":"abnormal meiosis I","termid":"FYPO:0003603"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000054","FYPO:0005447","FYPO:0000631","FYPO:0000002"],"is_obsolete":false,"name":"abnormal initial meiotic spindle pole body separation in meiosis I","synonyms":[{"name":"abnormal initial meiotic spindle pole body separation in first meiotic nuclear division","type":"exact"},{"name":"abnormal initial mitotic SPB separation in meiosis I","type":"exact"}],"termid":"FYPO:0007080"}


id: PBO:0040978
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BCL2 interacting protein like","termid":"PBO:0040978"}


id: PBO:0113095
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Diacylglycerol kinase; localized to the endoplasmic reticulum (ER); overproduction induces enlargement of ER-like membrane structures, stimulates the mevalonate/ergosterol pathway and suppresses a temperature-sensitive sly1 mutation; contains a CTP transferase domain","termid":"PBO:0113095"}


id: PBO:0110475
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ETFRF1 pseudogene 1","termid":"PBO:0110475"}


id: PBO:0076355
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"synaptotagmin like 2","termid":"PBO:0076355"}


id: GO:0160205
data:
  {"annotated_genes":["SJAG_00827"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[62215],"is_not":false,"summary":null,"term":"GO:0160205"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: [ADP-thiazole synthase]-L-cysteine + glycine + NAD(+) = [ADP-thiazole synthase]-dehydroalanine + ADP-5-ethyl-4-methylthiazole-2-carboxylate + 2 H(+) + 3 H2O + nicotinamide.","definition_xrefs":["RHEA:55708"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pentosyltransferase activity","termid":"GO:0016763"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00827":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016757"}],"interesting_parent_ids":["GO:0016740","GO:0003824","GO:0016757","GO:0003674"],"is_obsolete":false,"name":"cysteine-dependent adenosine diphosphate thiazole synthase activity","references_by_uniquename":{"GO_REF:0000003":null},"secondary_identifiers":["EC:2.4.2.60"],"synonyms":[{"name":"ADP-thiazole synthase activity","type":"related"},{"name":"suicide thiamine thiazole synthase activity","type":"exact"}],"termid":"GO:0160205","terms_by_termid":{"GO:0160205":null}}


id: FYPO:0006237
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 cells contain a normal (i.e. indistinguishable from wild type) number of half-mer polysomes in the cytosol. A half-mer polysome is a complex consisting of an mRNA bound to a single small ribosomal subunit, followed by one or more complete bound ribosomes.","definition_xrefs":["PMID:18065650","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal level of macromolecular complex","termid":"FYPO:0006235"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal cytosolic half-mer polysome level","synonyms":[{"name":"cytosolic half-mer polysomes present at normal level","type":"exact"},{"name":"normal cytosolic half-mer polysome level during mitotic cell cycle","type":"related"},{"name":"normal cytosolic half-mer polysome level during vegetative growth","type":"exact"},{"name":"normal cytosolic halfmer polysome level","type":"exact"},{"name":"normal level of cytosolic half-mer polysomes","type":"related"}],"termid":"FYPO:0006237"}


id: MONDO:0000048
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete immunoglobulin A deficiency (obsolete MONDO:0000048)","termid":"MONDO:0000048","xrefs":{"Monarch":{"xref_id":"0000048"}}}


id: GO:0009715
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of chalcone, phenyl steryl ketone or its hydroxylated derivatives.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenylpropanoid biosynthetic process","termid":"GO:0009699"},{"relation_name":"is_a","term_name":"chalcone metabolic process","termid":"GO:0009714"},{"relation_name":"is_a","term_name":"ketone biosynthetic process","termid":"GO:0042181"},{"relation_name":"is_a","term_name":"olefinic compound biosynthetic process","termid":"GO:0120255"}],"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:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0019748","GO:0044281"],"is_obsolete":false,"name":"chalcone biosynthetic process","synonyms":[{"name":"chalcone anabolism","type":"exact"},{"name":"chalcone biosynthesis","type":"exact"},{"name":"chalcone formation","type":"exact"},{"name":"chalcone synthesis","type":"exact"}],"termid":"GO:0009715"}


id: PBO:0004001
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin-like protein modifier Ned8","termid":"PBO:0004001"}


id: PBO:0090604
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"wybutosine biosynthesis protein Tyw1","termid":"PBO:0090604"}


id: MONDO:0006282
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm arising from the endothelial cells of the lymphatic vessels.","definition_xrefs":["NCIT:C3205"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sarcoma","termid":"MONDO:0005089"}],"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":"lymphangiosarcoma","secondary_identifiers":["ICDO:9170/3","MEDGEN:6154","EFO:1000339","SCTID:403986008","ICD9:171.9","MESH:D008204","UMLS:C0024224","DOID:2689"],"synonyms":[{"name":"Stewart-Treves syndrome","type":"exact"},{"name":"lymphangioendothelial sarcoma","type":"exact"},{"name":"lymphangiosarcoma","type":"exact"},{"name":"lymphangiosarcoma of Stewart and Treves","type":"related"},{"name":"lymphangiosarcoma, malignant","type":"exact"},{"name":"malignant lymphangioendothelioma","type":"exact"}],"termid":"MONDO:0006282","xrefs":{"Monarch":{"xref_id":"0006282"}}}


id: MONDO:0030448
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"immunodeficiency disease","termid":"MONDO:0021094"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"immunodeficiency 86","secondary_identifiers":["MEDGEN:1794205","OMIM:619549","UMLS:C5561995"],"synonyms":[{"name":"IMD86","type":"exact"}],"termid":"MONDO:0030448","xrefs":{"Monarch":{"xref_id":"0030448"}}}


id: PBO:0077495
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 214","termid":"PBO:0077495"}


id: MONDO:0020752
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"juvenile myoclonic epilepsy","termid":"MONDO:0009696"},{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myoclonic epilepsy, juvenile, susceptibility to, 1","secondary_identifiers":["MEDGEN:342587","UMLS:C1850778"],"synonyms":[{"name":"EJM1","type":"exact"}],"termid":"MONDO:0020752","xrefs":{"Monarch":{"xref_id":"0020752"}}}


id: PBO:0111776
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Yip1 family","termid":"PBO:0111776"}


id: GO:0035640
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The specific behavior of an organism in response to a novel environment or stimulus.","definition_xrefs":["PMID:11682103","GOC:BHF","GOC:pr","PMID:9767169"],"direct_ancestors":[{"relation_name":"is_a","term_name":"behavior","termid":"GO:0007610"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"exploration behavior","synonyms":[{"name":"exploration behaviour","type":"exact"},{"name":"exploratory behavior","type":"exact"},{"name":"exploratory behaviour","type":"exact"},{"name":"open-field behavior","type":"narrow"}],"termid":"GO:0035640"}


id: MONDO:0009173
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, genetic, gastroenterological disease characterized by early-onset failure to thrive, edema, hypoproteinemia, diarrhea and fat malabsorption (or steatorrhea) in the presence of very low or absent trypsin activity in duodenal fluid. Celiac disease, or other pancreatic or mucosal disorders, may be associated.","definition_xrefs":["Orphanet:168601"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"digestive system disorder","termid":"MONDO:0004335"}],"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":"congenital enteropathy due to enteropeptidase deficiency","secondary_identifiers":["SCTID:190952002","MEDGEN:82802","MESH:C562649","NANDO:2200910","GARD:17038","ICD9:277.89","OMIM:226200","UMLS:C0268416","DOID:0111667"],"synonyms":[{"name":"congenital enterokinase deficiency","type":"exact"},{"name":"enterokinase deficiency","type":"related"},{"name":"enteropeptidase deficiency","type":"related"}],"termid":"MONDO:0009173","xrefs":{"Monarch":{"xref_id":"0009173"}}}


id: PBO:0088551
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar polyphosphatase","termid":"PBO:0088551"}


id: MONDO:0006294
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A primary or metastatic malignant neoplasm affecting the pleura. A representative example of primary malignant pleural neoplasm is the malignant pleural mesothelioma. A representative example of metastatic malignant neoplasm to the pleura is metastatic carcinoma that has spread to the pleura from another anatomic site.","definition_xrefs":["NCIT:C3547"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete connective tissue cancer (obsolete MONDO:0002176)","termid":"MONDO:0002176"},{"relation_name":"is_a","term_name":"respiratory system cancer","termid":"MONDO:0000376"},{"relation_name":"is_a","term_name":"thoracic cancer","termid":"MONDO:0003274"},{"relation_name":"is_a","term_name":"pleural neoplasm","termid":"MONDO:0021065"}],"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":"pleural cancer","secondary_identifiers":["DOID:5158","EFO:1000362","ICD9:163","ICD9:163.8","ICD10CM:C38.4","MEDGEN:56307","UMLS:C0153494","SCTID:363433009","ICD9:163.9"],"synonyms":[{"name":"cancer of pleura","type":"exact"},{"name":"cancer of the pleura","type":"exact"},{"name":"malignant neoplasm of pleura","type":"exact"},{"name":"malignant neoplasm of the pleura","type":"exact"},{"name":"malignant pleura neoplasm","type":"exact"},{"name":"malignant pleural neoplasm","type":"exact"},{"name":"malignant pleural tumor","type":"exact"},{"name":"malignant pleural tumour","type":"exact"},{"name":"malignant tumor of pleura","type":"exact"},{"name":"malignant tumor of the pleura","type":"exact"},{"name":"malignant tumour of pleura","type":"exact"},{"name":"malignant tumour of the pleura","type":"exact"},{"name":"neoplasm of pleura","type":"broad"},{"name":"pleura cancer","type":"exact"},{"name":"pleural cancer","type":"exact"},{"name":"pleural tumor","type":"broad"},{"name":"pleural tumour","type":"broad"}],"termid":"MONDO:0006294","xrefs":{"Monarch":{"xref_id":"0006294"}}}


id: GO:0061666
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of UFM1 to a substrate protein via the reaction X-UFM1 + S = X + S-UFM1, where X is either an E2 or E3 enzyme, the X-UFM1 linkage is a thioester bond, and the S-UFM1 linkage is an isopeptide bond between the C-terminal amino acid of UFM1 and the epsilon-amino group of lysine residues in the substrate.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ubiquitin-like protein ligase activity","termid":"GO:0061659"},{"relation_name":"is_a","term_name":"UFM1 transferase activity","termid":"GO:0071568"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0019787"},{"rel_name":"is_a","termid":"GO:0016746"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0019787","GO:0016746","GO:0140096","GO:0003824"],"is_obsolete":false,"name":"UFM1 ligase activity","synonyms":[{"name":"E3","type":"broad"}],"termid":"GO:0061666"}


id: PBO:0080874
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"YOD1 deubiquitinase","termid":"PBO:0080874"}


id: PBO:0089671
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sporulation specific Rab GEF Spo13","termid":"PBO:0089671"}


id: GO:0004503
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-tyrosine + O2 = L-DOPAquinone + H2O. This reaction can use both monophenols (such as tyrosine) and catechols (o-diphenols) as substrates.","definition_xrefs":["RHEA:18117","PMID:4965136"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, another compound as one donor, and incorporation of one atom of oxygen","termid":"GO:0016716"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"tyrosinase activity","secondary_identifiers":["EC:1.14.18.1","MetaCyc:MONOPHENOL-MONOOXYGENASE-RXN"],"synonyms":[{"name":"L-tyrosine monooxygenase activity","type":"exact"},{"name":"N-acetyl-6-hydroxytryptophan oxidase activity","type":"related"},{"name":"catecholase","type":"related"},{"name":"chlorogenic acid oxidase activity","type":"related"},{"name":"chlorogenic oxidase activity","type":"related"},{"name":"cresolase activity","type":"related"},{"name":"dopa oxidase","type":"related"},{"name":"monophenol monooxidase activity","type":"related"},{"name":"monophenol monooxygenase activity","type":"exact"},{"name":"monophenol oxidase activity","type":"related"},{"name":"monophenol oxygenase","type":"exact"},{"name":"monophenolase activity","type":"related"},{"name":"o-diphenol oxidase activity","type":"related"},{"name":"o-diphenol oxidoreductase","type":"related"},{"name":"o-diphenol:O2 oxidoreductase activity","type":"related"},{"name":"phenol oxidase activity","type":"broad"},{"name":"phenolase activity","type":"broad"},{"name":"prophenol oxidase activity","type":"related"},{"name":"prophenoloxidase activity","type":"related"},{"name":"pyrocatechol oxidase","type":"broad"},{"name":"tyrosine-dopa oxidase activity","type":"related"}],"termid":"GO:0004503"}


id: GO:0071082
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of an alpha9-beta1 integrin complex bound to the extracellular matrix protein tenascin.","definition_xrefs":["PMID:9565552"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005886"],"is_obsolete":false,"name":"alpha9-beta1 integrin-tenascin complex","synonyms":[{"name":"ITGA9-ITGB1-TNC complex","type":"narrow"}],"termid":"GO:0071082"}


id: FYPO:0002285
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cell morphology phenotype observed in the vegetative growth phase of the life cycle in which a cell is elongated during a cellular response to hydrogen peroxide.","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete elongated cell during cellular response to hydrogen peroxide (obsolete FYPO:0002285)","synonyms":[{"name":"elongated cell during cellular response to H2O2","type":"exact"},{"name":"elongated cell during cellular response to hydrogen peroxide during mitotic cell cycle","type":"related"},{"name":"elongated cell during cellular response to hydrogen peroxide during vegetative growth","type":"exact"},{"name":"elongated in response to hydrogen peroxide","type":"exact"}],"termid":"FYPO:0002285"}


id: PBO:0000747
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SNARE Bet1 (predicted)","termid":"PBO:0000747"}


id: MONDO:0023243
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The Glass-Chapman-Hockley syndrome is a very rare disease. To date, the syndrome has only been reported in one family with five members affected in three generations. The first patients were two brothers that had an abnormally-shaped head due to coronal craniosynostosis. Their mother, maternal aunt, and maternal grandmother were also found to have the syndrome. The signs and symptoms varied from person to person; however, the signs and symptoms included coronal craniosynostosis, small middle part of the face (midfacial hypoplasia), and short fingers (brachydactyly).The inheritance is thought to be autosomal dominant. No genes have been identified for this syndrome. Treatment included surgery to correct the craniosynostosis. No issues with development and normal intelligence were reported. This is an n-of-1 use case where only one patient or family has been described with this disorder.","definition_xrefs":["GARD:0002479"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"craniosynostosis","termid":"MONDO:0015469"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0005497"],"is_obsolete":false,"name":"glass-chapman-hockley syndrome","secondary_identifiers":["Orphanet:1535","SCTID:720814001"],"synonyms":[{"name":"craniosynostosis - dysmorphism - brachydactyly","type":"related"},{"name":"craniosynostosis brachydactyly","type":"related"},{"name":"craniosynostosis with facial dysmorphism and brachydactyly syndrome","type":"exact"},{"name":"craniosynostosis-dysmorphism-brachydactyly syndrome","type":"related"},{"name":"glass chapman hockley syndrome","type":"related"}],"termid":"MONDO:0023243","xrefs":{"Monarch":{"xref_id":"0023243"}}}


id: GO:0140844
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of ADP-ribose groups to the glutamate-2 residue of the N-terminal tail of histone H2B (or an equivalent residue).","definition_xrefs":["PMID:27530147"],"direct_ancestors":[{"relation_name":"is_a","term_name":"NAD+-protein-glutamate ADP-ribosyltransferase activity","termid":"GO:0140807"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0140096","GO:0016740","GO:0016757","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"NAD+-histone H2BE2 glutamate ADP-ribosyltransferase activity","synonyms":[{"name":"NAD+-histone H2B-E2 glutamate ADP-ribosyltransferase activity","type":"exact"},{"name":"NAD+-histone-glutamate ADP-ribosyltransferase activity (H2B-E2 specific)","type":"exact"}],"termid":"GO:0140844"}


id: PBO:0053976
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 1288","termid":"PBO:0053976"}


id: PBO:0082057
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3-deoxy-D-arabino-heptulosonate-7-phosphate (DAHP) synthase; catalyzes the first step in aromatic amino acid biosynthesis and is feedback-inhibited by phenylalanine or high concentration of tyrosine or tryptophan","termid":"PBO:0082057"}


id: GO:0070224
data:
  {"annotated_genes":["SJAG_02599"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[78007],"is_not":false,"summary":null,"term":"GO:0070224"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: H2S (hydrogen sulfide) + a quinone = S0 (sulfane sulfur) + a hydroquinone.","definition_xrefs":["RHEA:30239"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on a sulfur group of donors, quinone or similar compound as acceptor","termid":"GO:0016672"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02599":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"sulfide:quinone oxidoreductase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-1614665","MetaCyc:R17-RXN"],"synonyms":[{"name":"sulfide-quinone reductase activity","type":"exact"},{"name":"sulphide:quinone oxidoreductase activity","type":"exact"}],"termid":"GO:0070224","terms_by_termid":{"GO:0070224":null}}


id: MONDO:0001171
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute form of salpingo-oophoritis.","definition_xrefs":["MONDO:patterns/acute"],"direct_ancestors":[{"relation_name":"is_a","term_name":"salpingo-oophoritis","termid":"MONDO:0001172"},{"relation_name":"is_a","term_name":"acute salpingitis","termid":"MONDO:0001173"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acute salpingo-oophoritis","secondary_identifiers":["UMLS:C0156327","ICD9:614.0","MEDGEN:510243","DOID:10971","SCTID:266581008"],"synonyms":[{"name":"acute salpingitis and oophoritis","type":"exact"},{"name":"salpingo-oophoritis, acute","type":"exact"}],"termid":"MONDO:0001171","xrefs":{"Monarch":{"xref_id":"0001171"}}}


id: GO:1901259
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any rRNA processing that takes place in chloroplast.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rRNA processing","termid":"GO:0006364"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0042254"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0044085","GO:0010467","GO:0042254"],"is_obsolete":false,"name":"chloroplast rRNA processing","termid":"GO:1901259"}


id: GO:0032743
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of interleukin-2 production.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cytokine production","termid":"GO:0001819"},{"relation_name":"is_a","term_name":"regulation of interleukin-2 production","termid":"GO:0032663"},{"relation_name":"positively_regulates","term_name":"interleukin-2 production","termid":"GO:0032623"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"positive regulation of interleukin-2 production","secondary_identifiers":["GO:0045086","GO:1900042"],"synonyms":[{"name":"activation of interleukin-2 production","type":"narrow"},{"name":"positive regulation of IL-2 production","type":"exact"},{"name":"positive regulation of interleukin-2 biosynthetic process","type":"narrow"},{"name":"positive regulation of interleukin-2 secretion","type":"narrow"},{"name":"stimulation of interleukin-2 production","type":"narrow"},{"name":"up regulation of interleukin-2 production","type":"exact"},{"name":"up-regulation of interleukin-2 production","type":"exact"},{"name":"upregulation of interleukin-2 production","type":"exact"}],"termid":"GO:0032743"}


id: PBO:0072374
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S27a","termid":"PBO:0072374"}


id: GO:2001289
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving lipid X, 2,3-diacylglucosamine 1-phosphate.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino sugar metabolic process","termid":"GO:0006040"},{"relation_name":"is_a","term_name":"phosphate-containing compound metabolic process","termid":"GO:0006796"},{"relation_name":"is_a","term_name":"organophosphate metabolic process","termid":"GO:0019637"}],"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":"lipid X metabolic process","synonyms":[{"name":"2,3-Bis(3-hydroxytetradecanoyl)-beta-D-glucosaminyl 1-phosphate metabolic process","type":"related"},{"name":"2,3-Bis(3-hydroxytetradecanoyl)-beta-D-glucosaminyl 1-phosphate metabolism","type":"related"},{"name":"2,3-Bis(beta-hydoroxymyristoyl)-beta-D-glucosaminyl 1-phosphate metabolic process","type":"related"},{"name":"2,3-Bis(beta-hydoroxymyristoyl)-beta-D-glucosaminyl 1-phosphate metabolism","type":"related"},{"name":"2-deoxy-3-O-[(3R)-3-hydroxytetradecanoyl]-2-{[(3R)-3-hydroxytetradecanoyl]amino}-1-O-phosphono-alpha-D-glucopyranose metabolic process","type":"exact"},{"name":"2-deoxy-3-O-[(3R)-3-hydroxytetradecanoyl]-2-{[(3R)-3-hydroxytetradecanoyl]amino}-1-O-phosphono-alpha-D-glucopyranose metabolism","type":"exact"},{"name":"lipid X metabolism","type":"exact"}],"termid":"GO:2001289"}


id: PBO:0079349
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tweety family member 2","termid":"PBO:0079349"}


id: MOD:01945
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that forms (2-aminosuccinimidyl)-3-sulfanylpropanoic acid by crosslinking either an aspartic acid residue or an asparagine residue with the following cysteine residue.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"2-aminosuccinimide ring crosslinked residues","termid":"MOD:01944"},{"relation_name":"is_a","term_name":"crosslinked L-cysteine residue","termid":"MOD:02044"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"2-(2-aminosuccinimidyl)-3-sulfanylpropanoic acid","termid":"MOD:01945"}


id: PBO:0030985
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_metabolic_process","termid":"PBO:0030985"}


id: PBO:0001413
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptionally regulates trr1","termid":"PBO:0001413"}


id: GO:0048269
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A multimeric enzyme complex composed of variable numbers of catalytic alpha subunits, and noncatalytic beta subunits. The beta subunits are believed to have a regulatory function. The enzyme complex catalyzes the synthesis of S-adenosylmethionine (AdoMet), which is the major methyl group donor, participating in the methylation of proteins, DNA, RNA, phospholipids, and other small molecules.","definition_xrefs":["PMID:25075345","PMID:10644686","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular protein-containing complex","termid":"GO:0140535"},{"relation_name":"is_a","term_name":"transferase complex","termid":"GO:1990234"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"methionine adenosyltransferase complex","synonyms":[{"name":"MAT complex","type":"exact"}],"termid":"GO:0048269"}


id: GO:0034765
data:
  {"annotated_genes":["SJAG_04551","SJAG_00296","SJAG_03631"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[93031,115220],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905949"},{"annotations":[103964],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905665"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the directed movement of ions from one side of a membrane to the other.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transmembrane transport","termid":"GO:0034762"},{"relation_name":"is_a","term_name":"regulation of monoatomic ion transport","termid":"GO:0043269"},{"relation_name":"regulates","term_name":"monoatomic ion transmembrane transport","termid":"GO:0034220"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00296":null,"SJAG_03631":null,"SJAG_04551":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0055085","GO:0008150"],"is_obsolete":false,"name":"regulation of monoatomic ion transmembrane transport","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"regulation of ion membrane transport","type":"exact"},{"name":"regulation of ion transmembrane transport","type":"broad"},{"name":"regulation of transmembrane ion transport","type":"exact"}],"termid":"GO:0034765","terms_by_termid":{"GO:1905665":null,"GO:1905949":null}}


id: GO:0007232
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals generated in response to osmotic change, as mediated through a Sho1 osmosensor system.","definition_xrefs":["GOC:jl","PMID:26787842"],"direct_ancestors":[{"relation_name":"is_a","term_name":"osmosensory signaling pathway","termid":"GO:0007231"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"osmosensory signaling pathway via Sho1 osmosensor","synonyms":[{"name":"osmosensory signalling pathway via Sho1 osmosensor","type":"exact"},{"name":"signal transduction during osmotic stress via Sho1 osmosensor","type":"exact"}],"termid":"GO:0007232"}


id: PBO:0058926
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA let-7e","termid":"PBO:0058926"}


id: GO:0003132
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that mediates the transfer of information from mesodermal cells to endodermal cells that contributes to heart induction.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mesodermal-endodermal cell signaling","termid":"GO:0003131"},{"relation_name":"part_of","term_name":"heart induction","termid":"GO:0003129"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"mesodermal-endodermal cell signaling involved in heart induction","synonyms":[{"name":"mesodermal-endodermal cell signalling involved in heart induction","type":"exact"}],"termid":"GO:0003132"}


id: MONDO:0020282
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete metabolic disease with macular cherry-red spot (obsolete MONDO:0020282)","secondary_identifiers":["Orphanet:98714"],"termid":"MONDO:0020282","xrefs":{"Monarch":{"xref_id":"0020282"}}}


id: PATO:0000644
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A increased size quality inhering in an organ or tissue by virtue of the bearer's exhibiting increased number of cells.","definition_xrefs":["Wikipedia:http://en.wikipedia.org/wiki/Hyperplastic"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased size","termid":"PATO:0000586"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hyperplastic","secondary_identifiers":["PATO:0000943"],"synonyms":[{"name":"hyperplasia","type":"exact"},{"name":"overdeveloped","type":"related"}],"termid":"PATO:0000644"}


id: SO:0000278
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A transcript that is bound by a nucleic acid.","definition_xrefs":["SO:xp"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"bound_by_nucleic_acid","termid":"SO:0000876"},{"relation_name":"is_a","term_name":"transcript","termid":"SO:0000673"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcript_bound_by_nucleic_acid","synonyms":[{"name":"transcript bound by nucleic acid","type":"exact"}],"termid":"SO:0000278"}


id: GO:1900094
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any regulation of transcription from RNA polymerase II promoter that is involved in determination of left/right symmetry.","definition_xrefs":["GOC:BHF","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of transcription from RNA polymerase II promoter involved in determination of left/right symmetry (obsolete GO:1900094)","synonyms":[{"name":"global transcription regulation from Pol II promoter of determination of left/right asymmetry","type":"related"},{"name":"global transcription regulation from Pol II promoter of determination of left/right symmetry","type":"related"},{"name":"regulation of gene-specific transcription from RNA polymerase II promoter of determination of left/right asymmetry","type":"related"},{"name":"regulation of gene-specific transcription from RNA polymerase II promoter of determination of left/right symmetry","type":"related"},{"name":"regulation of global transcription from Pol II promoter of determination of left/right asymmetry","type":"related"},{"name":"regulation of global transcription from Pol II promoter of determination of left/right symmetry","type":"related"},{"name":"regulation of transcription from Pol II promoter of determination of left/right asymmetry","type":"exact"},{"name":"regulation of transcription from Pol II promoter of determination of left/right symmetry","type":"exact"},{"name":"regulation of transcription from RNA polymerase II promoter of determination of left/right asymmetry","type":"exact"},{"name":"regulation of transcription from RNA polymerase II promoter of determination of left/right symmetry","type":"exact"},{"name":"regulation of transcription from RNA polymerase II promoter, global of determination of left/right asymmetry","type":"related"},{"name":"regulation of transcription from RNA polymerase II promoter, global of determination of left/right symmetry","type":"related"}],"termid":"GO:1900094"}


id: PBO:0043840
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"carnitine palmitoyltransferase 2 pseudogene 1","termid":"PBO:0043840"}


id: PBO:0025516
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein phosphatase PP1, Dis2","termid":"PBO:0025516"}


id: GO:0102408
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: hexadecanedioyl-CoA + sn-glycerol 3-phosphate = coenzyme A + sn-2-C16:0-DCA-LPA.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete sn-2-glycerol-3-phosphate C16:0-DCA-CoA acyl transferase activity (obsolete GO:0102408)","termid":"GO:0102408"}


id: MOD:01333
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-isoleucine residue to 6x(13)C labeled L-isoleucine.","definition_xrefs":["PubMed:12766232","PubMed:12716131","Unimod:188#I"],"direct_ancestors":[{"relation_name":"is_a","term_name":"6x(13)C labeled residue","termid":"MOD:00544"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"6x(13)C labeled L-isoleucine","synonyms":[{"name":"13C(6) Silac label","type":"related"},{"name":"Label:13C(6)","type":"related"}],"termid":"MOD:01333"}


id: GO:0048225
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An extracellular matrix part that consists of fatty acid-derived polymers, including both aromatic and aliphatic components. The suberin network is found in specialized plant cell walls, where it is laid down between the primary wall and plasma membrane, forms protective and wound-healing layers, and provides a water-impermeable diffusion barrier.","definition_xrefs":["PMID:7706282","PMID:18440267","GOC:jid","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"secondary cell wall","termid":"GO:0009531"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005618"}],"interesting_parent_ids":["GO:0005575","GO:0005618"],"is_obsolete":false,"name":"suberin network","termid":"GO:0048225"}


id: MONDO:0013787
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":"psychomotor retardation, epilepsy, and craniofacial dysmorphism","secondary_identifiers":["OMIM:614501","UMLS:C3281055","MEDGEN:482685"],"synonyms":[{"name":"PMRED","type":"related"},{"name":"neurodevelopmental disorder with hypotonia, craniofacial abnormalities, and seizures","type":"exact"},{"name":"psychomotor retardation, epilepsy, and craniofacial dysmorphism","type":"exact"}],"termid":"MONDO:0013787","xrefs":{"Monarch":{"xref_id":"0013787"}}}


id: PBO:0073892
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 12 member 8","termid":"PBO:0073892"}


id: GO:0072068
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the late distal convoluted tubule over time, from its formation to the mature structure. The late distal convoluted tubule contains DCT cells and intercalated (IC) alpha and beta cells and is vasopressin-sensitive.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nephron epithelium development","termid":"GO:0072009"},{"relation_name":"part_of","term_name":"distal convoluted tubule development","termid":"GO:0072025"}],"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":"late distal convoluted tubule development","termid":"GO:0072068"}


id: PBO:0050278
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histocompatibility minor HB-1","termid":"PBO:0050278"}


id: PBO:0076248
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SUV39H2 divergent transcript","termid":"PBO:0076248"}


id: FYPO:0007617
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to sodium azide (NaN3). Cells stop growing (and may die) at a concentration of sodium azide that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000139","FYPO:0000003","FYPO:0002683","FYPO:0005447"],"is_obsolete":false,"name":"sensitive to sodium azide","synonyms":[{"name":"sensitive to NaN3","type":"exact"},{"name":"sensitive to sodium azide during mitotic cell cycle","type":"related"},{"name":"sensitive to sodium azide during vegetative growth","type":"exact"}],"termid":"FYPO:0007617"}


id: GO:0019656
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The anaerobic chemical reactions and pathways resulting in the enzymatic breakdown of D-glucose to D-lactate and ethanol, yielding energy in the form of adenosine triphosphate (ATP) at the rate of one ATP per glucose molecule.","definition_xrefs":["MetaCyc:P122-PWY","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ethanol metabolic process","termid":"GO:0006067"},{"relation_name":"is_a","term_name":"glucose catabolic process to lactate","termid":"GO:0019659"},{"relation_name":"is_a","term_name":"non-glycolytic fermentation","termid":"GO:0019662"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006091"},{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006091","GO:0005975","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"glucose catabolic process to D-lactate and ethanol","synonyms":[{"name":"glucose fermentation to D-lactate and ethanol","type":"exact"},{"name":"heterofermentation","type":"exact"},{"name":"heterofermentative lactate fermentation","type":"exact"},{"name":"heterofermentative pathway","type":"exact"},{"name":"heterolactate fermentation","type":"exact"},{"name":"heterolactic fermentation","type":"exact"}],"termid":"GO:0019656"}


id: GO:0052364
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways performed by an organism in its symbiont resulting in the breakdown of substances. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["ISBN:0198547684"],"gene_count":0,"genotype_count":0,"name":"obsolete catabolism by host of substance in symbiont (obsolete GO:0052364)","termid":"GO:0052364"}


id: FYPO:0005706
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the duration of progression through anaphase B of mitosis is longer than normal. Anaphase B is the stage of mitosis in which the polar microtubules elongate and the two poles of the spindle move farther apart.","definition_xrefs":["PomBase:mah","GO:0000092"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased duration of mitotic anaphase","termid":"FYPO:0000618"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000002","FYPO:0000631","FYPO:0005447"],"is_obsolete":false,"name":"increased duration of mitotic anaphase B","synonyms":[{"name":"delayed mitotic anaphase B progression","type":"related"},{"name":"increased duration of anaphase B during mitotic cell cycle","type":"exact"},{"name":"increased duration of mitotic anaphase B during vegetative growth","type":"exact"},{"name":"increased duration of mitotic anaphase B progression","type":"exact"},{"name":"prolonged mitotic anaphase B","type":"exact"}],"termid":"FYPO:0005706"}


id: PBO:0059814
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CYB pseudogene 40","termid":"PBO:0059814"}


id: PBO:0040798
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"basic helix-loop-helix family member b9 pseudogene 1","termid":"PBO:0040798"}


id: MONDO:0005763
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infections with viruses of the family flaviviridae.","definition_xrefs":["MESH:D018178"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary viral infectious disease","termid":"MONDO:0100329"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Flaviviridae infectious disease","secondary_identifiers":["SCTID:111865007","EFO:0007274"],"synonyms":[{"name":"Flaviviridae caused disease or disorder","type":"exact"},{"name":"Flaviviridae disease or disorder","type":"exact"}],"termid":"MONDO:0005763","xrefs":{"Monarch":{"xref_id":"0005763"}}}


id: PBO:0052435
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kinesin light chain 2","termid":"PBO:0052435"}


id: GO:0010704
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cell cycle process in which the 5' to 3' exonucleolytic resection of the DNA at the site of the break to form a 3' single-strand DNA overhang resulting in the transfer of genetic information from one helix to another.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meiotic DNA double-strand break processing","termid":"GO:0000706"},{"relation_name":"part_of","term_name":"meiotic gene conversion","termid":"GO:0006311"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006281"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006310"},{"rel_name":"part_of","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0008150","GO:0007049","GO:0006259","GO:0006310","GO:0006281"],"is_obsolete":false,"name":"meiotic DNA double-strand break processing involved in meiotic gene conversion","termid":"GO:0010704"}


id: MONDO:0859592
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An anaplastic oligodendroglioma that has material basis in IDH gene family mutation and combined whole-arm losses of 1p and 19q (1p/19q codeletion).","definition_xrefs":["DOID:0080882"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anaplastic oligodendroglioma","termid":"MONDO:0016696"}],"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":"IDH-mutant and 1p/19q-codeleted oligodendroglioma","secondary_identifiers":["MEDGEN:926090","NCIT:C129318","UMLS:C4288558"],"termid":"MONDO:0859592","xrefs":{"Monarch":{"xref_id":"0859592"}}}


id: PBO:0069125
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 375, pseudogene","termid":"PBO:0069125"}


id: MOD:00394
data:
  {"annotated_genes":["SJAG_02522","SJAG_00733"],"annotation_feature_type":"gene","cv_annotations":{"PSI-MOD":[{"annotations":[82275,82318],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MOD:00050"}]},"cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a hydrogen atom with an acetyl group.","definition_xrefs":["PubMed:11999733","PubMed:12175151","Unimod:1","PubMed:15350136","DeltaMass:0","PubMed:11857757","PubMed:14730666"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acylated residue","termid":"MOD:00649"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00733":null,"SJAG_02522":null},"genotype_count":0,"is_obsolete":false,"name":"acetylated residue","references_by_uniquename":{"PMID:36408920":null},"synonyms":[{"name":"AcRes","type":"exact"},{"name":"Acetyl","type":"related"},{"name":"Acetylation","type":"related"},{"name":"Acetylation (N terminus, N epsilon of Lysine, O of Serine) (Ac)","type":"exact"}],"termid":"MOD:00394","terms_by_termid":{"MOD:00050":null}}


id: MONDO:1010431
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Atherosclerosis that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"atherosclerosis, non-human animal","termid":"MONDO:1010008"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"atherosclerosis, domestic cat","secondary_identifiers":["OMIA:000080-9685"],"termid":"MONDO:1010431","xrefs":{"Monarch":{"xref_id":"1010431"}}}


id: PBO:0088366
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"succinate dehydrogenase (ubiquinone) iron-sulfur protein subunit","termid":"PBO:0088366"}


id: GO:0008012
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"The action of a molecule that contributes to the structural integrity of the chitin-based cuticle of an adult organism. An example of this is found in Drosophila melanogaster.","definition_xrefs":["GOC:mah","GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"structural constituent of chitin-based cuticle","termid":"GO:0005214"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005198"}],"interesting_parent_ids":["GO:0003674","GO:0005198"],"is_obsolete":false,"name":"structural constituent of adult chitin-based cuticle","synonyms":[{"name":"structural constituent of adult cuticle","type":"broad"}],"termid":"GO:0008012"}


id: GO:0102930
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: geranyl diphosphate + 4-hydroxybenzoic acid = 3-geranyl-4-hydroxybenzoate + diphosphoric acid.","definition_xrefs":["RHEA:27854","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity, transferring alkyl or aryl (other than methyl) groups","termid":"GO:0016765"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016765"},{"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:0016740","GO:0003824","GO:0016765"],"is_obsolete":false,"name":"4-hydroxybenzoate geranyltransferase activity","secondary_identifiers":["EC:2.5.1.93","MetaCyc:RXN-8920"],"termid":"GO:0102930"}


id: GO:0043171
data:
  {"annotated_genes":["SJAG_01088","SJAG_00181","SJAG_01430"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[74384,79377,116311],"is_not":false,"summary":null,"term":"GO:0043171"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of peptides, compounds of 2 or more (but usually less than 100) amino acids where the alpha carboxyl group of one is bound to the alpha amino group of another.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptide metabolic process","termid":"GO:0006518"},{"relation_name":"is_a","term_name":"catabolic process","termid":"GO:0009056"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00181":null,"SJAG_01088":null,"SJAG_01430":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"peptide catabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"peptide breakdown","type":"exact"},{"name":"peptide catabolism","type":"exact"},{"name":"peptide degradation","type":"exact"}],"termid":"GO:0043171","terms_by_termid":{"GO:0043171":null}}


id: GO:0021830
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of interneurons from the subpallium to the cortex during forebrain development.","definition_xrefs":["PMID:12626695","GOC:dph","GO_REF:0000021","GOC:cls","GOC:jid","GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"substrate-independent telencephalic tangential interneuron migration","termid":"GO:0021843"}],"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":"interneuron migration from the subpallium to the cortex","termid":"GO:0021830"}


id: GO:0044843
data:
  {"annotated_genes":["SJAG_03699","SJAG_00996","SJAG_00991","SJAG_00169","SJAG_02026","SJAG_03591","SJAG_01187","SJAG_03160","SJAG_05346","SJAG_02723","SJAG_02810","SJAG_01210","SJAG_01401","SJAG_01311","SJAG_00100","SJAG_03681","SJAG_01825","SJAG_04140","SJAG_00071","SJAG_03048","SJAG_02404"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[75860,110200,113889],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000082"},{"annotations":[110733,90756,104181,103440,117764],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0031568"},{"annotations":[93121,111518],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0031571"},{"annotations":[93972,95140,93558,100691],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:2000134"},{"annotations":[107804,118937,108490,111031,107642,104196],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1900087"},{"annotations":[76717,117200,78467,117766,110739,93564],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0007089"}]},"cv_name":"biological_process","definition":"The cell cycle process by which a cell in G1 phase commits to S phase.","definition_xrefs":["GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell cycle phase transition","termid":"GO:0044770"}],"gene_count":21,"genes_by_uniquename":{"SJAG_00071":null,"SJAG_00100":null,"SJAG_00169":null,"SJAG_00991":null,"SJAG_00996":null,"SJAG_01187":null,"SJAG_01210":null,"SJAG_01311":null,"SJAG_01401":null,"SJAG_01825":null,"SJAG_02026":null,"SJAG_02404":null,"SJAG_02723":null,"SJAG_02810":null,"SJAG_03048":null,"SJAG_03160":null,"SJAG_03591":null,"SJAG_03681":null,"SJAG_03699":null,"SJAG_04140":null,"SJAG_05346":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":"cell cycle G1/S phase transition","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0044843","terms_by_termid":{"GO:0000082":null,"GO:0007089":null,"GO:0031568":null,"GO:0031571":null,"GO:1900087":null,"GO:2000134":null}}


id: PBO:0005488
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone H2B Htb1","termid":"PBO:0005488"}


id: GO:1900135
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of renin secretion into blood stream.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein secretion","termid":"GO:0050714"},{"relation_name":"is_a","term_name":"regulation of renin secretion into blood stream","termid":"GO:1900133"},{"relation_name":"positively_regulates","term_name":"renin secretion into blood stream","termid":"GO:0002001"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"positive regulation of renin secretion into blood stream","synonyms":[{"name":"activation of renin release into blood stream","type":"narrow"},{"name":"activation of renin secretion into blood stream","type":"narrow"},{"name":"positive regulation of renin release into blood stream","type":"exact"},{"name":"up regulation of renin release into blood stream","type":"exact"},{"name":"up regulation of renin secretion into blood stream","type":"exact"},{"name":"up-regulation of renin release into blood stream","type":"exact"},{"name":"up-regulation of renin secretion into blood stream","type":"exact"},{"name":"upregulation of renin release into blood stream","type":"exact"},{"name":"upregulation of renin secretion into blood stream","type":"exact"}],"termid":"GO:1900135"}


id: FYPO:0007810
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which the amount, distribution, and morphology of cytoplasmic microtubules is normal (i.e. indistinguishable from wild type) during a cellular response to a pheromone.","definition_xrefs":["PomBase:mah","PMID:11950884"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cytoplasmic microtubules","termid":"FYPO:0007809"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal cytoplasmic microtubules during cellular response to pheromone","synonyms":[{"name":"normal cytoplasmic microtubule morphology during cellular response to pheromone","type":"exact"},{"name":"normal cytoplasmic microtubule structure during cellular response to pheromone","type":"narrow"},{"name":"normal cytoplasmic microtubules during mating projection formation","type":"related"},{"name":"normal cytoplasmic microtubules during response to pheromone","type":"exact"},{"name":"normal microtubules during cellular response to pheromone","type":"exact"}],"termid":"FYPO:0007810"}


id: MONDO:0002413
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Glycogenosis due to glucose-6-phosphatase (G6P) deficiency or glycogen storage disease, (GSD), type 1, is a group of inherited metabolic diseases, including types a and b, and characterized by poor tolerance to fasting, growth retardation and hepatomegaly resulting from accumulation of glycogen and fat in the liver.","definition_xrefs":["Orphanet:364"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete nephropathy secondary to a storage or other metabolic disease (obsolete MONDO:0019743)","termid":"MONDO:0019743"},{"relation_name":"is_a","term_name":"disorder of glycogen metabolism","termid":"MONDO:0002412"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0037792"],"is_obsolete":false,"name":"glycogen storage disease I","secondary_identifiers":["DOID:0081329","ICD10CM:E74.01","NANDO:2200538","NORD:1193","SCTID:7265005","UMLS:C0017920","GARD:16523","MEDGEN:6640","MedDRA:10018464","MESH:D005953","NANDO:1200840","NCIT:C84733","MONDO:0018220","NANDO:1201018"],"synonyms":[{"name":"G6P deficiency","type":"exact"},{"name":"GSD due to G6P deficiency","type":"exact"},{"name":"GSD type 1","type":"exact"},{"name":"GSD type I","type":"exact"},{"name":"GSD1","type":"exact"},{"name":"Glycogen Storage Disease Type I","type":"exact"},{"name":"deficiency of glucose-6-phosphatase","type":"exact"},{"name":"glycogen storage disease I","type":"exact"},{"name":"glycogen storage disease due to G6P deficiency","type":"exact"},{"name":"glycogen storage disease due to glucose-6-phosphatase deficiency","type":"exact"},{"name":"glycogen storage disease type 1","type":"exact"},{"name":"glycogen storage disease type I","type":"exact"},{"name":"glycogen storage disease, type I","type":"exact"},{"name":"glycogenosis type 1","type":"exact"},{"name":"glycogenosis type I","type":"exact"},{"name":"hepatorenal glycogenosis","type":"exact"},{"name":"von Gierke disease","type":"exact"},{"name":"von Gierke's disease","type":"exact"}],"termid":"MONDO:0002413","xrefs":{"Monarch":{"xref_id":"0002413"}}}


id: GO:0072005
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the identity of a kidney is maintained. Identity is considered to be the aggregate of characteristics by which a structure is recognized.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"maintenance of animal organ identity","termid":"GO:0048496"},{"relation_name":"part_of","term_name":"kidney rudiment formation","termid":"GO:0072003"}],"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":"maintenance of kidney identity","synonyms":[{"name":"maintenance of kidney anlage identity","type":"related"}],"termid":"GO:0072005"}


id: MONDO:0008982
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hereditary macular disorder, usually presenting between the ages of 30-60, characterized by a large area of atrophy in the center of the macula and the loss or absence of photoreceptors, retinal pigment epithelium and choriocapillaris in this area, resulting in a progressive decrease in visual acuity.","definition_xrefs":["Orphanet:75377"],"direct_ancestors":[{"relation_name":"is_a","term_name":"optic choroid disorder","termid":"MONDO:0001898"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"central areolar choroidal dystrophy","secondary_identifiers":["ICD10CM:H31.22","MESH:C535358","NANDO:1200939","SCTID:312918002","MEDGEN:283932","OMIMPS:215500","icd11.foundation:2018537024","GARD:10049","ICD9:363.54","SCTID:231996009","UMLS:C1536451"],"synonyms":[{"name":"CACD","type":"exact"},{"name":"CACD1","type":"related"},{"name":"areolar atrophy of the macula","type":"exact"},{"name":"central areolar choroidal sclerosis","type":"exact"},{"name":"choroidal dystrophy","type":"exact"},{"name":"choroidal dystrophy central areolar","type":"related"},{"name":"choroidal dystrophy, central areolar, 1","type":"related"}],"termid":"MONDO:0008982","xrefs":{"Monarch":{"xref_id":"0008982"}}}


id: GO:0002785
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of antimicrobial peptide production.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of production of molecular mediator of immune response","termid":"GO:0002701"},{"relation_name":"is_a","term_name":"regulation of antimicrobial peptide production","termid":"GO:0002784"},{"relation_name":"is_a","term_name":"negative regulation of antimicrobial humoral response","termid":"GO:0008348"},{"relation_name":"negatively_regulates","term_name":"antimicrobial peptide production","termid":"GO:0002775"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"negative regulation of antimicrobial peptide production","synonyms":[{"name":"down regulation of antimicrobial peptide production","type":"exact"},{"name":"down-regulation of antimicrobial peptide production","type":"exact"},{"name":"downregulation of antimicrobial peptide production","type":"exact"},{"name":"inhibition of antimicrobial peptide production","type":"narrow"}],"termid":"GO:0002785"}


id: PBO:0116802
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DEAD/H-box helicase 11 like 13","termid":"PBO:0116802"}


id: PBO:0064137
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyruvate kinase M1/2 pseudogene 4","termid":"PBO:0064137"}


id: MONDO:0001323
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Transient bilateral swelling of breast tissue in a neonate that results from the waning influence of maternal estrogen.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gynecomastia disorder","termid":"MONDO:0001571"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"infant gynecomastia","secondary_identifiers":["SCTID:34831003","DOID:11603","MEDGEN:258541","UMLS:C1449721","ICD10CM:P83.4","ICD9:778.7"],"synonyms":[{"name":"breast engorgement in newborn","type":"exact"},{"name":"neonatal gynaecomastia","type":"exact"}],"termid":"MONDO:0001323","xrefs":{"Monarch":{"xref_id":"0001323"}}}


id: PBO:0074320
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SMAD9 intronic transcript 1","termid":"PBO:0074320"}


id: PBO:0044744
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DExD-box helicase 21","termid":"PBO:0044744"}


id: PBO:0083734
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential chromatin-associated protein; involved in initiation of DNA replication; required for association of MCM2-7 complex with replication origins; required to stabilize catalytic subunit of DNA polymerase-alpha; coordinates function of replication fork helicase; self-associates through its N-terminal domain","termid":"PBO:0083734"}


id: PBO:0084435
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAL-activator protein; transcription factor; part of the complex locus MAL6, plays a positive role in the regulation of maltose fermentation","termid":"PBO:0084435"}


id: MONDO:0011166
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lymphedema-atrial septal defects-facial changes syndrome is characterized by congenital lymphoedema of the lower limbs, atrial septal defect and a characteristic facies (a round face with a prominent forehead, a flat nasal bridge with a broad nasal tip, epicanthal folds, a thin upper lip and a cleft chin). It has been described in two brothers and a sister. Transmission appears to be autosomal recessive.","definition_xrefs":["Orphanet:86915"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"primary lymphedema","termid":"MONDO:0019175"}],"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":"lymphedema-atrial septal defects-facial changes syndrome","secondary_identifiers":["UMLS:C2677167","GARD:284","MEDGEN:383042","MESH:C535539","MESH:C567398","OMIM:601927","SCTID:721978002"],"synonyms":[{"name":"Irons Bhan syndrome","type":"related"},{"name":"Irons-Bhan syndrome","type":"exact"},{"name":"Irons-Bianchi syndrome","type":"exact"},{"name":"autosomal recessive syndrome of lymphedema, hydroceles, atrial septal defect, and characteristic facial changes","type":"related"},{"name":"lymphedema, CARDIAC septal defects, and characteristic facies","type":"related"},{"name":"lymphedema, atrial septal defect, and characteristic facial changes","type":"related"},{"name":"lymphedema, atrial septal defect, and characteristic facies","type":"related"}],"termid":"MONDO:0011166","xrefs":{"Monarch":{"xref_id":"0011166"}}}


id: MONDO:1012972
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hereditary neurological disease that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"nervous system disorder, non-human animal","termid":"MONDO:1011336"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hereditary neurological disease, non-human animal","termid":"MONDO:1012972","xrefs":{"Monarch":{"xref_id":"1012972"}}}


id: PBO:0088871
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SNARE associated Golgi protein","termid":"PBO:0088871"}


id: MONDO:0032747
data:
  {"annotated_genes":["SJAG_01156"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88936],"is_not":false,"summary":null,"term":"MONDO:0032747"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hydatidiform mole","termid":"MONDO:0006248"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01156":null},"genotype_count":0,"is_obsolete":false,"name":"hydatidiform mole, recurrent, 4","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:18368","UMLS:C5193094","OMIM:618432","MEDGEN:1677210"],"synonyms":[{"name":"HYDATIDIFORM MOLE, RECURRENT, 4","type":"related"},{"name":"HYDM4","type":"related"}],"termid":"MONDO:0032747","terms_by_termid":{"MONDO:0032747":null},"xrefs":{"Monarch":{"xref_id":"0032747"}}}


id: GO:1900781
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of the indole alkaloid fumiquinazoline C.","definition_xrefs":["GOC:TermGenie","GOC:di","PMID:20225828"],"direct_ancestors":[{"relation_name":"is_a","term_name":"indole alkaloid biosynthetic process","termid":"GO:0035835"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0019748"],"is_obsolete":false,"name":"fumiquinazoline C biosynthetic process","secondary_identifiers":["GO:1900779","GO:1900775","GO:1900773"],"synonyms":[{"name":"fumiquinazoline C anabolism","type":"exact"},{"name":"fumiquinazoline C biosynthesis","type":"exact"},{"name":"fumiquinazoline C formation","type":"exact"},{"name":"fumiquinazoline C metabolic process","type":"broad"},{"name":"fumiquinazoline C metabolism","type":"broad"},{"name":"fumiquinazoline C synthesis","type":"exact"},{"name":"fumiquinazoline biosynthesis","type":"exact"},{"name":"fumiquinazoline biosynthetic process","type":"broad"},{"name":"fumiquinazoline metabolic process","type":"broad"},{"name":"fumiquinazoline metabolism","type":"broad"},{"name":"fumiquinazolines synthesis","type":"related"}],"termid":"GO:1900781"}


id: PBO:0091416
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by S. cerevisiae ELO3","termid":"PBO:0091416"}


id: GO:0016875
data:
  {"annotated_genes":["SJAG_03545","SJAG_01797","SJAG_04738","SJAG_01159","SJAG_01522","SJAG_00420","SJAG_04285","SJAG_03626","SJAG_04409","SJAG_04840","SJAG_02236","SJAG_02263","SJAG_01197","SJAG_04473","SJAG_00443","SJAG_04762","SJAG_04482","SJAG_01235","SJAG_00103","SJAG_16456","SJAG_00488","SJAG_02517","SJAG_02206","SJAG_02615","SJAG_02977","SJAG_00653","SJAG_02015","SJAG_01352","SJAG_01259","SJAG_04856","SJAG_03071","SJAG_03585","SJAG_02428","SJAG_03277","SJAG_04094","SJAG_00243"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[77615],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004813"},{"annotations":[70869],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004812"},{"annotations":[78113],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004814"},{"annotations":[104088,106907],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004816"},{"annotations":[78473,78382],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004815"},{"annotations":[74192],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004817"},{"annotations":[72026,74607],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004818"},{"annotations":[81905],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004819"},{"annotations":[74687],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004820"},{"annotations":[80372],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004821"},{"annotations":[73155,77051],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004822"},{"annotations":[77611,79811],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004823"},{"annotations":[73543,75354],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004824"},{"annotations":[79891,71126],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004825"},{"annotations":[80424,80783,79444],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004826"},{"annotations":[72479,79076],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004827"},{"annotations":[74713,78535],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004828"},{"annotations":[75460,72452],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004829"},{"annotations":[73017,71746],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004830"},{"annotations":[72508,80564],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004831"},{"annotations":[71589,71816],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004832"}]},"cv_name":"molecular_function","definition":"Catalysis of the joining of two molecules via a carbon-oxygen bond, with the concomitant hydrolysis of the diphosphate bond in ATP or a similar triphosphate.","definition_xrefs":["EC:6.1.-.-"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ligase activity","termid":"GO:0016874"}],"gene_count":36,"genes_by_uniquename":{"SJAG_00103":null,"SJAG_00243":null,"SJAG_00420":null,"SJAG_00443":null,"SJAG_00488":null,"SJAG_00653":null,"SJAG_01159":null,"SJAG_01197":null,"SJAG_01235":null,"SJAG_01259":null,"SJAG_01352":null,"SJAG_01522":null,"SJAG_01797":null,"SJAG_02015":null,"SJAG_02206":null,"SJAG_02236":null,"SJAG_02263":null,"SJAG_02428":null,"SJAG_02517":null,"SJAG_02615":null,"SJAG_02977":null,"SJAG_03071":null,"SJAG_03277":null,"SJAG_03545":null,"SJAG_03585":null,"SJAG_03626":null,"SJAG_04094":null,"SJAG_04285":null,"SJAG_04409":null,"SJAG_04473":null,"SJAG_04482":null,"SJAG_04738":null,"SJAG_04762":null,"SJAG_04840":null,"SJAG_04856":null,"SJAG_16456":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016874"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016874"],"is_obsolete":false,"name":"ligase activity, forming carbon-oxygen bonds","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000043":null,"GO_REF:0000107":null},"termid":"GO:0016875","terms_by_termid":{"GO:0004812":null,"GO:0004813":null,"GO:0004814":null,"GO:0004815":null,"GO:0004816":null,"GO:0004817":null,"GO:0004818":null,"GO:0004819":null,"GO:0004820":null,"GO:0004821":null,"GO:0004822":null,"GO:0004823":null,"GO:0004824":null,"GO:0004825":null,"GO:0004826":null,"GO:0004827":null,"GO:0004828":null,"GO:0004829":null,"GO:0004830":null,"GO:0004831":null,"GO:0004832":null}}


id: GO:0036129
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that decreases the frequency, rate or extent of transcription from an RNA polymerase II promoter as a result of a hydrogen peroxide (H2O2) stimulus.","definition_xrefs":["GOC:al"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of transcription from RNA polymerase II promoter in response to hydrogen peroxide (obsolete GO:0036129)","termid":"GO:0036129"}


id: GO:0098855
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A cation ion channel with a preference for K+ over Na+ ions, which is activated by membrane hyperpolarization, and consists of a tetramer of HCN family members. Some members of this family (HCN1, HCN2 and HCN4) are also activated when cAMP binds to their cyclic nucleotide binding domain (CNBD). Channel complexes of this family play an important role in the control of pacemaker activity in the heart.","definition_xrefs":["PMID:20829353"],"direct_ancestors":[{"relation_name":"is_a","term_name":"voltage-gated potassium channel complex","termid":"GO:0008076"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005886"],"is_obsolete":false,"name":"HCN channel complex","secondary_identifiers":["GO:1990759","GO:1990746"],"synonyms":[{"name":"HCN1 channel complex","type":"narrow"},{"name":"HCN2 channel complex","type":"narrow"},{"name":"HCN3 channel complex","type":"narrow"},{"name":"HCN4 channel complex","type":"narrow"},{"name":"K/Na hyperpolarization-activated channel 3 complex","type":"narrow"},{"name":"K/Na hyperpolarization-activated cyclic nucleotide-gated channel 1 complex","type":"narrow"},{"name":"K/Na hyperpolarization-activated cyclic nucleotide-gated channel 2 complex","type":"narrow"},{"name":"K/Na hyperpolarization-activated cyclic nucleotide-gated channel 4 complex","type":"narrow"},{"name":"K/Na hyperpolarization-activated cyclic nucleotide-gated channel complex","type":"exact"},{"name":"potassium/sodium hyperpolarization-activated channel 3 complex","type":"narrow"},{"name":"potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1 complex","type":"narrow"},{"name":"potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 complex","type":"narrow"},{"name":"potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 tetramer","type":"related"},{"name":"potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 4 complex","type":"narrow"},{"name":"potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 4 tetramer","type":"related"},{"name":"potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel complex","type":"exact"}],"termid":"GO:0098855"}


id: GO:0019085
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The first phase of viral transcription that occurs after entry of the virus into the host cell, but prior to viral genome replication. It involves the transcription of genes for non-structural proteins, and for lytic viruses, the early gene products are involved in establishing control over the host cell.","definition_xrefs":["GOC:bf","GOC:jh2","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral transcription","termid":"GO:0019083"}],"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":"early viral transcription","synonyms":[{"name":"immediate early viral mRNA transcription","type":"related"}],"termid":"GO:0019085"}


id: GO:0046016
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process involving glucose that activates or increases the rate of transcription.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon catabolite activation of transcription","termid":"GO:0045991"},{"relation_name":"is_a","term_name":"regulation of transcription by glucose","termid":"GO:0046015"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006351"},{"rel_name":"regulates","termid":"GO:0006351"},{"rel_name":"is_a","termid":"GO:0006355"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0006351","GO:0006355","GO:0010467"],"is_obsolete":false,"name":"positive regulation of transcription by glucose","synonyms":[{"name":"activation of transcription by glucose","type":"narrow"},{"name":"stimulation of transcription by glucose","type":"narrow"},{"name":"up regulation of transcription by glucose","type":"exact"},{"name":"up-regulation of transcription by glucose","type":"exact"},{"name":"upregulation of transcription by glucose","type":"exact"}],"termid":"GO:0046016"}


id: FYPO:0001688
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which vegetative cell population growth is normal (i.e. indistinguishable from wild type) in a medium containing brefeldin A.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal vegetative cell population growth","termid":"FYPO:0001357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0002058"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0002060","FYPO:0000003","FYPO:0000139","FYPO:0002057","FYPO:0002058"],"is_obsolete":false,"name":"normal growth on brefeldin A","synonyms":[{"name":"normal cell population growth in presence of brefeldin A","type":"exact"},{"name":"normal cell population growth on BFA","type":"exact"},{"name":"normal cell population growth on brefeldin A","type":"exact"},{"name":"normal cellular response to brefeldin A","type":"related"},{"name":"normal vegetative cell population growth on brefeldin A","type":"exact"}],"termid":"FYPO:0001688"}


id: PBO:0059342
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein S10 pseudogene 1","termid":"PBO:0059342"}


id: PBO:0045080
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DLGAP5 pseudogene 1","termid":"PBO:0045080"}


id: PBO:0064390
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PMS1 homolog 2, mismatch repair system component pseudogene 12","termid":"PBO:0064390"}


id: PBO:0031189
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_growth_during_cellular_response_to_salt_stress","termid":"PBO:0031189"}


id: GO:0071339
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that can methylate lysine-4 of histone H3. MLL1/MLL is the catalytic methyltransferase subunit, and the complex also contains the core components ASH2L, HCFC1/HCF1 WDR5 and RBBP5.","definition_xrefs":["GOC:sp","PMID:15960975"],"direct_ancestors":[{"relation_name":"is_a","term_name":"MLL1/2 complex","termid":"GO:0044665"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005654"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005654","GO:0005575","GO:0032991","GO:0005634"],"is_obsolete":false,"name":"MLL1 complex","termid":"GO:0071339"}


id: PR:Q10202
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- dbp3 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q10202"],"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":"ATP-dependent RNA helicase dbp3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC17D1.06","synonyms":[{"name":"Spom972h-dbp3","type":"exact"}],"termid":"PR:Q10202"}


id: MONDO:0007686
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Gray platelet syndrome (GPS) is a rare inherited bleeding disorder characterized by macrothrombocytopenia, myelofibrosis, splenomegaly and typical gray appearance of platelets on Wright stained peripheral blood smear.","definition_xrefs":["Orphanet:721"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited bleeding disorder, platelet-type","termid":"MONDO:0000009"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"alpha granule disease","termid":"MONDO:0020117"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"gray platelet syndrome","secondary_identifiers":["SCTID:51720005","GARD:2562","DOID:0111044","MESH:D055652","icd11.foundation:1818085572","NCIT:C84741","MEDGEN:82900","UMLS:C0272302","OMIM:139090"],"synonyms":[{"name":"Alpha storage pool deficiency","type":"exact"},{"name":"BDPLT4","type":"exact"},{"name":"GPS","type":"exact"},{"name":"bleeding disorder, Platelet-type, 4","type":"related"},{"name":"gray platelet syndrome","type":"exact"},{"name":"marked decrease or absence of alpha-granules and of platelet-specific alpha-granule proteins","type":"related"},{"name":"platelet alpha-granule deficiency","type":"exact"},{"name":"platelet-type bleeding disorder 4","type":"exact"}],"termid":"MONDO:0007686","xrefs":{"Monarch":{"xref_id":"0007686"}}}


id: FYPO:0001790
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which plasmids are lost at the same frequency as in wild-type cells. Plasmid loss occurs when one or both daughter cells do not inherit copies of a plasmid from the mother cell, and may result from failure of plasmid replication or segregation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell phenotype","termid":"FYPO:0000002"},{"relation_name":"is_a","term_name":"normal vegetative phenotype","termid":"FYPO:0001312"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal plasmid loss","termid":"FYPO:0001790"}


id: GO:0047189
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 3-amino-L-alanine + oxalyl-CoA = N(3)-oxalyl-L-2,3-diaminopropanoate + CoA.","definition_xrefs":["RHEA:13465"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyltransferase activity, transferring groups other than amino-acyl groups","termid":"GO:0016747"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0016746","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"2,3-diaminopropionate N-oxalyltransferase activity","secondary_identifiers":["MetaCyc:2.3.1.58-RXN","EC:2.3.1.58","KEGG_REACTION:R04211"],"synonyms":[{"name":"ODAP synthase activity","type":"related"},{"name":"oxalyl-CoA:L-2,3-diaminopropanoate 3-N-oxalyltransferase activity","type":"related"},{"name":"oxalyl-CoA:L-2,3-diaminopropanoate N3-oxalyltransferase activity","type":"related"},{"name":"oxalyl-CoA:L-alpha,beta-diaminopropionic acid oxalyltransferase activity","type":"related"},{"name":"oxalyldiaminopropionate synthase activity","type":"related"},{"name":"oxalyldiaminopropionic synthase activity","type":"related"}],"termid":"GO:0047189"}


id: PBO:0005348
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NuA4 histone acetyltransferase complex subunit Vid21","termid":"PBO:0005348"}


id: PBO:0064174
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phospholipase A2 group X","termid":"PBO:0064174"}


id: GO:0021545
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the cranial nerves over time, from its formation to the mature structure. The cranial nerves are composed of twelve pairs of nerves that emanate from the nervous tissue of the hindbrain. These nerves are sensory, motor, or mixed in nature, and provide the motor and general sensory innervation of the head, neck and viscera. They mediate vision, hearing, olfaction and taste and carry the parasympathetic innervation of the autonomic ganglia that control visceral functions.","definition_xrefs":["GOC:cls","GOC:dgh","ISBN:0838580343","GOC:jid","GOC:dph","GO_REF:0000021"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nerve development","termid":"GO:0021675"}],"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":"cranial nerve development","termid":"GO:0021545"}


id: PBO:0003948
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved fungal mitochondrial protein","termid":"PBO:0003948"}


id: PBO:0003906
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translation initiation factor eIF1","termid":"PBO:0003906"}


id: PBO:0069599
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 876, pseudogene","termid":"PBO:0069599"}


id: PBO:0061608
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear casein kinase and cyclin dependent kinase substrate 1 pseudogene 1","termid":"PBO:0061608"}


id: PBO:0091366
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rad57 facilitates Rad51 assembly at damage sites independently of Swi5","termid":"PBO:0091366"}


id: PBO:0082469
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Calmodulin-binding actin-associated protein; roles in endocytic membrane tabulation and constriction, and exocytosis; N-BAR domain protein that interacts with Rvs161p to regulate actin cytoskeleton, endocytosis, and viability following starvation or osmotic stress; recruited to bud tips by Gyl1p and Gyp5p during polarized growth; homolog of mammalian amphiphysin; necessary for efficient trafficking of CoQ6 to mitochondria","termid":"PBO:0082469"}


id: PBO:0031761
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-cell_cycle_arrest_in_mitotic_G2_phase","termid":"PBO:0031761"}


id: GO:0051291
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of creating protein oligomers, compounds composed of a small number, usually between three and ten, of component monomers that are not all identical. Oligomers may be formed by the polymerization of a number of monomers or the depolymerization of a large protein polymer.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein complex oligomerization","termid":"GO:0051259"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0044085","GO:0065003","GO:0008150"],"is_obsolete":false,"name":"protein heterooligomerization","synonyms":[{"name":"protein heterooligomer assembly","type":"exact"},{"name":"protein heterooligomer biosynthesis","type":"exact"},{"name":"protein heterooligomer biosynthetic process","type":"exact"},{"name":"protein heterooligomer formation","type":"exact"}],"termid":"GO:0051291"}


id: FYPO:0006579
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to manganese. Cells stop growing (and may die) at a concentration of manganese ions that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0002683","FYPO:0005447","FYPO:0000139","FYPO:0000003","FYPO:0001985"],"is_obsolete":false,"name":"sensitive to manganese","synonyms":[{"name":"hypersensitive to manganese","type":"exact"},{"name":"sensitive to manganese during mitotic cell cycle","type":"related"},{"name":"sensitive to manganese during vegetative growth","type":"exact"},{"name":"sensitive to manganese ions","type":"exact"}],"termid":"FYPO:0006579"}


id: MONDO:1010931
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Polymyositis that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polymyositis, non-human animal","termid":"MONDO:1010203"},{"relation_name":"is_a","term_name":"myopathy, dog","termid":"MONDO:1010917"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polymyositis, dog","secondary_identifiers":["OMIA:001874-9615"],"termid":"MONDO:1010931","xrefs":{"Monarch":{"xref_id":"1010931"}}}


id: GO:0008817
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 ATP + 2 corrinoid + reduced [electron-transfer flavoprotein] = 2 adenosylcorrinoid + 3 H+ + oxidized [electron-transfer flavoprotein] + 2 triphosphate. The corrinoid can be cob(II)yrinate a,c diamide, cob(II)inamide or cob(II)alamin.","definition_xrefs":["PMID:5946606","PMID:19933577"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity, transferring alkyl or aryl (other than methyl) groups","termid":"GO:0016765"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016765"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016765","GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"corrinoid adenosyltransferase activity","secondary_identifiers":["Reactome:R-HSA-3322125","EC:2.5.1.17","Reactome:R-HSA-3159253","KEGG_REACTION:R05218","GO:0043784"],"synonyms":[{"name":"ATP:cob(I)alamin Co-beta-adenosyltransferase activity","type":"narrow"},{"name":"ATP:cob(I)alamin cobeta-adenosyltransferase activity","type":"related"},{"name":"ATP:cob(I)yrinic acid-a,c-diamide cobeta-adenosyltransferase activity","type":"narrow"},{"name":"ATP:corrinoid adenosyltransferase activity","type":"related"},{"name":"aquacob(I)alamin adenosyltransferase activity","type":"narrow"},{"name":"aquocob(I)alamin vitamin B12s adenosyltransferase activity","type":"narrow"},{"name":"cob(I)alamin adenosyltransferase activity","type":"narrow"},{"name":"cob(I)yrinic acid a,c-diamide adenosyltransferase activity","type":"narrow"},{"name":"cob(II)yrinic acid a,c-diamide reductase activity","type":"narrow"},{"name":"cob(II)yrinic acid-a,c-diamide:FMN oxidoreductase activity","type":"narrow"},{"name":"vitamin B12s adenosyltransferase activity","type":"related"}],"termid":"GO:0008817"}


id: PBO:0076005
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"STIM2 antisense RNA 1","termid":"PBO:0076005"}


id: FYPO:0004208
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of H3-K4 specific histone methyltransferase activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone methyltransferase activity","termid":"FYPO:0004783"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000641","FYPO:0000654","FYPO:0005447","FYPO:0000002","FYPO:0000652","FYPO:0000707","FYPO:0000661","FYPO:0001985"],"is_obsolete":false,"name":"abnormal histone methyltransferase activity (H3-K4 specific)","synonyms":[{"name":"abnormal H3-K4 specific histone methyltransferase activity","type":"exact"}],"termid":"FYPO:0004208"}


id: PBO:0029742
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-spherical_cell","termid":"PBO:0029742"}


id: GO:0008801
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: beta-D-glucose 1-phosphate = beta-D-glucose 6-phosphate.","definition_xrefs":["EC:5.4.2.6","RHEA:20113"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular phosphotransferase activity","termid":"GO:0016868"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016853","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"beta-phosphoglucomutase activity","secondary_identifiers":["KEGG_REACTION:R02728","MetaCyc:BETA-PHOSPHOGLUCOMUTASE-RXN"],"synonyms":[{"name":"beta-D-glucose 1,6-phosphomutase activity","type":"related"}],"termid":"GO:0008801"}


id: GO:0035591
data:
  {"annotated_genes":["SJAG_04943","SJAG_01047","SJAG_03625","SJAG_01199","SJAG_01605","SJAG_02098","SJAG_04503","SJAG_04671","SJAG_00317","SJAG_03081","SJAG_01188","SJAG_00209","SJAG_04509","SJAG_01464","SJAG_02332","SJAG_03602","SJAG_04259","SJAG_03342","SJAG_04666"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[76031,77644,89722,91060,94246,94659,95756,100250,101009,101184,108936,113293,114332,115651,119000],"is_not":false,"summary":null,"term":"GO:0035591"},{"annotations":[101793,71798,119239],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005078"},{"annotations":[77041],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030159"}]},"cv_name":"molecular_function","definition":"The binding activity of a molecule that brings together two or more molecules in a signaling pathway, permitting those molecules to function in a coordinated way. Adaptor molecules themselves do not have catalytic activity.","definition_xrefs":["PMID:19104498","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-macromolecule adaptor activity","termid":"GO:0030674"}],"gene_count":19,"genes_by_uniquename":{"SJAG_00209":null,"SJAG_00317":null,"SJAG_01047":null,"SJAG_01188":null,"SJAG_01199":null,"SJAG_01464":null,"SJAG_01605":null,"SJAG_02098":null,"SJAG_02332":null,"SJAG_03081":null,"SJAG_03342":null,"SJAG_03602":null,"SJAG_03625":null,"SJAG_04259":null,"SJAG_04503":null,"SJAG_04509":null,"SJAG_04666":null,"SJAG_04671":null,"SJAG_04943":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0030674"},{"rel_name":"is_a","termid":"GO:0060090"}],"interesting_parent_ids":["GO:0003674","GO:0030674","GO:0060090"],"is_obsolete":false,"name":"signaling adaptor activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"signaling protein recruiting activity","type":"exact"},{"name":"signaling scaffold activity","type":"related"},{"name":"signalling adaptor activity","type":"exact"}],"termid":"GO:0035591","terms_by_termid":{"GO:0005078":null,"GO:0030159":null,"GO:0035591":null}}


id: PR:Q9Y7N9
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC1450.12 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9Y7N9"],"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":"PX domain-containing protein C1450.12 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1450.12","synonyms":[{"name":"Spom972h-SPCC1450.12","type":"exact"}],"termid":"PR:Q9Y7N9"}


id: PBO:0046670
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"estrogen-related receptor alpha pseudogene 2","termid":"PBO:0046670"}


id: PBO:0031625
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_ascospore_wall_assembly","termid":"PBO:0031625"}


id: PBO:0055364
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 2793","termid":"PBO:0055364"}


id: PR:Q9C0Y4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- agl1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9C0Y4"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha-glucosidase Agl1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAPB24D3.10c","synonyms":[{"name":"SPAPB24D3.10c","type":"related"},{"name":"Spom972h-agl1","type":"exact"},{"name":"agl","type":"related"},{"name":"maltase (Schizosaccharomyces pombe 972h-)","type":"broad"}],"termid":"PR:Q9C0Y4"}


id: GO:0060657
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency, or extent of mammary gland cord elongation as a result of a signal being created by a mesenchymal cell that is a precursor to the mammary fat and its subsequent reception and interpretation by an mammary cord epithelial cell.","definition_xrefs":["GOC:dph","PMID:12558599"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-cell signaling","termid":"GO:0007267"},{"relation_name":"is_a","term_name":"regulation of developmental growth","termid":"GO:0048638"},{"relation_name":"regulates","term_name":"mammary gland cord elongation","termid":"GO:0060654"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"regulation of mammary gland cord elongation by mammary fat precursor cell-epithelial cell signaling","synonyms":[{"name":"regulation of mammary gland cord elongation by mammary fat precursor cell-epithelial cell signalling","type":"exact"}],"termid":"GO:0060657"}


id: PBO:0056369
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitogen-activated protein kinase 6 pseudogene 6","termid":"PBO:0056369"}


id: FYPO:0007319
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which stress granule assembly occurs to a lower extent than normal when the cell is subject to glucose starvation.","definition_xrefs":["PomBase:mah","PMID:32071154"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal stress granule assembly","termid":"FYPO:0007318"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"decreased stress granule assembly during glucose starvation","synonyms":[{"name":"decreased stress granule assembly during cellular response to glucose starvation","type":"exact"},{"name":"decreased stress granule assembly during glucose depletion","type":"exact"},{"name":"decreased stress granule assembly during glucose deprivation","type":"exact"},{"name":"decreased stress granule assembly during glucose limitation","type":"related"},{"name":"reduced stress granule assembly during glucose starvation","type":"exact"}],"termid":"FYPO:0007319"}


id: GO:0055002
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a striated muscle cell over time, from its formation to the mature structure. Striated muscle cells contain fibers that are divided by transverse bands into striations, and cardiac and skeletal muscle are types of striated muscle.","definition_xrefs":["CL:0000737","GOC:devbiol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscle cell development","termid":"GO:0055001"},{"relation_name":"part_of","term_name":"striated muscle cell differentiation","termid":"GO:0051146"}],"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":"striated muscle cell development","termid":"GO:0055002"}


id: GO:0044634
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents, or reduces the frequency, rate or extent of complement activation by the alternative pathway, in a different organism.","definition_xrefs":["GOC:jl","PMID:20837040"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of complement activation, alternative pathway in another organism (obsolete GO:0044634)","synonyms":[{"name":"negative regulation of complement activation, alternative pathway in other organism","type":"exact"}],"termid":"GO:0044634"}


id: MONDO:0003038
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Loss or impairment of the ability to write (letters, syllables, words, or phrases) due to an injury to a specific cerebral area or occasionally due to emotional factors. This condition rarely occurs in isolation, and often accompanies aphasia. (From Adams et al., Principles of Neurology, 6th ed, p485; apa, Thesaurus of Psychological Index Terms, 1994)","definition_xrefs":["MESH:D000381"],"direct_ancestors":[{"relation_name":"is_a","term_name":"writing disorder","termid":"MONDO:0000599"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dysgraphia","secondary_identifiers":["DOID:4540","MEDGEN:115942","NCIT:C182452","UMLS:C0234144","HP:0010526"],"synonyms":[{"name":"dysgraphia","type":"exact"},{"name":"dysgraphia (disease)","type":"exact"}],"termid":"MONDO:0003038","xrefs":{"Monarch":{"xref_id":"0003038"}}}


id: PBO:0075027
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 115-38","termid":"PBO:0075027"}


id: FYPO:0005107
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A regulation phenotype observed in the vegetative growth phase of the life cycle in which regulation of mitotic DNA replication initiation is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal regulation of mitotic cell cycle","termid":"FYPO:0001928"},{"relation_name":"is_a","term_name":"normal regulation of DNA replication","termid":"FYPO:0002995"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257","FYPO:0001312","FYPO:0001320"],"is_obsolete":false,"name":"normal regulation of mitotic DNA replication initiation","synonyms":[{"name":"normal regulation of DNA replication initiation during mitotic cell cycle","type":"exact"},{"name":"normal regulation of DNA replication initiation involved in mitotic cell cycle DNA replication","type":"exact"},{"name":"normal regulation of mitotic DNA replication initiation during vegetative growth","type":"exact"}],"termid":"FYPO:0005107"}


id: GO:1901566
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of organonitrogen compound.","definition_xrefs":["GOC:TermGenie","GOC:pr"],"gene_count":0,"genotype_count":0,"name":"obsolete organonitrogen compound biosynthetic process (obsolete GO:1901566)","termid":"GO:1901566"}


id: PBO:0061298
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NPC intracellular cholesterol transporter 1","termid":"PBO:0061298"}


id: SO:0001031
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Reverse is an attribute of the feature, where the feature is in the 3' to 5' direction. Again could be applied to primer.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"direction_attribute","termid":"SO:0001029"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"reverse","termid":"SO:0001031"}


id: PBO:0113422
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase II subunit B12.6; contacts DNA; mutations affect transcription start site selection and fidelity of transcription; positively regulates ATG1 transcription as a key regulator of autophagy","termid":"PBO:0113422"}


id: MONDO:0008643
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":"veins, pattern of, on anterior thorax","secondary_identifiers":["OMIM:192400","UMLS:C1860490","MEDGEN:348117"],"synonyms":[{"name":"veins, pattern of, on anterior thorax","type":"exact"}],"termid":"MONDO:0008643","xrefs":{"Monarch":{"xref_id":"0008643"}}}


id: GO:0003843
data:
  {"annotated_genes":["SJAG_05285","SJAG_02222","SJAG_00876","SJAG_01288","SJAG_03587"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[76524,77582,81752,115023],"is_not":false,"summary":null,"term":"GO:0003843"},{"annotations":[117684],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140752"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-glucose + [(1->3)-beta-D-glucosyl](n) = UDP + [(1->3)-beta-D-glucosyl](n+1).","definition_xrefs":["EC:2.4.1.34"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glucosyltransferase activity","termid":"GO:0035251"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00876":null,"SJAG_01288":null,"SJAG_02222":null,"SJAG_03587":null,"SJAG_05285":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0016757","GO:0003824"],"is_obsolete":false,"name":"1,3-beta-D-glucan synthase activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["RHEA:21476","GO:0009981","MetaCyc:13-BETA-GLUCAN-SYNTHASE-RXN"],"synonyms":[{"name":"(1,3)-beta-glucan (callose) synthase activity","type":"related"},{"name":"1,3-beta-D-glucan synthetase activity","type":"related"},{"name":"1,3-beta-D-glucan-UDP glucosyltransferase activity","type":"related"},{"name":"1,3-beta-glucan synthase activity","type":"related"},{"name":"1,3-beta-glucan-uridine diphosphoglucosyltransferase activity","type":"related"},{"name":"GS-II","type":"related"},{"name":"UDP-glucose-1,3-beta-D-glucan glucosyltransferase activity","type":"related"},{"name":"UDP-glucose-1,3-beta-glucan glucosyltransferase activity","type":"related"},{"name":"UDP-glucose-beta-glucan glucosyltransferase activity","type":"related"},{"name":"UDP-glucose:(1,3)beta-glucan synthase activity","type":"related"},{"name":"UDP-glucose:1,3-beta-D-glucan 3-beta-D-glucosyltransferase activity","type":"related"},{"name":"UDPglucose-1,3-beta-D-glucan glucosyltransferase activity","type":"related"},{"name":"UDPglucose:1,3-beta-D-glucan 3-beta-D-glucosyltransferase activity","type":"related"},{"name":"beta-1,3-glucan synthase activity","type":"exact"},{"name":"beta-1,3-glucan synthetase activity","type":"related"},{"name":"callose synthase activity","type":"exact"},{"name":"callose synthetase activity","type":"related"},{"name":"paramylon synthetase","type":"related"},{"name":"uridine diphosphoglucose-1,3-beta-glucan glucosyltransferase activity","type":"related"}],"termid":"GO:0003843","terms_by_termid":{"GO:0003843":null,"GO:0140752":null}}


id: MONDO:0032852
data:
  {"annotated_genes":["SJAG_04621"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88655],"is_not":false,"summary":null,"term":"MONDO:0032852"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital myopathy","termid":"MONDO:0019952"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04621":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"myopathy, congenital, with structured cores and z-line abnormalities","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5231445","DOID:0081342","OMIM:618654","MEDGEN:1684705"],"synonyms":[{"name":"MYOCOZ","type":"related"},{"name":"MYOPATHY, CONGENITAL, WITH STRUCTURED CORES AND Z-LINE ABNORMALITIES","type":"related"},{"name":"Multiple Structured Core Disease","type":"related"},{"name":"myopathy, congenital with structured cores and z-line abnormalities","type":"exact"}],"termid":"MONDO:0032852","terms_by_termid":{"MONDO:0032852":null},"xrefs":{"Monarch":{"xref_id":"0032852"}}}


id: PBO:0082821
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Conserved NAPDH-dependent diflavin reductase; component of an early step in the cytosolic Fe-S protein assembly (CIA) machinery; transfers electrons from NADPH to the Fe-S cluster of Dre2p; plays a pro-death role under oxidative stress; Tah18p-dependent nitric oxide synthesis confers high-temperature stress tolerance; possible target for development of antifungal drugs","termid":"PBO:0082821"}


id: MONDO:0859354
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"thyroid hormone metabolism, abnormal","termid":"MONDO:0031432"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thyroid hormone metabolism, abnormal, 3","secondary_identifiers":["OMIM:620198","UMLS:C5774292","MEDGEN:1824065"],"termid":"MONDO:0859354","xrefs":{"Monarch":{"xref_id":"0859354"}}}


id: PBO:0031622
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_sporulation","termid":"PBO:0031622"}


id: MONDO:0018886
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete listeriosis (obsolete MONDO:0018886)","termid":"MONDO:0018886","xrefs":{"Monarch":{"xref_id":"0018886"}}}


id: GO:0030118
data:
  {"annotated_genes":["SJAG_02177","SJAG_00379","SJAG_01167","SJAG_00800","SJAG_04565","SJAG_01809","SJAG_02805","SJAG_00104","SJAG_04931","SJAG_02282","SJAG_04609","SJAG_04517","SJAG_04644"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[114641,114853,79369,62802],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030121"},{"annotations":[58661,76197,80009,110173],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030122"},{"annotations":[64552],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030131"},{"annotations":[66612,59068],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030130"},{"annotations":[78603],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071439"},{"annotations":[75567,81522],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030125"}]},"cv_name":"cellular_component","definition":"A membrane coat found on coated pits and some coated vesicles; consists of polymerized clathrin triskelions, each comprising three clathrin heavy chains and three clathrin light chains, linked to the membrane via one of the AP adaptor complexes.","definition_xrefs":["PMID:11252894","PMID:9531549","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane coat","termid":"GO:0030117"}],"gene_count":13,"genes_by_uniquename":{"SJAG_00104":null,"SJAG_00379":null,"SJAG_00800":null,"SJAG_01167":null,"SJAG_01809":null,"SJAG_02177":null,"SJAG_02282":null,"SJAG_02805":null,"SJAG_04517":null,"SJAG_04565":null,"SJAG_04609":null,"SJAG_04644":null,"SJAG_04931":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005737","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"clathrin coat","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["NIF_Subcellular:sao879919129","Wikipedia:Clathrin","GO:0016190"],"synonyms":[{"name":"clathrin cage","type":"exact"}],"termid":"GO:0030118","terms_by_termid":{"GO:0030121":null,"GO:0030122":null,"GO:0030125":null,"GO:0030130":null,"GO:0030131":null,"GO:0071439":null}}


id: GO:0160237
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-alanyl-D-alanine + H2O = 2 D-alanine.","definition_xrefs":["PMID:7873524","RHEA:20661"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dipeptidase activity","termid":"GO:0016805"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0008233"},{"rel_name":"is_a","termid":"GO:0140096"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016787","GO:0140096","GO:0008233"],"is_obsolete":false,"name":"D-Ala-D-Ala dipeptidase activity","secondary_identifiers":["EC:3.4.13.22"],"synonyms":[{"name":"D-alanyl-D-alanine dipeptidase activity","type":"exact"}],"termid":"GO:0160237"}


id: MONDO:0006720
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Neoplasms containing cyst-like formations or producing mucin or serum.","definition_xrefs":["MESH:D018297"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial neoplasm","termid":"MONDO:0005626"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cystic, mucinous, and serous neoplasm","secondary_identifiers":["EFO:1000889","UMLS:C0206767","MEDGEN:61678"],"termid":"MONDO:0006720","xrefs":{"Monarch":{"xref_id":"0006720"}}}


id: PBO:0089952
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sphingolipid biosynthesis protein","termid":"PBO:0089952"}


id: GO:0018553
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 3-(2,3-dihydroxyphenyl)propionate + O2 = 2-hydroxy-6-keto-nona-2,4-dienedioate.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete 3-(2,3-dihydroxyphenyl)propionate 1,2-dioxygenase activity (obsolete GO:0018553)","termid":"GO:0018553"}


id: MONDO:0022622
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital disorder of glycosylation","termid":"MONDO:0015286"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0024322","MONDO:0005066"],"is_obsolete":false,"name":"congenital disorder of glycosylation syndrome type 4","secondary_identifiers":["GARD:1174"],"synonyms":[{"name":"CDG syndrome type 4","type":"exact"},{"name":"congenital disorder of glycosylation syndrome type 4","type":"exact"}],"termid":"MONDO:0022622","xrefs":{"Monarch":{"xref_id":"0022622"}}}


id: PBO:0069164
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 416, pseudogene","termid":"PBO:0069164"}


id: PR:O42997
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC27B12.07 gene.","definition_xrefs":["UniProtKB:O42997","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 C27B12.07 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC27B12.07","synonyms":[{"name":"Spom972h-SPBC27B12.07","type":"exact"}],"termid":"PR:O42997"}


id: PBO:0041484
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 11 open reading frame 97","termid":"PBO:0041484"}


id: GO:0009672
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: auxin(out) + H+(out) = auxin(in) + H+(in).","definition_xrefs":["PMID:8688077"],"direct_ancestors":[{"relation_name":"is_a","term_name":"solute:proton symporter activity","termid":"GO:0015295"},{"relation_name":"is_a","term_name":"auxin transmembrane transporter activity","termid":"GO:0080161"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"auxin:proton symporter activity","synonyms":[{"name":"auxin:hydrogen symporter activity","type":"exact"}],"termid":"GO:0009672"}


id: PBO:0042916
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CF transmembrane conductance regulator","termid":"PBO:0042916"}


id: GO:0046405
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: glycerol = 3-hydroxypropanal + H2O.","definition_xrefs":["EC:4.2.1.30","PMID:18307109"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydro-lyase activity","termid":"GO:0016836"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016829","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"glycerol dehydratase activity","secondary_identifiers":["MetaCyc:GLYCEROL-DEHYDRATASE-RXN","RHEA:19765"],"synonyms":[{"name":"glycerol dehydrase activity","type":"related"},{"name":"glycerol hydro-lyase (3-hydroxypropanal-forming)","type":"related"},{"name":"glycerol hydro-lyase activity","type":"related"}],"termid":"GO:0046405"}


id: PBO:0028013
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_protein_localization_to_microtubule_cytoskeleton","termid":"PBO:0028013"}


id: PBO:0088486
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"splicing factor Cxr1","termid":"PBO:0088486"}


id: GO:0036484
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The characteristic movement of trunk neural crest cells from the neural tube to other locations in the vertebrate embryo.","definition_xrefs":["PMID:2387238","GOC:bf","GOC:mat","GOC:PARL"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neural crest cell migration","termid":"GO:0001755"},{"relation_name":"part_of","term_name":"trunk segmentation","termid":"GO:0035290"}],"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":"trunk neural crest cell migration","synonyms":[{"name":"trunk NCC migration","type":"exact"}],"termid":"GO:0036484"}


id: GO:0060109
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The fluid-filled cuticle layer that lies between the cortical and basal layers and is characterized by the presence of regularly spaced columnar struts that lie on either side of the annular furrows and link the two surrounding layers. In C. elegans, a defined medial layer is found only in adult animals.","definition_xrefs":["ISSN:15518507","GOC:kmv","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"cuticular extracellular matrix","termid":"GO:0060102"}],"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":"medial layer of collagen and cuticulin-based cuticle extracellular matrix","synonyms":[{"name":"medial layer struts","type":"related"}],"termid":"GO:0060109"}


id: GO:0019243
data:
  {"annotated_genes":["SJAG_02988","SJAG_04674","SJAG_01596","SJAG_04726"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[61740,74579,76209,104618],"is_not":false,"summary":null,"term":"GO:0019243"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of methylglyoxal, CH3-CO-CHO, into D-lactate via the intermediate S-lactoyl-glutathione. Glutathione is used in the first step of the pathway and then regenerated in the second step.","definition_xrefs":["GOC:dph","GOC:ai","PMID:2198020"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methylglyoxal catabolic process to lactate","termid":"GO:0061727"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01596":null,"SJAG_02988":null,"SJAG_04674":null,"SJAG_04726":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098754"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0098754","GO:0044281"],"is_obsolete":false,"name":"methylglyoxal catabolic process to D-lactate via S-lactoyl-glutathione","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:PWY-5386"],"synonyms":[{"name":"D-lactate biosynthesis from methylglyoxal","type":"broad"},{"name":"D-lactate biosynthetic process from methylglyoxal","type":"broad"},{"name":"glyoxalase system","type":"related"},{"name":"methylglyoxal breakdown to D-lactate","type":"broad"},{"name":"methylglyoxal catabolism to D-lactate via S-lactoyl-glutathione","type":"exact"},{"name":"methylglyoxal degradation to D-lactate","type":"broad"},{"name":"methylglyoxal detoxification","type":"related"}],"termid":"GO:0019243","terms_by_termid":{"GO:0019243":null}}


id: PBO:0086963
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Regulatory gamma subunit of fatty acid synthase (FAS); ATPase dedicated chaperone that adapts proteasome assembly to stress; induced upon stress; interacts with Rpt6p to assist its pairing to Rpt3p and early steps in proteasome biogenesis; associates with ribosomes; heterozygous deletion demonstrated increases in chromosome instability in a rad9 deletion background; protein abundance is decreased upon intracellular iron depletion","termid":"PBO:0086963"}


id: MONDO:0011320
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An extremely rare syndrome characterized by the association of radioulnar synostosis with microcephaly, scoliosis, short stature and intellectual deficit.","definition_xrefs":["Orphanet:3268"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"radioulnar synostosis-microcephaly-scoliosis syndrome","secondary_identifiers":["MEDGEN:400399","UMLS:C1863881","OMIM:603438","GARD:394"],"synonyms":[{"name":"Giuffre-Tsukahara syndrome","type":"exact"},{"name":"Giuffré-Tsukahara syndrome","type":"exact"},{"name":"Tsukahara syndrome","type":"exact"},{"name":"Tsukahara syndrome of radioulnar synostosis, short stature, microcephaly, scoliosis, and intellectual disability","type":"related"},{"name":"Tsukahara syndrome of radioulnar synostosis, short stature, microcephaly, scoliosis, and mental retardation","type":"related"},{"name":"radioulnar synostosis with microcephaly, short stature, scoliosis, and intellectual disability","type":"related"},{"name":"radioulnar synostosis with microcephaly, short stature, scoliosis, and mental retardation","type":"related"}],"termid":"MONDO:0011320","xrefs":{"Monarch":{"xref_id":"0011320"}}}


id: PBO:0043252
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CLDN10 antisense RNA 1","termid":"PBO:0043252"}


id: PBO:0048822
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein subunit gamma 7","termid":"PBO:0048822"}


id: MONDO:0018255
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spondylometaphyseal dysplasia","termid":"MONDO:0016763"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spondylometaphyseal dysplasia, Czarny-Ratajczak type","secondary_identifiers":["Orphanet:370019","GARD:21587"],"termid":"MONDO:0018255","xrefs":{"Monarch":{"xref_id":"0018255"}}}


id: PBO:0058706
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6834","termid":"PBO:0058706"}


id: GO:0044513
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which an organism alters or subverts a G protein-coupled receptor signaling pathway in another organism via the action of a venom.","definition_xrefs":["GOC:fj","GOC:jl","PMID:8405712"],"direct_ancestors":[{"relation_name":"is_a","term_name":"venom-mediated perturbation of signal transduction","termid":"GO:0044509"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"venom-mediated perturbation of G protein-coupled receptor signaling pathway","synonyms":[{"name":"envenomation resulting in modulation of G protein-coupled receptor activity in another organism","type":"narrow"},{"name":"envenomation resulting in modulation of G protein-coupled receptor activity in other organism","type":"exact"},{"name":"envenomation resulting in modulation of G-protein coupled receptor activity in other organism","type":"exact"}],"termid":"GO:0044513"}


id: GO:1900112
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of histone H3-K9 trimethylation.","definition_xrefs":["GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of histone H3-K9 trimethylation (obsolete GO:1900112)","termid":"GO:1900112"}


id: PBO:0057901
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3202-2","termid":"PBO:0057901"}


id: PBO:0002643
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1.1.1.25","termid":"PBO:0002643"}


id: PBO:0042544
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclin dependent kinase 9","termid":"PBO:0042544"}


id: GO:1903191
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of glyoxal.","definition_xrefs":["GOC:PARL","GO_REF:0000068","GOC:bf","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aldehyde biosynthetic process","termid":"GO:0046184"},{"relation_name":"is_a","term_name":"glyoxal metabolic process","termid":"GO:1903189"}],"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":"glyoxal biosynthetic process","synonyms":[{"name":"glyoxal anabolism","type":"exact"},{"name":"glyoxal biosynthesis","type":"exact"},{"name":"glyoxal formation","type":"exact"},{"name":"glyoxal synthesis","type":"exact"}],"termid":"GO:1903191"}


id: PBO:0017569
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diacylglycerol cholinephosphotransferase/ diacylglycerol ethanolaminesphotransferase Ept1 (predicted)","termid":"PBO:0017569"}


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:mtg_sensu","GOC:bf"],"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: PBO:0030420
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_sterol_binding","termid":"PBO:0030420"}


id: GO:0015432
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: bile acid(in) + ATP + H2O -> bile acid(out) + ADP + phosphate.","definition_xrefs":["RHEA:50048"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bile acid transmembrane transporter activity","termid":"GO:0015125"},{"relation_name":"is_a","term_name":"ATPase-coupled monocarboxylic acid transmembrane transporter activity","termid":"GO:0033285"},{"relation_name":"is_a","term_name":"ATPase-coupled lipid transmembrane transporter activity","termid":"GO:0034040"},{"relation_name":"is_a","term_name":"ABC-type transporter activity","termid":"GO:0140359"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"ABC-type bile acid transporter activity","secondary_identifiers":["TC:3.A.1.207.2","Reactome:R-HSA-194153","Reactome:R-HSA-5678517","Reactome:R-HSA-193362"],"synonyms":[{"name":"ATP-dependent bile acid transmembrane transporter activity","type":"related"},{"name":"ATPase-coupled bile acid transmembrane transporter activity","type":"related"},{"name":"bile acid porter activity","type":"narrow"},{"name":"bile acid-exporting ATPase activity","type":"narrow"}],"termid":"GO:0015432"}


id: SO:0001406
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A post translationally modified arginine amino acid feature.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified_amino_acid_feature","termid":"SO:0001385"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"modified_L_arginine","secondary_identifiers":["MOD:00902"],"synonyms":[{"name":"ModArg","type":"exact"},{"name":"modified L arginine","type":"exact"},{"name":"modified L-arginine","type":"exact"}],"termid":"SO:0001406"}


id: PBO:0084087
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Guanine nucleotide exchange factor for the GTPase Gtr1p; subunit of the HOPS endocytic tethering complex; vacuole membrane protein; functions as a Rab GTPase effector, interacting with both GTP- and GDP-bound conformations of Ypt7p; facilitates tethering and promotes membrane fusion events at the late endosome and vacuole; required for both membrane and protein trafficking; component of vacuole-mitochondrion contacts (vCLAMPs) important for lipid transfer between organelles","termid":"PBO:0084087"}


id: PBO:0110121
data:
  {"annotation_feature_type":"gene","cv_name":"pubprop_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_file_curator","termid":"PBO:0110121"}


id: PBO:0038392
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_during","termid":"PBO:0038392"}


id: MONDO:0014503
data:
  {"annotated_genes":["SJAG_05212"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88502],"is_not":false,"summary":null,"term":"MONDO:0014503"}]},"cv_name":"mondo","definition":"Any autosomal recessive congenital cerebellar ataxia in which the cause of the disease is a mutation in the CWF19L1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"autosomal recessive congenital cerebellar ataxia","termid":"MONDO:0020043"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05212":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005559"],"is_obsolete":false,"name":"autosomal recessive spinocerebellar ataxia 17","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:863738","UMLS:C4015301","Orphanet:453521","OMIM:616127","DOID:0080064","GARD:17786"],"synonyms":[{"name":"CWF19L1 autosomal recessive congenital cerebellar ataxia","type":"exact"},{"name":"SCAR17","type":"exact"},{"name":"autosomal recessive cerebellar ataxia due to CWF19L1 deficiency","type":"related"},{"name":"autosomal recessive congenital cerebellar ataxia caused by mutation in CWF19L1","type":"exact"},{"name":"autosomal recessive spinocerebellar ataxia type 17","type":"exact"},{"name":"spinocerebellar ataxia autosomal recessive type 17","type":"exact"},{"name":"spinocerebellar ataxia, autosomal recessive 17","type":"related"},{"name":"spinocerebellar ataxia, autosomal recessive type 17","type":"exact"}],"termid":"MONDO:0014503","terms_by_termid":{"MONDO:0014503":null},"xrefs":{"Monarch":{"xref_id":"0014503"}}}


id: PBO:0063088
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"progestin and adipoQ receptor family member 6","termid":"PBO:0063088"}


id: PBO:0058235
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4524a","termid":"PBO:0058235"}


id: MONDO:1011413
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Paroxysmal nocturnal hemoglobinuria that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of glycosylation, non-human animal","termid":"MONDO:1011314"},{"relation_name":"is_a","term_name":"renal disease, non-human animal","termid":"MONDO:1011909"},{"relation_name":"is_a","term_name":"anemia, non-human animal","termid":"MONDO:1012981"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paroxysmal nocturnal hemoglobinuria, non-human animal","secondary_identifiers":["OMIA:002372"],"termid":"MONDO:1011413","xrefs":{"Monarch":{"xref_id":"1011413"}}}


id: PBO:0029760
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-viable_after_spore_germination_with_elongated_germ_tube","termid":"PBO:0029760"}


id: MONDO:0005873
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infections of the nervous system caused by fungi of the genus aspergillus, most commonly aspergillus fumigatus. Aspergillus infections may occur in immunocompetent hosts, but are more prevalent in individuals with immunologic deficiency syndromes. The organism may spread to the nervous system from focal infections in the lung, mastoid region, sinuses, inner ear, bones, eyes, gastrointestinal tract, and heart. Sinus infections may be locally invasive and enter the intracranial compartment, producing meningitis, fungal; cranial neuropathies; and abscesses in the frontal lobes of the brain. (From Joynt, Clinical Neurology, 1998, Ch 27, pp62-3)","definition_xrefs":["MESH:D020953"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aspergillosis","termid":"MONDO:0005657"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuroaspergillosis","secondary_identifiers":["UMLS:C0752342","DOID:13565","MEDGEN:199873"],"termid":"MONDO:0005873","xrefs":{"Monarch":{"xref_id":"0005873"}}}


id: PBO:0000637
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SWI/SNF complex subunit Snf30","termid":"PBO:0000637"}


id: PBO:0068223
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 530","termid":"PBO:0068223"}


id: PBO:0049220
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GRK3 antisense RNA 1","termid":"PBO:0049220"}


id: PBO:0031168
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_amino_acid_import","termid":"PBO:0031168"}


id: PBO:0108683
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RabGAP Gyp7","termid":"PBO:0108683"}


id: PBO:0116604
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lung cancer associated lncRNA targeting TOP2A","termid":"PBO:0116604"}


id: PBO:0017842
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutathione transmembrane transporter Pgt1","termid":"PBO:0017842"}


id: MONDO:0005155
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder characterized by replacement of the liver parenchyma with fibrous tissue and regenerative nodules. It is usually caused by alcoholism, hepatitis B, and hepatitis C. Complications include the development of ascites, esophageal varices, bleeding, and hepatic encephalopathy.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"liver disorder","termid":"MONDO:0005154"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0002515","MONDO:0004335"],"is_obsolete":false,"name":"cirrhosis of liver","secondary_identifiers":["MEDGEN:7368","NANDO:2200937","SCTID:19943007","EFO:0001422","ICD9:571.5","UMLS:C0023890","NCIT:C2951","MESH:D008103","NANDO:2100268","DOID:5082"],"synonyms":[{"name":"cirrhosis","type":"exact"},{"name":"cirrhosis of liver","type":"exact"},{"name":"liver cirrhosis","type":"related"}],"termid":"MONDO:0005155","xrefs":{"Monarch":{"xref_id":"0005155"}}}


id: MONDO:0003218
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A lesion in which the normally situated glands are partially or completely replaced by atypical cells with malignant characteristics.","definition_xrefs":["NCIT:C4123"],"direct_ancestors":[{"relation_name":"is_a","term_name":"in situ carcinoma","termid":"MONDO:0004647"},{"relation_name":"is_a","term_name":"adenocarcinoma","termid":"MONDO:0004970"}],"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":"adenocarcinoma in situ","secondary_identifiers":["UMLS:C0334276","MESH:D065311","ONCOTREE:AIS","MEDGEN:87203","DOID:4943","ICDO:8140/2"],"synonyms":[{"name":"AIS","type":"related"},{"name":"adenocarcinoma in situ","type":"exact"}],"termid":"MONDO:0003218","xrefs":{"Monarch":{"xref_id":"0003218"}}}


id: PBO:0054564
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 1966","termid":"PBO:0054564"}


id: PBO:0001931
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial inner membrane protein involved in cytochrome c oxidase assembly Cox16 (predicted)","termid":"PBO:0001931"}


id: PR:O13682
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- swr1 gene.","definition_xrefs":["UniProtKB:O13682","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":"helicase swr1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC11E3.01c","synonyms":[{"name":"Spom972h-swr1","type":"exact"}],"termid":"PR:O13682"}


id: PBO:0072889
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"strawberry notch homolog 1","termid":"PBO:0072889"}


id: PBO:0050843
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inhibitor of Bruton tyrosine kinase","termid":"PBO:0050843"}


id: GO:0045977
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of progression through the embryonic mitotic cell cycle.","definition_xrefs":["GOC:go_curators","GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mitotic cell cycle, embryonic","termid":"GO:0009794"},{"relation_name":"is_a","term_name":"positive regulation of mitotic cell cycle","termid":"GO:0045931"},{"relation_name":"positively_regulates","term_name":"mitotic cell cycle, embryonic","termid":"GO:0045448"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"positive regulation of mitotic cell cycle, embryonic","synonyms":[{"name":"activation of mitotic cell cycle, embryonic","type":"narrow"},{"name":"positive regulation of embryonic mitotic cell cycle","type":"exact"},{"name":"positive regulation of embryonic mitotic cell cycle progression","type":"exact"},{"name":"positive regulation of progression through embryonic mitotic cell cycle","type":"exact"},{"name":"stimulation of mitotic cell cycle, embryonic","type":"narrow"},{"name":"up regulation of mitotic cell cycle, embryonic","type":"exact"},{"name":"up-regulation of mitotic cell cycle, embryonic","type":"exact"},{"name":"upregulation of mitotic cell cycle, embryonic","type":"exact"}],"termid":"GO:0045977"}


id: FYPO:0001962
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which a protein phosphatase activity is absent.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein phosphatase activity","termid":"FYPO:0001756"},{"relation_name":"is_a","term_name":"abolished phosphatase activity","termid":"FYPO:0004303"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0000654","FYPO:0001985","FYPO:0000652","FYPO:0000707"],"is_obsolete":false,"name":"abolished protein phosphatase activity","synonyms":[{"name":"protein phosphatase activity abolished","type":"exact"}],"termid":"FYPO:0001962"}


id: GO:0008457
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: UDP-N-acetyl-D-glucosamine + beta-D-galactosyl-1,4-N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,4-beta-D-glucosylceramide = UDP + N-acetyl-D-glucosaminyl-1,3-beta-D-galactosyl-1,4-N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,4-beta-D-glucosylceramide.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete beta-galactosyl-N-acetylglucosaminylgalactosylglucosyl-ceramide beta-1,3-acetylglucosaminyltransferase activity (obsolete GO:0008457)","synonyms":[{"name":"UDP-N-acetyl-D-glucosamine:beta-D-galactosyl-1,4-N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,4-beta-D-glucosylceramide beta-1,3-acetylglucosaminyltransferase activity","type":"exact"},{"name":"poly-N-acetyllactosamine extension enzyme activity","type":"broad"}],"termid":"GO:0008457"}


id: PBO:0074110
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 29 member 2","termid":"PBO:0074110"}


id: PBO:0084086
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Guanine nucleotide exchange factor for Gpa1p; amplifies G protein signaling; functions as a chaperone under ATP-depleted oxidative stress conditions; subunit of GET complex, involved in ATP dependent Golgi to ER trafficking and insertion of tail-anchored (TA) proteins into ER membrane under non-stress conditions; binds as dimer to transmembrane domain (TMD) cargo, shielding TMDs from aqueous solvent; protein abundance increases under DNA replication stress","termid":"PBO:0084086"}


id: PBO:0049326
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"general transcription factor IIB","termid":"PBO:0049326"}


id: MONDO:1012085
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"tetragametic chimerism, non-human animal","termid":"MONDO:1011918"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tetragametic chimerism, cattle","secondary_identifiers":["OMIA:000393-9913"],"termid":"MONDO:1012085","xrefs":{"Monarch":{"xref_id":"1012085"}}}


id: GO:0016328
data:
  {"annotated_genes":["SJAG_00053","SJAG_01564","SJAG_02613","SJAG_03247","SJAG_04413"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[92218,93295,99269,119395,120558],"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:hb","GOC:pr","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":5,"genes_by_uniquename":{"SJAG_00053":null,"SJAG_01564":null,"SJAG_02613":null,"SJAG_03247":null,"SJAG_04413":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0005575"}],"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: PBO:0046344
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 2","termid":"PBO:0046344"}


id: GO:0075136
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of the symbiont or its cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of detecting molecules of its host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biological process involved in interaction with host","termid":"GO:0051701"},{"relation_name":"is_a","term_name":"response to other organism","termid":"GO:0051707"}],"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 host","synonyms":[{"name":"response of symbiont to host","type":"related"}],"termid":"GO:0075136"}


id: PBO:0084723
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial inner membrane protein; required for assembly of cytochrome c oxidase","termid":"PBO:0084723"}


id: GO:0034573
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: didemethylisoproturon + H2O = carbamic acid + 4-isopropylaniline.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete didemethylisoproturon amidohydrolase activity (obsolete GO:0034573)","termid":"GO:0034573"}


id: PBO:0081073
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger DHHC-type palmitoyltransferase 5","termid":"PBO:0081073"}


id: GO:0003416
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The increase in size or mass of an endochondral bone that contributes to the shaping of the bone.","definition_xrefs":["GOC:ascb_2009","GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bone growth","termid":"GO:0098868"}],"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":"endochondral bone growth","termid":"GO:0003416"}


id: PBO:0077640
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thioredoxin related transmembrane protein 4","termid":"PBO:0077640"}


id: MONDO:0019053
data:
  {"annotated_genes":["SJAG_02848","SJAG_05950","SJAG_03440","SJAG_04823","SJAG_03781","SJAG_02384","SJAG_00702","SJAG_04763","SJAG_02693","SJAG_00326","SJAG_02619","SJAG_01165","SJAG_00891","SJAG_02997","SJAG_04146","SJAG_02788","SJAG_03324"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87753],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013571"},{"annotations":[88094],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009958"},{"annotations":[87311,87310],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013726"},{"annotations":[89052],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013948"},{"annotations":[88682],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054549"},{"annotations":[89053],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013949"},{"annotations":[89051],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013950"},{"annotations":[89054],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013951"},{"annotations":[89055],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013952"},{"annotations":[89013,89012],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013967"},{"annotations":[88642],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008953"},{"annotations":[89003],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011101"},{"annotations":[88630],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008954"},{"annotations":[88914],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008736"},{"annotations":[89035],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013927"},{"annotations":[89037],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013930"},{"annotations":[89038],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013931"},{"annotations":[89040],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013936"},{"annotations":[89042],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013937"},{"annotations":[89043],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013938"},{"annotations":[89041],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013939"},{"annotations":[89046],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013942"},{"annotations":[89044],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013943"},{"annotations":[89049],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013945"},{"annotations":[88091],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009959"},{"annotations":[87828],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008972"},{"annotations":[87673],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014743"}]},"cv_name":"mondo","definition":"A group of congenital disorders of lipid metabolism, caused by loss of the normal peroxisomes. Signs and symptoms include developmental delays, intellectual disability, characteristic facial dysmorphic features, hepatomegaly, and hypotonia.","definition_xrefs":["NCIT:C85005"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"metabolic epilepsy","termid":"MONDO:0100033"},{"relation_name":"is_a","term_name":"inborn errors of metabolism","termid":"MONDO:0019052"}],"gene_count":17,"genes_by_uniquename":{"SJAG_00326":null,"SJAG_00702":null,"SJAG_00891":null,"SJAG_01165":null,"SJAG_02384":null,"SJAG_02619":null,"SJAG_02693":null,"SJAG_02788":null,"SJAG_02848":null,"SJAG_02997":null,"SJAG_03324":null,"SJAG_03440":null,"SJAG_03781":null,"SJAG_04146":null,"SJAG_04763":null,"SJAG_04823":null,"SJAG_05950":null},"genotype_count":0,"in_subsets":["pombe_mondo_slim"],"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"peroxisomal disease","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD9:277.89","MEDGEN:129185","DOID:906","NANDO:2100166","Orphanet:68373","NANDO:1200758","SCTID:238059005","UMLS:C0282528","icd11.foundation:782299726","GARD:18885","ICD9:277.86"],"synonyms":[{"name":"disorder of peroxisomal function","type":"exact"},{"name":"peroxisomal disease","type":"exact"},{"name":"peroxisomal disorder","type":"exact"},{"name":"peroxisomal function disorder","type":"exact"}],"termid":"MONDO:0019053","terms_by_termid":{"MONDO:0008736":null,"MONDO:0008953":null,"MONDO:0008954":null,"MONDO:0008972":null,"MONDO:0009958":null,"MONDO:0009959":null,"MONDO:0011101":null,"MONDO:0013571":null,"MONDO:0013726":null,"MONDO:0013927":null,"MONDO:0013930":null,"MONDO:0013931":null,"MONDO:0013936":null,"MONDO:0013937":null,"MONDO:0013938":null,"MONDO:0013939":null,"MONDO:0013942":null,"MONDO:0013943":null,"MONDO:0013945":null,"MONDO:0013948":null,"MONDO:0013949":null,"MONDO:0013950":null,"MONDO:0013951":null,"MONDO:0013952":null,"MONDO:0013967":null,"MONDO:0014743":null,"MONDO:0054549":null},"xrefs":{"Monarch":{"xref_id":"0019053"}}}


id: PBO:0083632
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EH domain-containing protein involved in endocytosis; actin cytoskeletal organization and cell wall morphogenesis; forms a complex with Sla1p and Pan1p","termid":"PBO:0083632"}


id: MONDO:0002265
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Motor behavior that is repetitive, often seemingly driven, and nonfunctional. This behavior markedly interferes with normal activities or results in severe bodily self-injury. The behavior is not due to the direct physiological effects of a substance or a general medical condition. (dsm-iv, 1994)","definition_xrefs":["MESH:D019956"],"direct_ancestors":[{"relation_name":"is_a","term_name":"specific developmental disorder","termid":"MONDO:0000592"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"stereotypic movement disorder","secondary_identifiers":["ICD9:307.3","SCTID:5507002","MEDGEN:21320","UMLS:C0038273","DOID:2303"],"synonyms":[{"name":"stereotyped repetitive movements","type":"exact"},{"name":"stereotyped repetitive movements NOS (finding)","type":"exact"},{"name":"stereotypy habit disorder","type":"exact"}],"termid":"MONDO:0002265","xrefs":{"Monarch":{"xref_id":"0002265"}}}


id: PBO:0016520
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae CAK1","termid":"PBO:0016520"}


id: FYPO:0002781
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which transcription occurs to a greater extent than normal during a cellular response to nitric oxide. All genes, or a specific subset of genes, may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased transcription during vegetative growth","termid":"FYPO:0000780"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0006551","FYPO:0000294","FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"increased transcription during cellular response to nitric oxide","synonyms":[{"name":"increased transcription during cellular response to NO during vegetative growth","type":"exact"},{"name":"increased transcription during cellular response to nitric oxide during mitotic cell cycle","type":"related"},{"name":"increased transcription during cellular response to nitric oxide during vegetative growth","type":"exact"},{"name":"increased transcription during cellular response to nitric oxide stress","type":"related"}],"termid":"FYPO:0002781"}


id: PBO:0117015
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KIAA1191 antisense RNA 1","termid":"PBO:0117015"}


id: PBO:0064200
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"placenta associated 8","termid":"PBO:0064200"}


id: GO:0016287
data:
  {"annotated_genes":["SJAG_02654","SJAG_03305"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[71825,72289],"is_not":false,"summary":null,"term":"GO:0016287"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: acyl-CoA + glycerone phosphate = 1-acylglycerone 3-phosphate + CoA.","definition_xrefs":["RHEA:17657","EC:2.3.1.42"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-acetyltransferase activity","termid":"GO:0016413"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02654":null,"SJAG_03305":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016746","GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"glycerone-phosphate O-acyltransferase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["KEGG_REACTION:R01013","Reactome:R-HSA-75879","MetaCyc:2.3.1.42-RXN","Reactome:R-HSA-1483002"],"synonyms":[{"name":"acyl-CoA:glycerone-phosphate O-acyltransferase activity","type":"related"},{"name":"dihydroxyacetone phosphate acyltransferase activity","type":"related"}],"termid":"GO:0016287","terms_by_termid":{"GO:0016287":null}}


id: MONDO:0000470
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease involving the endocardium.","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":"endocardium disorder","secondary_identifiers":["DOID:0050825","MEDGEN:678520","UMLS:C0854140","SCTID:123596001"],"synonyms":[{"name":"disease of endocardium","type":"exact"},{"name":"disease or disorder of endocardium","type":"exact"},{"name":"disorder of endocardium","type":"exact"},{"name":"endocardial disease","type":"exact"},{"name":"endocardiopathy","type":"related"},{"name":"endocardium disease","type":"exact"},{"name":"endocardium disease or disorder","type":"exact"}],"termid":"MONDO:0000470","xrefs":{"Monarch":{"xref_id":"0000470"}}}


id: MONDO:1010022
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ventricular septal defect that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of development or morphogenesis, non-human animal","termid":"MONDO:1011313"},{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"heart disorder, non-human animal","termid":"MONDO:1012982"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ventricular septal defect, non-human animal","secondary_identifiers":["OMIA:001041"],"termid":"MONDO:1010022","xrefs":{"Monarch":{"xref_id":"1010022"}}}


id: MOD:00774
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"Natural or modified residues with a mass of 243.02-243.03 Da.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"residues isobaric at a resolution below 0.01 Da","termid":"MOD:00770"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"residues isobaric at 243.02-243.03 Da","termid":"MOD:00774"}


id: FYPO:0001610
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of L-lysine measured in the vacuole is lower than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased level of substance in vacuole","termid":"FYPO:0001602"},{"relation_name":"is_a","term_name":"decreased cellular lysine level","termid":"FYPO:0001619"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"decreased vacuolar lysine level","synonyms":[{"name":"decreased level of lysine in vacuole","type":"exact"},{"name":"decreased vacuolar L-lysine level","type":"exact"},{"name":"decreased vacuolar lysine level during mitotic cell cycle","type":"related"},{"name":"decreased vacuolar lysine level during vegetative growth","type":"exact"},{"name":"reduced level of lysine in vacuole","type":"exact"},{"name":"reduced vacuolar lysine level","type":"exact"}],"termid":"FYPO:0001610"}


id: PBO:0042787
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"centrosomal protein 152","termid":"PBO:0042787"}


id: GO:0060854
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of the coordinated growth and sprouting of lymph vessels giving rise to the organized lymphatic system.","definition_xrefs":["GOC:tb","GOC:sdb_2009","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"branching morphogenesis of an epithelial tube","termid":"GO:0048754"},{"relation_name":"part_of","term_name":"lymphangiogenesis","termid":"GO:0001946"}],"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":"branching involved in lymph vessel morphogenesis","synonyms":[{"name":"patterning of lymph vessels","type":"broad"}],"termid":"GO:0060854"}


id: PBO:0001502
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA ligase Trl1 (predicted)","termid":"PBO:0001502"}


id: PR:Q9UUE2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- cnt5 gene.","definition_xrefs":["UniProtKB:Q9UUE2","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":"protein csx2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC17G9.08c","synonyms":[{"name":"Spom972h-cnt5","type":"exact"}],"termid":"PR:Q9UUE2"}


id: MOD:00310
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-arginine residue to N5-methyl-L-arginine.","definition_xrefs":["PubMed:9792625","RESID:AA0305","PubMed:11875433","PubMed:9873020"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monomethylated L-arginine","termid":"MOD:00414"},{"relation_name":"is_a","term_name":"N-methylated residue","termid":"MOD:00602"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00427"}],"interesting_parent_ids":["MOD:00427"],"is_obsolete":false,"name":"N5-methyl-L-arginine","synonyms":[{"name":"(2S)-2-amino-5-(N-methylcarbamimidamido)pentanoic acid","type":"exact"},{"name":"MOD_RES N5-methylarginine","type":"exact"},{"name":"Methyl","type":"related"},{"name":"Methylation","type":"related"},{"name":"N5-carbamimidoyl-N5-methyl-L-ornithine","type":"exact"},{"name":"N5-methyl-L-arginine","type":"exact"},{"name":"N5-methylated L-arginine","type":"exact"},{"name":"N5Me1Arg","type":"exact"},{"name":"delta-N-methylarginine","type":"exact"}],"termid":"MOD:00310"}


id: PBO:0062205
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 5 subfamily A member 2","termid":"PBO:0062205"}


id: PBO:0120347
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WRN antisense RNA 1","termid":"PBO:0120347"}


id: PR:P41391
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A ran GTPase-activating protein 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO02096"],"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":"ran GTPase-activating protein 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC22E12.07","secondary_identifiers":["UniProtKB:P41391"],"synonyms":[{"name":"Spom972h-RANGAP1","type":"exact"},{"name":"protein rna1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P41391"}


id: GO:0042302
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"The action of a molecule that contributes to the structural integrity of a cuticle.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"structural molecule activity","termid":"GO:0005198"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005198"}],"interesting_parent_ids":["GO:0003674","GO:0005198"],"is_obsolete":false,"name":"structural constituent of cuticle","termid":"GO:0042302"}


id: GO:1902935
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a protein is transported to, or maintained in, a location within a septin ring.","definition_xrefs":["GO_REF:0000087","PMID:16325501","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization to cytoskeleton","termid":"GO:0044380"},{"relation_name":"is_a","term_name":"protein localization to cell cortex","termid":"GO:0072697"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"protein localization to septin ring","synonyms":[{"name":"protein localisation in septin ring","type":"exact"},{"name":"protein localisation to septin ring","type":"exact"},{"name":"protein localization in septin ring","type":"exact"}],"termid":"GO:1902935"}


id: SO:0001332
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Wybutosine is a modified guanosine base feature.","direct_ancestors":[{"relation_name":"is_a","term_name":"modified_guanosine","termid":"SO:0001276"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"wybutosine","secondary_identifiers":["RNAMOD:037"],"synonyms":[{"name":"yW","type":"exact"}],"termid":"SO:0001332"}


id: PBO:0003287
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HIRA interacting protein","termid":"PBO:0003287"}


id: GO:1903203
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of oxidative stress-induced neuron death.","definition_xrefs":["GOC:bf","GOC:PARL","GOC:TermGenie","GO_REF:0000058"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of oxidative stress-induced neuron death (obsolete GO:1903203)","synonyms":[{"name":"regulation of neuron death in response to oxidative stress","type":"exact"},{"name":"regulation of neuronal cell death in response to oxidative stress","type":"exact"}],"termid":"GO:1903203"}


id: PBO:0088877
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"copper-binding protein of the mitochondrial inner membrane Cmc2","termid":"PBO:0088877"}


id: PBO:0065337
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protogenin","termid":"PBO:0065337"}


id: GO:2001110
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of lens epithelial cell proliferation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of epithelial cell proliferation","termid":"GO:0050680"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"is_a","term_name":"regulation of lens epithelial cell proliferation","termid":"GO:2001109"},{"relation_name":"negatively_regulates","term_name":"lens epithelial cell proliferation","termid":"GO:0097166"}],"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 lens epithelial cell proliferation","termid":"GO:2001110"}


id: PBO:0063766
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphate regulating endopeptidase X-linked","termid":"PBO:0063766"}


id: MONDO:0016078
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital arteriovenous fistula","termid":"MONDO:0020296"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital systemic arteriovenous fistula","secondary_identifiers":["GARD:18758","Orphanet:2039","UMLS:C5191839","MEDGEN:1679454"],"termid":"MONDO:0016078","xrefs":{"Monarch":{"xref_id":"0016078"}}}


id: MONDO:0015714
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"central precocious puberty","termid":"MONDO:0019165"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"secondary central precocious puberty","secondary_identifiers":["Orphanet:169618"],"termid":"MONDO:0015714","xrefs":{"Monarch":{"xref_id":"0015714"}}}


id: PBO:0075162
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nuclear ribonucleoprotein polypeptide C pseudogene 18","termid":"PBO:0075162"}


id: GO:0004776
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: GTP + succinate + CoA = GDP + succinyl-CoA + phosphate.","definition_xrefs":["RHEA:22120"],"direct_ancestors":[{"relation_name":"is_a","term_name":"succinate-CoA ligase activity","termid":"GO:0004774"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016874","GO:0003824"],"is_obsolete":false,"name":"succinate-CoA ligase (GDP-forming) activity","secondary_identifiers":["Reactome:R-HSA-71775","EC:6.2.1.4","KEGG_REACTION:R00432","MetaCyc:SUCCINATE--COA-LIGASE-GDP-FORMING-RXN"],"synonyms":[{"name":"succinate:CoA ligase (GDP-forming) activity","type":"related"},{"name":"succinyl CoA synthetase activity","type":"related"},{"name":"succinyl coenzyme A synthetase","type":"broad"},{"name":"succinyl coenzyme A synthetase (GDP-forming) activity","type":"related"},{"name":"succinyl coenzyme A synthetase (guanosine diphosphate-forming) activity","type":"related"},{"name":"succinyl-CoA synthetase (GDP-forming) activity","type":"related"}],"termid":"GO:0004776"}


id: PBO:0045599
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"double homeobox 4 like 10 (pseudogene)","termid":"PBO:0045599"}


id: PBO:0077903
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tryptase pseudogene 1","termid":"PBO:0077903"}


id: PBO:0088879
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TIP41 type 2a phosphatase regulator Tip41","termid":"PBO:0088879"}


id: PBO:0064465
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA polymerase delta 2, accessory subunit pseudogene 1","termid":"PBO:0064465"}


id: MONDO:0010797
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pearson syndrome is characterized by refractory sideroblastic anemia, vacuolization of bone marrow precursors and exocrine pancreatic dysfunction.","definition_xrefs":["Orphanet:699"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"constitutional neutropenia","termid":"MONDO:0015134"},{"relation_name":"excluded_subClassOf","term_name":"obsolete metabolic disorder with intestinal involvement (obsolete MONDO:0015188)","termid":"MONDO:0015188"},{"relation_name":"excluded_subClassOf","term_name":"obsolete syndrome with hypoparathyroidism (obsolete MONDO:0015895)","termid":"MONDO:0015895"},{"relation_name":"excluded_subClassOf","term_name":"obsolete mitochondrial oxidative phosphorylation disorder due to a large-scale single deletion of mitochondrial DNA (obsolete MONDO:0016792)","termid":"MONDO:0016792"},{"relation_name":"excluded_subClassOf","term_name":"inherited sideroblastic anemia","termid":"MONDO:0020099"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pearson syndrome","secondary_identifiers":["DOID:0060067","UMLS:C0342784","MEDGEN:87459","SCTID:237985009","ICD9:277.87","NCIT:C115326","MedDRA:10062941","icd11.foundation:452521132","GARD:7343","OMIM:557000"],"synonyms":[{"name":"Pearson marrow-pancreas syndrome","type":"exact"},{"name":"Pearson's marrow/pancreas syndrome","type":"related"},{"name":"Pearson's syndrome","type":"related"},{"name":"sideroblastic Anaemia with marrow cell vacuolization and exocrine pancreatic dysfunction","type":"related"},{"name":"sideroblastic Anemia with marrow cell vacuolization and exocrine pancreatic dysfunction","type":"related"},{"name":"sideroblastic anaemia with marrow cell vacuolization and exocrine pancreatic dysfunction (formerly)","type":"related"},{"name":"sideroblastic anemia with marrow cell vacuolization and exocrine pancreatic dysfunction (formerly)","type":"related"}],"termid":"MONDO:0010797","xrefs":{"Monarch":{"xref_id":"0010797"}}}


id: PBO:0046336
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ectonucleotide pyrophosphatase/phosphodiesterase 1","termid":"PBO:0046336"}


id: FYPO:0008057
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed  ability of an enzyme to catalyze consecutive reactions without releasing the substrate (i.e. template) is abnormal.","direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal catalytic activity","termid":"FYPO:0000661"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000661"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0000661","FYPO:0001985","FYPO:0000654","FYPO:0000652"],"is_obsolete":false,"name":"abnormal enzyme processivity","termid":"FYPO:0008057"}


id: GO:0002621
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of non-professional antigen presenting cell antigen processing and presentation.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of antigen processing and presentation","termid":"GO:0002579"},{"relation_name":"is_a","term_name":"regulation of non-professional antigen presenting cell antigen processing and presentation","termid":"GO:0002619"},{"relation_name":"positively_regulates","term_name":"non-professional antigen presenting cell antigen processing and presentation","termid":"GO:0002473"}],"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 non-professional antigen presenting cell antigen processing and presentation","synonyms":[{"name":"activation of non-professional antigen presenting cell antigen processing and presentation","type":"narrow"},{"name":"stimulation of non-professional antigen presenting cell antigen processing and presentation","type":"narrow"},{"name":"up regulation of non-professional antigen presenting cell antigen processing and presentation","type":"exact"},{"name":"up-regulation of non-professional antigen presenting cell antigen processing and presentation","type":"exact"},{"name":"upregulation of non-professional antigen presenting cell antigen processing and presentation","type":"exact"}],"termid":"GO:0002621"}


id: PBO:0042248
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-C motif chemokine receptor 10","termid":"PBO:0042248"}


id: PBO:0080923
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta pseudogene 1","termid":"PBO:0080923"}


id: MONDO:0033864
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":"movement disorder","termid":"MONDO:0005395"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome","secondary_identifiers":["UMLS:C4748715","GARD:17962","Orphanet:522077","MEDGEN:1648431","OMIM:618218"],"synonyms":[{"name":"Baker-Gordon syndrome","type":"exact"}],"termid":"MONDO:0033864","xrefs":{"Monarch":{"xref_id":"0033864"}}}


id: PBO:0087058
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribosomal 60S subunit protein L28; homologous to mammalian ribosomal protein L27A and bacterial L15; may have peptidyl transferase activity; can mutate to cycloheximide resistance","termid":"PBO:0087058"}


id: GO:0072220
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the metanephric descending thin limb over time, from its formation to the mature structure. The metanephric descending thin limb is a part of the metanephric loop of Henle situated just after the proximal straight tubule (S3). It extends to the tip of the metanephric loop of Henle.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"descending thin limb development","termid":"GO:0072022"},{"relation_name":"part_of","term_name":"metanephric loop of Henle development","termid":"GO:0072236"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"metanephric descending thin limb development","termid":"GO:0072220"}


id: GO:2000522
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of immunological synapse formation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cellular process","termid":"GO:0048522"},{"relation_name":"is_a","term_name":"regulation of immunological synapse formation","termid":"GO:2000520"},{"relation_name":"positively_regulates","term_name":"immunological synapse formation","termid":"GO:0001771"}],"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 immunological synapse formation","synonyms":[{"name":"positive regulation of formation of immunological synapse","type":"exact"}],"termid":"GO:2000522"}


id: PBO:0060576
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NBPF member 12","termid":"PBO:0060576"}


id: PBO:0070387
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rhophilin associated tail protein 1B","termid":"PBO:0070387"}


id: GO:0070943
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed killing of a symbiont target cell by a neutrophil. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["ISBN:0781765196","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"killing by host of symbiont cells","termid":"GO:0051873"},{"relation_name":"is_a","term_name":"neutrophil mediated cytotoxicity","termid":"GO:0070942"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"neutrophil-mediated killing of symbiont cell","synonyms":[{"name":"neutrophil mediated killing of symbiont cell","type":"exact"}],"termid":"GO:0070943"}


id: PBO:0027894
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_histone_methyltransferase_activity_(H3-K4_specific)","termid":"PBO:0027894"}


id: GO:0032059
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A cell extension caused by localized decoupling of the cytoskeleton from the plasma membrane and characterized by rapid formation, rounded shape, and scarcity of organelles within the protrusion. Blebs are formed during apoptosis and other cellular processes, including cell locomotion, cell division, and as a result of physical or chemical stresses.","definition_xrefs":["GOC:mtg_apoptosis","PMID:12083798","PMID:16624291","Wikipedia:Bleb_(cell_biology)"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane bounded cell projection","termid":"GO:0120025"}],"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":"bleb","synonyms":[{"name":"plasma membrane bleb","type":"exact"}],"termid":"GO:0032059"}


id: GO:0035415
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of mitotic prometaphase, the stage following prophase in mitosis (in higher eukaryotes) during which the nuclear envelope is disrupted and breaks into membrane vesicles, and the spindle microtubules enter the nuclear region.","definition_xrefs":["GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of mitotic prometaphase (obsolete GO:0035415)","synonyms":[{"name":"regulation of mitotic prometaphase","type":"exact"}],"termid":"GO:0035415"}


id: PBO:0047230
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 230 member B","termid":"PBO:0047230"}


id: PBO:0076124
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"syntaxin binding protein 6","termid":"PBO:0076124"}


id: GO:0043576
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the process of gaseous exchange between an organism and its environment.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of multicellular organismal process","termid":"GO:0051239"},{"relation_name":"regulates","term_name":"respiratory gaseous exchange by respiratory system","termid":"GO:0007585"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of respiratory gaseous exchange","termid":"GO:0043576"}


id: GO:0102172
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 4alpha-hydroxymethyl,4beta,14alpha-dimethyl-9beta,19-cyclo-5alpha-ergost-24(241)-en-3beta-ol + NADH + O2 + H+ = 4alpha-formyl,4beta,14alpha-dimethyl-9beta,19-cyclo-5alpha-ergost-24(241)-en-3beta-ol + NAD + 2 H2O.","definition_xrefs":["RHEA:58860","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen","termid":"GO:0016709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"4alpha-hydroxymethyl,4beta,14alpha-dimethyl-9beta,19-cyclo-5alpha-ergost-24(241)-en-3beta-ol-4alpha-methyl oxidase activity","secondary_identifiers":["MetaCyc:RXN-11925"],"termid":"GO:0102172"}


id: PBO:0075502
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spermatogenesis and centriole associated 1 like","termid":"PBO:0075502"}


id: GO:0001955
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A developmental process, independent of morphogenetic (shape) change, that is required for a blood vessel to attain its fully functional state.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure maturation","termid":"GO:0071695"},{"relation_name":"part_of","term_name":"blood vessel development","termid":"GO:0001568"}],"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":"blood vessel maturation","termid":"GO:0001955"}


id: PBO:0064966
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRAME family member 19","termid":"PBO:0064966"}


id: PBO:0114089
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F1-FO ATP synthase peripheral stalk-membrane subunit, Atp4","termid":"PBO:0114089"}


id: GO:1990078
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that inhibits multiple events of replication initiation during one replication cycle.","definition_xrefs":["PMID:21708944","GOC:bhm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"replisome","termid":"GO:0030894"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"part_of","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0005694","GO:0032991"],"is_obsolete":false,"name":"replication inhibiting complex","termid":"GO:1990078"}


id: GO:0044079
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont alters or subverts the regulated release of a neurotransmitter from a cell in its host organism.","definition_xrefs":["MITRE:tk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host cellular process","termid":"GO:0044068"}],"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 neurotransmitter secretion","synonyms":[{"name":"modification by symbiont of host neurotransmitter secretion","type":"exact"},{"name":"modulation by symbiont of host neurotransmitter secretion","type":"exact"},{"name":"modulation of host neurotransmitter secretion by symbiont","type":"exact"},{"name":"regulation by symbiont of host neurotransmitter secretion","type":"exact"}],"termid":"GO:0044079"}


id: GO:0071446
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 salicylic acid stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to salicylic acid","termid":"GO:0009751"},{"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 salicylic acid stimulus","synonyms":[{"name":"cellular response to salicylate stimulus","type":"exact"}],"termid":"GO:0071446"}


id: PBO:0058148
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4444-1","termid":"PBO:0058148"}


id: PBO:0068521
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 116, pseudogene","termid":"PBO:0068521"}


id: GO:2000548
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of dendritic cell dendrite assembly.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of plasma membrane bounded cell projection assembly","termid":"GO:0120033"},{"relation_name":"is_a","term_name":"regulation of dendritic cell dendrite assembly","termid":"GO:2000547"},{"relation_name":"negatively_regulates","term_name":"dendritic cell dendrite assembly","termid":"GO:0097026"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"negative regulation of dendritic cell dendrite assembly","synonyms":[{"name":"negative regulation of dendritic extension","type":"related"}],"termid":"GO:2000548"}


id: SO:0000181
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A match against a translated sequence.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide_match","termid":"SO:0000347"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translated_nucleotide_match","synonyms":[{"name":"translated nucleotide match","type":"exact"}],"termid":"SO:0000181"}


id: GO:0004034
data:
  {"annotated_genes":["SJAG_03818","SJAG_02951"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[115584,115585],"is_not":false,"summary":null,"term":"GO:0004034"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: alpha-D-glucose = beta-D-glucose. Also acts on L-arabinose, D-xylose, D-galactose, maltose and lactose.","definition_xrefs":["EC:5.1.3.3"],"direct_ancestors":[{"relation_name":"is_a","term_name":"racemase and epimerase activity, acting on carbohydrates and derivatives","termid":"GO:0016857"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02951":null,"SJAG_03818":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016853","GO:0003824"],"is_obsolete":false,"name":"aldose 1-epimerase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:ALDOSE-1-EPIMERASE-RXN","Reactome:R-HSA-9931853","Reactome:R-HSA-9931926"],"synonyms":[{"name":"aldose mutarotase activity","type":"related"},{"name":"mutarotase activity","type":"related"}],"termid":"GO:0004034","terms_by_termid":{"GO:0004034":null}}


id: PBO:0066692
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RMDN2 antisense RNA 1","termid":"PBO:0066692"}


id: GO:0051541
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving elastin, a glycoprotein which is randomly coiled and crosslinked to form elastic fibers that are found in connective tissue.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycoprotein metabolic process","termid":"GO:0009100"}],"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":"elastin metabolic process","synonyms":[{"name":"elastin metabolism","type":"exact"}],"termid":"GO:0051541"}


id: PBO:0062808
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oxysterol binding protein like 8","termid":"PBO:0062808"}


id: PBO:0034026
data:
  {"annotation_feature_type":"gene","cv_name":"pubprop_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"canto_curator_name","termid":"PBO:0034026"}


id: PBO:0087603
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the CCR4-NOT1 core complex; this complex has multiple roles in the regulation of mRNA levels including regulation of transcription and destabilization of mRNA by deadenylation; basal transcription factor that increases initiation and elongation; activates the ATPase activity of Dhh1p, resulting in processing body disassembly","termid":"PBO:0087603"}


id: PBO:0047201
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 217 member A pseudogene 1","termid":"PBO:0047201"}


id: PBO:0029712
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_5-fluorouracil","termid":"PBO:0029712"}


id: PBO:0076226
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPT7 like, STAGA complex subunit gamma","termid":"PBO:0076226"}


id: PBO:0064202
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"placenta associated 9","termid":"PBO:0064202"}


id: GO:0140091
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A muscle cell-specific SWI/SNF-type complex that contains eight to fourteen proteins, including both conserved (core) and nonconserved components; contains the ATPase product of either the SMARCA4/BAF190A/BRG1 gene, the mammalian ortholog of the yeast SNF2 gene, or the SMARCA2/BAF190B/BRM gene, the mammalian ortholog of the Drosophila brm (brahma) gene, or an ortholog of either of these genes, and the muscle-specific product of the DPF3/BAF45C gene or an ortholog thereof.","definition_xrefs":["PMID:11175787","PMID:15525990","PMID:8895581","GO:bhm","PMID:8804307","PMID:12620226"],"direct_ancestors":[{"relation_name":"is_a","term_name":"SWI/SNF superfamily-type complex","termid":"GO:0070603"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005694","GO:0032991","GO:0005634","GO:0005575"],"is_obsolete":false,"name":"mBAF complex","synonyms":[{"name":"muscle-specific BAF complex","type":"exact"},{"name":"muscle-specific SWI/SNF complex","type":"exact"},{"name":"muscle-type BAF complex","type":"exact"},{"name":"muscle-type SWI/SNF complex","type":"exact"}],"termid":"GO:0140091"}


id: MONDO:0037251
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A chronic congestive enlargement of the spleen leading to the destruction of blood cells resulting in pancytopenia.","definition_xrefs":["PMID:35800794"],"direct_ancestors":[{"relation_name":"is_a","term_name":"splenic disorder","termid":"MONDO:0002332"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"congestive splenomegaly","secondary_identifiers":["UMLS:C0154307","MESH:C537903","SCTID:19058002","GARD:5888","MEDGEN:56339"],"synonyms":[{"name":"Banti syndrome","type":"exact"},{"name":"Banti's disease","type":"exact"},{"name":"Banti's spleen","type":"exact"},{"name":"Banti's syndrome","type":"exact"},{"name":"fibrocongestive splenomegaly","type":"related"},{"name":"idiopathic congestive splenomegaly","type":"related"},{"name":"idiopathic portal hypertension","type":"related"}],"termid":"MONDO:0037251","xrefs":{"Monarch":{"xref_id":"0037251"}}}


id: MONDO:0020146
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete major induction processes eye anomaly (obsolete MONDO:0020146)","secondary_identifiers":["Orphanet:98554"],"termid":"MONDO:0020146","xrefs":{"Monarch":{"xref_id":"0020146"}}}


id: MONDO:0010782
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"myopathy, lactic acidosis, and sideroblastic anemia","termid":"MONDO:0000863"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005066","MONDO:0005336","MONDO:0002280","MONDO:0004069"],"is_obsolete":false,"name":"myopathy, lactic acidosis, and sideroblastic anemia 3","secondary_identifiers":["MEDGEN:903059","GARD:15312","OMIM:500011","UMLS:C4225415","DOID:0111184"],"synonyms":[{"name":"MLASA3","type":"related"},{"name":"myopathy, lactic acidosis, and sideroblastic anaemia type 3","type":"exact"},{"name":"myopathy, lactic acidosis, and sideroblastic anemia 3","type":"exact"},{"name":"myopathy, lactic acidosis, and sideroblastic anemia type 3","type":"exact"}],"termid":"MONDO:0010782","xrefs":{"Monarch":{"xref_id":"0010782"}}}


id: MONDO:0017482
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"humeral agenesis/hypoplasia","termid":"MONDO:0017440"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"humeral agenesis/hypoplasia, unilateral","secondary_identifiers":["Orphanet:295061"],"synonyms":[{"name":"humeral intercalary meromelia, unilateral","type":"exact"}],"termid":"MONDO:0017482","xrefs":{"Monarch":{"xref_id":"0017482"}}}


id: PBO:0091561
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by S. cerevisiae LIA1","termid":"PBO:0091561"}


id: PBO:0001151
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcium/calmodulin-dependent protein kinase Cmk1","termid":"PBO:0001151"}


id: PBO:0043881
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CREB/ATF bZIP transcription factor","termid":"PBO:0043881"}


id: PBO:0040843
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BLM RecQ like helicase","termid":"PBO:0040843"}


id: FYPO:0005205
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the rate or occurrence of DNA polymerase processivity factor activity is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal DNA polymerase processivity factor activity","termid":"FYPO:0004499"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000652","FYPO:0000707"],"is_obsolete":false,"name":"increased DNA polymerase processivity factor activity","termid":"FYPO:0005205"}


id: FYPO:0002596
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 histone H2A phosphorylation occurs to a greater extent than normal. All histone H2A phosphorylation may be affected, or phosphorylation of specific sites on histone H2A may be increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone phosphorylation during vegetative growth","termid":"FYPO:0002591"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0002494","FYPO:0002274","FYPO:0005447","FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"increased histone H2A phosphorylation during vegetative growth","synonyms":[{"name":"increased histone H2A phosphorylation during mitotic cell cycle","type":"related"}],"termid":"FYPO:0002596"}


id: PBO:0112975
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase, Alg7","termid":"PBO:0112975"}


id: MONDO:0005194
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infection with any of the rotaviruses. Specific infections include human infantile diarrhea, neonatal calf diarrhea, and epidemic diarrhea of infant mice.","definition_xrefs":["MESH:D012400"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary viral infectious disease","termid":"MONDO:0100329"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rotavirus infection","secondary_identifiers":["SCTID:18624000","MEDGEN:19835","ICD9:078.89","EFO:0002622","UMLS:C0035869"],"synonyms":[{"name":"Rotavirus caused disease or disorder","type":"exact"},{"name":"Rotavirus disease or disorder","type":"exact"},{"name":"Rotavirus infectious disease","type":"exact"}],"termid":"MONDO:0005194","xrefs":{"Monarch":{"xref_id":"0005194"}}}


id: PBO:0047811
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"forkhead box M1","termid":"PBO:0047811"}


id: PBO:0109460
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER membrane protein required for translocation of Man5GlcNac2-PP-Dol from the cytoplasmic side to the lumenal side of the ER Rft1","termid":"PBO:0109460"}


id: FYPO:0000163
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which macroautophagy is abnormal. Macroautophagy is the major pathway by which cells digest parts of their own cytoplasm.","definition_xrefs":["GO:0016236","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal autophagy","termid":"FYPO:0008082"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"abnormal macroautophagy","secondary_identifiers":["FYPO:0000379"],"synonyms":[{"name":"abnormal autophagy","type":"broad"},{"name":"autophagy: abnormal","type":"broad"}],"termid":"FYPO:0000163"}


id: MONDO:0010818
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any retinitis pigmentosa in which the cause of the disease is a mutation in the CRB1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinitis pigmentosa","termid":"MONDO:0019200"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0005066","MONDO:0005328"],"is_obsolete":false,"name":"retinitis pigmentosa 12","secondary_identifiers":["OMIM:600105","DOID:0110358","GARD:10376","MEDGEN:374019","MESH:C563999","ICD10CM:H35.5","UMLS:C1838647"],"synonyms":[{"name":"CRB1 retinitis pigmentosa","type":"exact"},{"name":"RP 12","type":"related"},{"name":"RP with or without Pprpe","type":"related"},{"name":"RP with or without preserved Paraarteriole retinal pigment epithelium","type":"related"},{"name":"RP12","type":"exact"},{"name":"retinitis pigmentosa 12","type":"exact"},{"name":"retinitis pigmentosa caused by mutation in CRB1","type":"exact"},{"name":"retinitis pigmentosa type 12","type":"exact"},{"name":"retinitis pigmentosa with or without Paraarteriolar preservation of retinal pigment epithelium","type":"related"},{"name":"retinitis pigmentosa-12","type":"exact"}],"termid":"MONDO:0010818","xrefs":{"Monarch":{"xref_id":"0010818"}}}


id: GO:0008664
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis the reaction: a 3'-end 2',3'-cyclophospho-ribonucleotide-RNA + H2O = a 3'-end 2'-phospho-ribonucleotide-RNA + H+.","definition_xrefs":["PMID:25239919","RHEA:11828"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphoric diester hydrolase activity","termid":"GO:0008081"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016788"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016788","GO:0016787"],"is_obsolete":false,"name":"RNA 2',3'-cyclic 3'-phosphodiesterase activity","secondary_identifiers":["EC:3.1.4.58"],"synonyms":[{"name":"2'-5' RNA ligase activity","type":"narrow"}],"termid":"GO:0008664"}


id: PBO:0049769
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 7","termid":"PBO:0049769"}


id: GO:0032335
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the regulated release of activin from a cell.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of hormone secretion","termid":"GO:0046883"},{"relation_name":"regulates","term_name":"activin secretion","termid":"GO:0032333"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0023052","GO:0006810"],"is_obsolete":false,"name":"regulation of activin secretion","termid":"GO:0032335"}


id: PBO:0077262
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane p24 trafficking protein 10 pseudogene 2","termid":"PBO:0077262"}


id: GO:0015988
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The transport of protons across a membrane and against an electrochemical gradient, using energy from a source such as ATP hydrolysis, light, or electron transport.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proton transmembrane transport","termid":"GO:1902600"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0055085","GO:0008150"],"is_obsolete":false,"name":"energy coupled proton transmembrane transport, against electrochemical gradient","termid":"GO:0015988"}


id: PBO:0090860
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell surface adhesion protein for conjugation","termid":"PBO:0090860"}


id: PBO:0005051
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.3.1.20","termid":"PBO:0005051"}


id: PBO:0052402
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3","termid":"PBO:0052402"}


id: PBO:0109547
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SIP/FAR complex subunit Csc2","termid":"PBO:0109547"}


id: PBO:0071094
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 96","termid":"PBO:0071094"}


id: GO:0044500
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 decrease of the force with which blood travels through the circulatory system of the bitten/stung organism.","definition_xrefs":["GOC:fj","GOC:jl","PMID:19837656"],"gene_count":0,"genotype_count":0,"name":"obsolete venom-mediated decrease in blood pressure in another organism (obsolete GO:0044500)","synonyms":[{"name":"envenomation resulting in negative regulation of blood pressure in another organism","type":"exact"},{"name":"envenomation resulting in negative regulation of blood pressure in other organism","type":"exact"},{"name":"hypotensive activity in other organism","type":"exact"}],"termid":"GO:0044500"}


id: FYPO:0006197
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype observed in the vegetative growth phase of the life cycle in which a cell is inviable, has one nucleus, and has normal length but a greater diameter than normal.","definition_xrefs":["PMID:20805322","PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"mononucleate vegetative cell","termid":"FYPO:0000060"},{"relation_name":"has_part","term_name":"normal vegetative cell length","termid":"FYPO:0003503"},{"relation_name":"is_a","term_name":"mononucleate vegetative cell","termid":"FYPO:0000060"},{"relation_name":"is_a","term_name":"inviable vegetative cell with normal cell morphology","termid":"FYPO:0002199"},{"relation_name":"is_a","term_name":"inviable vegetative cell with abnormal cell morphology","termid":"FYPO:0002273"},{"relation_name":"is_a","term_name":"normal vegetative cell length","termid":"FYPO:0003503"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000004","FYPO:0000257","FYPO:0001320","FYPO:0000005","FYPO:0001985","FYPO:0001312"],"is_obsolete":false,"name":"inviable mononucleate vegetative cell, with normal cell length and increased cell diameter","synonyms":[{"name":"inviable mononucleate cell, with normal cell length and increased cell diameter, during vegetative growth","type":"exact"},{"name":"inviable mononucleate vegetative cell, with increased cell diameter and normal cell length","type":"exact"},{"name":"inviable mononucleate vegetative cell, with normal cell length and increased cell diameter during mitotic cell cycle","type":"related"},{"name":"inviable mononucleate vegetative cell, with normal length and increased diameter","type":"exact"},{"name":"inviable swollen mononucleate vegetative cell, with normal cell length","type":"related"},{"name":"lethal; mononucleate vegetative cell, with normal cell length and increased cell diameter","type":"exact"}],"termid":"FYPO:0006197"}


id: PBO:0109647
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"taxilin gamma Y-linked (pseudogene)","termid":"PBO:0109647"}


id: MONDO:0010728
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A syndrome characterized by the association of skeletal abnormalities, cutis laxa, craniostenosis, ambiguous genitalia, psychomotor retardation and facial abnormalities. So far, it has been described in two males (maternal first cousins). The mode of inheritance was suggested to be X-linked recessive.","definition_xrefs":["Orphanet:3134"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"excluded_subClassOf","term_name":"syndromic craniosynostosis","termid":"MONDO:0015338"},{"relation_name":"excluded_subClassOf","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"},{"relation_name":"excluded_subClassOf","term_name":"inherited cutis laxa","termid":"MONDO:0100237"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SCARF syndrome","secondary_identifiers":["SCTID:734173003","icd11.foundation:1075253748","MEDGEN:326461","UMLS:C1839321","OMIM:312830","GARD:247","MESH:C536625"],"synonyms":[{"name":"SCARF syndrome","type":"exact"},{"name":"skeletal abnormalities, cutis laxa, craniostenosis, ambiguous genitalia, retardation, and Facial abnormalities","type":"related"}],"termid":"MONDO:0010728","xrefs":{"Monarch":{"xref_id":"0010728"}}}


id: MONDO:0000847
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete pycnodysostosis (obsolete MONDO:0000847)","termid":"MONDO:0000847","xrefs":{"Monarch":{"xref_id":"0000847"}}}


id: PBO:0079302
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 1","termid":"PBO:0079302"}


id: PBO:0000090
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intergenic RNA (predicted)","termid":"PBO:0000090"}


id: PBO:0084713
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial inner membrane insertase; mediates the insertion of both mitochondrial- and nuclear-encoded proteins from the matrix into the inner membrane; also has a role in insertion of carrier proteins into the inner membrane; acts as a voltage-gated ion channel, activated by substrate peptides; interacts with mitochondrial ribosomes; conserved from bacteria to animals","termid":"PBO:0084713"}


id: MONDO:0019468
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A slow-growing type of leukemia (blood cancer) in which too many lymphocytes are found in the bone marrow and/or blood. The T-cell is specified as the defective cell line.","definition_xrefs":["NCIT:C70649"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mature T-cell and NK-cell non-Hodgkin lymphoma","termid":"MONDO:0000430"},{"relation_name":"is_a","term_name":"prolymphocytic leukemia","termid":"MONDO:0001023"},{"relation_name":"is_a","term_name":"precursor T-lymphoblastic lymphoma/leukemia","termid":"MONDO:0003537"},{"relation_name":"is_a","term_name":"T-cell acute lymphoblastic leukemia","termid":"MONDO:0004963"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"T-cell prolymphocytic leukemia","secondary_identifiers":["Orphanet:86871","ICDO:9834/3","UMLS:C2363142","MEDGEN:391707","GARD:13731","DOID:0081042","EFO:1000560","icd11.foundation:352523899","MedDRA:10042985","NCIT:C4752","ONCOTREE:TPLL","SCTID:277545003","SCTID:277567002","MESH:D015461"],"synonyms":[{"name":"CLL, T-cell","type":"exact"},{"name":"T cell CLL","type":"exact"},{"name":"T cell chronic lymphocytic leukaemia","type":"exact"},{"name":"T cell chronic lymphocytic leukemia","type":"exact"},{"name":"T cell prolymphocytic leukaemia","type":"exact"},{"name":"T cell prolymphocytic leukemia","type":"exact"},{"name":"T prolymphocytic leukaemia","type":"exact"},{"name":"T prolymphocytic leukemia","type":"exact"},{"name":"T-PLL","type":"exact"},{"name":"T-cell CLL","type":"exact"},{"name":"T-cell chronic lymphocytic leukaemia","type":"exact"},{"name":"T-cell chronic lymphocytic leukemia","type":"exact"},{"name":"T-cell prolymphocytic leukemia","type":"exact"},{"name":"TPLL","type":"related"},{"name":"chronic T-cell leukaemia","type":"narrow"},{"name":"chronic T-cell leukemia","type":"narrow"},{"name":"chronic T-cell lymphocytic leukaemia","type":"narrow"},{"name":"chronic T-cell lymphocytic leukemia","type":"narrow"},{"name":"leukemia, T-cell, chronic","type":"related"}],"termid":"MONDO:0019468","xrefs":{"Monarch":{"xref_id":"0019468"}}}


id: GO:1904305
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of gastro-intestinal system smooth muscle contraction.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:10821044"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of smooth muscle contraction","termid":"GO:0045986"},{"relation_name":"is_a","term_name":"regulation of gastro-intestinal system smooth muscle contraction","termid":"GO:1904304"},{"relation_name":"negatively_regulates","term_name":"gastro-intestinal system smooth muscle contraction","termid":"GO:0014831"}],"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 gastro-intestinal system smooth muscle contraction","synonyms":[{"name":"down regulation of gastro-intestinal system smooth muscle contraction","type":"exact"},{"name":"down-regulation of gastro-intestinal system smooth muscle contraction","type":"exact"},{"name":"downregulation of gastro-intestinal system smooth muscle contraction","type":"exact"},{"name":"inhibition of gastro-intestinal system smooth muscle contraction","type":"narrow"}],"termid":"GO:1904305"}


id: PBO:0074692
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, H/ACA box 70B","termid":"PBO:0074692"}


id: PBO:0078018
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 8","termid":"PBO:0078018"}


id: PBO:0080280
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vomeronasal 1 receptor 43 pseudogene","termid":"PBO:0080280"}


id: PBO:0110504
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA methyltransferase subunit 11-2 pseudogene 8","termid":"PBO:0110504"}


id: PBO:0058272
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4650-1","termid":"PBO:0058272"}


id: PBO:0063091
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"progestin and adipoQ receptor family member 9","termid":"PBO:0063091"}


id: PBO:0062430
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 7 subfamily E member 91 pseudogene","termid":"PBO:0062430"}


id: MONDO:0015586
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Benign familial mesial temporal lobe epilepsy is a rare epilepsy characterized by seizures with viscerosensory or experential auras, onset in adolescence or early adulthood and good prognosis. It is defined as at least 24 months of seizure freedom with or without antiepileptic medication.","definition_xrefs":["Orphanet:163717"],"gene_count":0,"genotype_count":0,"name":"obsolete benign familial mesial temporal lobe epilepsy (obsolete MONDO:0015586)","synonyms":[{"name":"benign FMTLE","type":"exact"}],"termid":"MONDO:0015586","xrefs":{"Monarch":{"xref_id":"0015586"}}}


id: PBO:0108605
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-regulates_characteristic","termid":"PBO:0108605"}


id: PBO:0071568
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L35a pseudogene 34","termid":"PBO:0071568"}


id: PBO:0056424
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MARCO like","termid":"PBO:0056424"}


id: GO:0042297
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A behavioral process whose outcome is a relatively long-lasting behavioral change whereby an organism modifies innate vocalizations to imitate sounds produced by others.","definition_xrefs":["PMID:16418265","GOC:dos","GOC:BHF","GOC:rl","PMID:17035521"],"direct_ancestors":[{"relation_name":"is_a","term_name":"auditory behavior","termid":"GO:0031223"},{"relation_name":"is_a","term_name":"imitative learning","termid":"GO:0098596"},{"relation_name":"is_a","term_name":"learned vocalization behavior or vocal learning","termid":"GO:0098598"}],"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":"vocal learning","secondary_identifiers":["Wikipedia:Vocal_learning"],"termid":"GO:0042297"}


id: PBO:0067290
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 375, pseudogene","termid":"PBO:0067290"}


id: PBO:0058289
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4664","termid":"PBO:0058289"}


id: MONDO:0859198
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, impaired intellectual development, microcephaly, hypotonia, and ocular anomalies","secondary_identifiers":["UMLS:C5561998","OMIM:619557","MEDGEN:1794208"],"termid":"MONDO:0859198","xrefs":{"Monarch":{"xref_id":"0859198"}}}


id: MONDO:0971032
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An acquired metabolic disease that is characterized by ethanol fermentation in the bladder and the absence of alcoholic intoxication.","definition_xrefs":["DOID:0081456"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acquired metabolic disease","termid":"MONDO:0006504"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"bladder fermentation syndrome","termid":"MONDO:0971032","xrefs":{"Monarch":{"xref_id":"0971032"}}}


id: PBO:0041619
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcium binding protein 5","termid":"PBO:0041619"}


id: PBO:0066915
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 217","termid":"PBO:0066915"}


id: MONDO:0004965
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma that arises from epithelial cells of the acinar cell","direct_ancestors":[{"relation_name":"is_a","term_name":"adenocarcinoma","termid":"MONDO:0004970"}],"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":"acinar cell carcinoma","secondary_identifiers":["MEDGEN:61660","MESH:D018267","DOID:3025","EFO:0000216","icd11.foundation:1322159869","ONCOTREE:ACCC","NCIT:C3768","UMLS:C0206685","ICDO:8550/3"],"synonyms":[{"name":"ACCC","type":"related"},{"name":"acinar adenocarcinoma","type":"exact"},{"name":"acinar carcinoma","type":"exact"},{"name":"acinar cell adenocarcinoma","type":"exact"},{"name":"acinar cell carcinoma","type":"exact"},{"name":"acinar cell carcinoma (morphologic abnormality)","type":"exact"},{"name":"acinic cell adenocarcinoma","type":"exact"},{"name":"acinic cell carcinoma","type":"exact"},{"name":"acinic cell tumor","type":"related"},{"name":"acinic cell tumour","type":"related"},{"name":"carcinoma of acinar cell","type":"exact"},{"name":"carcinoma, acinar cell, malignant","type":"exact"}],"termid":"MONDO:0004965","xrefs":{"Monarch":{"xref_id":"0004965"}}}


id: GO:0102489
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: GTP + 2 H2O = GMP + 2 hydrogenphosphate + 2 H+.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete GTP phosphohydrolase activity (obsolete GO:0102489)","termid":"GO:0102489"}


id: GO:0071432
data:
  {"annotated_genes":["SJAG_04398"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[94995],"is_not":false,"summary":null,"term":"GO:0071432"}]},"cv_name":"biological_process","definition":"The formation of a mature peptide mating pheromone by proteolysis and/or modification of a peptide precursor, occurring in the context of conjugation with cellular fusion.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptide pheromone maturation","termid":"GO:0007323"},{"relation_name":"positively_regulates","term_name":"conjugation with cellular fusion","termid":"GO:0000747"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04398":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0000747"},{"rel_name":"positively_regulates","termid":"GO:0000747"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0051604"}],"interesting_parent_ids":["GO:0008150","GO:0051604","GO:0000747","GO:0010467"],"is_obsolete":false,"name":"peptide mating pheromone maturation involved in positive regulation of conjugation with cellular fusion","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"a-factor processing (proteolytic)","type":"narrow"},{"name":"alpha-factor maturation","type":"narrow"},{"name":"mating-type peptide pheromone maturation involved in conjugation with cellular fusion","type":"exact"},{"name":"peptide mating pheromone formation involved in conjugation with cellular fusion","type":"exact"},{"name":"peptide mating pheromone processing involved in conjugation with cellular fusion","type":"exact"}],"termid":"GO:0071432","terms_by_termid":{"GO:0071432":null}}


id: PBO:0064554
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proopiomelanocortin","termid":"PBO:0064554"}


id: MONDO:0017116
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital hydrocephalus","termid":"MONDO:0016349"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"congenital communicating hydrocephalus","secondary_identifiers":["Orphanet:269505","GARD:20998","UMLS:C5679774","MEDGEN:1842324"],"synonyms":[{"name":"congenital non-obstructive hydrocephalus","type":"exact"}],"termid":"MONDO:0017116","xrefs":{"Monarch":{"xref_id":"0017116"}}}


id: GO:0042333
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a motile cell or organism in response to the presence of an oxidizable substrate, for example, fructose.","definition_xrefs":["GOC:jl","PMID:11029423"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chemotaxis","termid":"GO:0006935"},{"relation_name":"is_a","term_name":"energy taxis","termid":"GO:0009453"}],"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":"chemotaxis to oxidizable substrate","synonyms":[{"name":"taxis in response to oxidizable substrate","type":"exact"}],"termid":"GO:0042333"}


id: PBO:0031207
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-monopolar_actin_cortical_patch_localization","termid":"PBO:0031207"}


id: PBO:0085976
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; proposed involvement in transport based on mass spectrometry analysis of copurifying proteins; null mutant is viable","termid":"PBO:0085976"}


id: PBO:0053366
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 278","termid":"PBO:0053366"}


id: MONDO:0005812
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An acute viral infection of the respiratory tract, occurring in isolated cases, in epidemics, or in pandemics; it is caused by serologically different strains of viruses (influenzaviruses) designated A, B, and C, has a 3-day incubation period, and usually lasts for 3 to 10 days. It is marked by inflammation of the nasal mucosa, pharynx, and conjunctiva; headache; myalgia; often fever, chills, and prostration; and occasionally involvement of the myocardium or central nervous system.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral respiratory tract infection","termid":"MONDO:0024352"},{"relation_name":"is_a","term_name":"primary viral infectious disease","termid":"MONDO:0100329"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"influenza","secondary_identifiers":["DOID:8469","ICD9:487","SCTID:61700007","NCIT:C53482","MESH:D007251","MESH:D009976","UMLS:C0021400","EFO:0007328","MEDGEN:9466","ICD9:487.8","icd11.foundation:145723401"],"synonyms":[{"name":"Influenza with other manifestations","type":"exact"},{"name":"flu","type":"exact"},{"name":"influenza infection","type":"exact"},{"name":"influenza with non-respiratory manifestation","type":"exact"},{"name":"orthomyxoviridae caused disease or disorder","type":"exact"},{"name":"orthomyxoviridae disease or disorder","type":"exact"},{"name":"orthomyxoviridae infectious disease","type":"exact"}],"termid":"MONDO:0005812","xrefs":{"Monarch":{"xref_id":"0005812"}}}


id: PBO:0082260
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Amino acid permease; involved in uptake of cysteine, leucine, isoleucine and valine; BAP3 has a paralog, BAP2, that arose from the whole genome duplication","termid":"PBO:0082260"}


id: GO:0047798
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + cyclomaltodextrin = linear maltodextrin.","definition_xrefs":["EC:3.2.1.54","MetaCyc:CYCLOMALTODEXTRINASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, hydrolyzing O-glycosyl compounds","termid":"GO:0004553"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016787","GO:0003674","GO:0016798","GO:0003824"],"is_obsolete":false,"name":"cyclomaltodextrinase activity","secondary_identifiers":["RHEA:23980"],"synonyms":[{"name":"cyclodextrinase activity","type":"related"},{"name":"cycloheptaglucanase activity","type":"related"},{"name":"cyclohexaglucanase activity","type":"related"},{"name":"cyclomaltodextrin dextrin-hydrolase (decyclizing)","type":"related"}],"termid":"GO:0047798"}


id: PBO:0038642
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acyl-CoA thioesterase 9","termid":"PBO:0038642"}


id: PBO:0050139
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group box 1 pseudogene 49","termid":"PBO:0050139"}


id: FYPO:0006981
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which the levels and proportions of polysaccharides in the cell wall are normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah","PMID:30389790"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal subcellular component during vegetative growth","termid":"FYPO:0001313"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257","FYPO:0001320"],"is_obsolete":false,"name":"normal cell wall polysaccharide composition during vegetative growth","synonyms":[{"name":"normal cell wall polysaccharide composition during mitotic cell cycle","type":"related"}],"termid":"FYPO:0006981"}


id: PBO:0057878
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3182","termid":"PBO:0057878"}


id: GO:1902857
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of non-motile cilium assembly.","definition_xrefs":["GOC:cilia","GOC:kmv","GOC:TermGenie","PMID:23807208","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cilium assembly","termid":"GO:0045724"},{"relation_name":"is_a","term_name":"regulation of non-motile cilium assembly","termid":"GO:1902855"},{"relation_name":"positively_regulates","term_name":"non-motile cilium assembly","termid":"GO:1905515"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0044085","GO:0008150"],"is_obsolete":false,"name":"positive regulation of non-motile cilium assembly","synonyms":[{"name":"activation of immotile primary cilium assembly","type":"narrow"},{"name":"activation of nonmotile primary cilia assembly","type":"related"},{"name":"activation of nonmotile primary cilium assembly","type":"narrow"},{"name":"activation of sensory cilium assembly","type":"narrow"},{"name":"activation of sensory cilium biogenesis","type":"related"},{"name":"positive regulation of immotile primary cilium assembly","type":"related"},{"name":"positive regulation of nonmotile primary cilia assembly","type":"related"},{"name":"positive regulation of nonmotile primary cilium assembly","type":"related"},{"name":"positive regulation of sensory cilium assembly","type":"related"},{"name":"positive regulation of sensory cilium biogenesis","type":"related"},{"name":"up regulation of immotile primary cilium assembly","type":"related"},{"name":"up regulation of nonmotile primary cilia assembly","type":"related"},{"name":"up regulation of nonmotile primary cilium assembly","type":"related"},{"name":"up regulation of sensory cilium assembly","type":"related"},{"name":"up regulation of sensory cilium biogenesis","type":"related"},{"name":"up-regulation of immotile primary cilium assembly","type":"related"},{"name":"up-regulation of nonmotile primary cilia assembly","type":"related"},{"name":"up-regulation of nonmotile primary cilium assembly","type":"related"},{"name":"up-regulation of sensory cilium assembly","type":"related"},{"name":"up-regulation of sensory cilium biogenesis","type":"related"},{"name":"upregulation of immotile primary cilium assembly","type":"related"},{"name":"upregulation of nonmotile primary cilia assembly","type":"related"},{"name":"upregulation of nonmotile primary cilium assembly","type":"related"},{"name":"upregulation of sensory cilium assembly","type":"related"},{"name":"upregulation of sensory cilium biogenesis","type":"related"}],"termid":"GO:1902857"}


id: PBO:0061064
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sodium/potassium transporting ATPase interacting 3","termid":"PBO:0061064"}


id: GO:0090303
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency, or extent of the series of events that restore integrity to a damaged tissue, following an injury.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of wound healing","termid":"GO:0061041"},{"relation_name":"is_a","term_name":"positive regulation of response to wounding","termid":"GO:1903036"},{"relation_name":"positively_regulates","term_name":"wound healing","termid":"GO:0042060"}],"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 wound healing","termid":"GO:0090303"}


id: PBO:0084318
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Karyopherin; a carrier protein involved in nuclear import of proteins; importin beta homolog","termid":"PBO:0084318"}


id: PBO:0084613
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Merged ORF; YER108C has been merged into YER109C because it has been demonstrated that they correspond to a mutated FLO8 gene with an A to G transition at position 431 in strain S288C, changing amino acid 144 from a Trp to a stop","termid":"PBO:0084613"}


id: GO:0051140
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of natural killer T cell proliferation.","definition_xrefs":["ISBN:0781735149","PMID:9133426","PMID:12154375"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of alpha-beta T cell proliferation","termid":"GO:0046640"},{"relation_name":"is_a","term_name":"regulation of NK T cell activation","termid":"GO:0051133"},{"relation_name":"regulates","term_name":"NK T cell proliferation","termid":"GO:0001866"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of NK T cell proliferation","synonyms":[{"name":"regulation of NK T lymphocyte proliferation","type":"exact"},{"name":"regulation of NK T-cell proliferation","type":"exact"},{"name":"regulation of NK T-lymphocyte proliferation","type":"exact"},{"name":"regulation of NKT cell proliferation","type":"exact"},{"name":"regulation of NT cell proliferation","type":"exact"},{"name":"regulation of natural T cell proliferation","type":"exact"},{"name":"regulation of natural killer T cell proliferation","type":"exact"}],"termid":"GO:0051140"}


id: GO:0002852
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of T cell mediated cytotoxicity directed against a tumor cell target.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of T cell mediated cytotoxicity","termid":"GO:0001914"},{"relation_name":"is_a","term_name":"regulation of T cell mediated immune response to tumor cell","termid":"GO:0002840"},{"relation_name":"regulates","term_name":"T cell mediated cytotoxicity directed against tumor cell target","termid":"GO:0002419"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of T cell mediated cytotoxicity directed against tumor cell target","termid":"GO:0002852"}


id: PBO:0064640
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphopantothenoylcysteine decarboxylase","termid":"PBO:0064640"}


id: SO:0002154
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A genomic region where there is an exchange of genetic material with another genomic region, occurring in somatic cells.","definition_xrefs":["NCBI:cf","SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"recombination_feature","termid":"SO:0000298"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitotic_recombination_region","synonyms":[{"name":"INSDC_feature:misc_recomb","type":"broad"},{"name":"INSDC_qualifier:mitotic","type":"exact"},{"name":"INSDC_qualifier:mitotic_recombination","type":"exact"},{"name":"mitotic recombination region","type":"exact"}],"termid":"SO:0002154"}


id: GO:0035121
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which the anatomical structures of the tail are generated and organized. The tail is the hindmost part of some animals.","definition_xrefs":["ISBN:0198612001"],"gene_count":0,"genotype_count":0,"name":"obsolete tail morphogenesis (obsolete GO:0035121)","synonyms":[{"name":"tail morphogenesis","type":"exact"}],"termid":"GO:0035121"}


id: MONDO:0004143
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A WHO grade I meningioma characterized by the presence of psammoma bodies that predominate over the meningeal cells.","definition_xrefs":["NCIT:C4331"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meningioma","termid":"MONDO:0016642"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"psammomatous meningioma","secondary_identifiers":["DOID:7210","MEDGEN:90815","UMLS:C0334607","ICDO:9533/0"],"synonyms":[{"name":"psammomatous meningioma (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0004143","xrefs":{"Monarch":{"xref_id":"0004143"}}}


id: GO:0031419
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to cobalamin (vitamin B12), a water-soluble vitamin characterized by possession of a corrin nucleus containing a cobalt atom.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vitamin binding","termid":"GO:0019842"},{"relation_name":"is_a","term_name":"tetrapyrrole binding","termid":"GO:0046906"},{"relation_name":"is_a","term_name":"heterocyclic compound binding","termid":"GO:1901363"}],"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":"cobalamin binding","synonyms":[{"name":"vitamin B12 binding","type":"exact"}],"termid":"GO:0031419"}


id: PR:O14037
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC2C4.04c gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14037"],"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":"UPF0538 protein C2C4.04c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC2C4.04c","synonyms":[{"name":"Spom972h-SPAC2C4.04c","type":"exact"}],"termid":"PR:O14037"}


id: MONDO:0018972
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare epithelial tumor of stomach (obsolete MONDO:0018972)","secondary_identifiers":["Orphanet:63443"],"synonyms":[{"name":"rare gastric epithelial tumor","type":"exact"}],"termid":"MONDO:0018972","xrefs":{"Monarch":{"xref_id":"0018972"}}}


id: MONDO:0016962
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete partial duplication of the long arm of chromosome 11 (obsolete MONDO:0016962)","termid":"MONDO:0016962","xrefs":{"Monarch":{"xref_id":"0016962"}}}


id: GO:0035283
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Division of the central nervous system into a series of semi-repetitive parts or segments.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"segmentation","termid":"GO:0035282"},{"relation_name":"part_of","term_name":"central nervous system development","termid":"GO:0007417"}],"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":"central nervous system segmentation","termid":"GO:0035283"}


id: MONDO:0012208
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"keratinopathic ichthyosis","termid":"MONDO:0017266"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"congenital reticular ichthyosiform erythroderma","secondary_identifiers":["GARD:17305","Orphanet:281190","MEDGEN:777141","icd11.foundation:565254051","UMLS:C3665704","MESH:C563781","OMIM:609165","SCTID:703504006"],"synonyms":[{"name":"Aarau disease","type":"related"},{"name":"CRIE","type":"exact"},{"name":"IWC","type":"exact"},{"name":"erythroderma, ichthyosiform, congenital reticular","type":"related"},{"name":"erythrokeratoderma, reticular","type":"related"},{"name":"ichthyosis variegata","type":"exact"},{"name":"ichthyosis with confetti","type":"exact"}],"termid":"MONDO:0012208","xrefs":{"Monarch":{"xref_id":"0012208"}}}


id: PBO:0049793
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HCK proto-oncogene, Src family tyrosine kinase","termid":"PBO:0049793"}


id: PR:Q9Y7T8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A proteasome subunit beta type-3 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO04477","PANTHER:PTHR11599:SF7"],"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":"proteasome subunit beta type-3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC63.12c","secondary_identifiers":["UniProtKB:Q9Y7T8"],"synonyms":[{"name":"Spom972h-PSMB3","type":"exact"}],"termid":"PR:Q9Y7T8"}


id: GO:0043365
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + dihydroflavodoxin + [formate C-acetyltransferase]-glycine = 5'-deoxyadenosine + L-methionine + flavodoxin semiquinone + [formate C-acetyltransferase]-glycin-2-yl radical.","definition_xrefs":["EC:1.97.1.4","GOC:jl","PMID:18307109"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycyl-radical enzyme activating activity","termid":"GO:0043364"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"[formate-C-acetyltransferase]-activating enzyme activity","secondary_identifiers":["MetaCyc:TDCEACT-RXN","GO:0008862","RHEA:19225"],"synonyms":[{"name":"PFL activase activity","type":"related"},{"name":"PFL-glycine:S-adenosyl-L-methionine H transferase (flavodoxin-oxidizing, S-adenosyl-L-methionine-cleaving) activity","type":"related"},{"name":"[pyruvate formate-lyase]-activating enzyme activity","type":"related"},{"name":"formate C-acetyltransferase-glycine dihydroflavodoxin:S-adenosyl-L-methionine oxidoreductase (S-adenosyl-L-methionine cleaving)","type":"related"},{"name":"formate acetyltransferase activating enzyme activity","type":"related"},{"name":"formate acetyltransferase-glycine dihydroflavodoxin:S-adenosyl-L-methionine oxidoreductase (S-adenosyl-L-methionine cleaving) activity","type":"related"},{"name":"formate-C-acetyltransferase-activating enzyme","type":"related"},{"name":"pyruvate formate-lyase-activating enzyme","type":"related"}],"termid":"GO:0043365"}


id: PBO:0044723
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DEAD/H-box helicase 11 like 10 (pseudogene)","termid":"PBO:0044723"}


id: MONDO:0012223
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":"hypotrichosis, progressive patterned scalp, with wiry hair, onycholysis, and cleft lip/palate","secondary_identifiers":["MEDGEN:324538","MESH:C563765","OMIM:609250","UMLS:C1836521"],"synonyms":[{"name":"Marie Unna-like scalp hypotrichosis","type":"related"},{"name":"hypotrichosis, progressive patterned scalp, with wiry hair, onycholysis, and cleft lip/palate","type":"exact"}],"termid":"MONDO:0012223","xrefs":{"Monarch":{"xref_id":"0012223"}}}


id: PBO:0063408
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PDCL3 pseudogene 4","termid":"PBO:0063408"}


id: MONDO:0015225
data:
  {"annotated_genes":["SJAG_00875","SJAG_05194","SJAG_03703","SJAG_00773","SJAG_03847","SJAG_01665","SJAG_00853","SJAG_02096","SJAG_01863","SJAG_02431","SJAG_03106","SJAG_00992","SJAG_03379","SJAG_01065","SJAG_04697"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88487],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032903"},{"annotations":[88317],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030281"},{"annotations":[87796],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0975826"},{"annotations":[87479],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030847"},{"annotations":[88941,88940],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032751"},{"annotations":[88324],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008822"},{"annotations":[87601],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014248"},{"annotations":[88948,88947],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008338"},{"annotations":[88972,88973],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0020746"},{"annotations":[87916],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100104"},{"annotations":[88989,88990],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008675"},{"annotations":[88829],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010532"},{"annotations":[87760],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012750"},{"annotations":[87970],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009670"},{"annotations":[87266],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012656"},{"annotations":[87208],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014552"},{"annotations":[87591],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014806"},{"annotations":[87590],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014807"},{"annotations":[87459,87460],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008016"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital limb malformation","termid":"MONDO:0019054"}],"gene_count":15,"genes_by_uniquename":{"SJAG_00773":null,"SJAG_00853":null,"SJAG_00875":null,"SJAG_00992":null,"SJAG_01065":null,"SJAG_01665":null,"SJAG_01863":null,"SJAG_02096":null,"SJAG_02431":null,"SJAG_03106":null,"SJAG_03379":null,"SJAG_03703":null,"SJAG_03847":null,"SJAG_04697":null,"SJAG_05194":null},"genotype_count":0,"is_obsolete":false,"name":"arthrogryposis syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:D001176","GARD:19870","Orphanet:109007","icd11.foundation:1692487835"],"synonyms":[{"name":"arthrogryposis syndrome","type":"exact"}],"termid":"MONDO:0015225","terms_by_termid":{"MONDO:0008016":null,"MONDO:0008338":null,"MONDO:0008675":null,"MONDO:0008822":null,"MONDO:0009670":null,"MONDO:0010532":null,"MONDO:0012656":null,"MONDO:0012750":null,"MONDO:0014248":null,"MONDO:0014552":null,"MONDO:0014806":null,"MONDO:0014807":null,"MONDO:0020746":null,"MONDO:0030281":null,"MONDO:0030847":null,"MONDO:0032751":null,"MONDO:0032903":null,"MONDO:0100104":null,"MONDO:0975826":null},"xrefs":{"Monarch":{"xref_id":"0015225"}}}


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":["PRO:DNx","OMA:SCHPO03309","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:0010156
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Formation and development of sporocyte, the haploid spores of angiosperms which are initiated by the differentiation of a subset of floral cells into sporocytes, which then undergo meiotic divisions to form microspores and megaspores.","definition_xrefs":["PMID:10465788"],"gene_count":0,"genotype_count":0,"name":"obsolete sporocyte morphogenesis (obsolete GO:0010156)","synonyms":[{"name":"sporocyte morphogenesis","type":"exact"}],"termid":"GO:0010156"}


id: PBO:0057286
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 506","termid":"PBO:0057286"}


id: PBO:0077425
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 161B pseudogene 1","termid":"PBO:0077425"}


id: GO:1903859
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of dendrite extension.","definition_xrefs":["PMID:24898855","GOC:pad","GOC:TermGenie","GO_REF:0000058","GOC:PARL"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell growth","termid":"GO:0001558"},{"relation_name":"is_a","term_name":"regulation of cell morphogenesis","termid":"GO:0022604"},{"relation_name":"is_a","term_name":"regulation of developmental growth","termid":"GO:0048638"},{"relation_name":"regulates","term_name":"dendrite extension","termid":"GO:0097484"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of dendrite extension","termid":"GO:1903859"}


id: PBO:0040170
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ASNS pseudogene 1","termid":"PBO:0040170"}


id: SO:0002001
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A segment of non-homology between a and alpha mating alleles, found at all three mating loci (HML, MAT, and HMR), has two forms (Ya and Yalpha).","definition_xrefs":["SGD:jd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mating_type_region_motif","termid":"SO:0001999"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Y_region","synonyms":[{"name":"Y-region","type":"exact"}],"termid":"SO:0002001"}


id: GO:0140754
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in intracellular membranes are reorganized by viral proteins that perturb membrane integrity and can cause an extensive rearrangement of cellular membranes, forming membranous webs, which are thought to be the site of replication or certain viruses, for example the HPV virus.","definition_xrefs":["PMID:19376974"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host membrane","termid":"GO:0141171"}],"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":"reorganization of cellular membranes to establish viral sites of replication","termid":"GO:0140754"}


id: PBO:0059388
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein S23 pseudogene 1","termid":"PBO:0059388"}


id: MOD:00017
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts a source amino acid residue to a glycine.","definition_xrefs":["ChEBI:29947","PubMed:6692818","PubMed:1310545","RESID:AA0008","DeltaMass:0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"natural, standard, encoded residue","termid":"MOD:01441"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycine residue","synonyms":[{"name":"Gly","type":"exact"},{"name":"aminoacetic acid","type":"exact"},{"name":"aminoethanoic acid","type":"exact"},{"name":"azanylethanoic acid","type":"exact"},{"name":"glycine","type":"exact"},{"name":"glycocoll","type":"exact"}],"termid":"MOD:00017"}


id: FYPO:0007937
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the number of sites of DNA breakpoint junctions is greater than normal during stationary phase.","direct_ancestors":[{"relation_name":"is_a","term_name":"increased number of DNA breakpoint junctions","termid":"FYPO:0007936"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002"],"is_obsolete":false,"name":"increased number of DNA breakpoint junctions during stationary phase","termid":"FYPO:0007937"}


id: PBO:0044749
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DEAD-box helicase 28","termid":"PBO:0044749"}


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


id: PBO:0053706
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 908","termid":"PBO:0053706"}


id: PBO:0078110
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor associated transmembrane adaptor 1","termid":"PBO:0078110"}


id: MONDO:0007002
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease involving the trochlear nerve.","direct_ancestors":[{"relation_name":"is_a","term_name":"cranial nerve neuropathy","termid":"MONDO:0003569"},{"relation_name":"is_a","term_name":"peripheral nervous system disorder","termid":"MONDO:0003620"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trochlear nerve disorder","secondary_identifiers":["DOID:13864","MedDRA:10074765","SCTID:20610004","MESH:D020432","MEDGEN:888203","UMLS:C4048184","NCIT:C78395","ICD9:378.53"],"synonyms":[{"name":"IVth cranial nerve disorder","type":"exact"},{"name":"IVth nerve disorder","type":"exact"},{"name":"disease of trochlear nerve","type":"exact"},{"name":"disease or disorder of trochlear nerve","type":"exact"},{"name":"disorder of trochlear nerve","type":"exact"},{"name":"superior oblique muscle innervation disorder","type":"exact"},{"name":"trochlear nerve disease","type":"exact"},{"name":"trochlear nerve disease or disorder","type":"exact"},{"name":"trochlear nerve disorder","type":"exact"}],"termid":"MONDO:0007002","xrefs":{"Monarch":{"xref_id":"0007002"}}}


id: GO:0005359
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: glucose(out) + H(out)+ = glucose(in) + H(in)+. In low-affinity transport the transporter is able to bind the solute only if it is present at very high concentrations. Symporter activity enables the active transport of a solute across a membrane by a mechanism whereby two or more species are transported together in the same direction in a tightly coupled process not directly linked to a form of energy other than chemiosmotic energy.","definition_xrefs":["GOC:mtg_transport"],"direct_ancestors":[{"relation_name":"is_a","term_name":"D-glucose:proton symporter activity","termid":"GO:0005356"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"low-affinity D-glucose:proton symporter activity","synonyms":[{"name":"low-affinity glucose:proton symporter activity","type":"exact"},{"name":"low-affinity hydrogen/glucose transporter activity","type":"broad"},{"name":"low-affinity hydrogen:glucose symporter activity","type":"exact"},{"name":"low-affinity hydrogen:glucose transporter activity","type":"broad"}],"termid":"GO:0005359"}


id: PATO:0001395
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A diploidy quality inhering in a bearer in by virtue of belonging in a species whose one of the sexes has haploid cells and the other has diploid cells.","definition_xrefs":["Wikipedia:http://en.wikipedia.org/wiki/Haplodiploid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diploid","termid":"PATO:0001394"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"haplodiploid","termid":"PATO:0001395"}


id: PBO:0089692
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Swr1 complex histone chaperone module subunit, SNF2 family ATP-dependent chromatin remodeller Swr1","termid":"PBO:0089692"}


id: MONDO:0011898
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Charcot-Marie-Tooth disease recessive intermediate A","termid":"MONDO:0012014"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005244"],"is_obsolete":false,"name":"Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomal recessive","secondary_identifiers":["MEDGEN:375113","OMIM:607706","UMLS:C1843183"],"synonyms":[{"name":"CMT2 with vocal cord paresis, autosomal recessive","type":"related"},{"name":"Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomal recessive","type":"exact"},{"name":"Charcot-Marie-Tooth disease, type 4A, axonal form","type":"related"},{"name":"Charcot-Marie-Tooth neuropathy, axonal, with vocal cord paresis, autosomal recessive","type":"related"}],"termid":"MONDO:0011898","xrefs":{"Monarch":{"xref_id":"0011898"}}}


id: PBO:0027899
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_snRNA_level","termid":"PBO:0027899"}


id: GO:0004850
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: uridine + phosphate = uracil + alpha-D-ribose 1-phosphate.","definition_xrefs":["EC:2.4.2.3"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine-nucleoside phosphorylase activity","termid":"GO:0016154"}],"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:0016757"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0016757","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"uridine phosphorylase activity","secondary_identifiers":["Reactome:R-HSA-74376","RHEA:24388","Reactome:R-HSA-74372","MetaCyc:URPHOS-RXN"],"synonyms":[{"name":"UPH","type":"related"},{"name":"UPase activity","type":"related"},{"name":"UrdPase activity","type":"related"},{"name":"pyrimidine phosphorylase activity","type":"broad"},{"name":"uridine:phosphate alpha-D-ribosyltransferase activity","type":"related"}],"termid":"GO:0004850"}


id: PBO:0004738
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein phosphatase (predicted)","termid":"PBO:0004738"}


id: PBO:0080049
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"USP21 pseudogene 1","termid":"PBO:0080049"}


id: GO:0015861
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of cytidine, cytosine riboside, into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine nucleoside transport","termid":"GO:0015864"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"cytidine transport","termid":"GO:0015861"}


id: PBO:0000924
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleoporin Nup40","termid":"PBO:0000924"}


id: PBO:0073055
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SCYL2 pseudogene 1","termid":"PBO:0073055"}


id: GO:0035469
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Determination of the asymmetric location of the pancreas with respect to the left and right halves of the organism.","definition_xrefs":["PMID:12702646","GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"determination of left/right symmetry","termid":"GO:0007368"},{"relation_name":"part_of","term_name":"pancreas development","termid":"GO:0031016"}],"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":"determination of pancreatic left/right asymmetry","termid":"GO:0035469"}


id: PR:Q09688
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mug121 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q09688"],"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":"meiotically up-regulated gene 121 protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC13C5.06c","synonyms":[{"name":"Spom972h-mug121","type":"exact"}],"termid":"PR:Q09688"}


id: MONDO:0021227
data:
  {"annotated_genes":["SJAG_03429","SJAG_02398","SJAG_01895","SJAG_03920","SJAG_00260","SJAG_01671"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88524],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009050"},{"annotations":[87628],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008192"},{"annotations":[88833],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011121"},{"annotations":[88733],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011544"},{"annotations":[87415],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007273"},{"annotations":[87625],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013602"}]},"cv_name":"mondo","definition":"A neoplasm (disease) that involves the adrenal gland.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endocrine gland neoplasm","termid":"MONDO:0002082"},{"relation_name":"is_a","term_name":"adrenal gland disorder","termid":"MONDO:0005495"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00260":null,"SJAG_01671":null,"SJAG_01895":null,"SJAG_02398":null,"SJAG_03429":null,"SJAG_03920":null},"genotype_count":0,"is_obsolete":false,"name":"adrenal gland neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:100091","GARD:19765","UMLS:C0001624","EFO:0003850","MEDGEN:1352","ONCOTREE:ADRENAL_GLAND","NCIT:C2859"],"synonyms":[{"name":"ADRENAL_GLAND","type":"related"},{"name":"adrenal gland neoplasm (disease)","type":"exact"},{"name":"adrenal gland tumor","type":"exact"},{"name":"adrenal gland tumour","type":"exact"},{"name":"adrenal neoplasm","type":"exact"},{"name":"adrenal neoplasms","type":"exact"},{"name":"adrenal tumor","type":"exact"},{"name":"adrenal tumour","type":"exact"},{"name":"adrenal/paraganglial tumor","type":"related"},{"name":"adrenal/paraganglial tumour","type":"related"},{"name":"neoplasm of adrenal gland","type":"exact"},{"name":"neoplasm of the adrenal gland","type":"exact"},{"name":"tumor of adrenal gland","type":"exact"},{"name":"tumor of the adrenal gland","type":"exact"},{"name":"tumour of adrenal gland","type":"exact"},{"name":"tumour of the adrenal gland","type":"exact"}],"termid":"MONDO:0021227","terms_by_termid":{"MONDO:0007273":null,"MONDO:0008192":null,"MONDO:0009050":null,"MONDO:0011121":null,"MONDO:0011544":null,"MONDO:0013602":null},"xrefs":{"Monarch":{"xref_id":"0021227"}}}


id: MONDO:0009413
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"common variable immunodeficiency","termid":"MONDO:0015517"}],"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, common variable, 2","secondary_identifiers":["GARD:15184","MEDGEN:461704","OMIM:240500","UMLS:C3150354","DOID:0081145"],"synonyms":[{"name":"CVID2","type":"related"},{"name":"antibody deficiency due to TACI defect","type":"related"},{"name":"hypogammaglobulinemia due to TACI deficiency","type":"related"},{"name":"immunodeficiency, common variable, 2","type":"exact"},{"name":"immunodeficiency, common variable, type 2","type":"exact"}],"termid":"MONDO:0009413","xrefs":{"Monarch":{"xref_id":"0009413"}}}


id: GO:0010148
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Release of water by the plant into the air as water vapor mainly through leaves.","definition_xrefs":["GOC:sm","ISBN:0879015322"],"direct_ancestors":[{"relation_name":"is_a","term_name":"water transport","termid":"GO:0006833"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"transpiration","secondary_identifiers":["Wikipedia:Transpiration"],"termid":"GO:0010148"}


id: PBO:0045107
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA meiotic recombinase 1","termid":"PBO:0045107"}


id: GO:1905865
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of Atg1/ULK1 kinase complex assembly.","definition_xrefs":["GOC:autophagy","GOC:TermGenie","GO_REF:0000058","GOC:mf","PMID:26567215"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein-containing complex assembly","termid":"GO:0031333"},{"relation_name":"is_a","term_name":"regulation of Atg1/ULK1 kinase complex assembly","termid":"GO:1905864"},{"relation_name":"negatively_regulates","term_name":"Atg1/ULK1 kinase complex assembly","termid":"GO:1904745"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0065003"},{"rel_name":"negatively_regulates","termid":"GO:0065003"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0065003","GO:0008150","GO:0044085"],"is_obsolete":false,"name":"negative regulation of Atg1/ULK1 kinase complex assembly","synonyms":[{"name":"down regulation of ATG1 kinase complex assembly","type":"exact"},{"name":"down regulation of ATG1 kinase complex formation","type":"exact"},{"name":"down regulation of ATG1-ATG13 complex assembly","type":"exact"},{"name":"down regulation of ATG1-ATG13 complex formation","type":"exact"},{"name":"down regulation of ATG1/ULK1 kinase complex assembly","type":"exact"},{"name":"down regulation of ATG1/ULK1 kinase complex formation","type":"exact"},{"name":"down regulation of ATG1/ULK1 signaling complex assembly","type":"exact"},{"name":"down regulation of ATG1/ULK1 signaling complex formation","type":"exact"},{"name":"down regulation of Atg1p signalling complex assembly","type":"exact"},{"name":"down regulation of Atg1p signalling complex formation","type":"exact"},{"name":"down regulation of ULK1 signaling complex assembly","type":"exact"},{"name":"down regulation of ULK1 signaling complex formation","type":"exact"},{"name":"down regulation of ULK1-ATG13-FIP200 complex assembly","type":"exact"},{"name":"down regulation of ULK1-ATG13-FIP200 complex formation","type":"exact"},{"name":"down regulation of ULK1-ATG13-RB1CC1 complex assembly","type":"exact"},{"name":"down regulation of ULK1-ATG13-RB1CC1 complex formation","type":"exact"},{"name":"down-regulation of ATG1 kinase complex assembly","type":"exact"},{"name":"down-regulation of ATG1 kinase complex formation","type":"exact"},{"name":"down-regulation of ATG1-ATG13 complex assembly","type":"exact"},{"name":"down-regulation of ATG1-ATG13 complex formation","type":"exact"},{"name":"down-regulation of ATG1/ULK1 kinase complex assembly","type":"exact"},{"name":"down-regulation of ATG1/ULK1 kinase complex formation","type":"exact"},{"name":"down-regulation of ATG1/ULK1 signaling complex assembly","type":"exact"},{"name":"down-regulation of ATG1/ULK1 signaling complex formation","type":"exact"},{"name":"down-regulation of Atg1p signalling complex assembly","type":"exact"},{"name":"down-regulation of Atg1p signalling complex formation","type":"exact"},{"name":"down-regulation of ULK1 signaling complex assembly","type":"exact"},{"name":"down-regulation of ULK1 signaling complex formation","type":"exact"},{"name":"down-regulation of ULK1-ATG13-FIP200 complex assembly","type":"exact"},{"name":"down-regulation of ULK1-ATG13-FIP200 complex formation","type":"exact"},{"name":"down-regulation of ULK1-ATG13-RB1CC1 complex assembly","type":"exact"},{"name":"down-regulation of ULK1-ATG13-RB1CC1 complex formation","type":"exact"},{"name":"downregulation of ATG1 kinase complex assembly","type":"exact"},{"name":"downregulation of ATG1 kinase complex formation","type":"exact"},{"name":"downregulation of ATG1-ATG13 complex assembly","type":"exact"},{"name":"downregulation of ATG1-ATG13 complex formation","type":"exact"},{"name":"downregulation of ATG1/ULK1 kinase complex assembly","type":"exact"},{"name":"downregulation of ATG1/ULK1 kinase complex formation","type":"exact"},{"name":"downregulation of ATG1/ULK1 signaling complex assembly","type":"exact"},{"name":"downregulation of ATG1/ULK1 signaling complex formation","type":"exact"},{"name":"downregulation of Atg1p signalling complex assembly","type":"exact"},{"name":"downregulation of Atg1p signalling complex formation","type":"exact"},{"name":"downregulation of ULK1 signaling complex assembly","type":"exact"},{"name":"downregulation of ULK1 signaling complex formation","type":"exact"},{"name":"downregulation of ULK1-ATG13-FIP200 complex assembly","type":"exact"},{"name":"downregulation of ULK1-ATG13-FIP200 complex formation","type":"exact"},{"name":"downregulation of ULK1-ATG13-RB1CC1 complex assembly","type":"exact"},{"name":"downregulation of ULK1-ATG13-RB1CC1 complex formation","type":"exact"},{"name":"inhibition of ATG1 kinase complex assembly","type":"narrow"},{"name":"inhibition of ATG1 kinase complex formation","type":"narrow"},{"name":"inhibition of ATG1-ATG13 complex assembly","type":"narrow"},{"name":"inhibition of ATG1-ATG13 complex formation","type":"narrow"},{"name":"inhibition of ATG1/ULK1 kinase complex assembly","type":"narrow"},{"name":"inhibition of ATG1/ULK1 kinase complex formation","type":"narrow"},{"name":"inhibition of ATG1/ULK1 signaling complex assembly","type":"narrow"},{"name":"inhibition of ATG1/ULK1 signaling complex formation","type":"narrow"},{"name":"inhibition of Atg1p signalling complex assembly","type":"narrow"},{"name":"inhibition of Atg1p signalling complex formation","type":"narrow"},{"name":"inhibition of ULK1 signaling complex assembly","type":"narrow"},{"name":"inhibition of ULK1 signaling complex formation","type":"narrow"},{"name":"inhibition of ULK1-ATG13-FIP200 complex assembly","type":"narrow"},{"name":"inhibition of ULK1-ATG13-FIP200 complex formation","type":"narrow"},{"name":"inhibition of ULK1-ATG13-RB1CC1 complex assembly","type":"narrow"},{"name":"inhibition of ULK1-ATG13-RB1CC1 complex formation","type":"narrow"},{"name":"negative regulation of ATG1 kinase complex assembly","type":"exact"},{"name":"negative regulation of ATG1 kinase complex formation","type":"exact"},{"name":"negative regulation of ATG1-ATG13 complex assembly","type":"exact"},{"name":"negative regulation of ATG1-ATG13 complex formation","type":"exact"},{"name":"negative regulation of ATG1/ULK1 kinase complex formation","type":"exact"},{"name":"negative regulation of ATG1/ULK1 signaling complex assembly","type":"exact"},{"name":"negative regulation of ATG1/ULK1 signaling complex formation","type":"exact"},{"name":"negative regulation of Atg1p signalling complex assembly","type":"exact"},{"name":"negative regulation of Atg1p signalling complex formation","type":"exact"},{"name":"negative regulation of ULK1 signaling complex assembly","type":"exact"},{"name":"negative regulation of ULK1 signaling complex formation","type":"exact"},{"name":"negative regulation of ULK1-ATG13-FIP200 complex assembly","type":"exact"},{"name":"negative regulation of ULK1-ATG13-FIP200 complex formation","type":"exact"},{"name":"negative regulation of ULK1-ATG13-RB1CC1 complex assembly","type":"exact"},{"name":"negative regulation of ULK1-ATG13-RB1CC1 complex formation","type":"exact"}],"termid":"GO:1905865"}


id: GO:0001309
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Progressive reduction in length of the telomeres, the termini of eukaryotic chromosomes, that occurs as part of the cellular aging process.","definition_xrefs":["PMID:9891807","GOC:jh"],"gene_count":0,"genotype_count":0,"name":"obsolete age-dependent telomere shortening (obsolete GO:0001309)","synonyms":[{"name":"age-dependent telomere shortening","type":"exact"}],"termid":"GO:0001309"}


id: GO:0016015
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Acts as a trigger for a pattern specification process when present at a specific concentration within a gradient.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"receptor ligand activity","termid":"GO:0048018"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0140677"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0098772","GO:0140677","GO:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"morphogen activity","termid":"GO:0016015"}


id: GO:0080078
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of a methyl group from S-adenosyl-L-methionine to the oxygen atom of a tricaffeoyl spermidine molecule.","definition_xrefs":["PMID:19077165"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-methyltransferase activity","termid":"GO:0008171"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016740","GO:0016741","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"tricaffeoyl spermidine:S-adenosyl-L-methionine O-methyltransferase activity","termid":"GO:0080078"}


id: MONDO:0021631
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A astrocytoma (excluding glioblastoma) that involves the brain.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"astrocytoma (excluding glioblastoma)","termid":"MONDO:0019781"},{"relation_name":"is_a","term_name":"primary brain neoplasm","termid":"MONDO:0021632"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"brain astrocytoma","secondary_identifiers":["MEDGEN:811330","SCTID:254938000","UMLS:C3695127","NCIT:C60780"],"synonyms":[{"name":"astrocytoma (excluding glioblastoma) of brain","type":"exact"},{"name":"brain astrocytoma","type":"exact"},{"name":"brain astrocytoma (excluding glioblastoma)","type":"exact"}],"termid":"MONDO:0021631","xrefs":{"Monarch":{"xref_id":"0021631"}}}


id: PBO:0085955
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; null mutant lacks mitochondrial DNA and cannot grow on glycerol; the authentic, non-tagged protein is detected in highly purified mitochondria in high-throughput studies","termid":"PBO:0085955"}


id: MONDO:0016850
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Atypical Norrie disease due to monosomy Xp11.3 is a rare chromosomal anomaly syndrome, resulting from the partial deletion of the short arm of chromosome X, principally characterized by classical Norrie disease (bilateral, severe retinal malformations and opacity of the lens leading to congenital blindness, on occasion associated with progressive sensorineural deafness and intellectual disability), microcephaly, hypotonia, psychomotor and growth delay, moderate to severe mental handicap and disruptive behavior. Clinical phenotype is highly variable and immunodeficiency, epilepsy and hypogonadism have also been reported.","definition_xrefs":["Orphanet:261501"],"direct_ancestors":[{"relation_name":"is_a","term_name":"partial monosomy of the short arm of chromosome X","termid":"MONDO:0017004"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"atypical Norrie disease due to monosomy Xp11.3","secondary_identifiers":["SCTID:733626002","GARD:20782","MEDGEN:1377538","ICD10CM:H35.5","UMLS:C4518083"],"synonyms":[{"name":"atypical Norrie disease due to Xp11.3 microdeletion","type":"exact"},{"name":"atypical Norrie disease due to del(X)(p11.3)","type":"exact"}],"termid":"MONDO:0016850","xrefs":{"Monarch":{"xref_id":"0016850"}}}


id: GO:0106243
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 9alpha-copalyl diphosphate = diphosphate + syn-isopimara-7,15-diene.","definition_xrefs":["PMID:29315936","GOC:emb","RHEA:62188"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-oxygen lyase activity, acting on phosphates","termid":"GO:0016838"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016829","GO:0003824"],"is_obsolete":false,"name":"syn-isopimara-7,15-diene synthase activity","termid":"GO:0106243"}


id: GO:0018425
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of O3-(N-acetylglucosamine-1-phosphoryl)-L-serine. The recovery of O-phosphorylserine from acid hydrolysates suggests N-acetylglucosamine-1-phosphate residues are esterified to peptidyl serines through phosphoester bonds.","definition_xrefs":["RESID:AA0296"],"gene_count":0,"genotype_count":0,"name":"obsolete O3-(N-acetylglucosamine-1-phosphoryl)-L-serine biosynthetic process (obsolete GO:0018425)","synonyms":[{"name":"O3-(N-acetylglucosamine-1-phosphoryl)-L-serine anabolism","type":"exact"},{"name":"O3-(N-acetylglucosamine-1-phosphoryl)-L-serine biosynthesis","type":"exact"},{"name":"O3-(N-acetylglucosamine-1-phosphoryl)-L-serine formation","type":"exact"},{"name":"O3-(N-acetylglucosamine-1-phosphoryl)-L-serine synthesis","type":"exact"}],"termid":"GO:0018425"}


id: PBO:0069112
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 361, pseudogene","termid":"PBO:0069112"}


id: GO:0003842
data:
  {"annotated_genes":["SJAG_02235"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[79868],"is_not":false,"summary":null,"term":"GO:0003842"}]},"cv_name":"molecular_function","definition":"L-glutamate 5-semialdehyde + NAD+ + H2O = L-glutamate + NADH + 2 H+.","definition_xrefs":["RHEA:30235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor","termid":"GO:0016620"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02235":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"L-glutamate gamma-semialdehyde dehydrogenase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["MetaCyc:RXN-14116","EC:1.2.1.88","Reactome:R-HSA-70679","Reactome:R-HSA-9929439","Reactome:R-HSA-6784402"],"synonyms":[{"name":"1-pyrroline dehydrogenase","type":"broad"},{"name":"1-pyrroline-5-carboxylate dehydrogenase activity","type":"related"},{"name":"1-pyrroline-5-carboxylate:NAD+ oxidoreductase activity","type":"related"},{"name":"L-pyrroline-5-carboxylate-NAD+ oxidoreductase activity","type":"related"},{"name":"delta1-pyrroline-5-carboxylate dehydrogenase activity","type":"related"},{"name":"pyrroline-5-carboxylate dehydrogenase activity","type":"related"},{"name":"pyrroline-5-carboxylic acid dehydrogenase activity","type":"related"}],"termid":"GO:0003842","terms_by_termid":{"GO:0003842":null}}


id: MONDO:0003304
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An elongated and multinodular neurofibroma, formed when the tumor involves either multiple trunks of a plexus or multiple fascicles of a large nerve, such as the sciatic. Some plexiform neurofibromas resemble a bag of worms, others produce a massive ropy enlargement of the nerve. (Adapted from WHO.)","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neurofibroma","termid":"MONDO:0016755"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plexiform neurofibroma","secondary_identifiers":["ICD9:215.9","MEDGEN:64640","HP:0009732","ICDO:9550/0","NCIT:C3797","MESH:D018318","UMLS:C0206728","SCTID:403818001","DOID:5151"],"synonyms":[{"name":"plexiform neurofibroma","type":"exact"},{"name":"plexiform neurofibroma (disease)","type":"exact"}],"termid":"MONDO:0003304","xrefs":{"Monarch":{"xref_id":"0003304"}}}


id: PATO:0001149
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001149 susceptibility value (obsolete PATO:0001149)","termid":"PATO:0001149"}


id: PBO:0075694
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SRD5A3 antisense RNA 1","termid":"PBO:0075694"}


id: GO:1990500
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that causes translational repression in Drosophila. Prevents assembly of ribosomes at the mRNA by interfacing with a sequence-specific RNA-binding protein leading to recruitment of the CCR4 complex and consequently, reduction of the mRNA's poly(A) tail length. The complex is also required for dorso-ventral pattern formation in the embryo.","definition_xrefs":["GOC:bhm","PMID:14723848"],"direct_ancestors":[{"relation_name":"is_a","term_name":"translation repressor complex","termid":"GO:1903502"},{"relation_name":"part_of","term_name":"P-body","termid":"GO:0000932"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0000932"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0000932","GO:0032991","GO:0005737","GO:0005575"],"is_obsolete":false,"name":"eif4e-cup complex","synonyms":[{"name":"eukaryotic translation initiation factor 4E-cup complex","type":"exact"}],"termid":"GO:1990500"}


id: PBO:0084916
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Modulator of cell separation and mitotic exit; inhibits separation through Ub-dependent Ace2p proteolysis; part of a daughter-specific switch induced by the mitotic exit network that inhibits exit and resets the cell cycle after the execution of  MEN function, blocking Tem1p and Cdc15 association; required for chromosome stability and multiple mitotic checkpoints; regulated by SCF; haploid transcription regulated by Ste12p; contains 12 degenerate leucine-rich repeat motifs and an atypical F-box","termid":"PBO:0084916"}


id: GO:0009626
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The rapid, localized death of plant cells in response to invasion by a pathogen.","definition_xrefs":["ISBN:0582227089"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to stress","termid":"GO:0033554"},{"relation_name":"is_a","term_name":"symbiont-induced defense-related programmed cell death","termid":"GO:0034050"},{"relation_name":"is_a","term_name":"innate immune response","termid":"GO:0045087"}],"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":"plant-type hypersensitive response","synonyms":[{"name":"HR","type":"broad"},{"name":"HR-PCD","type":"exact"},{"name":"plant hypersensitive response","type":"exact"}],"termid":"GO:0009626"}


id: GO:0098544
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in which a protein complex is maintained in a location and prevented from moving elsewhere. These include sequestration, stabilization to prevent transport elsewhere and the active retrieval of protein complexes that move away.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"maintenance of location","termid":"GO:0051235"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"maintenance of protein complex location","termid":"GO:0098544"}


id: PBO:0044901
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"derlin 3","termid":"PBO:0044901"}


id: MONDO:0006178
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A solitary fibrous tumor characterized by the presence of areas of abrupt transition to high grade sarcoma.","definition_xrefs":["NCIT:C79948"],"direct_ancestors":[{"relation_name":"is_a","term_name":"solitary fibrous tumor","termid":"MONDO:0016238"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dedifferentiated solitary fibrous tumor","secondary_identifiers":["EFO:1000214","UMLS:C2699572","MEDGEN:396654"],"termid":"MONDO:0006178","xrefs":{"Monarch":{"xref_id":"0006178"}}}


id: FYPO:0004095
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein in a cell is normal (i.e. indistinguishable from wild type) during the meiotic cell cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization","termid":"FYPO:0003627"},{"relation_name":"is_a","term_name":"normal cellular process during meiotic cell cycle","termid":"FYPO:0007277"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal protein localization during meiotic cell cycle","synonyms":[{"name":"normal protein localisation during meiotic cell cycle","type":"exact"}],"termid":"FYPO:0004095"}


id: GO:0044389
data:
  {"annotated_genes":["SJAG_03843","SJAG_02253","SJAG_00803","SJAG_00452","SJAG_01134","SJAG_01226","SJAG_03643","SJAG_01686","SJAG_04335","SJAG_01365","SJAG_02591","SJAG_00615","SJAG_01540","SJAG_00032","SJAG_03575"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[77191],"is_not":false,"summary":null,"term":"GO:0044389"},{"annotations":[77404,78750,80264,72154,80933,68728,73587,74636,76656,80829,80973,81484,82060,74773],"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:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005515","GO:0005488","GO:0003674"],"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: PBO:0044722
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DEAD/H-box helicase 11 like 9 (pseudogene)","termid":"PBO:0044722"}


id: MONDO:0002638
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplasm involving a glossopharyngeal nerve.","definition_xrefs":["MONDO:patterns/neoplasm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cranial nerve neoplasm","termid":"MONDO:0002633"},{"relation_name":"is_a","term_name":"glossopharyngeal nerve disorder","termid":"MONDO:0002639"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glossopharyngeal nerve neoplasm","secondary_identifiers":["DOID:3417","ICD9:239.7","MEDGEN:224734","NCIT:C5828","SCTID:126975006","UMLS:C1263900"],"synonyms":[{"name":"IXth cranial nerve neoplasms","type":"exact"},{"name":"IXth cranial nerve tumors","type":"exact"},{"name":"IXth cranial nerve tumours","type":"exact"},{"name":"Ninth cranial nerve neoplasm","type":"exact"},{"name":"Ninth cranial nerve neoplasms","type":"exact"},{"name":"Ninth cranial nerve tumor","type":"exact"},{"name":"Ninth cranial nerve tumors","type":"exact"},{"name":"Ninth cranial nerve tumour","type":"exact"},{"name":"Ninth cranial nerve tumours","type":"exact"},{"name":"glossopharyngeal nerve neoplasm","type":"exact"},{"name":"glossopharyngeal nerve neoplasm (disease)","type":"exact"},{"name":"glossopharyngeal nerve neoplasms","type":"exact"},{"name":"glossopharyngeal nerve tumor","type":"exact"},{"name":"glossopharyngeal nerve tumors","type":"exact"},{"name":"glossopharyngeal nerve tumour","type":"exact"},{"name":"glossopharyngeal nerve tumours","type":"exact"},{"name":"neoplasm of Ninth cranial nerve","type":"exact"},{"name":"neoplasm of glossopharyngeal nerve","type":"exact"},{"name":"neoplasm of the Ninth cranial nerve","type":"exact"},{"name":"neoplasm of the glossopharyngeal nerve","type":"exact"},{"name":"tumor of Ninth cranial nerve","type":"exact"},{"name":"tumor of glossopharyngeal nerve","type":"exact"},{"name":"tumor of the Ninth cranial nerve","type":"exact"},{"name":"tumor of the glossopharyngeal nerve","type":"exact"},{"name":"tumour of Ninth cranial nerve","type":"exact"},{"name":"tumour of glossopharyngeal nerve","type":"exact"},{"name":"tumour of the Ninth cranial nerve","type":"exact"},{"name":"tumour of the glossopharyngeal nerve","type":"exact"}],"termid":"MONDO:0002638","xrefs":{"Monarch":{"xref_id":"0002638"}}}


id: MONDO:0008690
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"xeroderma pigmentosum","termid":"MONDO:0019600"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0021190"},{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005066","MONDO:0021190"],"is_obsolete":false,"name":"xeroderma pigmentosum, autosomal dominant, mild","secondary_identifiers":["MESH:C565989","OMIM:194400","MEDGEN:395440","UMLS:C1860231"],"synonyms":[{"name":"xeroderma pigmentosum, autosomal dominant, mild","type":"exact"}],"termid":"MONDO:0008690","xrefs":{"Monarch":{"xref_id":"0008690"}}}


id: PBO:0027328
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_degradation_of_ribosomal_proteins","termid":"PBO:0027328"}


id: GO:0043720
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 3-keto-5-aminohexanoate + acetyl-CoA = L-3-aminobutyryl-CoA + acetoacetate.","definition_xrefs":["MetaCyc:R125-RXN","PMID:13064"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyltransferase activity, transferring groups other than amino-acyl groups","termid":"GO:0016747"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016746"},{"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:0016746","GO:0003674","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"3-keto-5-aminohexanoate cleavage activity","secondary_identifiers":["RHEA:31555"],"synonyms":[{"name":"3-keto-5-aminohexanoate cleavage enzyme","type":"exact"}],"termid":"GO:0043720"}


id: GO:0051994
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of a methyl group to the phosphorus atom of an acceptor molecule.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methyltransferase activity","termid":"GO:0008168"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016741"},{"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:0016741","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"P-methyltransferase activity","termid":"GO:0051994"}


id: PR:O94598
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sec5 gene.","definition_xrefs":["UniProtKB:O94598","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":"exocyst complex component sec5 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC622.10c","synonyms":[{"name":"Spom972h-sec5","type":"exact"}],"termid":"PR:O94598"}


id: GO:0072574
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The multiplication or reproduction of hepatocytes, resulting in the expansion of a cell population. Hepatocytes form the main structural component of the liver. They are specialized epithelial cells that are organized into interconnected plates called lobules.","definition_xrefs":["CL:0000182","GOC:mah","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial cell proliferation involved in liver morphogenesis","termid":"GO:0072575"}],"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":"hepatocyte proliferation","termid":"GO:0072574"}


id: PBO:0003264
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pig-N (predicted)","termid":"PBO:0003264"}


id: FYPO:0001174
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A vegetative cell population growth phenotype in which cells grow normally (i.e. indistinguishably from wild type) in a medium containing sucrose as the carbon source.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal vegetative cell population growth","termid":"FYPO:0001357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0002057","FYPO:0002058","FYPO:0002060","FYPO:0000257","FYPO:0000139"],"is_obsolete":false,"name":"normal growth on sucrose carbon source","synonyms":[{"name":"normal cell population growth on sucrose carbon source","type":"exact"},{"name":"normal vegetative cell population growth on sucrose carbon source","type":"exact"}],"termid":"FYPO:0001174"}


id: PBO:0042422
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell division cycle 27 pseudogene 6","termid":"PBO:0042422"}


id: PBO:0038495
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ABCC5 antisense RNA 1","termid":"PBO:0038495"}


id: PBO:0072353
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S26 pseudogene 39","termid":"PBO:0072353"}


id: GO:0009276
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The peptidoglycan layer of the Gram-negative cell envelope. In Gram-negative cells the peptidoglycan is relatively thin (1-2nm) and is linked to the outer membrane by lipoproteins. In Gram-negative cells the peptidoglycan is too thin to retain the primary stain in the Gram staining procedure and therefore cells appear red after Gram stain.","definition_xrefs":["GOC:mlg","ISBN:0815108893"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidoglycan-based cell wall","termid":"GO:0009274"},{"relation_name":"part_of","term_name":"cell envelope","termid":"GO:0030313"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005618"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005618","GO:0005575"],"is_obsolete":false,"name":"Gram-negative-bacterium-type cell wall","synonyms":[{"name":"1-2nm peptidoglycan-based cell wall","type":"exact"},{"name":"cell wall inner membrane","type":"exact"}],"termid":"GO:0009276"}


id: PBO:0059106
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MORN repeat containing 2","termid":"PBO:0059106"}


id: GO:0046179
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of keto-D-gluconate, the anion of keto-D-gluconic acid, an aldonic acid derived from glucose.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"keto-D-gluconate metabolic process","termid":"GO:0019525"},{"relation_name":"is_a","term_name":"ketogluconate biosynthetic process","termid":"GO:0046180"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0005975","GO:0044281"],"is_obsolete":false,"name":"keto-D-gluconate biosynthetic process","synonyms":[{"name":"keto-D-gluconate anabolism","type":"exact"},{"name":"keto-D-gluconate biosynthesis","type":"exact"},{"name":"keto-D-gluconate formation","type":"exact"},{"name":"keto-D-gluconate synthesis","type":"exact"}],"termid":"GO:0046179"}


id: GO:0050612
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: A + arsenite + H2O = AH(2) + arsenate + 2 H+.","definition_xrefs":["GOC:rynl"],"gene_count":0,"genotype_count":0,"name":"obsolete arsenate reductase (donor) activity (obsolete GO:0050612)","termid":"GO:0050612"}


id: PBO:0072247
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S20 pseudogene 22","termid":"PBO:0072247"}


id: GO:0120216
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A cartilage extracellular matrix complex that mediates interactions between major components of the extracellular matrix such as collagens and proteoglycans and contributes to their fibrillar network. Exists as an obligate homotrimer.","definition_xrefs":["PMID:9699631","GOC:bhm","PMID:10367731","PMID:15075323"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"extracellular matrix","termid":"GO:0031012"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"matrilin complex","synonyms":[{"name":"matrilin family complex","type":"related"},{"name":"matrilin-1 complex","type":"narrow"},{"name":"matrilin-2 complex","type":"narrow"},{"name":"matrilin-3 complex","type":"narrow"},{"name":"matrilin-4 complex","type":"narrow"}],"termid":"GO:0120216"}


id: PBO:0077358
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 97 pseudogene 2","termid":"PBO:0077358"}


id: GO:0042294
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of URM1 from one protein to another via the reaction X-URM1 + Y = Y-URM1 + X, where both X-URM1 and Y-URM1 are covalent linkages.","definition_xrefs":["GOC:mah","PMID:12826404"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ubiquitin-like protein transferase activity","termid":"GO:0019787"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0019787"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016746","GO:0019787","GO:0016740","GO:0003824","GO:0003674","GO:0140096"],"is_obsolete":false,"name":"URM1 transferase activity","termid":"GO:0042294"}


id: GO:1902712
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex which is capable of G protein-coupled GABA receptor activity. In human, it is usually a heterodimer composed of GABA-B receptor subunits 1 and 2.","definition_xrefs":["GOC:TermGenie","GO_REF:0000088","GOC:bhm","PMID:18790874"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor dimeric complex","termid":"GO:0038037"},{"relation_name":"is_a","term_name":"GABA receptor complex","termid":"GO:1902710"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005886","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"G protein-coupled GABA receptor complex","synonyms":[{"name":"G-protein coupled GABA receptor complex","type":"exact"}],"termid":"GO:1902712"}


id: PBO:0049171
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GRAPL long non-coding downstream RNA","termid":"PBO:0049171"}


id: FYPO:0006045
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 mitotic sister chromatid biorientation begins later than normal.","definition_xrefs":["PomBase:mah","PMID:27146110"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic sister chromatid biorientation","termid":"FYPO:0000326"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0000641"},{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000337"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0000631","FYPO:0001320","FYPO:0001985","FYPO:0000138","FYPO:0000337","FYPO:0000641"],"is_obsolete":false,"name":"delayed onset of mitotic sister chromatid biorientation","synonyms":[{"name":"delayed mitotic sister chromatid biorientation","type":"exact"},{"name":"delayed onset of mitotic sister chromatid biorientation during vegetative growth","type":"exact"},{"name":"delayed onset of sister chromatid biorientation during mitotic cell cycle","type":"related"},{"name":"mitotic sister chromatid biorientation delayed","type":"exact"}],"termid":"FYPO:0006045"}


id: PBO:0090625
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"external invertase, beta-fructofuranosidase Inv1","termid":"PBO:0090625"}


id: PBO:0058488
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5682","termid":"PBO:0058488"}


id: GO:0043640
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of benzoate, by its hydroxylation to cis-1,2-dihydroxybenzoate followed by dehydrogenation to catechol.","definition_xrefs":["MetaCyc:PWY-2503","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benzoate catabolic process","termid":"GO:0043639"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"benzoate catabolic process via hydroxylation","synonyms":[{"name":"benzoate breakdown via hydroxylation","type":"exact"},{"name":"benzoate degradation via hydroxylation","type":"exact"}],"termid":"GO:0043640"}


id: MONDO:0001960
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Alpers syndrome (obsolete MONDO:0001960)","termid":"MONDO:0001960","xrefs":{"Monarch":{"xref_id":"0001960"}}}


id: GO:0050651
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of dermatan sulfate proteoglycans, which consist of a core protein linked to a dermatan sulfate glycosaminoglycan. The dermatan sulfate chain is composed of the repeating disaccharide unit beta-(1,4)-D-hexuronic acid-beta-(1,3)-N-acetyl-D-galactosamine. Tthe former can be a mixture of sulfated and nonsulfated D-glucuronic and L-iduronic acids, and the latter can be O-sulfated. Dermatan sulfate chains are covalently linked to serine/threonine residues (O-linked) of the core protein via a tetrasaccharide linker sequence (xylose-galactose-galactose-glucuronate).","definition_xrefs":["PMID:17239763"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proteoglycan biosynthetic process","termid":"GO:0030166"},{"relation_name":"is_a","term_name":"dermatan sulfate proteoglycan metabolic process","termid":"GO:0050655"},{"relation_name":"is_a","term_name":"protein O-linked xylosylation","termid":"GO:0180064"}],"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":"dermatan sulfate proteoglycan biosynthetic process","secondary_identifiers":["MetaCyc:PWY-6568"],"synonyms":[{"name":"chondroitin sulfate B proteoglycan biosynthesis","type":"exact"},{"name":"chondroitin sulfate B proteoglycan biosynthetic process","type":"exact"},{"name":"dermatan sulfate proteoglycan anabolism","type":"exact"},{"name":"dermatan sulfate proteoglycan biosynthesis","type":"exact"},{"name":"dermatan sulfate proteoglycan formation","type":"exact"},{"name":"dermatan sulfate proteoglycan synthesis","type":"exact"},{"name":"dermatan sulphate proteoglycan biosynthesis","type":"exact"},{"name":"dermatan sulphate proteoglycan biosynthetic process","type":"exact"}],"termid":"GO:0050651"}


id: GO:0046725
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process where the infecting virus reduces the levels of viral proteins in a cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation by virus of viral protein levels in host cell","termid":"GO:0046719"},{"relation_name":"is_a","term_name":"negative regulation of viral process","termid":"GO:0048525"}],"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 by virus of viral protein levels in host cell","synonyms":[{"name":"down regulation of viral protein levels in host cell","type":"exact"},{"name":"down-regulation of viral protein levels in host cell","type":"exact"},{"name":"downregulation of viral protein levels in host cell","type":"exact"},{"name":"inhibition of viral protein levels in host cell","type":"narrow"},{"name":"negative regulation of viral protein levels","type":"exact"}],"termid":"GO:0046725"}


id: PBO:0064177
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phospholipase A2 group XD, pseudogene","termid":"PBO:0064177"}


id: PBO:0015677
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PAt1 Compensation","termid":"PBO:0015677"}


id: GO:0035095
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in the behavior of an organism as a result of a nicotine stimulus.","definition_xrefs":["ISBN:0198506732","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adult behavior","termid":"GO:0030534"},{"relation_name":"part_of","term_name":"response to nicotine","termid":"GO:0035094"}],"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":"behavioral response to nicotine","synonyms":[{"name":"behavioural response to nicotine","type":"exact"}],"termid":"GO:0035095"}


id: GO:0001302
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process associated with progression of the cell from its inception to the end of its lifespan that occurs as the cell continues cycles of growth and division.","definition_xrefs":["GOC:jh","PMID:12044934"],"gene_count":0,"genotype_count":0,"name":"obsolete replicative cell aging (obsolete GO:0001302)","synonyms":[{"name":"replicative cell ageing","type":"exact"}],"termid":"GO:0001302"}


id: PBO:0013782
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diphosphomevalonate decarboxylase mvd1 (predicted)","termid":"PBO:0013782"}


id: PBO:0050188
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group nucleosome binding domain 1 pseudogene 5","termid":"PBO:0050188"}


id: MONDO:0017549
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"humero-radio-ulnar synostosis","termid":"MONDO:0017983"}],"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":"humero-radio-ulnar synostosis, bilateral","secondary_identifiers":["Orphanet:295207","MEDGEN:1744773","UMLS:C5438978","icd11.foundation:557249772"],"synonyms":[{"name":"humero-radio-ulnar fusion, bilateral","type":"exact"}],"termid":"MONDO:0017549","xrefs":{"Monarch":{"xref_id":"0017549"}}}


id: FYPO:0003289
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 medial cortical nodes is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to medial cortex during vegetative growth","termid":"FYPO:0000731"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000138","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"abnormal protein localization to medial cortical node","synonyms":[{"name":"abnormal protein localisation to medial cortical node","type":"exact"},{"name":"abnormal protein localization to cortical medial dot","type":"exact"},{"name":"abnormal protein localization to cytokinetic nodes","type":"related"},{"name":"abnormal protein localization to medial cortical node during mitotic cell cycle","type":"related"},{"name":"abnormal protein localization to medial cortical node during vegetative growth","type":"exact"},{"name":"abnormal protein localization to medial cortical nodes","type":"exact"},{"name":"abnormal protein recruitment to medial cortical node","type":"related"}],"termid":"FYPO:0003289"}


id: PBO:0055893
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat containing 14","termid":"PBO:0055893"}


id: MONDO:0001185
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder characterized by a retrospective gap in memory of important personal information, usually of a traumatic or stressful nature; the memory loss far exceeds ordinary forgetfulness and is not the result of substance use or the consequence of a medical condition.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dissociative disorder","termid":"MONDO:0001160"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dissociative amnesia","secondary_identifiers":["DOID:11037","ICD9:300.12","SCTID:84209002","icd11.foundation:626975732","MEDGEN:66743","UMLS:C0236795","NCIT:C94328","ICD10CM:F44.0"],"synonyms":[{"name":"psychogenic amnesia","type":"exact"}],"termid":"MONDO:0001185","xrefs":{"Monarch":{"xref_id":"0001185"}}}


id: FYPO:0002437
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 cells form actin cables that are thicker than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal actin cable morphology","termid":"FYPO:0002031"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0004803"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0004803","FYPO:0000002","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"thick actin cables","synonyms":[{"name":"increased actin cable thickness","type":"exact"},{"name":"thick actin cables during mitotic cell cycle","type":"related"},{"name":"thick actin cables during vegetative growth","type":"exact"},{"name":"thick formin-nucleated actin cables","type":"exact"}],"termid":"FYPO:0002437"}


id: PBO:0004384
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphatidylinositol-3,4,5-trisphosphate3-phosphatasePtn1","termid":"PBO:0004384"}


id: PBO:0076098
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"syntaxin 4","termid":"PBO:0076098"}


id: PBO:0029620
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_ATP-dependent_3'-5'_DNA_helicase_activity","termid":"PBO:0029620"}


id: GO:2000052
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of non-canonical Wnt-activated signaling pathway.","definition_xrefs":["GOC:yaf","GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of Wnt signaling pathway","termid":"GO:0030177"},{"relation_name":"is_a","term_name":"regulation of non-canonical Wnt signaling pathway","termid":"GO:2000050"},{"relation_name":"positively_regulates","term_name":"non-canonical Wnt signaling pathway","termid":"GO:0035567"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of non-canonical Wnt signaling pathway","synonyms":[{"name":"positive regulation of beta-catenin-independent Wnt receptor signaling pathway","type":"exact"},{"name":"positive regulation of non-canonical Wnt receptor signaling pathway","type":"exact"},{"name":"positive regulation of non-canonical Wnt receptor signalling pathway","type":"exact"},{"name":"positive regulation of non-canonical Wnt-activated signaling pathway","type":"exact"}],"termid":"GO:2000052"}


id: GO:0008428
data:
  {"annotated_genes":["SJAG_02594"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[90648],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0060698"}]},"cv_name":"molecular_function","definition":"Binds to and stops, prevents or reduces the activity of ribonuclease.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclease inhibitor activity","termid":"GO:0140721"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02594":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0004857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0140678"},{"rel_name":"is_a","termid":"GO:0098772"}],"interesting_parent_ids":["GO:0003674","GO:0030234","GO:0140678","GO:0098772","GO:0004857"],"is_obsolete":false,"name":"ribonuclease inhibitor activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"RNA nuclease inhibitor activity","type":"exact"}],"termid":"GO:0008428","terms_by_termid":{"GO:0060698":null}}


id: PBO:0073177
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"selenoprotein I","termid":"PBO:0073177"}


id: FYPO:0006538
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype in which a cell is shaped in the form of a spheroid during a cellular response to a pheromone. In spheroid cells, there is much less difference between the long and short axes of the cell than in wild type. Spheroid cells may shorter than normal, with approximately the same diameter as normal, or they may be enlarged.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spheroid cell","termid":"FYPO:0001955"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000005"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0000005"],"is_obsolete":false,"name":"spheroid cell during cellular response to pheromone","synonyms":[{"name":"cell morphology, round cells during cellular response to pheromone","type":"related"},{"name":"cell morphology, rounded cells during cellular response to pheromone","type":"related"},{"name":"rounded cell during cellular response to pheromone","type":"exact"}],"termid":"FYPO:0006538"}


id: MONDO:0018160
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited malignant tumor that originates in the nuclear layer of the retina. A predisposition to retinoblastoma has been associated with 13q14 cytogenetic abnormalities. Patients with the inherited form appear to be at increased risk for secondary nonocular malignancies such as osteosarcoma, malignant fibrous histiocytoma, and fibrosarcoma.","definition_xrefs":["NCIT:C8495"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinoblastoma","termid":"MONDO:0008380"},{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"},{"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:0004992"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005328"],"is_obsolete":false,"name":"hereditary retinoblastoma","secondary_identifiers":["Orphanet:357027","DOID:4648","UMLS:C0751483","MEDGEN:155869","GARD:17544","OMIM:180200"],"synonyms":[{"name":"RB1","type":"exact"},{"name":"familial retinoblastoma","type":"exact"},{"name":"hereditary retinoblastoma","type":"exact"},{"name":"retinoblastoma, autosomal dominant, somatic mutation","type":"exact"},{"name":"retinoblastoma, trilateral, autosomal dominant, somatic mutation","type":"exact"}],"termid":"MONDO:0018160","xrefs":{"Monarch":{"xref_id":"0018160"}}}


id: PBO:0089390
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U3 snoRNP-associated protein Utp11","termid":"PBO:0089390"}


id: MONDO:0010015
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any anterior segment dysgenesis in which the cause of the disease is a mutation in the PXDN gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anterior segment dysgenesis","termid":"MONDO:0019503"},{"relation_name":"is_a","term_name":"sclerocornea","termid":"MONDO:0019629"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"anterior segment dysgenesis 7","secondary_identifiers":["Orphanet:289499","UMLS:C3151617","GARD:17327","DOID:0080612","MEDGEN:462967","OMIM:269400"],"synonyms":[{"name":"ASGD7","type":"related"},{"name":"CCMCO","type":"exact"},{"name":"COPOA","type":"related"},{"name":"PXDN anterior segment dysgenesis","type":"exact"},{"name":"PXDN-related ocular dysgenesis","type":"exact"},{"name":"anterior segment dysgenesis 7","type":"exact"},{"name":"anterior segment dysgenesis 7, with sclerocornea","type":"exact"},{"name":"anterior segment dysgenesis caused by mutation in PXDN","type":"exact"},{"name":"congenital cataract microcornea with corneal opacity","type":"related"},{"name":"corneal opacification and other ocular anomalies","type":"related"},{"name":"corneal opacification with Other ocular anomalies","type":"related"},{"name":"corneal opacification with other ocular anomalies","type":"related"},{"name":"sclerocornea with Other ocular anomalies","type":"related"},{"name":"sclerocornea with other ocular anomalies","type":"exact"}],"termid":"MONDO:0010015","xrefs":{"Monarch":{"xref_id":"0010015"}}}


id: GO:0140121
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a Lewy body.","definition_xrefs":["PMID:15158159"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inclusion body assembly","termid":"GO:0070841"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044085","GO:0008150"],"is_obsolete":false,"name":"Lewy body formation","termid":"GO:0140121"}


id: PBO:0000059
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pseudogene malic acid transport protein","termid":"PBO:0000059"}


id: PBO:0040591
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BACH1 intronic transcript 1","termid":"PBO:0040591"}


id: PR:Q09745
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC12C2.04 gene.","definition_xrefs":["UniProtKB:Q09745","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 C12C2.04 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC12C2.04","synonyms":[{"name":"Spom972h-SPBC12C2.04","type":"exact"}],"termid":"PR:Q09745"}


id: GO:0090160
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of substances from the Golgi to lysosomes.","definition_xrefs":["GOC:tb","GOC:ascb_2009","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Golgi to vacuole transport","termid":"GO:0006896"},{"relation_name":"is_a","term_name":"lysosomal transport","termid":"GO:0007041"},{"relation_name":"is_a","term_name":"cytosolic transport","termid":"GO:0016482"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0016192","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"Golgi to lysosome transport","termid":"GO:0090160"}


id: PBO:0029350
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-altered_tRNA_level_during_vegetative_growth","termid":"PBO:0029350"}


id: PBO:0030570
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_cellular_serine_level","termid":"PBO:0030570"}


id: GO:0140052
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 an oxidized lipoprotein particle stimulus.","definition_xrefs":["GOC:aruk","PMID:20037584","GOC:BHF","PMID:27607416"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to low-density lipoprotein particle stimulus","termid":"GO:0071404"}],"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 oxidised low-density lipoprotein particle stimulus","synonyms":[{"name":"cellular response to ox-LDL particle stimulus","type":"exact"},{"name":"cellular response to oxLDL particle stimulus","type":"exact"},{"name":"cellular response to oxidised LDL particle stimulus","type":"exact"},{"name":"cellular response to oxidized LDL particle stimulus","type":"exact"},{"name":"cellular response to oxidized low-density lipoprotein particle stimulus","type":"exact"}],"termid":"GO:0140052"}


id: FYPO:0000046
data:
  {"alleles_by_uniquename":{"SJAG_00266:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00266","name":"atf1delta","uniquename":"SJAG_00266:allele-1"},"SJAG_00409:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00409","name":"gpd1delta","uniquename":"SJAG_00409:allele-1"},"SJAG_00514:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00514","name":"scd1delta","uniquename":"SJAG_00514:allele-1"},"SJAG_01794:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01794","name":"scd2delta","uniquename":"SJAG_01794:allele-1"},"SJAG_01946:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01946","name":"cem1delta","uniquename":"SJAG_01946:allele-1"},"SJAG_02527:allele-1":{"allele_type":"disruption","description":"RNA sequencing revealed that only the 5' end of the disrupted allele showed low RNA expression and coverage","gene_uniquename":"SJAG_02527","name":"lig4::KanMX6","uniquename":"SJAG_02527:allele-1"},"SJAG_02592:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02592","name":"sty1delta","uniquename":"SJAG_02592:allele-1"},"SJAG_03198:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03198","name":"oar2delta","uniquename":"SJAG_03198:allele-1"},"SJAG_03198:allele-2":{"allele_type":"amino_acid_mutation","description":"Y189D cold sensitive","gene_uniquename":"SJAG_03198","name":"oar2-51","uniquename":"SJAG_03198:allele-2"},"SJAG_03198:allele-3":{"allele_type":"amino_acid_mutation","description":"R72A,L75A,R106A,L109A","gene_uniquename":"SJAG_03198","name":"oar2-dm12","synonyms":[{"name":"destruction box mutations","reference":"PMID:23786411","type":"exact"}],"uniquename":"SJAG_03198:allele-3"},"SJAG_03360:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03360","name":"shc1delta","uniquename":"SJAG_03360:allele-1"},"SJAG_03453:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03453","name":"ras1delta","uniquename":"SJAG_03453:allele-1"},"SJAG_04464:allele-1":{"allele_type":"amino_acid_mutation","description":"R152C","gene_uniquename":"SJAG_04464","name":"pim1-R152C","synonyms":[{"name":"Inferred CDK-phospho-mimic mutation","reference":"PMID:28954740","type":"exact"}],"uniquename":"SJAG_04464:allele-1"},"SJAG_04697:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04697","name":"gms1delta","uniquename":"SJAG_04697:allele-1"},"SJAG_04703:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04703","name":"for3delta","uniquename":"SJAG_04703:allele-1"},"SJAG_05207:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_05207","name":"cmp7delta","uniquename":"SJAG_05207:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[121009],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0005883"},{"annotations":[121396,121384],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0004481"},{"annotations":[121509,121224],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000082"},{"annotations":[120984,120986,120985,121455,121000],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000080"},{"annotations":[121480,121066,121476,121472,121212],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001355"},{"annotations":[121076],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001408"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell population phenotype in which cell population growth is decreased relative to normal. Decreased growth may reflect a reduced growth rate (i.e. slower growth), growth that occurs to a lesser extent than normal, or both. Cell population growth refers to an increase in the number of cells in the population as individual cells grow and divide.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell population growth","termid":"FYPO:0000045"},{"relation_name":"is_a","term_name":"viable cell 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sequencing revealed that only the 5' end of the disrupted allele showed low RNA expression and coverage)[Knockdown]","display_uniquename":"lig4::KanMX6-RNA_sequencing_revealed_that_only_the_5'_end_of_the_disrupted_allele_showed_low_RNA_expression_and_coverage-disruption-expression-knockdown","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02527:allele-1","expression":"Knockdown"}]}]},"oar2-51-Y189D_cold_sensitive-amino_acid_mutation-expression-overexpression":{"display_name":"oar2-51(Y189D cold sensitive)[Overexpression]","display_uniquename":"oar2-51-Y189D_cold_sensitive-amino_acid_mutation-expression-overexpression","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03198:allele-2","expression":"Overexpression"}]}]},"oar2-dm12-R72A,L75A,R106A,L109A-amino_acid_mutation-expression-overexpression":{"display_name":"oar2-dm12(R72A,L75A,R106A,L109A 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type"}]}]},"ras1delta":{"display_name":"ras1delta","display_uniquename":"ras1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03453:allele-1","expression":"Null"}]}]},"scd1delta":{"display_name":"scd1delta","display_uniquename":"scd1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00514:allele-1","expression":"Null"}]}]},"scd2delta":{"display_name":"scd2delta","display_uniquename":"scd2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01794:allele-1","expression":"Null"}]}]},"shc1delta":{"display_name":"shc1delta","display_uniquename":"shc1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03360:allele-1","expression":"Null"}]}]},"sty1delta":{"display_name":"sty1delta","display_uniquename":"sty1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02592:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0002058","FYPO:0001985","FYPO:0000003","FYPO:0002057","FYPO:0000139"],"is_obsolete":false,"name":"decreased cell population growth","references_by_uniquename":{"PMID:23786411":null,"PMID:28954740":null,"PMID:29566183":null,"PMID:30726171":null,"PMID:31150379":null,"PMID:32243490":null,"PMID:36058798":null,"PMID:37164017":null,"PMID:37233261":null,"PMID:40195311":null},"secondary_identifiers":["FYPO:0000222"],"single_locus_annotated_genes":["SJAG_05207","SJAG_04464","SJAG_03198","SJAG_03453","SJAG_04703","SJAG_00514","SJAG_00409","SJAG_02527","SJAG_01946","SJAG_04697","SJAG_00266","SJAG_01794","SJAG_02592","SJAG_03360"],"single_locus_genotype_uniquenames":["gpd1delta","oar2delta","gms1delta","ras1delta","oar2-dm12-R72A,L75A,R106A,L109A-amino_acid_mutation-expression-overexpression","sty1delta","cem1delta","atf1delta","lig4::KanMX6-RNA_sequencing_revealed_that_only_the_5'_end_of_the_disrupted_allele_showed_low_RNA_expression_and_coverage-disruption-expression-knockdown","scd1delta","pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type","shc1delta","cmp7delta","scd2delta","for3delta","oar2-51-Y189D_cold_sensitive-amino_acid_mutation-expression-overexpression"],"synonyms":[{"name":"aerobic growth defects","type":"related"},{"name":"decreased aerobic cell population growth","type":"narrow"},{"name":"decreased growth","type":"broad"},{"name":"reduced aerobic cell population growth","type":"narrow"},{"name":"reduced cell population growth","type":"exact"},{"name":"slow aerobic cell population growth","type":"narrow"}],"termid":"FYPO:0000046","terms_by_termid":{"FYECO:0000004":null,"FYECO:0000005":null,"FYECO:0000006":null,"FYECO:0000117":null,"FYECO:0000137":null,"FYPO:0000080":null,"FYPO:0000082":null,"FYPO:0001355":null,"FYPO:0001408":null,"FYPO:0004481":null,"FYPO:0005883":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null}}


id: PBO:0058281
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4658","termid":"PBO:0058281"}


id: PBO:0120127
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Glutathione-dependent oxidoreductase; mitochondrial matrix protein and subunit of an iron-sulfur assembly complex with Bol1p acting at a late stage in iron-sulfur center biogenesis; acts as a central hub in iron-sulfur cluster intermediate trafficking within mitochondria and export to the cytoplasm; hydroperoxide and superoxide-radical responsive; monothiol glutaredoxin subfamily member along with Grx3p and Grx4p","termid":"PBO:0120127"}


id: PBO:0078485
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Ile (anticodon AAT) 5-5","termid":"PBO:0078485"}


id: PBO:0058404
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4774","termid":"PBO:0058404"}


id: MONDO:0006755
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Abnormal thyroid function tests, low triiodothyronine with elevated reverse triiodothyronine, in the setting of non-thyroidal illness.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"thyroid gland disorder","termid":"MONDO:0003240"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"euthyroid sick syndrome","secondary_identifiers":["EFO:1000931","MEDGEN:41908","ICD9:790.94","MESH:D005067","UMLS:C0015190","DOID:2856","NCIT:C113170","ICD10CM:E07.81","MedDRA:10015549","SCTID:237542005"],"synonyms":[{"name":"euthyroid sick syndrome","type":"exact"},{"name":"sick euthyroid syndrome","type":"exact"},{"name":"sick-euthyroid syndrome","type":"exact"}],"termid":"MONDO:0006755","xrefs":{"Monarch":{"xref_id":"0006755"}}}


id: GO:1901285
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of 5,6,7,8-tetrahydromethanopterin.","definition_xrefs":["GOC:TermGenie","GOC:yaf","UniPathway:UPA00065"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dicarboxylic acid biosynthetic process","termid":"GO:0043650"},{"relation_name":"is_a","term_name":"5,6,7,8-tetrahydromethanopterin metabolic process","termid":"GO:1901283"},{"relation_name":"is_a","term_name":"tetrahydromethanopterin biosynthetic process","termid":"GO:2001118"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0042559"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0042559","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"5,6,7,8-tetrahydromethanopterin biosynthetic process","synonyms":[{"name":"5,6,7,8-tetrahydromethanopterin anabolism","type":"exact"},{"name":"5,6,7,8-tetrahydromethanopterin biosynthesis","type":"exact"},{"name":"5,6,7,8-tetrahydromethanopterin formation","type":"exact"},{"name":"5,6,7,8-tetrahydromethanopterin synthesis","type":"exact"}],"termid":"GO:1901285"}


id: GO:0016247
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binds to and modulates the activity of a channel. A channel catalyzes energy-independent facilitated diffusion, mediated by passage of a solute through a transmembrane aqueous pore or channel.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transporter regulator activity","termid":"GO:0141108"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0098772","GO:0003674"],"is_obsolete":false,"name":"channel regulator activity","termid":"GO:0016247"}


