# terms

id: PBO:0018174
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"structure-specific DNA nuclease regulator Pxd1","termid":"PBO:0018174"}


id: PBO:0003185
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.6.1.2","termid":"PBO:0003185"}


id: MONDO:0012670
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the LRTOMT gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0019497"}],"interesting_parent_ids":["MONDO:0019497","MONDO:0006025"],"is_obsolete":false,"name":"autosomal recessive nonsyndromic hearing loss 63","secondary_identifiers":["OMIM:611451","UMLS:C1969621","DOID:0110515","GARD:22627","MEDGEN:409872","MESH:C566951"],"synonyms":[{"name":"DFNB63","type":"narrow"},{"name":"LRTOMT autosomal recessive nonsyndromic deafness","type":"narrow"},{"name":"autosomal recessive deafness 63","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 63","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness caused by mutation in LRTOMT","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 63","type":"narrow"},{"name":"autosomal recessive nonsyndromic hearing loss 63","type":"exact"},{"name":"deafness, autosomal recessive 63","type":"narrow"},{"name":"deafness, autosomal recessive type 63","type":"narrow"}],"termid":"MONDO:0012670","xrefs":{"Monarch":{"xref_id":"0012670"}}}


id: MONDO:0002751
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma that arises from glandular epithelial cells of the urinary bladder","direct_ancestors":[{"relation_name":"is_a","term_name":"adenocarcinoma","termid":"MONDO:0004970"},{"relation_name":"is_a","term_name":"urinary bladder carcinoma","termid":"MONDO:0004986"}],"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":"bladder adenocarcinoma","secondary_identifiers":["SCTID:255110003","UMLS:C0279682","NCIT:C4032","EFO:1000125","DOID:3711","ONCOTREE:BLAD","MEDGEN:76014"],"synonyms":[{"name":"adenocarcinoma of bladder","type":"exact"},{"name":"adenocarcinoma of the bladder","type":"exact"},{"name":"adenocarcinoma of the urinary bladder","type":"exact"},{"name":"adenocarcinoma of urinary bladder","type":"exact"},{"name":"blad","type":"related"},{"name":"bladder adenocarcinoma","type":"exact"},{"name":"urinary bladder adenocarcinoma","type":"exact"}],"termid":"MONDO:0002751","xrefs":{"Monarch":{"xref_id":"0002751"}}}


id: PBO:0113355
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein required for proper cell fusion and cell morphology; acts as phosphorylation-regulated noise suppressor of pheromone signaling pathway; forms a complex with Bud14p and Kel2p that regulates Bnr1p (formin) to affect actin cable assembly, cytokinesis, and polarized growth; functions in a complex with Kel2p to negatively regulate mitotic exit, interacts with Tem1p and Lte1p; localizes to regions of polarized growth; potential Cdc28p substrate","termid":"PBO:0113355"}


id: PBO:0047431
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FCF1 pseudogene 2","termid":"PBO:0047431"}


id: GO:0030174
data:
  {"annotated_genes":["SJAG_03160","SJAG_03438","SJAG_03695","SJAG_03048","SJAG_00364","SJAG_03720","SJAG_01210","SJAG_02162"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[104191,110737,99588],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903467"},{"annotations":[119144,113893],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903468"},{"annotations":[118094,104197,108455,90875],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904514"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of initiation of DNA-dependent DNA replication; the process in which DNA becomes competent to replicate. In eukaryotes, replication competence is established in early G1 and lost during the ensuing S phase.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of DNA-templated DNA replication","termid":"GO:0090329"},{"relation_name":"regulates","term_name":"DNA replication initiation","termid":"GO:0006270"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00364":null,"SJAG_01210":null,"SJAG_02162":null,"SJAG_03048":null,"SJAG_03160":null,"SJAG_03438":null,"SJAG_03695":null,"SJAG_03720":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006259"},{"rel_name":"regulates","termid":"GO:0006260"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006259","GO:0006260"],"is_obsolete":false,"name":"regulation of DNA-templated DNA replication initiation","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"DNA replication licencing","type":"exact"},{"name":"DNA replication licensing","type":"exact"},{"name":"regulation of DNA replication initiation","type":"broad"},{"name":"regulation of DNA-dependent DNA replication initiation","type":"exact"}],"termid":"GO:0030174","terms_by_termid":{"GO:1903467":null,"GO:1903468":null,"GO:1904514":null}}


id: MONDO:0017353
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Neonatal glycine encephalopathy is a frequent, usually severe form of glycine encephalopathy (GE) characterized by coma, apnea, hypotonia, seizure and myoclonic jerks in the neonatal period, and subsequent developmental delay.","definition_xrefs":["Orphanet:289857"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycine encephalopathy","termid":"MONDO:0011612"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0005066"],"is_obsolete":false,"name":"neonatal glycine encephalopathy","secondary_identifiers":["GARD:17332","icd11.foundation:414151121","MEDGEN:1785446","NANDO:1200985","UMLS:C5548200"],"synonyms":[{"name":"classic glycine encephalopathy","type":"exact"},{"name":"neonatal NKH","type":"exact"},{"name":"neonatal non-ketotic hyperglycinemia","type":"exact"}],"termid":"MONDO:0017353","xrefs":{"Monarch":{"xref_id":"0017353"}}}


id: PBO:0078346
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Glu (CTC) 12-1","termid":"PBO:0078346"}


id: PBO:0089661
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phospholipid-translocating ATPase complex Lem3 family subunit","termid":"PBO:0089661"}


id: PBO:0055707
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lectin, mannose binding 2","termid":"PBO:0055707"}


id: GO:0043156
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Structural changes to eukaryotic chromatin occurring as a result of cation stress, an increase or decrease in the concentration of positively charged ions in the environment.","definition_xrefs":["GOC:jl","PMID:14762213","GOC:vw"],"gene_count":0,"genotype_count":0,"name":"obsolete chromatin remodeling in response to cation stress (obsolete GO:0043156)","termid":"GO:0043156"}


id: GO:0009897
data:
  {"annotated_genes":["SJAG_04685","SJAG_02260","SJAG_00254","SJAG_00310","SJAG_04851","SJAG_00109","SJAG_00415","SJAG_03640","SJAG_00784","SJAG_04875","SJAG_01086","SJAG_02173","SJAG_02916","SJAG_04238","SJAG_00096","SJAG_04789","SJAG_04209","SJAG_01290","SJAG_04850","SJAG_05272","SJAG_01835","SJAG_00340","SJAG_03204","SJAG_01029","SJAG_02093","SJAG_02435"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[58769,65243,91738,91932,95859,96656,96668,96669,96670,97095,104060,104067,104068,105820,108390,114887,115599,116237,116336,116613,117465,118132,119205,119641,120216,120653],"is_not":false,"summary":null,"term":"GO:0009897"}]},"cv_name":"cellular_component","definition":"The leaflet of the plasma membrane that faces away from the cytoplasm and any proteins embedded or anchored in it or attached to its surface.","definition_xrefs":["GOC:tb","GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"side of membrane","termid":"GO:0098552"},{"relation_name":"part_of","term_name":"plasma membrane","termid":"GO:0005886"},{"relation_name":"part_of","term_name":"cell surface","termid":"GO:0009986"}],"gene_count":26,"genes_by_uniquename":{"SJAG_00096":null,"SJAG_00109":null,"SJAG_00254":null,"SJAG_00310":null,"SJAG_00340":null,"SJAG_00415":null,"SJAG_00784":null,"SJAG_01029":null,"SJAG_01086":null,"SJAG_01290":null,"SJAG_01835":null,"SJAG_02093":null,"SJAG_02173":null,"SJAG_02260":null,"SJAG_02435":null,"SJAG_02916":null,"SJAG_03204":null,"SJAG_03640":null,"SJAG_04209":null,"SJAG_04238":null,"SJAG_04685":null,"SJAG_04789":null,"SJAG_04850":null,"SJAG_04851":null,"SJAG_04875":null,"SJAG_05272":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0009986"}],"interesting_parent_ids":["GO:0005886","GO:0005575","GO:0009986"],"is_obsolete":false,"name":"external side of plasma membrane","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"external leaflet of plasma membrane","type":"exact"},{"name":"juxtamembrane","type":"broad"},{"name":"outer surface of cytoplasmic membrane","type":"exact"}],"termid":"GO:0009897","terms_by_termid":{"GO:0009897":null}}


id: PBO:0026782
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_cell_cycle_progression_following_cellular_response_to_hydroxyurea","termid":"PBO:0026782"}


id: GO:0035927
data:
  {"annotated_genes":["SJAG_03358"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[80895],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016031"}]},"cv_name":"biological_process","definition":"The process in which a rRNA, ribosomal ribonucleic acid, is transported from the cytosol into the mitochondrial matrix.","definition_xrefs":["GOC:ans","PMID:20691904"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA transport","termid":"GO:0050658"},{"relation_name":"is_a","term_name":"transmembrane transport","termid":"GO:0055085"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03358":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0008150","GO:0055085","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"RNA import into mitochondrion","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"cytoplasmic RNA import into mitochondrion","type":"narrow"},{"name":"nuclear-encoded RNA import into mitochondrion","type":"narrow"}],"termid":"GO:0035927","terms_by_termid":{"GO:0016031":null}}


id: GO:0036315
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 sterol stimulus.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to sterol","termid":"GO:0036314"},{"relation_name":"is_a","term_name":"cellular response to lipid","termid":"GO:0071396"},{"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 sterol","termid":"GO:0036315"}


id: PBO:0053607
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 640","termid":"PBO:0053607"}


id: PATO:0000044
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A physical quality which inheres in a bearer by virtue of the number of the bearer's repetitive actions in a particular time.","definition_xrefs":["Wikipedia:http://en.wikipedia.org/wiki/frequency"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rate","termid":"PATO:0000161"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"frequency","termid":"PATO:0000044"}


id: PR:Q9UQX0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A superoxide dismutase [Mn], mitochondrial that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO01332","PANTHER:PTHR11404:SF5"],"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":"superoxide dismutase [Mn], mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1486.01","secondary_identifiers":["UniProtKB:Q9UQX0"],"synonyms":[{"name":"Spom972h-SOD2","type":"exact"}],"termid":"PR:Q9UQX0"}


id: MONDO:0700166
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A sexually transmitted tumor arising from histiocytes and occurring in dogs.","definition_xrefs":["NCIT:C162473"],"direct_ancestors":[{"relation_name":"is_a","term_name":"venereal tumors, veterinary","termid":"MONDO:0025478"},{"relation_name":"is_a","term_name":"canine neoplasm","termid":"MONDO:0700139"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"canine transmissible venereal tumor","termid":"MONDO:0700166","xrefs":{"Monarch":{"xref_id":"0700166"}}}


id: GO:0090167
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in which disassembled Golgi vesicles are localized into daughter cells upon cell division.","definition_xrefs":["GOC:tb","GOC:dph","GOC:ascb_2009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Golgi organization","termid":"GO:0007030"},{"relation_name":"is_a","term_name":"Golgi localization","termid":"GO:0051645"},{"relation_name":"part_of","term_name":"Golgi inheritance","termid":"GO:0048313"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"Golgi distribution to daughter cells","synonyms":[{"name":"Golgi apparatus distribution to daughter cells","type":"exact"}],"termid":"GO:0090167"}


id: MONDO:0011464
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Spinocerebellar ataxia type 11 (SCA11) is a subtype of autosomal dominant cerebellar ataxia type III (ADCA type III) characterized by the early-onset of cerebellar signs, eye movement abnormalities and pyramidal signs.","definition_xrefs":["Orphanet:98767"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant cerebellar ataxia type III","termid":"MONDO:0019793"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0000426","MONDO:0002039"],"is_obsolete":false,"name":"spinocerebellar ataxia type 11","secondary_identifiers":["GARD:10475","MESH:C565772","DOID:0050961","icd11.foundation:743674840","UMLS:C1858351","SCTID:719207000","MEDGEN:346799","OMIM:604432"],"synonyms":[{"name":"SCA11","type":"exact"},{"name":"spinocerebellar ataxia 11","type":"related"},{"name":"spinocerebellar ataxia type 11","type":"exact"}],"termid":"MONDO:0011464","xrefs":{"Monarch":{"xref_id":"0011464"}}}


id: GO:0070287
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with ferritin, and delivering ferritin into the cell via endocytosis.","definition_xrefs":["PMID:19154717","PMID:17459943","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cargo receptor activity","termid":"GO:0038024"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038024"}],"interesting_parent_ids":["GO:0003674","GO:0038024"],"is_obsolete":false,"name":"ferritin receptor activity","synonyms":[{"name":"ferritin complex receptor activity","type":"exact"}],"termid":"GO:0070287"}


id: MONDO:0030923
data:
  {"annotated_genes":["SJAG_04489","SJAG_03345"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88537],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013501"},{"annotations":[87108],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010936"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited neurodegenerative disorder","termid":"MONDO:0024237"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03345":null,"SJAG_04489":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"frontotemporal dementia and/or amyotrophic lateral sclerosis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIMPS:105500"],"termid":"MONDO:0030923","terms_by_termid":{"MONDO:0010936":null,"MONDO:0013501":null},"xrefs":{"Monarch":{"xref_id":"0030923"}}}


id: GO:0034920
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: pyrene + 2 H+ + 2 e- + O2 = cis-4,5-dihydroxy-4,5-dihydropyrene.","definition_xrefs":["UM-BBD_reactionID:r0934"],"gene_count":0,"genotype_count":0,"name":"obsolete pyrene dioxygenase activity (obsolete GO:0034920)","termid":"GO:0034920"}


id: PBO:0078328
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor delta variable 3","termid":"PBO:0078328"}


id: PBO:0081909
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 876, pseudogene","termid":"PBO:0081909"}


id: PBO:0089149
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin-protein ligase E3, human RNF126 ortholog","termid":"PBO:0089149"}


id: PBO:0084263
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Integral ER membrane protein with type-III transmembrane domains; required for maintenance of ER zinc homeostasis; required for post-translational SRP-independent protein translocation into the ER; necessary for efficient targeting of Trm1p tRNA methyltransferase to the inner nuclear membrane; mutations cause defects in cortical ER morphology in both the mother and daughter cells","termid":"PBO:0084263"}


id: MONDO:0043089
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute posterior multifocal placoid pigment epitheliopathy (APMPPE) is an acquired, inflammatory eye condition affecting the retina, retinal pigment epithelium (pigmented layer of the retina), and choroid. It usually affects both eyes and is characterized by multiple, yellow-white lesions in the back of the eye. The condition can significantly impair visual acuity if the macula is involved. APMPPE typically resolves on its own in weeks to months. While the cause is unknown, about a third of cases appear to develop after a flu-like illness. Non-ocular symptoms are uncommon, but cerebral vasculitis can be present and may cause permanent and/or severe neurological complications.","definition_xrefs":["GARD:0002183"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"},{"relation_name":"is_a","term_name":"multifocal choroiditis","termid":"MONDO:0023833"}],"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":"acute posterior multifocal placoid pigment epitheliopathy","secondary_identifiers":["ICD10CM:H30.14","MEDGEN:56348","GARD:2183","icd11.foundation:2036282532","NORD:1101","SCTID:89188001","UMLS:C0154884"],"synonyms":[{"name":"AMPPE","type":"related"},{"name":"APMPPE","type":"related"},{"name":"Epitheliopathy, Acute Posterior Multifocal Placoid Pigment","type":"exact"},{"name":"acute multifocal placoid pigment epitheliopathy","type":"related"},{"name":"acute placoid pigment epitheliopathy","type":"related"},{"name":"acute posterior multifocal placoid pigment epitheliopathy","type":"exact"},{"name":"amppe - acute multifocal placoid pigment epitheliopathy","type":"related"},{"name":"apmppe","type":"related"},{"name":"epitheliopathy, acute posterior multifocal placoid pigment","type":"related"},{"name":"multifocal placoid pigment epitheliopathy","type":"related"},{"name":"pigment epitheliopathy, disseminated retinitis and retinochoroiditis","type":"related"}],"termid":"MONDO:0043089","xrefs":{"Monarch":{"xref_id":"0043089"}}}


id: PBO:0077436
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 170A","termid":"PBO:0077436"}


id: GO:0032099
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that reduces appetite.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of response to food","termid":"GO:0032096"},{"relation_name":"is_a","term_name":"regulation of appetite","termid":"GO:0032098"}],"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 appetite","synonyms":[{"name":"appetite suppression","type":"related"},{"name":"down regulation of appetite","type":"exact"},{"name":"down-regulation of appetite","type":"exact"},{"name":"downregulation of appetite","type":"exact"},{"name":"inhibition of appetite","type":"narrow"},{"name":"negative regulation of hunger","type":"related"}],"termid":"GO:0032099"}


id: PBO:0090636
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"40S ribosomal protein S4","termid":"PBO:0090636"}


id: MONDO:1011760
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"integumentary system disorder, non-human animal","termid":"MONDO:1011328"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"symmetrical onychomadesis, non-human animal","secondary_identifiers":["OMIA:001989"],"termid":"MONDO:1011760","xrefs":{"Monarch":{"xref_id":"1011760"}}}


id: MONDO:0016726
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete neuronal tumor (obsolete MONDO:0016726)","secondary_identifiers":["Orphanet:251924"],"termid":"MONDO:0016726","xrefs":{"Monarch":{"xref_id":"0016726"}}}


id: GO:0001532
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with interleukin-21 and transmitting the signal from one side of the membrane to the other to initiate a change in cell activity.","definition_xrefs":["GOC:jl","GOC:signaling"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine receptor activity","termid":"GO:0004896"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0038023","GO:0003674"],"is_obsolete":false,"name":"interleukin-21 receptor activity","synonyms":[{"name":"IL-21 receptor activity","type":"exact"},{"name":"IL-21R","type":"exact"}],"termid":"GO:0001532"}


id: GO:0008304
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete eukaryotic translation initiation factor 4 complex (obsolete GO:0008304)","synonyms":[{"name":"eIF-4","type":"exact"},{"name":"eukaryotic translation initiation factor 4 complex","type":"exact"}],"termid":"GO:0008304"}


id: PBO:0088969
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger C2H2-type, human ZNF277 ortholog, implicated in transcriptional regulation","termid":"PBO:0088969"}


id: MONDO:0030716
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spermatogenic failure","termid":"MONDO:0004983"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"spermatogenic failure 66","secondary_identifiers":["UMLS:C5676945","DOID:0070565","OMIM:619799","MEDGEN:1806298"],"synonyms":[{"name":"SPGF66","type":"exact"},{"name":"spermatogenic failure 66","type":"exact"}],"termid":"MONDO:0030716","xrefs":{"Monarch":{"xref_id":"0030716"}}}


id: GO:0140055
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A histone reader that recognizes a histone H4 acetylated at lysine 8.","definition_xrefs":["PMID:17996705"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H4 reader activity","termid":"GO:0140008"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0060090"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140566"},{"rel_name":"is_a","termid":"GO:0030674"}],"interesting_parent_ids":["GO:0030674","GO:0003674","GO:0140566","GO:0060090"],"is_obsolete":false,"name":"histone H4K8ac reader activity","synonyms":[{"name":"H4K8ac modified histone binding","type":"narrow"}],"termid":"GO:0140055"}


id: PBO:0078597
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripartite motif containing 60 pseudogene 10, Y-linked","termid":"PBO:0078597"}


id: GO:0015652
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: quaternary ammonium group(out) + H+(out) = quaternary ammonium group(in) + H+(in).","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"solute:proton symporter activity","termid":"GO:0015295"},{"relation_name":"is_a","term_name":"quaternary ammonium group transmembrane transporter activity","termid":"GO:0015651"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0003674","GO:0022857","GO:0005215"],"is_obsolete":false,"name":"quaternary ammonium group:proton symporter activity","synonyms":[{"name":"quaternary ammonium group:hydrogen symporter activity","type":"exact"}],"termid":"GO:0015652"}


id: PBO:0090861
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Arf GAP, GTPase activating protein for Arf6, Ucp3","termid":"PBO:0090861"}


id: GO:0106289
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of deadenylation-dependent decapping of nuclear-transcribed mRNA.","definition_xrefs":["PMID:32354837"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of deadenylation-dependent decapping of nuclear-transcribed mRNA","termid":"GO:0106288"},{"relation_name":"is_a","term_name":"negative regulation of mRNA catabolic process","termid":"GO:1902373"},{"relation_name":"negatively_regulates","term_name":"deadenylation-dependent decapping of nuclear-transcribed mRNA","termid":"GO:0000290"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0010467"},{"rel_name":"negatively_regulates","termid":"GO:0016071"},{"rel_name":"regulates","termid":"GO:0016071"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150","GO:0016071"],"is_obsolete":false,"name":"negative regulation of deadenylation-dependent decapping of nuclear-transcribed mRNA","termid":"GO:0106289"}


id: GO:0016831
data:
  {"annotated_genes":["SJAG_03743","SJAG_03632","SJAG_02902","SJAG_04842","SJAG_03349","SJAG_01455","SJAG_04109","SJAG_00043","SJAG_02176","SJAG_00937","SJAG_03524","SJAG_01081","SJAG_02980","SJAG_04627","SJAG_00721","SJAG_03164","SJAG_02734"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[91451],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120539"},{"annotations":[79592],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004014"},{"annotations":[78906],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004163"},{"annotations":[81365],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004351"},{"annotations":[70059],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004425"},{"annotations":[77492],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004586"},{"annotations":[75799],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004590"},{"annotations":[120390],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008948"},{"annotations":[62749,72639,80909],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004609"},{"annotations":[91194],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004633"},{"annotations":[65436],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004638"},{"annotations":[75622,72916,73239],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004737"},{"annotations":[76659],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004853"}]},"cv_name":"molecular_function","definition":"Catalysis of the nonhydrolytic addition or removal of a carboxyl group to or from a compound.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-carbon lyase activity","termid":"GO:0016830"}],"gene_count":17,"genes_by_uniquename":{"SJAG_00043":null,"SJAG_00721":null,"SJAG_00937":null,"SJAG_01081":null,"SJAG_01455":null,"SJAG_02176":null,"SJAG_02734":null,"SJAG_02902":null,"SJAG_02980":null,"SJAG_03164":null,"SJAG_03349":null,"SJAG_03524":null,"SJAG_03632":null,"SJAG_03743":null,"SJAG_04109":null,"SJAG_04627":null,"SJAG_04842":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0003824","GO:0016829","GO:0003674"],"is_obsolete":false,"name":"carboxy-lyase activity","references_by_uniquename":{"GO_REF:0000003":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-6787757","Reactome:R-HSA-6814165","Reactome:R-HSA-71223","EC:4.1.1.-"],"synonyms":[{"name":"decarboxylase activity","type":"exact"}],"termid":"GO:0016831","terms_by_termid":{"GO:0004014":null,"GO:0004163":null,"GO:0004351":null,"GO:0004425":null,"GO:0004586":null,"GO:0004590":null,"GO:0004609":null,"GO:0004633":null,"GO:0004638":null,"GO:0004737":null,"GO:0004853":null,"GO:0008948":null,"GO:0120539":null}}


id: GO:0005021
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with a vascular endothelial growth factor (VEGF) receptor ligand and transmitting the signal across the plasma membrane to initiate a change in cell activity.","definition_xrefs":["GOC:signaling","GOC:mah","PMID:19909239"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane receptor protein tyrosine kinase activity","termid":"GO:0004714"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0004672"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016301"}],"interesting_parent_ids":["GO:0016301","GO:0140096","GO:0038023","GO:0003824","GO:0003674","GO:0004672","GO:0016740"],"is_obsolete":false,"name":"vascular endothelial growth factor receptor activity","secondary_identifiers":["GO:0036326","GO:0036330","GO:0036327","GO:0036328","GO:0036329"],"synonyms":[{"name":"VEGF receptor activity","type":"exact"},{"name":"VEGF-A-activated receptor activity","type":"narrow"},{"name":"VEGF-B-activated receptor activity","type":"narrow"},{"name":"VEGF-C-activated receptor activity","type":"narrow"},{"name":"VEGF-D-activated receptor activity","type":"narrow"},{"name":"VEGF-E-activated receptor activity","type":"narrow"},{"name":"VEGF-activated receptor activity","type":"exact"},{"name":"VEGFR activity","type":"exact"},{"name":"vascular endothelial growth factor E-activated receptor activity","type":"exact"},{"name":"vascular endothelial growth factor-activated receptor activity","type":"exact"}],"termid":"GO:0005021"}


id: PBO:0073902
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLC14A2 antisense RNA 1","termid":"PBO:0073902"}


id: MONDO:0003303
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-metastasizing encapsulated neoplasm arising from nerves in the gallbladder. Morphologically, it is characterized by the presence of fibroblasts and Schwann cells.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gallbladder cancer","termid":"MONDO:0005411"},{"relation_name":"is_a","term_name":"neurofibroma","termid":"MONDO:0016755"},{"relation_name":"is_a","term_name":"peripheral nervous system cancer","termid":"MONDO:0021089"},{"relation_name":"is_a","term_name":"malignant glioma","termid":"MONDO:0100342"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0002515","MONDO:0004992"],"is_obsolete":false,"name":"neurofibroma of gallbladder","secondary_identifiers":["NCIT:C5746","UMLS:C1333751","MEDGEN:232540","DOID:5150"],"synonyms":[{"name":"gall bladder neurofibroma","type":"exact"},{"name":"gallbladder neurofibroma","type":"exact"},{"name":"neurofibroma of gall bladder","type":"exact"},{"name":"neurofibroma of gallbladder","type":"exact"},{"name":"neurofibroma of the gallbladder","type":"exact"}],"termid":"MONDO:0003303","xrefs":{"Monarch":{"xref_id":"0003303"}}}


id: PBO:0065358
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prosaposin like 1","termid":"PBO:0065358"}


id: GO:0008622
data:
  {"annotated_genes":["SJAG_04879","SJAG_01823","SJAG_02908","SJAG_02667"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[109178,111785,115422,117263],"is_not":false,"summary":null,"term":"GO:0008622"}]},"cv_name":"cellular_component","definition":"A heterotetrameric DNA polymerase complex that catalyzes processive DNA synthesis in the absence of PCNA, but is further stimulated in the presence of PCNA. The complex contains a large catalytic subunit and three small subunits, and is best characterized in Saccharomyces, in which the subunits are named Pol2p, Dpb2p, Dpb3p, and Dpb4p. Some evidence suggests that DNA polymerase epsilon is the leading strand polymerase; it is also involved in nucleotide-excision repair and mismatch repair.","definition_xrefs":["PMID:9745046","PMID:15814431"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA polymerase complex","termid":"GO:0042575"},{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"},{"relation_name":"part_of","term_name":"nuclear chromosome","termid":"GO:0000228"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01823":null,"SJAG_02667":null,"SJAG_02908":null,"SJAG_04879":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005694"}],"interesting_parent_ids":["GO:0005634","GO:0005575","GO:0005694","GO:0032991"],"is_obsolete":false,"name":"epsilon DNA polymerase complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"DNA polymerase epsilon complex","type":"exact"}],"termid":"GO:0008622","terms_by_termid":{"GO:0008622":null}}


id: GO:0004263
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the preferential cleavage of Tyr-Xaa > Trp-Xaa > Phe-Xaa > Leu-Xaa.","definition_xrefs":["ISBN:0198506732"],"gene_count":0,"genotype_count":0,"name":"obsolete chymotrypsin activity (obsolete GO:0004263)","synonyms":[{"name":"alpha-chymar","type":"related"},{"name":"alpha-chymar ophth","type":"related"},{"name":"alpha-chymotrypsin A","type":"related"},{"name":"alpha-chymotrypsin activity","type":"narrow"},{"name":"avazyme","type":"related"},{"name":"chymar","type":"related"},{"name":"chymotest","type":"related"},{"name":"chymotrypsin A activity","type":"narrow"},{"name":"chymotrypsin B activity","type":"narrow"},{"name":"chymotrypsin activity","type":"exact"},{"name":"chymotrypsins A and B","type":"related"},{"name":"enzeon","type":"related"},{"name":"quimar","type":"related"},{"name":"quimotrase activity","type":"related"}],"termid":"GO:0004263"}


id: PR:O94534
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- alp14 gene.","definition_xrefs":["UniProtKB:O94534","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":"spindle pole body component alp14 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC895.07","synonyms":[{"name":"Spom972h-alp14","type":"exact"},{"name":"altered polarity protein 14 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94534"}


id: PBO:0005147
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bis(5'-nucleosidyl)-tetraphosphatase","termid":"PBO:0005147"}


id: PBO:0077112
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translocase of inner mitochondrial membrane 21","termid":"PBO:0077112"}


id: MONDO:0005369
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A slow growing neuroendocrine tumor, composed of uniform, round, or polygonal cells having monotonous, centrally located nuclei and small nucleoli, infrequent mitoses, and no necrosis. The tumor may show a variety of patterns, such as solid, trabecular, and acinar. Electron microscopy shows small secretory granules. Immunohistochemical studies reveal NSE, as well as chromogranin immunoreactivity. Malignant histology (cellular pleomorphism, hyperchromatic nuclei, prominent nucleoli, necrosis, and mitoses) can occasionally be seen. Such cases may have an aggressive clinical course. Gastrointestinal tract and lung are common sites of involvement.","definition_xrefs":["NCIT:C2915"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuroendocrine neoplasm","termid":"MONDO:0019496"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"carcinoid tumor","secondary_identifiers":["HP:0100570","UMLS:C0007095","ICD9:209.60","EFO:0004243","ICDO:8240/3","ICDO:8241/3","MEDGEN:2838","MESH:D002276","NANDO:2200396","SCTID:443492008"],"synonyms":[{"name":"NET G1","type":"exact"},{"name":"carcinoid","type":"exact"},{"name":"carcinoid tumor","type":"exact"},{"name":"carcinoid tumor (disease)","type":"exact"},{"name":"carcinoid tumour (disease)","type":"exact"},{"name":"neuroendocrine neoplasm G1","type":"exact"},{"name":"neuroendocrine tumor G1","type":"exact"},{"name":"neuroendocrine tumour G1","type":"exact"}],"termid":"MONDO:0005369","xrefs":{"Monarch":{"xref_id":"0005369"}}}


id: GO:0046075
data:
  {"annotated_genes":["SJAG_04665","SJAG_04657","SJAG_04627"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[94252,72780,70216],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006235"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving dTTP, deoxyribosylthymine triphosphate.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine deoxyribonucleoside triphosphate metabolic process","termid":"GO:0009211"},{"relation_name":"is_a","term_name":"pyrimidine deoxyribonucleotide metabolic process","termid":"GO:0009219"}],"gene_count":3,"genes_by_uniquename":{"SJAG_04627":null,"SJAG_04657":null,"SJAG_04665":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0055086"],"is_obsolete":false,"name":"dTTP metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000107":null},"synonyms":[{"name":"dTTP metabolism","type":"exact"}],"termid":"GO:0046075","terms_by_termid":{"GO:0006235":null}}


id: PR:P33075
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An adenylate kinase 2, mitochondrial that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR23359:SF22","PRO:DNx","OMA:SCHPO00933"],"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":"adenylate kinase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4G9.03","secondary_identifiers":["UniProtKB:P33075"],"synonyms":[{"name":"ATP-AMP transphosphorylase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"ATP:AMP phosphotransferase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-AK2","type":"exact"},{"name":"adenylate kinase cytosolic and mitochondrial (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"adenylate monophosphate kinase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P33075"}


id: FYPO:0003125
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the occurrence of translational initiation in the cytoplasm is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased translation","termid":"FYPO:0001798"},{"relation_name":"is_a","term_name":"abnormal cytoplasmic translation","termid":"FYPO:0003124"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985","FYPO:0005447","FYPO:0006551"],"is_obsolete":false,"name":"decreased cytoplasmic translational initiation","synonyms":[{"name":"decreased cytoplasmic translation initiation","type":"exact"},{"name":"decreased cytoplasmic translational initiation during mitotic cell cycle","type":"related"},{"name":"decreased cytoplasmic translational initiation during vegetative growth","type":"exact"},{"name":"reduced cytoplasmic translational initiation","type":"exact"}],"termid":"FYPO:0003125"}


id: PBO:0076273
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"synaptonemal complex central element protein 1 like","termid":"PBO:0076273"}


id: GO:0075151
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which the symbiont organism activates, maintains or increases the frequency, rate or extent of its receptor-mediated signal transduction as a result of detecting molecules of its host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of receptor-mediated signal transduction in response to host (obsolete GO:0075151)","synonyms":[{"name":"positive regulation of symbiont receptor-mediated signal transduction in response to host","type":"exact"}],"termid":"GO:0075151"}


id: MONDO:0010179
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Isolated right ventricular hypoplasia (IRVH) is a rare congenital heart malformation characterized by underdevelopment of the right ventricle associated with patent foramen ovale or interauricular communication and normally developed tricuspid and pulmonary valves. IRVH manifests with severe cyanosis, congestive heart failure, and in severe cases, death in early infancy.","definition_xrefs":["Orphanet:439"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"hypoplastic right heart syndrome","termid":"MONDO:0020291"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"isolated right ventricular hypoplasia","secondary_identifiers":["MEDGEN:336377","SCTID:718135001","MESH:C535682","OMIM:277200","GARD:4721","UMLS:C1848587"],"synonyms":[{"name":"Irvh","type":"related"},{"name":"hypoplasia of the right ventricle","type":"related"},{"name":"isolated hypoplasia of the right ventricle","type":"related"},{"name":"right ventricle hypoplasia","type":"related"},{"name":"right ventricular hypoplasia","type":"related"},{"name":"right ventricular hypoplasia, isolated","type":"related"}],"termid":"MONDO:0010179","xrefs":{"Monarch":{"xref_id":"0010179"}}}


id: MONDO:0033619
data:
  {"annotated_genes":["SJAG_04821"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87502],"is_not":false,"summary":null,"term":"MONDO:0033619"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"ALG14-congenital disorder of glycosylation","termid":"MONDO:0100559"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04821":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0024322"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0024322"],"is_obsolete":false,"name":"myopathy, epilepsy, and progressive cerebral atrophy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5436652","MEDGEN:1759100","OMIM:619036"],"synonyms":[{"name":"MEPCA","type":"exact"}],"termid":"MONDO:0033619","terms_by_termid":{"MONDO:0033619":null},"xrefs":{"Monarch":{"xref_id":"0033619"}}}


id: PBO:0074058
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLC25A36 pseudogene 1","termid":"PBO:0074058"}


id: PBO:0085121
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nucleolar protein; essential for processing and maturation of 27S pre-rRNA and large ribosomal subunit biogenesis; constituent of 66S pre-ribosomal particles; contains four RNA recognition motifs (RRMs); human ortholog RBM28 implicated in ANE syndrome","termid":"PBO:0085121"}


id: PBO:0062686
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 51 subfamily A member 7","termid":"PBO:0062686"}


id: PBO:0084525
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Member of the conserved GPN-loop GTPase family; has a role in transport of RNA polymerase II to the nucleus; exhibits GTP-dependent binding to PolII; has ATPase activity; involved in sister chromatid cohesion; phosphorylated by the Pcl1p-Pho85p kinase complex; human homolog XAB1 interacts with human RNA polymerase II; protein abundance increases in response to DNA replication stress","termid":"PBO:0084525"}


id: FYPO:0000422
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the occurrence of endocytosis is decreased. A phenotype may affect endocytosis of all cargoes, or of specific cargo such as a particular protein.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_output","term_name":"increased protein level in plasma membrane","termid":"FYPO:0003504"},{"relation_name":"is_a","term_name":"abnormal endocytosis during vegetative growth","termid":"FYPO:0000034"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0001320","FYPO:0000138","FYPO:0001985"],"is_obsolete":false,"name":"decreased endocytosis during vegetative growth","synonyms":[{"name":"decreased endocytosis during mitotic cell cycle","type":"related"},{"name":"decreased protein internalization during vegetative growth","type":"narrow"},{"name":"endocytosis: decreased during vegetative growth","type":"related"},{"name":"reduced actin-mediated endocytosis during vegetative growth","type":"exact"},{"name":"reduced endocytosis during vegetative growth","type":"exact"}],"termid":"FYPO:0000422"}


id: PBO:0088309
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutathione S-transferase","termid":"PBO:0088309"}


id: GO:0010419
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving the side chains of pectic rhamnogalacturonan II. A number of structurally distinct di- and oligosaccharides can be attached to the C-3 and C-2 of the backbone, respectively.","definition_xrefs":["GOC:tair_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rhamnogalacturonan II metabolic process","termid":"GO:0010396"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0005975"],"is_obsolete":false,"name":"rhamnogalacturonan II side chain metabolic process","synonyms":[{"name":"rhamnogalacturonan II side chain metabolism","type":"exact"}],"termid":"GO:0010419"}


id: GO:1901390
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of transforming growth factor beta activation.","definition_xrefs":["GOC:TermGenie","GOC:sl"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of transforming growth factor beta activation (obsolete GO:1901390)","synonyms":[{"name":"activation of L-TGF-beta activation","type":"exact"},{"name":"activation of TGF-B activation","type":"exact"},{"name":"activation of TGF-beta activation","type":"exact"},{"name":"activation of TGFB activation","type":"exact"},{"name":"activation of TGFbeta activation","type":"exact"},{"name":"activation of latent TGF-beta activation","type":"exact"},{"name":"activation of transforming growth factor beta activation","type":"narrow"},{"name":"positive regulation of L-TGF-beta activation","type":"exact"},{"name":"positive regulation of TGF-B activation","type":"exact"},{"name":"positive regulation of TGF-beta activation","type":"exact"},{"name":"positive regulation of TGFB activation","type":"exact"},{"name":"positive regulation of TGFbeta activation","type":"exact"},{"name":"positive regulation of latent TGF-beta activation","type":"exact"},{"name":"up regulation of L-TGF-beta activation","type":"exact"},{"name":"up regulation of TGF-B activation","type":"exact"},{"name":"up regulation of TGF-beta activation","type":"exact"},{"name":"up regulation of TGFB activation","type":"exact"},{"name":"up regulation of TGFbeta activation","type":"exact"},{"name":"up regulation of latent TGF-beta activation","type":"exact"},{"name":"up regulation of transforming growth factor beta activation","type":"exact"},{"name":"up-regulation of L-TGF-beta activation","type":"exact"},{"name":"up-regulation of TGF-B activation","type":"exact"},{"name":"up-regulation of TGF-beta activation","type":"exact"},{"name":"up-regulation of TGFB activation","type":"exact"},{"name":"up-regulation of TGFbeta activation","type":"exact"},{"name":"up-regulation of latent TGF-beta activation","type":"exact"},{"name":"up-regulation of transforming growth factor beta activation","type":"exact"},{"name":"upregulation of L-TGF-beta activation","type":"exact"},{"name":"upregulation of TGF-B activation","type":"exact"},{"name":"upregulation of TGF-beta activation","type":"exact"},{"name":"upregulation of TGFB activation","type":"exact"},{"name":"upregulation of TGFbeta activation","type":"exact"},{"name":"upregulation of latent TGF-beta activation","type":"exact"},{"name":"upregulation of transforming growth factor beta activation","type":"exact"}],"termid":"GO:1901390"}


id: MONDO:0016396
data:
  {"annotated_genes":["SJAG_04084","SJAG_04321"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88098],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013853"},{"annotations":[88703],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014485"}]},"cv_name":"mondo","definition":"Pontocerebellar hypoplasia type 1 (PCH1), also known as Norman's disease, is a clinically and genetically heterogeneous group of autosomal recessive disorders with a prenatal onset characterized by diffuse muscular atrophy secondary to pontocerebellar hypoplasia and spinal cord anterior horn cell degeneration resulting in early death.","definition_xrefs":["Orphanet:2254"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental anomaly of metabolic origin","termid":"MONDO:0015327"},{"relation_name":"is_a","term_name":"bulbospinal muscular atrophy","termid":"MONDO:0016113"},{"relation_name":"is_a","term_name":"autosomal recessive non-syndromic intellectual disability","termid":"MONDO:0019502"},{"relation_name":"is_a","term_name":"pontocerebellar hypoplasia","termid":"MONDO:0020135"}],"gene_count":2,"genes_by_uniquename":{"SJAG_04084":null,"SJAG_04321":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0020022"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0037792","MONDO:0006025","MONDO:0005559","MONDO:0005066","MONDO:0020022"],"is_obsolete":false,"name":"pontocerebellar hypoplasia type 1","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:10704","icd11.foundation:1227773923","MESH:C548069","SCTID:718610008","UMLS:C5442006","DOID:0112322","MEDGEN:1780208"],"synonyms":[{"name":"MRT32","type":"exact"},{"name":"Norman disease","type":"exact"},{"name":"PCH1","type":"exact"},{"name":"mental retardation, autosomal recessive 32","type":"related"}],"termid":"MONDO:0016396","terms_by_termid":{"MONDO:0013853":null,"MONDO:0014485":null},"xrefs":{"Monarch":{"xref_id":"0016396"}}}


id: GO:0099072
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that regulates the the local concentration of neurotransmitter receptor at the postsynaptic membrane.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of biological quality","termid":"GO:0065008"}],"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 postsynaptic membrane neurotransmitter receptor levels","termid":"GO:0099072"}


id: PBO:0084022
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Glycosylphosphatidylinositol (GPI)-anchored cell wall endoglucanase; localizes in birth scars; required for proper cell separation after cytokinesis; expression is activated by Swi5p and tightly regulated in a cell cycle-dependent manner","termid":"PBO:0084022"}


id: MONDO:0015109
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mitral valve disorder","termid":"MONDO:0003767"},{"relation_name":"is_a","term_name":"congenital mitral valve insufficiency and/or stenosis","termid":"MONDO:0019817"}],"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":"congenital anomaly of the mitral subvalvular apparatus","secondary_identifiers":["GARD:19784","UMLS:C3164517","MEDGEN:756923","icd11.foundation:498751490","Orphanet:101932"],"termid":"MONDO:0015109","xrefs":{"Monarch":{"xref_id":"0015109"}}}


id: GO:0001664
data:
  {"annotated_genes":["SJAG_02233","SJAG_02444"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[75950,82143],"is_not":false,"summary":null,"term":"GO:0001664"}]},"cv_name":"molecular_function","definition":"Binding to a G protein-coupled receptor.","definition_xrefs":["GOC:ceb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"signaling receptor binding","termid":"GO:0005102"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02233":null,"SJAG_02444":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"G protein-coupled receptor binding","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-500717"],"synonyms":[{"name":"G protein coupled receptor binding","type":"exact"},{"name":"G protein coupled receptor ligand","type":"narrow"},{"name":"G-protein coupled receptor binding","type":"exact"},{"name":"G-protein-coupled receptor ligand","type":"narrow"}],"termid":"GO:0001664","terms_by_termid":{"GO:0001664":null}}


id: PATO:0000885
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000885 male fertility value (obsolete PATO:0000885)","termid":"PATO:0000885"}


id: GO:0106078
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: succinyl-CoA + histone = CoA + succinyl-histone.","definition_xrefs":["PMID:29211711"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptide N-succinyltransferase activity","termid":"GO:0106075"},{"relation_name":"is_a","term_name":"histone modifying activity","termid":"GO:0140993"}],"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:0003824"},{"rel_name":"is_a","termid":"GO:0016746"}],"interesting_parent_ids":["GO:0016740","GO:0003824","GO:0140096","GO:0016746","GO:0003674"],"is_obsolete":false,"name":"histone succinyltransferase activity","termid":"GO:0106078"}


id: PBO:0070784
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L12 pseudogene 14","termid":"PBO:0070784"}


id: PBO:0060734
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase complex assembly factor 3","termid":"PBO:0060734"}


id: GO:0045770
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of asymmetric cell division.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of asymmetric cell division","termid":"GO:0009786"},{"relation_name":"is_a","term_name":"positive regulation of cell division","termid":"GO:0051781"},{"relation_name":"positively_regulates","term_name":"asymmetric cell division","termid":"GO:0008356"}],"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 asymmetric cell division","synonyms":[{"name":"activation of asymmetric cell division","type":"narrow"},{"name":"stimulation of asymmetric cell division","type":"narrow"},{"name":"up regulation of asymmetric cell division","type":"exact"},{"name":"up-regulation of asymmetric cell division","type":"exact"},{"name":"upregulation of asymmetric cell division","type":"exact"}],"termid":"GO:0045770"}


id: PBO:0031674
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_secretion","termid":"PBO:0031674"}


id: PBO:0030918
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_cell_cortex_morphology_during_vegetative_growth","termid":"PBO:0030918"}


id: PR:O14334
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A prefoldin subunit 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO02984","PANTHER:PTHR20903:SF0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prefoldin subunit 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1D7.01","secondary_identifiers":["UniProtKB:O14334"],"synonyms":[{"name":"Spom972h-PFDN1","type":"exact"}],"termid":"PR:O14334"}


id: PBO:0084214
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Homodimeric subunit of autophagy-specific PtdIns-3-kinase complex I; required for the integrity of the active PtdIns-3-kinase complex I by maintaining an association between Vps15p-Vps34p and Atg14p-Vps30p subcomplexes; localizes to the pre-autophagosomal structure (PAS) in an Atg14p-dependent manner; ATG38 is non-essential but is required for macroautophagy","termid":"PBO:0084214"}


id: GO:0018342
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The covalent attachment of a prenyl group to a protein; geranyl, farnesyl, or geranylgeranyl groups may be added.","definition_xrefs":["GOC:di","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein modification process","termid":"GO:0036211"},{"relation_name":"is_a","term_name":"prenylation","termid":"GO:0097354"}],"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":"protein prenylation","secondary_identifiers":["GO:0018346"],"synonyms":[{"name":"C-terminal protein prenylation","type":"narrow"},{"name":"protein amino acid prenylation","type":"exact"}],"termid":"GO:0018342"}


id: PBO:0080676
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WHAMM pseudogene 3","termid":"PBO:0080676"}


id: PBO:0045318
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"double C2 domain alpha","termid":"PBO:0045318"}


id: PBO:0047684
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibronectin leucine rich transmembrane protein 1","termid":"PBO:0047684"}


id: PBO:0063600
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peroxisomal biogenesis factor 12 pseudogene 1","termid":"PBO:0063600"}


id: RO:HOM0000060
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Between-species paralogy that involves single copy paralogs resulting from reciprocal gene loss.","direct_ancestors":[{"relation_name":"is_a","term_name":"in_1_to_1_homology_relationship_with","termid":"RO:HOM0000019"},{"relation_name":"is_a","term_name":"in_between-species_paralogy_relationship_with","termid":"RO:HOM0000050"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"in_apparent_orthology_relationship_with","synonyms":[{"name":"1:1 paralogy","type":"exact"},{"name":"apparent 1:1 orthology","type":"exact"},{"name":"apparent orthologous to","type":"exact"},{"name":"pseudoorthology","type":"exact"}],"termid":"RO:HOM0000060"}


id: PBO:0061976
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 2 subfamily AP member 1","termid":"PBO:0061976"}


id: PBO:0080187
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vitamin D receptor","termid":"PBO:0080187"}


id: MONDO:0018480
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"carcinoma of esophagus","termid":"MONDO:0019086"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"carcinoma of esophagus, salivary gland type","secondary_identifiers":["MEDGEN:1678006","GARD:21741","Orphanet:418945","UMLS:C5190854"],"synonyms":[{"name":"esophageal carcinoma, salivary gland type","type":"exact"}],"termid":"MONDO:0018480","xrefs":{"Monarch":{"xref_id":"0018480"}}}


id: PBO:0076729
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcobalamin 2","termid":"PBO:0076729"}


id: GO:0102872
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 1-palmitoyl-2-linoleoyl-phosphatidylcholine + O2 + a reduced electron acceptor = 1-16:0-2-18:3-phosphatidylcholine + 2 H2O + an oxidized electron acceptor.","definition_xrefs":["PMID:8102138","GOC:pz","PMID:15538555"],"gene_count":0,"genotype_count":0,"name":"obsolete 1-16:0-2-18:2-phosphatidylcholine desaturase activity (obsolete GO:0102872)","termid":"GO:0102872"}


id: GO:1902382
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of 11-oxo-beta-amyrin.","definition_xrefs":["PMID:22128119","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pentacyclic triterpenoid catabolic process","termid":"GO:0019741"},{"relation_name":"is_a","term_name":"ketone catabolic process","termid":"GO:0042182"},{"relation_name":"is_a","term_name":"11-oxo-beta-amyrin metabolic process","termid":"GO:1902381"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0006629"],"is_obsolete":false,"name":"11-oxo-beta-amyrin catabolic process","synonyms":[{"name":"11-oxo-beta-amyrin breakdown","type":"exact"},{"name":"11-oxo-beta-amyrin catabolism","type":"exact"},{"name":"11-oxo-beta-amyrin degradation","type":"exact"}],"termid":"GO:1902382"}


id: GO:2001194
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of lysine biosynthetic process via alpha-aminoadipate and saccharopine.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of lysine biosynthetic process via aminoadipic acid","termid":"GO:1902986"},{"relation_name":"regulates","term_name":"lysine biosynthetic process via alpha-aminoadipate and saccharopine","termid":"GO:0051975"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006520"},{"rel_name":"regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0006520"],"is_obsolete":false,"name":"regulation of lysine biosynthetic process via alpha-aminoadipate and saccharopine","synonyms":[{"name":"regulation of lysine biosynthesis via aminoadipic acid and saccharopine","type":"exact"},{"name":"regulation of lysine biosynthetic process via aminoadipic acid and saccharopine","type":"exact"}],"termid":"GO:2001194"}


id: GO:0102264
data:
  {"annotated_genes":["SJAG_03236"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[106521],"is_not":false,"summary":null,"term":"GO:0102264"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: a 5,6-dihydrouracil20 in tRNA + NAD(P) = H+ + a uracil20 in tRNA + NAD(P)H.","definition_xrefs":["EC:1.3.1.91","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA dihydrouridine synthase activity","termid":"GO:0017150"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03236":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140101"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0140101","GO:0140098","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"tRNA-dihydrouridine20 synthase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:RXN-12456"],"termid":"GO:0102264","terms_by_termid":{"GO:0102264":null}}


id: MONDO:0013909
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"human herpesvirus 8, susceptibility to","secondary_identifiers":["MEDGEN:766754","OMIM:614836","UMLS:C3553840"],"synonyms":[{"name":"HHV-8, susceptibility to","type":"related"},{"name":"HHV8S","type":"exact"},{"name":"HUMAN HERPESVIRUS 8, susceptibility to","type":"related"}],"termid":"MONDO:0013909","xrefs":{"Monarch":{"xref_id":"0013909"}}}


id: SO:0000075
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An attribute to describe a gene when the 3' region overlaps with another gene's 3' region.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"overlapping","termid":"SO:0000068"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"three_prime_three_prime_overlap","synonyms":[{"name":"three prime-three prime overlap","type":"exact"}],"termid":"SO:0000075"}


id: GO:0030677
data:
  {"annotated_genes":["SJAG_03234","SJAG_01369","SJAG_02547","SJAG_00306","SJAG_04582","SJAG_01623","SJAG_02553","SJAG_06613","SJAG_04916","SJAG_03796","SJAG_00955"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[117164,64547,92898,120472,72917,117252,61025,106381,101303,73150,73486],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005655"}]},"cv_name":"cellular_component","definition":"A ribonucleoprotein complex that catalyzes cleavage of the leader sequence of precursor tRNAs (pre-tRNAs), generating the mature 5' end of tRNAs.","definition_xrefs":["PMID:12045094","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endoribonuclease complex","termid":"GO:1902555"},{"relation_name":"is_a","term_name":"ribonucleoprotein complex","termid":"GO:1990904"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00306":null,"SJAG_00955":null,"SJAG_01369":null,"SJAG_01623":null,"SJAG_02547":null,"SJAG_02553":null,"SJAG_03234":null,"SJAG_03796":null,"SJAG_04582":null,"SJAG_04916":null,"SJAG_06613":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"ribonuclease P complex","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"RNase P complex","type":"exact"}],"termid":"GO:0030677","terms_by_termid":{"GO:0005655":null}}


id: PBO:0086841
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein with similarity to asparagine synthetases; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm; YML096W is not an essential gene and partially overlaps the verified gene RAD10","termid":"PBO:0086841"}


id: PBO:0030011
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-meiosis_and_sporulation_in_haploid","termid":"PBO:0030011"}


id: MONDO:0015653
data:
  {"annotated_genes":["SJAG_00686","SJAG_02774","SJAG_01507"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87903],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0034106"},{"annotations":[88501],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0044319"},{"annotations":[88917],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0958231"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"epilepsy","termid":"MONDO:0005027"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00686":null,"SJAG_01507":null,"SJAG_02774":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"monogenic epilepsy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5680430","GARD:20086","MEDGEN:1842675","Orphanet:166472"],"synonyms":[{"name":"monogenic disease with epilepsy","type":"exact"}],"termid":"MONDO:0015653","terms_by_termid":{"MONDO:0034106":null,"MONDO:0044319":null,"MONDO:0958231":null},"xrefs":{"Monarch":{"xref_id":"0015653"}}}


id: PBO:0004456
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"19S proteasome regulatory subunit Rpn2 (predicted)","termid":"PBO:0004456"}


id: GO:0080171
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of a lytic vacuole.","definition_xrefs":["PMID:20729380"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vacuole organization","termid":"GO:0007033"}],"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":"lytic vacuole organization","synonyms":[{"name":"lytic vacuolar assembly","type":"narrow"},{"name":"lytic vacuole biogenesis","type":"related"},{"name":"lytic vacuole organisation","type":"exact"},{"name":"lytic vacuole organization and biogenesis","type":"related"}],"termid":"GO:0080171"}


id: GO:1902526
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of protein monoubiquitination.","definition_xrefs":["GOC:TermGenie","PMID:21931591"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein ubiquitination","termid":"GO:0031397"},{"relation_name":"is_a","term_name":"regulation of protein monoubiquitination","termid":"GO:1902525"},{"relation_name":"negatively_regulates","term_name":"protein monoubiquitination","termid":"GO:0006513"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0070647"},{"rel_name":"negatively_regulates","termid":"GO:0070647"}],"interesting_parent_ids":["GO:0008150","GO:0070647"],"is_obsolete":false,"name":"negative regulation of protein monoubiquitination","synonyms":[{"name":"down regulation of protein monoubiquitination","type":"exact"},{"name":"down regulation of protein monoubiquitinylation","type":"exact"},{"name":"down regulation of protein monoubiquitylation","type":"exact"},{"name":"down-regulation of protein monoubiquitination","type":"exact"},{"name":"down-regulation of protein monoubiquitinylation","type":"exact"},{"name":"down-regulation of protein monoubiquitylation","type":"exact"},{"name":"downregulation of protein monoubiquitination","type":"exact"},{"name":"downregulation of protein monoubiquitinylation","type":"exact"},{"name":"downregulation of protein monoubiquitylation","type":"exact"},{"name":"inhibition of protein monoubiquitination","type":"narrow"},{"name":"inhibition of protein monoubiquitinylation","type":"narrow"},{"name":"inhibition of protein monoubiquitylation","type":"narrow"},{"name":"negative regulation of protein monoubiquitinylation","type":"exact"},{"name":"negative regulation of protein monoubiquitylation","type":"exact"}],"termid":"GO:1902526"}


id: MONDO:0021169
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hemangioma characterized by the presence of epithelioid endothelial cells.","definition_xrefs":["NCIT:C4298"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hemangioma","termid":"MONDO:0006500"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"epithelioid hemangioma","secondary_identifiers":["UMLS:C0205788","DOID:474","MEDGEN:61449","ICDO:9125/0","Orphanet:675396"],"synonyms":[{"name":"epithelioid haemangioma","type":"exact"},{"name":"epithelioid hemangioma","type":"exact"},{"name":"histiocytoid hemangioma","type":"exact"}],"termid":"MONDO:0021169","xrefs":{"Monarch":{"xref_id":"0021169"}}}


id: PBO:0091698
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by S. cerevisiae sgt1","termid":"PBO:0091698"}


id: MONDO:0034147
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete neonatal epileptic encephalopathy due to glutaminase deficiency (obsolete MONDO:0034147)","termid":"MONDO:0034147","xrefs":{"Monarch":{"xref_id":"0034147"}}}


id: PBO:0081223
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger MYM-type containing 3","termid":"PBO:0081223"}


id: GO:0050431
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to TGF-beta, transforming growth factor beta, a multifunctional peptide that controls proliferation, differentiation and other functions in many cell types.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"growth factor binding","termid":"GO:0019838"},{"relation_name":"is_a","term_name":"cytokine binding","termid":"GO:0019955"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"transforming growth factor beta binding","synonyms":[{"name":"TGF-beta binding","type":"exact"},{"name":"TGFbeta binding","type":"exact"},{"name":"transforming growth factor beta ligand binding to type I receptor","type":"related"},{"name":"transforming growth factor beta ligand binding to type II receptor","type":"related"}],"termid":"GO:0050431"}


id: GO:1902644
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving tertiary alcohol.","definition_xrefs":["GO_REF:0000068","GOC:mengo_curators","GOC:TermGenie","PMID:11288200"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alcohol metabolic process","termid":"GO:0006066"}],"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":"tertiary alcohol metabolic process","synonyms":[{"name":"tertiary alcohol metabolism","type":"exact"}],"termid":"GO:1902644"}


id: GO:0019884
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which an antigen-presenting cell expresses antigen (peptide or lipid) of exogenous origin on its cell surface in association with an MHC protein complex.","definition_xrefs":["ISBN:0781735149","GOC:add","PMID:15771591","PMID:15928678"],"direct_ancestors":[{"relation_name":"is_a","term_name":"antigen processing and presentation","termid":"GO:0019882"}],"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":"antigen processing and presentation of exogenous antigen","synonyms":[{"name":"antigen presentation, exogenous antigen","type":"exact"}],"termid":"GO:0019884"}


id: GO:0072076
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The biological process whose specific outcome is the progression of a nephrogenic mesenchyme from an initial condition to its mature state. This process begins with the formation of nephrogenic mesenchyme and ends with the mature structure. Nephrogenic mesenchyme is the tissue made up of loosely connected mesenchymal cells in the nephron.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kidney mesenchyme development","termid":"GO:0072074"},{"relation_name":"part_of","term_name":"nephron development","termid":"GO:0072006"}],"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":"nephrogenic mesenchyme development","termid":"GO:0072076"}


id: PBO:0077046
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"THRAP3 pseudogene 1","termid":"PBO:0077046"}


id: PBO:0076740
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"t-complex 11 like 2","termid":"PBO:0076740"}


id: MONDO:0800127
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare hereditary amyloidosis that incorporates deposition of amyloid microfibril material in the lung parenchyma.","definition_xrefs":["PMID:29038189"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary amyloidosis","termid":"MONDO:0018634"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0021179"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0021179","MONDO:0005066"],"is_obsolete":false,"name":"pulmonary amyloidosis","secondary_identifiers":["UMLS:C0700376","MEDGEN:675153"],"termid":"MONDO:0800127","xrefs":{"Monarch":{"xref_id":"0800127"}}}


id: MONDO:0014638
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Fanconi anemia in which the cause of the disease is a mutation in the UBE2T gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Fanconi anemia","termid":"MONDO:0019391"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0021190"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0002280","MONDO:0021190","MONDO:0005066","MONDO:0005046"],"is_obsolete":false,"name":"Fanconi anemia complementation group T","secondary_identifiers":["UMLS:C4084840","GARD:16111","DOID:0111081","MEDGEN:896157","OMIM:616435"],"synonyms":[{"name":"FANCT","type":"exact"},{"name":"Fanconi Anemia, complementation group type T","type":"exact"},{"name":"Fanconi anaemia caused by mutation in UBE2T","type":"exact"},{"name":"Fanconi anaemia complementation group type T","type":"exact"},{"name":"Fanconi anemia caused by mutation in UBE2T","type":"exact"},{"name":"Fanconi anemia complementation group type T","type":"exact"},{"name":"Fanconi anemia, complementation group T","type":"related"},{"name":"UBE2T Fanconi anaemia","type":"exact"},{"name":"UBE2T Fanconi anemia","type":"exact"}],"termid":"MONDO:0014638","xrefs":{"Monarch":{"xref_id":"0014638"}}}


id: GO:0061529
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regulated release of epinephrine by a cell in which the epinephrine acts as a neurotransmitter.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epinephrine secretion","termid":"GO:0048242"},{"relation_name":"is_a","term_name":"catecholamine secretion, neurotransmission","termid":"GO:0160043"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0023052","GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"epinephrine secretion, neurotransmission","synonyms":[{"name":"adrenaline secretion, neurotransmission","type":"exact"}],"termid":"GO:0061529"}


id: PBO:0005061
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.3.1.12","termid":"PBO:0005061"}


id: PBO:0003101
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA export factor, cytoplasmic nucleoporin Gle1","termid":"PBO:0003101"}


id: PBO:0041360
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C4BPA pseudogene 3","termid":"PBO:0041360"}


id: MONDO:0009465
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare form of intestinal atresia characterized by the presence of numerous atresic segments in the small bowel (duodenum) or large bowel and leading to symptoms of intestinal obstruction: vomiting, abdominal bloating and inability to pass meconium in newborns.","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete syndromic intestinal malformation (obsolete MONDO:0015212)","termid":"MONDO:0015212"},{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"multiple intestinal atresia","secondary_identifiers":["GARD:3013","MedDRA:10028210","MEDGEN:65090","Orphanet:2300","SCTID:95472001","ICD9:751.8","MESH:C562441","DOID:14671","UMLS:C0220744"],"synonyms":[{"name":"CID-MIA/early-onset IBD","type":"related"},{"name":"GIDID","type":"related"},{"name":"combined immunodeficiency-enteropathy spectrum","type":"related"},{"name":"familial intestinal polyatresia syndrome","type":"related"},{"name":"gastrointestinal defects and immunodeficiency syndrome","type":"related"},{"name":"intestinal atresia multiple","type":"related"},{"name":"intestinal atresia, multiple","type":"related"},{"name":"intestinal atresia, multiple and/or inflammatory bowel disease with or without immunodeficiency","type":"related"},{"name":"multiple gastrointestinal atresias","type":"exact"},{"name":"multiple intestinal atresia","type":"exact"}],"termid":"MONDO:0009465","xrefs":{"Monarch":{"xref_id":"0009465"}}}


id: PBO:0045475
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dorsal root ganglia homeobox","termid":"PBO:0045475"}


id: GO:0034912
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: phthalate 3,4-cis-dihydrodiol + NAD+ = 3,4-dihydroxyphthalate + NADH + H+.","definition_xrefs":["UM-BBD_reactionID:r1445"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor","termid":"GO:0016628"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"phthalate 3,4-cis-dihydrodiol dehydrogenase activity","secondary_identifiers":["MetaCyc:RXN5F9-56"],"termid":"GO:0034912"}


id: PBO:0054289
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 1680","termid":"PBO:0054289"}


id: PBO:0067647
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 822, pseudogene","termid":"PBO:0067647"}


id: GO:1905303
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of macropinocytosis.","definition_xrefs":["GO_REF:0000058","GOC:PARL","PMID:18691641","GOC:TermGenie","GOC:pad"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of pinocytosis","termid":"GO:0048549"},{"relation_name":"is_a","term_name":"regulation of macropinocytosis","termid":"GO:1905301"},{"relation_name":"positively_regulates","term_name":"macropinocytosis","termid":"GO:0044351"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0016192"],"is_obsolete":false,"name":"positive regulation of macropinocytosis","synonyms":[{"name":"activation of macropinocytosis","type":"narrow"},{"name":"up regulation of macropinocytosis","type":"exact"},{"name":"up-regulation of macropinocytosis","type":"exact"},{"name":"upregulation of macropinocytosis","type":"exact"}],"termid":"GO:1905303"}


id: GO:0016853
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id: GO:0001760
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-amino-3-carboxymuconate 6-semialdehyde + H+ = 2-aminomuconate 6-semialdehyde + CO2.","definition_xrefs":["RHEA:16557","EC:4.1.1.45"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxy-lyase activity","termid":"GO:0016831"}],"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":"aminocarboxymuconate-semialdehyde decarboxylase activity","secondary_identifiers":["KEGG_REACTION:R04323","MetaCyc:AMINO-CARBOXYMUCONATE-SEMIALDEHYDE-RXN"],"synonyms":[{"name":"2-amino-3-(3-oxoprop-1-en-1-yl)but-2-enedioate carboxy-lyase (2-aminomuconate-semialdehyde-forming)","type":"related"},{"name":"2-amino-3-(3-oxoprop-1-en-1-yl)but-2-enedioate carboxy-lyase activity","type":"related"},{"name":"2-amino-3-(3-oxoprop-2-enyl)but-2-enedioate carboxy-lyase activity","type":"related"},{"name":"ACMSD activity","type":"exact"},{"name":"alpha-amino-beta-carboxymuconate-epsilon-semialdehade decarboxylase activity","type":"related"},{"name":"alpha-amino-beta-carboxymuconate-epsilon-semialdehyde beta-decarboxylase activity","type":"related"},{"name":"picolinic acid carboxylase activity","type":"related"},{"name":"picolinic acid decarboxylase activity","type":"related"}],"termid":"GO:0001760"}


id: PBO:0051023
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"insulin like growth factor binding protein 3","termid":"PBO:0051023"}


id: PBO:0036071
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_histone_H3-K9_methylation_during_vegetative_growth","termid":"PBO:0036071"}


id: FYPO:0004033
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to chromatin at tRNA genes is increased.","definition_xrefs":["PomBase:mah","PMID:25392932"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein localization to chromatin at ncRNA genes","termid":"FYPO:0007011"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000138","FYPO:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"increased protein localization to chromatin at tRNA genes","synonyms":[{"name":"increased protein localisation to chromatin at tRNA genes","type":"exact"},{"name":"increased protein localization to chromatin at tRNA genes during mitotic cell cycle","type":"related"},{"name":"increased protein localization to chromatin at tRNA genes during vegetative growth","type":"exact"},{"name":"increased protein localization to chromatin at transfer RNA genes","type":"exact"}],"termid":"FYPO:0004033"}


id: GO:0060108
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The extracellular matrix part that is a regularly spaced indentation in the outer cortical layer of the cuticle. The pattern of annular furrows corresponds to sites of invaginations in hypodermal cell membranes that, in turn, correspond to submembranous regions where actin microfilament bundles assemble early in lethargus, the first phase of the molting cycle in which activity and feeding decline.","definition_xrefs":["GOC:dph","GOC:kmv","ISSN:15518507"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"cortical layer of collagen and cuticulin-based cuticle extracellular matrix","termid":"GO:0060106"}],"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":"annular furrow extracellular matrix","termid":"GO:0060108"}


id: PBO:0000836
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sulfite reductase Sir1","termid":"PBO:0000836"}


id: FYPO:0001438
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 tetracycline.","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:0002058"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0002060"}],"interesting_parent_ids":["FYPO:0002058","FYPO:0000139","FYPO:0000003","FYPO:0002057","FYPO:0000257","FYPO:0002060"],"is_obsolete":false,"name":"normal growth on tetracycline","synonyms":[{"name":"normal cell population growth in presence of tetracycline","type":"exact"},{"name":"normal cell population growth on tetracycline","type":"exact"},{"name":"normal cellular response to tetracycline","type":"related"},{"name":"normal vegetative cell population growth on tetracycline","type":"exact"}],"termid":"FYPO:0001438"}


id: PBO:0072501
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein SA pseudogene 30","termid":"PBO:0072501"}


id: GO:0051391
data:
  {"annotated_genes":["SJAG_01877","SJAG_01638"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[74123,109158],"is_not":false,"summary":null,"term":"GO:0051391"}]},"cv_name":"biological_process","definition":"The modification of tRNA structure by addition of an acetyl group to tRNA. An acetyl group is CH3CO-, derived from acetic [ethanoic] acid.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA modification","termid":"GO:0006400"},{"relation_name":"is_a","term_name":"RNA acetylation","termid":"GO:1990884"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01638":null,"SJAG_01877":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0006399"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150","GO:0006399"],"is_obsolete":false,"name":"tRNA acetylation","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0051391","terms_by_termid":{"GO:0051391":null}}


id: PBO:0061195
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nicotinamide nucleotide transhydrogenase","termid":"PBO:0061195"}


id: GO:0031798
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a type 1 metabotropic glutamate receptor.","definition_xrefs":["GOC:mah","GOC:nln"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled glutamate receptor binding","termid":"GO:0035256"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"type 1 metabotropic glutamate receptor binding","synonyms":[{"name":"type 1 metabotropic glutamate receptor ligand","type":"narrow"}],"termid":"GO:0031798"}


id: GO:0032160
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Arrays of septin filaments, or bars, found in a series of filamentous structures. Such structures have been observed in the prospore membrane during spore formation in S. cerevisiae and in the chlamydospore membrane during chlamydospore formation in C. albicans.","definition_xrefs":["PMID:16151244","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"septin cytoskeleton","termid":"GO:0032156"},{"relation_name":"part_of","term_name":"cytoskeleton","termid":"GO:0005856"}],"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":"septin filament array","synonyms":[{"name":"septin bar","type":"related"}],"termid":"GO:0032160"}


id: PBO:0005248
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retromer complex subunit Vps5","termid":"PBO:0005248"}


id: MONDO:0003403
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A classification of testicular cancers that arise in specialized sex cells called germ cells. Nonseminomas include embryonal carcinoma, teratoma, choriocarcinoma, and yolk sac tumor.","definition_xrefs":["NCIT:C5027"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malignant testicular germ cell tumor","termid":"MONDO:0003510"},{"relation_name":"is_a","term_name":"testicular non-seminomatous germ cell tumor","termid":"MONDO:0006447"}],"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":"testicular non-seminomatous germ cell cancer","secondary_identifiers":["MEDGEN:233162","UMLS:C1334625","DOID:5345"],"synonyms":[{"name":"malignant non-seminomatous germ cell cancer of testis","type":"exact"},{"name":"malignant non-seminomatous germ cell cancer of the testis","type":"exact"},{"name":"malignant non-seminomatous germ cell neoplasm of testis","type":"exact"},{"name":"malignant non-seminomatous germ cell neoplasm of the testis","type":"exact"},{"name":"malignant non-seminomatous germ cell tumor of testis","type":"exact"},{"name":"malignant non-seminomatous germ cell tumor of the testis","type":"exact"},{"name":"malignant non-seminomatous germ cell tumour of testis","type":"exact"},{"name":"malignant non-seminomatous germ cell tumour of the testis","type":"exact"},{"name":"malignant testicular non-seminomatous germ cell neoplasm","type":"exact"},{"name":"malignant testicular non-seminomatous germ cell tumor","type":"exact"},{"name":"malignant testicular non-seminomatous germ cell tumour","type":"exact"},{"name":"testicular germ cell tumor non-seminomatous, malignant","type":"exact"},{"name":"testicular germ cell tumour non-seminomatous, malignant","type":"exact"},{"name":"testicular non-seminomatous germ cell cancer","type":"exact"},{"name":"testicular non-seminomatous germ cell tumor, malignant","type":"exact"},{"name":"testicular non-seminomatous malignant germ cell neoplasm","type":"exact"}],"termid":"MONDO:0003403","xrefs":{"Monarch":{"xref_id":"0003403"}}}


id: GO:0070263
data:
  {"annotated_genes":["SJAG_01975","SJAG_01755","SJAG_04723","SJAG_04720","SJAG_00239"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[104542,104795,104796,108691,118427],"is_not":false,"summary":null,"term":"GO:0070263"}]},"cv_name":"cellular_component","definition":"The side of the fungal-type cell wall that is opposite to the side that faces the cell and its contents.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"external side of cell wall","termid":"GO:0010339"},{"relation_name":"part_of","term_name":"fungal-type cell wall","termid":"GO:0009277"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00239":null,"SJAG_01755":null,"SJAG_01975":null,"SJAG_04720":null,"SJAG_04723":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005618"},{"rel_name":"part_of","termid":"GO:0009986"}],"interesting_parent_ids":["GO:0009986","GO:0005618","GO:0005575"],"is_obsolete":false,"name":"external side of fungal-type cell wall","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0070263","terms_by_termid":{"GO:0070263":null}}


id: MONDO:0002218
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cancer that involves the temporal lobe.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerebral hemisphere cancer","termid":"MONDO:0002731"},{"relation_name":"is_a","term_name":"neoplasm of temporal lobe","termid":"MONDO:0021372"}],"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":"temporal lobe cancer","secondary_identifiers":["UMLS:C0153636","ICD9:191.2","MEDGEN:509347","SCTID:363468009","DOID:2135","ICD10CM:C71.2"],"synonyms":[{"name":"cancer of temporal lobe","type":"exact"},{"name":"malignant neoplasm of temporal lobe","type":"exact"},{"name":"malignant temporal lobe neoplasm","type":"exact"},{"name":"temporal lobe cancer","type":"exact"},{"name":"temporal lobe neoplasm","type":"related"},{"name":"tumour of temporal lobe","type":"related"}],"termid":"MONDO:0002218","xrefs":{"Monarch":{"xref_id":"0002218"}}}


id: PBO:0002840
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAP kinase kinase kinase Win1","termid":"PBO:0002840"}


id: MONDO:0001888
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A usually large cell non-Hodgkin lymphoma of B-cell phenotype, arising from the anus. Lymphomas originating from the anal region are rare in the general population, but they are seen with a higher frequency in HIV-positive patients, particularly homosexual men.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anus cancer","termid":"MONDO:0001879"},{"relation_name":"is_a","term_name":"rectum lymphoma","termid":"MONDO:0002166"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005570","MONDO:0004335"],"is_obsolete":false,"name":"anus lymphoma","secondary_identifiers":["MEDGEN:272308","DOID:14139","NCIT:C5601","UMLS:C1332268"],"synonyms":[{"name":"anal lymphoma","type":"exact"},{"name":"anus lymphoma","type":"exact"},{"name":"lymphoma of anus","type":"exact"},{"name":"lymphoma of the anus","type":"exact"},{"name":"primary anal lymphoma","type":"exact"}],"termid":"MONDO:0001888","xrefs":{"Monarch":{"xref_id":"0001888"}}}


id: FYPO:0004574
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","gene_count":0,"genotype_count":0,"name":"OBSOLETE FYPO:0004574 DEPRECATED increased subtelomere-derived RNA level (obsolete FYPO:0004574)","termid":"FYPO:0004574"}


id: GO:1901452
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of response to benzene.","definition_xrefs":["GOC:TermGenie","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of response to stimulus","termid":"GO:0048585"},{"relation_name":"is_a","term_name":"regulation of response to benzene","termid":"GO:1901451"},{"relation_name":"negatively_regulates","term_name":"response to benzene","termid":"GO:1901423"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of response to benzene","synonyms":[{"name":"down regulation of response to benzene","type":"exact"},{"name":"down-regulation of response to benzene","type":"exact"},{"name":"downregulation of response to benzene","type":"exact"},{"name":"inhibition of response to benzene","type":"narrow"}],"termid":"GO:1901452"}


id: GO:0052895
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: N1-acetylspermine + oxygen + H2O = N1-acetylspermidine + 3-aminopropanal + hydrogen peroxide.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete N1-acetylspermine:oxygen oxidoreductase (N1-acetylspermidine-forming) activity (obsolete GO:0052895)","termid":"GO:0052895"}


id: MONDO:0009339
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital bile acid synthesis defect type 2 (BAS defect type 2) is an anomaly of bile acid synthesis characterized by severe and rapidly progressive cholestatic liver disease, and malabsorption of fat and fat-soluble vitamins.","definition_xrefs":["Orphanet:79303"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital bile acid synthesis defect","termid":"MONDO:0018841"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002525"}],"interesting_parent_ids":["MONDO:0002525","MONDO:0005066"],"is_obsolete":false,"name":"congenital bile acid synthesis defect 2","secondary_identifiers":["UMLS:C1856127","DOID:0111069","MESH:C535443","GARD:10045","OMIM:235555","MEDGEN:383840"],"synonyms":[{"name":"AKR1D1 congenital bile acid synthesis defect","type":"exact"},{"name":"BASD2","type":"exact"},{"name":"CBAS2","type":"exact"},{"name":"bile acid synthesis defect, congenital, 2","type":"related"},{"name":"bile acid synthesis defect, congenital, type 2","type":"exact"},{"name":"cholestasis with Delta(4)-3-oxosteroid 5-Beta-reductase deficiency","type":"related"},{"name":"cholestasis with delta(4)-3-oxosteroid 5-beta-reductase deficiency","type":"exact"},{"name":"congenital bile acid synthesis defect caused by mutation in AKR1D1","type":"exact"},{"name":"congenital bile acid synthesis defect type 2","type":"exact"},{"name":"congenital bile acid synthesis defect, type 2","type":"related"}],"termid":"MONDO:0009339","xrefs":{"Monarch":{"xref_id":"0009339"}}}


id: PBO:0003708
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dolichol-phosphate mannosyltransferase subunit 2 (predicted)","termid":"PBO:0003708"}


id: FYPO:0001448
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 trehalose measured in a cell is too low to detect.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"altered level of substance in cell during vegetative growth","termid":"FYPO:0001323"},{"relation_name":"is_a","term_name":"altered cellular trehalose level","termid":"FYPO:0001446"}],"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:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"trehalose absent from cell during heat shock","synonyms":[{"name":"absent trehalose","type":"exact"},{"name":"trehalose absent from cell during heat shock during mitotic cell cycle","type":"related"},{"name":"trehalose absent from cell during vegetative growth and during heat shock","type":"exact"}],"termid":"FYPO:0001448"}


id: PBO:0066196
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA binding motif protein 15","termid":"PBO:0066196"}


id: GO:0016494
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with a C-X-C chemokine and transmitting the signal from one side of the membrane to the other to initiate a change in cell activity. A C-X-C chemokine has a single amino acid between the first two cysteines of the characteristic four cysteine motif.","definition_xrefs":["GOC:signaling","PMID:8662823"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chemokine receptor activity","termid":"GO:0004950"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0038023","GO:0003674"],"is_obsolete":false,"name":"C-X-C chemokine receptor activity","termid":"GO:0016494"}


id: PBO:0027933
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_H3-K9_dimethylation_at_centromere","termid":"PBO:0027933"}


id: PBO:0086164
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein required for rRNA maturation and ribosomal subunit biogenesis; required for 18S rRNA maturation; also required for small ribosomal subunit biogenesis; cosediments with pre-ribosomal particles; mutation decreases efficiency of +1 Ty1 frameshifting and transposition, and affects budding pattern","termid":"PBO:0086164"}


id: GO:0099505
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the potential difference across a presynaptic membrane.","definition_xrefs":["GOC:ef","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of membrane potential","termid":"GO:0042391"}],"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 presynaptic membrane potential","synonyms":[{"name":"regulation of pre-synaptic membrane potential","type":"exact"}],"termid":"GO:0099505"}


id: GO:1903618
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of transdifferentiation.","definition_xrefs":["GOC:TermGenie","PMID:22118091","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell differentiation","termid":"GO:0045595"},{"relation_name":"regulates","term_name":"transdifferentiation","termid":"GO:0060290"}],"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 transdifferentiation","termid":"GO:1903618"}


id: MONDO:0013386
data:
  {"annotated_genes":["SJAG_00365"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88836],"is_not":false,"summary":null,"term":"MONDO:0013386"}]},"cv_name":"mondo","definition":"Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the MSRB3 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00365":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0019497","MONDO:0006025"],"is_obsolete":false,"name":"autosomal recessive nonsyndromic hearing loss 74","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:22638","OMIM:613718","DOID:0110523","MEDGEN:453237","UMLS:C2239351"],"synonyms":[{"name":"DFNB74","type":"narrow"},{"name":"MSRB3 autosomal recessive nonsyndromic deafness","type":"narrow"},{"name":"autosomal recessive deafness 74","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 74","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness caused by mutation in MSRB3","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 74","type":"narrow"},{"name":"deafness, autosomal recessive 74","type":"narrow"},{"name":"deafness, autosomal recessive type 74","type":"narrow"}],"termid":"MONDO:0013386","terms_by_termid":{"MONDO:0013386":null},"xrefs":{"Monarch":{"xref_id":"0013386"}}}


id: PBO:0003902
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial translation initiation factor (predicted)","termid":"PBO:0003902"}


id: GO:0061818
data:
  {"annotated_genes":["SJAG_00195"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[100294],"is_not":false,"summary":null,"term":"GO:0061818"}]},"cv_name":"biological_process","definition":"The process of assisting in the folding of tRNAs into the correct tertiary structure.","definition_xrefs":["GOC:dph","PMID:27849601"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA folding","termid":"GO:0034337"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00195":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"tRNA folding","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0061818","terms_by_termid":{"GO:0061818":null}}


id: GO:0051554
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving flavonols, a member of a class of vascular pigments formed by consecutive oxidative processes from the flavonoid intermediates flavanones and dihydroflavonols. Flavonols are the most widespread of the flavonoids and have a wide array of physiological activities.","definition_xrefs":["PMID:11402179"],"direct_ancestors":[{"relation_name":"is_a","term_name":"flavone metabolic process","termid":"GO:0051552"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"flavonol metabolic process","synonyms":[{"name":"flavonol metabolism","type":"exact"}],"termid":"GO:0051554"}


id: MONDO:0009661
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Mucopolysaccharidosis type 6 (MPS 6) is a lysosomal storage disease with progressive multisystem involvement, associated with a deficiency of arylsulfatase B (ASB) leading to the accumulation of dermatan sulfate.","definition_xrefs":["Orphanet:583"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"eye disorder","termid":"MONDO:0005328"},{"relation_name":"is_a","term_name":"mucopolysaccharidosis","termid":"MONDO:0019249"},{"relation_name":"is_a","term_name":"lysosomal storage disease with skeletal involvement","termid":"MONDO:0800088"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0002561"}],"interesting_parent_ids":["MONDO:0002561","MONDO:0005066","MONDO:0037792","MONDO:0005328"],"is_obsolete":false,"name":"mucopolysaccharidosis type 6","secondary_identifiers":["NANDO:1200109","MedDRA:10056892","NANDO:1200108","icd11.foundation:1288379621","OMIM:253200","MEDGEN:44514","DOID:12800","SCTID:69463008","SCTID:52677002","NORD:1405","GARD:7095","NANDO:1200110","NANDO:2200551","NCIT:C61264","UMLS:C0026709","MESH:D009087"],"synonyms":[{"name":"ARSB deficiency","type":"exact"},{"name":"ASB deficiency","type":"exact"},{"name":"Arsb deficiency","type":"related"},{"name":"MPS 6","type":"related"},{"name":"MPS VI","type":"related"},{"name":"MPS VI - Maroteaux-Lamy syndrome","type":"exact"},{"name":"MPS6","type":"exact"},{"name":"MPSVI","type":"exact"},{"name":"Maroteaux - Lamy syndrome","type":"exact"},{"name":"Maroteaux Lamy Syndrome","type":"exact"},{"name":"Maroteaux Lamy syndrome","type":"related"},{"name":"Maroteaux-Lamy disease","type":"exact"},{"name":"Maroteaux-Lamy syndrome","type":"exact"},{"name":"Mucopoly-saccharidosis type VI","type":"related"},{"name":"N-acetylgalactosamine 4-sulfatase deficiency","type":"exact"},{"name":"N-acetylgalactosamine-4-sulfatase deficiency","type":"related"},{"name":"arylsulfatase B deficiency","type":"exact"},{"name":"deficiency of N-acetylgalactosamine-4-sulfatase","type":"exact"},{"name":"mucopolysaccharidosis VI","type":"related"},{"name":"mucopolysaccharidosis type VI","type":"exact"},{"name":"mucopolysaccharidosis type VI (Maroteaux-Lamy)","type":"exact"}],"termid":"MONDO:0009661","xrefs":{"Monarch":{"xref_id":"0009661"}}}


id: MONDO:1012333
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hemophagocytic syndrome, non-human animal","termid":"MONDO:1011697"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hemophagocytic syndrome, domestic cat","secondary_identifiers":["OMIA:001229-9685"],"termid":"MONDO:1012333","xrefs":{"Monarch":{"xref_id":"1012333"}}}


id: PBO:0055149
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 2568","termid":"PBO:0055149"}


id: GO:0160227
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An oligosaccharyltransferase complex that contains STT3B as the catalytic subunit.","definition_xrefs":["PMID:39509507","PMID:31831667"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oligosaccharyltransferase complex","termid":"GO:0008250"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005783"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005789"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0005789","GO:0005783","GO:0032991"],"is_obsolete":false,"name":"oligosaccharyltransferase complex B","synonyms":[{"name":"OST-B","type":"exact"}],"termid":"GO:0160227"}


id: MONDO:0022945
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deafness peripheral neuropathy arterial disease","termid":"MONDO:0022945","xrefs":{"Monarch":{"xref_id":"0022945"}}}


id: PBO:0069147
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 398, pseudogene","termid":"PBO:0069147"}


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


id: MONDO:0010817
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the KCNQ4 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant nonsyndromic hearing loss","termid":"MONDO:0019587"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0019497","MONDO:0000426"],"is_obsolete":false,"name":"autosomal dominant nonsyndromic hearing loss 2A","secondary_identifiers":["DOID:0110558","OMIM:600101","GARD:18099","UMLS:C2677637","MEDGEN:436997","MESH:C567441"],"synonyms":[{"name":"DFNA2A","type":"narrow"},{"name":"KCNQ4 autosomal dominant nonsyndromic deafness","type":"narrow"},{"name":"autosomal dominant deafness 2A","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness 2A","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness caused by mutation in KCNQ4","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness type 2A","type":"narrow"},{"name":"deafness, autosomal dominant 2A","type":"narrow"},{"name":"deafness, autosomal dominant 2a","type":"narrow"},{"name":"deafness, autosomal dominant type 2A","type":"narrow"}],"termid":"MONDO:0010817","xrefs":{"Monarch":{"xref_id":"0010817"}}}


id: PATO:0000480
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000480 positive regulation (obsolete PATO:0000480)","termid":"PATO:0000480"}


id: PR:000027569
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A histone H3 that is a translation product of the Schizosaccharomyces pombe 972h- hht1 gene or a 1:1 ortholog thereof in fungi.","definition_xrefs":["PRO:CNA"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein","termid":"PR:000000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fungal histone H3.1","pombase_gene_id":"SPAC1834.04","synonyms":[{"name":"hht1","type":"exact"}],"termid":"PR:000027569"}


id: GO:0003325
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a pancreatic PP cell over time, from its formation to the mature structure. A pancreatic polypeptide-producing cell is a cell in the pancreas that produces pancreatic polypeptide.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial cell development","termid":"GO:0002064"},{"relation_name":"part_of","term_name":"pancreatic PP cell differentiation","termid":"GO:0003312"}],"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":"pancreatic PP cell development","termid":"GO:0003325"}


id: PBO:0071155
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L22 pseudogene 20","termid":"PBO:0071155"}


id: GO:0010970
data:
  {"annotated_genes":["SJAG_00140","SJAG_02561","SJAG_03673","SJAG_01863","SJAG_02336","SJAG_01297","SJAG_03437","SJAG_01613","SJAG_02286","SJAG_04001","SJAG_02761","SJAG_02731","SJAG_01224","SJAG_00918","SJAG_05220","SJAG_00594","SJAG_04143","SJAG_03540","SJAG_00332","SJAG_01371","SJAG_02651","SJAG_02737","SJAG_00851","SJAG_00113","SJAG_02045","SJAG_01546","SJAG_01662","SJAG_05266","SJAG_00368","SJAG_01370","SJAG_05319","SJAG_02431","SJAG_04597","SJAG_03073","SJAG_05185","SJAG_01775","SJAG_01211","SJAG_00397"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[92964],"is_not":false,"summary":null,"term":"GO:0010970"},{"annotations":[97025,93662,105080,99392,102547,93198,92806,104789,112906,113257,118809,89571,115806],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030989"},{"annotations":[113080,103257,108424],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032118"},{"annotations":[99467,101048],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090561"},{"annotations":[93200,99394,101049,78071,89575],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000743"},{"annotations":[96227],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1902854"},{"annotations":[105568],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0099117"},{"annotations":[102206,105724,120548,110107],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140210"},{"annotations":[92794,98589,102343,90957,91564,118780,110730,100440,111740,115957,109343],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990976"},{"annotations":[106372,106705],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047496"}]},"cv_name":"biological_process","definition":"The movement of organelles or other particles from one location in the cell to another along microtubules, driven by motor activity.","definition_xrefs":["GOC:dph","GOC:mah","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microtubule-based movement","termid":"GO:0007018"},{"relation_name":"is_a","term_name":"cytoskeleton-dependent intracellular transport","termid":"GO:0030705"},{"relation_name":"is_a","term_name":"microtubule-based transport","termid":"GO:0099111"}],"gene_count":38,"genes_by_uniquename":{"SJAG_00113":null,"SJAG_00140":null,"SJAG_00332":null,"SJAG_00368":null,"SJAG_00397":null,"SJAG_00594":null,"SJAG_00851":null,"SJAG_00918":null,"SJAG_01211":null,"SJAG_01224":null,"SJAG_01297":null,"SJAG_01370":null,"SJAG_01371":null,"SJAG_01546":null,"SJAG_01613":null,"SJAG_01662":null,"SJAG_01775":null,"SJAG_01863":null,"SJAG_02045":null,"SJAG_02286":null,"SJAG_02336":null,"SJAG_02431":null,"SJAG_02561":null,"SJAG_02651":null,"SJAG_02731":null,"SJAG_02737":null,"SJAG_02761":null,"SJAG_03073":null,"SJAG_03437":null,"SJAG_03540":null,"SJAG_03673":null,"SJAG_04001":null,"SJAG_04143":null,"SJAG_04597":null,"SJAG_05185":null,"SJAG_05220":null,"SJAG_05266":null,"SJAG_05319":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"transport along microtubule","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"establishment of localization by movement along microtubule","type":"exact"},{"name":"microtubule-based transport","type":"broad"},{"name":"movement along microtubule","type":"exact"}],"termid":"GO:0010970","terms_by_termid":{"GO:0000743":null,"GO:0010970":null,"GO:0030989":null,"GO:0032118":null,"GO:0047496":null,"GO:0090561":null,"GO:0099117":null,"GO:0140210":null,"GO:1902854":null,"GO:1990976":null}}


id: PBO:0077388
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 128","termid":"PBO:0077388"}


id: GO:1901248
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of lung ciliated cell differentiation.","definition_xrefs":["GOC:BHF","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of epithelial cell differentiation","termid":"GO:0030858"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"is_a","term_name":"regulation of lung ciliated cell differentiation","termid":"GO:1901246"},{"relation_name":"positively_regulates","term_name":"lung ciliated cell differentiation","termid":"GO:0061141"}],"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 lung ciliated cell differentiation","synonyms":[{"name":"activation of lung ciliated cell differentiation","type":"narrow"},{"name":"up regulation of lung ciliated cell differentiation","type":"exact"},{"name":"up-regulation of lung ciliated cell differentiation","type":"exact"},{"name":"upregulation of lung ciliated cell differentiation","type":"exact"}],"termid":"GO:1901248"}


id: GO:0032897
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of viral transcription.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of viral transcription","termid":"GO:0046782"},{"relation_name":"is_a","term_name":"negative regulation of viral process","termid":"GO:0048525"},{"relation_name":"negatively_regulates","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":"negative regulation of viral transcription","synonyms":[{"name":"down regulation of viral transcription","type":"exact"},{"name":"down-regulation of viral transcription","type":"exact"},{"name":"downregulation of viral transcription","type":"exact"},{"name":"inhibition of viral transcription","type":"narrow"}],"termid":"GO:0032897"}


id: PBO:0034125
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_symptom","termid":"PBO:0034125"}


id: PBO:0056394
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAPRE1 pseudogene 1","termid":"PBO:0056394"}


id: FYPO:0003780
data:
  {"alleles_by_uniquename":{"SJAG_03250:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03250","name":"sst4delta","uniquename":"SJAG_03250:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[121291],"is_not":false,"summary":null,"term":"FYPO:0003780"}]},"cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which the size, shape, or structure of all or part of the nuclear envelope is normal (i.e. indistinguishable from wild type) during mitosis.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal nuclear envelope morphology","termid":"FYPO:0003751"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03250":null},"genotype_count":1,"genotypes_by_uniquename":{"sst4delta":{"display_name":"sst4delta","display_uniquename":"sst4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03250:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0000257"],"is_obsolete":false,"name":"normal nuclear envelope morphology during mitosis","references_by_uniquename":{"PMID:32109380":null},"single_locus_annotated_genes":["SJAG_03250"],"single_locus_genotype_uniquenames":["sst4delta"],"synonyms":[{"name":"normal nuclear envelope morphology during mitosis during vegetative growth","type":"exact"},{"name":"normal nuclear envelope morphology during mitotic M phase","type":"related"},{"name":"normal nuclear envelope morphology during mitotic nuclear division","type":"exact"},{"name":"normal nuclear membrane morphology during mitosis","type":"narrow"}],"termid":"FYPO:0003780","terms_by_termid":{"FYPO:0003780":null}}


id: PR:O14006
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC29A4.03c gene.","definition_xrefs":["UniProtKB:O14006","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":"37S ribosomal protein S9, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC29A4.03c","synonyms":[{"name":"Spom972h-SPAC29A4.03c","type":"exact"}],"termid":"PR:O14006"}


id: GO:0001688
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete cytoplasmic dynein intermediate chain (obsolete GO:0001688)","synonyms":[{"name":"cytoplasmic dynein intermediate chain","type":"exact"}],"termid":"GO:0001688"}


id: MONDO:0100338
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"urinary system disorder","termid":"MONDO:0002118"},{"relation_name":"is_a","term_name":"infectious disease","termid":"MONDO:0005550"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"urinary tract infection","secondary_identifiers":["MEDGEN:52943","DOID:0080784","EFO:0003103","MESH:D014552","UMLS:C0042029"],"synonyms":[{"name":"urinary tract infection (disease)","type":"exact"}],"termid":"MONDO:0100338","xrefs":{"Monarch":{"xref_id":"0100338"}}}


id: PBO:0026946
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_sunitinib","termid":"PBO:0026946"}


id: MONDO:0015279
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete hereditary predisposition to infections (obsolete MONDO:0015979)","termid":"MONDO:0015979"},{"relation_name":"is_a","term_name":"inborn error of immunity","termid":"MONDO:0003778"},{"relation_name":"is_a","term_name":"hereditary skin disorder","termid":"MONDO:0100118"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005093"],"is_obsolete":false,"name":"chronic mucocutaneous candidiasis","secondary_identifiers":["Orphanet:1334","SCTID:234568006","UMLS:C0006845","HP:0002728","GARD:1077","icd11.foundation:2120780687","MedDRA:10009007","NANDO:1200363","MEDGEN:2426","OMIMPS:114580","DOID:2058","NANDO:2200764","MESH:D002178","NCIT:C34444"],"synonyms":[{"name":"CANDF","type":"exact"},{"name":"CMC","type":"exact"},{"name":"chronic mucocutaneous candidiasis","type":"exact"},{"name":"chronic mucocutaneous candidiasis (disease)","type":"exact"},{"name":"familial CMC","type":"exact"},{"name":"familial candidiasis","type":"exact"},{"name":"familial chronic mucocutaneous candidiasis","type":"exact"}],"termid":"MONDO:0015279","xrefs":{"Monarch":{"xref_id":"0015279"}}}


id: GO:0032871
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of karyogamy, the creation of a single nucleus from multiple nuclei as a result of membrane fusion.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of nucleus organization","termid":"GO:1903353"},{"relation_name":"regulates","term_name":"karyogamy","termid":"GO:0000741"}],"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 karyogamy","termid":"GO:0032871"}


id: GO:1900714
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of violaceol I biosynthetic process.","definition_xrefs":["GOC:TermGenie","GOC:di"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of small molecule metabolic process","termid":"GO:0062014"},{"relation_name":"is_a","term_name":"negative regulation of secondary metabolite biosynthetic process","termid":"GO:1900377"},{"relation_name":"is_a","term_name":"regulation of violaceol I biosynthetic process","termid":"GO:1900713"},{"relation_name":"negatively_regulates","term_name":"violaceol I biosynthetic process","termid":"GO:1900590"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0019748"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0019748"],"is_obsolete":false,"name":"negative regulation of violaceol I biosynthetic process","synonyms":[{"name":"down regulation of violaceol I anabolism","type":"exact"},{"name":"down regulation of violaceol I biosynthesis","type":"exact"},{"name":"down regulation of violaceol I biosynthetic process","type":"exact"},{"name":"down regulation of violaceol I formation","type":"exact"},{"name":"down regulation of violaceol I synthesis","type":"exact"},{"name":"down-regulation of violaceol I anabolism","type":"exact"},{"name":"down-regulation of violaceol I biosynthesis","type":"exact"},{"name":"down-regulation of violaceol I biosynthetic process","type":"exact"},{"name":"down-regulation of violaceol I formation","type":"exact"},{"name":"down-regulation of violaceol I synthesis","type":"exact"},{"name":"downregulation of violaceol I anabolism","type":"exact"},{"name":"downregulation of violaceol I biosynthesis","type":"exact"},{"name":"downregulation of violaceol I biosynthetic process","type":"exact"},{"name":"downregulation of violaceol I formation","type":"exact"},{"name":"downregulation of violaceol I synthesis","type":"exact"},{"name":"inhibition of violaceol I anabolism","type":"exact"},{"name":"inhibition of violaceol I biosynthesis","type":"exact"},{"name":"inhibition of violaceol I biosynthetic process","type":"narrow"},{"name":"inhibition of violaceol I formation","type":"exact"},{"name":"inhibition of violaceol I synthesis","type":"exact"},{"name":"negative regulation of violaceol I anabolism","type":"exact"},{"name":"negative regulation of violaceol I biosynthesis","type":"exact"},{"name":"negative regulation of violaceol I formation","type":"exact"},{"name":"negative regulation of violaceol I synthesis","type":"exact"}],"termid":"GO:1900714"}


id: MONDO:0001242
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A clotting condition characterized as a disruption in the homeostatic balance of the coagulation and fibrinolytic systems presenting as a pathological activation of coagulation mechanisms leading to the formation of small clots inside the blood vessels throughout the body of the newborn.","definition_xrefs":["NCIT:C111856"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disseminated intravascular coagulation","termid":"MONDO:0001243"}],"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":"disseminated intravascular coagulation in newborn","secondary_identifiers":["UMLS:C0158992","MEDGEN:510687","ICD9:776.2","DOID:11246","SCTID:34417008"],"synonyms":[{"name":"DIC in newborn","type":"exact"},{"name":"disseminated intravascular coagulation in newborn","type":"exact"},{"name":"neonatal disseminated intravascular coagulation","type":"exact"}],"termid":"MONDO:0001242","xrefs":{"Monarch":{"xref_id":"0001242"}}}


id: PBO:0026807
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_protein_localization_to_linear_element","termid":"PBO:0026807"}


id: GO:0051632
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the directed movement of acetylcholine into a cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of acetylcholine uptake","termid":"GO:0051631"},{"relation_name":"is_a","term_name":"negative regulation of amine transport","termid":"GO:0051953"},{"relation_name":"negatively_regulates","term_name":"acetylcholine uptake","termid":"GO:0051630"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"negative regulation of acetylcholine uptake","synonyms":[{"name":"down regulation of acetylcholine uptake","type":"exact"},{"name":"down-regulation of acetylcholine uptake","type":"exact"},{"name":"downregulation of acetylcholine uptake","type":"exact"},{"name":"negative regulation of acetylcholine import","type":"exact"}],"termid":"GO:0051632"}


id: PBO:0065612
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PTP4A1 pseudogene 6","termid":"PBO:0065612"}


id: PBO:0041980
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil domain containing 24","termid":"PBO:0041980"}


id: SO:0000335
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A mRNA with a minus 2 frameshift.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"minus_2_frameshift","termid":"SO:0000867"},{"relation_name":"is_a","term_name":"mRNA_with_frameshift","termid":"SO:0000108"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mRNA_with_minus_2_frameshift","synonyms":[{"name":"mRNA with minus 2 frameshift","type":"exact"}],"termid":"SO:0000335"}


id: PBO:0068706
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U4 small nuclear 87, pseudogene","termid":"PBO:0068706"}


id: PBO:0073080
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"succinate dehydrogenase complex flavoprotein subunit A","termid":"PBO:0073080"}


id: FYPO:0003264
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A spindle phenotype in which the meiotic spindles in adjacent dividing nuclei overlap during meiosis I. The order of nuclei in the resulting ascus differs from normal as a result.","definition_xrefs":["PomBase:mah","PMID:24196444"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal meiotic spindle","termid":"FYPO:0000734"}],"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":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0000120"},{"rel_name":"is_a","termid":"FYPO:0002399"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0000054","FYPO:0001985","FYPO:0000120","FYPO:0002399"],"is_obsolete":false,"name":"overlapping meiosis I spindles","synonyms":[{"name":"overlapping spindles at meiosis I","type":"exact"},{"name":"overlapping spindles during first meiotic nuclear division","type":"exact"}],"termid":"FYPO:0003264"}


id: MONDO:0019147
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The infection of a fly larva (maggot) in human tissue, which most commonly occurs in tropical climates. Affected tissues most commonly include skin, especially if open wounds are present, nasal passages, ears, and eyes.","definition_xrefs":["NCIT:C128400"],"direct_ancestors":[{"relation_name":"is_a","term_name":"parasitic ectoparasitic infectious disease","termid":"MONDO:0002875"}],"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":"myiasis","secondary_identifiers":["ICD10CM:B87","MedDRA:10028586","DOID:11080","Orphanet:75110","GARD:18924","EFO:0007389","icd11.foundation:1367149207","MEDGEN:10148","SCTID:60412004","ICD9:134.0","MESH:D009198","UMLS:C0027030"],"synonyms":[{"name":"infestation by fly larvae","type":"exact"},{"name":"infestation by maggots","type":"exact"},{"name":"maggot infestation","type":"exact"},{"name":"myiasis, unspecified","type":"exact"}],"termid":"MONDO:0019147","xrefs":{"Monarch":{"xref_id":"0019147"}}}


id: GO:0050652
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The elongation of dermatan sulfate proteoglycan chains by alternate addition of N-acetylhexosamine and GlcUA residues to the GAG-protein linkage region tetrasaccharide of dermatan sulfate.","definition_xrefs":["PMID:11788602","GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete dermatan sulfate proteoglycan biosynthetic process, chain elongation (obsolete GO:0050652)","synonyms":[{"name":"chondroitin sulfate B proteoglycan biosynthesis, polysaccharide chain biosynthesis","type":"exact"},{"name":"chondroitin sulfate B proteoglycan biosynthesis, polysaccharide chain biosynthetic process","type":"exact"},{"name":"chondroitin sulfate B proteoglycan chain elongation","type":"exact"},{"name":"dermatan sulfate proteoglycan anabolism, polysaccharide chain anabolism","type":"exact"},{"name":"dermatan sulfate proteoglycan biosynthetic process, polysaccharide chain biosynthetic process","type":"exact"},{"name":"dermatan sulfate proteoglycan chain elongation","type":"exact"},{"name":"dermatan sulfate proteoglycan formation, polysaccharide chain biosynthesis","type":"exact"},{"name":"dermatan sulfate proteoglycan formation, polysaccharide chain formation","type":"exact"},{"name":"dermatan sulfate proteoglycan synthesis, polysaccharide chain synthesis","type":"exact"},{"name":"dermatan sulphate proteoglycan biosynthesis, polysaccharide chain biosynthesis","type":"exact"},{"name":"dermatan sulphate proteoglycan biosynthesis, polysaccharide chain biosynthetic process","type":"exact"}],"termid":"GO:0050652"}


id: PBO:0064149
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plakophilin 2","termid":"PBO:0064149"}


id: FYPO:0007996
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in mitotic interphase in which cells form actin cables that are thinner than normal. This is evidence by lower actin fluorescence signal and is likely due to the presence of fewer actin filaments than normal.","definition_xrefs":["PMID:15184402","PomBase:mlr"],"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:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0004803"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0004803","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"thin actin cables","termid":"FYPO:0007996"}


id: MONDO:0013101
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"excluded_subClassOf","term_name":"skin basal cell carcinoma","termid":"MONDO:0005341"},{"relation_name":"is_a","term_name":"basal cell carcinoma, susceptibility to","termid":"MONDO:0100047"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"basal cell carcinoma, susceptibility to, 2","secondary_identifiers":["UMLS:C2751606","MEDGEN:442769","OMIM:613058"],"synonyms":[{"name":"BCC2","type":"exact"},{"name":"basal cell carcinoma, susceptibility to, 2","type":"exact"}],"termid":"MONDO:0013101","xrefs":{"Monarch":{"xref_id":"0013101"}}}


id: GO:0052114
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The responsive adjustment of an organism to the pH conditions in or around its host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete adaptation to host pH environment (obsolete GO:0052114)","synonyms":[{"name":"adaptation to host pH environment","type":"exact"},{"name":"pH tolerance to host environment","type":"exact"}],"termid":"GO:0052114"}


id: GO:0006328
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete AT binding (obsolete GO:0006328)","synonyms":[{"name":"AT binding","type":"exact"}],"termid":"GO:0006328"}


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


id: PBO:0054142
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 1508","termid":"PBO:0054142"}


id: GO:1903427
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of reactive oxygen species biosynthetic process.","definition_xrefs":["GOC:bf","GOC:TermGenie","GO_REF:0000058","GOC:PARL","PMID:24252804"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of biosynthetic process","termid":"GO:0009890"},{"relation_name":"is_a","term_name":"regulation of reactive oxygen species biosynthetic process","termid":"GO:1903426"},{"relation_name":"is_a","term_name":"negative regulation of reactive oxygen species metabolic process","termid":"GO:2000378"},{"relation_name":"negatively_regulates","term_name":"reactive oxygen species biosynthetic process","termid":"GO:1903409"}],"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 reactive oxygen species biosynthetic process","synonyms":[{"name":"down regulation of ROS formation","type":"related"},{"name":"down regulation of ROS generation","type":"related"},{"name":"down regulation of reactive oxygen species anabolism","type":"exact"},{"name":"down regulation of reactive oxygen species biosynthesis","type":"exact"},{"name":"down regulation of reactive oxygen species biosynthetic process","type":"exact"},{"name":"down regulation of reactive oxygen species formation","type":"exact"},{"name":"down regulation of reactive oxygen species generation","type":"related"},{"name":"down regulation of reactive oxygen species synthesis","type":"exact"},{"name":"down-regulation of ROS formation","type":"related"},{"name":"down-regulation of ROS generation","type":"related"},{"name":"down-regulation of reactive oxygen species anabolism","type":"exact"},{"name":"down-regulation of reactive oxygen species biosynthesis","type":"exact"},{"name":"down-regulation of reactive oxygen species biosynthetic process","type":"exact"},{"name":"down-regulation of reactive oxygen species formation","type":"exact"},{"name":"down-regulation of reactive oxygen species generation","type":"related"},{"name":"down-regulation of reactive oxygen species synthesis","type":"exact"},{"name":"downregulation of ROS formation","type":"related"},{"name":"downregulation of ROS generation","type":"related"},{"name":"downregulation of reactive oxygen species anabolism","type":"exact"},{"name":"downregulation of reactive oxygen species biosynthesis","type":"exact"},{"name":"downregulation of reactive oxygen species biosynthetic process","type":"exact"},{"name":"downregulation of reactive oxygen species formation","type":"exact"},{"name":"downregulation of reactive oxygen species generation","type":"related"},{"name":"downregulation of reactive oxygen species synthesis","type":"exact"},{"name":"inhibition of ROS formation","type":"related"},{"name":"inhibition of ROS generation","type":"related"},{"name":"inhibition of reactive oxygen species anabolism","type":"narrow"},{"name":"inhibition of reactive oxygen species biosynthesis","type":"narrow"},{"name":"inhibition of reactive oxygen species biosynthetic process","type":"narrow"},{"name":"inhibition of reactive oxygen species formation","type":"narrow"},{"name":"inhibition of reactive oxygen species generation","type":"related"},{"name":"inhibition of reactive oxygen species synthesis","type":"narrow"},{"name":"negative regulation of ROS formation","type":"related"},{"name":"negative regulation of ROS generation","type":"related"},{"name":"negative regulation of reactive oxygen species anabolism","type":"exact"},{"name":"negative regulation of reactive oxygen species biosynthesis","type":"exact"},{"name":"negative regulation of reactive oxygen species formation","type":"exact"},{"name":"negative regulation of reactive oxygen species generation","type":"related"},{"name":"negative regulation of reactive oxygen species synthesis","type":"exact"},{"name":"prevention of ROS generation","type":"exact"}],"termid":"GO:1903427"}


id: PBO:0073729
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"stem-loop binding protein","termid":"PBO:0073729"}


id: SO:0000380
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A small catalytic RNA motif that catalyzes self-cleavage reaction. Its name comes from its secondary structure which resembles a carpenter's hammer. The hammerhead ribozyme is involved in the replication of some viroid and some satellite RNAs.","definition_xrefs":["PMID:2436805"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"ribozymic","termid":"SO:0001186"},{"relation_name":"is_a","term_name":"RNA_motif","termid":"SO:0000715"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hammerhead_ribozyme","secondary_identifiers":["http://en.wikipedia.org/wiki/Hammerhead_ribozyme"],"synonyms":[{"name":"INSDC_feature:ncRNA","type":"broad"},{"name":"INSDC_qualifier:hammerhead_ribozyme","type":"exact"},{"name":"hammerhead ribozyme","type":"exact"}],"termid":"SO:0000380"}


id: MONDO:0800290
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Li-fraumeni-like syndrome","secondary_identifiers":["MEDGEN:382523","UMLS:C2675080"],"synonyms":[{"name":"LFL","type":"exact"}],"termid":"MONDO:0800290","xrefs":{"Monarch":{"xref_id":"0800290"}}}


id: SO:0100010
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An experimental region wherean analysis has been run and not produced any annotation.","definition_xrefs":["EBIBS:GAR"],"direct_ancestors":[{"relation_name":"is_a","term_name":"experimental_result_region","termid":"SO:0000703"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"no_output","synonyms":[{"name":"no output","type":"exact"}],"termid":"SO:0100010"}


id: PBO:0052886
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin associated protein 9-9","termid":"PBO:0052886"}


id: GO:1900130
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of lipid binding.","definition_xrefs":["GOC:pm","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of lipid binding (obsolete GO:1900130)","termid":"GO:1900130"}


id: GO:0120336
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The portion of the radial spoke 1 that is orthogonal to the elongated stalk and which projects towards the central pair of microtubules within the ciliary axoneme.","definition_xrefs":["PMID:22754630","PMID:348711799","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"radial spoke head","termid":"GO:0001535"},{"relation_name":"part_of","term_name":"radial spoke 1","termid":"GO:0120333"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"radial spoke head 1","synonyms":[{"name":"radial spokehead 1","type":"exact"}],"termid":"GO:0120336"}


id: MONDO:0007080
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Familial hyperaldosteronism type I (FH-I) is a rare heritable, glucocorticoid remediable form of primary aldosteronism (PA) characterized by early-onset hypertension, hyperaldosteronism, variable hypokalemia, low plasma renin activity (PRA), and abnormal production of 18-oxocortisol and 18-hydroxycortisol.","definition_xrefs":["Orphanet:403"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial hyperaldosteronism","termid":"MONDO:0016525"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glucocorticoid-remediable aldosteronism","secondary_identifiers":["GARD:2790","MEDGEN:824577","DOID:14080","UMLS:C3838731","ICD10CM:E26.02","ICD9:255.11","OMIM:103900","MESH:C563177"],"synonyms":[{"name":"ACTH-dependent hyperaldosteronism syndrome","type":"related"},{"name":"FH 1","type":"related"},{"name":"FH-I","type":"exact"},{"name":"FH1","type":"exact"},{"name":"GRA","type":"exact"},{"name":"HALD1","type":"related"},{"name":"aldosteronism, glucocorticoid-remediable","type":"exact"},{"name":"aldosteronism, sensitive to dexamethasone","type":"related"},{"name":"dexamethasone sensitive hypertension","type":"related"},{"name":"dexamethasone-sensitive hypertension","type":"exact"},{"name":"familial hyperaldosteronism type 1","type":"exact"},{"name":"familial hyperaldosteronism type I","type":"related"},{"name":"glucocorticoid sensitive hypertension","type":"related"},{"name":"glucocorticoid-remediable aldosteronism","type":"exact"},{"name":"glucocorticoid-sensitive hypertension","type":"exact"},{"name":"glucocorticoid-suppressible hyperaldosteronism","type":"related"},{"name":"hyperaldosteronism, familial type 1","type":"related"},{"name":"hyperaldosteronism, familial, type 1","type":"related"},{"name":"hyperaldosteronism, familial, type I","type":"related"}],"termid":"MONDO:0007080","xrefs":{"Monarch":{"xref_id":"0007080"}}}


id: PBO:0028730
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_cellular_L-ergothioneine_level","termid":"PBO:0028730"}


id: GO:0051162
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving L-arabitol, the pentitol derived from arabinose or lyxose by reduction of the aldehyde group.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"arabitol metabolic process","termid":"GO:0051161"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"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:0008150","GO:0005975","GO:0044281"],"is_obsolete":false,"name":"L-arabitol metabolic process","synonyms":[{"name":"L-arabitol metabolism","type":"exact"}],"termid":"GO:0051162"}


id: MONDO:0015808
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Folliculotropic mycosis fungoides is a rare variant of mycosis fungoides (MF), a form of cutaneous T-cell lymphoma, and is characterized by the presence of folliculotropic infiltrates in patch-plaque lesions usually involving the head and neck area.","definition_xrefs":["Orphanet:178512"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"mycosis fungoides","termid":"MONDO:0009691"},{"relation_name":"is_a","term_name":"secondary catabolic mucinosis of skin","termid":"MONDO:0021655"},{"relation_name":"is_a","term_name":"mycosis fungoides variant","termid":"MONDO:0045071"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0004992","MONDO:0005570"],"is_obsolete":false,"name":"folliculotropic mycosis fungoides","secondary_identifiers":["NCIT:C35685","MEDGEN:302080","icd11.foundation:1335995469","UMLS:C1627767","ICD9:701.8","GARD:20154","SCTID:404109006"],"synonyms":[{"name":"alopecia mucinosa (t cell lymphoma)","type":"related"},{"name":"follicular mucinosis type mycosis fungoides","type":"exact"},{"name":"follicular mycosis fungoides","type":"exact"},{"name":"folliculotropic mycosis fungoides","type":"exact"},{"name":"mycosis fungoides-associated follicular mucinosis","type":"exact"}],"termid":"MONDO:0015808","xrefs":{"Monarch":{"xref_id":"0015808"}}}


id: PBO:0029116
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_cell_cycle_phase","termid":"PBO:0029116"}


id: GO:0102618
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: oryzalexin D + NAD(P) = oryzalexin B + H+ + NAD(P)H.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete oryzalexin B synthase activity (obsolete GO:0102618)","termid":"GO:0102618"}


id: GO:1900884
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of tridecane biosynthetic process.","definition_xrefs":["GOC:TermGenie","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of tridecane metabolic process","termid":"GO:1900893"},{"relation_name":"is_a","term_name":"regulation of alkane biosynthetic process","termid":"GO:1901577"},{"relation_name":"regulates","term_name":"tridecane biosynthetic process","termid":"GO:1900632"}],"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 tridecane biosynthetic process","synonyms":[{"name":"regulation of tridecane anabolism","type":"exact"},{"name":"regulation of tridecane biosynthesis","type":"exact"},{"name":"regulation of tridecane formation","type":"exact"},{"name":"regulation of tridecane synthesis","type":"exact"}],"termid":"GO:1900884"}


id: PBO:0044705
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DDX5 pseudogene 1","termid":"PBO:0044705"}


id: PBO:0071602
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L36a pseudogene 19","termid":"PBO:0071602"}


id: PBO:0062081
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 4 subfamily A member 12 pseudogene","termid":"PBO:0062081"}


id: FYPO:0000562
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 cellular respiration does not occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular respiration","termid":"FYPO:0000078"},{"relation_name":"is_a","term_name":"abolished cellular process","termid":"FYPO:0005449"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"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:0001985","FYPO:0000002","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"abolished cellular respiration","synonyms":[{"name":"abolished cellular respiration during mitotic cell cycle","type":"related"},{"name":"absent respiratory metabolism","type":"exact"},{"name":"cellular respiration abolished","type":"exact"},{"name":"cellular respiration abolished during vegetative growth","type":"exact"},{"name":"respiration abolished","type":"broad"},{"name":"respiratory metabolism abolished","type":"exact"},{"name":"respiratory metabolism: absent","type":"related"}],"termid":"FYPO:0000562"}


id: MONDO:0012687
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"eye disorder","termid":"MONDO:0005328"}],"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":"familial cavitary optic disk anomaly","secondary_identifiers":["MEDGEN:370593","MESH:C566924","GARD:17822","Orphanet:464760","OMIM:611543","UMLS:C1969063"],"synonyms":[{"name":"CODA","type":"related"},{"name":"cavitary optic DISC anomalies","type":"related"},{"name":"familial CODA","type":"exact"}],"termid":"MONDO:0012687","xrefs":{"Monarch":{"xref_id":"0012687"}}}


id: FYPO:0003771
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the plasma membrane surrounding the cell tip is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein localization to cell tip during vegetative growth","termid":"FYPO:0001586"},{"relation_name":"is_a","term_name":"decreased protein localization to plasma membrane during vegetative growth","termid":"FYPO:0008198"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0000138","FYPO:0001320"],"is_obsolete":false,"name":"decreased protein localization to plasma membrane of cell tip during vegetative growth","synonyms":[{"name":"decreased protein localisation to plasma membrane of cell tip during vegetative growth","type":"exact"},{"name":"decreased protein localization in plasma membrane of cell tip during vegetative growth","type":"exact"},{"name":"decreased protein localization to plasma membrane of cell end during vegetative growth","type":"exact"},{"name":"decreased protein localization to plasma membrane of cell tip during mitotic cell cycle","type":"related"},{"name":"reduced protein localization to plasma membrane of cell tip during vegetative growth","type":"exact"}],"termid":"FYPO:0003771"}


id: SO:0001787
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant that causes a change at the 5th base pair after the start of the intron in the orientation of the transcript.","definition_xrefs":["EBI:gr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"splice_site_variant","termid":"SO:0001629"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"splice_donor_5th_base_variant","synonyms":[{"name":"splice donor 5th base variant","type":"exact"}],"termid":"SO:0001787"}


id: PBO:0045916
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EF-hand calcium binding domain 11","termid":"PBO:0045916"}


id: PBO:0044618
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"discoidin, CUB and LCCL domain containing 1","termid":"PBO:0044618"}


id: PBO:0082152
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Adapter protein for pexophagy and the Cvt targeting pathway; directs receptor-bound cargo to the phagophore assembly site (PAS) for packaging into vesicles; required for recruiting other proteins to the PAS; recruits Dnm1p to facilitate fission of mitochondria that are destined for removal by mitophagy","termid":"PBO:0082152"}


id: MONDO:0975841
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary gingival fibromatosis","termid":"MONDO:0016070"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibromatosis, gingival, 6","secondary_identifiers":["OMIM:620999"],"termid":"MONDO:0975841","xrefs":{"Monarch":{"xref_id":"0975841"}}}


id: MONDO:0010195
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Weissenbacher-Zweymuller syndrome (obsolete MONDO:0010195)","termid":"MONDO:0010195","xrefs":{"Monarch":{"xref_id":"0010195"}}}


id: PBO:0109258
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 120 member A opposite strand","termid":"PBO:0109258"}


id: PBO:0092000
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane spermidine family transmembrane transporter","termid":"PBO:0092000"}


id: PATO:0000448
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000448 high percentage (obsolete PATO:0000448)","termid":"PATO:0000448"}


id: GO:0035834
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving an indole alkaloid, an alkaloid containing an indole skeleton.","definition_xrefs":["GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alkaloid metabolic process","termid":"GO:0009820"}],"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":"indole alkaloid metabolic process","synonyms":[{"name":"indole alkaloid metabolism","type":"exact"}],"termid":"GO:0035834"}


id: GO:0071880
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An adenylate cyclase-activating G protein-coupled receptor signaling pathway initiated by a ligand binding to an adrenergic receptor on the surface of the target cell, and ending with the regulation of a downstream cellular process.","definition_xrefs":["GOC:mah","GOC:signaling","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenylate cyclase-activating G protein-coupled receptor signaling pathway","termid":"GO:0007189"},{"relation_name":"is_a","term_name":"adrenergic receptor signaling pathway","termid":"GO:0071875"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"adenylate cyclase-activating adrenergic receptor signaling pathway","synonyms":[{"name":"activation of adenylate cyclase activity by adrenergic receptor signaling pathway","type":"related"},{"name":"activation of adenylate cyclase activity by adrenergic receptor signalling pathway","type":"exact"},{"name":"adrenergic receptor, adenylate cyclase activating pathway","type":"exact"},{"name":"adrenergic receptor, adenylyl cyclase activating pathway","type":"exact"}],"termid":"GO:0071880"}


id: PBO:0072285
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S24 pseudogene 3","termid":"PBO:0072285"}


id: GO:1902208
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of bacterial-type flagellum assembly.","definition_xrefs":["GOC:jl","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell projection assembly","termid":"GO:0060491"},{"relation_name":"is_a","term_name":"regulation of organelle assembly","termid":"GO:1902115"},{"relation_name":"regulates","term_name":"bacterial-type flagellum assembly","termid":"GO:0044780"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0044085","GO:0008150"],"is_obsolete":false,"name":"regulation of bacterial-type flagellum assembly","synonyms":[{"name":"regulation of bacterial flagellum assembly","type":"exact"}],"termid":"GO:1902208"}


id: PBO:0059990
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND4L pseudogene 10","termid":"PBO:0059990"}


id: PBO:0042184
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclin B2","termid":"PBO:0042184"}


id: GO:0034163
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of toll-like receptor 9 signaling pathway.","definition_xrefs":["GOC:add","PMID:16551253","PMID:17328678"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytoplasmic pattern recognition receptor signaling pathway","termid":"GO:0039531"},{"relation_name":"regulates","term_name":"toll-like receptor 9 signaling pathway","termid":"GO:0034162"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"regulation of toll-like receptor 9 signaling pathway","synonyms":[{"name":"regulation of TLR9 signaling pathway","type":"exact"},{"name":"regulation of toll-like receptor 9 signalling pathway","type":"exact"}],"termid":"GO:0034163"}


id: MOD:00241
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-asparagine residue to N4-hydroxymethyl-L-asparagine.","definition_xrefs":["RESID:AA0236","Unimod:414"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N4-glycosyl-L-asparagine","termid":"MOD:00160"}],"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":"N4-hydroxymethyl-L-asparagine","synonyms":[{"name":"(2S)-2-amino-4-[(hydroxymethyl)amino]-4-oxobutanoic acid","type":"exact"},{"name":"2-amino-N4-hydroxymethylbutanediamic acid","type":"exact"},{"name":"Hydroxymethyl","type":"related"},{"name":"N(gamma)-hydroxymethylasparagine","type":"exact"},{"name":"N4-hydroxymethyl-L-asparagine","type":"exact"},{"name":"N4-hydroxymethylasparagine","type":"exact"},{"name":"beta-hydroxymethylasparagine","type":"exact"},{"name":"hydroxymethyl","type":"related"}],"termid":"MOD:00241"}


id: PBO:0086746
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; potential Cdc28p substrate; null mutant displays increased resistance to antifungal agents gliotoxin, cycloheximide and H2O2","termid":"PBO:0086746"}


id: PBO:0050143
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group box 2 pseudogene 1","termid":"PBO:0050143"}


id: GO:0042571
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An immunoglobulin complex that is secreted into extracellular space and found in mucosal areas or other tissues or circulating in the blood or lymph. In its canonical form, a circulating immunoglobulin complex is composed of two identical heavy chains and two identical light chains, held together by disulfide bonds. Some forms of are polymers of the basic structure and contain additional components such as J-chain and the secretory component.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immunoglobulin complex","termid":"GO:0019814"},{"relation_name":"part_of","term_name":"extracellular space","termid":"GO:0005615"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005576"}],"interesting_parent_ids":["GO:0005576","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"immunoglobulin complex, circulating","secondary_identifiers":["Wikipedia:Antibody"],"synonyms":[{"name":"antibody","type":"exact"}],"termid":"GO:0042571"}


id: GO:0060748
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The branching process in which the mammary gland ducts form tertiary branches off of the secondary branches as part of diestrus and pregnancy.","definition_xrefs":["PMID:18614704","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"part_of","term_name":"mammary gland branching involved in pregnancy","termid":"GO:0060745"}],"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":"tertiary branching involved in mammary gland duct morphogenesis","termid":"GO:0060748"}


id: MONDO:0010729
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"X-linked mental retardation, Schimke type, is characterized by intellectual deficit, growth retardation with short stature, deafness and ophthalmoplegia. Choreoathetosis with muscle spasticity generally appears during childhood. It has been described in four boys, three of whom were from the same family. Transmission is X-linked.","definition_xrefs":["Orphanet:85285"],"direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"X-linked intellectual disability, Schimke type","secondary_identifiers":["GARD:9288","MESH:C536630","OMIM:312840","MEDGEN:374193","SCTID:719010001","UMLS:C1839320"],"synonyms":[{"name":"Schimke X-linked intellectual disability syndrome","type":"related"},{"name":"Schimke X-linked mental retardation syndrome","type":"related"},{"name":"childhood-onset choreoathetosis with spasticity, postnatal microcephaly, growth and intellectual disability, ophthalmoplegia, and deafness","type":"related"},{"name":"childhood-onset choreoathetosis with spasticity, postnatal microcephaly, growth and mental retardation, ophthalmoplegia, and deafness","type":"related"},{"name":"choreoathetosis with intellectual disability X- linked","type":"related"},{"name":"choreoathetosis with intellectual disability, X-linked","type":"related"},{"name":"choreoathetosis with mental retardation X- linked","type":"related"},{"name":"choreoathetosis with mental retardation, X-linked","type":"related"},{"name":"progressive basal ganglion dysfunction, mental and growth retardation, external ophthalmoplegia, postnatal microcephaly and deafness","type":"related"}],"termid":"MONDO:0010729","xrefs":{"Monarch":{"xref_id":"0010729"}}}


id: PBO:0072687
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RUN domain containing 3B","termid":"PBO:0072687"}


id: PATO:0001649
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A curvature quality inhering in a bearer by virtue of the bearer's being curved towards the side.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"curved","termid":"PATO:0000406"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"curved lateral","termid":"PATO:0001649"}


id: PBO:0016531
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lanosterol synthase Erg7","termid":"PBO:0016531"}


id: PBO:0031856
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-haploinsufficient","termid":"PBO:0031856"}


id: MONDO:0017426
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"non-syndromic polydactyly","termid":"MONDO:0011348"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"postaxial polydactyly of fingers","secondary_identifiers":["Orphanet:294942","UMLS:C0431904","icd11.foundation:1146378807","GARD:12460","MEDGEN:609221","SCTID:205131007"],"synonyms":[{"name":"postaxial polydactyly of hand","type":"exact"}],"termid":"MONDO:0017426","xrefs":{"Monarch":{"xref_id":"0017426"}}}


id: GO:0051467
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events by which a steroid hormone stimulus is received by a cell and converted into a molecular signal.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detection of hormone stimulus","termid":"GO:0009720"},{"relation_name":"is_a","term_name":"response to steroid hormone","termid":"GO:0048545"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"detection of steroid hormone stimulus","termid":"GO:0051467"}


id: PBO:0065077
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prickle planar cell polarity protein 4","termid":"PBO:0065077"}


id: GO:0036411
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A trimeric protein complex containing a H-NS homodimer and a Cnu monomer. In bacteria, this complex negatively regulates transcription of a range of genes.","definition_xrefs":["GOC:bhm","PMID:18189420","PMID:22358512"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcription repressor complex","termid":"GO:0017053"}],"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:0032991","GO:0005575"],"is_obsolete":false,"name":"H-NS-Cnu complex","termid":"GO:0036411"}


id: PBO:0070728
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L9 pseudogene 33","termid":"PBO:0070728"}


id: PBO:0004197
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AP-2 adaptor complex subunit Aps2 (predicted)","termid":"PBO:0004197"}


id: PBO:0059610
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ATP6 pseudogene 22","termid":"PBO:0059610"}


id: GO:0045972
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the regulated release of juvenile hormone.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of juvenile hormone secretion","termid":"GO:0007558"},{"relation_name":"is_a","term_name":"negative regulation of lipid transport","termid":"GO:0032369"},{"relation_name":"is_a","term_name":"negative regulation of hormone secretion","termid":"GO:0046888"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"negatively_regulates","term_name":"juvenile hormone secretion","termid":"GO:0045443"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052","GO:0006810"],"is_obsolete":false,"name":"negative regulation of juvenile hormone secretion","synonyms":[{"name":"down regulation of juvenile hormone secretion","type":"exact"},{"name":"down-regulation of juvenile hormone secretion","type":"exact"},{"name":"downregulation of juvenile hormone secretion","type":"exact"},{"name":"inhibition of juvenile hormone secretion","type":"narrow"}],"termid":"GO:0045972"}


id: PBO:0075257
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sorting nexin 18 pseudogene 10","termid":"PBO:0075257"}


id: GO:0010338
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that gives rise to a leaf. This process pertains to the initial formation of a structure from unspecified parts.","definition_xrefs":["GOC:tair_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plant organ development","termid":"GO:0099402"},{"relation_name":"is_a","term_name":"plant organ formation","termid":"GO:1905393"},{"relation_name":"part_of","term_name":"leaf morphogenesis","termid":"GO:0009965"}],"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":"leaf formation","termid":"GO:0010338"}


id: GO:0050126
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: N-carbamoylputrescine + H2O + 2 H+ = CO2 + NH4 + putrescine.","definition_xrefs":["RHEA:22284","EC:3.5.1.53"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides","termid":"GO:0016811"}],"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:0016787"},{"rel_name":"is_a","termid":"GO:0016810"}],"interesting_parent_ids":["GO:0016787","GO:0003674","GO:0016810","GO:0003824"],"is_obsolete":false,"name":"N-carbamoylputrescine amidase activity","secondary_identifiers":["KEGG_REACTION:R01152","MetaCyc:N-CARBAMOYLPUTRESCINE-AMIDASE-RXN"],"synonyms":[{"name":"N-carbamoylputrescine amidohydrolase activity","type":"related"},{"name":"NCP","type":"related"},{"name":"carbamoylputrescine hydrolase activity","type":"related"}],"termid":"GO:0050126"}


id: GO:0003813
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the selective cleavage of Arg-Ser bond in complement component C3 alpha-chain to form C3a and C3b, and Arg bond in complement component C5 alpha-chain to form C5a and C5b.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete classical-complement-pathway C3/C5 convertase activity (obsolete GO:0003813)","synonyms":[{"name":"C3 convertase activity","type":"broad"},{"name":"C42","type":"related"},{"name":"C423","type":"related"},{"name":"C4b,2a","type":"related"},{"name":"C4b,2a,3b","type":"related"},{"name":"C5 convertase activity","type":"broad"},{"name":"classical-complement-pathway C3/C5 convertase activity","type":"exact"},{"name":"complement C2 activity","type":"broad"},{"name":"complement C3 convertase activity","type":"related"},{"name":"complement C42","type":"related"}],"termid":"GO:0003813"}


id: RO:HOM0000011
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Historical homology that involves genes that diverged after a duplication event.","direct_ancestors":[{"relation_name":"is_a","term_name":"in_historical_homology_relationship_with","termid":"RO:HOM0000007"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"in_paralogy_relationship_with","synonyms":[{"name":"paralogous to","type":"exact"}],"termid":"RO:HOM0000011"}


id: PBO:0083433
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the uncharacterized ORF YIL060W","termid":"PBO:0083433"}


id: PBO:0042489
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cadherin 12 pseudogene 2","termid":"PBO:0042489"}


id: GO:0086055
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that mediates signaling interactions between a Purkinje myocyte and a ventricular cardiac muscle cell by transfer of current between their adjacent cytoplasms via intercellular protein channels.","definition_xrefs":["GOC:BHF","GOC:mtg_cardiac_conduct_nov11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell communication by electrical coupling involved in cardiac conduction","termid":"GO:0086064"},{"relation_name":"is_a","term_name":"Purkinje myocyte to ventricular cardiac muscle cell communication","termid":"GO:0086068"}],"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":"Purkinje myocyte to ventricular cardiac muscle cell communication by electrical coupling","termid":"GO:0086055"}


id: GO:0070188
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A nuclear telomere cap complex that is formed by the association of the Stn1 and Ten1 proteins with telomeric DNA; in some species a third protein is present.","definition_xrefs":["GOC:vw","PMID:19064932","GOC:mah","PMID:17715303"],"gene_count":0,"genotype_count":0,"name":"obsolete Stn1-Ten1 complex (obsolete GO:0070188)","termid":"GO:0070188"}


id: GO:0045818
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the chemical reactions and pathways resulting in the breakdown of glycogen.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of glycogen catabolic process","termid":"GO:0005981"},{"relation_name":"is_a","term_name":"negative regulation of catabolic process","termid":"GO:0009895"},{"relation_name":"is_a","term_name":"negative regulation of glycogen metabolic process","termid":"GO:0070874"},{"relation_name":"negatively_regulates","term_name":"glycogen catabolic process","termid":"GO:0005980"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006091"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006091"},{"rel_name":"negatively_regulates","termid":"GO:0005975"},{"rel_name":"regulates","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0006091","GO:0005975","GO:0008150"],"is_obsolete":false,"name":"negative regulation of glycogen catabolic process","synonyms":[{"name":"down regulation of glycogen catabolic process","type":"exact"},{"name":"down-regulation of glycogen catabolic process","type":"exact"},{"name":"downregulation of glycogen catabolic process","type":"exact"},{"name":"inhibition of glycogen catabolic process","type":"narrow"},{"name":"negative regulation of glycogen breakdown","type":"exact"},{"name":"negative regulation of glycogen catabolism","type":"exact"},{"name":"negative regulation of glycogen degradation","type":"exact"},{"name":"negative regulation of glycogenolysis","type":"exact"}],"termid":"GO:0045818"}


id: GO:1901328
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a cytochalasin B stimulus.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"},{"relation_name":"is_a","term_name":"response to oxygen-containing compound","termid":"GO:1901700"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to cytochalasin B","termid":"GO:1901328"}


id: GO:0034146
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by a ligand binding to toll-like receptor 5.","definition_xrefs":["PMID:16551253","PMID:17328678","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell surface toll-like receptor signaling pathway","termid":"GO:0140895"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"toll-like receptor 5 signaling pathway","secondary_identifiers":["Reactome:R-HSA-168176"],"synonyms":[{"name":"TLR5 signaling pathway","type":"exact"},{"name":"toll-like receptor 5 signalling pathway","type":"exact"}],"termid":"GO:0034146"}


id: GO:0038182
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with an extracellular bile acid and transmitting the signal across the membrane by activating an associated G-protein; promotes the exchange of GDP for GTP on the alpha subunit of a heterotrimeric G-protein complex.","definition_xrefs":["PMID:32480317","PMID:12524422","PMID:35415765","PMID:36409000"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor activity","termid":"GO:0004930"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"G protein-coupled bile acid receptor activity","secondary_identifiers":["Wikipedia:G_protein-coupled_bile_acid_receptor"],"synonyms":[{"name":"G-protein coupled bile acid receptor activity","type":"exact"},{"name":"cell surface bile acid receptor","type":"broad"},{"name":"lithocholic acid receptor activity","type":"broad"},{"name":"membrane bile acid receptor activity","type":"broad"}],"termid":"GO:0038182"}


id: GO:0047276
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: beta-D-galactosyl-(1,4)-beta-N-acetyl-D-glucosaminyl-R + UDP-galactose = alpha-D-galactosyl-(1,3)-beta-D-galactosyl-(1,4)-beta-N-acetyl-D-glucosaminyl-R + UDP.","definition_xrefs":["EC:2.4.1.87","RHEA:13013"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-galactosyltransferase activity","termid":"GO:0035250"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016740","GO:0016757","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"N-acetyllactosaminide 3-alpha-galactosyltransferase activity","secondary_identifiers":["GO:0003946","MetaCyc:2.4.1.151-RXN"],"synonyms":[{"name":"N-acetyllactosaminide alpha-1,3-galactosyltransferase activity","type":"exact"},{"name":"UDP-Gal:Gal-beta-1->4GlcNAc-R alpha-1->3-galactosyltransferase activity","type":"related"},{"name":"UDP-Gal:Galbeta1->4GlcNAc-R alpha1->3-galactosyltransferase activity","type":"related"},{"name":"UDP-Gal:N-acetyllactosaminide alpha(1,3)-galactosyltransferase activity","type":"related"},{"name":"UDP-Gal:N-acetyllactosaminide alpha-(1,3)-galactosyltransferase activity","type":"related"},{"name":"UDP-Gal:N-acetyllactosaminide alpha-1,3-D-galactosyltransferase activity","type":"related"},{"name":"UDP-Gal:beta-D-Gal(1,4)-D-GlcNAc alpha(1,3)-galactosyltransferase activity","type":"related"},{"name":"UDP-Gal:beta-D-Gal(1,4)-D-GlcNAc alpha-(1,3)-galactosyltransferase activity","type":"related"},{"name":"UDP-galactose-acetyllactosamine alpha-D-galactosyltransferase activity","type":"related"},{"name":"UDP-galactose:N-acetyllactosaminide 3-alpha-D-galactosyltransferase activity","type":"related"},{"name":"UDPgalactose:beta-D-galactosyl-beta-1,4-N-acetyl-D-glucosaminyl-glycopeptide alpha-1,3-D-galactosyltransferase activity","type":"related"},{"name":"alpha-galactosyltransferase activity","type":"related"},{"name":"beta-D-galactosyl-N-acetylglucosaminylglycopeptide alpha-1,3-galactosyltransferase activity","type":"related"},{"name":"beta-galactosyl-N-acetylglucosaminylglycopeptide alpha-1,3-galactosyltransferase activity","type":"exact"},{"name":"glucosaminylglycopeptide alpha-1,3-galactosyltransferase activity","type":"related"},{"name":"uridine diphosphogalactose-acetyllactosamine alpha-1->3-galactosyltransferase activity","type":"related"},{"name":"uridine diphosphogalactose-acetyllactosamine alpha1->3-galactosyltransferase activity","type":"related"},{"name":"uridine diphosphogalactose-acetyllactosamine galactosyltransferase activity","type":"related"},{"name":"uridine diphosphogalactose-galactosylacetylglucosaminylgalactosyl-glucosylceramide galactosyltransferase activity","type":"related"},{"name":"uridine diphosphogalactose-galactosylacetylglucosaminylgalactosylglucosylceramide galactosyltransferase activity","type":"related"}],"termid":"GO:0047276"}


id: PBO:0067382
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 484, pseudogene","termid":"PBO:0067382"}


id: FYPO:0005951
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which nucleosome occupancy is lower than normal in chromatin regions where RNA polymerase II actively transcribes genes. Nucleosome occupancy measures the tendency for DNA in a given region to be packaged into nucleosomes.","definition_xrefs":["PomBase:mah","PMID:28218250"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased nucleosome occupancy in euchromatin","termid":"FYPO:0005516"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000641","FYPO:0005447","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"decreased nucleosome occupancy at highly transcribed RNA polymerase II genes","synonyms":[{"name":"decreased nucleosome occupancy at highly transcribed RNA polymerase II genes during mitotic cell cycle","type":"related"},{"name":"decreased nucleosome occupancy at highly transcribed RNA polymerase II genes during vegetative growth","type":"exact"},{"name":"reduced nucleosome occupancy at highly transcribed RNA polymerase II genes","type":"exact"}],"termid":"FYPO:0005951"}


id: GO:0010296
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: protein C-terminal S-farnesyl-L-cysteine methyl ester + H2O = protein C-terminal S-farnesyl-L-cysteine + methanol + H+.","definition_xrefs":["PMID:16870359","RHEA:48520"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein methylesterase activity","termid":"GO:0051723"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0016788","GO:0003824","GO:0140096"],"is_obsolete":false,"name":"prenylcysteine methylesterase activity","secondary_identifiers":["MetaCyc:RXN-8409"],"termid":"GO:0010296"}


id: GO:0072192
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of an epithelial cell in the urothelium. The urothelium is the epithelial tube of the ureter.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial cell differentiation","termid":"GO:0030855"},{"relation_name":"part_of","term_name":"ureter urothelium development","termid":"GO:0072190"}],"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":"ureter epithelial cell differentiation","termid":"GO:0072192"}


id: PBO:0056579
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"multiple C2 and transmembrane domain containing 2","termid":"PBO:0056579"}


id: GO:0044861
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a protein into a plasma membrane raft.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein transport into membrane raft","termid":"GO:0032596"},{"relation_name":"is_a","term_name":"protein localization to plasma membrane raft","termid":"GO:0044860"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0061024"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0061024","GO:0006810"],"is_obsolete":false,"name":"protein transport into plasma membrane raft","termid":"GO:0044861"}


id: GO:0002040
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The extension of new blood vessels from existing vessels into avascular tissues, this process includes the specialization of endothelial cells into leading tip and stalk cells, proliferation and migration of the endothelial cells and cell adhesion resulting in angiogenic sprout fusion or lumen formation.","definition_xrefs":["PMID:16391003","PMID:23031691"],"direct_ancestors":[{"relation_name":"is_a","term_name":"angiogenesis","termid":"GO:0001525"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"sprouting angiogenesis","termid":"GO:0002040"}


id: MONDO:0017059
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A disease that has its basis in the disruption of neural tube closure.","definition_xrefs":["MONDO:design_pattern"],"gene_count":0,"genotype_count":0,"name":"obsolete neural tube closure defect (obsolete MONDO:0017059)","secondary_identifiers":["Orphanet:268357"],"synonyms":[{"name":"disorder of neural tube closure","type":"exact"},{"name":"neural tube closure disease","type":"exact"}],"termid":"MONDO:0017059","xrefs":{"Monarch":{"xref_id":"0017059"}}}


id: MONDO:0043287
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Obstruction of the blood flow in the superior vena cava caused by a malignant neoplasm, thrombosis, or aneurysm. It is a medical emergency requiring immediate treatment. Signs and symptoms include swelling and cyanosis of the face, neck, and upper arms, cough, orthopnea, and headache.","definition_xrefs":["NCIT:C3396"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"vascular disorder","termid":"MONDO:0005385"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"superior vena cava syndrome","secondary_identifiers":["UMLS:C0038833","MESH:D013479","MEDGEN:52576","SCTID:63363004"],"synonyms":[{"name":"SVC obstruction","type":"related"},{"name":"SVC syndrome","type":"related"},{"name":"SVCS","type":"related"},{"name":"superior vena cava obstruction","type":"related"},{"name":"superior vena cava syndrome","type":"exact"},{"name":"superior vena cava thrombosis","type":"related"}],"termid":"MONDO:0043287","xrefs":{"Monarch":{"xref_id":"0043287"}}}


id: PBO:0039733
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"apolipoprotein C4","termid":"PBO:0039733"}


id: PBO:0071434
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L31 pseudogene 40","termid":"PBO:0071434"}


id: GO:0007115
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete bud site selection/establishment of cell polarity (sensu Saccharomyces) (obsolete GO:0007115)","synonyms":[{"name":"bud site selection/establishment of cell polarity (sensu Saccharomyces)","type":"exact"}],"termid":"GO:0007115"}


id: PBO:0081860
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 792","termid":"PBO:0081860"}


id: PBO:0114288
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peroxisome mebbrane ubiquitin conjugating enzyme E2 Ubc16 Pex4","termid":"PBO:0114288"}


id: GO:1904086
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of epiboly involved in gastrulation with mouth forming second.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:24892953"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of morphogenesis of an epithelium","termid":"GO:1905330"},{"relation_name":"regulates","term_name":"epiboly involved in gastrulation with mouth forming second","termid":"GO:0055113"}],"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 epiboly involved in gastrulation with mouth forming second","termid":"GO:1904086"}


id: GO:0070762
data:
  {"annotated_genes":["SJAG_01834","SJAG_03200"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[75745,121444],"is_not":false,"summary":null,"term":"GO:0070762"}]},"cv_name":"cellular_component","definition":"A subcomplex of the nuclear pore complex (NPC) that spans the nuclear membrane and anchors the NPC to the nuclear envelope. In S. cerevisiae, the transmembrane ring is composed of Pom152p, Pom34p, and Ndc1p. In vertebrates, it is composed of Gp210, Ndc1, and Pom121. Components are arranged in 8-fold symmetrical 'spokes' around the central transport channel. A single 'spoke', can be isolated and is sometime referred to as the Ndc1 complex.","definition_xrefs":["PMID:22419078","PMID:19524430","GOC:dgf","PMID:18046406","PMID:20947011"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"},{"relation_name":"part_of","term_name":"nuclear pore","termid":"GO:0005643"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01834":null,"SJAG_03200":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"part_of","termid":"GO:0005643"},{"rel_name":"part_of","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005634","GO:0005643","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"nuclear pore transmembrane ring","references_by_uniquename":{"GO_REF:0000033":null,"PMID:21733045":null},"synonyms":[{"name":"NDC1 complex","type":"exact"},{"name":"NDC1 subcomplex","type":"exact"}],"termid":"GO:0070762","terms_by_termid":{"GO:0070762":null}}


id: PATO:0000851
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000851 absolute auditory threshold (obsolete PATO:0000851)","termid":"PATO:0000851"}


id: FYPO:0003616
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 fluphenazine. Cells stop growing (and may die) at a concentration of fluphenazine 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:0000139"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0001985","FYPO:0002683","FYPO:0000139","FYPO:0005447"],"is_obsolete":false,"name":"sensitive to fluphenazine","synonyms":[{"name":"hypersensitive to fluphenazine","type":"exact"},{"name":"sensitive to fluphenazine during mitotic cell cycle","type":"related"},{"name":"sensitive to fluphenazine during vegetative growth","type":"exact"}],"termid":"FYPO:0003616"}


id: MONDO:0024889
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign epithelial neoplasm of the female reproductive system arising from mesonephric remnants.","definition_xrefs":["NCIT:C4294"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"benign reproductive system neoplasm","termid":"MONDO:0000383"},{"relation_name":"is_a","term_name":"kidney benign neoplasm","termid":"MONDO:0002513"},{"relation_name":"is_a","term_name":"mesonephric neoplasm","termid":"MONDO:0024888"},{"relation_name":"is_a","term_name":"benign epithelial neoplasm","termid":"MONDO:0036976"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"benign mesonephroma","secondary_identifiers":["MEDGEN:87259","DOID:2616","UMLS:C0334530","ICDO:9110/0"],"synonyms":[{"name":"Mesonephroma, benign","type":"exact"},{"name":"Mesonephroma, benign (morphologic abnormality)","type":"exact"},{"name":"Wolffian duct adenoma","type":"exact"},{"name":"benign Mesonephroma","type":"exact"},{"name":"benign mesonephric neoplasm","type":"exact"},{"name":"mesonephric adenoma","type":"exact"},{"name":"mesonephric duct adenoma","type":"exact"},{"name":"mesonephric neoplasm, benign","type":"exact"}],"termid":"MONDO:0024889","xrefs":{"Monarch":{"xref_id":"0024889"}}}


id: MONDO:0016622
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Melhem-Fahl syndrome was described in two siblings born to consanguineous parents in 1985 and was characterized by the presence of 15 dorsal vertebrae and rib pairs. No other cases have been documented since the initial report.","definition_xrefs":["Orphanet:2482"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"dysostosis","termid":"MONDO:0018234"}],"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":"Melhem-Fahl syndrome","secondary_identifiers":["MEDGEN:444059","SCTID:732263008","icd11.foundation:999539082","UMLS:C2931453","GARD:3462","MESH:C537238"],"synonyms":[{"name":"Melhem Fahl syndrome","type":"related"},{"name":"fifteen dorsal vertebrae and rib pairs","type":"related"}],"termid":"MONDO:0016622","xrefs":{"Monarch":{"xref_id":"0016622"}}}


id: PBO:0072641
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA 2',3'-cyclic phosphate and 5'-OH ligase","termid":"PBO:0072641"}


id: GO:0106180
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the translocation of hydrons (hydron being the general name for H+ in its natural abundance).","definition_xrefs":["GOC:hjd"],"gene_count":0,"genotype_count":0,"name":"obsolete translocase activity of hydrons (obsolete GO:0106180)","termid":"GO:0106180"}


id: PBO:0110464
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ACTR2 pseudogene 2","termid":"PBO:0110464"}


id: MONDO:0100438
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A retinopathy caused by biallelic variants in the AIPL1 gene.","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited retinal dystrophy","termid":"MONDO:0019118"}],"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":"AIPL1-related retinopathy","synonyms":[{"name":"AIPL1 Leber congenital amaurosis","type":"narrow"},{"name":"AIPL1 retinopathy","type":"exact"},{"name":"LCA4","type":"narrow"},{"name":"Leber congenital amaurosis 4","type":"narrow"},{"name":"Leber congenital amaurosis caused by mutation in AIPL1","type":"narrow"},{"name":"Leber congenital amaurosis type 4","type":"narrow"},{"name":"amaurosis congenita of Leber, type 4","type":"narrow"},{"name":"cone-rod dystrophy","type":"narrow"},{"name":"cone-rod dystrophy, AIPL1-related","type":"narrow"},{"name":"retinitis pigmentosa, juvenile","type":"narrow"},{"name":"retinitis pigmentosa, juvenile, AIPL1-related","type":"narrow"}],"termid":"MONDO:0100438","xrefs":{"Monarch":{"xref_id":"0100438"}}}


id: MONDO:0024292
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A polypoid tumor that arises from any part of the gastrointestinal tract and protrudes into the lumen. Representative examples include adenomatous polyps, hyperplastic polyps, and hamartomatous polyps.","definition_xrefs":["NCIT:C35516"],"direct_ancestors":[{"relation_name":"is_a","term_name":"digestive system disorder","termid":"MONDO:0004335"},{"relation_name":"is_a","term_name":"polyp","termid":"MONDO:0005079"}],"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":"gastrointestinal polyp","secondary_identifiers":["UMLS:C1257915","MEDGEN:219797"],"synonyms":[{"name":"GI polyp","type":"exact"},{"name":"gastrointestinal polyp","type":"exact"},{"name":"gastrointestinal tract polyp","type":"exact"}],"termid":"MONDO:0024292","xrefs":{"Monarch":{"xref_id":"0024292"}}}


id: SO:0000002
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A folded sequence.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biological_region","termid":"SO:0001411"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sequence_secondary_structure","synonyms":[{"name":"INSDC_feature:misc_structure","type":"exact"},{"name":"sequence secondary structure","type":"exact"}],"termid":"SO:0000002"}


id: PBO:0082233
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alpha-glucosidase; weak, but broad substrate specificity for alpha-1,4- and alpha-1,6-glucosides; member of IMA isomaltase family; not required for isomaltose utilization, but Ima3p overexpression allows the ima1 null mutant to grow on isomaltose; lower activitiy and thermostability in vitro than Ima2p despite sequence difference of only 3 amino acids; cleaves alpha-1,3 linkage of nigerose and turanose, but not alpha-1,5 of leucrose; identical to IMA4","termid":"PBO:0082233"}


id: PBO:0056839
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MGAT4 family member D","termid":"PBO:0056839"}


id: GO:0019909
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Binds to and modulates of the activity of [pyruvate dehydrogenase (lipoamide)] phosphatase.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete [pyruvate dehydrogenase (lipoamide)] phosphatase regulator activity (obsolete GO:0019909)","synonyms":[{"name":"[pyruvate dehydrogenase (lipoamide)] phosphatase, intrinsic regulator activity","type":"narrow"}],"termid":"GO:0019909"}


id: PBO:0048626
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GIPC PDZ domain containing family member 2","termid":"PBO:0048626"}


id: FYPO:0004829
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of a phosphatase activity is decreased during a cellular response to adenine starvation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased phosphatase activity","termid":"FYPO:0004304"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0000654","FYPO:0001985","FYPO:0000652","FYPO:0000661","FYPO:0000707"],"is_obsolete":false,"name":"decreased phosphatase activity during cellular response to adenine starvation","synonyms":[{"name":"decreased phosphatase activity during adenine starvation","type":"exact"},{"name":"reduced phosphatase activity during cellular response to adenine starvation","type":"exact"}],"termid":"FYPO:0004829"}


id: PBO:0051715
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"insulin induced gene 2","termid":"PBO:0051715"}


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


id: PBO:0032703
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_level_of_histone_H3_in_cell","termid":"PBO:0032703"}


id: GO:0071106
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which adenosine 3',5'-bisphosphate is transported across a membrane.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine ribonucleotide transport","termid":"GO:0015868"},{"relation_name":"is_a","term_name":"adenine nucleotide transport","termid":"GO:0051503"},{"relation_name":"is_a","term_name":"purine-containing compound transmembrane transport","termid":"GO:0072530"},{"relation_name":"is_a","term_name":"nucleotide transmembrane transport","termid":"GO:1901679"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0051179","GO:0055085","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"adenosine 3',5'-bisphosphate transmembrane transport","synonyms":[{"name":"adenosine 3',5'-bisphosphate membrane transport","type":"exact"},{"name":"adenosine 3',5'-diphosphate transport","type":"exact"},{"name":"adenosine 3'-phosphate-5'-phosphate transmembrane transport","type":"exact"}],"termid":"GO:0071106"}


id: PBO:0079081
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-iMet (anticodon CAT) 2-1","termid":"PBO:0079081"}


id: PBO:0074723
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 80C","termid":"PBO:0074723"}


id: PBO:0038372
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-facultative_parasite_of","termid":"PBO:0038372"}


id: GO:0086097
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A phospholipase C-activating G protein-coupled receptor signaling pathway initiated by angiotensin binding to its receptor on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["GOC:mtg_cardiac_conduct_nov11","GOC:bf","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phospholipase C-activating G protein-coupled receptor signaling pathway","termid":"GO:0007200"},{"relation_name":"is_a","term_name":"angiotensin-activated signaling pathway","termid":"GO:0038166"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"phospholipase C-activating angiotensin-activated signaling pathway","synonyms":[{"name":"Gq-coupled angiotensin receptor signaling pathway","type":"exact"},{"name":"PLC-activating angiotensin receptor signaling pathway","type":"exact"},{"name":"angiotensin-mediated signaling pathway via activation of phospholipase C","type":"exact"},{"name":"phospholipase C-activating angiotensin receptor signaling pathway","type":"exact"},{"name":"phospholipase C-activating angiotensin-mediated signaling pathway","type":"related"}],"termid":"GO:0086097"}


id: PBO:0071926
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S4X pseudogene 3","termid":"PBO:0071926"}


id: PBO:0044079
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cystatin pseudogene 1","termid":"PBO:0044079"}


id: PBO:0028521
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_histone_H3-K9_acetylation","termid":"PBO:0028521"}


id: FYPO:0007780
data:
  {"alleles_by_uniquename":{"SJAG_00124:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00124","name":"SJAG_00124delta","uniquename":"SJAG_00124:allele-1"},"SJAG_01787:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01787","name":"pck1delta","uniquename":"SJAG_01787:allele-1"},"SJAG_02013:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02013","name":"pyp1delta","uniquename":"SJAG_02013:allele-1"},"SJAG_04551:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04551","name":"pmk1delta","uniquename":"SJAG_04551:allele-1"},"SJAG_04551:allele-2":{"allele_type":"amino_acid_insertion","description":"82-NITCIYDLDIIINPYNFNEVYIYEE-105","gene_uniquename":"SJAG_04551","name":"Pmk1Sj(ins82-105)","uniquename":"SJAG_04551:allele-2"},"SJAG_04551:allele-3":{"allele_type":"other","description":"Pmk1 from S. pombe","gene_uniquename":"SJAG_04551","name":"Pmk1Sp","uniquename":"SJAG_04551:allele-3"},"SJAG_04551:allele-4":{"allele_type":"partial_amino_acid_deletion","description":"Pmk1 from S. pombe with deleted residues 82-105","gene_uniquename":"SJAG_04551","name":"Pmk1Sp(delta82-105)","uniquename":"SJAG_04551:allele-4"},"SJAG_04697:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04697","name":"gms1delta","uniquename":"SJAG_04697:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[121159],"is_not":false,"summary":null,"term":"FYPO:0007780"}],"single_locus_phenotype":[{"annotations":[121147,121163,121168,121171,121413,121415,121511],"is_not":false,"summary":null,"term":"FYPO:0007780"}]},"cv_name":"fission_yeast_phenotype","definition":"A phenotype in which the mycelium formed by fission yeast undergoing hyphal growth covers a smaller area than normal.","definition_xrefs":["PMID:31150379","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal hyphal growth","termid":"FYPO:0007773"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00124":null,"SJAG_01787":null,"SJAG_02013":null,"SJAG_04551":null,"SJAG_04697":null},"genotype_count":8,"genotypes_by_uniquename":{"Pmk1Sj(ins82-105)-82-NITCIYDLDIIINPYNFNEVYIYEE-105-amino_acid_insertion-expression-not_assayed_or_wild_type":{"display_name":"Pmk1Sj(ins82-105)(82-NITCIYDLDIIINPYNFNEVYIYEE-105)","display_uniquename":"Pmk1Sj(ins82-105)-82-NITCIYDLDIIINPYNFNEVYIYEE-105-amino_acid_insertion-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04551:allele-2","expression":"Not assayed or wild type"}]}]},"Pmk1Sp(delta82-105)-Pmk1_from_S._pombe_with_deleted_residues_82-105-partial_amino_acid_deletion-expression-not_assayed_or_wild_type":{"display_name":"Pmk1Sp(delta82-105)(Pmk1 from S. pombe with deleted residues 82-105 Δaa)","display_uniquename":"Pmk1Sp(delta82-105)-Pmk1_from_S._pombe_with_deleted_residues_82-105-partial_amino_acid_deletion-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04551:allele-4","expression":"Not assayed or wild type"}]}]},"Pmk1Sp-Pmk1_from_S._pombe-other-expression-not_assayed_or_wild_type":{"display_name":"Pmk1Sp(Pmk1 from S. pombe)","display_uniquename":"Pmk1Sp-Pmk1_from_S._pombe-other-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04551:allele-3","expression":"Not assayed or wild type"}]}]},"SJAG_00124delta":{"display_name":"SJAG_00124delta","display_uniquename":"SJAG_00124delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00124:allele-1","expression":"Null"}]}]},"gms1delta":{"display_name":"gms1delta","display_uniquename":"gms1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04697:allele-1","expression":"Null"}]}]},"pck1delta__pmk1delta":{"display_name":"pck1delta pmk1delta","display_uniquename":"pck1delta__pmk1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01787:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_04551:allele-1","expression":"Null"}]}]},"pmk1delta":{"display_name":"pmk1delta","display_uniquename":"pmk1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04551:allele-1","expression":"Null"}]}]},"pyp1delta":{"display_name":"pyp1delta","display_uniquename":"pyp1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02013:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0007773"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0007773","FYPO:0000002"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_04551","SJAG_01787"],"name":"decreased mycelial expansion","references_by_uniquename":{"PMID:31150379":null,"PMID:34198697":null,"PMID:36058798":null},"single_locus_annotated_genes":["SJAG_00124","SJAG_04551","SJAG_02013","SJAG_04697"],"single_locus_genotype_uniquenames":["pmk1delta","pyp1delta","Pmk1Sp-Pmk1_from_S._pombe-other-expression-not_assayed_or_wild_type","SJAG_00124delta","gms1delta","Pmk1Sj(ins82-105)-82-NITCIYDLDIIINPYNFNEVYIYEE-105-amino_acid_insertion-expression-not_assayed_or_wild_type","Pmk1Sp(delta82-105)-Pmk1_from_S._pombe_with_deleted_residues_82-105-partial_amino_acid_deletion-expression-not_assayed_or_wild_type"],"termid":"FYPO:0007780","terms_by_termid":{"FYECO:0000137":null,"FYECO:0000314":null,"FYPO:0007780":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null}}


id: GO:1990724
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A homodimeric protein complex that is capable of binding a range of carbohydrates and is involved in anti-inflammatory and pro-apoptotic processes.","definition_xrefs":["PMID:18777589","PMID:8262940","GOC:bhm","PMID:15476813"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein complex involved in cell-cell adhesion","termid":"GO:0098635"}],"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:0032991","GO:0005575"],"is_obsolete":false,"name":"galectin complex","synonyms":[{"name":"galectin-1 complex","type":"narrow"},{"name":"galectin-2 complex","type":"narrow"}],"termid":"GO:1990724"}


id: PBO:0088060
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ubiquitin-protein ligase (E3); controls septin dynamics, spindle position checkpoint (SPOC) with ligase Dma2p by regulating recruitment of Elm1p to bud neck; regulates levels of eIF2 subunit Gcd11p, as well as abundance, localization, and ubiquitination of Cdk inhibitory kinase Swe1p; ubiquitinates cyclin Pcl1p; ortholog of human RNF8, similar to human Chfr; contains FHA, RING fingers; DMA1 has a paralog, DMA2, that arose from the whole genome duplication","termid":"PBO:0088060"}


id: GO:0010939
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the rate, frequency or extent of necrotic cell death. Necrotic cell death is a cell death process that is morphologically characterized by a gain in cell volume (oncosis), swelling of organelles, plasma membrane rupture and subsequent loss of intracellular contents.","definition_xrefs":["PMID:16507998"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of necrotic cell death (obsolete GO:0010939)","termid":"GO:0010939"}


id: PBO:0060845
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuronal growth regulator 1","termid":"PBO:0060845"}


id: PBO:0039380
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adenosine monophosphate deaminase 3","termid":"PBO:0039380"}


id: PBO:0070910
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L17 pseudogene 18","termid":"PBO:0070910"}


id: PBO:0074675
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 59B","termid":"PBO:0074675"}


id: MONDO:0005712
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Nystagmus present at birth or caused by lesions sustained in utero or at the time of birth. It is usually pendular, and is associated with albinism and conditions characterized by early loss of central vision. Inheritance patterns may be X-linked, autosomal dominant, or recessive. (Adams et al., Principles of Neurology, 6th ed, p275)","definition_xrefs":["MESH:D020417"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"pathologic nystagmus","termid":"MONDO:0004843"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"congenital nystagmus","secondary_identifiers":["icd11.foundation:1626567380","MEDGEN:195995","ICD9:379.51","EFO:0007217","ICD10CM:H55.01","OMIMPS:310700","DOID:9649","HP:0000639","Orphanet:651","UMLS:C0700501","SCTID:64635004"],"synonyms":[{"name":"congenital idiopathic nystagmus","type":"exact"},{"name":"congenital pathologic nystagmus","type":"exact"},{"name":"motor congenital nystagmus","type":"exact"},{"name":"nystagmus","type":"broad"},{"name":"nystagmus, congenital","type":"exact"}],"termid":"MONDO:0005712","xrefs":{"Monarch":{"xref_id":"0005712"}}}


id: PBO:0091472
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sucrose alpha-glucosidase Suc2","termid":"PBO:0091472"}


id: PBO:0044446
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome P450 family 4 subfamily F member 24, pseudogene","termid":"PBO:0044446"}


id: MONDO:0008124
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"omphalocele","termid":"MONDO:0019015"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"omphalocele, autosomal","secondary_identifiers":["OMIM:164750","UMLS:C3277235","MEDGEN:478865","GARD:18586"],"synonyms":[{"name":"chromosome 1P31 Duplication syndrome","type":"related"},{"name":"omphalocele due to duplication of 1p31.3, isolated cases","type":"exact"},{"name":"omphalocele, autosomal","type":"exact"},{"name":"paraomphalocele","type":"related"},{"name":"type - epigastric - defect in the cephalic fold","type":"related"},{"name":"type - hypogastric - defect in the caudal fold","type":"related"}],"termid":"MONDO:0008124","xrefs":{"Monarch":{"xref_id":"0008124"}}}


id: PBO:0001537
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HbrB family protein","termid":"PBO:0001537"}


id: FYPO:0005577
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the phosphorylation of one or more specific proteins occurs to a lower extent than normal during the meiotic cell cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein phosphorylation","termid":"FYPO:0002679"},{"relation_name":"is_a","term_name":"abnormal protein phosphorylation during meiotic cell cycle","termid":"FYPO:0006765"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0002274","FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0002494"],"is_obsolete":false,"name":"decreased protein phosphorylation during meiotic cell cycle","synonyms":[{"name":"reduced protein phosphorylation during meiotic cell cycle","type":"exact"}],"termid":"FYPO:0005577"}


id: PBO:0004915
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PMT4 subfamily","termid":"PBO:0004915"}


id: MONDO:0002357
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm involving the hepatic flexure of colon.","direct_ancestors":[{"relation_name":"is_a","term_name":"ascending colon cancer","termid":"MONDO:0002238"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992"],"is_obsolete":false,"name":"hepatic flexure cancer","secondary_identifiers":["DOID:260","ICD10CM:C18.3","ICD9:153.0","MEDGEN:509289","SCTID:363407001","UMLS:C0153433"],"synonyms":[{"name":"Ca hepatic flexure - colon","type":"exact"},{"name":"cancer of hepatic flexure of colon","type":"exact"},{"name":"hepatic flexure of colon cancer","type":"exact"},{"name":"malignant hepatic flexure of colon neoplasm","type":"exact"},{"name":"malignant neoplasm of hepatic flexure","type":"exact"},{"name":"malignant neoplasm of hepatic flexure of colon","type":"exact"},{"name":"malignant tumor of hepatic flexure","type":"exact"},{"name":"malignant tumour of hepatic flexure","type":"exact"}],"termid":"MONDO:0002357","xrefs":{"Monarch":{"xref_id":"0002357"}}}


id: GO:0048705
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the skeleton are generated and organized.","definition_xrefs":["GOC:dph","GOC:dsf","GOC:jid","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"animal organ morphogenesis","termid":"GO:0009887"},{"relation_name":"part_of","term_name":"skeletal system development","termid":"GO:0001501"}],"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":"skeletal system morphogenesis","synonyms":[{"name":"skeletal morphogenesis","type":"exact"}],"termid":"GO:0048705"}


id: PBO:0042710
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CELSR1 pseudogene 1","termid":"PBO:0042710"}


id: GO:0030484
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The contractile fibers, composed of actin, myosin, and associated proteins, found in cells of smooth or striated muscle.","definition_xrefs":["ISBN:0815316194","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete muscle fiber (obsolete GO:0030484)","synonyms":[{"name":"muscle fiber","type":"exact"},{"name":"muscle fibre","type":"exact"}],"termid":"GO:0030484"}


id: GO:0031362
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the plasma membrane consisting of the gene products that are tethered to the external side of the membrane only by a covalently attached anchor, such as a lipid group embedded in the membrane. Gene products with peptide sequences that are embedded in the membrane are excluded from this grouping.","definition_xrefs":["GOC:mah","GOC:dos"],"gene_count":0,"genotype_count":0,"name":"obsolete anchored component of external side of plasma membrane (obsolete GO:0031362)","synonyms":[{"name":"anchored to external leaflet of plasma membrane","type":"exact"},{"name":"anchored to external side of plasma membrane","type":"exact"}],"termid":"GO:0031362"}


id: GO:0047837
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-xylose + NADP+ = D-xylono-1,5-lactone + H+ + NADPH.","definition_xrefs":["RHEA:22000"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"D-xylose 1-dehydrogenase (NADP+) activity","secondary_identifiers":["EC:1.1.1.179","KEGG_REACTION:R01430","MetaCyc:D-XYLOSE-1-DEHYDROGENASE-NADP+-RXN"],"synonyms":[{"name":"D-xylose (nicotinamide adenine dinucleotide phosphate) dehydrogenase activity","type":"related"},{"name":"D-xylose-NADP dehydrogenase activity","type":"related"},{"name":"D-xylose:NADP+ 1-oxidoreductase activity","type":"related"},{"name":"D-xylose:NADP+ oxidoreductase activity","type":"related"}],"termid":"GO:0047837"}


id: MONDO:0006075
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign soft tissue lesion arising from the adrenal gland. It is composed of mature adipose and hematopoietic/lymphoid tissues.","definition_xrefs":["NCIT:C3736"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign neoplasm of adrenal gland","termid":"MONDO:0021511"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adrenal gland myelolipoma","secondary_identifiers":["UMLS:C0206635","EFO:1000074","MEDGEN:64623","MESH:D018209","ICDO:8870/0","SCTID:719049003"],"synonyms":[{"name":"MYELOLIPOMA, benign","type":"exact"},{"name":"Myelolipoma","type":"exact"},{"name":"adrenal gland myelolipoma","type":"exact"}],"termid":"MONDO:0006075","xrefs":{"Monarch":{"xref_id":"0006075"}}}


id: MONDO:0859325
data:
  {"annotated_genes":["SJAG_00071","SJAG_04853"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87364,87365],"is_not":false,"summary":null,"term":"MONDO:0859325"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"genetic developmental and epileptic encephalopathy","termid":"MONDO:0100062"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00071":null,"SJAG_04853":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"},{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0005027","MONDO:0700092"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy 109","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0070378","MEDGEN:1824036","UMLS:C5774263","OMIM:620145"],"termid":"MONDO:0859325","terms_by_termid":{"MONDO:0859325":null},"xrefs":{"Monarch":{"xref_id":"0859325"}}}


id: SO:0001408
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The C-terminal residues of a polypeptide which are exchanged for a GPI-anchor.","definition_xrefs":["EBI:rh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cleaved_peptide_region","termid":"SO:0100011"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"SO:0000839"}],"interesting_parent_ids":["SO:0000839"],"is_obsolete":false,"name":"cleaved_for_gpi_anchor_region","synonyms":[{"name":"cleaved for gpi anchor region","type":"exact"}],"termid":"SO:0001408"}


id: PBO:0089608
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosome assembly protein Sqt1","termid":"PBO:0089608"}


id: PBO:0117209
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane sulfite efflux transmembrane transporter Ssu4","termid":"PBO:0117209"}


id: PBO:0044638
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"decapping mRNA 1A","termid":"PBO:0044638"}


id: GO:0042995
data:
  {"annotated_genes":["SJAG_03596","SJAG_02379","SJAG_01978","SJAG_04100","SJAG_04621","SJAG_00938","SJAG_03688","SJAG_01794","SJAG_02222","SJAG_03011","SJAG_00514","SJAG_02718","SJAG_04509","SJAG_00667","SJAG_02228","SJAG_00279","SJAG_00700","SJAG_01769","SJAG_01943","SJAG_02169","SJAG_00870","SJAG_02924","SJAG_04901","SJAG_03357","SJAG_03444","SJAG_01017","SJAG_01215","SJAG_04781","SJAG_05285","SJAG_03646","SJAG_01993","SJAG_00185","SJAG_04982","SJAG_04723","SJAG_00663","SJAG_01732","SJAG_02989","SJAG_04001","SJAG_00677","SJAG_04887","SJAG_04470","SJAG_04703","SJAG_02351","SJAG_02700","SJAG_03145","SJAG_02486","SJAG_03453","SJAG_00845","SJAG_05001","SJAG_01171","SJAG_01888"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[59524,79001],"is_not":false,"summary":null,"term":"GO:0042995"},{"annotations":[113217],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005937"},{"annotations":[90906,109905,95634,94323,118033,97182,121516,101366,109966,113168,101968,116481,103762,92652,90089,103761,95828],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990819"},{"annotations":[89951,100793],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070250"},{"annotations":[96313,101931,107839,117827],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032175"},{"annotations":[98677,105072,107932,110899,80454,116181,117674,77309,71883,94396,110689,89700,92528,78058,75691,73922,100709,99534,92482,108692,108993,79530,99728],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0043332"},{"annotations":[98190,112041],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070867"},{"annotations":[81321],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005902"}]},"cv_name":"cellular_component","definition":"A prolongation or process extending from a cell, e.g. a flagellum or axon.","definition_xrefs":["GOC:jl","PMID:16318917"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"}],"gene_count":51,"genes_by_uniquename":{"SJAG_00185":null,"SJAG_00279":null,"SJAG_00514":null,"SJAG_00663":null,"SJAG_00667":null,"SJAG_00677":null,"SJAG_00700":null,"SJAG_00845":null,"SJAG_00870":null,"SJAG_00938":null,"SJAG_01017":null,"SJAG_01171":null,"SJAG_01215":null,"SJAG_01732":null,"SJAG_01769":null,"SJAG_01794":null,"SJAG_01888":null,"SJAG_01943":null,"SJAG_01978":null,"SJAG_01993":null,"SJAG_02169":null,"SJAG_02222":null,"SJAG_02228":null,"SJAG_02351":null,"SJAG_02379":null,"SJAG_02486":null,"SJAG_02700":null,"SJAG_02718":null,"SJAG_02924":null,"SJAG_02989":null,"SJAG_03011":null,"SJAG_03145":null,"SJAG_03357":null,"SJAG_03444":null,"SJAG_03453":null,"SJAG_03596":null,"SJAG_03646":null,"SJAG_03688":null,"SJAG_04001":null,"SJAG_04100":null,"SJAG_04470":null,"SJAG_04509":null,"SJAG_04621":null,"SJAG_04703":null,"SJAG_04723":null,"SJAG_04781":null,"SJAG_04887":null,"SJAG_04901":null,"SJAG_04982":null,"SJAG_05001":null,"SJAG_05285":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"cell projection","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000043":null,"GO_REF:0000107":null,"PMID:36148799":null},"synonyms":[{"name":"cell process","type":"broad"},{"name":"cellular process","type":"broad"},{"name":"cellular projection","type":"exact"}],"termid":"GO:0042995","terms_by_termid":{"GO:0005902":null,"GO:0005937":null,"GO:0032175":null,"GO:0042995":null,"GO:0043332":null,"GO:0070250":null,"GO:0070867":null,"GO:1990819":null}}


id: PATO:0002346
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A concave 3-D shape quality inhering in a bearer by virtue of the bearer's having two connected parts, roughly spherical, of different sizes.","definition_xrefs":["PATOC:MH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"concave 3-D shape","termid":"PATO:0002008"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"snowman-shaped","termid":"PATO:0002346"}


id: GO:0150033
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of protein localization to lysosome.","definition_xrefs":["GOC:bc","GOC:aruk","PMID:24305806"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein localization to lysosome","termid":"GO:0150031"},{"relation_name":"is_a","term_name":"negative regulation of protein localization","termid":"GO:1903828"},{"relation_name":"negatively_regulates","term_name":"protein localization to lysosome","termid":"GO:0061462"}],"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 protein localization to lysosome","termid":"GO:0150033"}


id: MONDO:0017641
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete miscellaneous movement disorder due to neurodegenerative disease (obsolete MONDO:0017641)","secondary_identifiers":["Orphanet:306695"],"termid":"MONDO:0017641","xrefs":{"Monarch":{"xref_id":"0017641"}}}


id: PBO:0077740
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transducer of ERBB2, 1","termid":"PBO:0077740"}


id: GO:0050789
data:
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id: GO:0097231
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id: PBO:0113072
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id: MONDO:1011588
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  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Porphyria that occurs in pig.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"porphyria, non-human animal","termid":"MONDO:1011418"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"porphyria, pig","secondary_identifiers":["OMIA:000815-9823"],"termid":"MONDO:1011588","xrefs":{"Monarch":{"xref_id":"1011588"}}}


id: GO:0046538
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id: PBO:0062772
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id: MONDO:0015918
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  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Rare neurodegenerative disease.","gene_count":0,"genotype_count":0,"name":"obsolete rare neurodegenerative disease (obsolete MONDO:0015918)","secondary_identifiers":["Orphanet:182070"],"synonyms":[{"name":"rare neurodegenerative disease","type":"exact"}],"termid":"MONDO:0015918","xrefs":{"Monarch":{"xref_id":"0015918"}}}


id: PR:G2TRK9
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  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- new13 gene.","definition_xrefs":["PRO:DNx","UniProtKB:G2TRK9"],"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 new13 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4D7.14","synonyms":[{"name":"Spom972h-new13","type":"exact"}],"termid":"PR:G2TRK9"}


id: PBO:0049435
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GUSB pseudogene 12","termid":"PBO:0049435"}


id: GO:0099079
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id: GO:0035624
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which a receptor is activated by another receptor. Receptor transactivation can occur through different mechanisms and includes cross-talk between signaling pathways where one receptor activates a receptor for a different ligand, and also activation of subunits within a receptor oligomer.","definition_xrefs":["PMID:21063387","GOC:BHF","PMID:16870826","GOC:al","GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete receptor transactivation (obsolete GO:0035624)","termid":"GO:0035624"}


id: GO:0141170
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of positive regulation of 5-methylcytosine DNA demethylation, direct 5-methylcytosine excision pathway.","definition_xrefs":["PMID:36478523"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of DNA metabolic process","termid":"GO:0051054"},{"relation_name":"positively_regulates","term_name":"chromosomal 5-methylcytosine DNA demethylation, direct 5-methylcytosine excision pathway","termid":"GO:0141169"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006259","GO:0008150"],"is_obsolete":false,"name":"positive regulation of 5-methylcytosine DNA demethylation, direct 5-methylcytosine excision pathway","termid":"GO:0141170"}


id: MONDO:1012598
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Oculocutaneous albinism that occurs in rabbits due to a mutation in the TYR gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oculocutaneous albinism, non-human animal","termid":"MONDO:1012579"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oculocutaneous albinism, TYR-related, rabbit","secondary_identifiers":["OMIA:000202-9986"],"synonyms":[{"name":"coat/skin colour, oculocutaneous albinism type I (OCA1), TYR-related in Oryctolagus cuniculus (rabbit)","type":"exact"}],"termid":"MONDO:1012598","xrefs":{"Monarch":{"xref_id":"1012598"}}}


id: GO:0110157
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  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An extracellular complex that binds lipoprotein receptors VLDLR and APOER2, cadherin-related neuronal receptors (CNRs) or alpha3beta1 integrin and induces various downstream, reelin-dependent, phosphorylation cascades. It ultimately affects polarization, differentiation, neuronal migration and layer formation in the embryonic brain and neuron growth, maturation, and synaptic activity in the postnatal and adult brain.","definition_xrefs":["GOC:bhm","PMID:21844191","PMID:28887403"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"extracellular space","termid":"GO:0005615"}],"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:0005576"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005576"],"is_obsolete":false,"name":"reelin complex","termid":"GO:0110157"}


id: PBO:0001765
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  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ABC transporter family","termid":"PBO:0001765"}


id: PBO:0091440
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id: PBO:0040141
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id: PBO:0062249
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id: GO:0006187
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of dGTP, deoxyguanosine triphosphate (2'-deoxyguanosine 5'-triphosphate) from other compounds, including gGDP, deoxyguanosine diphosphate.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dGDP metabolic process","termid":"GO:0046066"},{"relation_name":"is_a","term_name":"dGTP biosynthetic process","termid":"GO:0046071"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"dGTP biosynthetic process from dGDP","synonyms":[{"name":"dGTP anabolism from dGDP","type":"exact"},{"name":"dGTP formation from dGDP","type":"exact"},{"name":"dGTP synthesis from dGDP","type":"exact"}],"termid":"GO:0006187"}


id: PBO:0034307
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-electrically_synapsed_to","termid":"PBO:0034307"}


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


id: MOD:01508
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces the N6-hydrogen atom of a lysine residue with the Applied Biosystems iTRAQ4plex-117 reporter+balance group.","definition_xrefs":["OMSSA:212","Unimod:889#K","OMSSA:177","Unimod:214#K"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iTRAQ4plex-117, mTRAQ heavy, reporter+balance reagent acylated residue","termid":"MOD:01506"},{"relation_name":"is_a","term_name":"iTRAQ4plex reporter+balance reagent N-acylated residue","termid":"MOD:01709"},{"relation_name":"is_a","term_name":"N6-acylated L-lysine","termid":"MOD:01875"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01875"}],"interesting_parent_ids":["MOD:01875"],"is_obsolete":false,"name":"iTRAQ4plex-117, mTRAQ heavy, reporter+balance reagent N6-acylated lysine","synonyms":[{"name":"(4-methylpiperazin-1-yl)acetyl","type":"exact"},{"name":"Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry","type":"related"},{"name":"Applied Biosystems mTRAQ(TM) reagent","type":"related"},{"name":"Representative mass and accurate mass for 116 & 117","type":"related"},{"name":"iTRAQ","type":"related"},{"name":"iTRAQ117K","type":"exact"},{"name":"iTRAQ4plex","type":"related"},{"name":"mTRAQ heavy","type":"related"},{"name":"mTRAQ heavy on K","type":"exact"}],"termid":"MOD:01508"}


id: PBO:0075608
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spondin 2","termid":"PBO:0075608"}


id: PBO:0062883
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"OVCA2 serine hydrolase domain containing","termid":"PBO:0062883"}


id: PBO:0117388
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"patatin like domain 6, lysophospholipase","termid":"PBO:0117388"}


id: GO:0009128
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of purine nucleoside monophosphate, a compound consisting of a purine base linked to a ribose or deoxyribose sugar esterified with phosphate on the sugar.","definition_xrefs":["ISBN:0198506732","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside monophosphate catabolic process","termid":"GO:0009125"},{"relation_name":"is_a","term_name":"purine nucleoside monophosphate metabolic process","termid":"GO:0009126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"purine nucleoside monophosphate catabolic process","synonyms":[{"name":"purine nucleoside monophosphate breakdown","type":"exact"},{"name":"purine nucleoside monophosphate catabolism","type":"exact"},{"name":"purine nucleoside monophosphate degradation","type":"exact"}],"termid":"GO:0009128"}


id: GO:0045918
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of cytolysis.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytolysis","termid":"GO:0042268"},{"relation_name":"is_a","term_name":"negative regulation of cellular process","termid":"GO:0048523"},{"relation_name":"negatively_regulates","term_name":"cytolysis","termid":"GO:0019835"}],"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 cytolysis","synonyms":[{"name":"down regulation of cytolysis","type":"exact"},{"name":"down-regulation of cytolysis","type":"exact"},{"name":"downregulation of cytolysis","type":"exact"},{"name":"inhibition of cytolysis","type":"narrow"}],"termid":"GO:0045918"}


id: FYECO:0000368
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which tamoxifen was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ tamoxifen","termid":"FYECO:0000368"}


id: MONDO:0009892
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chuvash erythrocytosis is a rare, genetic, congenital secondary polycythemia disorder characterized by increased hemoglobin, hematocrit and erythropoietin serum levels and normal oxygen affinity, which usually manifests with headache, dizziness, dyspnea and/or plethora. Patients present an increased risk of hemorrhage, thrombosis and early death.","definition_xrefs":["Orphanet:238557"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial polycythemia","termid":"MONDO:0001115"},{"relation_name":"is_a","term_name":"congenital secondary polycythemia","termid":"MONDO:0016540"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"Chuvash polycythemia","secondary_identifiers":["OMIM:263400","MEDGEN:332974","GARD:17176","UMLS:C1837915","DOID:0060474","MESH:C563918"],"synonyms":[{"name":"Chuvash erythrocytosis","type":"related"},{"name":"Chuvash erythromatosis","type":"exact"},{"name":"Chuvash polycythemia","type":"exact"},{"name":"Chuvash type polycythemia","type":"exact"},{"name":"ECYT2","type":"related"},{"name":"VHL familial polycythemia","type":"exact"},{"name":"Von Hippel-Lindau-dependent polycythemia","type":"exact"},{"name":"autosomal recessive benign erythrocytosis","type":"exact"},{"name":"erythrocytosis, autosomal recessive benign","type":"related"},{"name":"erythrocytosis, familial, 2","type":"related"},{"name":"erythrocytosis, familial, type 2","type":"exact"},{"name":"familial erythrocytosis 2","type":"exact"},{"name":"familial polycythemia caused by mutation in VHL","type":"exact"},{"name":"polycythemia, Chuvash type","type":"related"},{"name":"polycythemia, VHL-dependent","type":"related"}],"termid":"MONDO:0009892","xrefs":{"Monarch":{"xref_id":"0009892"}}}


id: GO:0007096
data:
  {"annotated_genes":["SJAG_03126","SJAG_01050","SJAG_01801","SJAG_04464","SJAG_00082","SJAG_02736","SJAG_04597","SJAG_03048","SJAG_04943"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[72053,72912,78318,112869],"is_not":false,"summary":null,"term":"GO:0007096"},{"annotations":[80673],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031578"},{"annotations":[104188],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001100"},{"annotations":[91813,95564,104195,113817],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031536"}]},"cv_name":"biological_process","definition":"Any process involved in the progression from anaphase/telophase to G1 that is associated with a conversion from high to low mitotic CDK activity.","definition_xrefs":["GOC:rn"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mitotic cell cycle phase transition","termid":"GO:1901990"},{"relation_name":"regulates","term_name":"exit from mitosis","termid":"GO:0010458"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00082":null,"SJAG_01050":null,"SJAG_01801":null,"SJAG_02736":null,"SJAG_03048":null,"SJAG_03126":null,"SJAG_04464":null,"SJAG_04597":null,"SJAG_04943":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044772"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0044772","GO:0007049"],"is_obsolete":false,"name":"regulation of exit from mitosis","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-176409"],"termid":"GO:0007096","terms_by_termid":{"GO:0001100":null,"GO:0007096":null,"GO:0031536":null,"GO:0031578":null}}


id: PBO:0079980
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"USP9Y pseudogene 18","termid":"PBO:0079980"}


id: MONDO:0011251
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":"facial dysmorphism, cleft palate, hearing loss, and camptodactyly","secondary_identifiers":["OMIM:602556","MEDGEN:400705","MESH:C566524","UMLS:C1865203"],"synonyms":[{"name":"facial dysmorphism, cleft palate, hearing loss, and camptodactyly","type":"exact"}],"termid":"MONDO:0011251","xrefs":{"Monarch":{"xref_id":"0011251"}}}


id: PBO:0030108
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_cellular_threonine_level","termid":"PBO:0030108"}


id: PBO:0041310
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C2orf49 divergent transcript","termid":"PBO:0041310"}


id: PR:O94385
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pom152 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94385"],"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":"nucleoporin pom152 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC29A10.07","synonyms":[{"name":"Spom972h-pom152","type":"exact"}],"termid":"PR:O94385"}


id: PBO:0057068
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 149","termid":"PBO:0057068"}


id: PATO:0001287
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A color consisting of red and brown hue.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brown","termid":"PATO:0000952"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"red brown","termid":"PATO:0001287"}


id: MONDO:1040026
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm that has spread to the brain from another anatomic site.","definition_xrefs":["PMID:29262201"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brain cancer","termid":"MONDO:0001657"},{"relation_name":"is_a","term_name":"metastatic malignant neoplasm","termid":"MONDO:0024880"}],"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":"metastatic malignant neoplasm in the brain","secondary_identifiers":["MEDGEN:113095","UMLS:C0220650"],"termid":"MONDO:1040026","xrefs":{"Monarch":{"xref_id":"1040026"}}}


id: SO:0000178
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The DNA region of a group of adjacent genes whose transcription is coordinated on one or several mutually overlapping transcription units transcribed in the same direction and sharing at least one gene.","definition_xrefs":["SO:ma"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gene_group","termid":"SO:0005855"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"operon","secondary_identifiers":["http://en.wikipedia.org/wiki/Operon"],"synonyms":[{"name":"INSDC_feature:operon","type":"exact"}],"termid":"SO:0000178"}


id: PBO:0076245
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sushi domain containing 6","termid":"PBO:0076245"}


id: MONDO:0011915
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial mitral valve prolapse","termid":"MONDO:0008004"}],"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":"mitral valve prolapse, myxomatous 2","secondary_identifiers":["GARD:15421","MEDGEN:335856","MESH:C564326","OMIM:607829","UMLS:C1843003"],"synonyms":[{"name":"MMVP2","type":"exact"},{"name":"MVP2","type":"related"},{"name":"mitral valve prolapse 2","type":"related"},{"name":"mitral valve prolapse, myxomatous 2","type":"exact"},{"name":"myxomatous mitral valve prolapse 2","type":"related"}],"termid":"MONDO:0011915","xrefs":{"Monarch":{"xref_id":"0011915"}}}


