# terms

id: PBO:0071018
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 20","termid":"PBO:0071018"}


id: GO:0051036
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the volume of an endosome, a membrane-bounded organelle that carries materials newly ingested by endocytosis.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of vesicle size","termid":"GO:0097494"}],"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 endosome size","synonyms":[{"name":"endosome enlargement","type":"related"}],"termid":"GO:0051036"}


id: MONDO:0001604
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"eyelid disorder","termid":"MONDO:0003382"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"lagophthalmos","secondary_identifiers":["ICD9:374.2","SCTID:60735000","icd11.foundation:1200365909","ICD9:374.20","UMLS:C0152226","ICD10CM:H02.2","MEDGEN:57517","DOID:12959"],"termid":"MONDO:0001604","xrefs":{"Monarch":{"xref_id":"0001604"}}}


id: PBO:0063155
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paired box 1","termid":"PBO:0063155"}


id: PBO:0047824
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"forkhead box O4","termid":"PBO:0047824"}


id: PBO:0027454
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_triphosphatase_activity","termid":"PBO:0027454"}


id: PBO:0056602
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MDM4 regulator of p53","termid":"PBO:0056602"}


id: PBO:0061198
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NIN1 (RPN12) binding protein 1 homolog","termid":"PBO:0061198"}


id: GO:0034085
data:
  {"annotated_genes":["SJAG_00796","SJAG_01644"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[71832],"is_not":false,"summary":null,"term":"GO:0034085"},{"annotations":[74827],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034087"}]},"cv_name":"biological_process","definition":"The process in which the sister chromatids of a replicated chromosome become associated with each other during S phase.","definition_xrefs":["GOC:jh","GOC:mah","PMID:14623866"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell cycle process","termid":"GO:0022402"},{"relation_name":"part_of","term_name":"sister chromatid cohesion","termid":"GO:0007062"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00796":null,"SJAG_01644":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"establishment of sister chromatid cohesion","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0034085","terms_by_termid":{"GO:0034085":null,"GO:0034087":null}}


id: GO:0070038
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + rRNA = S-adenosyl-L-homocysteine + rRNA containing N3-methylpseudouridine.","definition_xrefs":["GOC:imk","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rRNA (pseudouridine) methyltransferase activity","termid":"GO:0070037"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0140098","GO:0016741","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"rRNA (pseudouridine-N3-)-methyltransferase activity","termid":"GO:0070038"}


id: GO:0106212
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cell cycle process in which centromeres dissociate from the spindle pole body, contributing to the rearrangement of chromosomes into the orientation characteristic of meiotic prophase I.","definition_xrefs":["PMID:27611693","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome organization involved in meiotic cell cycle","termid":"GO:0070192"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"centromere detachment from spindle pole body involved in meiotic chromosome organization","synonyms":[{"name":"centromere detachment from SPB involved in meiotic chromosome organization","type":"exact"},{"name":"centromere detachment from spindle pole body involved in chromosome organization involved in meiotic cell cycle","type":"exact"}],"termid":"GO:0106212"}


id: PBO:0055412
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 2842","termid":"PBO:0055412"}


id: MONDO:1012491
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"lethal arthrogryposis syndrome, non-human animal","termid":"MONDO:1011968"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lethal arthrogryposis syndrome, cattle","secondary_identifiers":["OMIA:001953-9913"],"termid":"MONDO:1012491","xrefs":{"Monarch":{"xref_id":"1012491"}}}


id: GO:0015889
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of cobalamin (vitamin B12), a water-soluble vitamin characterized by possession of a corrin nucleus containing a cobalt atom, into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vitamin transport","termid":"GO:0051180"},{"relation_name":"is_a","term_name":"nitrogen compound transport","termid":"GO:0071705"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"cobalamin transport","secondary_identifiers":["Reactome:R-HSA-9758881","Reactome:R-HSA-9758890"],"synonyms":[{"name":"vitamin B12 transport","type":"exact"}],"termid":"GO:0015889"}


id: MONDO:0013338
data:
  {"annotated_genes":["SJAG_00488","SJAG_04409"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86810,86811],"is_not":false,"summary":null,"term":"MONDO:0013338"}]},"cv_name":"mondo","definition":"Autosomal recessive intermediate Charcot-Marie-Tooth disease type B is an extremely rare subtype of autosomal recessive intermediate Charcot-Marie-Tooth (CMT) disease characterized by a CMT neuropathy associated with developmental delay, self-abusive behavior, dysmorphic features and vestibular Schwannoma. Motor nerve conduction velocities demonstrate features of both demyelinating and axonal pathology.","definition_xrefs":["Orphanet:254334"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive intermediate Charcot-Marie-Tooth disease","termid":"MONDO:0017058"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00488":null,"SJAG_04409":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005244"],"is_obsolete":false,"name":"Charcot-Marie-Tooth disease recessive intermediate B","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0110204","MEDGEN:462247","UMLS:C3150897","GARD:12454","OMIM:613641"],"synonyms":[{"name":"CMTRIB","type":"exact"},{"name":"Charcot-Marie-Tooth disease caused by mutation in KARS","type":"exact"},{"name":"Charcot-Marie-Tooth disease recessive intermediate type B","type":"exact"},{"name":"Charcot-Marie-Tooth disease, recessive Intermediate type B","type":"exact"},{"name":"Charcot-Marie-Tooth disease, recessive intermediate B","type":"related"},{"name":"Charcot-Marie-Tooth disease, recessive intermediate, B","type":"related"},{"name":"Charcot-Marie-Tooth neuropathy recessive intermediate B","type":"exact"},{"name":"Charcot-Marie-Tooth neuropathy, recessive Intermediate B","type":"related"},{"name":"KARS Charcot-Marie-Tooth disease","type":"exact"},{"name":"RI-CMT type B","type":"exact"},{"name":"RI-CMTB","type":"exact"},{"name":"autosomal recessive intermediate Charcot-Marie-Tooth disease type B","type":"exact"}],"termid":"MONDO:0013338","terms_by_termid":{"MONDO:0013338":null},"xrefs":{"Monarch":{"xref_id":"0013338"}}}


id: PBO:0029570
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_spore","termid":"PBO:0029570"}


id: PBO:0071346
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L29 pseudogene 4","termid":"PBO:0071346"}


id: PBO:0046384
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EOLA1 divergent transcript","termid":"PBO:0046384"}


id: MOD:00401
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that is produced by formation of an adduct of a cysteine residue with the Gygi isotope-coded affinity tag d0 reagent.","definition_xrefs":["PubMed:10504701","Unimod:8#C"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isotope tagged reagent derivatized residue","termid":"MOD:01426"},{"relation_name":"is_a","term_name":"isotope tagged sufhydryl reagent modified cysteine","termid":"MOD:01820"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"Gygi ICAT(TM) d0 modified cysteine","synonyms":[{"name":"Gygi ICAT(TM) d0","type":"related"},{"name":"ICAT-G","type":"related"}],"termid":"MOD:00401"}


id: PBO:0060686
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NDST1 antisense RNA 1","termid":"PBO:0060686"}


id: GO:1905231
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 borneol stimulus.","definition_xrefs":["GOC:TermGenie","GO_REF:0000071","PMID:26593909"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to lipid","termid":"GO:0071396"},{"relation_name":"is_a","term_name":"response to borneol","termid":"GO:1905230"}],"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 borneol","termid":"GO:1905231"}


id: PBO:0082797
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the yeast dynactin complex; consisting of Nip100p, Jnm1p, and Arp1p; required for proper nuclear migration and spindle partitioning during mitotic anaphase B","termid":"PBO:0082797"}


id: MONDO:0016041
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital microgastria is a rare malformation where the embryological development of the stomach is interrupted, leading to an abnormally small foregut in newborns and characterized by extreme feeding intolerance and malnutrition along with growth retardation and death if untreated. It is usually associated with multiple congenital anomalies.","definition_xrefs":["Orphanet:199293"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital microgastria","secondary_identifiers":["MEDGEN:82732","ICD9:750.7","GARD:20330","icd11.foundation:1695007532","SCTID:83714006","UMLS:C0266150"],"termid":"MONDO:0016041","xrefs":{"Monarch":{"xref_id":"0016041"}}}


id: PBO:0052560
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kynurenine 3-monooxygenase","termid":"PBO:0052560"}


id: SO:0001990
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A 5' UTR variant where a premature start codon is moved.","definition_xrefs":["SANGER:am"],"direct_ancestors":[{"relation_name":"is_a","term_name":"5_prime_UTR_premature_start_codon_variant","termid":"SO:0001983"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"five_prime_UTR_premature_start_codon_location_variant","termid":"SO:0001990"}


id: GO:0030817
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of the nucleotide cAMP (cyclic AMP, adenosine 3',5'-cyclophosphate).","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of cAMP biosynthetic process (obsolete GO:0030817)","synonyms":[{"name":"regulation of 3',5' cAMP biosynthesis","type":"exact"},{"name":"regulation of 3',5' cAMP biosynthetic process","type":"exact"},{"name":"regulation of 3',5'-cAMP biosynthesis","type":"exact"},{"name":"regulation of 3',5'-cAMP biosynthetic process","type":"exact"},{"name":"regulation of adenosine 3',5'-cyclophosphate biosynthesis","type":"exact"},{"name":"regulation of adenosine 3',5'-cyclophosphate biosynthetic process","type":"exact"},{"name":"regulation of cAMP anabolism","type":"exact"},{"name":"regulation of cAMP biosynthesis","type":"exact"},{"name":"regulation of cAMP formation","type":"exact"},{"name":"regulation of cAMP synthesis","type":"exact"},{"name":"regulation of cyclic AMP biosynthesis","type":"exact"},{"name":"regulation of cyclic AMP biosynthetic process","type":"exact"}],"termid":"GO:0030817"}


id: GO:0046667
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Programmed cell death that occurs in the retina to remove excess cells between ommatidia, thus resulting in a hexagonal lattice, precise with respect to cell number and position surrounding each ommatidium.","definition_xrefs":["PMID:12006672"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinal cell programmed cell death","termid":"GO:0046666"},{"relation_name":"part_of","term_name":"compound eye morphogenesis","termid":"GO:0001745"}],"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":"compound eye retinal cell programmed cell death","termid":"GO:0046667"}


id: PBO:0076086
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"steroid sulfatase (microsomal) pseudogene 1","termid":"PBO:0076086"}


id: GO:1902891
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of root hair elongation.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","GOC:als","PMID:22329353"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell growth","termid":"GO:0030308"},{"relation_name":"is_a","term_name":"negative regulation of developmental growth","termid":"GO:0048640"},{"relation_name":"is_a","term_name":"regulation of root hair elongation","termid":"GO:1902890"},{"relation_name":"is_a","term_name":"negative regulation of cell maturation","termid":"GO:1903430"},{"relation_name":"negatively_regulates","term_name":"root hair elongation","termid":"GO:0048767"}],"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 root hair elongation","synonyms":[{"name":"down regulation of root hair elongation","type":"exact"},{"name":"down-regulation of root hair elongation","type":"exact"},{"name":"downregulation of root hair elongation","type":"exact"},{"name":"inhibition of root hair elongation","type":"narrow"}],"termid":"GO:1902891"}


id: PBO:0048777
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"guanosine monophosphate reductase 2","termid":"PBO:0048777"}


id: PBO:0049591
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H3 clustered histone 9, pseudogene","termid":"PBO:0049591"}


id: PATO:0001677
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An efficiency quality inhering in a bearer by virtue of the bearer's lacking efficiency.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"efficiency","termid":"PATO:0001029"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inefficient","termid":"PATO:0001677"}


id: FYPO:0001357
data:
  {"alleles_by_uniquename":{"SJAG_00426:allele-1":{"allele_type":"amino_acid_mutation","description":"P363S","gene_uniquename":"SJAG_00426","name":"bbl1-P363S","uniquename":"SJAG_00426:allele-1"},"SJAG_00601:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00601","name":"rip1delta","uniquename":"SJAG_00601:allele-1"},"SJAG_01355:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01355","name":"cox6delta","uniquename":"SJAG_01355:allele-1"},"SJAG_01946:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01946","name":"cem1delta","uniquename":"SJAG_01946:allele-1"},"SJAG_03198:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03198","name":"oar2delta","uniquename":"SJAG_03198:allele-1"},"SJAG_03198:allele-2":{"allele_type":"amino_acid_mutation","description":"Y189D cold sensitive","gene_uniquename":"SJAG_03198","name":"oar2-51","uniquename":"SJAG_03198:allele-2"},"SJAG_03198:allele-3":{"allele_type":"amino_acid_mutation","description":"R72A,L75A,R106A,L109A","gene_uniquename":"SJAG_03198","name":"oar2-dm12","synonyms":[{"name":"destruction box mutations","reference":"PMID:23786411","type":"exact"}],"uniquename":"SJAG_03198:allele-3"},"SJAG_03575:allele-1":{"allele_type":"amino_acid_mutation","description":"E548K ts","gene_uniquename":"SJAG_03575","name":"apc2-361","uniquename":"SJAG_03575:allele-1"},"SJAG_03720:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03720","name":"tel1delta","uniquename":"SJAG_03720:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[119134,119135,119136,119138],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000674"}],"single_locus_phenotype":[{"annotations":[119143,119144,119145,119169],"is_not":false,"summary":null,"term":"FYPO:0001357"},{"annotations":[119316],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001690"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell population phenotype in which a population of cells grows normally (i.e. indistinguishably from wild type) in the vegetative growth phase of the life cycle. 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id: GO:1904936
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The orderly movement of an interneuron from one site to another.","definition_xrefs":["GOC:ah","GO_REF:0000091","GOC:TermGenie","PMID:18622031"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuron migration","termid":"GO:0001764"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"interneuron migration","synonyms":[{"name":"inter neuron migration","type":"exact"},{"name":"inter-neuron migration","type":"exact"}],"termid":"GO:1904936"}


id: PBO:0083092
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-binding transcription factor required for activating GAL genes; responds to galactose; repressed by Gal80p and activated by Gal3p","termid":"PBO:0083092"}


id: GO:0009119
data:
  {"annotated_genes":["SJAG_00694","SJAG_02959","SJAG_03096","SJAG_03881","SJAG_03771","SJAG_00044","SJAG_02580","SJAG_01673","SJAG_02582","SJAG_06634","SJAG_01859","SJAG_01070","SJAG_00134"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[88641],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046086"},{"annotations":[87346,87347],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006154"},{"annotations":[90309],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046085"},{"annotations":[116579],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006169"},{"annotations":[69702,69542],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009972"},{"annotations":[69687],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006190"},{"annotations":[73297,66396,93520,61722],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006166"},{"annotations":[73170],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046132"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving any ribonucleoside, a nucleoside in which purine or pyrimidine base is linked to a ribose (beta-D-ribofuranose) molecule.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside metabolic process","termid":"GO:0009116"}],"gene_count":13,"genes_by_uniquename":{"SJAG_00044":null,"SJAG_00134":null,"SJAG_00694":null,"SJAG_01070":null,"SJAG_01673":null,"SJAG_01859":null,"SJAG_02580":null,"SJAG_02582":null,"SJAG_02959":null,"SJAG_03096":null,"SJAG_03771":null,"SJAG_03881":null,"SJAG_06634":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0044281","GO:0055086","GO:0008150"],"is_obsolete":false,"name":"ribonucleoside metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000043":null,"GO_REF:0000107":null},"synonyms":[{"name":"ribonucleoside metabolism","type":"exact"}],"termid":"GO:0009119","terms_by_termid":{"GO:0006154":null,"GO:0006166":null,"GO:0006169":null,"GO:0006190":null,"GO:0009972":null,"GO:0046085":null,"GO:0046086":null,"GO:0046132":null}}


id: PBO:0029707
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_after_spore_germination,_without_cell_division","termid":"PBO:0029707"}


id: GO:0030882
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a lipid antigen.","definition_xrefs":["PMID:14500461"],"direct_ancestors":[{"relation_name":"is_a","term_name":"antigen binding","termid":"GO:0003823"},{"relation_name":"is_a","term_name":"lipid binding","termid":"GO:0008289"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0008289"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0008289","GO:0005488"],"is_obsolete":false,"name":"lipid antigen binding","termid":"GO:0030882"}


id: GO:0001956
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the regulated release of a neurotransmitter.","definition_xrefs":["GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of neurotransmitter secretion","termid":"GO:0046928"},{"relation_name":"is_a","term_name":"positive regulation of synaptic transmission","termid":"GO:0050806"},{"relation_name":"is_a","term_name":"positive regulation of neurotransmitter transport","termid":"GO:0051590"},{"relation_name":"is_a","term_name":"positive regulation of secretion by cell","termid":"GO:1903532"},{"relation_name":"positively_regulates","term_name":"neurotransmitter secretion","termid":"GO:0007269"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0006810","GO:0023052","GO:0008150"],"is_obsolete":false,"name":"positive regulation of neurotransmitter secretion","synonyms":[{"name":"activation of neurotransmitter secretion","type":"narrow"},{"name":"stimulation of neurotransmitter secretion","type":"narrow"},{"name":"up regulation of neurotransmitter secretion","type":"exact"},{"name":"up-regulation of neurotransmitter secretion","type":"exact"},{"name":"upregulation of neurotransmitter secretion","type":"exact"}],"termid":"GO:0001956"}


id: PBO:0007992
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase type 2A, intrinsic regulator Rrd1 (predicted)","termid":"PBO:0007992"}


id: GO:0090523
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: NADPH + H+ + 2 ferricytochrome b(5) = NADP+ + 2 ferrocytochrome b(5).","definition_xrefs":["RHEA:64576","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytochrome-b5 reductase activity, acting on NAD(P)H","termid":"GO:0004128"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"cytochrome-b5 reductase activity, acting on NADPH","synonyms":[{"name":"cytochrome-b5 reductase activity","type":"broad"}],"termid":"GO:0090523"}


id: GO:1905812
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of motor neuron axon guidance.","definition_xrefs":["PMID:18434533","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of axon guidance","termid":"GO:1902667"},{"relation_name":"regulates","term_name":"motor neuron axon guidance","termid":"GO:0008045"}],"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 motor neuron axon guidance","synonyms":[{"name":"regulation of motoneuron axon guidance","type":"exact"},{"name":"regulation of motor axon guidance","type":"exact"},{"name":"regulation of motor axon pathfinding","type":"exact"}],"termid":"GO:1905812"}


id: FYPO:0004319
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of a cyclin-dependent protein kinase activity is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein kinase activity","termid":"FYPO:0002700"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000661"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000707","FYPO:0000652","FYPO:0000654","FYPO:0000661"],"is_obsolete":false,"name":"increased cyclin-dependent protein kinase activity","termid":"FYPO:0004319"}


id: PBO:0004627
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MCM complex subunit Mcm7","termid":"PBO:0004627"}


id: PR:Q9HDT8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCP20C8.01c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9HDT8"],"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":"UPF0612 protein P20C8.01c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCP20C8.01c","synonyms":[{"name":"Spom972h-SPCP20C8.01c","type":"exact"}],"termid":"PR:Q9HDT8"}


id: PBO:0051309
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin kappa variable 1/OR2-1 (pseudogene)","termid":"PBO:0051309"}


id: MONDO:0013914
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hypogonadotropic hypogonadism that has material basis in homozygous mutation in the GNRH1 gene on chromosome 8p21.","definition_xrefs":["DOID:0090072","PMID:19535795"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypogonadotropic hypogonadism","termid":"MONDO:0018555"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypogonadotropic hypogonadism 12 with or without anosmia","secondary_identifiers":["OMIM:227200","OMIM:614841","UMLS:C1856897","ICD10CM:E23.0","MEDGEN:347328","GARD:276","MESH:C535764"],"synonyms":[{"name":"FIGD","type":"related"},{"name":"HH12","type":"related"},{"name":"eunuchoidism familial hypogonadotropic","type":"related"},{"name":"eunuchoidism, familial hypogonadotropic","type":"exact"},{"name":"familial hypogonadotrophic eunuchoidism","type":"exact"},{"name":"familial hypogonadotropic eunuchoidism","type":"related"},{"name":"familial idiopathic gonadotrpin deficiency","type":"exact"},{"name":"gonadotropin deficiency familial idiopathic","type":"related"},{"name":"gonadotropin deficiency, familial idiopathic","type":"related"},{"name":"hypogonadotropic hypogonadism 12 with or without anosmia","type":"exact"}],"termid":"MONDO:0013914","xrefs":{"Monarch":{"xref_id":"0013914"}}}


id: PBO:0084124
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Heterotrimeric nascent polypeptide-associated complex beta3 subunit; complex binds ribosomes via its beta-subunits in close proximity to nascent polypeptides; interacts with Caf130p of the CCR4-NOT complex; similar to human BTF3; BTT1 has a paralog, EGD1, that arose from the whole genome duplication","termid":"PBO:0084124"}


id: GO:0050551
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: geranyl diphosphate = diphosphate + myrcene.","definition_xrefs":["RHEA:16965","EC:4.2.3.15"],"direct_ancestors":[{"relation_name":"is_a","term_name":"terpene synthase activity","termid":"GO:0010333"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016829"],"is_obsolete":false,"name":"myrcene synthase activity","secondary_identifiers":["MetaCyc:RXN-5110","KEGG_REACTION:R02009"],"synonyms":[{"name":"geranyl-diphosphate diphosphate-lyase (myrcene-forming) activity","type":"exact"}],"termid":"GO:0050551"}


id: PR:Q9UUA4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sec66 gene.","definition_xrefs":["UniProtKB:Q9UUA4","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":"translocation protein sec66 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC409.21","synonyms":[{"name":"Spom972h-sec66","type":"exact"}],"termid":"PR:Q9UUA4"}


id: MONDO:0013549
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":"N-acetylaspartate deficiency","secondary_identifiers":["MEDGEN:481346","OMIM:614063","UMLS:C3279716"],"synonyms":[{"name":"N-acetylaspartate deficiency","type":"exact"},{"name":"NACED","type":"related"},{"name":"hypoacetylaspartia","type":"related"},{"name":"naa deficiency","type":"related"}],"termid":"MONDO:0013549","xrefs":{"Monarch":{"xref_id":"0013549"}}}


id: PBO:0030432
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_tRNA_methyltransferase_activity","termid":"PBO:0030432"}


id: GO:0090527
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A process that is carried out at the cellular level which results in dynamic structural changes to the arrangement of actin filaments.","definition_xrefs":["GOC:dph","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete actin filament reorganization (obsolete GO:0090527)","termid":"GO:0090527"}


id: FYPO:0001374
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the medial cortex of a spore is abolished.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to medial cortex","termid":"FYPO:0001371"},{"relation_name":"is_a","term_name":"abnormal protein localization to medial cortex in spores","termid":"FYPO:0001372"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0000138"],"is_obsolete":false,"name":"abolished protein localization to medial cortex in spores","synonyms":[{"name":"protein localisation to medial cortex abolished in spores","type":"exact"},{"name":"protein localization to medial cortex abolished in spores","type":"exact"},{"name":"protein localization to medial ring abolished in spores","type":"exact"}],"termid":"FYPO:0001374"}


id: GO:0070506
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with a high-density lipoprotein particle and delivering the high-density lipoprotein into the cell via endocytosis.","definition_xrefs":["PMID:9211901","GOC:rl","GOC:bf","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipoprotein particle receptor activity","termid":"GO:0030228"}],"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":"high-density lipoprotein particle receptor activity","synonyms":[{"name":"HDL receptor","type":"exact"},{"name":"high-density lipoprotein receptor activity","type":"exact"}],"termid":"GO:0070506"}


id: GO:0007260
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of introducing a phosphate group to a tyrosine residue of a STAT (Signal Transducer and Activator of Transcription) protein.","definition_xrefs":["GOC:jl","PMID:10918594"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidyl-tyrosine phosphorylation","termid":"GO:0018108"},{"relation_name":"part_of","term_name":"cell surface receptor signaling pathway via JAK-STAT","termid":"GO:0007259"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"tyrosine phosphorylation of STAT protein","secondary_identifiers":["GO:0042503","GO:0042502","GO:0042505","GO:0042506","GO:0042508","GO:0042504","GO:0042507"],"synonyms":[{"name":"tyrosine phosphorylation of Stat1 protein","type":"narrow"},{"name":"tyrosine phosphorylation of Stat2 protein","type":"narrow"},{"name":"tyrosine phosphorylation of Stat3 protein","type":"narrow"},{"name":"tyrosine phosphorylation of Stat4 protein","type":"narrow"},{"name":"tyrosine phosphorylation of Stat5 protein","type":"narrow"},{"name":"tyrosine phosphorylation of Stat6 protein","type":"narrow"},{"name":"tyrosine phosphorylation of Stat7 protein","type":"narrow"}],"termid":"GO:0007260"}


id: MONDO:0016712
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Classic medulloblastoma is a histological variant of medulloblastoma, an embryonic malignancy, having a midline location, occurring most often in children and manifesting with variable symptoms such as headaches, nausea, vomiting and ataxia.","definition_xrefs":["Orphanet:251867"],"direct_ancestors":[{"relation_name":"is_a","term_name":"medulloblastoma","termid":"MONDO:0007959"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"classic medulloblastoma","secondary_identifiers":["SCTID:699704002","icd11.foundation:1548011794","UMLS:C1707400","NCIT:C54039","GARD:17216","MEDGEN:353541"],"synonyms":[{"name":"classic medulloblastoma","type":"exact"}],"termid":"MONDO:0016712","xrefs":{"Monarch":{"xref_id":"0016712"}}}


id: GO:0140109
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A histone reader that recognizes a histone H3 monomethylated at lysine 4.","definition_xrefs":["PMID:29255264","PMID:18840606"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H3 reader activity","termid":"GO:0140006"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140566"},{"rel_name":"is_a","termid":"GO:0030674"},{"rel_name":"is_a","termid":"GO:0060090"}],"interesting_parent_ids":["GO:0003674","GO:0140566","GO:0060090","GO:0030674"],"is_obsolete":false,"name":"histone H3K4me1 reader activity","synonyms":[{"name":"H3-K4me1 modified histone binding","type":"narrow"},{"name":"H3K4me1 modified histone binding","type":"narrow"}],"termid":"GO:0140109"}


id: MONDO:0005109
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An infection caused by the human immunodeficiency virus.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral sexually transmitted disease","termid":"MONDO:0021682"},{"relation_name":"is_a","term_name":"lentivirus infection","termid":"MONDO:0022034"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HIV infectious disease","secondary_identifiers":["ICD9:042","ICD9:042-042.99","EFO:0000764","MESH:D015658","DOID:526","ICD10CM:B20-B20","NANDO:2200810","NCIT:C3108","SCTID:86406008","MEDGEN:5583","UMLS:C0019693"],"synonyms":[{"name":"HIV infection","type":"exact"},{"name":"Human immunodeficiency virus caused disease or disorder","type":"exact"},{"name":"Human immunodeficiency virus disease or disorder","type":"exact"},{"name":"Human immunodeficiency virus infectious disease","type":"exact"},{"name":"human immunodeficiency virus infectious disease","type":"related"}],"termid":"MONDO:0005109","xrefs":{"Monarch":{"xref_id":"0005109"}}}


id: GO:0141066
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which an organism effects a change that impairs the structure or function of the host extracellular matrix.","definition_xrefs":["PMID:2404867","PMID:11982763","PMID:21115719","PMID:25865874"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated disruption of host cellular anatomical structure","termid":"GO:0052008"},{"relation_name":"is_a","term_name":"disruption of extracellular matrix of another organism","termid":"GO:0141041"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated disruption of host extracellular matrix","synonyms":[{"name":"disruption of host extracellular matrix","type":"broad"}],"termid":"GO:0141066"}


id: GO:0098528
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a skeletal muscle fiber cell. Skeletal muscle fiber differentiation starts with myoblast fusion and the appearance of specific cell markers (this is the cell development step). Then individual skeletal muscle fibers fuse to form bigger myotubes and start to contract.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myotube differentiation","termid":"GO:0014902"},{"relation_name":"is_a","term_name":"skeletal muscle cell differentiation","termid":"GO:0035914"}],"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 muscle fiber differentiation","termid":"GO:0098528"}


id: PBO:0036517
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear cap-binding complex variant subunit Cbc3","termid":"PBO:0036517"}


id: PBO:0054141
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 1507","termid":"PBO:0054141"}


id: GO:0097383
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: dIDP + H2O = dIMP + H+ + phosphate.","definition_xrefs":["GOC:pde","PMID:20385596","RHEA:35211"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside diphosphate phosphatase activity","termid":"GO:0017110"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"dIDP phosphatase activity","secondary_identifiers":["Reactome:R-HSA-2509793"],"synonyms":[{"name":"deoxyinosine-diphosphatase activity","type":"related"}],"termid":"GO:0097383"}


id: FYPO:0003964
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of a glutathione disulfide oxidoreductase activity is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased oxidoreductase activity","termid":"FYPO:0000690"},{"relation_name":"is_a","term_name":"abnormal glutathione disulfide oxidoreductase activity","termid":"FYPO:0003963"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0000707","FYPO:0000654","FYPO:0000652","FYPO:0001985"],"is_obsolete":false,"name":"decreased glutathione disulfide oxidoreductase activity","synonyms":[{"name":"reduced glutathione disulfide oxidoreductase activity","type":"exact"}],"termid":"FYPO:0003964"}


id: MONDO:1010572
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Diabetes mellitus that occurs in long-tailed chinchilla.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diabetes mellitus, non-human animal","termid":"MONDO:1010052"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diabetes mellitus, long-tailed chinchilla","secondary_identifiers":["OMIA:000279-34839"],"termid":"MONDO:1010572","xrefs":{"Monarch":{"xref_id":"1010572"}}}


id: PBO:0069249
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 504, pseudogene","termid":"PBO:0069249"}


id: MONDO:0013301
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Aromatase deficiency disrupts the synthesis of estradiol, resulting in hirsutism of mothers during gestation of an affected child; pseudohermaphroditism and virilization in women; and tall stature, osteoporosis and obesity in men.","definition_xrefs":["Orphanet:91"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete hereditary 46,XX disorder of sex development (obsolete MONDO:0957024)","termid":"MONDO:0957024"},{"relation_name":"is_a","term_name":"inherited primary ovarian failure","termid":"MONDO:0019852"},{"relation_name":"is_a","term_name":"pregnancy disorder","termid":"MONDO:0024575"}],"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":"aromatase deficiency","secondary_identifiers":["OMIM:613546","UMLS:C1960539","GARD:365","icd11.foundation:260189446","MEDGEN:743307","MESH:C537436","NCIT:C120144"],"synonyms":[{"name":"aromatase deficiency","type":"exact"},{"name":"congenital estrogen deficiency","type":"exact"},{"name":"congenital oestrogen deficiency","type":"exact"},{"name":"pseudohermaphroditism, female, due to placental aromatase deficiency","type":"related"}],"termid":"MONDO:0013301","xrefs":{"Monarch":{"xref_id":"0013301"}}}


id: GO:0072439
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of events in which information about whether DNA replication is complete is received and converted into a molecular signal, contributing to a meiotic DNA replication checkpoint.","definition_xrefs":["GOC:mtg_cell_cycle"],"gene_count":0,"genotype_count":0,"name":"obsolete detection of stimulus involved in meiotic DNA replication checkpoint (obsolete GO:0072439)","synonyms":[{"name":"meiotic DNA replication checkpoint sensor mechanism","type":"related"},{"name":"meiotic DNA replication checkpoint sensor process","type":"related"},{"name":"sensing involved in meiotic DNA replication checkpoint","type":"related"}],"termid":"GO:0072439"}


id: PR:Q9USJ5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- hem12 gene.","definition_xrefs":["UniProtKB:Q9USJ5","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":"uroporphyrinogen decarboxylase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC4B3.05c","synonyms":[{"name":"Spom972h-hem12","type":"exact"},{"name":"UPD (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"URO-D (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9USJ5"}


id: FYPO:0000775
data:
  {"alleles_by_uniquename":{"SJAG_00610:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00610","name":"pck2delta","uniquename":"SJAG_00610:allele-1"},"SJAG_01787:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01787","name":"pck1delta","uniquename":"SJAG_01787: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-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"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[118916],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0002033"},{"annotations":[118908,118912],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001838"},{"annotations":[118902],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001038"}]},"cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the phosphorylation of one or more specific proteins, or of specific protein sites, is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein modification during vegetative growth","termid":"FYPO:0000329"},{"relation_name":"is_a","term_name":"abnormal protein phosphorylation","termid":"FYPO:0002677"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00610":null,"SJAG_01787":null,"SJAG_04551":null},"genotype_count":4,"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"}]}]},"pck1delta":{"display_name":"pck1delta","display_uniquename":"pck1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01787:allele-1","expression":"Null"}]}]},"pck2delta":{"display_name":"pck2delta","display_uniquename":"pck2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00610:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002494"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0002494","FYPO:0001985","FYPO:0002274","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"abnormal protein phosphorylation during vegetative growth","references_by_uniquename":{"PMID:34198697":null},"single_locus_annotated_genes":["SJAG_04551","SJAG_00610","SJAG_01787"],"single_locus_genotype_uniquenames":["Pmk1Sp(delta82-105)-Pmk1_from_S._pombe_with_deleted_residues_82-105-partial_amino_acid_deletion-expression-not_assayed_or_wild_type","pck1delta","Pmk1Sj(ins82-105)-82-NITCIYDLDIIINPYNFNEVYIYEE-105-amino_acid_insertion-expression-not_assayed_or_wild_type","pck2delta"],"synonyms":[{"name":"abnormal protein phosphorylation during mitotic cell cycle","type":"related"}],"termid":"FYPO:0000775","terms_by_termid":{"FYPO:0001038":null,"FYPO:0001838":null,"FYPO:0002033":null}}


id: MONDO:1011852
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder, non-human animal","termid":"MONDO:1011336"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neurogenic muscular atrophy, non-human animal","secondary_identifiers":["OMIA:000719"],"termid":"MONDO:1011852","xrefs":{"Monarch":{"xref_id":"1011852"}}}


id: PBO:0066215
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA binding motif protein 22 pseudogene 11","termid":"PBO:0066215"}


id: FYPO:0007443
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 endoplasmic reticulum is abolished, and the protein is present in the cytosol instead.","definition_xrefs":["PMID:32320462","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to endoplasmic reticulum during vegetative growth","termid":"FYPO:0003777"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0005447","FYPO:0000138","FYPO:0000002"],"is_obsolete":false,"name":"abolished protein localization to endoplasmic reticulum membrane, with protein mislocalized to cytosol","synonyms":[{"name":"abolished protein localization to ER membrane, with protein mislocalized to cytosol","type":"exact"},{"name":"abolished protein localization to endoplasmic reticulum membrane, with protein mislocalized to cytosol during mitotic cell cycle","type":"related"},{"name":"abolished protein localization to endoplasmic reticulum membrane, with protein mislocalized to cytosol during vegetative growth","type":"exact"}],"termid":"FYPO:0007443"}


id: GO:0034559
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: bisphenol A + NADH + H+ + O2 = 1,2-bis(4-hydroxyphenyl)-2-propanol + NAD+ + H2O.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete bisphenol A hydroxylase B activity (obsolete GO:0034559)","termid":"GO:0034559"}


id: PBO:0054137
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 1503","termid":"PBO:0054137"}


id: MONDO:0006443
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete tenosynovial giant cell tumor (obsolete MONDO:0006443)","termid":"MONDO:0006443","xrefs":{"Monarch":{"xref_id":"0006443"}}}


id: GO:0002653
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of tolerance induction dependent upon immune response.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of tolerance induction","termid":"GO:0002644"},{"relation_name":"is_a","term_name":"regulation of tolerance induction dependent upon immune response","termid":"GO:0002652"},{"relation_name":"is_a","term_name":"negative regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains","termid":"GO:0002823"},{"relation_name":"negatively_regulates","term_name":"tolerance induction dependent upon immune response","termid":"GO:0002461"}],"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 tolerance induction dependent upon immune response","synonyms":[{"name":"down regulation of tolerance induction dependent upon immune response","type":"exact"},{"name":"down-regulation of tolerance induction dependent upon immune response","type":"exact"},{"name":"downregulation of tolerance induction dependent upon immune response","type":"exact"},{"name":"inhibition of tolerance induction dependent upon immune response","type":"narrow"},{"name":"negative regulation of immune response-dependent tolerance induction","type":"exact"}],"termid":"GO:0002653"}


id: PBO:0046223
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"elongin C pseudogene 16","termid":"PBO:0046223"}


id: MONDO:0009617
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal recessive primary microcephaly in which the cause of the disease is a mutation in the MCPH1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive primary microcephaly","termid":"MONDO:0016660"},{"relation_name":"is_a","term_name":"microcephaly with intellectual disability","termid":"MONDO:0100200"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0700092"],"is_obsolete":false,"name":"microcephaly 1, primary, autosomal recessive","secondary_identifiers":["Orphanet:52183","UMLS:C1855081","DOID:0070285","GARD:15198","MEDGEN:344415","MESH:C565384","OMIM:251200"],"synonyms":[{"name":"MCPH1","type":"related"},{"name":"MCPH1 autosomal recessive primary microcephaly","type":"exact"},{"name":"PCC syndrome","type":"related"},{"name":"autosomal recessive primary microcephaly caused by mutation in MCPH1","type":"exact"},{"name":"microcephaly 1, primary, autosomal recessive","type":"exact"},{"name":"premature chromosome condensation syndrome","type":"related"},{"name":"premature chromosome condensation with microcephaly and intellectual disability","type":"related"},{"name":"premature chromosome condensation with microcephaly and mental retardation","type":"related"}],"termid":"MONDO:0009617","xrefs":{"Monarch":{"xref_id":"0009617"}}}


id: PBO:0049237
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GRM7 antisense RNA 1","termid":"PBO:0049237"}


id: PBO:0086566
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; conserved among S. cerevisiae strains; YOL085C is not an essential gene; partially overlaps dubious ORF YOL085W-A","termid":"PBO:0086566"}


id: GO:0060262
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate frequency or extent of the covalent attachment of a palmitoyl group to the N-terminal amino acid residue of a protein.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of N-terminal protein palmitoylation","termid":"GO:0060254"},{"relation_name":"is_a","term_name":"negative regulation of protein lipidation","termid":"GO:1903060"},{"relation_name":"negatively_regulates","term_name":"N-terminal protein palmitoylation","termid":"GO:0006500"}],"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 N-terminal protein palmitoylation","termid":"GO:0060262"}


id: MONDO:0002730
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A kidney neoplasm that occurs during childhood.","definition_xrefs":["MONDO:design_pattern"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"kidney cancer","termid":"MONDO:0002367"},{"relation_name":"is_a","term_name":"childhood neoplasm","termid":"MONDO:0021079"},{"relation_name":"is_a","term_name":"kidney neoplasm","termid":"MONDO:0021163"}],"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":"childhood kidney neoplasm","secondary_identifiers":["DOID:3675","MEDGEN:232356","NCIT:C6563","UMLS:C1333003"],"synonyms":[{"name":"childhood kidney neoplasm","type":"exact"},{"name":"childhood kidney tumor","type":"exact"},{"name":"childhood kidney tumour","type":"exact"},{"name":"childhood renal neoplasm","type":"exact"},{"name":"childhood renal tumor","type":"exact"},{"name":"childhood renal tumour","type":"exact"},{"name":"kidney neoplasm","type":"broad"},{"name":"kidney neoplasm of childhood","type":"exact"},{"name":"paediatric kidney neoplasm","type":"exact"},{"name":"paediatric kidney tumour","type":"exact"},{"name":"paediatric renal neoplasm","type":"exact"},{"name":"paediatric renal tumour","type":"exact"},{"name":"pediatric kidney neoplasm","type":"exact"},{"name":"pediatric kidney tumor","type":"exact"},{"name":"pediatric renal neoplasm","type":"exact"},{"name":"pediatric renal tumor","type":"exact"}],"termid":"MONDO:0002730","xrefs":{"Monarch":{"xref_id":"0002730"}}}


id: GO:1903628
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of dUTP diphosphatase activity.","definition_xrefs":["GO_REF:0000059","GOC:TermGenie","PMID:1315924"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of dUTP diphosphatase activity (obsolete GO:1903628)","synonyms":[{"name":"down regulation of dUTP diphosphatase activity","type":"exact"},{"name":"down regulation of dUTP nucleotidohydrolase activity","type":"exact"},{"name":"down regulation of dUTP pyrophosphatase activity","type":"exact"},{"name":"down regulation of dUTPase activity","type":"exact"},{"name":"down regulation of deoxyuridine-triphosphatase activity","type":"exact"},{"name":"down regulation of desoxyuridine 5'-triphosphatase activity","type":"exact"},{"name":"down regulation of desoxyuridine 5'-triphosphate nucleotidohydrolase activity","type":"exact"},{"name":"down-regulation of dUTP diphosphatase activity","type":"exact"},{"name":"down-regulation of dUTP nucleotidohydrolase activity","type":"exact"},{"name":"down-regulation of dUTP pyrophosphatase activity","type":"exact"},{"name":"down-regulation of dUTPase activity","type":"exact"},{"name":"down-regulation of deoxyuridine-triphosphatase activity","type":"exact"},{"name":"down-regulation of desoxyuridine 5'-triphosphatase activity","type":"exact"},{"name":"down-regulation of desoxyuridine 5'-triphosphate nucleotidohydrolase activity","type":"exact"},{"name":"downregulation of dUTP diphosphatase activity","type":"exact"},{"name":"downregulation of dUTP nucleotidohydrolase activity","type":"exact"},{"name":"downregulation of dUTP pyrophosphatase activity","type":"exact"},{"name":"downregulation of dUTPase activity","type":"exact"},{"name":"downregulation of deoxyuridine-triphosphatase activity","type":"exact"},{"name":"downregulation of desoxyuridine 5'-triphosphatase activity","type":"exact"},{"name":"downregulation of desoxyuridine 5'-triphosphate nucleotidohydrolase activity","type":"exact"},{"name":"inhibition of dUTP diphosphatase activity","type":"narrow"},{"name":"inhibition of dUTP nucleotidohydrolase activity","type":"narrow"},{"name":"inhibition of dUTP pyrophosphatase activity","type":"narrow"},{"name":"inhibition of dUTPase activity","type":"narrow"},{"name":"inhibition of deoxyuridine-triphosphatase activity","type":"narrow"},{"name":"inhibition of desoxyuridine 5'-triphosphatase activity","type":"narrow"},{"name":"inhibition of desoxyuridine 5'-triphosphate nucleotidohydrolase activity","type":"narrow"},{"name":"negative regulation of dUTP nucleotidohydrolase activity","type":"exact"},{"name":"negative regulation of dUTP pyrophosphatase activity","type":"exact"},{"name":"negative regulation of dUTPase activity","type":"exact"},{"name":"negative regulation of deoxyuridine-triphosphatase activity","type":"exact"},{"name":"negative regulation of desoxyuridine 5'-triphosphatase activity","type":"exact"},{"name":"negative regulation of desoxyuridine 5'-triphosphate nucleotidohydrolase activity","type":"exact"}],"termid":"GO:1903628"}


id: PBO:0061096
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuroligin 1","termid":"PBO:0061096"}


id: PBO:0052414
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3","termid":"PBO:0052414"}


id: MONDO:0014091
data:
  {"annotated_genes":["SJAG_02564"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84882],"is_not":false,"summary":null,"term":"MONDO:0014091"}]},"cv_name":"mondo","definition":"Any mitochondrial complex deficiency in which the cause of the disease is a mutation in the ATP5F1A gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial complex deficiency","termid":"MONDO:0000066"},{"relation_name":"is_a","term_name":"mitochondrial proton-transporting ATP synthase complex deficiency","termid":"MONDO:0014471"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02564":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005066"],"is_obsolete":false,"name":"mitochondrial complex V (ATP synthase) deficiency nuclear type 4B","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:815229","UMLS:C3808899","DOID:0070462","OMIM:615228","GARD:18667"],"synonyms":[{"name":"ATP5F1A mitochondrial complex deficiency","type":"exact"},{"name":"MC5DN4B","type":"exact"},{"name":"mitochondrial Complex 5 (ATP synthase) deficiency, ATP5A1 type","type":"related"},{"name":"mitochondrial Complex 5 (ATP synthase) deficiency, nuclear type 4","type":"related"},{"name":"mitochondrial complex V (ATP synthase) deficiency, nuclear type 4","type":"related"},{"name":"mitochondrial complex deficiency caused by mutation in ATP5F1A","type":"exact"}],"termid":"MONDO:0014091","terms_by_termid":{"MONDO:0014091":null},"xrefs":{"Monarch":{"xref_id":"0014091"}}}


id: PBO:0039370
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AMMECR1 intronic transcript 1","termid":"PBO:0039370"}


id: PBO:0018249
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PI31 proteasome inhibitor Fub1 (predicted)","termid":"PBO:0018249"}


id: PR:Q7LL04
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC1494.01 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q7LL04"],"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":"UPF0676 protein C1494.01 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1494.01","synonyms":[{"name":"Spom972h-SPCC1494.01","type":"exact"}],"termid":"PR:Q7LL04"}


id: PBO:0011990
data:
  {"annotation_feature_type":"gene","cv_name":"species_dist","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"orthologous to S. cerevisiae YKR022C","termid":"PBO:0011990"}


id: PBO:0091217
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sub-telomeric 5Tm protein family","termid":"PBO:0091217"}


id: GO:0034014
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 triglyceride stimulus.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to lipid","termid":"GO:0033993"},{"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 triglyceride","synonyms":[{"name":"response to triacylglyceride","type":"exact"},{"name":"response to triacylglycerol","type":"exact"}],"termid":"GO:0034014"}


id: MONDO:0021373
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplasm (disease) that involves the parietal lobe.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neoplasm of cerebral hemisphere","termid":"MONDO:0021374"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neoplasm of parietal lobe","secondary_identifiers":["NCIT:C5573","SCTID:126956001","MEDGEN:266073","UMLS:C1263888"],"synonyms":[{"name":"neoplasm of parietal lobe","type":"exact"},{"name":"neoplasm of the parietal lobe","type":"exact"},{"name":"parietal lobe neoplasm","type":"exact"},{"name":"parietal lobe neoplasm (disease)","type":"exact"},{"name":"parietal lobe tumor","type":"exact"},{"name":"parietal lobe tumour","type":"exact"},{"name":"tumor of parietal lobe","type":"exact"},{"name":"tumor of the parietal lobe","type":"exact"},{"name":"tumour of parietal lobe","type":"exact"},{"name":"tumour of the parietal lobe","type":"exact"}],"termid":"MONDO:0021373","xrefs":{"Monarch":{"xref_id":"0021373"}}}


id: PBO:0077816
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tumor protein p53 inducible protein 13","termid":"PBO:0077816"}


id: PBO:0116220
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5-oxoprolinase (ATP-hydrolyzing), Oxp2","termid":"PBO:0116220"}


id: GO:0141044
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The global programming of epigenetic modifications following binucleate central cell fertilization. This involves DNA methylation at the silent allele. In the endosperm, maternal genomes are hypomethylated compared with the paternal genome.","definition_xrefs":["PMID:10580004","PMID:18700816","PMID:16469697","PMID:16527743","PMID:28118754"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epigenetic programming in the zygotic pronuclei","termid":"GO:0044725"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006325"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0006325","GO:0010467","GO:0008150"],"is_obsolete":false,"name":"epigenetic programming in the endosperm","synonyms":[{"name":"epigenetic reprogramming in the endosperm","type":"exact"}],"termid":"GO:0141044"}


id: GO:0071094
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of an alpha6-beta4 integrin complex bound to the cell surface protein CD9.","definition_xrefs":["PMID:10711425"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005886","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"alpha6-beta4 integrin-CD9 complex","synonyms":[{"name":"ITGA6-ITGB4-CD9 complex","type":"narrow"}],"termid":"GO:0071094"}


id: GO:0046336
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of ethanolamine (2-aminoethanol), an important water-soluble base of phospholipid (phosphatidylethanolamine).","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ethanolamine metabolic process","termid":"GO:0006580"},{"relation_name":"is_a","term_name":"primary alcohol catabolic process","termid":"GO:0034310"},{"relation_name":"is_a","term_name":"biogenic amine catabolic process","termid":"GO:0042402"},{"relation_name":"is_a","term_name":"primary amino compound catabolic process","termid":"GO:1901161"}],"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":"ethanolamine catabolic process","synonyms":[{"name":"ethanolamine breakdown","type":"exact"},{"name":"ethanolamine catabolism","type":"exact"},{"name":"ethanolamine degradation","type":"exact"}],"termid":"GO:0046336"}


id: MONDO:0014867
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Spinocerebellar ataxia type 43 is a rare autosomal dominant cerebellar ataxia type I disorder characterized by late adult-onset of slowly progressive cerebellar ataxia, typically presenting with balance and gait disturbances, in association with axonal peripheral neuropathy resulting in reduced/absent deep tendon reflexes and sensory impairment. Lower limb pain and amyotrophy may be present, as well as various cerebellar signs, including dysarthria, nystagmus, hypometric saccades and tremor.","definition_xrefs":["Orphanet:497764"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant cerebellar ataxia","termid":"MONDO:0020380"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0002039","MONDO:0005559"],"is_obsolete":false,"name":"spinocerebellar ataxia 43","secondary_identifiers":["OMIM:617018","MEDGEN:934730","DOID:0111745","UMLS:C4310763","GARD:17917"],"synonyms":[{"name":"MME autosomal dominant cerebellar ataxia","type":"exact"},{"name":"SCA43","type":"exact"},{"name":"autosomal dominant cerebellar ataxia caused by mutation in MME","type":"exact"},{"name":"spinocerebellar ataxia 43","type":"exact"},{"name":"spinocerebellar ataxia 43; SCA43","type":"exact"},{"name":"spinocerebellar ataxia type 43","type":"exact"}],"termid":"MONDO:0014867","xrefs":{"Monarch":{"xref_id":"0014867"}}}


id: PBO:0073349
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SERPINB9 antisense RNA 1","termid":"PBO:0073349"}


id: GO:0071014
data:
  {"annotated_genes":["SJAG_01408","SJAG_05235","SJAG_00911","SJAG_02295","SJAG_05212","SJAG_02905","SJAG_05025","SJAG_03469","SJAG_04385","SJAG_01810","SJAG_01214","SJAG_04055","SJAG_00446","SJAG_03687","SJAG_00639","SJAG_02843","SJAG_00206","SJAG_04117","SJAG_04898","SJAG_02078","SJAG_00564","SJAG_01301","SJAG_01186","SJAG_00322","SJAG_02304","SJAG_04694","SJAG_04427","SJAG_00147","SJAG_00859","SJAG_00563","SJAG_00414","SJAG_02317","SJAG_03301","SJAG_02279","SJAG_02227","SJAG_02844","SJAG_01008","SJAG_04783","SJAG_04497","SJAG_03601","SJAG_03210","SJAG_03427","SJAG_03711","SJAG_01870","SJAG_02722","SJAG_00597"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[69567,71932,72495,77519,77693,78063,87536,88080,88087,93140,94679,94931,95092,95145,95351,96197,96592,97763,98197,98264,98798,100386,102292,102455,103786,104269,105273,105630,106299,106921,107395,108981,109813,110369,111029,111486,112840,115236,115237,115704,116619,116958,118632],"is_not":false,"summary":null,"term":"GO:0071014"},{"annotations":[78320,108621,57335],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071008"}]},"cv_name":"cellular_component","definition":"A spliceosomal complex that is formed following the release of the spliced product from the post-spliceosomal complex and contains the excised intron and three snRNPs, either U2 or U12, U5, and either U6 or U6atac.","definition_xrefs":["ISBN:0879695897","GOC:ab","GOC:krc","GOC:mah","PMID:19239890","PMID:20149226"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spliceosomal complex","termid":"GO:0005681"}],"gene_count":46,"genes_by_uniquename":{"SJAG_00147":null,"SJAG_00206":null,"SJAG_00322":null,"SJAG_00414":null,"SJAG_00446":null,"SJAG_00563":null,"SJAG_00564":null,"SJAG_00597":null,"SJAG_00639":null,"SJAG_00859":null,"SJAG_00911":null,"SJAG_01008":null,"SJAG_01186":null,"SJAG_01214":null,"SJAG_01301":null,"SJAG_01408":null,"SJAG_01810":null,"SJAG_01870":null,"SJAG_02078":null,"SJAG_02227":null,"SJAG_02279":null,"SJAG_02295":null,"SJAG_02304":null,"SJAG_02317":null,"SJAG_02722":null,"SJAG_02843":null,"SJAG_02844":null,"SJAG_02905":null,"SJAG_03210":null,"SJAG_03301":null,"SJAG_03427":null,"SJAG_03469":null,"SJAG_03601":null,"SJAG_03687":null,"SJAG_03711":null,"SJAG_04055":null,"SJAG_04117":null,"SJAG_04385":null,"SJAG_04427":null,"SJAG_04497":null,"SJAG_04694":null,"SJAG_04783":null,"SJAG_04898":null,"SJAG_05025":null,"SJAG_05212":null,"SJAG_05235":null},"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:0005634"}],"interesting_parent_ids":["GO:0005634","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"post-mRNA release spliceosomal complex","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"mammalian spliceosomal complex I","type":"narrow"}],"termid":"GO:0071014","terms_by_termid":{"GO:0071008":null,"GO:0071014":null}}


id: GO:1905539
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of postsynapse to nucleus signaling pathway.","definition_xrefs":["ISBN:9780071120005","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of signal transduction","termid":"GO:0009966"},{"relation_name":"regulates","term_name":"postsynapse to nucleus signaling pathway","termid":"GO:0099527"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"regulation of postsynapse to nucleus signaling pathway","synonyms":[{"name":"regulation of postsynaptic signaling to nucleus","type":"exact"}],"termid":"GO:1905539"}


id: PBO:0077646
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TNF alpha induced protein 3","termid":"PBO:0077646"}


id: MONDO:0060592
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sweeney-Cox syndrome","secondary_identifiers":["DOID:0080538","OMIM:617746","UMLS:C4540299","MEDGEN:1625659"],"synonyms":[{"name":"SWCOS","type":"related"},{"name":"Sweeney-Cox syndrome","type":"exact"}],"termid":"MONDO:0060592","xrefs":{"Monarch":{"xref_id":"0060592"}}}


id: GO:0050096
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: threo-3-methyl-L-aspartate = mesaconate + NH4.","definition_xrefs":["RHEA:12829","EC:4.3.1.2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ammonia-lyase activity","termid":"GO:0016841"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016829","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"methylaspartate ammonia-lyase activity","secondary_identifiers":["KEGG_REACTION:R03696","MetaCyc:METHYLASPARTATE-AMMONIA-LYASE-RXN"],"synonyms":[{"name":"3-methylaspartase activity","type":"related"},{"name":"L-threo-3-methylaspartate ammonia-lyase (mesaconate-forming)","type":"related"},{"name":"L-threo-3-methylaspartate ammonia-lyase activity","type":"related"},{"name":"beta-methylaspartase activity","type":"related"}],"termid":"GO:0050096"}


id: GO:0046108
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving uridine, uracil riboside, a ribonucleoside very widely distributed but occurring almost entirely as phosphoric esters in ribonucleotides and ribonucleic acids.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine ribonucleoside metabolic process","termid":"GO:0046131"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0055086","GO:0008150"],"is_obsolete":false,"name":"uridine metabolic process","synonyms":[{"name":"uridine metabolism","type":"exact"}],"termid":"GO:0046108"}


id: GO:1900085
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of peptidyl-tyrosine autophosphorylation.","definition_xrefs":["GOC:bf","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein autophosphorylation","termid":"GO:0031953"},{"relation_name":"is_a","term_name":"negative regulation of peptidyl-tyrosine phosphorylation","termid":"GO:0050732"},{"relation_name":"is_a","term_name":"regulation of peptidyl-tyrosine autophosphorylation","termid":"GO:1900084"},{"relation_name":"negatively_regulates","term_name":"peptidyl-tyrosine autophosphorylation","termid":"GO:0038083"}],"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 peptidyl-tyrosine autophosphorylation","synonyms":[{"name":"down regulation of peptidyl-tyrosine autophosphorylation","type":"exact"},{"name":"down regulation of receptor tyrosine kinase autophosphorylation","type":"narrow"},{"name":"down regulation of tyrosine autophosphorylation","type":"exact"},{"name":"down-regulation of peptidyl-tyrosine autophosphorylation","type":"exact"},{"name":"down-regulation of receptor tyrosine kinase autophosphorylation","type":"narrow"},{"name":"down-regulation of tyrosine autophosphorylation","type":"exact"},{"name":"downregulation of peptidyl-tyrosine autophosphorylation","type":"exact"},{"name":"downregulation of receptor tyrosine kinase autophosphorylation","type":"narrow"},{"name":"downregulation of tyrosine autophosphorylation","type":"exact"},{"name":"inhibition of peptidyl-tyrosine autophosphorylation","type":"narrow"},{"name":"inhibition of receptor tyrosine kinase autophosphorylation","type":"narrow"},{"name":"inhibition of tyrosine autophosphorylation","type":"narrow"},{"name":"negative regulation of receptor tyrosine kinase autophosphorylation","type":"narrow"},{"name":"negative regulation of tyrosine autophosphorylation","type":"exact"}],"termid":"GO:1900085"}


id: PR:Q8WZJ8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rpc31 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q8WZJ8"],"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":"DNA-directed RNA polymerase III subunit rpc31 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC839.12","synonyms":[{"name":"DNA-directed RNA polymerase III 31 kDa polypeptide (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"RNA polymerase III subunit C31 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-rpc31","type":"exact"}],"termid":"PR:Q8WZJ8"}


id: PR:P87245
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- kms1 gene.","definition_xrefs":["UniProtKB:P87245","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":"karyogamy meiotic segregation protein 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC3A11.05c","synonyms":[{"name":"Spom972h-kms1","type":"exact"}],"termid":"PR:P87245"}


id: MONDO:0012857
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"disseminated superficial actinic porokeratosis","termid":"MONDO:0019212"}],"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":"porokeratosis 5, disseminated superficial actinic type","secondary_identifiers":["MESH:C567356","UMLS:C2676769","MEDGEN:382935","OMIM:612293","GARD:15551"],"synonyms":[{"name":"POROK5","type":"exact"},{"name":"porokeratosis 5, disseminated superficial actinic","type":"exact"},{"name":"porokeratosis 5, disseminated superficial actinic type","type":"exact"},{"name":"porokeratosis, disseminated superficial actinic, 3","type":"related"}],"termid":"MONDO:0012857","xrefs":{"Monarch":{"xref_id":"0012857"}}}


id: PR:Q8WZJ9
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A solute carrier family 35 member B1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR10778:SF10","OMA:SCHPO02527","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UDP-galactose transporter homolog 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC839.11c","secondary_identifiers":["UniProtKB:Q8WZJ9"],"synonyms":[{"name":"Spom972h-SLC35B1","type":"exact"}],"termid":"PR:Q8WZJ9"}


id: GO:0045492
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of xylan, a polymer containing a beta-1,4-linked D-xylose backbone.","definition_xrefs":["PMID:11931668","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"xylan metabolic process","termid":"GO:0045491"},{"relation_name":"is_a","term_name":"cell wall polysaccharide biosynthetic process","termid":"GO:0070592"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0071554"},{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0071554","GO:0008150","GO:0005975"],"is_obsolete":false,"name":"xylan biosynthetic process","synonyms":[{"name":"xylan anabolism","type":"exact"},{"name":"xylan biosynthesis","type":"exact"},{"name":"xylan formation","type":"exact"},{"name":"xylan synthesis","type":"exact"}],"termid":"GO:0045492"}


id: GO:0010529
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that decreases the frequency, rate or extent of transposition. Transposition results in the movement of discrete segments of DNA between nonhomologous sites.","definition_xrefs":["GOC:tb","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of transposition (obsolete GO:0010529)","termid":"GO:0010529"}


id: PBO:0041751
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cullin associated and neddylation dissociated 1","termid":"PBO:0041751"}


id: PBO:0085765
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein kinase of unknown cellular role; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm; interacts with rRNA transcription and ribosome biogenesis factors and the long chain fatty acyl-CoA synthetase Faa3p; FRK1 has a paralog, KIN4, that arose from the whole genome duplication","termid":"PBO:0085765"}


id: PBO:0052299
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KH RNA binding domain containing, signal transduction associated 3","termid":"PBO:0052299"}


id: _global:causal_agent_in_process
data:
  {"annotation_feature_type":"gene","cv_name":"external","definition":"A relationship between a material entity and a process where the material entity has some causal role that influences the process","direct_ancestors":[{"relation_name":"is_a","term_name":"causal_relation_between_material_entity_and_a_process","termid":"_global:causal_relation_between_material_entity_and_a_process"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"causal_agent_in_process","secondary_identifiers":["RO:0002500"],"termid":"_global:causal_agent_in_process"}


id: PBO:0077802
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thymocyte selection associated high mobility group box","termid":"PBO:0077802"}


id: MONDO:0014856
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the TRMT10C gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"combined oxidative phosphorylation deficiency","termid":"MONDO:0000732"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005066"],"is_obsolete":false,"name":"combined oxidative phosphorylation defect type 30","secondary_identifiers":["OMIM:616974","DOID:0111471","GARD:17864","MEDGEN:1799028","UMLS:C5567605","Orphanet:478042"],"synonyms":[{"name":"COXPD30","type":"exact"},{"name":"TRMT10C combined oxidative phosphorylation deficiency","type":"exact"},{"name":"combined oxidative phosphorylation deficiency 30","type":"exact"},{"name":"combined oxidative phosphorylation deficiency caused by mutation in TRMT10C","type":"exact"},{"name":"combined oxidative phosphorylation deficiency type 30","type":"exact"}],"termid":"MONDO:0014856","xrefs":{"Monarch":{"xref_id":"0014856"}}}


id: PBO:0042699
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CUGBP Elav-like family member 1","termid":"PBO:0042699"}


id: PBO:0088277
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"delta-1-pyrroline-5-carboxylate reductase Pro3","termid":"PBO:0088277"}


id: GO:0047505
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (-)-menthol + H+ + NADPH + O2 = 1,4-menthane-3,8-diol + H2O + NADP+.","definition_xrefs":["RHEA:11648","EC:1.14.13.46"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen","termid":"GO:0016709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"(-)-menthol monooxygenase activity","secondary_identifiers":["KEGG_REACTION:R02178","MetaCyc:--MENTHOL-MONOOXYGENASE-RXN"],"synonyms":[{"name":"(-)-menthol,NADPH:oxygen oxidoreductase (8-hydroxylating)","type":"related"},{"name":"l-menthol monooxygenase activity","type":"related"}],"termid":"GO:0047505"}


id: GO:1902854
data:
  {"annotated_genes":["SJAG_04597"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[94174],"is_not":false,"summary":null,"term":"GO:1902854"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of nuclear migration during mitotic telophase.","definition_xrefs":["GOC:TermGenie","PMID:23087209","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of nuclear migration along microtubule","termid":"GO:1902840"},{"relation_name":"is_a","term_name":"regulation of nuclear migration during mitotic telophase","termid":"GO:1902852"},{"relation_name":"positively_regulates","term_name":"nuclear migration during mitotic telophase","termid":"GO:0090561"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04597":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"positive regulation of nuclear migration during mitotic telophase","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"activation of nuclear migration during mitotic telophase","type":"narrow"},{"name":"up regulation of nuclear migration during mitotic telophase","type":"exact"},{"name":"up-regulation of nuclear migration during mitotic telophase","type":"exact"},{"name":"upregulation of nuclear migration during mitotic telophase","type":"exact"}],"termid":"GO:1902854","terms_by_termid":{"GO:1902854":null}}


id: GO:0071209
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a U7 small nuclear RNA (U7 snRNA).","definition_xrefs":["GOC:mah","PMID:12975319"],"direct_ancestors":[{"relation_name":"is_a","term_name":"snRNA binding","termid":"GO:0017069"}],"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:0003723"}],"interesting_parent_ids":["GO:0005488","GO:0003723","GO:0003674"],"is_obsolete":false,"name":"U7 snRNA binding","termid":"GO:0071209"}


id: GO:2001103
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a maltohexaoseacetate into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hexasaccharide transport","termid":"GO:2001102"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"maltohexaose transport","termid":"GO:2001103"}


id: PBO:0027254
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_vegetative_cell_growth","termid":"PBO:0027254"}


id: MONDO:0000369
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An extrapulmonary tuberculosis that is located in gastrointestinal tract, located in peritoneum, located in omentum, located in mesentery, located in liver, located in spleen or located in pancreas.","definition_xrefs":["DOID:0050599"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extrapulmonary tuberculosis","termid":"MONDO:0000368"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"abdominal tuberculosis","secondary_identifiers":["SCTID:447330002","ICD9:014.80","UMLS:C0740652","MEDGEN:677012"],"synonyms":[{"name":"tuberculosis of abdomen","type":"exact"}],"termid":"MONDO:0000369","xrefs":{"Monarch":{"xref_id":"0000369"}}}


id: GO:1990659
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process of binding or confining manganese ions such that they are separated from other components of a biological system.","definition_xrefs":["GOC:bhm","PMID:25417112"],"gene_count":0,"genotype_count":0,"name":"obsolete sequestering of manganese ion (obsolete GO:1990659)","synonyms":[{"name":"manganese ion retention","type":"exact"},{"name":"manganese ion sequestering","type":"exact"},{"name":"manganese ion sequestration","type":"exact"},{"name":"manganese ion storage","type":"exact"},{"name":"retention of manganese ion","type":"exact"},{"name":"sequestration of manganese ion","type":"exact"},{"name":"storage of manganese ion","type":"exact"}],"termid":"GO:1990659"}


id: GO:0002701
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of the production of molecular mediator of immune response.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of immune effector process","termid":"GO:0002698"},{"relation_name":"is_a","term_name":"regulation of production of molecular mediator of immune response","termid":"GO:0002700"},{"relation_name":"is_a","term_name":"negative regulation of gene expression","termid":"GO:0010629"},{"relation_name":"negatively_regulates","term_name":"production of molecular mediator of immune response","termid":"GO:0002440"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"negative regulation of production of molecular mediator of immune response","synonyms":[{"name":"down regulation of production of molecular mediator of immune response","type":"exact"},{"name":"down-regulation of production of molecular mediator of immune response","type":"exact"},{"name":"downregulation of production of molecular mediator of immune response","type":"exact"},{"name":"inhibition of production of molecular mediator of immune response","type":"narrow"}],"termid":"GO:0002701"}


id: PBO:0050377
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 1","termid":"PBO:0050377"}


id: PBO:0077818
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tumor protein p53 inducible nuclear protein 2","termid":"PBO:0077818"}


id: MONDO:0004861
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"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":"ophthalmia nodosa","secondary_identifiers":["DOID:9722","ICD9:360.14","SCTID:12371008","icd11.foundation:691596189","UMLS:C0154775","MEDGEN:509654"],"termid":"MONDO:0004861","xrefs":{"Monarch":{"xref_id":"0004861"}}}


id: GO:0009722
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events in which a cytokinin stimulus is received by a cell and converted into a molecular signal.","definition_xrefs":["GOC:sm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detection of hormone stimulus","termid":"GO:0009720"},{"relation_name":"is_a","term_name":"response to cytokinin","termid":"GO:0009735"}],"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 cytokinin stimulus","synonyms":[{"name":"perception of cytokinin stimulus","type":"related"}],"termid":"GO:0009722"}


id: PBO:0004939
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ran GTPase Spi1","termid":"PBO:0004939"}


id: GO:0106125
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A matrix composed of planar membranes, vesicles and lipid inclusions within the reservosome.","definition_xrefs":["PMID:15521631","GOC:ach","PMID:18452191","PMID:21818313","PMID:19288526","PMID:22425988","PMID:12204365"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"reservosome","termid":"GO:0106123"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005773"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005773","GO:0005737","GO:0005575"],"is_obsolete":false,"name":"reservosome matrix","termid":"GO:0106125"}


id: GO:1902752
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of renal amino acid absorption.","definition_xrefs":["GO_REF:0000058","PMID:1526373","GOC:hjd","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of renal system process","termid":"GO:0098801"},{"relation_name":"regulates","term_name":"renal amino acid absorption","termid":"GO:1990297"}],"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 renal amino acid absorption","termid":"GO:1902752"}


id: GO:0006670
data:
  {"annotated_genes":["SJAG_04178","SJAG_01057","SJAG_02706","SJAG_02305","SJAG_00880","SJAG_02429"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[105749,109463,76656,78689,96660,73517],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046512"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving sphingosine (sphing-4-enine), trans-D-erytho-2-amino-octadec-4-ene-1,3-diol, a long chain amino diol sphingoid base that occurs in most sphingolipids in animal tissues.","definition_xrefs":["GOC:ma","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diol metabolic process","termid":"GO:0034311"},{"relation_name":"is_a","term_name":"sphingoid metabolic process","termid":"GO:0046519"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00880":null,"SJAG_01057":null,"SJAG_02305":null,"SJAG_02429":null,"SJAG_02706":null,"SJAG_04178":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0006629","GO:0008150"],"is_obsolete":false,"name":"sphingosine metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"(4E)-sphing-4-enine metabolic process","type":"exact"},{"name":"(4E)-sphing-4-enine metabolism","type":"exact"},{"name":"sphing-4-enine metabolic process","type":"exact"},{"name":"sphing-4-enine metabolism","type":"exact"},{"name":"sphingosine metabolism","type":"exact"}],"termid":"GO:0006670","terms_by_termid":{"GO:0046512":null}}


id: GO:0060695
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate, frequency, or extent of cholesterol transporter activity.","definition_xrefs":["GOC:tb","GOC:BHF","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of lipid transporter activity","termid":"GO:0110114"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"negative regulation of cholesterol transporter activity","termid":"GO:0060695"}


id: MONDO:0011588
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited blood coagulation disease characterized by autosomal dominant inheritance of mildly increased bleeding, platelet aggregation defect, and impaired conversion of arachidonic acid to thromboxane A2 in platelets due to deficiency in PTGS1 activity.","definition_xrefs":["DOID:0111058","PMID:8562397"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited bleeding disorder, platelet-type","termid":"MONDO:0000009"},{"relation_name":"is_a","term_name":"inherited blood coagulation disorder","termid":"MONDO:0021181"}],"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":"platelet-type bleeding disorder 12","secondary_identifiers":["MESH:C567786","MEDGEN:414043","OMIM:605735","UMLS:C2751535"],"synonyms":[{"name":"BDPLT12","type":"exact"},{"name":"PGHS1 deficiency","type":"exact"},{"name":"bleeding disorder, platelet-type, 12","type":"related"},{"name":"platelet COX1 deficiency","type":"exact"},{"name":"platelet cyclooxygenase 1 deficiency","type":"exact"},{"name":"platelet prostaglandin-endoperoxide synthase 1 deficiency","type":"exact"},{"name":"prostaglandin-endoperoxide synthase 1 deficiency, platelet","type":"related"}],"termid":"MONDO:0011588","xrefs":{"Monarch":{"xref_id":"0011588"}}}


id: SO:0001917
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A kind of transcription_initiation_cluster defined by the clustering of CAGE tags on a sequence region.","definition_xrefs":["SO:andrewgibson","PMID:16645617"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcription_start_cluster","termid":"SO:0001915"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CAGE_cluster","synonyms":[{"name":"CAGE cluster","type":"exact"},{"name":"CAGE peak","type":"exact"},{"name":"CAGE_peak","type":"exact"},{"name":"INSDC_feature:misc_feature","type":"broad"},{"name":"INSDC_note:CAGE_cluster","type":"exact"}],"termid":"SO:0001917"}


id: GO:0045862
data:
  {"annotated_genes":["SJAG_03048","SJAG_02723","SJAG_01131","SJAG_01544","SJAG_03699","SJAG_01210","SJAG_00642","SJAG_00071","SJAG_00712","SJAG_04477","SJAG_00766","SJAG_01489","SJAG_00077"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89720],"is_not":false,"summary":null,"term":"GO:0045862"},{"annotations":[88705],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905786"},{"annotations":[61445,67031,66808,68057,65544,68400],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901800"},{"annotations":[102134,106415,116814,108648,111460],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032436"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the hydrolysis of a peptide bond or bonds within a protein.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of proteolysis","termid":"GO:0030162"},{"relation_name":"is_a","term_name":"positive regulation of protein metabolic process","termid":"GO:0051247"},{"relation_name":"positively_regulates","term_name":"proteolysis","termid":"GO:0006508"}],"gene_count":13,"genes_by_uniquename":{"SJAG_00071":null,"SJAG_00077":null,"SJAG_00642":null,"SJAG_00712":null,"SJAG_00766":null,"SJAG_01131":null,"SJAG_01210":null,"SJAG_01489":null,"SJAG_01544":null,"SJAG_02723":null,"SJAG_03048":null,"SJAG_03699":null,"SJAG_04477":null},"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 proteolysis","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000108":null},"synonyms":[{"name":"activation of proteolysis","type":"narrow"},{"name":"positive regulation of peptidolysis","type":"exact"},{"name":"stimulation of proteolysis","type":"narrow"},{"name":"up regulation of proteolysis","type":"exact"},{"name":"up-regulation of proteolysis","type":"exact"},{"name":"upregulation of proteolysis","type":"exact"}],"termid":"GO:0045862","terms_by_termid":{"GO:0032436":null,"GO:0045862":null,"GO:1901800":null,"GO:1905786":null}}


id: GO:0045860
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of protein kinase activity.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein phosphorylation","termid":"GO:0001934"},{"relation_name":"is_a","term_name":"positive regulation of kinase activity","termid":"GO:0033674"},{"relation_name":"is_a","term_name":"regulation of protein kinase activity","termid":"GO:0045859"}],"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 protein kinase activity","synonyms":[{"name":"stimulation of protein kinase activity","type":"narrow"},{"name":"up regulation of protein kinase activity","type":"exact"},{"name":"up-regulation of protein kinase activity","type":"exact"},{"name":"upregulation of protein kinase activity","type":"exact"}],"termid":"GO:0045860"}


id: GO:1903050
data:
  {"annotated_genes":["SJAG_04477","SJAG_01528","SJAG_03048","SJAG_01544","SJAG_02723","SJAG_02485","SJAG_01131","SJAG_01210","SJAG_03699","SJAG_00766","SJAG_01489","SJAG_00642","SJAG_00052","SJAG_02244","SJAG_00712","SJAG_00475","SJAG_00071"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[102112],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905785"},{"annotations":[77351,77843],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904293"},{"annotations":[106708,77033],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032435"},{"annotations":[88705],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905786"},{"annotations":[61445,68400,66808,68057,65544,67031],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901800"},{"annotations":[108648,106415,116814,111460,102134],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032436"},{"annotations":[114374],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032434"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of proteolysis involved in cellular catabolic process.","definition_xrefs":["GOC:rl","PMID:18307834","GOC:BHF","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of proteolysis","termid":"GO:0030162"},{"relation_name":"regulates","term_name":"proteolysis involved in protein catabolic process","termid":"GO:0051603"}],"gene_count":17,"genes_by_uniquename":{"SJAG_00052":null,"SJAG_00071":null,"SJAG_00475":null,"SJAG_00642":null,"SJAG_00712":null,"SJAG_00766":null,"SJAG_01131":null,"SJAG_01210":null,"SJAG_01489":null,"SJAG_01528":null,"SJAG_01544":null,"SJAG_02244":null,"SJAG_02485":null,"SJAG_02723":null,"SJAG_03048":null,"SJAG_03699":null,"SJAG_04477":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of proteolysis involved in protein catabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000108":null},"synonyms":[{"name":"regulation of peptidolysis during cellular protein catabolic process","type":"related"},{"name":"regulation of peptidolysis during cellular protein catabolism","type":"related"},{"name":"regulation of peptidolysis involved in cellular protein catabolic process","type":"exact"},{"name":"regulation of peptidolysis involved in cellular protein catabolism","type":"exact"},{"name":"regulation of proteolysis during cellular protein catabolic process","type":"related"},{"name":"regulation of proteolysis during cellular protein catabolism","type":"related"},{"name":"regulation of proteolysis involved in cellular protein catabolic process","type":"exact"}],"termid":"GO:1903050","terms_by_termid":{"GO:0032434":null,"GO:0032435":null,"GO:0032436":null,"GO:1901800":null,"GO:1904293":null,"GO:1905785":null,"GO:1905786":null}}


id: MONDO:0025163
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A congenital reproductive abnormality in white female offspring (heifers) in certain breeds of cattle, such as Belgian Blue and Shorthorn. The white color is inherited as a recessive trait which is associated with defects in the female reproductive tract (Muellerian system). These heifers are usually sterile.","definition_xrefs":["MESH:D050072"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cattle disease","termid":"MONDO:0024913"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"white heifer disease","secondary_identifiers":["SCTID:82642007"],"synonyms":[{"name":"disease, White heifer","type":"related"}],"termid":"MONDO:0025163","xrefs":{"Monarch":{"xref_id":"0025163"}}}


id: SO:0000295
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A type of spliceosomal intron spliced by the U12 spliceosome, that includes U11, U12, U4atac/U6atac and U5 snRNAs.","definition_xrefs":["PMID:9428511"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spliceosomal_intron","termid":"SO:0000662"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U12_intron","synonyms":[{"name":"U12 intron","type":"exact"},{"name":"U12-dependent intron","type":"exact"}],"termid":"SO:0000295"}


id: PBO:0066311
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RBPJ pseudogene 5","termid":"PBO:0066311"}


id: PBO:0082676
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the EKC/KEOPS protein complex; EKC/KEOPS complex is required for t6A tRNA modification and telomeric TG1-3 recombination; may have role in transcription; implicated in osmotic stress response; other complex members are Kae1p, Cgi121p, Pcc1p, and Bud32p","termid":"PBO:0082676"}


id: PBO:0062101
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 B member 1","termid":"PBO:0062101"}


id: MONDO:0012051
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"chronic periodontitis","termid":"MONDO:0005593"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"periodontitis, aggressive, 2","secondary_identifiers":["UMLS:C1969478","MEDGEN:370671","MESH:C566946","OMIM:608526"],"synonyms":[{"name":"periodontitis, aggressive, 2","type":"exact"},{"name":"periodontitis, aggressive, type 2","type":"exact"}],"termid":"MONDO:0012051","xrefs":{"Monarch":{"xref_id":"0012051"}}}


id: MONDO:0016111
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete non-dystrophic myopathy with collagen 6 anomaly (obsolete MONDO:0016111)","secondary_identifiers":["Orphanet:206659"],"termid":"MONDO:0016111","xrefs":{"Monarch":{"xref_id":"0016111"}}}


id: MONDO:0014092
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A schizophrenia that has material basis in a mutation of SLC1A1 on chromosome 9p24.2.","definition_xrefs":["DOID:0070093"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"schizophrenia","termid":"MONDO:0005090"},{"relation_name":"is_a","term_name":"schizophrenia, susceptibility to","termid":"MONDO:0100182"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"schizophrenia 18","secondary_identifiers":["OMIM:615232","UMLS:C3808913","MEDGEN:815243"],"synonyms":[{"name":"SCZD18","type":"exact"},{"name":"chromosome 7q36.3 Duplication syndrome, 362-Kb","type":"exact"},{"name":"schizoaffective disorder","type":"related"},{"name":"schizophrenia 18","type":"exact"},{"name":"schizophrenia 18 with or without an affective disorder","type":"related"},{"name":"schizophrenia susceptibility 18","type":"exact"},{"name":"schizophrenia type 18","type":"exact"}],"termid":"MONDO:0014092","xrefs":{"Monarch":{"xref_id":"0014092"}}}


id: GO:1905166
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of lysosomal protein catabolic process.","definition_xrefs":["GOC:TermGenie","GOC:PARL","GOC:bf","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein catabolic process in the vacuole","termid":"GO:1904351"},{"relation_name":"is_a","term_name":"regulation of lysosomal protein catabolic process","termid":"GO:1905165"},{"relation_name":"negatively_regulates","term_name":"lysosomal protein catabolic process","termid":"GO:1905146"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0030163"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0030163"}],"interesting_parent_ids":["GO:0030163","GO:0008150"],"is_obsolete":false,"name":"negative regulation of lysosomal protein catabolic process","synonyms":[{"name":"down regulation of cellular protein breakdown in lysosome","type":"exact"},{"name":"down regulation of cellular protein catabolic process in lysosome","type":"exact"},{"name":"down regulation of cellular protein catabolism in lysosome","type":"exact"},{"name":"down regulation of cellular protein degradation in lysosome","type":"exact"},{"name":"down regulation of lysosomal protein catabolic process","type":"exact"},{"name":"down regulation of lysosomal protein catabolism","type":"exact"},{"name":"down regulation of lysosomal protein degradation","type":"exact"},{"name":"down regulation of lysosomal proteolysis","type":"related"},{"name":"down regulation of proteolysis within lysosome","type":"related"},{"name":"down-regulation of cellular protein breakdown in lysosome","type":"exact"},{"name":"down-regulation of cellular protein catabolic process in lysosome","type":"exact"},{"name":"down-regulation of cellular protein catabolism in lysosome","type":"exact"},{"name":"down-regulation of cellular protein degradation in lysosome","type":"exact"},{"name":"down-regulation of lysosomal protein catabolic process","type":"exact"},{"name":"down-regulation of lysosomal protein catabolism","type":"exact"},{"name":"down-regulation of lysosomal protein degradation","type":"exact"},{"name":"down-regulation of lysosomal proteolysis","type":"related"},{"name":"down-regulation of proteolysis within lysosome","type":"related"},{"name":"downregulation of cellular protein breakdown in lysosome","type":"exact"},{"name":"downregulation of cellular protein catabolic process in lysosome","type":"exact"},{"name":"downregulation of cellular protein catabolism in lysosome","type":"exact"},{"name":"downregulation of cellular protein degradation in lysosome","type":"exact"},{"name":"downregulation of lysosomal protein catabolic process","type":"exact"},{"name":"downregulation of lysosomal protein catabolism","type":"exact"},{"name":"downregulation of lysosomal protein degradation","type":"exact"},{"name":"downregulation of lysosomal proteolysis","type":"related"},{"name":"downregulation of proteolysis within lysosome","type":"related"},{"name":"inhibition of cellular protein breakdown in lysosome","type":"narrow"},{"name":"inhibition of cellular protein catabolic process in lysosome","type":"narrow"},{"name":"inhibition of cellular protein catabolism in lysosome","type":"narrow"},{"name":"inhibition of cellular protein degradation in lysosome","type":"narrow"},{"name":"inhibition of lysosomal protein catabolic process","type":"narrow"},{"name":"inhibition of lysosomal protein catabolism","type":"narrow"},{"name":"inhibition of lysosomal protein degradation","type":"narrow"},{"name":"inhibition of lysosomal proteolysis","type":"related"},{"name":"inhibition of proteolysis within lysosome","type":"related"},{"name":"negative regulation of cellular protein breakdown in lysosome","type":"exact"},{"name":"negative regulation of cellular protein catabolic process in lysosome","type":"exact"},{"name":"negative regulation of cellular protein catabolism in lysosome","type":"exact"},{"name":"negative regulation of cellular protein degradation in lysosome","type":"exact"},{"name":"negative regulation of lysosomal protein catabolism","type":"exact"},{"name":"negative regulation of lysosomal protein degradation","type":"exact"},{"name":"negative regulation of lysosomal proteolysis","type":"related"},{"name":"negative regulation of proteolysis within lysosome","type":"related"}],"termid":"GO:1905166"}


id: PBO:0033760
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_duration_of_meiosis_I","termid":"PBO:0033760"}


id: GO:1905680
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of innate immunity memory response.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of innate immune response","termid":"GO:0045088"},{"relation_name":"regulates","term_name":"innate immunity memory response","termid":"GO:0090714"}],"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 innate immunity memory response","termid":"GO:1905680"}


id: PBO:0088407
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Golgi zinc importer, CDF family, Cis4","termid":"PBO:0088407"}


id: MONDO:0017443
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital absence of both forearm and hand is a rare developmental defect during embryogenesis characterized by unilateral or bilateral arrest of proximal to distal development of the upper limb, leading to a transverse deficiency with absence of the forearm, wrist and hand. A short below-the-elbow amputation is most commonly observed and the residual limb is usually well cushioned, with rudimentary nubbins or dumpling possibly found on the end.","definition_xrefs":["Orphanet:294979"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"},{"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":"congenital absence of both forearm and hand","secondary_identifiers":["GARD:21194","ICD10CM:Q71.2","icd11.foundation:810894993","MEDGEN:727129","UMLS:C1306663"],"synonyms":[{"name":"radio-ulnar terminal transverse meromelia","type":"exact"}],"termid":"MONDO:0017443","xrefs":{"Monarch":{"xref_id":"0017443"}}}


id: MONDO:0100291
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"T acute lymphoblastic leukemia in which the blasts have unique immunophenotypic and genetic characteristics suggesting only limited early T-cell differentiation.","definition_xrefs":["NCIT:C130043"],"direct_ancestors":[{"relation_name":"is_a","term_name":"T-cell acute lymphoblastic leukemia","termid":"MONDO:0004963"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"early T cell progenitor acute lymphoblastic leukemia","secondary_identifiers":["UMLS:C4329780","MEDGEN:1385175"],"synonyms":[{"name":"ETP ALL","type":"exact"},{"name":"ETP-ALL","type":"exact"},{"name":"early T acute lymphoblastic leukaemia","type":"exact"},{"name":"early T acute lymphoblastic leukemia","type":"exact"},{"name":"early T-cell precursor acute lymphoblastic leukaemia","type":"exact"},{"name":"early T-cell precursor acute lymphoblastic leukemia","type":"exact"},{"name":"early T-cell precursor lymphoblastic leukaemia","type":"exact"},{"name":"early T-cell precursor lymphoblastic leukemia","type":"exact"}],"termid":"MONDO:0100291","xrefs":{"Monarch":{"xref_id":"0100291"}}}


id: PBO:0049930
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hedgehog acyltransferase like","termid":"PBO:0049930"}


id: PBO:0114533
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone H3-H4 chaperone (ATP-dependent) Abo2","termid":"PBO:0114533"}


id: MONDO:0060591
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":"immunodeficiency, developmental delay, and hypohomocysteinemia","secondary_identifiers":["UMLS:C4540293","MEDGEN:1616061","OMIM:617744"],"synonyms":[{"name":"IMDDHH","type":"related"},{"name":"immunodeficiency, developmental delay, and hypohomocysteinemia","type":"exact"}],"termid":"MONDO:0060591","xrefs":{"Monarch":{"xref_id":"0060591"}}}


id: PBO:0059043
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"multimerin 2","termid":"PBO:0059043"}


id: MOD:00671
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a residue hydroxyl group with a acyloxy group.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acylated residue","termid":"MOD:00649"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"O-acylated residue","synonyms":[{"name":"OAcylRes","type":"exact"}],"termid":"MOD:00671"}


id: PBO:0048385
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"granule associated Rac and RHOG effector 1","termid":"PBO:0048385"}


id: MONDO:0035363
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete IRF2BPL-related regressive neurodevelopmental disorder-dystonia-seizures syndrome (obsolete MONDO:0035363)","termid":"MONDO:0035363","xrefs":{"Monarch":{"xref_id":"0035363"}}}


id: PBO:0062544
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 9 subfamily I member 3 pseudogene","termid":"PBO:0062544"}


id: MONDO:0002984
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare cutaneous lesion composed of eosinophilic histiocytes, which are often multinucleated. The lesions are yellow-brown papules affecting any part of the body. Patients are usually adult men. The prognosis is excellent. -- 2003","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histiocytosis","termid":"MONDO:0002637"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"reticulohistiocytic granuloma","secondary_identifiers":["UMLS:C0035290","ICD9:277.89","DOID:4394","MESH:D015616","MEDGEN:48431","NCIT:C3356","SCTID:404162004"],"synonyms":[{"name":"Reticulohistiocytoma","type":"exact"},{"name":"reticulohistiocytic granuloma (morphologic abnormality)","type":"exact"},{"name":"solitary Reticulohistiocytoma","type":"exact"},{"name":"solitary histiocytoma","type":"related"},{"name":"solitary reticulohistiocytoma","type":"exact"},{"name":"solitary reticulohistiocytosis","type":"related"}],"termid":"MONDO:0002984","xrefs":{"Monarch":{"xref_id":"0002984"}}}


id: GO:0062083
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with a MHC class Ib molecule of the HLA-G subclass to mediate signaling that inhibits activation of a lymphocyte.","definition_xrefs":["DOI:10.1002/9780470015902.a0024246"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inhibitory MHC class Ib receptor activity","termid":"GO:0062080"}],"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:0003674","GO:0038023"],"is_obsolete":false,"name":"HLA-G specific inhibitory MHC class Ib receptor activity","termid":"GO:0062083"}


id: GO:0062030
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops or decreases the rate, frequency or extent of stress-granule assembly, the aggregation, arrangement and bonding together of proteins and RNA molecules to form a stress granule.","definition_xrefs":["PMID:20180778"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of stress granule assembly","termid":"GO:0062028"},{"relation_name":"is_a","term_name":"negative regulation of organelle assembly","termid":"GO:1902116"},{"relation_name":"negatively_regulates","term_name":"stress granule assembly","termid":"GO:0034063"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"negative regulation of stress granule assembly","termid":"GO:0062030"}


id: MONDO:0033046
data:
  {"annotated_genes":["SJAG_01354"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85185],"is_not":false,"summary":null,"term":"MONDO:0033046"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Meier-Gorlin syndrome","termid":"MONDO:0016817"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01354":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"Meier-Gorlin syndrome 8","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0080255","MEDGEN:1390366","OMIM:617564","UMLS:C4479655"],"synonyms":[{"name":"MGORS8","type":"related"},{"name":"Meier-Gorlin syndrome 8","type":"exact"}],"termid":"MONDO:0033046","terms_by_termid":{"MONDO:0033046":null},"xrefs":{"Monarch":{"xref_id":"0033046"}}}


id: MONDO:0005765
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A viral infectious disease that results in infection in cattle and swine, has material basis in foot-and-mouth disease virus, which is transmitted by contaminated fomites, or transmitted by ingestion of food contaminated with infected meat or animal products. The infection results in formation of vesicles in the mouth, or on the feet and has symptom lameness.","definition_xrefs":["EFO:0007277"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cattle disease","termid":"MONDO:0024913"},{"relation_name":"is_a","term_name":"swine disease","termid":"MONDO:0024990"},{"relation_name":"is_a","term_name":"viral infectious disease, non-human animal","termid":"MONDO:0700053"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"foot and mouth disease","secondary_identifiers":["icd11.foundation:1008730501","MESH:D005536"],"termid":"MONDO:0005765","xrefs":{"Monarch":{"xref_id":"0005765"}}}


id: PBO:0078083
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trafficking protein particle complex subunit 2L","termid":"PBO:0078083"}


id: MONDO:0009998
data:
  {"annotated_genes":["SJAG_02879"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84982],"is_not":false,"summary":null,"term":"MONDO:0009998"}]},"cv_name":"mondo","definition":"Richieri Costa-Pereira syndrome is characterized by short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies (including hypoplastic thumbs), and clubfoot. It has been described in 14 Brazilian families and in one unrelated French patient. Prominent low set ears and a highly arched palate were also observed. Transmission is autosomal recessive.","definition_xrefs":["Orphanet:3102"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"},{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02879":null},"genotype_count":0,"is_obsolete":false,"name":"Richieri Costa-Pereira syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:4718","icd11.foundation:107084177","OMIM:268305","MESH:C535677","MEDGEN:336581","SCTID:723998001","UMLS:C1849348"],"synonyms":[{"name":"ROBIN sequence with cleft mandible and limb anomalies","type":"related"},{"name":"Richieri Costa Pereira syndrome","type":"related"},{"name":"Richieri Costa-Pereira syndrome","type":"exact"},{"name":"Richieri-Costa and Pereira form of acrofacial dysostosis","type":"related"},{"name":"Richieri-Costa-Pereira syndrome","type":"related"},{"name":"short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfoot","type":"related"},{"name":"short stature-Pierre Robin sequence-cleft mandible-hand anomalies clubfoot syndrome","type":"exact"},{"name":"short stature-Pierre Robin syndrome-cleft mandible-hand anomalies clubfoot syndrome","type":"exact"}],"termid":"MONDO:0009998","terms_by_termid":{"MONDO:0009998":null},"xrefs":{"Monarch":{"xref_id":"0009998"}}}


id: PBO:0002846
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ca2+/Mn2+ transporting P-type ATPase P5 type Cta5","termid":"PBO:0002846"}


id: SO:0001434
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A cassette pseudogene is a kind of gene in an inactive form which may recombine at a telomeric locus to form a functional copy.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non_processed_pseudogene","termid":"SO:0001760"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cassette_pseudogene","synonyms":[{"name":"cassette pseudogene","type":"exact"},{"name":"cassette type psedogene","type":"related"}],"termid":"SO:0001434"}


id: MONDO:0000522
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete inflammatory myofibroblastic tumor (obsolete MONDO:0000522)","termid":"MONDO:0000522","xrefs":{"Monarch":{"xref_id":"0000522"}}}


id: PBO:0074994
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 115-5","termid":"PBO:0074994"}


id: PBO:0034546
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_cellular_phosphatidic_acid_level","termid":"PBO:0034546"}


id: GO:0061493
data:
  {"annotated_genes":["SJAG_02795","SJAG_02246","SJAG_04901"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[96616,98027,99610],"is_not":false,"summary":null,"term":"GO:0061493"}]},"cv_name":"cellular_component","definition":"One of three laminate structures that form the mitotic spindle pole body; the inner plaque is on the nuclear face of the spindle pole body.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"central plaque of spindle pole body","termid":"GO:0005823"},{"relation_name":"part_of","term_name":"mitotic spindle pole body","termid":"GO:0044732"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02246":null,"SJAG_02795":null,"SJAG_04901":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005816"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0015630"}],"interesting_parent_ids":["GO:0005816","GO:0005575","GO:0015630"],"is_obsolete":false,"name":"central plaque of mitotic spindle pole body","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0061493","terms_by_termid":{"GO:0061493":null}}


id: PBO:0050399
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein C like 4","termid":"PBO:0050399"}


id: PBO:0062986
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PACRG antisense RNA 1","termid":"PBO:0062986"}


id: GO:0035822
data:
  {"annotated_genes":["SJAG_02724","SJAG_02079","SJAG_01495","SJAG_01601","SJAG_02556","SJAG_02226","SJAG_00247","SJAG_02460","SJAG_01076","SJAG_02267","SJAG_03221","SJAG_01419","SJAG_01677","SJAG_02828","SJAG_03097","SJAG_05239"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[116542,88924,105829,114765,110572,100339,97181,110051,87692,89052,95932,98881,106390,118503,108269],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007534"},{"annotations":[89053,100305],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006311"}]},"cv_name":"biological_process","definition":"A DNA recombination process that results in the unidirectional transfer of genetic material from a donor sequence to a highly homologous acceptor. The resulting acceptor sequence is identical to that of the donor.","definition_xrefs":["GOC:mah","PMID:17846636"],"direct_ancestors":[{"relation_name":"is_a","term_name":"homologous recombination","termid":"GO:0035825"}],"gene_count":16,"genes_by_uniquename":{"SJAG_00247":null,"SJAG_01076":null,"SJAG_01419":null,"SJAG_01495":null,"SJAG_01601":null,"SJAG_01677":null,"SJAG_02079":null,"SJAG_02226":null,"SJAG_02267":null,"SJAG_02460":null,"SJAG_02556":null,"SJAG_02724":null,"SJAG_02828":null,"SJAG_03097":null,"SJAG_03221":null,"SJAG_05239":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006310"},{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006259","GO:0006310","GO:0008150"],"is_obsolete":false,"name":"gene conversion","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0035822","terms_by_termid":{"GO:0006311":null,"GO:0007534":null}}


id: PBO:0075428
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sperm associated antigen 17","termid":"PBO:0075428"}


id: GO:1905358
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of snRNA pseudouridine synthesis.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:27268497"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of RNA metabolic process","termid":"GO:0051254"},{"relation_name":"is_a","term_name":"regulation of snRNA pseudouridine synthesis","termid":"GO:1905356"},{"relation_name":"positively_regulates","term_name":"snRNA pseudouridine synthesis","termid":"GO:0031120"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0016073"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0016073"}],"interesting_parent_ids":["GO:0016073","GO:0008150"],"is_obsolete":false,"name":"positive regulation of snRNA pseudouridine synthesis","synonyms":[{"name":"activation of snRNA pseudouridine synthesis","type":"narrow"},{"name":"up regulation of snRNA pseudouridine synthesis","type":"exact"},{"name":"up-regulation of snRNA pseudouridine synthesis","type":"exact"},{"name":"upregulation of snRNA pseudouridine synthesis","type":"exact"}],"termid":"GO:1905358"}


id: PBO:0082461
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Calcineurin A; one isoform (the other is Cmp2p) of the catalytic subunit of calcineurin, a Ca++/calmodulin-regulated protein phosphatase which regulates Crz1p (a stress-response transcription factor), the other calcineurin subunit is CNB1; regulates the function of Aly1p alpha-arrestin; CNA1 has a paralog, CMP2, that arose from the whole genome duplication","termid":"PBO:0082461"}


id: GO:1903220
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of malate dehydrogenase (decarboxylating) (NADP+) activity.","definition_xrefs":["GOC:TermGenie","GOC:sart","GO_REF:0000059","PMID:12398416"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of malate dehydrogenase (decarboxylating) (NADP+) activity (obsolete GO:1903220)","synonyms":[{"name":"activation of 'malic' enzyme","type":"related"},{"name":"activation of (S)-malate:NADP+ oxidoreductase (oxaloacetate-decarboxylating)","type":"narrow"},{"name":"activation of L-malate:NADP oxidoreductase activity","type":"narrow"},{"name":"activation of NADP-linked decarboxylating malic enzyme","type":"related"},{"name":"activation of NADP-malic enzyme activity","type":"narrow"},{"name":"activation of NADP-specific malate dehydrogenase activity","type":"narrow"},{"name":"activation of NADP-specific malic enzyme","type":"related"},{"name":"activation of malate dehydrogenase (NADP, decarboxylating)","type":"narrow"},{"name":"activation of malate dehydrogenase (decarboxylating) (NADP+) activity","type":"narrow"},{"name":"activation of malate dehydrogenase (decarboxylating, NADP)","type":"narrow"},{"name":"positive regulation of 'malic' enzyme","type":"related"},{"name":"positive regulation of (S)-malate:NADP+ oxidoreductase (oxaloacetate-decarboxylating)","type":"exact"},{"name":"positive regulation of L-malate:NADP oxidoreductase activity","type":"exact"},{"name":"positive regulation of NADP-linked decarboxylating malic enzyme","type":"related"},{"name":"positive regulation of NADP-malic enzyme activity","type":"exact"},{"name":"positive regulation of NADP-specific malate dehydrogenase activity","type":"exact"},{"name":"positive regulation of NADP-specific malic enzyme","type":"related"},{"name":"positive regulation of malate dehydrogenase (NADP, decarboxylating)","type":"exact"},{"name":"positive regulation of malate dehydrogenase (decarboxylating, NADP)","type":"exact"},{"name":"up regulation of 'malic' enzyme","type":"related"},{"name":"up regulation of (S)-malate:NADP+ oxidoreductase (oxaloacetate-decarboxylating)","type":"exact"},{"name":"up regulation of L-malate:NADP oxidoreductase activity","type":"exact"},{"name":"up regulation of NADP-linked decarboxylating malic enzyme","type":"related"},{"name":"up regulation of NADP-malic enzyme activity","type":"exact"},{"name":"up regulation of NADP-specific malate dehydrogenase activity","type":"exact"},{"name":"up regulation of NADP-specific malic enzyme","type":"related"},{"name":"up regulation of malate dehydrogenase (NADP, decarboxylating)","type":"exact"},{"name":"up regulation of malate dehydrogenase (decarboxylating) (NADP+) activity","type":"exact"},{"name":"up regulation of malate dehydrogenase (decarboxylating, NADP)","type":"exact"},{"name":"up-regulation of 'malic' enzyme","type":"related"},{"name":"up-regulation of (S)-malate:NADP+ oxidoreductase (oxaloacetate-decarboxylating)","type":"exact"},{"name":"up-regulation of L-malate:NADP oxidoreductase activity","type":"exact"},{"name":"up-regulation of NADP-linked decarboxylating malic enzyme","type":"related"},{"name":"up-regulation of NADP-malic enzyme activity","type":"exact"},{"name":"up-regulation of NADP-specific malate dehydrogenase activity","type":"exact"},{"name":"up-regulation of NADP-specific malic enzyme","type":"related"},{"name":"up-regulation of malate dehydrogenase (NADP, decarboxylating)","type":"exact"},{"name":"up-regulation of malate dehydrogenase (decarboxylating) (NADP+) activity","type":"exact"},{"name":"up-regulation of malate dehydrogenase (decarboxylating, NADP)","type":"exact"},{"name":"upregulation of 'malic' enzyme","type":"related"},{"name":"upregulation of (S)-malate:NADP+ oxidoreductase (oxaloacetate-decarboxylating)","type":"exact"},{"name":"upregulation of L-malate:NADP oxidoreductase activity","type":"exact"},{"name":"upregulation of NADP-linked decarboxylating malic enzyme","type":"related"},{"name":"upregulation of NADP-malic enzyme activity","type":"exact"},{"name":"upregulation of NADP-specific malate dehydrogenase activity","type":"exact"},{"name":"upregulation of NADP-specific malic enzyme","type":"related"},{"name":"upregulation of malate dehydrogenase (NADP, decarboxylating)","type":"exact"},{"name":"upregulation of malate dehydrogenase (decarboxylating) (NADP+) activity","type":"exact"},{"name":"upregulation of malate dehydrogenase (decarboxylating, NADP)","type":"exact"}],"termid":"GO:1903220"}


id: PBO:0049498
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H2A clustered histone 5, pseudogene","termid":"PBO:0049498"}


id: PBO:0081767
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 699","termid":"PBO:0081767"}


id: GO:0086018
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that mediates the transfer of information from an SA node cardiomyocyte to an atrial cardiomyocyte.","definition_xrefs":["GOC:mtg_cardiac_conduct_nov11","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-cell signaling involved in cardiac conduction","termid":"GO:0086019"},{"relation_name":"is_a","term_name":"SA node cell to atrial cardiac muscle cell communication","termid":"GO:0086070"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"SA node cell to atrial cardiac muscle cell signaling","synonyms":[{"name":"SA node cardiac muscle cell to atrial cardiac muscle cell signalling","type":"exact"},{"name":"SA node cardiomyocyte to atrial cardiomyocyte signalling","type":"exact"},{"name":"SAN cardiomyocyte to atrial cardiomyocyte signalling","type":"exact"},{"name":"sinoatrial node cardiomyocyte to atrial cardiomyocyte signalling","type":"exact"},{"name":"sinus node cardiomyocyte to atrial cardiomyocyte signalling","type":"narrow"}],"termid":"GO:0086018"}


id: GO:0051171
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of the chemical reactions and pathways involving nitrogen or nitrogenous compounds.","definition_xrefs":["GOC:tb","GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of nitrogen compound metabolic process (obsolete GO:0051171)","termid":"GO:0051171"}


id: GO:0042219
data:
  {"annotated_genes":["SJAG_00903","SJAG_03316","SJAG_01612","SJAG_02100","SJAG_04858"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[102013,76405,73453,78341],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006751"},{"annotations":[74188],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006660"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of compounds derived from amino acids, organic acids containing one or more amino substituents.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified amino acid metabolic process","termid":"GO:0006575"},{"relation_name":"is_a","term_name":"catabolic process","termid":"GO:0009056"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00903":null,"SJAG_01612":null,"SJAG_02100":null,"SJAG_03316":null,"SJAG_04858":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"modified amino acid catabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"amino acid derivative catabolic process","type":"exact"},{"name":"cellular amino acid derivative breakdown","type":"exact"},{"name":"cellular amino acid derivative catabolic process","type":"exact"},{"name":"cellular amino acid derivative catabolism","type":"exact"},{"name":"cellular amino acid derivative degradation","type":"exact"},{"name":"cellular modified amino acid breakdown","type":"exact"},{"name":"cellular modified amino acid catabolic process","type":"exact"},{"name":"cellular modified amino acid catabolism","type":"exact"},{"name":"cellular modified amino acid degradation","type":"exact"},{"name":"modified amino acid catabolism","type":"exact"}],"termid":"GO:0042219","terms_by_termid":{"GO:0006660":null,"GO:0006751":null}}


id: PBO:0041363
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 4 open reading frame 17","termid":"PBO:0041363"}


id: PBO:0059386
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein S22 pseudogene 1","termid":"PBO:0059386"}


id: MONDO:0800491
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neonatal/infantile epilepsy syndrome characterized by frequent drug-resistant seizures that begin ≤3 months of age, with abnormal interictal EEG and neurological examination.","direct_ancestors":[{"relation_name":"is_a","term_name":"neonatal/infantile-onset epilepsy syndrome with developmental and epileptic encephalopathy","termid":"MONDO:0800490"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"early-infantile DEE","synonyms":[{"name":"EIDEE","type":"exact"},{"name":"early-infantile developmental and epileptic encephalopathy syndrome","type":"exact"}],"termid":"MONDO:0800491","xrefs":{"Monarch":{"xref_id":"0800491"}}}


id: PBO:0058392
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4764","termid":"PBO:0058392"}


id: PBO:0109228
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KLF3 pseudogene 2","termid":"PBO:0109228"}


id: SO:0002357
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A physically clustered group of two or more genes in a particular genome that together encode a biosynthetic pathway for the production of a specialized metabolite (including its chemical variants).","definition_xrefs":["PMID:26284661"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biological_region","termid":"SO:0001411"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"biosynthetic_gene_cluster","synonyms":[{"name":"Metabolic gene cluster","type":"exact"}],"termid":"SO:0002357"}


id: PBO:0001090
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA Glycine","termid":"PBO:0001090"}


id: PBO:0004028
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Golgi transport complex subunit Cog5 (predicted)","termid":"PBO:0004028"}


id: GO:1902557
data:
  {"annotated_genes":["SJAG_03334"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[101116],"is_not":false,"summary":null,"term":"GO:1902557"}]},"cv_name":"molecular_function","definition":"Enables the transfer of 5'-adenylyl sulfate from one side of a membrane to the other.","definition_xrefs":["PMID:24296033","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenine nucleotide transmembrane transporter activity","termid":"GO:0000295"},{"relation_name":"is_a","term_name":"purine ribonucleotide transmembrane transporter activity","termid":"GO:0005346"},{"relation_name":"is_a","term_name":"organic anion transmembrane transporter activity","termid":"GO:0008514"},{"relation_name":"is_a","term_name":"sulfur compound transmembrane transporter activity","termid":"GO:1901682"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03334":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"5'-adenylyl sulfate transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1902557","terms_by_termid":{"GO:1902557":null}}


id: MONDO:0017174
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Machado-Joseph disease type 1 is a rare, usually severe subtype of Machado-Joseph disease (SCA3/MJD) characterized by the presence of marked pyramidal and extrapyramidal signs.","definition_xrefs":["Orphanet:276238"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Machado-Joseph disease","termid":"MONDO:0007182"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0005559","MONDO:0002039"],"is_obsolete":false,"name":"Machado-Joseph disease type 1","secondary_identifiers":["icd11.foundation:1094680019","UMLS:C0751668","MEDGEN:155610","GARD:21048","SCTID:91953003"],"synonyms":[{"name":"SCA3, Joseph type","type":"exact"},{"name":"azorean disease, type i","type":"exact"},{"name":"spinocerebellar ataxia type 3, Joseph type","type":"exact"}],"termid":"MONDO:0017174","xrefs":{"Monarch":{"xref_id":"0017174"}}}


id: MONDO:0015095
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Peters anomaly","termid":"MONDO:0011414"}],"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":"Peters anomaly-cataract syndrome","secondary_identifiers":["MEDGEN:419463","Orphanet:101033","UMLS:C2931652","MESH:C537885"],"termid":"MONDO:0015095","xrefs":{"Monarch":{"xref_id":"0015095"}}}


id: FYPO:0001164
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A vegetative cell population growth phenotype in which cells grow normally (i.e. indistinguishably from wild type) in a medium containing glucose as the carbon source.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal vegetative cell population growth","termid":"FYPO:0001357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0002060","FYPO:0002057","FYPO:0000257","FYPO:0000003","FYPO:0002058","FYPO:0000139"],"is_obsolete":false,"name":"normal growth on glucose carbon source","synonyms":[{"name":"normal cell population growth on glucose carbon source","type":"exact"},{"name":"normal vegetative cell population growth on dextrose carbon source","type":"exact"},{"name":"normal vegetative cell population growth on glucose carbon source","type":"exact"}],"termid":"FYPO:0001164"}


id: BFO:0000063
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"x precedes y if and only if the time point at which x ends is before or equivalent to the time point at which y starts. Formally: x precedes y iff ω(x) <= α(y), where α is a function that maps a process to a start point, and ω is a function that maps a process to an end point.","direct_ancestors":[{"relation_name":"is_a","term_name":"temporally_related_to","termid":"RO:0002222"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"precedes","termid":"BFO:0000063"}


id: SO:0000845
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region of sequence which is a promoter for RNA polymerase III type 1.","definition_xrefs":["SO:ke"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:0000845 RNApol_III_promoter_type_1_region (obsolete SO:0000845)","termid":"SO:0000845"}


id: GO:1902804
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of synaptic vesicle transport.","definition_xrefs":["PMID:23527112","GOC:TermGenie","GO_REF:0000058","GOC:kmv"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cellular process","termid":"GO:0048523"},{"relation_name":"is_a","term_name":"negative regulation of transport","termid":"GO:0051051"},{"relation_name":"is_a","term_name":"regulation of synaptic vesicle transport","termid":"GO:1902803"},{"relation_name":"negatively_regulates","term_name":"synaptic vesicle transport","termid":"GO:0048489"}],"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"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"negative regulation of synaptic vesicle transport","synonyms":[{"name":"down regulation of synaptic vesicle fission","type":"related"},{"name":"down regulation of synaptic vesicle fusion","type":"related"},{"name":"down regulation of synaptic vesicle transport","type":"exact"},{"name":"down-regulation of synaptic vesicle fission","type":"related"},{"name":"down-regulation of synaptic vesicle fusion","type":"related"},{"name":"down-regulation of synaptic vesicle transport","type":"exact"},{"name":"downregulation of synaptic vesicle fission","type":"related"},{"name":"downregulation of synaptic vesicle fusion","type":"related"},{"name":"downregulation of synaptic vesicle transport","type":"exact"},{"name":"inhibition of synaptic vesicle fission","type":"related"},{"name":"inhibition of synaptic vesicle fusion","type":"related"},{"name":"inhibition of synaptic vesicle transport","type":"narrow"},{"name":"negative regulation of synaptic vesicle fission","type":"related"},{"name":"negative regulation of synaptic vesicle fusion","type":"related"}],"termid":"GO:1902804"}


id: PBO:0074933
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 100","termid":"PBO:0074933"}


id: MONDO:0015736
data:
  {"annotated_genes":["SJAG_03379","SJAG_03145","SJAG_04887"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85061],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008070"},{"annotations":[84935],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012239"},{"annotations":[86494],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009725"}]},"cv_name":"mondo","definition":"Intermediate nemaline myopathy is a type of nemaline myopathy (NM) that shows features of typical NM in neonates with a more severe progression.","definition_xrefs":["Orphanet:171433"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"myopathy","termid":"MONDO:0005336"},{"relation_name":"is_a","term_name":"qualitative or quantitative defects of alpha-actin","termid":"MONDO:0016193"},{"relation_name":"is_a","term_name":"qualitative or quantitative defects of nebulin","termid":"MONDO:0016194"},{"relation_name":"is_a","term_name":"qualitative or quantitative defects of tropomyosin","termid":"MONDO:0017303"}],"gene_count":3,"genes_by_uniquename":{"SJAG_03145":null,"SJAG_03379":null,"SJAG_04887":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0005336"],"is_obsolete":false,"name":"intermediate nemaline myopathy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1803914","UMLS:C5680452","GARD:12823","icd11.foundation:1667070006"],"synonyms":[{"name":"Intermediate congenital NM","type":"related"},{"name":"Intermediate congenital nemaline myopathy","type":"related"}],"termid":"MONDO:0015736","terms_by_termid":{"MONDO:0008070":null,"MONDO:0009725":null,"MONDO:0012239":null},"xrefs":{"Monarch":{"xref_id":"0015736"}}}


id: PBO:0078862
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TRPC6 pseudogene 10","termid":"PBO:0078862"}


id: PBO:0072172
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S15 pseudogene 9","termid":"PBO:0072172"}


id: GO:0004691
data:
  {"annotated_genes":["SJAG_04312"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[73020],"is_not":false,"summary":null,"term":"GO:0004691"}]},"cv_name":"molecular_function","definition":"cAMP-dependent catalysis of the reaction: ATP + a protein = ADP + a phosphoprotein.","definition_xrefs":["PMID:35805104","PMID:32935175","PMID:35053423"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cyclic nucleotide-dependent protein kinase activity","termid":"GO:0004690"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04312":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0004672"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016301","GO:0016740","GO:0004672","GO:0140096","GO:0003674"],"is_obsolete":false,"name":"cAMP-dependent protein kinase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-177284","Reactome:R-HSA-177275","EC:2.7.11.11","Reactome:R-HSA-5610720","Reactome:R-HSA-5687088","Reactome:R-HSA-432232","Reactome:R-HSA-5617182","GO:0008602","Reactome:R-HSA-9838321","Reactome:R-HSA-913451","Reactome:R-HSA-9861318","Reactome:R-HSA-5610741","Reactome:R-HSA-163676","Reactome:R-HSA-163773","Reactome:R-HSA-163672","Reactome:R-HSA-5610717","Reactome:R-HSA-5617179"],"synonyms":[{"name":"3',5' cAMP-dependent protein kinase activity","type":"exact"},{"name":"3',5'-cAMP-dependent protein kinase activity","type":"exact"},{"name":"AMPK","type":"related"},{"name":"ATP:protein phosphotransferase (cAMP-dependent) activity","type":"related"},{"name":"PKA","type":"related"},{"name":"PKA C","type":"related"},{"name":"STK22","type":"related"},{"name":"adenosine 3',5'-cyclophosphate-dependent protein kinase activity","type":"exact"},{"name":"cAMP-dependent protein kinase, intrinsic catalyst activity","type":"exact"},{"name":"cyclic AMP-dependent protein kinase activity","type":"exact"},{"name":"protein kinase A activity","type":"broad"}],"termid":"GO:0004691","terms_by_termid":{"GO:0004691":null}}


id: PBO:0066941
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 243","termid":"PBO:0066941"}


id: FYPO:0004355
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the phosphorylation of one or more specific proteins, or of specific protein sites, occurs to a greater extent than normal during mitosis.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein phosphorylation during vegetative growth","termid":"FYPO:0001038"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0001320","FYPO:0002494","FYPO:0000002","FYPO:0002274"],"is_obsolete":false,"name":"increased protein phosphorylation during mitosis","synonyms":[{"name":"increased protein phosphorylation during mitosis during vegetative growth","type":"exact"},{"name":"increased protein phosphorylation during mitotic M phase","type":"related"},{"name":"increased protein phosphorylation during mitotic nuclear division","type":"exact"},{"name":"increased protein/peptide phosphorylation during mitosis","type":"exact"}],"termid":"FYPO:0004355"}


id: PBO:0042484
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cadherin 9","termid":"PBO:0042484"}


id: GO:0010071
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The specification of a meristem which will give rise to a primary or lateral root.","definition_xrefs":["GOC:tb","GOC:ascb_2009","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"is_a","term_name":"embryonic meristem initiation","termid":"GO:0090421"},{"relation_name":"part_of","term_name":"root morphogenesis","termid":"GO:0010015"},{"relation_name":"part_of","term_name":"embryonic meristem development","termid":"GO:0048508"}],"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":"root meristem specification","termid":"GO:0010071"}


id: PBO:0069425
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 689, pseudogene","termid":"PBO:0069425"}


id: PBO:0086395
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative cytochrome b5 reductase, localized to the plasma membrane; may be involved in regulation of lifespan; required for maturation of Gas1p and Pho8p, proposed to be involved in protein trafficking; PGA3 has a paralog, AIM33, that arose from the whole genome duplication","termid":"PBO:0086395"}


id: MONDO:0000646
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-metastasizing neoplasm that arises from the ovary. Representative examples include serous cystadenoma, mucinous cystadenoma, clear cell adenofibroma, benign Brenner tumor, thecoma, and fibroma.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign female reproductive system neoplasm","termid":"MONDO:0000624"},{"relation_name":"is_a","term_name":"ovarian neoplasm","termid":"MONDO:0021068"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ovarian benign neoplasm","secondary_identifiers":["MEDGEN:14058","NCIT:C2895","UMLS:C0004997","SCTID:92260003","DOID:0060112","EFO:1000116"],"synonyms":[{"name":"benign neoplasm of ovary","type":"exact"},{"name":"benign neoplasm of the ovary","type":"exact"},{"name":"benign ovarian neoplasm","type":"exact"},{"name":"benign ovarian tumor","type":"exact"},{"name":"benign ovarian tumour","type":"exact"},{"name":"benign tumor of ovary","type":"exact"},{"name":"benign tumor of the ovary","type":"exact"},{"name":"benign tumour of ovary","type":"exact"},{"name":"benign tumour of the ovary","type":"exact"},{"name":"ovary benign neoplasm","type":"exact"}],"termid":"MONDO:0000646","xrefs":{"Monarch":{"xref_id":"0000646"}}}


id: GO:0019914
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Modulation of the activity of the enzyme cyclin-dependent protein kinase activating kinase.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein kinase regulator activity","termid":"GO:0019887"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0030234"}],"interesting_parent_ids":["GO:0030234","GO:0098772","GO:0003674"],"is_obsolete":false,"name":"cyclin-dependent protein kinase activating kinase regulator activity","synonyms":[{"name":"cyclin-dependent protein kinase activating kinase, intrinsic regulator activity","type":"narrow"}],"termid":"GO:0019914"}


id: MONDO:0018274
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"GM3 synthase deficiency is characterized by recurrent seizures (epilepsy) and problems with brain development. Within the first few weeks after birth, affected infants become irritable and develop feeding difficulties and vomiting that prevent them from growing and gaining weight at the usual rate. Seizures begin within the first year of life and worsen over time. Multiple types of seizures are possible, including generalized tonic-clonic seizures (also known as grand mal seizures), which cause muscle rigidity, convulsions, and loss of consciousness. Some affected children also experience prolonged episodes of seizure activity called nonconvulsive status epilepticus. The seizures associated with GM3 synthase deficiency tend to be resistant (refractory) to treatment with antiseizure medications.","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"skin disorder","termid":"MONDO:0005093"},{"relation_name":"excluded_subClassOf","term_name":"skin pigmentation disorder","termid":"MONDO:0019288"},{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"inborn disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylation","termid":"MONDO:0017748"},{"relation_name":"is_a","term_name":"disorder of phospholipids, sphingolipids and fatty acids biosynthesis","termid":"MONDO:0018117"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0002525"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0024322","MONDO:0002525","MONDO:0006025"],"is_obsolete":false,"name":"GM3 synthase deficiency","secondary_identifiers":["OMIM:609056","Orphanet:370938","Orphanet:370933","DOID:0060470","Orphanet:171714","MEDGEN:323005","SCTID:722762005","GARD:12059","UMLS:C1836824"],"synonyms":[{"name":"Amish infantile epilepsy syndrome","type":"exact"},{"name":"GM3 synthase deficiency","type":"exact"},{"name":"SPDRS","type":"exact"},{"name":"ST3GAL5-CDG","type":"exact"},{"name":"disorder of lactosylceramide alpha-2,3-sialyltransferase activity","type":"exact"},{"name":"epilepsy syndrome, infantile-onset symptomatic","type":"exact"},{"name":"infantile-onset symptomatic epilepsy syndrome - developmental stagnation - blindness","type":"exact"},{"name":"infantile-onset symptomatic epilepsy syndrome-developmental stagnation-blindness syndrome","type":"exact"},{"name":"lactosylceramide alpha-2,3-sialyltransferase activity disease","type":"exact"},{"name":"salt & pepper syndrome","type":"exact"},{"name":"salt and pepper developmental regression syndrome","type":"exact"},{"name":"salt and pepper mental retardation syndrome","type":"related"},{"name":"salt-and-pepper syndrome","type":"exact"}],"termid":"MONDO:0018274","xrefs":{"Monarch":{"xref_id":"0018274"}}}


id: GO:0002950
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: an N-acyl-sphingoid base + CDP-ethanolamine = an N-acyl-sphingoid 1-phosphoethanolamine + CMP + H+.","definition_xrefs":["EC:2.7.8.48","PMID:25667419"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphotransferase activity, for other substituted phosphate groups","termid":"GO:0016780"}],"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:0016780"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016740","GO:0016780"],"is_obsolete":false,"name":"ceramide phosphoethanolamine synthase activity","secondary_identifiers":["Reactome:R-HSA-8959462","RHEA:45896"],"termid":"GO:0002950"}


id: PBO:0056717
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mesenchyme homeobox 2","termid":"PBO:0056717"}


id: PBO:0089475
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyridoxal phosphate-dependent transferase, unknown specificity, implicated in sulfur compound metabolism","termid":"PBO:0089475"}


id: PBO:0002440
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iron-sulphur cluster biogenesis protein (predicted)","termid":"PBO:0002440"}


id: PBO:0044617
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dendritic cell associated nuclear protein 1","termid":"PBO:0044617"}


id: MONDO:0019990
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Non-amyloid fibrillary glomerulopathy (non-amyloid FGP) is a rare cause of glomerulonephritis (GN) characterized by glomerular accumulation of non-amyloid fibrils in the mesangium and the glomerular (and rarely tubular) basement membrane, that mainly presents with renal insufficiency, micro-hematuria and nephrotic range proteinuria. Non-amyloid FGP and immunotactoid glomerulopathy (ITG) are often grouped together as pathogenetically related diseases.","definition_xrefs":["Orphanet:97566"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immunotactoid or fibrillary glomerulopathy","termid":"MONDO:0019605"}],"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":"non-amyloid fibrillary glomerulopathy","secondary_identifiers":["MEDGEN:907201","UMLS:C4273674","NORD:2024","SCTID:718192000","GARD:12740"],"synonyms":[{"name":"Congo red-negative amyloidosis-like glomerulopathy","type":"exact"},{"name":"Fibrillary Glomerulonephritis ","type":"exact"},{"name":"fibrillary glomerulonephritis","type":"related"},{"name":"non-amyloid fibrillary glomerulonephritis","type":"exact"}],"termid":"MONDO:0019990","xrefs":{"Monarch":{"xref_id":"0019990"}}}


id: PBO:0081270
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 34","termid":"PBO:0081270"}


id: GO:0051799
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of hair follicle development.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of developmental process","termid":"GO:0051093"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"is_a","term_name":"regulation of hair follicle development","termid":"GO:0051797"},{"relation_name":"negatively_regulates","term_name":"hair follicle development","termid":"GO:0001942"}],"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 hair follicle development","synonyms":[{"name":"down regulation of hair follicle development","type":"exact"},{"name":"down-regulation of hair follicle development","type":"exact"},{"name":"downregulation of hair follicle development","type":"exact"},{"name":"inhibition of hair follicle development","type":"narrow"}],"termid":"GO:0051799"}


id: PBO:0085335
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Phosphatidylserine synthase; functions in phospholipid biosynthesis; transcriptionally repressed by myo-inositol and choline","termid":"PBO:0085335"}


id: GO:0010979
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the rate, frequency or extent of vitamin D 24-hydroxylase activity. Vitamin D 24-hydroxylase activity catalyzes the hydroxylation of C-24 of any form of vitamin D.","definition_xrefs":["GOC:BHF","GOC:dph","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of vitamin D 24-hydroxylase activity (obsolete GO:0010979)","termid":"GO:0010979"}


id: PBO:0042563
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclin dependent kinase like 5","termid":"PBO:0042563"}


id: SO:0000663
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region that can be transcribed into a transfer RNA (tRNA).","direct_ancestors":[{"relation_name":"is_a","term_name":"non_protein_coding","termid":"SO:0000011"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA_encoding","synonyms":[{"name":"tRNA encoding","type":"exact"}],"termid":"SO:0000663"}


id: SO:0000774
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A transmissible element containing genes involved in metabolism, analogous to the pathogenicity islands of gram negative bacteria.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"genomic_island","termid":"SO:0000772"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metabolic_island","synonyms":[{"name":"metabolic island","type":"exact"}],"termid":"SO:0000774"}


id: GO:0044519
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that begins with venom being forced into an organism by the bite or sting of another organism, and ends with the resultant modulation of the activity of a vasoactive intestinal polypeptide receptor in the bitten organism.","definition_xrefs":["GOC:fj","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"envenomation resulting in modulation of receptor activity in another organism","termid":"GO:0044511"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"envenomation resulting in modulation of vasoactive intestinal polypeptide receptor activity in another organism","synonyms":[{"name":"envenomation resulting in modulation of VIP receptor activity in other organism","type":"exact"},{"name":"envenomation resulting in modulation of vasoactive intestinal polypeptide receptor activity in other organism","type":"exact"},{"name":"envenomation resulting in regulation of VIP receptor activity in other organism","type":"exact"},{"name":"envenomation resulting in regulation of vasoactive intestinal polypeptide receptor activity in other organism","type":"exact"}],"termid":"GO:0044519"}


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


id: GO:0034080
data:
  {"annotated_genes":["SJAG_04038","SJAG_03867","SJAG_04696","SJAG_03619","SJAG_00873","SJAG_05273","SJAG_00045","SJAG_04989","SJAG_00307","SJAG_03183","SJAG_02908","SJAG_00756","SJAG_01611","SJAG_04581","SJAG_02303","SJAG_00684","SJAG_02872","SJAG_03905","SJAG_02119","SJAG_04547"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[70003,71213,79680,88632,89827,92557,94456,95227,98899,99151,101820,102658,106121,107098,112858,113963,114823,116210,117438,118556],"is_not":false,"summary":null,"term":"GO:0034080"}]},"cv_name":"biological_process","definition":"The formation of chromatin containing the histone H3 variant CENP-A to form centromeric chromatin. This specialised chromatin occurs at centromeric region in point centromeres, and the central core in modular centromeres.","definition_xrefs":["PMID:18158900","PMID:19217403","PMID:35422390","GOC:mah","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromatin remodeling at centromere","termid":"GO:0031055"},{"relation_name":"part_of","term_name":"centromere complex assembly","termid":"GO:0034508"}],"gene_count":20,"genes_by_uniquename":{"SJAG_00045":null,"SJAG_00307":null,"SJAG_00684":null,"SJAG_00756":null,"SJAG_00873":null,"SJAG_01611":null,"SJAG_02119":null,"SJAG_02303":null,"SJAG_02872":null,"SJAG_02908":null,"SJAG_03183":null,"SJAG_03619":null,"SJAG_03867":null,"SJAG_03905":null,"SJAG_04038":null,"SJAG_04547":null,"SJAG_04581":null,"SJAG_04696":null,"SJAG_04989":null,"SJAG_05273":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0065003"},{"rel_name":"is_a","termid":"GO:0006325"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044085","GO:0065003","GO:0006325","GO:0008150"],"is_obsolete":false,"name":"CENP-A containing chromatin assembly","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0034509","GO:0061641","Reactome:R-HSA-606279"],"synonyms":[{"name":"CENP-A containing chromatin organization","type":"related"},{"name":"CENP-A containing nucleosome assembly","type":"related"},{"name":"CENP-A containing nucleosome assembly at centromere","type":"exact"},{"name":"CENP-A deposition","type":"related"},{"name":"CENP-A loading","type":"related"},{"name":"CenH3-containing nucleosome assembly at centromere","type":"related"},{"name":"DNA replication-independent nucleosome assembly at centromere","type":"exact"},{"name":"centromere specific nucleosome exchange","type":"related"},{"name":"centromere-specific histone exchange","type":"exact"},{"name":"centromeric DNA replication-independent nucleosome assembly","type":"exact"},{"name":"centromeric chromatin organization","type":"related"}],"termid":"GO:0034080","terms_by_termid":{"GO:0034080":null}}


id: PBO:0049802
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypocretin receptor 1","termid":"PBO:0049802"}


id: MONDO:0016938
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndrome caused by partial chromosomal duplication","termid":"MONDO:0000762"},{"relation_name":"is_a","term_name":"chromosome 20 disorder","termid":"MONDO:0700025"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partial trisomy of chromosome 20","secondary_identifiers":["UMLS:C4518509","MEDGEN:1377617","SCTID:726360002","GARD:20858","Orphanet:262692"],"synonyms":[{"name":"partial duplication of chromosome 20","type":"exact"},{"name":"partial trisomy of chromosome type 20","type":"exact"}],"termid":"MONDO:0016938","xrefs":{"Monarch":{"xref_id":"0016938"}}}


id: GO:0140261
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein-containing complex that monoubiquitinates histone H2A on K119, thus it facilitates the maintenance of the transcriptionally repressive state of some genes, such as BCL6. It consists of the corepressor BCOR or BCORL1, a Polycomb group (PcG) and a SCF ubiquitin ligase subcomplexes. In mammals, the core subunits of the complex include the PcG and PcG-associated proteins NSPC1, RING1, RNF2, and RYBP and the components of the SCF ubiquitin ligase, SKP1, and FBXL10.","definition_xrefs":["PMID:22325352","PMID:16943429","PMID:24515802"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear ubiquitin ligase complex","termid":"GO:0000152"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005634","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"BCOR complex","synonyms":[{"name":"BCL6 corepressor (BCOR) complex","type":"exact"},{"name":"BCOR/BCORL1 complex","type":"exact"},{"name":"PRC1.1 complex","type":"exact"},{"name":"non-canonical BCOR-PRC1.1 complex","type":"exact"},{"name":"non-canonical PRC1-BCOR complex","type":"exact"}],"termid":"GO:0140261"}


id: PBO:0046965
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 83 member C","termid":"PBO:0046965"}


id: PBO:0065713
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PVR cell adhesion molecule","termid":"PBO:0065713"}


id: PBO:0047108
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 157 member A","termid":"PBO:0047108"}


id: GO:0002784
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of antimicrobial peptide production.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of production of molecular mediator of immune response","termid":"GO:0002700"},{"relation_name":"is_a","term_name":"regulation of antimicrobial humoral response","termid":"GO:0002759"},{"relation_name":"regulates","term_name":"antimicrobial peptide production","termid":"GO:0002775"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"regulation of antimicrobial peptide production","termid":"GO:0002784"}


id: GO:0004177
data:
  {"annotated_genes":["SJAG_03022","SJAG_01088","SJAG_01896","SJAG_06636","SJAG_00969","SJAG_00181","SJAG_03744","SJAG_02033"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[63549,62171],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004239"},{"annotations":[64254,57774,72493,63548,74088,97599,114197,60080],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070006"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of a single N-terminal amino acid residue from a polypeptide chain.","definition_xrefs":["PMID:24157837","EC:3.4.11.-"],"direct_ancestors":[{"relation_name":"is_a","term_name":"exopeptidase activity","termid":"GO:0008238"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00181":null,"SJAG_00969":null,"SJAG_01088":null,"SJAG_01896":null,"SJAG_02033":null,"SJAG_03022":null,"SJAG_03744":null,"SJAG_06636":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008233"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0008233","GO:0140096","GO:0016787","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"aminopeptidase activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000003":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["https://www.ebi.ac.uk/merops/about/glossary.shtml#AMINOPEPTIDASE","Reactome:R-HSA-2534096","MetaCyc:RXN0-5052","Reactome:R-HSA-1236954","Reactome:R-HSA-983162"],"termid":"GO:0004177","terms_by_termid":{"GO:0004239":null,"GO:0070006":null}}


id: MONDO:0018915
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete pneumococcal meningitis (obsolete MONDO:0018915)","termid":"MONDO:0018915","xrefs":{"Monarch":{"xref_id":"0018915"}}}


id: PBO:0053180
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LEM domain containing 3","termid":"PBO:0053180"}


id: GO:1903023
data:
  {"annotated_genes":["SJAG_02736","SJAG_02169"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[116671],"is_not":false,"summary":null,"term":"GO:1903023"},{"annotations":[90491],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903024"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of formation of an ascospore-type prospore membrane.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:11405625"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell cycle process","termid":"GO:0010564"},{"relation_name":"is_a","term_name":"regulation of cellular component biogenesis","termid":"GO:0044087"},{"relation_name":"is_a","term_name":"regulation of developmental process","termid":"GO:0050793"},{"relation_name":"is_a","term_name":"regulation of cellular component organization","termid":"GO:0051128"},{"relation_name":"is_a","term_name":"regulation of reproductive process","termid":"GO:2000241"},{"relation_name":"regulates","term_name":"ascospore-type prospore membrane formation","termid":"GO:0032120"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02169":null,"SJAG_02736":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0061024"}],"interesting_parent_ids":["GO:0044085","GO:0007049","GO:0008150","GO:0061024"],"is_obsolete":false,"name":"regulation of ascospore-type prospore membrane formation","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"regulation of FSM assembly","type":"exact"},{"name":"regulation of FSM biosynthesis","type":"exact"},{"name":"regulation of FSM formation","type":"exact"},{"name":"regulation of ascospore-type prospore membrane assembly","type":"related"},{"name":"regulation of forespore membrane biosynthesis","type":"exact"},{"name":"regulation of forespore membrane formation","type":"exact"}],"termid":"GO:1903023","terms_by_termid":{"GO:1903023":null,"GO:1903024":null}}


id: PBO:0016092
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"centromere protein Mis20/Eic2","termid":"PBO:0016092"}


id: GO:0048807
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of female genitalia are generated and organized.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"genitalia morphogenesis","termid":"GO:0035112"},{"relation_name":"part_of","term_name":"female genitalia development","termid":"GO:0030540"}],"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":"female genitalia morphogenesis","synonyms":[{"name":"female genital morphogenesis","type":"related"}],"termid":"GO:0048807"}


id: PBO:0090152
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cul4-RING E3 complex WD repeat protein subunit Ddb1","termid":"PBO:0090152"}


id: MONDO:0100512
data:
  {"annotated_genes":["SJAG_01649","SJAG_02658"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86821],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008758"},{"annotations":[85411],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009747"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial DNA depletion syndrome","termid":"MONDO:0018158"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01649":null,"SJAG_02658":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005066"],"is_obsolete":false,"name":"mitochondrial DNA depletion syndrome, hepatocerebral form","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:C580039","Orphanet:254871","icd11.foundation:1285620325","MEDGEN:777993","GARD:20769","UMLS:C3711385"],"synonyms":[{"name":"deoxyguanosine kinase deficiency","type":"exact"},{"name":"mtDNA depletion syndrome, hepatocerebral form","type":"exact"}],"termid":"MONDO:0100512","terms_by_termid":{"MONDO:0008758":null,"MONDO:0009747":null},"xrefs":{"Monarch":{"xref_id":"0100512"}}}


id: MONDO:0012374
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":"brachyphalangy, polydactyly, and tibial aplasia/hypoplasia","secondary_identifiers":["OMIM:609945","MESH:C537100","UMLS:C1864965","MEDGEN:355340"],"synonyms":[{"name":"brachyphalangy, polydactyly and absent tibiae","type":"related"},{"name":"brachyphalangy, polydactyly, and tibial aplasia/hypoplasia","type":"exact"}],"termid":"MONDO:0012374","xrefs":{"Monarch":{"xref_id":"0012374"}}}


id: FYPO:0006921
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the frequency of gene conversion at replication fork barriers is decreased.","definition_xrefs":["PMID:31149897","PMID:28586299","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased gene conversion during vegetative growth","termid":"FYPO:0000185"},{"relation_name":"is_a","term_name":"decreased DNA recombination at mitotic DNA replication fork barriers","termid":"FYPO:0006920"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000293","FYPO:0000002","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"decreased gene conversion at mitotic DNA replication fork barriers","synonyms":[{"name":"decreased gene conversion at mitotic DNA replication fork barriers during mitotic cell cycle","type":"related"},{"name":"decreased gene conversion at mitotic DNA replication fork barriers during vegetative growth","type":"exact"},{"name":"reduced gene conversion at mitotic DNA replication fork barriers","type":"exact"}],"termid":"FYPO:0006921"}


id: PBO:0050072
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homeobox containing 1","termid":"PBO:0050072"}


id: PBO:0056639
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mediator complex subunit 14 pseudogene 1","termid":"PBO:0056639"}


id: GO:0048071
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Establishment of a pattern of pigment in one sex that is not observed in the other sex.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"is_a","term_name":"developmental pigmentation","termid":"GO:0048066"},{"relation_name":"part_of","term_name":"sex differentiation","termid":"GO:0007548"}],"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":"sex-specific pigmentation","termid":"GO:0048071"}


id: PBO:0070721
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L9 pseudogene 26","termid":"PBO:0070721"}


id: PR:O14118
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- efm3 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14118"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein-lysine N-methyltransferase efm3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC3A11.03","synonyms":[{"name":"Spom972h-efm3","type":"exact"},{"name":"elongation factor methyltransferase 3 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14118"}


id: SO:0000650
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Cytosolic SSU rRNA is an RNA component of the small subunit of cytosolic ribosomes.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"derives_from","term_name":"rRNA_small_subunit_primary_transcript","termid":"SO:0000255"},{"relation_name":"is_a","term_name":"cytosolic_rRNA","termid":"SO:0002343"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytosolic_SSU_rRNA","synonyms":[{"name":"cytosolic SSU rRNA","type":"exact"},{"name":"cytosolic SSU ribosomal RNA","type":"exact"},{"name":"cytosolic small subunit rRNA","type":"exact"}],"termid":"SO:0000650"}


id: GO:0045429
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of nitric oxide.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of biosynthetic process","termid":"GO:0009891"},{"relation_name":"is_a","term_name":"regulation of nitric oxide biosynthetic process","termid":"GO:0045428"},{"relation_name":"is_a","term_name":"positive regulation of nitric oxide metabolic process","termid":"GO:1904407"},{"relation_name":"positively_regulates","term_name":"nitric oxide biosynthetic process","termid":"GO:0006809"}],"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 nitric oxide biosynthetic process","synonyms":[{"name":"activation of nitric oxide biosynthetic process","type":"narrow"},{"name":"positive regulation of nitric oxide anabolism","type":"exact"},{"name":"positive regulation of nitric oxide biosynthesis","type":"exact"},{"name":"positive regulation of nitric oxide formation","type":"exact"},{"name":"positive regulation of nitric oxide synthesis","type":"exact"},{"name":"stimulation of nitric oxide biosynthetic process","type":"narrow"},{"name":"up regulation of nitric oxide biosynthetic process","type":"exact"},{"name":"up-regulation of nitric oxide biosynthetic process","type":"exact"},{"name":"upregulation of nitric oxide biosynthetic process","type":"exact"}],"termid":"GO:0045429"}


id: MONDO:0044982
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"pseudoallergy","termid":"MONDO:0044981"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"drug pseudoallergy","secondary_identifiers":["UMLS:C3662272","SCTID:609398007","MEDGEN:783426"],"synonyms":[{"name":"drug allergy","type":"related"},{"name":"drug pseudoallergy","type":"exact"}],"termid":"MONDO:0044982","xrefs":{"Monarch":{"xref_id":"0044982"}}}


id: PBO:0027246
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-polyadenylated_25S_rRNA_absent_from_cell","termid":"PBO:0027246"}


id: PBO:0069787
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1073, pseudogene","termid":"PBO:0069787"}


id: GO:0003027
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that modulates blood pressure by the action of chemoreceptors found in the carotid bodies and their resultant modulation of the vasomotor center. Chemoreceptors respond to oxygen, carbon dioxide and hydrogen ions.","definition_xrefs":["GOC:dph","GOC:mtg_cardio","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of systemic arterial blood pressure by chemoreceptor signaling","termid":"GO:0001979"}],"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 systemic arterial blood pressure by carotid body chemoreceptor signaling","synonyms":[{"name":"carotid body chemoreceptor regulation of systemic arterial blood pressure","type":"exact"},{"name":"carotid body chemoreceptor response to lowering of systemic arterial blood pressure","type":"exact"},{"name":"regulation of systemic arterial blood pressure by carotid body chemoreceptor signalling","type":"exact"},{"name":"vagal reflex","type":"broad"}],"termid":"GO:0003027"}


id: MONDO:0021035
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"alopecia - intellectual disability syndrome","termid":"MONDO:0008756"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alopecia-intellectual disability syndrome 1","secondary_identifiers":["MEDGEN:349263","UMLS:C1859878","DOID:0080628","OMIM:203650"],"synonyms":[{"name":"APMR","type":"broad"},{"name":"APMR1","type":"exact"},{"name":"alopecia-intellectual disability syndrome 1","type":"exact"},{"name":"alopecia-mental retardation syndrome 1","type":"exact"}],"termid":"MONDO:0021035","xrefs":{"Monarch":{"xref_id":"0021035"}}}


id: GO:0034182
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the extent to which the association between sister chromatids of a replicated chromosome is maintained during a mitotic cell cycle.","definition_xrefs":["GOC:vw","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of maintenance of sister chromatid cohesion","termid":"GO:0034091"},{"relation_name":"regulates","term_name":"maintenance of mitotic sister chromatid cohesion","termid":"GO:0034088"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"regulation of maintenance of mitotic sister chromatid cohesion","termid":"GO:0034182"}


id: GO:1990547
data:
  {"annotated_genes":["SJAG_00547"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[67596],"is_not":false,"summary":null,"term":"GO:1990547"}]},"cv_name":"biological_process","definition":"The process in which a phosphate ion is transported across a mitochondrial membrane, into or out of the mitochondrion.","definition_xrefs":["PMID:9099701"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphate ion transmembrane transport","termid":"GO:0035435"},{"relation_name":"is_a","term_name":"mitochondrial transmembrane transport","termid":"GO:1990542"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00547":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0055085","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"mitochondrial phosphate ion transmembrane transport","references_by_uniquename":{"GO_REF:0000002":null},"termid":"GO:1990547","terms_by_termid":{"GO:1990547":null}}


id: FYPO:0008324
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular phenotype observed in the vegetative growth phase of the life cycle in which the total cytosolic ribosome content (monosomes + polysomes) in a cell is lower than normal.","definition_xrefs":["PMID:39358553","PomBase:pc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"altered level of macromolecular complex during vegetative growth","termid":"FYPO:0003684"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"decreased cytosolic ribosome content","termid":"FYPO:0008324"}


id: GO:0051663
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of the nucleus to a specific location within a cell during the establishment and maintenance of the dorsal/ventral axis of the oocyte.","definition_xrefs":["GOC:tb","GOC:ai","GOC:dph","GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleus localization","termid":"GO:0051647"},{"relation_name":"part_of","term_name":"oocyte dorsal/ventral axis specification","termid":"GO:0007310"}],"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":"oocyte nucleus localization involved in oocyte dorsal/ventral axis specification","secondary_identifiers":["GO:0051662"],"synonyms":[{"name":"establishment and maintenance of oocyte nucleus localization during oocyte axis determination","type":"exact"},{"name":"oocyte axis determination, oocyte nucleus localization","type":"exact"},{"name":"oocyte nucleus localisation involved in oocyte dorsal/ventral axis specification","type":"exact"},{"name":"oocyte nucleus localization during oocyte axis determination","type":"related"},{"name":"oocyte nucleus localization involved in oocyte dorsal-ventral axis specification","type":"exact"},{"name":"oocyte nucleus localization involved in oocyte dorsal/ventral axis determination","type":"exact"},{"name":"oocyte nucleus localization involved in oocyte dorsoventral axis specification","type":"exact"}],"termid":"GO:0051663"}


id: MONDO:0009429
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":"hypophosphatemia, renal, with intracerebral calcifications","secondary_identifiers":["MEDGEN:383776","OMIM:241519","UMLS:C1855809","MESH:C565478"],"synonyms":[{"name":"hypophosphatemia, renal, with intracerebral calcifications","type":"exact"}],"termid":"MONDO:0009429","xrefs":{"Monarch":{"xref_id":"0009429"}}}


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


id: GO:1901182
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of camalexin biosynthetic process.","definition_xrefs":["GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of camalexin biosynthetic process (obsolete GO:1901182)","synonyms":[{"name":"regulation of camalexin anabolism","type":"exact"},{"name":"regulation of camalexin biosynthesis","type":"exact"},{"name":"regulation of camalexin formation","type":"exact"},{"name":"regulation of camalexin synthesis","type":"exact"}],"termid":"GO:1901182"}


id: MONDO:1010889
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any neuronal ceroid lipofuscinosis that occurs in sheep due to a mutation in the CLN5 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuronal ceroid lipofuscinosis, sheep","termid":"MONDO:1011578"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuronal ceroid lipofuscinosis, CLN5-related, sheep","secondary_identifiers":["OMIA:001482-9940"],"synonyms":[{"name":"CLN5","type":"exact"},{"name":"neuronal ceroid lipofuscinosis, 5, sheep","type":"related"}],"termid":"MONDO:1010889","xrefs":{"Monarch":{"xref_id":"1010889"}}}


id: MONDO:0002547
data:
  {"annotated_genes":["SJAG_04213","SJAG_01111"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87081,87082],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0024517"}]},"cv_name":"mondo","definition":"A benign or malignant neoplasm arising from the perineural cells in the sheaths surrounding the nerves. Representative examples include neurofibroma, schwannoma, and malignant peripheral nerve sheath tumor.","definition_xrefs":["NCIT:C4972"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peripheral nervous system neoplasm","termid":"MONDO:0001406"},{"relation_name":"is_a","term_name":"glioma","termid":"MONDO:0021042"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01111":null,"SJAG_04213":null},"genotype_count":0,"is_obsolete":false,"name":"nerve sheath neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:D018317","MEDGEN:64639","UMLS:C0206727","ONCOTREE:NST","DOID:3193"],"synonyms":[{"name":"neoplasm of nerve sheath","type":"exact"},{"name":"neoplasm of the nerve sheath","type":"exact"},{"name":"nerve sheath neoplasm","type":"exact"},{"name":"nerve sheath tumor","type":"exact"},{"name":"nerve sheath tumour","type":"exact"},{"name":"peripheral nerve sheath neoplasm","type":"exact"},{"name":"tumor of nerve sheath","type":"exact"},{"name":"tumour of nerve sheath","type":"exact"}],"termid":"MONDO:0002547","terms_by_termid":{"MONDO:0024517":null},"xrefs":{"Monarch":{"xref_id":"0002547"}}}


id: PBO:0001818
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome b2 (L-lactate cytochrome-c oxidoreductase) (predicted)","termid":"PBO:0001818"}


id: PBO:0047122
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FAM167A antisense RNA 1","termid":"PBO:0047122"}


id: GO:0016734
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 8 reduced ferredoxin + 8 H+ + N2 + 16 ATP = 8 oxidized ferredoxin + 2 NH3 + 16 ADP + 16 phosphate.","definition_xrefs":["EC:1.18.6.1"],"gene_count":0,"genotype_count":0,"name":"obsolete molybdenum-iron nitrogenase activity (obsolete GO:0016734)","synonyms":[{"name":"molybdenum-iron nitrogenase activity","type":"exact"}],"termid":"GO:0016734"}


id: PBO:0043283
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-type lectin domain family 4 member G","termid":"PBO:0043283"}


id: GO:0036423
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (2E,6E)-farnesyl diphosphate + 3 isopentenyl diphosphate = 3 diphosphate + all-trans-hexaprenyl diphosphate.","definition_xrefs":["RHEA:27559"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prenyl diphosphate synthase activity","termid":"GO:0120531"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016765"}],"interesting_parent_ids":["GO:0003674","GO:0016765","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"hexaprenyl-diphosphate synthase ((2E,6E)-farnesyl-diphosphate specific) activity","secondary_identifiers":["MetaCyc:TRANS-PENTAPRENYLTRANSFERASE-RXN","KEGG_REACTION:R09245","EC:2.5.1.83"],"synonyms":[{"name":"HexPS activity","type":"exact"},{"name":"hexaprenyl diphosphate synthase activity","type":"broad"},{"name":"hexaprenyl pyrophosphate synthetase activity","type":"broad"}],"termid":"GO:0036423"}


id: FYPO:0004599
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 rate, or speed, of DNA replication is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic DNA replication","termid":"FYPO:0001343"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0000293","FYPO:0000631","FYPO:0000002","FYPO:0001320","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"increased rate of DNA replication during vegetative growth","synonyms":[{"name":"increased rate of DNA replication during mitotic cell cycle","type":"related"}],"termid":"FYPO:0004599"}


id: PBO:0087584
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the Anaphase-Promoting Complex/Cyclosome (APC/C); necessary for maintaining sister chromatid cohesion in prophase I of meiosis by inhibiting premature ubiquitination and subsequent degradation of substrates by the APC(Ama1) ubiquitin ligase","termid":"PBO:0087584"}


id: GO:1905529
data:
  {"annotated_genes":["SJAG_03970"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[87852],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905530"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of uracil import across plasma membrane.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:26536126"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transmembrane transport","termid":"GO:0034762"},{"relation_name":"regulates","term_name":"uracil import across plasma membrane","termid":"GO:0098721"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03970":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0055085","GO:0008150"],"is_obsolete":false,"name":"regulation of uracil import across plasma membrane","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1905529","terms_by_termid":{"GO:1905530":null}}


id: PATO:0001108
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001108 relative amplitude value (obsolete PATO:0001108)","termid":"PATO:0001108"}


id: PBO:0053988
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 1305","termid":"PBO:0053988"}


id: PBO:0069354
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 614, pseudogene","termid":"PBO:0069354"}


id: GO:0140680
data:
  {"annotated_genes":["SJAG_03664"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[66751],"is_not":false,"summary":null,"term":"GO:0140680"}]},"cv_name":"molecular_function","definition":"Catalysis of the removal of a methyl group from a di- or a monomethyl-lysine residue at position 36 of the histone H3 protein. This is a dioxygenase reaction that is dependent on Fe(II) and 2-oxoglutarate.","definition_xrefs":["PMID:20531378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H3K36 demethylase activity","termid":"GO:0051864"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03664":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0032452"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0032452","GO:0003824","GO:0140096","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"histone H3K36me/H3K36me2 demethylase activity","references_by_uniquename":{"GO_REF:0000003":null},"secondary_identifiers":["EC:1.14.11.27","MetaCyc:RXN-13186","RHEA:42032"],"synonyms":[{"name":"histone H3-di/monomethyl-lysine-36 demethylase activity","type":"exact"},{"name":"histone H3K36me demethylase activity","type":"related"},{"name":"histone H3K36me2 demethylase activity","type":"broad"}],"termid":"GO:0140680","terms_by_termid":{"GO:0140680":null}}


id: GO:1900102
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of endoplasmic reticulum unfolded protein response.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of endoplasmic reticulum unfolded protein response","termid":"GO:1900101"},{"relation_name":"is_a","term_name":"negative regulation of intracellular signal transduction","termid":"GO:1902532"},{"relation_name":"is_a","term_name":"negative regulation of response to endoplasmic reticulum stress","termid":"GO:1903573"},{"relation_name":"negatively_regulates","term_name":"endoplasmic reticulum unfolded protein response","termid":"GO:0030968"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"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"],"is_obsolete":false,"name":"negative regulation of endoplasmic reticulum unfolded protein response","synonyms":[{"name":"down regulation of ER unfolded protein response","type":"exact"},{"name":"down regulation of SREBP-mediated signalling pathway","type":"related"},{"name":"down regulation of endoplasmic reticulum unfolded protein response","type":"exact"},{"name":"down regulation of erUPR","type":"exact"},{"name":"down-regulation of ER unfolded protein response","type":"exact"},{"name":"down-regulation of SREBP-mediated signalling pathway","type":"related"},{"name":"down-regulation of endoplasmic reticulum unfolded protein response","type":"exact"},{"name":"down-regulation of erUPR","type":"exact"},{"name":"downregulation of ER unfolded protein response","type":"exact"},{"name":"downregulation of SREBP-mediated signalling pathway","type":"related"},{"name":"downregulation of endoplasmic reticulum unfolded protein response","type":"exact"},{"name":"downregulation of erUPR","type":"exact"},{"name":"inhibition of ER unfolded protein response","type":"exact"},{"name":"inhibition of SREBP-mediated signalling pathway","type":"related"},{"name":"inhibition of endoplasmic reticulum unfolded protein response","type":"narrow"},{"name":"inhibition of erUPR","type":"exact"},{"name":"negative regulation of ER unfolded protein response","type":"exact"},{"name":"negative regulation of SREBP-mediated signalling pathway","type":"related"},{"name":"negative regulation of erUPR","type":"exact"}],"termid":"GO:1900102"}


id: PBO:0060283
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myosin heavy chain gene cluster antisense RNA","termid":"PBO:0060283"}


id: MONDO:0014206
data:
  {"annotated_genes":["SJAG_01159"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85612],"is_not":false,"summary":null,"term":"MONDO:0014206"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary pulmonary alveolar proteinosis","termid":"MONDO:0012580"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01159":null},"genotype_count":0,"is_obsolete":false,"name":"severe early-onset pulmonary alveolar proteinosis due to MARS deficiency","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:17746","UMLS:C4225400","MEDGEN:895551","OMIM:615486","Orphanet:440427"],"synonyms":[{"name":"ILLD","type":"related"},{"name":"PAP, Reunion island type","type":"exact"},{"name":"hereditary pulmonary alveolar proteinosis with hepatic involvement","type":"exact"},{"name":"infantile liver failure syndrome 2","type":"related"},{"name":"infantile liver failure syndrome 2, formerly","type":"related"},{"name":"interstitial lung and liver disease","type":"exact"},{"name":"pulmonary alveolar proteinosis, Reunion Island","type":"related"},{"name":"pulmonary alveolar proteinosis, Reunion island type","type":"exact"}],"termid":"MONDO:0014206","terms_by_termid":{"MONDO:0014206":null},"xrefs":{"Monarch":{"xref_id":"0014206"}}}


id: PR:Q9P7F4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC2E1P3.01 gene.","definition_xrefs":["UniProtKB:Q9P7F4","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":"zinc-type alcohol dehydrogenase-like protein C2E1P3.01 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC2E1P3.01","synonyms":[{"name":"Spom972h-SPAC2E1P3.01","type":"exact"}],"termid":"PR:Q9P7F4"}


id: PBO:0065328
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine protease 52, pseudogene","termid":"PBO:0065328"}


id: PBO:0079516
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TYMS opposite strand RNA","termid":"PBO:0079516"}


id: PBO:0002673
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"splicing associated factor Saf3","termid":"PBO:0002673"}


id: MONDO:0015471
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare epilepsy typically characterized by isolated focal motor and somatosensory seizures. Less frequently other focal seizure types, with or without secondary generalization, have been described. The seizures usually happen when the patient is awake and take a benign course. The condition is transitory, interictal examinations are normal, and there is usually no family history of epilepsy.","definition_xrefs":["Orphanet:1544"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adolescent-onset epilepsy syndrome","termid":"MONDO:0020073"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"benign focal seizures of adolescence","secondary_identifiers":["MEDGEN:896830","UMLS:C4275141","icd11.foundation:1800285392","SCTID:715425000","GARD:18728"],"synonyms":[{"name":"adolescent benign focal crisis","type":"exact"}],"termid":"MONDO:0015471","xrefs":{"Monarch":{"xref_id":"0015471"}}}


id: PR:O94242
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An aspartate--tRNA ligase, mitochondrial that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO04267"],"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":"aspartate--tRNA ligase, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC736.06","secondary_identifiers":["UniProtKB:O94242"],"synonyms":[{"name":"AspRS (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-DARS2","type":"exact"},{"name":"aspartyl-tRNA synthetase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94242"}


id: SO:0001062
data:
  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of a peptide chain which is cleaved off during the formation of the mature 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id: PBO:0047335
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibulin 1","termid":"PBO:0047335"}


id: GO:0120512
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (2E,6E)-farnesoate + O2 + reduced [NADPH--hemoprotein reductase] = H+ + H2O + juvenile hormone III carboxylate + oxidized [NADPH--hemoprotein reductase].","definition_xrefs":["RHEA:43724","PMID:22412378","PMID:38741075"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen","termid":"GO:0016712"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"farnesoate epoxidase activity","secondary_identifiers":["EC:1.14.14.128","MetaCyc:RXN-11770"],"synonyms":[{"name":"CYP15C1 activity","type":"related"}],"termid":"GO:0120512"}


id: MONDO:0012754
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  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"nanophthalmia","termid":"MONDO:0005514"}],"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":"nanophthalmos 3","secondary_identifiers":["GARD:18627","MESH:C567498","OMIM:611897","UMLS:C2678467","MEDGEN:395628"],"synonyms":[{"name":"NNO3","type":"exact"},{"name":"Nanophthalmia 3","type":"related"},{"name":"nanophthalmos 3","type":"exact"}],"termid":"MONDO:0012754","xrefs":{"Monarch":{"xref_id":"0012754"}}}


id: PBO:0053472
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  {"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 440","termid":"PBO:0053472"}


id: PBO:0067491
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 625, pseudogene","termid":"PBO:0067491"}


id: GO:0046360
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of 2-oxobutyrate, the anion of the organic acid 2-oxobutyric acid, which contains a ketone group on carbon 2.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"2-oxobutyrate metabolic process","termid":"GO:0046361"},{"relation_name":"is_a","term_name":"short-chain fatty acid biosynthetic process","termid":"GO:0051790"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"2-oxobutyrate biosynthetic process","synonyms":[{"name":"2-oxobutyrate anabolism","type":"exact"},{"name":"2-oxobutyrate biosynthesis","type":"exact"},{"name":"2-oxobutyrate formation","type":"exact"},{"name":"2-oxobutyrate synthesis","type":"exact"},{"name":"alpha-ketobutyrate biosynthesis","type":"exact"},{"name":"alpha-ketobutyrate biosynthetic process","type":"exact"}],"termid":"GO:0046360"}


id: FYECO:0000393
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which caspofungin was added to the medium or assay buffer in excess compared to standard medium or assay buffers at sub lethal dose for the assayed cell density.","definition_xrefs":["PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"+ caspofungin","termid":"FYECO:0000392"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ caspofungin SLD","termid":"FYECO:0000393"}


id: MONDO:0016974
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An epithelial neoplasm arising from the thymus. It may be associated with myasthenia gravis, pure red cell aplasia, and hypogammaglobulinemia. It includes thymoma type B1 which is a thymoma of low grade malignant potential, thymoma type B2 which is a thymoma of moderate malignancy, and thymoma type B3 which is also known as well differentiated thymic carcinoma.","definition_xrefs":["NCIT:C7114"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukocyte disorder","termid":"MONDO:0004805"},{"relation_name":"is_a","term_name":"thymoma","termid":"MONDO:0006456"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"thymoma type B","secondary_identifiers":["UMLS:C1328042","DOID:3282","Orphanet:263317","ICD10CM:D15.0","MEDGEN:231253","GARD:20893"],"synonyms":[{"name":"Dendritic cell thymoma","type":"exact"},{"name":"dendritic cell thymoma","type":"exact"},{"name":"dendritic cell thymoma (disease)","type":"exact"},{"name":"epithelioid thymoma","type":"exact"},{"name":"plump cell thymoma","type":"exact"},{"name":"primary thymic epithelial neoplasm type B","type":"exact"},{"name":"primary thymic epithelial tumor type B","type":"exact"},{"name":"primary thymic epithelial tumour type B","type":"exact"},{"name":"thymoma type B","type":"exact"}],"termid":"MONDO:0016974","xrefs":{"Monarch":{"xref_id":"0016974"}}}


id: PATO:0001827
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A biological sex quality inhering in an individual or a population by virtue of having internal reproductive organs of one sex and external sexual characteristics of the other sex.","definition_xrefs":["WordNet:WordNet"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenotypic sex","termid":"PATO:0001894"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pseudohermaphrodite","termid":"PATO:0001827"}


id: PBO:0041703
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calmodulin 1 pseudogene 1","termid":"PBO:0041703"}


id: GO:0075045
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of symbiont haustorium formation for nutrient acquisition from host. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of anatomical structure morphogenesis","termid":"GO:0022603"},{"relation_name":"is_a","term_name":"regulation of biological process involved in symbiotic interaction","termid":"GO:0043903"},{"relation_name":"is_a","term_name":"modulation of formation of structure involved in a symbiotic process","termid":"GO:0044145"},{"relation_name":"regulates","term_name":"formation of haustorium for nutrient acquisition","termid":"GO:0052094"}],"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 formation by symbiont of haustorium for nutrient acquisition from host","termid":"GO:0075045"}


id: PBO:0074486
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SMYD3 intronic transcript 1","termid":"PBO:0074486"}


id: PBO:0028406
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-viable_elongated_vegetative_cell_with_swollen_medial_region","termid":"PBO:0028406"}


id: MONDO:0000404
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete cell type cancer (obsolete MONDO:0000404)","termid":"MONDO:0000404","xrefs":{"Monarch":{"xref_id":"0000404"}}}


id: PBO:0026955
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_protein_localization_to_new_growing_cell_tip","termid":"PBO:0026955"}


id: MOD:01355
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces an O3 hydrogen atom of a threonine residue with a carbohydrate-like group composed of Hex1HexNAc1NeuAc1 linked through a glycosidic bond.","definition_xrefs":["Unimod:149#T"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Hex1HexNAc1NeuAc1 glycosylated residue","termid":"MOD:00517"},{"relation_name":"is_a","term_name":"modified L-threonine residue","termid":"MOD:00917"}],"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":"Hex1HexNAc1NeuAc1O-glycosylated threonine","synonyms":[{"name":"Hex(1)HexNAc(1)NeuAc(1)","type":"related"},{"name":"Hex1HexNAc1NeuAc1","type":"related"}],"termid":"MOD:01355"}


id: PBO:0060253
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MYCL pseudogene 3","termid":"PBO:0060253"}


id: FYPO:0005349
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the mitotic spindle pole body (SPB) moves rapidly back and forth to a greater extent and over a larger area than normal, causing increased chromosome movement. Normally, SPB oscillation occurs during mitotic interphase (as well as prophase) but is restricted to a small space.","definition_xrefs":["PMID:19001497","PomBase:mah","PMID:12390246"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal spindle pole body-led chromosome movement during mitotic interphase","termid":"FYPO:0005348"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"increased spindle pole body-led chromosome movement during mitotic interphase","synonyms":[{"name":"increased SPB-led chromosome movement during mitotic interphase","type":"exact"},{"name":"increased mitotic SPB oscillation during mitotic interphase","type":"exact"},{"name":"increased mitotic spindle pole body movement during mitotic interphase","type":"exact"},{"name":"increased mitotic spindle pole body oscillation during mitotic interphase","type":"exact"},{"name":"increased spindle pole body-led chromosome movement during interphase of mitotic cell cycle","type":"exact"},{"name":"increased spindle pole body-led chromosome movement during mitotic interphase during vegetative growth","type":"exact"}],"termid":"FYPO:0005349"}


id: PBO:0078748
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA methyltransferase 10B pseudogene 1","termid":"PBO:0078748"}


id: GO:0030913
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Formation of the junction between an axon and the glial cell that forms the myelin sheath. Paranodal junctions form at each paranode, i.e. at the ends of the unmyelinated nodes of Ranvier.","definition_xrefs":["PMID:14715942"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-cell junction assembly","termid":"GO:0007043"},{"relation_name":"is_a","term_name":"cellular component assembly involved in morphogenesis","termid":"GO:0010927"},{"relation_name":"part_of","term_name":"myelin assembly","termid":"GO:0032288"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"paranodal junction assembly","synonyms":[{"name":"paranodal axoglial junction formation","type":"exact"},{"name":"paranodal junction biosynthesis","type":"exact"},{"name":"paranodal junction formation","type":"exact"}],"termid":"GO:0030913"}


id: FYECO:0000134
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"The assay, or growth of cells, was conducted under strict anaerobic conditions.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping experimental environment","termid":"FYECO:0000132"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anaerobic environment","synonyms":[{"name":"- O","type":"exact"},{"name":"- oxygen","type":"exact"},{"name":"-O","type":"exact"},{"name":"-oxygen","type":"exact"},{"name":"anaerobiosis","type":"exact"},{"name":"minus oxygen","type":"exact"}],"termid":"FYECO:0000134"}


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":["GARD:18924","ICD9:134.0","MedDRA:10028586","MESH:D009198","Orphanet:75110","MEDGEN:10148","SCTID:60412004","icd11.foundation:1367149207","UMLS:C0027030","EFO:0007389","DOID:11080"],"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:0001816
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The appearance of a cytokine due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gene expression","termid":"GO:0010467"},{"relation_name":"is_a","term_name":"multicellular organismal process","termid":"GO:0032501"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"cytokine production","secondary_identifiers":["GO:0042107","GO:0050663","GO:0042032","GO:0042089"],"synonyms":[{"name":"cytokine biosynthetic process","type":"narrow"},{"name":"cytokine metabolic process","type":"narrow"},{"name":"cytokine secretion","type":"narrow"},{"name":"interferon production","type":"narrow"},{"name":"interferon secretion","type":"narrow"},{"name":"interleukin production","type":"narrow"},{"name":"interleukin secretion","type":"narrow"}],"termid":"GO:0001816"}


id: MONDO:0017682
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Intellectual disability-polydactyly-uncombable hair syndrome is a multiple congenital anomalies/dysmorphic syndrome characterized by intellectual disability, postaxial polydactyly, phalangeal hypoplasia, 2-3 toe syndactyly, uncombable hair and facial dysmorphism (including frontal bossing, hypotelorism, narrow palpebral fissures, nasal bridge and lips, prominent nasal root, large abnormal ears with prominent antihelix, poorly folded helix, underdeveloped lobule and antitragus, and micrognathia evolving into prognatism). Cryptorchidism, conductive hearing loss and progressive thoracic kyphosis were also reported.","definition_xrefs":["Orphanet:3082"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intellectual disability-polydactyly-uncombable hair syndrome","secondary_identifiers":["GARD:3141","MESH:C537615","UMLS:C2931547","MEDGEN:444082"],"synonyms":[{"name":"Kozlowski-Krajewska syndrome","type":"exact"},{"name":"intellectual disability, postaxial polydactyly, phalangeal hypoplasia, 2-3 toe syndactyly, unusual face, uncombable hair","type":"related"},{"name":"mental retardation, postaxial polydactyly, phalangeal hypoplasia, 2-3 toe syndactyly, unusual face, uncombable hair","type":"related"}],"termid":"MONDO:0017682","xrefs":{"Monarch":{"xref_id":"0017682"}}}


id: MONDO:0019824
data:
  {"annotated_genes":["SJAG_00301","SJAG_02829","SJAG_00321","SJAG_04398","SJAG_03597","SJAG_04110","SJAG_03698","SJAG_03418"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86094],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012794"},{"annotations":[86636],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008980"},{"annotations":[86722],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032787"},{"annotations":[85665,85666],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0026763"},{"annotations":[86763],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030886"},{"annotations":[85269],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009514"},{"annotations":[84979],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010961"},{"annotations":[86469],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014497"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"pituitary deficiency","termid":"MONDO:0015127"},{"relation_name":"is_a","term_name":"hereditary endocrine growth disease","termid":"MONDO:0015514"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00301":null,"SJAG_00321":null,"SJAG_02829":null,"SJAG_03418":null,"SJAG_03597":null,"SJAG_03698":null,"SJAG_04110":null,"SJAG_04398":null},"genotype_count":0,"is_obsolete":false,"name":"non-acquired pituitary hormone deficiency","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1842784","UMLS:C5681572","Orphanet:95488","ICD10CM:E23.0","GARD:19272"],"termid":"MONDO:0019824","terms_by_termid":{"MONDO:0008980":null,"MONDO:0009514":null,"MONDO:0010961":null,"MONDO:0012794":null,"MONDO:0014497":null,"MONDO:0026763":null,"MONDO:0030886":null,"MONDO:0032787":null},"xrefs":{"Monarch":{"xref_id":"0019824"}}}


id: MONDO:0001134
data:
  {"annotated_genes":["SJAG_03081"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87083],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007781"}]},"cv_name":"mondo","definition":"Hypertension that presents without an identifiable cause.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypertensive disorder","termid":"MONDO:0005044"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03081":null},"genotype_count":0,"is_obsolete":false,"name":"essential hypertension","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:10825","ICD9:401.9","MESH:D000075222","ICD9:401","UMLS:C0085580","SCTID:59621000","icd11.foundation:761947693","Orphanet:243761","MEDGEN:88442"],"synonyms":[{"name":"idiopathic hypertension","type":"exact"},{"name":"primary hypertension","type":"exact"}],"termid":"MONDO:0001134","terms_by_termid":{"MONDO:0007781":null},"xrefs":{"Monarch":{"xref_id":"0001134"}}}


id: PBO:0041278
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C1q and TNF related 4","termid":"PBO:0041278"}


id: MONDO:1012582
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inherited cone-rod dystrophy that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinal degeneration, non-human animal","termid":"MONDO:1010326"},{"relation_name":"is_a","term_name":"perceptual disorders, non-human animal","termid":"MONDO:1011343"},{"relation_name":"is_a","term_name":"hereditary neurological disease, non-human animal","termid":"MONDO:1012972"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cone-rod dystrophy, non-human animal","termid":"MONDO:1012582","xrefs":{"Monarch":{"xref_id":"1012582"}}}


id: PBO:0068598
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U2 small nuclear 49, pseudogene","termid":"PBO:0068598"}


id: FYPO:0006326
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the medial cortical nodes is decreased in the vegetative growth phase of the life cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein localization to medial cortex during vegetative growth","termid":"FYPO:0002557"},{"relation_name":"is_a","term_name":"abnormal protein localization to medial cortical node","termid":"FYPO:0003289"}],"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:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"decreased protein localization to medial cortical node","synonyms":[{"name":"decreased protein localisation to medial cortical node","type":"exact"},{"name":"decreased protein localization to cytokinetic nodes","type":"related"},{"name":"decreased protein localization to medial cortical node during mitotic cell cycle","type":"related"},{"name":"decreased protein localization to medial cortical node during vegetative growth","type":"exact"},{"name":"decreased protein recruitment to medial cortical node","type":"related"},{"name":"reduced protein localization to medial cortical node","type":"exact"}],"termid":"FYPO:0006326"}


id: GO:0001796
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of type IIa hypersensitivity, a type of inflammatory response.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of type II hypersensitivity","termid":"GO:0002892"},{"relation_name":"regulates","term_name":"type IIa hypersensitivity","termid":"GO:0001794"}],"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 type IIa hypersensitivity","termid":"GO:0001796"}


id: PBO:0027510
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_following_spore_germination,_single_cell_division,_unequal_chromosome_segregation","termid":"PBO:0027510"}


id: PBO:0075418
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sperm associated antigen 5","termid":"PBO:0075418"}


id: GO:0052141
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of a motile cell or organism towards a higher concentration of a specific chemical on or near 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 positive chemotaxis on or near host (obsolete GO:0052141)","termid":"GO:0052141"}


id: PBO:0054933
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 2347","termid":"PBO:0054933"}


id: PBO:0072788
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sarcoma antigen 3, pseudogene","termid":"PBO:0072788"}


id: PR:P22191
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPMIT.02 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P22191"],"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 cox1 intron-1 45.6 kDa protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPMIT.02","synonyms":[{"name":"Spom972h-SPMIT.02","type":"exact"},{"name":"maturase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P22191"}


id: GO:1905941
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of gonad development.","definition_xrefs":["GO_REF:0000058","PMID:15342467","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of developmental process","termid":"GO:0051094"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"is_a","term_name":"regulation of gonad development","termid":"GO:1905939"},{"relation_name":"is_a","term_name":"positive regulation of reproductive process","termid":"GO:2000243"},{"relation_name":"positively_regulates","term_name":"gonad development","termid":"GO:0008406"}],"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 gonad development","synonyms":[{"name":"activation of gonad development","type":"narrow"},{"name":"activation of gonadogenesis","type":"narrow"},{"name":"positive regulation of gonadogenesis","type":"exact"},{"name":"up regulation of gonad development","type":"exact"},{"name":"up regulation of gonadogenesis","type":"exact"},{"name":"up-regulation of gonad development","type":"exact"},{"name":"up-regulation of gonadogenesis","type":"exact"},{"name":"upregulation of gonad development","type":"exact"},{"name":"upregulation of gonadogenesis","type":"exact"}],"termid":"GO:1905941"}


id: PR:O94508
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An intron-binding protein aquarius that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02638","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":"pre-mRNA-splicing factor cwf11 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC646.02","secondary_identifiers":["UniProtKB:O94508"],"synonyms":[{"name":"Spom972h-AQR","type":"exact"},{"name":"complexed with cdc5 protein 11 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94508"}


id: PATO:0002161
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"Having two horns or horn-shaped branches.","definition_xrefs":["mondofacto:mondofacto"],"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":"bicornuate","termid":"PATO:0002161"}


id: PBO:0069441
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 706, pseudogene","termid":"PBO:0069441"}


id: GO:0141060
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The disruption of an anatomical structure of another organism, leading to damage or temporary subversion of that structure.","definition_xrefs":["GOC:pg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biological process involved in interspecies interaction between organisms","termid":"GO:0044419"}],"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":"disruption of anatomical structure in another organism","termid":"GO:0141060"}


id: PBO:0061770
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"OBI1 antisense RNA 1","termid":"PBO:0061770"}


id: PBO:0069670
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 947, pseudogene","termid":"PBO:0069670"}


id: GO:0010438
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 deprivation of sulfur.","definition_xrefs":["PMID:17420480"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to starvation","termid":"GO:0009267"}],"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 sulfur starvation","termid":"GO:0010438"}


id: MONDO:0014543
data:
  {"annotated_genes":["SJAG_03056"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85183],"is_not":false,"summary":null,"term":"MONDO:0014543"}]},"cv_name":"mondo","definition":"Any congenital myasthenic syndromes with glycosylation defect in which the cause of the disease is a mutation in the ALG2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital myasthenic syndrome with tubular aggregates","termid":"MONDO:0000182"},{"relation_name":"is_a","term_name":"ALG2-congenital disorder of glycosylation","termid":"MONDO:0011933"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03056":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0024322","MONDO:0005066"],"is_obsolete":false,"name":"congenital myasthenic syndrome 14","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0110669","MEDGEN:864034","GARD:18454","OMIM:616228","UMLS:C4015597"],"synonyms":[{"name":"ALG2 congenital myasthenic syndromes with glycosylation defect","type":"exact"},{"name":"CMS14","type":"exact"},{"name":"CMSTA3","type":"exact"},{"name":"congenital myasthenic syndrome 14","type":"exact"},{"name":"congenital myasthenic syndrome 14, with tubular aggregates","type":"exact"},{"name":"congenital myasthenic syndrome type 14","type":"exact"},{"name":"congenital myasthenic syndrome with tubular aggregates 3","type":"exact"},{"name":"congenital myasthenic syndromes with glycosylation defect caused by mutation in ALG2","type":"exact"},{"name":"myasthenic syndrome, congenital, 14","type":"related"},{"name":"myasthenic syndrome, congenital, 14, with tubular aggregates","type":"exact"},{"name":"myasthenic syndrome, congenital, type 14","type":"exact"},{"name":"myasthenic syndrome, congenital, with tubular aggregates 3","type":"related"}],"termid":"MONDO:0014543","terms_by_termid":{"MONDO:0014543":null},"xrefs":{"Monarch":{"xref_id":"0014543"}}}


id: MONDO:0000643
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-metastasizing neoplasm that arises from the vulva. Representative examples include cellular angiofibroma, melanocytic nevus, nodular hidradenoma, and Bartholin gland adenoma.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign female reproductive system neoplasm","termid":"MONDO:0000624"},{"relation_name":"is_a","term_name":"vulvar neoplasm","termid":"MONDO:0021049"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vulvar benign neoplasm","secondary_identifiers":["SCTID:92486005","UMLS:C0154003","DOID:0060109","MEDGEN:102301","NCIT:C3611"],"synonyms":[{"name":"benign neoplasm of the vulva","type":"exact"},{"name":"benign neoplasm of vulva","type":"exact"},{"name":"benign tumor of the vulva","type":"exact"},{"name":"benign tumor of vulva","type":"exact"},{"name":"benign tumour of the vulva","type":"exact"},{"name":"benign tumour of vulva","type":"exact"},{"name":"benign vulva neoplasm","type":"exact"},{"name":"benign vulva tumor","type":"exact"},{"name":"benign vulva tumour","type":"exact"},{"name":"benign vulval neoplasm","type":"exact"},{"name":"benign vulvar neoplasm","type":"exact"},{"name":"benign vulvar tumor","type":"exact"},{"name":"benign vulvar tumour","type":"exact"},{"name":"mammalian vulva benign neoplasm","type":"exact"},{"name":"vulva benign neoplasm","type":"exact"}],"termid":"MONDO:0000643","xrefs":{"Monarch":{"xref_id":"0000643"}}}


id: GO:0080032
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + methyl (-)-jasmonate = H+ + jasmonate + methanol.","definition_xrefs":["PMID:18467465","RHEA:55372","PMID:15233793"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxylic ester hydrolase activity","termid":"GO:0052689"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016788","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"methyl jasmonate esterase activity","secondary_identifiers":["MetaCyc:RXN-10767"],"synonyms":[{"name":"MEJA esterase activity","type":"exact"},{"name":"jasmonic acid methyl ester esterase activity","type":"exact"},{"name":"methyl JA esterase activity","type":"exact"}],"termid":"GO:0080032"}


id: PBO:0015254
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"E1 ubiquitin-like conjugating enzyme Atg7","termid":"PBO:0015254"}


id: GO:0006507
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The GPI anchor metabolic process that results in enzymatic cleavage of the anchor, releasing an anchored protein from the membrane.","definition_xrefs":["PMID:18811934","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete GPI anchor release (obsolete GO:0006507)","termid":"GO:0006507"}


id: PBO:0012236
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase type 2A Ppa1","termid":"PBO:0012236"}


id: GO:0051564
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the concentration of calcium ions in the smooth endoplasmic reticulum.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of endoplasmic reticulum calcium ion concentration","termid":"GO:0032470"},{"relation_name":"is_a","term_name":"smooth endoplasmic reticulum calcium ion homeostasis","termid":"GO:0051563"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098771"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0098771"],"is_obsolete":false,"name":"positive regulation of smooth endoplasmic reticulum calcium ion concentration","synonyms":[{"name":"elevation of calcium ion concentration in smooth endoplasmic reticulum","type":"exact"},{"name":"elevation of smooth ER calcium ion concentration","type":"exact"},{"name":"elevation of smooth endoplasmic reticulum calcium ion concentration","type":"exact"},{"name":"smooth endoplasmic reticulum calcium ion concentration elevation","type":"exact"}],"termid":"GO:0051564"}


id: PBO:0077285
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 30A","termid":"PBO:0077285"}


id: PBO:0069861
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1148, pseudogene","termid":"PBO:0069861"}


id: PATO:0000827
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000827 visual threshold value (obsolete PATO:0000827)","termid":"PATO:0000827"}


id: PBO:0060397
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NEDD4 binding protein 2 like 1","termid":"PBO:0060397"}


id: MOD:00236
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-asparagine residue to N4-(ADP-ribosyl)-L-asparagine.","definition_xrefs":["PubMed:2498316","PubMed:15842200","RESID:AA0231","Unimod:213#N"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenosine diphosphoribosyl (ADP-ribosyl) modified residue","termid":"MOD:00752"},{"relation_name":"is_a","term_name":"modified L-asparagine residue","termid":"MOD:00903"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N4-(ADP-ribosyl)-L-asparagine","synonyms":[{"name":"(S)-2-amino-4-([adenosine 5'-(trihydrogen diphosphate) 5'->5'-ester with alpha-D-ribofuranosyl]amino)-4-oxobutanoic acid","type":"exact"},{"name":"ADP Ribose addition","type":"related"},{"name":"ADP-Ribosyl","type":"related"},{"name":"MOD_RES ADP-ribosylasparagine","type":"exact"},{"name":"N4-(ADP-ribosyl)-L-asparagine","type":"exact"},{"name":"N4-[alpha-D-ribofuranoside 5'->5'-ester with adenosine 5'-(trihydrogen diphosphate)]-L-asparagine","type":"exact"},{"name":"N4-alpha-D-ribofuranosyl-L-asparagine 5'->5'-ester with adenosine 5'-(trihydrogen diphosphate)","type":"exact"}],"termid":"MOD:00236"}


id: PBO:0001929
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nicotinate phosphoribosyltransferase (predicted)","termid":"PBO:0001929"}


id: PBO:0050677
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock protein family A (Hsp70) member 8 pseudogene 4","termid":"PBO:0050677"}


id: PBO:0042083
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil domain containing 150","termid":"PBO:0042083"}


id: MONDO:1011078
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Urolithiasis that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"urolithiasis, non-human animal","termid":"MONDO:1010267"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"urolithiasis, dog","secondary_identifiers":["OMIA:001033-9615"],"termid":"MONDO:1011078","xrefs":{"Monarch":{"xref_id":"1011078"}}}


id: MONDO:0013113
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any metaphyseal anadysplasia in which the cause of the disease is a mutation in the MMP9 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metaphyseal anadysplasia","termid":"MONDO:0015177"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metaphyseal anadysplasia 2","secondary_identifiers":["MESH:C567771","GARD:15610","MEDGEN:414350","OMIM:613073","UMLS:C2751322"],"synonyms":[{"name":"MANDP2","type":"related"},{"name":"MMP9 metaphyseal anadysplasia","type":"exact"},{"name":"metaphyseal anadysplasia 2","type":"exact"},{"name":"metaphyseal anadysplasia caused by mutation in MMP9","type":"exact"},{"name":"metaphyseal anadysplasia type 2","type":"exact"}],"termid":"MONDO:0013113","xrefs":{"Monarch":{"xref_id":"0013113"}}}


id: PBO:0005315
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit L31 (predicted)","termid":"PBO:0005315"}


id: MONDO:1012454
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital myopathy with fiber-type disproportion, non-human animal","termid":"MONDO:1011804"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital myopathy with fiber-type disproportion, dog","secondary_identifiers":["OMIA:001796-9615"],"termid":"MONDO:1012454","xrefs":{"Monarch":{"xref_id":"1012454"}}}


id: GO:1901920
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any peptidyl-tyrosine dephosphorylation that is involved in activation of protein kinase activity.","definition_xrefs":["PMID:1756737","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-tyrosine dephosphorylation involved in activation of protein kinase activity (obsolete GO:1901920)","synonyms":[{"name":"peptidyl-tyrosine dephosphorylation involved in protein kinase activation","type":"related"}],"termid":"GO:1901920"}


id: PBO:0092031
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA Arginine (ucg), mitochondrial","termid":"PBO:0092031"}


id: GO:0042730
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that solubilizes fibrin in the bloodstream of a multicellular organism, chiefly by the proteolytic action of plasmin.","definition_xrefs":["GOC:jl","PMID:15842654"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of blood coagulation","termid":"GO:0030195"}],"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":"fibrinolysis","secondary_identifiers":["Reactome:R-HSA-75205","Wikipedia:Fibrinolysis"],"termid":"GO:0042730"}


id: MONDO:0100340
data:
  {"annotated_genes":["SJAG_03862"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85317],"is_not":false,"summary":null,"term":"MONDO:0100340"}]},"cv_name":"mondo","definition":"Any Friedreich ataxia in which the cause of the disease is a mutation in the FXN gene.","definition_xrefs":["OMIM:229300"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Friedreich ataxia","termid":"MONDO:0100339"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03862":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005559"],"is_obsolete":false,"name":"Friedreich ataxia 1","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0111218","MESH:C565561","MEDGEN:383962","UMLS:C1856689"],"synonyms":[{"name":"FRDA1","type":"exact"},{"name":"Friedreich ataxia","type":"broad"},{"name":"Friedreich ataxia 1","type":"exact"},{"name":"Friedreich ataxia type 1","type":"exact"}],"termid":"MONDO:0100340","terms_by_termid":{"MONDO:0100340":null},"xrefs":{"Monarch":{"xref_id":"0100340"}}}


id: PBO:0046779
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EXTL3 antisense RNA 1","termid":"PBO:0046779"}


id: PBO:0049375
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"general transcription factor IIIA pseudogene 5","termid":"PBO:0049375"}


id: PBO:0078599
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 12, Y-linked","termid":"PBO:0078599"}


id: MONDO:0004658
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A in situ carcinoma that involves the breast.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"in situ carcinoma","termid":"MONDO:0004647"},{"relation_name":"is_a","term_name":"breast carcinoma","termid":"MONDO:0004989"}],"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":"breast carcinoma in situ","secondary_identifiers":["UMLS:C0154084","NCIT:C3641","DOID:8791","ICD9:233.0","MESH:D000071960","MEDGEN:57817","SCTID:189336000"],"synonyms":[{"name":"breast cancer in situ","type":"exact"},{"name":"breast cancer stage 0","type":"exact"},{"name":"breast carcinoma in situ","type":"exact"},{"name":"breast in situ carcinoma","type":"exact"},{"name":"carcinoma in situ of breast","type":"exact"},{"name":"carcinoma in situ of the breast","type":"exact"},{"name":"in situ breast cancer","type":"exact"},{"name":"non-infiltrating breast carcinoma","type":"exact"},{"name":"non-infiltrating carcinoma of breast","type":"exact"},{"name":"non-infiltrating carcinoma of the breast","type":"exact"},{"name":"non-invasive breast carcinoma","type":"exact"},{"name":"non-invasive carcinoma of breast","type":"exact"},{"name":"non-invasive carcinoma of the breast","type":"exact"},{"name":"stage 0 breast cancer","type":"exact"},{"name":"stage 0 breast cancer aJCC v6","type":"exact"},{"name":"stage 0 breast cancer aJCC v6 and v7","type":"exact"},{"name":"stage 0 breast cancer aJCC v7","type":"exact"},{"name":"stage 0 breast carcinoma","type":"exact"},{"name":"stage 0 breast carcinoma in situ","type":"exact"},{"name":"stage 0 carcinoma of breast","type":"exact"},{"name":"stage 0 carcinoma of the breast","type":"exact"}],"termid":"MONDO:0004658","xrefs":{"Monarch":{"xref_id":"0004658"}}}


id: GO:1900245
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of MDA-5 signaling pathway.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of immune effector process","termid":"GO:0002699"},{"relation_name":"is_a","term_name":"regulation of MDA-5 signaling pathway","termid":"GO:0039533"},{"relation_name":"is_a","term_name":"positive regulation of pattern recognition receptor signaling pathway","termid":"GO:0062208"},{"relation_name":"is_a","term_name":"positive regulation of intracellular signal transduction","termid":"GO:1902533"},{"relation_name":"positively_regulates","term_name":"MDA-5 signaling pathway","termid":"GO:0039530"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of MDA-5 signaling pathway","synonyms":[{"name":"activation of IFIH1 signaling pathway","type":"narrow"},{"name":"activation of MDA-5 signaling pathway","type":"narrow"},{"name":"activation of MDA5 signaling pathway","type":"narrow"},{"name":"activation of melanoma differentiation-associated gene 5 signaling pathway","type":"narrow"},{"name":"positive regulation of IFIH1 signaling pathway","type":"exact"},{"name":"positive regulation of MDA-5 signalling pathway","type":"exact"},{"name":"positive regulation of MDA5 signaling pathway","type":"narrow"},{"name":"positive regulation of melanoma differentiation-associated gene 5 signaling pathway","type":"exact"},{"name":"up regulation of IFIH1 signaling pathway","type":"exact"},{"name":"up regulation of MDA-5 signaling pathway","type":"exact"},{"name":"up regulation of MDA5 signaling pathway","type":"narrow"},{"name":"up regulation of melanoma differentiation-associated gene 5 signaling pathway","type":"exact"},{"name":"up-regulation of IFIH1 signaling pathway","type":"exact"},{"name":"up-regulation of MDA-5 signaling pathway","type":"exact"},{"name":"up-regulation of MDA5 signaling pathway","type":"narrow"},{"name":"up-regulation of melanoma differentiation-associated gene 5 signaling pathway","type":"exact"},{"name":"upregulation of IFIH1 signaling pathway","type":"exact"},{"name":"upregulation of MDA-5 signaling pathway","type":"exact"},{"name":"upregulation of MDA5 signaling pathway","type":"narrow"},{"name":"upregulation of melanoma differentiation-associated gene 5 signaling pathway","type":"exact"}],"termid":"GO:1900245"}


id: GO:0045007
data:
  {"annotated_genes":["SJAG_02261"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[94623],"is_not":false,"summary":null,"term":"GO:0045007"}]},"cv_name":"biological_process","definition":"The disruption of the bond between the sugar in the backbone and the A or G base, causing the base to be removed and leaving a depurinated sugar.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"base-excision repair, AP site formation","termid":"GO:0006285"},{"relation_name":"is_a","term_name":"DNA modification","termid":"GO:0006304"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02261":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006281"},{"rel_name":"part_of","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006259","GO:0006281","GO:0008150"],"is_obsolete":false,"name":"depurination","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-73927","Wikipedia:Depurination"],"termid":"GO:0045007","terms_by_termid":{"GO:0045007":null}}


id: MONDO:0007782
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":"hyperthermia, cutaneous, with headaches and nausea","secondary_identifiers":["OMIM:145590","MEDGEN:374453","MESH:C564156","UMLS:C1840373"],"synonyms":[{"name":"farmer syndrome","type":"related"},{"name":"hyperthermia, cutaneous, with headaches and nausea","type":"exact"}],"termid":"MONDO:0007782","xrefs":{"Monarch":{"xref_id":"0007782"}}}


id: PBO:0081330
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 131","termid":"PBO:0081330"}


id: MONDO:0000516
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A chondroma that involves the phalanx.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bone benign neoplasm","termid":"MONDO:0000631"},{"relation_name":"is_a","term_name":"chondroma","termid":"MONDO:0002360"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phalanx chondroma","secondary_identifiers":["DOID:0050898"],"synonyms":[{"name":"phalanx chondroma","type":"exact"}],"termid":"MONDO:0000516","xrefs":{"Monarch":{"xref_id":"0000516"}}}


id: PBO:0046274
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"essential meiotic structure-specific endonuclease 1","termid":"PBO:0046274"}


id: PBO:0011425
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NuA4 complex phosphatidylinositol pseudokinase complex subunit Tra2","termid":"PBO:0011425"}


id: PBO:0090365
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear envelope Ish domain protein Ish1","termid":"PBO:0090365"}


id: MONDO:0000913
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hereditary spherocytosis in which the cause of the disease is a mutation in the SPTB gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary spherocytosis","termid":"MONDO:0019350"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0002280"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0002280"],"is_obsolete":false,"name":"hereditary spherocytosis type 2","secondary_identifiers":["GARD:16149","MEDGEN:436112","OMIM:616649","DOID:0110917","UMLS:C2674219"],"synonyms":[{"name":"HS2","type":"exact"},{"name":"SPH2","type":"exact"},{"name":"SPTB hereditary spherocytosis","type":"exact"},{"name":"hereditary spherocytosis 2","type":"exact"},{"name":"hereditary spherocytosis caused by mutation in SPTB","type":"exact"},{"name":"hereditary spherocytosis type 2","type":"exact"},{"name":"spherocytosis, hereditary, 2","type":"related"},{"name":"spherocytosis, type 2","type":"exact"}],"termid":"MONDO:0000913","xrefs":{"Monarch":{"xref_id":"0000913"}}}


id: FYPO:0006948
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of protein measured in a cell that is subject to glucose starvation is normal (i.e. indistinguishable from wild type). Total protein or a specific protein may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein level","termid":"FYPO:0004083"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal protein level during glucose starvation","synonyms":[{"name":"normal cellular protein level during glucose starvation","type":"exact"},{"name":"normal protein accumulation during glucose starvation","type":"related"},{"name":"normal protein level during glucose depletion","type":"exact"},{"name":"normal protein level during glucose deprivation","type":"exact"}],"termid":"FYPO:0006948"}


id: PBO:0071157
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L22 pseudogene 22","termid":"PBO:0071157"}


id: PBO:0049206
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamate ionotropic receptor NMDA type subunit 1","termid":"PBO:0049206"}


id: GO:1904691
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of type B pancreatic cell proliferation.","definition_xrefs":["PMID:24055447","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of epithelial cell proliferation","termid":"GO:0050680"},{"relation_name":"is_a","term_name":"regulation of type B pancreatic cell proliferation","termid":"GO:0061469"},{"relation_name":"negatively_regulates","term_name":"type B pancreatic cell proliferation","termid":"GO:0044342"}],"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 type B pancreatic cell proliferation","synonyms":[{"name":"down regulation of pancreatic B cell proliferation","type":"exact"},{"name":"down regulation of pancreatic beta cell proliferation","type":"exact"},{"name":"down regulation of type B pancreatic cell proliferation","type":"exact"},{"name":"down-regulation of pancreatic B cell proliferation","type":"exact"},{"name":"down-regulation of pancreatic beta cell proliferation","type":"exact"},{"name":"down-regulation of type B pancreatic cell proliferation","type":"exact"},{"name":"downregulation of pancreatic B cell proliferation","type":"exact"},{"name":"downregulation of pancreatic beta cell proliferation","type":"exact"},{"name":"downregulation of type B pancreatic cell proliferation","type":"exact"},{"name":"inhibition of pancreatic B cell proliferation","type":"narrow"},{"name":"inhibition of pancreatic beta cell proliferation","type":"narrow"},{"name":"inhibition of type B pancreatic cell proliferation","type":"narrow"},{"name":"negative regulation of pancreatic B cell proliferation","type":"exact"},{"name":"negative regulation of pancreatic beta cell proliferation","type":"exact"}],"termid":"GO:1904691"}


id: FYPO:0002894
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which transcription occurs to a lower extent than normal during a cellular response to calcium ions. All genes, or a specific subset of genes, may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased transcription during vegetative growth","termid":"FYPO:0000781"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000294"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000294","FYPO:0001320","FYPO:0006551","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"decreased transcription during cellular response to calcium ion","synonyms":[{"name":"decreased transcription during cellular response to calcium","type":"exact"},{"name":"decreased transcription during cellular response to calcium ion during mitotic cell cycle","type":"related"},{"name":"decreased transcription during cellular response to calcium ion during vegetative growth","type":"exact"},{"name":"decreased transcription in response to calcium","type":"exact"},{"name":"reduced transcription during cellular response to calcium ion","type":"exact"}],"termid":"FYPO:0002894"}


id: MONDO:0016112
data:
  {"annotated_genes":["SJAG_01939","SJAG_03345"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86493],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008178"},{"annotations":[85214],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010684"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"myopathy","termid":"MONDO:0005336"},{"relation_name":"is_a","term_name":"hereditary skeletal muscle disorder","termid":"MONDO:0700223"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01939":null,"SJAG_03345":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"hereditary inclusion-body myopathy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:20364","UMLS:C5680794","Orphanet:206662","MEDGEN:1843174"],"synonyms":[{"name":"cytoplasmic body myopathy","type":"related"},{"name":"inclusion myopathy","type":"exact"}],"termid":"MONDO:0016112","terms_by_termid":{"MONDO:0008178":null,"MONDO:0010684":null},"xrefs":{"Monarch":{"xref_id":"0016112"}}}


id: PBO:0059348
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein S14","termid":"PBO:0059348"}


id: GO:0090575
data:
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id: PBO:0058421
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id: PBO:0072235
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S20 pseudogene 10","termid":"PBO:0072235"}


id: PBO:0005380
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id: MONDO:0859260
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id: GO:0009338
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id: PBO:0045745
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endogenous Bornavirus like nucleoprotein 2","termid":"PBO:0045745"}


id: PBO:0072360
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S26 pseudogene 46","termid":"PBO:0072360"}


id: PBO:0016897
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id: GO:0009829
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events resulting in chemical or structural alterations of existing cell walls that contribute to fruit ripening.","definition_xrefs":["GOC:lr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plant-type cell wall modification","termid":"GO:0009827"},{"relation_name":"is_a","term_name":"cellular process involved in reproduction in multicellular organism","termid":"GO:0022412"},{"relation_name":"part_of","term_name":"fruit ripening","termid":"GO:0009835"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0071554"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0071554","GO:0008150"],"is_obsolete":false,"name":"cell wall modification involved in fruit ripening","synonyms":[{"name":"cell wall modification during ripening","type":"related"}],"termid":"GO:0009829"}


id: GO:1900474
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id: PBO:0043492
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"contactin 1","termid":"PBO:0043492"}


id: PBO:0001008
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial translation protein (predicted)","termid":"PBO:0001008"}


id: PBO:0028032
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  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_after_spore_germination,_multiple_cell_divisions,_chromosome_fragmentation_upon_segregation","termid":"PBO:0028032"}


id: GO:0018504
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  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: cis-1,2-dihydrobenzene-1,2-diol + NAD+ = catechol + NADH + H+.","definition_xrefs":["EC:1.3.1.19"],"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:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"cis-1,2-dihydrobenzene-1,2-diol dehydrogenase activity","secondary_identifiers":["RHEA:15457","UM-BBD_enzymeID:r0080","MetaCyc:1.3.1.19-RXN"],"synonyms":[{"name":"cis-1,2-dihydrobenzene-1,2-diol:NAD+ oxidoreductase activity","type":"related"},{"name":"cis-1,2-dihydrocyclohexa-3,5-diene (nicotinamide adenine dinucleotide) oxidoreductase activity","type":"related"},{"name":"cis-benzene glycol dehydrogenase activity","type":"related"}],"termid":"GO:0018504"}


id: GO:0060482
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The biological process whose specific outcome is the progression of a lobar bronchus from an initial condition to its mature state. This process begins with the formation of the lobar bronchus and ends with the mature structure. The lobar bronchus is the major airway within the respiratory tree that starts by division of the principal bronchi on both sides and ends at the point of its own subdivision into tertiary or segmental bronchi.","definition_xrefs":["GOC:dph","GOC:mtg_lung"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bronchus development","termid":"GO:0060433"}],"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":"lobar bronchus development","termid":"GO:0060482"}


id: MONDO:0000142
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  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete multiple congenital anomalies-hypotonia-seizures syndrome (obsolete MONDO:0000142)","termid":"MONDO:0000142","xrefs":{"Monarch":{"xref_id":"0000142"}}}


id: MONDO:0000600
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  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A specific phobia that involves an irrational fear of contracting a disease.","definition_xrefs":["DOID:0060048"],"direct_ancestors":[{"relation_name":"is_a","term_name":"specific phobia","termid":"MONDO:0012000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nosophobia","secondary_identifiers":["UMLS:C0522182","MEDGEN:637105"],"termid":"MONDO:0000600","xrefs":{"Monarch":{"xref_id":"0000600"}}}


id: PBO:0064433
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id: MONDO:0002320
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id: GO:0036424
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  {"annotated_genes":["SJAG_04449"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[60891],"is_not":false,"summary":null,"term":"GO:0036424"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: O-phospho-L-serine + H2O = L-serine + phosphate, on a free amino acid.","definition_xrefs":["RHEA:21208","PMID:9188776","PMID:25037224"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatase activity","termid":"GO:0016791"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04449":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:0016787"},{"rel_name":"is_a","termid":"GO:0016788"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0003824","GO:0016788"],"is_obsolete":false,"name":"L-phosphoserine phosphatase activity","references_by_uniquename":{"GO_REF:0000003":null},"secondary_identifiers":["MetaCyc:RXN0-5114","Reactome:R-HSA-977324","GO:0004647","KEGG_REACTION:R00582"],"synonyms":[{"name":"O-phosphoserine phosphohydrolase activity","type":"related"},{"name":"phosphoserine phosphatase activity","type":"related"}],"termid":"GO:0036424","terms_by_termid":{"GO:0036424":null}}


id: PBO:0084136
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"High-affinity copper transporter of plasma membrane; mediates nearly all copper uptake under low copper conditions; transcriptionally induced at low copper levels and degraded at high copper levels; protein increases in abundance and relocalizes from nucleus to plasma membrane upon DNA replication stress; human homolog SLC31A1 can complement a yeast ctr1 ctr3 double deletion","termid":"PBO:0084136"}


id: GO:0048889
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a neuromast support cell. Support cells are non-sensory cells of the neuromast that extend between the sensory hair cells from the basement membrane to the apical surface; they are surrounded by mantle cells.","definition_xrefs":["ISBN:0125296509"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"},{"relation_name":"part_of","term_name":"neuromast development","termid":"GO:0048884"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"neuromast support cell differentiation","termid":"GO:0048889"}


id: PBO:0063297
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protocadherin gamma subfamily C, 4","termid":"PBO:0063297"}


id: MONDO:0024276
data:
  {"annotated_genes":["SJAG_03677","SJAG_03453","SJAG_04067","SJAG_02049","SJAG_01144","SJAG_03787","SJAG_00440","SJAG_01970","SJAG_02231","SJAG_01151"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86940],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014937"},{"annotations":[86412],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007256"},{"annotations":[85931],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0003789"},{"annotations":[86550,86549,86551],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007763"},{"annotations":[85651],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012004"},{"annotations":[85628,87070,87071],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008566"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial neoplasm","termid":"MONDO:0005626"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00440":null,"SJAG_01144":null,"SJAG_01151":null,"SJAG_01970":null,"SJAG_02049":null,"SJAG_02231":null,"SJAG_03453":null,"SJAG_03677":null,"SJAG_03787":null,"SJAG_04067":null},"genotype_count":0,"is_obsolete":false,"name":"glandular cell neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0205854","NCIT:C7132","MEDGEN:64458","HP:0031493"],"synonyms":[{"name":"glandular cell epithelial neoplasm","type":"exact"},{"name":"glandular cell epithelium neoplasm","type":"exact"},{"name":"glandular cell neoplasm","type":"exact"},{"name":"glandular cell tumor","type":"exact"},{"name":"glandular cell tumour","type":"exact"}],"termid":"MONDO:0024276","terms_by_termid":{"MONDO:0003789":null,"MONDO:0007256":null,"MONDO:0007763":null,"MONDO:0008566":null,"MONDO:0012004":null,"MONDO:0014937":null},"xrefs":{"Monarch":{"xref_id":"0024276"}}}


id: MONDO:0015772
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Trisomy 8q is a very rare disorder characterized by duplication of the long arm of chromosome 8. The most commonly associated abnormalities include low birth weight, craniofacial abnormalities (prominent forehead, flat occiput, hypertelorism, upslanting palpebral fissures, ear and nose deformities, thin upper lips), congenital heart defects, skeletal defects, psychomotor retardation. Phenotypic features vary in relation to the duplication size.","definition_xrefs":["Orphanet:1752"],"direct_ancestors":[{"relation_name":"is_a","term_name":"partial duplication of the long arm of chromosome 8","termid":"MONDO:0016959"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trisomy 8q","secondary_identifiers":["NCIT:C36428","GARD:5362","icd11.foundation:573390171","MESH:C538020","UMLS:C0795829","MEDGEN:162775"],"synonyms":[{"name":"8q duplication","type":"related"},{"name":"8q trisomy","type":"related"},{"name":"Duplication 8q","type":"exact"},{"name":"chromosome 8q duplication","type":"related"},{"name":"partial trisomy 8q","type":"related"},{"name":"trisomy type 8q","type":"exact"}],"termid":"MONDO:0015772","xrefs":{"Monarch":{"xref_id":"0015772"}}}


id: GO:0030993
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A kinesin complex found in eukaryotic axonemes that contains two distinct plus end-directed kinesin motor proteins and at least one accessory subunit, and that functions in the anterograde transport of molecules (cargo) from the basal body to the distal tip of the axoneme.","definition_xrefs":["GOC:kmv","PMID:14570576"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"axoneme","termid":"GO:0005930"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0032991","GO:0005737","GO:0005575"],"is_obsolete":false,"name":"axonemal heterotrimeric kinesin-II complex","termid":"GO:0030993"}


id: SO:0000301
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A feature where recombination has occurred for the purpose of generating a diversity in the immune system.","direct_ancestors":[{"relation_name":"is_a","term_name":"recombination_feature_of_rearranged_gene","termid":"SO:0000300"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vertebrate_immune_system_gene_recombination_feature","synonyms":[{"name":"vertebrate immune system gene recombination feature","type":"exact"}],"termid":"SO:0000301"}


id: PBO:0038622
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alkaline ceramidase 3","termid":"PBO:0038622"}


id: PATO:0000215
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000215 respiratory function (obsolete PATO:0000215)","termid":"PATO:0000215"}


id: GO:1903387
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of homophilic cell adhesion.","definition_xrefs":["GO_REF:0000058","PMID:21724833","GOC:TermGenie","GOC:als"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell-cell adhesion","termid":"GO:0022409"},{"relation_name":"is_a","term_name":"regulation of homophilic cell adhesion","termid":"GO:1903385"},{"relation_name":"positively_regulates","term_name":"homophilic cell adhesion via plasma membrane adhesion molecules","termid":"GO:0007156"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0007155"},{"rel_name":"regulates","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"positive regulation of homophilic cell adhesion","synonyms":[{"name":"activation of homophilic cell adhesion","type":"narrow"},{"name":"up regulation of homophilic cell adhesion","type":"exact"},{"name":"up-regulation of homophilic cell adhesion","type":"exact"},{"name":"upregulation of homophilic cell adhesion","type":"exact"}],"termid":"GO:1903387"}


id: MONDO:0010917
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"chondrocalcinosis","termid":"MONDO:0001314"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"chondrocalcinosis 1","secondary_identifiers":["UMLS:C1833499","MESH:C535938","GARD:6048","MEDGEN:331527","OMIM:600668"],"synonyms":[{"name":"CCAL1","type":"exact"},{"name":"chondrocalcinosis 1","type":"exact"},{"name":"chondrocalcinosis with early-onset osteoarthritis","type":"related"}],"termid":"MONDO:0010917","xrefs":{"Monarch":{"xref_id":"0010917"}}}


id: PBO:0028358
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_mitotic_sister_chromatid_separation","termid":"PBO:0028358"}


id: GO:0001851
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a C3b product of the complement cascade.","definition_xrefs":["ISBN:0781735149","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"opsonin binding","termid":"GO:0001846"},{"relation_name":"is_a","term_name":"complement binding","termid":"GO:0001848"}],"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":"complement component C3b binding","termid":"GO:0001851"}


id: PR:Q9P7P6
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pdc102 gene.","definition_xrefs":["UniProtKB:Q9P7P6","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":"pyruvate decarboxylase C186.09 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC186.09","synonyms":[{"name":"Spom972h-pdc102","type":"exact"}],"termid":"PR:Q9P7P6"}


id: GO:1902049
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of neosartoricin.","definition_xrefs":["GOC:di","GOC:TermGenie","PMID:23368997"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenol-containing compound catabolic process","termid":"GO:0019336"},{"relation_name":"is_a","term_name":"polyketide catabolic process","termid":"GO:0030640"},{"relation_name":"is_a","term_name":"ketone catabolic process","termid":"GO:0042182"},{"relation_name":"is_a","term_name":"alcohol catabolic process","termid":"GO:0046164"},{"relation_name":"is_a","term_name":"neosartoricin metabolic process","termid":"GO:1902048"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0019748"],"is_obsolete":false,"name":"neosartoricin catabolic process","synonyms":[{"name":"neosartoricin breakdown","type":"exact"},{"name":"neosartoricin catabolism","type":"exact"},{"name":"neosartoricin degradation","type":"exact"}],"termid":"GO:1902049"}


id: PR:Q9USW8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mni1 gene.","definition_xrefs":["UniProtKB:Q9USW8","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C19C7.01 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC19C7.01","synonyms":[{"name":"Spom972h-mni1","type":"exact"}],"termid":"PR:Q9USW8"}


id: MONDO:0018512
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Any of the forms of epithelial tumor of colon that have a rare incidence.","definition_xrefs":["MONDO:patterns/rare"],"gene_count":0,"genotype_count":0,"name":"obsolete rare epithelial tumor of colon (obsolete MONDO:0018512)","secondary_identifiers":["Orphanet:423991"],"synonyms":[{"name":"rare epithelial tumor of colon","type":"exact"}],"termid":"MONDO:0018512","xrefs":{"Monarch":{"xref_id":"0018512"}}}


id: FYPO:0004878
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 one or more mitotically up-regulated RNAs measured in a cell is lower than normal (i.e. lower than observed in wild-type cells).","definition_xrefs":["PMID:18203864","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased RNA level during vegetative growth","termid":"FYPO:0001117"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0006551","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"decreased level of mitotically up-regulated gene mRNA during vegetative growth","synonyms":[{"name":"decreased level of mitotically up-regulated gene RNA during vegetative growth","type":"exact"},{"name":"decreased level of mitotically up-regulated gene mRNA during mitotic cell cycle","type":"related"},{"name":"decreased level of mitotically up-regulated gene transcripts during vegetative growth","type":"exact"},{"name":"decreased level of mitotically upregulated gene mRNA during vegetative growth","type":"exact"},{"name":"decreased mitotically up-regulated gene mRNA accumulation during vegetative growth","type":"related"},{"name":"reduced level of mitotically up-regulated gene mRNA during vegetative growth","type":"exact"}],"termid":"FYPO:0004878"}


id: MONDO:1010269
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypospadias that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of development or morphogenesis, non-human animal","termid":"MONDO:1011313"},{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"reproductive system disorder, non-human animal","termid":"MONDO:1011354"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypospadias, non-human animal","secondary_identifiers":["OMIA:001187"],"termid":"MONDO:1010269","xrefs":{"Monarch":{"xref_id":"1010269"}}}


id: FYPO:0000882
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 trimethylation of lysine at position 9 of histone H3 occurs to a lower extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone H3-K9 trimethylation during vegetative growth","termid":"FYPO:0000787"},{"relation_name":"is_a","term_name":"decreased histone H3-K9 methylation during vegetative growth","termid":"FYPO:0000872"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002274"}],"interesting_parent_ids":["FYPO:0002494","FYPO:0001985","FYPO:0002274","FYPO:0005447","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"decreased histone H3-K9 trimethylation during vegetative growth","synonyms":[{"name":"decreased histone H3 K9 trimethylation during vegetative growth","type":"exact"},{"name":"decreased histone H3-K9 trimethylation during mitotic cell cycle","type":"related"},{"name":"decreased histone H3K9 trimethylation during vegetative growth","type":"exact"},{"name":"decreased histone H3K9me3 during vegetative growth","type":"exact"},{"name":"decreased histone lysine H3 K9 trimethylation during vegetative growth","type":"exact"},{"name":"reduced histone H3-K9 trimethylation during vegetative growth","type":"exact"}],"termid":"FYPO:0000882"}


id: PBO:0111062
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pig-G, CP2 mannose-ethanolamine phosphotransferase GPI anchor biosynthesis protein Gpi7","termid":"PBO:0111062"}


id: PBO:0004218
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tricothiodystrophy disorder","termid":"PBO:0004218"}


id: MONDO:1011540
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypokalaemic periodic paralysis that occurs in lion.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypokalaemic periodic paralysis, non-human animal","termid":"MONDO:1011434"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypokalaemic periodic paralysis, lion","secondary_identifiers":["OMIA:001759-9689"],"termid":"MONDO:1011540","xrefs":{"Monarch":{"xref_id":"1011540"}}}


id: PR:Q10498
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- hgh1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q10498"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein HGH1 homolog (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC26F1.12c","synonyms":[{"name":"Spom972h-hgh1","type":"exact"}],"termid":"PR:Q10498"}


id: PBO:0085762
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein kinase of the PAK/Ste20 family, required for cell integrity; physically interacts with Cdc31p (centrin), which is a component of the spindle pole body; phosphorylates Cbk1p kinase after allosteric activation by Hym1p; part of the RAM network that regulates cellular polarity and morphogenesis","termid":"PBO:0085762"}


id: GO:0015927
data:
  {"annotated_genes":["SJAG_04859"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[71152],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004555"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of trehalose or a trehalose derivative.","definition_xrefs":["GOC:ai","PMID:31925485"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, hydrolyzing O-glycosyl compounds","termid":"GO:0004553"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04859":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016798","GO:0016787"],"is_obsolete":false,"name":"trehalase activity","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0015927","terms_by_termid":{"GO:0004555":null}}


id: GO:0019377
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of glycolipid, a class of 1,2-di-O-acylglycerols joined at oxygen 3 by a glycosidic linkage to a carbohydrate part (usually a mono-, di- or tri-saccharide).","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycolipid metabolic process","termid":"GO:0006664"},{"relation_name":"is_a","term_name":"membrane lipid catabolic process","termid":"GO:0046466"},{"relation_name":"is_a","term_name":"carbohydrate derivative catabolic process","termid":"GO:1901136"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"glycolipid catabolic process","synonyms":[{"name":"glycolipid breakdown","type":"exact"},{"name":"glycolipid catabolism","type":"exact"},{"name":"glycolipid degradation","type":"exact"}],"termid":"GO:0019377"}


id: GO:0015886
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of heme, any compound of iron complexed in a porphyrin (tetrapyrrole) ring, into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nitrogen compound transport","termid":"GO:0071705"},{"relation_name":"is_a","term_name":"iron coordination entity transport","termid":"GO:1901678"}],"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"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"heme transport","synonyms":[{"name":"haem transport","type":"exact"}],"termid":"GO:0015886"}


id: PR:O94324
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ppk31 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94324"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine-protein kinase ppk31 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC725.06c","synonyms":[{"name":"Spom972h-ppk31","type":"exact"},{"name":"meiotically up-regulated gene 25 protein (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94324"}


id: GO:1904008
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. 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 monosodium glutamate stimulus.","definition_xrefs":["PMID:20704590","GO_REF:0000071","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete response to monosodium glutamate (obsolete GO:1904008)","termid":"GO:1904008"}


id: MOD:00562
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Isotopic label","definition_xrefs":["Unimod:212","PubMed:12766232"],"direct_ancestors":[{"relation_name":"is_a","term_name":"(2)H deuterium tagged reagent","termid":"MOD:01431"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-ethyl iodoacetamide-d5","synonyms":[{"name":"N-ethyl iodoacetamide-d5","type":"related"},{"name":"NEIAA:2H(5)","type":"related"}],"termid":"MOD:00562"}


id: PBO:0043052
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CHP1 pseudogene 2","termid":"PBO:0043052"}


id: PR:Q9US13
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A 26S proteasome non-ATPase regulatory subunit 13 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR10539:SF0","OMA:SCHPO00842","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":"26S proteasome regulatory subunit rpn9 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC607.05","secondary_identifiers":["UniProtKB:Q9US13"],"synonyms":[{"name":"Spom972h-PSMD13","type":"exact"}],"termid":"PR:Q9US13"}


id: RO:0002472
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"A relationship between a piece of evidence a and some entity b, where b is  an information content entity, material entity or process, and \\nthe a supports either the existence of b, or the truth value of b.","direct_ancestors":[{"relation_name":"is_a","term_name":"related_via_evidence_or_inference_to","termid":"RO:0002616"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"is_evidence_for","termid":"RO:0002472"}


id: GO:0018423
data:
  {"annotated_genes":["SJAG_02660"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[75816],"is_not":false,"summary":null,"term":"GO:0018423"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + [protein]-L-leucine = S-adenosyl-L-homocysteine + [protein]-L-leucine methyl ester. This modification occurs only at the oxygen atoms of the free alpha carboxyl group of a leucine residue at the C-terminus of the protein.","definition_xrefs":["PMID:8514774"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein C-terminal carboxyl O-methyltransferase activity","termid":"GO:0003880"},{"relation_name":"is_a","term_name":"S-adenosylmethionine-dependent methyltransferase activity","termid":"GO:0008757"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02660":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0008276"},{"rel_name":"is_a","termid":"GO:0140096"}],"interesting_parent_ids":["GO:0003824","GO:0008276","GO:0016741","GO:0003674","GO:0016740","GO:0140096"],"is_obsolete":false,"name":"protein C-terminal leucine carboxyl O-methyltransferase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-8856945"],"synonyms":[{"name":"protein phosphatase methyltransferase activity","type":"narrow"},{"name":"protein-leucine O-methyltransferase activity","type":"exact"}],"termid":"GO:0018423","terms_by_termid":{"GO:0018423":null}}


id: MONDO:0016563
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"PSP-corticobasal syndrome (PSP-CBS) is an atypical variant of progressive supranuclear palsy (PSP), a rare late-onset neurodegenerative disease.","definition_xrefs":["Orphanet:240103"],"direct_ancestors":[{"relation_name":"is_a","term_name":"atypical progressive supranuclear palsy syndrome","termid":"MONDO:0020488"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"progressive supranuclear palsy-corticobasal syndrome","secondary_identifiers":["GARD:20648","MEDGEN:1781130","UMLS:C5548189"],"synonyms":[{"name":"PSP-CBS","type":"exact"},{"name":"PSP-corticobasal syndrome","type":"exact"}],"termid":"MONDO:0016563","xrefs":{"Monarch":{"xref_id":"0016563"}}}


id: PBO:0001380
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc ion transporter Zhf1","termid":"PBO:0001380"}


id: MOD:00459
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a residue alpha-amino- or alpha-imino-hydrogen with a 4x(13)C labeled succinyl group.","definition_xrefs":["PubMed:11857757","PubMed:12175151","Unimod:66#N-term"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alpha-amino succinylated residue","termid":"MOD:00457"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"4x(13)C labeled alpha-amino succinylated residue","synonyms":[{"name":"Succinic anhydride labeling reagent, heavy form (+4amu, 4C13), N-term & K","type":"related"},{"name":"Succinyl:13C(4)","type":"related"}],"termid":"MOD:00459"}


id: GO:0030426
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The migrating motile tip of a growing neuron projection, where actin accumulates, and the actin cytoskeleton is the most dynamic.","definition_xrefs":["ISBN:0815316194","GOC:aruk","PMID:10082468","GOC:bc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"site of polarized growth","termid":"GO:0030427"},{"relation_name":"part_of","term_name":"distal axon","termid":"GO:0150034"}],"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":"growth cone","secondary_identifiers":["Wikipedia:Growth_cone"],"termid":"GO:0030426"}


id: GO:0016711
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a flavonoid + NADPH + H+ + O2 = 3'-hydroxyflavonoid + NADP+ + H2O.","definition_xrefs":["EC:1.14.14.82"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen","termid":"GO:0016709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"flavonoid 3'-monooxygenase activity","secondary_identifiers":["MetaCyc:FLAVONOID-3-MONOOXYGENASE-RXN","RHEA:16337"],"synonyms":[{"name":"NADPH:flavonoid-3'-hydroxylase activity","type":"related"},{"name":"flavonoid 3'-hydroxylase activity","type":"related"},{"name":"flavonoid 3-hydroxylase","type":"related"},{"name":"flavonoid 3-monooxygenase","type":"related"},{"name":"flavonoid,NADPH:oxygen oxidoreductase (3'-hydroxylating)","type":"related"}],"termid":"GO:0016711"}


id: PBO:0073756
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 2 member 10","termid":"PBO:0073756"}


id: PBO:0050420
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein F pseudogene 1","termid":"PBO:0050420"}


id: GO:0030356
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete small cytoplasmic ribonucleoprotein (obsolete GO:0030356)","synonyms":[{"name":"scRNP","type":"exact"},{"name":"small cytoplasmic ribonucleoprotein","type":"exact"}],"termid":"GO:0030356"}


id: MONDO:0019541
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete non-infectious posterior uveitis (obsolete MONDO:0019541)","secondary_identifiers":["Orphanet:90061","icd11.foundation:2140734738"],"synonyms":[{"name":"non-infectious choroiditis","type":"exact"}],"termid":"MONDO:0019541","xrefs":{"Monarch":{"xref_id":"0019541"}}}


id: PBO:0057194
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIR365B and MIR4725 host gene","termid":"PBO:0057194"}


id: MONDO:0015182
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete congenital enteropathy involving intestinal mucosa development (obsolete MONDO:0015182)","secondary_identifiers":["Orphanet:104007"],"termid":"MONDO:0015182","xrefs":{"Monarch":{"xref_id":"0015182"}}}


id: PBO:0028656
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-S-shaped_cell","termid":"PBO:0028656"}


id: PBO:0064314
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phospholipid phosphatase 3","termid":"PBO:0064314"}


id: PBO:0063990
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi-interacting RNA cluster 24","termid":"PBO:0063990"}


id: GO:0047612
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a carboxylate + CoA + GTP = acyl-CoA + GDP + H+ + phosphate.","definition_xrefs":["RHEA:10968"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acid-thiol ligase activity","termid":"GO:0016878"}],"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:0016874"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016874"],"is_obsolete":false,"name":"acid-CoA ligase (GDP-forming) activity","secondary_identifiers":["MetaCyc:ACID--COA-LIGASE-GDP-FORMING-RXN","EC:6.2.1.10","KEGG_REACTION:R00394"],"synonyms":[{"name":"acid:CoA ligase (GDP-forming)","type":"related"},{"name":"acyl coenzyme A synthetase (guanosine diphosphate forming)","type":"related"},{"name":"acyl-CoA synthetase (GDP-forming) activity","type":"related"}],"termid":"GO:0047612"}


id: PBO:0048292
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"galactose-1-phosphate uridylyltransferase","termid":"PBO:0048292"}


id: PBO:0035875
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_histone_H3_acetylation_at_centromere_central_core_during_vegetative_growth","termid":"PBO:0035875"}


id: GO:0075512
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any clathrin-mediated endocytosis that is involved in the uptake of a virus into a host cell. Begins by invagination of a specific region of the host cell plasma membrane around the bound virus to form a clathrin-coated pit, which then pinches off to form a clathrin-coated endocytic vesicle containing the virus.","definition_xrefs":["VZ:957","GOC:bf","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"receptor-mediated endocytosis of virus by host cell","termid":"GO:0019065"},{"relation_name":"is_a","term_name":"clathrin-dependent endocytosis","termid":"GO:0072583"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0016192","GO:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"clathrin-dependent endocytosis of virus by host cell","secondary_identifiers":["GO:0075516"],"synonyms":[{"name":"clathrin-mediated endocytosis of virus by host cell","type":"exact"},{"name":"viral entry into host cell via clathrin-mediated endocytosis","type":"related"},{"name":"viral entry into host cell via clathrin-mediated endocytosis followed by endosome lysis","type":"narrow"},{"name":"viral penetration via clathrin-mediated endocytosis","type":"exact"}],"termid":"GO:0075512"}


id: PBO:0088857
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mating-type transcription factor (Pc-like)","termid":"PBO:0088857"}


id: PBO:0075406
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sperm acrosome associated 4","termid":"PBO:0075406"}


id: PBO:0069081
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 328, pseudogene","termid":"PBO:0069081"}


id: PBO:0057224
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 380","termid":"PBO:0057224"}


id: PBO:0047134
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 171 member B","termid":"PBO:0047134"}


id: GO:2000612
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of thyroid-stimulating hormone secretion.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of peptide hormone secretion","termid":"GO:0090276"},{"relation_name":"regulates","term_name":"thyroid-stimulating hormone secretion","termid":"GO:0070460"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"regulation of thyroid-stimulating hormone secretion","synonyms":[{"name":"regulation of TSH secretion","type":"exact"},{"name":"regulation of thyroid stimulating hormone secretion","type":"exact"}],"termid":"GO:2000612"}


id: MONDO:0100505
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Dermatitis caused by an allergic reaction to ingested food.","definition_xrefs":["NCIT:C34534"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dermatitis","termid":"MONDO:0002406"}],"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":"food dermatitis","synonyms":[{"name":"dermatitis due to food taken internally","type":"exact"}],"termid":"MONDO:0100505","xrefs":{"Monarch":{"xref_id":"0100505"}}}


id: PBO:0087776
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit Va of cytochrome c oxidase; cytochrome c oxidase is the terminal member of the mitochondrial inner membrane electron transport chain; Cox5Ap is predominantly expressed during aerobic growth while its isoform Vb (Cox5Bp) is expressed during anaerobic growth; COX5A has a paralog, COX5B, that arose from the whole genome duplication","termid":"PBO:0087776"}


id: MONDO:0003270
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete ganglioglioma (obsolete MONDO:0003270)","termid":"MONDO:0003270","xrefs":{"Monarch":{"xref_id":"0003270"}}}


id: MONDO:0014777
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hypotonia, infantile, with psychomotor retardation and characteristic facies in which the cause of the disease is a mutation in the UNC80 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypotonia, infantile, with psychomotor retardation and characteristic facies","termid":"MONDO:0014176"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0005559"],"is_obsolete":false,"name":"hypotonia, infantile, with psychomotor retardation and characteristic facies 2","secondary_identifiers":["MEDGEN:907651","GARD:18458","OMIM:616801","UMLS:C4225203"],"synonyms":[{"name":"IHPRF2","type":"exact"},{"name":"UNC80 hypotonia, infantile, with psychomotor retardation and characteristic facies","type":"exact"},{"name":"hypotonia, infantile, with psychomotor retardation and characteristic facies 2","type":"exact"},{"name":"hypotonia, infantile, with psychomotor retardation and characteristic facies 2; IHPRF2","type":"exact"},{"name":"hypotonia, infantile, with psychomotor retardation and characteristic facies caused by mutation in UNC80","type":"exact"},{"name":"hypotonia, infantile, with psychomotor retardation and characteristic facies type 2","type":"exact"}],"termid":"MONDO:0014777","xrefs":{"Monarch":{"xref_id":"0014777"}}}


id: PBO:0055562
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 2998","termid":"PBO:0055562"}


id: FYPO:0006193
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which the size, shape, or structure of the mating projection is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal subcellular component","termid":"FYPO:0001233"},{"relation_name":"output_of","term_name":"normal shmoo formation","termid":"FYPO:0000573"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"output_of","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal shmoo morphology","synonyms":[{"name":"normal conjugation tube morphology","type":"exact"},{"name":"normal mating projection morphology","type":"exact"}],"termid":"FYPO:0006193"}


id: PBO:0075797
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SS18 subunit of BAF chromatin remodeling complex","termid":"PBO:0075797"}


id: GO:0015649
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: 2-keto-3-deoxygluconate(out) + H+(out) = 2-keto-3-deoxygluconate(in) + H+(in).","definition_xrefs":["RHEA:29943","TC:2.A.10.1.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbohydrate:proton symporter activity","termid":"GO:0005351"},{"relation_name":"is_a","term_name":"monosaccharide transmembrane transporter activity","termid":"GO:0015145"},{"relation_name":"is_a","term_name":"secondary active monocarboxylate transmembrane transporter activity","termid":"GO:0015355"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"2-keto-3-deoxygluconate:proton symporter activity","secondary_identifiers":["MetaCyc:TRANS-RXN-113"],"synonyms":[{"name":"2-keto-3-deoxygluconate:hydrogen symporter activity","type":"exact"}],"termid":"GO:0015649"}


id: PBO:0068705
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U4 small nuclear 86, pseudogene","termid":"PBO:0068705"}


id: GO:0016990
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-arginine + H2O = L-citrulline + NH3.","definition_xrefs":["EC:3.5.3.6"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amidines","termid":"GO:0016813"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016810","GO:0016787","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"arginine deiminase activity","secondary_identifiers":["RHEA:19597","MetaCyc:ARGININE-DEIMINASE-RXN"],"synonyms":[{"name":"L-arginine deiminase activity","type":"related"},{"name":"L-arginine iminohydrolase activity","type":"related"},{"name":"arginine dihydrolase activity","type":"related"},{"name":"citrulline iminase activity","type":"related"}],"termid":"GO:0016990"}


id: MONDO:0030677
data:
  {"annotated_genes":["SJAG_00637"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86878],"is_not":false,"summary":null,"term":"MONDO:0030677"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Charcot-Marie-Tooth disease","termid":"MONDO:0015626"},{"relation_name":"is_a","term_name":"POLR3B-related disorder","termid":"MONDO:0700277"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00637":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"Charcot-Marie-Tooth disease, demyelinating, IIA 1I","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:619742","UMLS:C5676914","MEDGEN:1811493"],"synonyms":[{"name":"CMT1I","type":"exact"},{"name":"Charcot-Marie-Tooth disease neuropathy, IIA 1I","type":"exact"},{"name":"Charcot-Marie-Tooth disease, demyelinating, IIA 1I","type":"exact"}],"termid":"MONDO:0030677","terms_by_termid":{"MONDO:0030677":null},"xrefs":{"Monarch":{"xref_id":"0030677"}}}


id: GO:0102617
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: oryzalexin B + NAD(P) = oryzalexin C + H+ + NAD(P)H.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete oryzalexin C synthase (oryzalexin B dependent) activity (obsolete GO:0102617)","termid":"GO:0102617"}


id: GO:1990716
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Part of the 9+2 axoneme, that occurs in most motile cilia, consisting of the pair of two single central microtubules and their associated structures which include the central pair projections, the central pair bridges linking the two tubules, and the central pair caps which are attached to the distal or plus ends of the microtubules.","definition_xrefs":["PMID:21586547","PMID:9295136","GOC:cilia"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"axoneme","termid":"GO:0005930"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0005737"],"is_obsolete":false,"name":"axonemal central apparatus","termid":"GO:1990716"}


id: PBO:0029991
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-growth_auxotrophic_for_thiamine","termid":"PBO:0029991"}


id: PBO:0001600
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha-amylase homolog Mde5","termid":"PBO:0001600"}


id: GO:0080109
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: indole-3-acetonitrile + H2O = indole-3-acetamide.","definition_xrefs":["MetaCyc:RXN-7567","PMID:11607511","PMID:12430025"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nitrile hydratase activity","termid":"GO:0018822"}],"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:0003824","GO:0003674","GO:0016829"],"is_obsolete":false,"name":"indole-3-acetonitrile nitrile hydratase activity","secondary_identifiers":["KEGG_REACTION:R04020"],"termid":"GO:0080109"}


id: MONDO:0009421
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hypogonadism","termid":"MONDO:0002146"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypogonadism, male","secondary_identifiers":["MEDGEN:57480","UMLS:C0151721","ICD9:257.2","OMIM:241100","SCTID:48723006"],"synonyms":[{"name":"hypogonadism and testicular atrophy","type":"related"},{"name":"hypogonadism, male","type":"exact"}],"termid":"MONDO:0009421","xrefs":{"Monarch":{"xref_id":"0009421"}}}


id: PBO:0055192
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 2616","termid":"PBO:0055192"}


id: PBO:0028841
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-heterochromatin_assembly_beyond_boundary_element_IRC3L","termid":"PBO:0028841"}


id: GO:0080106
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 7-methylthiopropyl-glucosinolate = 7-methylsulfinylpropyl-glucosinolate.","definition_xrefs":["PMID:18799661"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen","termid":"GO:0016705"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"7-methylthiopropyl glucosinolate S-oxygenase activity","termid":"GO:0080106"}


id: MONDO:0001119
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cessation of menstruation before the age of 40. Symptoms include hot flashes, night sweats, mood swings, and decreased sex drive.","definition_xrefs":["NCIT:C80099"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary ovarian failure","termid":"MONDO:0005387"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"premature menopause","secondary_identifiers":["DOID:10787","MEDGEN:9963","MESH:D008594","UMLS:C0025322","ICD9:256.39","ICD9:256.31","EFO:0009005","SCTID:237788002"],"synonyms":[{"name":"POF","type":"exact"},{"name":"early menopause","type":"exact"},{"name":"menopause - premature","type":"exact"},{"name":"menopause praecox","type":"exact"},{"name":"premature menopause","type":"exact"},{"name":"premature ovarian failure","type":"exact"}],"termid":"MONDO:0001119","xrefs":{"Monarch":{"xref_id":"0001119"}}}


id: GO:0071897
data:
  {"annotated_genes":["SJAG_16460","SJAG_00814","SJAG_00611","SJAG_03906","SJAG_02527","SJAG_00573","SJAG_02194","SJAG_01677","SJAG_05239","SJAG_00198","SJAG_00939","SJAG_05979","SJAG_04266","SJAG_04586","SJAG_04791","SJAG_03855","SJAG_03685","SJAG_00406","SJAG_04190","SJAG_02658","SJAG_01378","SJAG_02199","SJAG_05197","SJAG_02818","SJAG_00153","SJAG_04089","SJAG_04877","SJAG_02667"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[59897,62909,63137,69260],"is_not":false,"summary":null,"term":"GO:0071897"},{"annotations":[78351],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000731"},{"annotations":[102578,76728,94994,108860],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904161"},{"annotations":[102629,60939,103978,66598,99067,70197],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070987"},{"annotations":[73057,74811,103979,70195,95633,77746,102630,77545],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042276"},{"annotations":[111506],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1904332"},{"annotations":[76715],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0032210"},{"annotations":[115690,79957,69465,107870,70353,113567,90403,80025],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007004"},{"annotations":[98064],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019985"}]},"cv_name":"biological_process","definition":"The biosynthetic process resulting in the formation of DNA.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA metabolic process","termid":"GO:0006259"},{"relation_name":"is_a","term_name":"nucleic acid biosynthetic process","termid":"GO:0141187"}],"gene_count":28,"genes_by_uniquename":{"SJAG_00153":null,"SJAG_00198":null,"SJAG_00406":null,"SJAG_00573":null,"SJAG_00611":null,"SJAG_00814":null,"SJAG_00939":null,"SJAG_01378":null,"SJAG_01677":null,"SJAG_02194":null,"SJAG_02199":null,"SJAG_02527":null,"SJAG_02658":null,"SJAG_02667":null,"SJAG_02818":null,"SJAG_03685":null,"SJAG_03855":null,"SJAG_03906":null,"SJAG_04089":null,"SJAG_04190":null,"SJAG_04266":null,"SJAG_04586":null,"SJAG_04791":null,"SJAG_04877":null,"SJAG_05197":null,"SJAG_05239":null,"SJAG_05979":null,"SJAG_16460":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006259","GO:0008150"],"is_obsolete":false,"name":"DNA biosynthetic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000108":null,"GO_REF:0000117":null},"synonyms":[{"name":"DNA anabolism","type":"exact"},{"name":"DNA biosynthesis","type":"exact"},{"name":"DNA formation","type":"exact"},{"name":"DNA synthesis","type":"exact"}],"termid":"GO:0071897","terms_by_termid":{"GO:0000731":null,"GO:0007004":null,"GO:0019985":null,"GO:0032210":null,"GO:0042276":null,"GO:0070987":null,"GO:0071897":null,"GO:1904161":null,"GO:1904332":null}}


id: PBO:0027377
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_vegetative_cell_with_nuclear_pore_aggregation_in_cytoplasm_during_mitotic_telophase","termid":"PBO:0027377"}


id: MONDO:0014996
data:
  {"annotated_genes":["SJAG_04704"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86782],"is_not":false,"summary":null,"term":"MONDO:0014996"}]},"cv_name":"mondo","definition":"Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the ELP2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive non-syndromic intellectual disability","termid":"MONDO:0019502"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04704":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0037792","MONDO:0005066"],"is_obsolete":false,"name":"intellectual disability, autosomal recessive 58","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0081220","GARD:13361","OMIM:617270","MEDGEN:934608","UMLS:C4310641"],"synonyms":[{"name":"ELP2 autosomal recessive non-syndromic intellectual disability","type":"exact"},{"name":"ELP2-related disorder","type":"related"},{"name":"MRT58","type":"exact"},{"name":"autosomal recessive intellectual disability 58","type":"related"},{"name":"autosomal recessive non-syndromic intellectual disability caused by mutation in ELP2","type":"exact"},{"name":"intellectual developmental disorder, autosomal recessive 58","type":"exact"},{"name":"intellectual disability, autosomal recessive 58","type":"exact"},{"name":"intellectual disability, autosomal recessive type 58","type":"exact"},{"name":"mental retardation, autosomal recessive 58","type":"exact"},{"name":"mental retardation, autosomal recessive type 58","type":"exact"}],"termid":"MONDO:0014996","terms_by_termid":{"MONDO:0014996":null},"xrefs":{"Monarch":{"xref_id":"0014996"}}}


