# terms

id: FYPO:0005019
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell cycle phenotype observed in the vegetative growth phase of the life cycle in which the duration of septum assembly is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal septum assembly","termid":"FYPO:0000673"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001320","FYPO:0001312","FYPO:0000002"],"is_obsolete":false,"name":"normal duration of septum assembly","synonyms":[{"name":"normal duration of division septum assembly","type":"exact"},{"name":"normal duration of septation","type":"broad"},{"name":"normal duration of septum assembly during mitotic cell cycle","type":"related"},{"name":"normal duration of septum assembly during vegetative growth","type":"exact"}],"termid":"FYPO:0005019"}


id: PR:O94290
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- cwf29 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94290"],"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":"U2 snRNP component ist3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC887.05c","synonyms":[{"name":"RNA-binding protein cwf29 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-cwf29","type":"exact"},{"name":"complexed with cdc5 protein 29 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94290"}


id: PBO:0045805
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EDRF1 divergent transcript","termid":"PBO:0045805"}


id: _global:existence_ends_during
data:
  {"annotation_feature_type":"gene","cv_name":"external","definition":"x existence ends during y if and only if the time point at which x ends is before or equivalent to the time point at which y ends and after or equivalent to the point at which y starts. Formally: x existence ends during y iff ω(x) <= ω(y) and ω(x) >= α(y).","direct_ancestors":[{"relation_name":"is_a","term_name":"existence_ends_during_or_before","termid":"_global:existence_ends_during_or_before"},{"relation_name":"is_a","term_name":"existence_overlaps","termid":"_global:existence_overlaps"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"existence_ends_during","secondary_identifiers":["RO:0002492"],"termid":"_global:existence_ends_during"}


id: GO:0047364
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (Z)-desulfoglucotropeolin + 3'-phosphoadenylyl sulfate = (Z)-glucotropeolin + adenosine 3',5'-bisphosphate + H+. Also converts (Z)-indolylmethyl desulfoglucosinolate to (Z)-glucobrassicin. This is the final step in the biosynthesis of the glucosinolate core structure.","definition_xrefs":["EC:2.8.2.24"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfotransferase activity","termid":"GO:0008146"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016782"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0003824","GO:0016782"],"is_obsolete":false,"name":"aromatic desulfoglucosinolate sulfotransferase activity","synonyms":[{"name":"3'-phosphoadenosine-5'-phosphosulfate:desulfoglucosinolate sulfotransferase activity","type":"related"},{"name":"3'-phosphoadenylyl-sulfate:desulfoglucosinolate sulfotransferase activity","type":"related"},{"name":"PAPS-desulfoglucosinolate sulfotransferase activity","type":"related"},{"name":"desulfoglucosinolate sulfotransferase activity","type":"broad"},{"name":"desulphoglucosinolate sulphotransferase activity","type":"exact"}],"termid":"GO:0047364"}


id: GO:0048306
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a protein or protein complex in the presence of calcium.","definition_xrefs":["PMID:10485905","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein binding","termid":"GO:0005515"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"calcium-dependent protein binding","termid":"GO:0048306"}


id: PBO:0040268
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"atlastin GTPase 3","termid":"PBO:0040268"}


id: PBO:0050336
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein A1pseudogene 38","termid":"PBO:0050336"}


id: PBO:0080154
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VCAN antisense RNA 1","termid":"PBO:0080154"}


id: GO:0042336
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Synthesis and deposition of a protein-based noncellular, hardened, or membranous secretion from an epithelial sheet, occurring as part of the molting cycle. Examples of this process are found in invertebrate species.","definition_xrefs":["GOC:dph","GOC:mtg_sensu","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete cuticle development involved in protein-based cuticle molting cycle (obsolete GO:0042336)","synonyms":[{"name":"cuticle anabolism during molting","type":"broad"},{"name":"cuticle biosynthetic process during molting","type":"broad"},{"name":"cuticle development involved in protein-based cuticle molting cycle","type":"exact"},{"name":"cuticle formation during molting","type":"broad"},{"name":"cuticle synthesis during molting","type":"broad"}],"termid":"GO:0042336"}


id: GO:0042027
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: peptidylproline (omega=180) = peptidylproline (omega=0).","definition_xrefs":["EC:5.2.1.8"],"gene_count":0,"genotype_count":0,"name":"obsolete cyclophilin-type peptidyl-prolyl cis-trans isomerase activity (obsolete GO:0042027)","synonyms":[{"name":"cyclophilin-type peptidyl-prolyl cis-trans isomerase activity","type":"exact"}],"termid":"GO:0042027"}


id: PBO:0059461
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mesogenin 1","termid":"PBO:0059461"}


id: MONDO:0010398
data:
  {"annotated_genes":["SJAG_04056"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86748],"is_not":false,"summary":null,"term":"MONDO:0010398"}]},"cv_name":"mondo","definition":"Any X-linked syndromic intellectual disability in which the cause of the disease is a mutation in the UPF3B gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04056":null},"genotype_count":0,"is_obsolete":false,"name":"syndromic X-linked intellectual disability 14","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:372646","UMLS:C1970822","MESH:C567063","OMIM:300676","DOID:0060821"],"synonyms":[{"name":"MRXS14","type":"related"},{"name":"UPF3B X-linked syndromic intellectual disability","type":"exact"},{"name":"X-linked syndromic intellectual disability caused by mutation in UPF3B","type":"exact"},{"name":"intellectual developmental disorder, X-linked syndromic 14, X-linked recessive","type":"exact"},{"name":"intellectual disability, X-linked, syndromic 14","type":"exact"},{"name":"intellectual disability, X-linked, syndromic type 14","type":"exact"},{"name":"mental retardation, X-linked, syndromic 14","type":"exact"},{"name":"mental retardation, X-linked, syndromic type 14","type":"exact"},{"name":"syndromic X-linked intellectual disability 14","type":"exact"},{"name":"syndromic X-linked intellectual disability type 14","type":"exact"}],"termid":"MONDO:0010398","terms_by_termid":{"MONDO:0010398":null},"xrefs":{"Monarch":{"xref_id":"0010398"}}}


id: PBO:0002284
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"20S proteasome component alpha 5, Pup2 (predicted)","termid":"PBO:0002284"}


id: SO:0001603
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant with in the CDS that causes a change in the resulting polypeptide sequence.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"translational_product_structure_variant","termid":"SO:0001598"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polypeptide_sequence_variant","synonyms":[{"name":"polypeptide sequence variant","type":"exact"}],"termid":"SO:0001603"}


id: GO:0047123
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: A + H2O + quinoline-4-carboxylate = 2-oxo-1,2-dihydroquinoline-4-carboxylate + AH(2).","definition_xrefs":["EC:1.3.99.19","RHEA:14949"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-CH group of donors","termid":"GO:0016627"}],"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:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"quinoline-4-carboxylate 2-oxidoreductase activity","secondary_identifiers":["MetaCyc:1.3.99.19-RXN","KEGG_REACTION:R05183"],"synonyms":[{"name":"quinoline-4-carboxylate:acceptor 2-oxidoreductase (hydroxylating)","type":"related"},{"name":"quinoline-4-carboxylic acid 2-oxidoreductase activity","type":"related"}],"termid":"GO:0047123"}


id: GO:0120032
data:
  {"annotated_genes":["SJAG_04509","SJAG_02379","SJAG_03453","SJAG_01794","SJAG_00514"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[92980,90359,110817,87410,89379],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902917"}]},"cv_name":"biological_process","definition":"Any process that modulates the rate, frequency, or extent of plasma membrane bounded cell projection assembly.","definition_xrefs":["GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell projection assembly","termid":"GO:0060491"},{"relation_name":"is_a","term_name":"regulation of plasma membrane bounded cell projection organization","termid":"GO:0120035"},{"relation_name":"regulates","term_name":"plasma membrane bounded cell projection assembly","termid":"GO:0120031"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00514":null,"SJAG_01794":null,"SJAG_02379":null,"SJAG_03453":null,"SJAG_04509":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0044085","GO:0008150"],"is_obsolete":false,"name":"regulation of plasma membrane bounded cell projection assembly","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0120032","terms_by_termid":{"GO:1902917":null}}


id: PBO:0051977
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IZUMO family member 4","termid":"PBO:0051977"}


id: SO:0000613
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A DNA sequence to which bacterial RNA polymerase binds, to begin transcription.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prokaryotic_promoter","termid":"SO:0002222"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bacterial_RNApol_promoter","synonyms":[{"name":"bacterial RNApol promoter","type":"exact"}],"termid":"SO:0000613"}


id: PR:O94306
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rpp21 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94306"],"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 C16C4.19 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC16C4.19","synonyms":[{"name":"Spom972h-rpp21","type":"exact"}],"termid":"PR:O94306"}


id: PBO:0058018
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3944","termid":"PBO:0058018"}


id: GO:0070197
data:
  {"annotated_genes":["SJAG_01777","SJAG_01263"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89275,105421],"is_not":false,"summary":null,"term":"GO:0070197"}]},"cv_name":"biological_process","definition":"The meiotic cell cycle process in which physical connections are formed between telomeric heterochromatin and the nuclear envelope, facilitating bouquet formation.","definition_xrefs":["PMID:18818742","GOC:pr","GOC:vw","GOC:jp"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome attachment to the nuclear envelope","termid":"GO:0097240"},{"relation_name":"is_a","term_name":"meiotic cell cycle process","termid":"GO:1903046"},{"relation_name":"part_of","term_name":"meiotic telomere tethering at nuclear periphery","termid":"GO:0044821"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01263":null,"SJAG_01777":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0140013"}],"interesting_parent_ids":["GO:0007049","GO:0051179","GO:0008150","GO:0140013"],"is_obsolete":false,"name":"meiotic attachment of telomere to nuclear envelope","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"attachment of telomeres to nuclear envelope","type":"broad"},{"name":"attachment of telomeric chromatin to nuclear envelope","type":"broad"}],"termid":"GO:0070197","terms_by_termid":{"GO:0070197":null}}


id: FYPO:0006440
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which a protein kinase activity is absent during a cellular response to hydroxyurea.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein kinase activity","termid":"FYPO:0001384"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0000652","FYPO:0000707","FYPO:0001985","FYPO:0000654"],"is_obsolete":false,"name":"abolished protein kinase activity during cellular response to hydroxyurea","synonyms":[{"name":"abolished protein kinase activity during cellular response to HU","type":"exact"},{"name":"protein kinase activity abolished during cellular response to hydroxyurea","type":"exact"}],"termid":"FYPO:0006440"}


id: PBO:0068995
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 239, pseudogene","termid":"PBO:0068995"}


id: PBO:0041478
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 11 open reading frame 71","termid":"PBO:0041478"}


id: MONDO:0007654
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":"genu valgum, st. Helena familial","secondary_identifiers":["MEDGEN:333980","OMIM:137370","MESH:C537685","UMLS:C1842052"],"synonyms":[{"name":"St. Helena familial genu valgum","type":"related"},{"name":"genu valgum, hereditary pubertal","type":"related"},{"name":"genu valgum, st Helena familial","type":"related"},{"name":"genu valgum, st. Helena familial","type":"exact"},{"name":"hereditary pubertal genu valgum","type":"related"},{"name":"severe 'knock-knees' and variable lesser malalignment at the elbows and wrists","type":"related"}],"termid":"MONDO:0007654","xrefs":{"Monarch":{"xref_id":"0007654"}}}


id: PBO:0003190
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.6.1.42","termid":"PBO:0003190"}


id: PBO:0070309
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNY1 pseudogene 15","termid":"PBO:0070309"}


id: MONDO:0022567
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":"cataract","termid":"MONDO:0005129"}],"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":"bhaskar jagannathan syndrome","secondary_identifiers":["UMLS:C2930901","MEDGEN:419280","MESH:C535437"],"termid":"MONDO:0022567","xrefs":{"Monarch":{"xref_id":"0022567"}}}


id: PBO:0034074
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-contributes_to_frequency_of_condition","termid":"PBO:0034074"}


id: MONDO:0012936
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leukemia, chronic lymphocytic, susceptibility to, 5","secondary_identifiers":["MEDGEN:436452","OMIM:612559","UMLS:C2675514"],"synonyms":[{"name":"Clls5","type":"related"},{"name":"leukemia, chronic lymphocytic susceptibility to, 5","type":"exact"},{"name":"leukemia, chronic lymphocytic, susceptibility to, 5","type":"exact"},{"name":"leukemia, chronic lymphocytic, susceptibility to, type 5","type":"exact"}],"termid":"MONDO:0012936","xrefs":{"Monarch":{"xref_id":"0012936"}}}


id: FYECO:0000124
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"Cells were grown to late exponential phase.","definition_xrefs":["PMID:10467002"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping growth timing","termid":"FYECO:0000122"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"growth to late exponential phase","termid":"FYECO:0000124"}


id: PBO:0044737
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DEAD-box helicase 18 pseudogene 5","termid":"PBO:0044737"}


id: GO:0003723
data:
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id: PBO:0078402
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id: FYPO:0001311
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id: MONDO:0004507
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id: GO:0015363
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id: PBO:0059307
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id: PBO:0064011
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id: GO:0018813
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id: PBO:0035882
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id: PBO:0075011
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id: PBO:0047654
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id: PBO:0040162
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id: PBO:0067830
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id: PBO:0004612
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id: PR:Q9Y7I8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- zuo1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9Y7I8"],"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":"zuotin (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1778.01c","synonyms":[{"name":"DnaJ-related protein zuo1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"J protein zuo1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-zuo1","type":"exact"},{"name":"ribosome-associated complex subunit zuo1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9Y7I8"}


id: GO:0061770
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a translation elongation factor, any polypeptide factor involved in the peptide elongation in ribosome-mediated translation.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein binding","termid":"GO:0005515"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"translation elongation factor binding","termid":"GO:0061770"}


id: GO:0050397
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: Watasenia luciferin + O2 = oxidized Watasenia luciferin + CO2 + light.","definition_xrefs":["EC:1.13.12.8","MetaCyc:WATASEMIA-LUCIFERIN-2-MONOOXYGENASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of one atom of oxygen (internal monooxygenases or internal mixed function oxidases)","termid":"GO:0016703"},{"relation_name":"is_a","term_name":"luciferin monooxygenase activity","termid":"GO:0045289"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"Watasenia-luciferin 2-monooxygenase activity","secondary_identifiers":["RHEA:18057"],"synonyms":[{"name":"Watasenia-luciferin:oxygen 2-oxidoreductase (decarboxylating)","type":"related"},{"name":"Watasenia-type luciferase activity","type":"related"},{"name":"luciferase activity","type":"broad"}],"termid":"GO:0050397"}


id: GO:0015441
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: ATP + H2O + beta-glucan(in) = ADP + phosphate + beta-glucan(out).","definition_xrefs":["RHEA:18453"],"direct_ancestors":[{"relation_name":"is_a","term_name":"beta-glucan transmembrane transporter activity","termid":"GO:0015160"},{"relation_name":"is_a","term_name":"ABC-type carbohydrate transporter activity","termid":"GO:0043211"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"ABC-type beta-glucan transporter activity","secondary_identifiers":["MetaCyc:3.6.3.42-RXN","EC:7.5.2.3"],"synonyms":[{"name":"ABC-type beta-glucan transporter","type":"related"},{"name":"ATP-dependent beta-glucan transporter activity","type":"related"},{"name":"ATPase-coupled beta-glucan transporter activity","type":"related"},{"name":"beta-glucan ABC transporter","type":"exact"},{"name":"beta-glucan-transporting ATPase activity","type":"related"}],"termid":"GO:0015441"}


id: MONDO:0971044
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Ehlers-Danlos syndrome","termid":"MONDO:0020066"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ehlers-Danlos syndrome, classic-like, 3","secondary_identifiers":["OMIM:620865"],"termid":"MONDO:0971044","xrefs":{"Monarch":{"xref_id":"0971044"}}}


id: PBO:0004708
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pet117 cytochrome c oxidase assemby protein (predicted)","termid":"PBO:0004708"}


id: PBO:0082009
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger SWIM-type containing 7","termid":"PBO:0082009"}


id: PBO:0002650
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histidine kinase Mak1","termid":"PBO:0002650"}


id: PBO:0055232
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 2659","termid":"PBO:0055232"}


id: PBO:0035972
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_invertase_activity","termid":"PBO:0035972"}


id: PBO:0058150
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4445","termid":"PBO:0058150"}


id: PBO:0082675
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 complex; EKC/KEOPS complex is required for t6A tRNA modification and telomeric TG1-3 recombination; may have role in transcription; Cgi121p is dispensable for tRNA modification; other complex members are Bud32p, Kae1p, Pcc1p, and Gon7p","termid":"PBO:0082675"}


id: PR:O42930
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- vps10 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O42930"],"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":"vacuolar protein sorting/targeting protein 10 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC16C6.06","synonyms":[{"name":"CPY receptor (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-vps10","type":"exact"},{"name":"carboxypeptidase Y receptor (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"sortilin vps10 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"vacuolar carboxypeptidase sorting receptor vps10 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O42930"}


id: PBO:0001276
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.1.1.36","termid":"PBO:0001276"}


id: PBO:0079134
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"t-SNARE domain containing 1","termid":"PBO:0079134"}


id: SO:0000593
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Most box C/D snoRNAs also contain long (>10 nt) sequences complementary to rRNA. Boxes C and D, as well as boxes C' and D', are usually located in close proximity, and form a structure known as the box C/D motif. This motif is important for snoRNA stability, processing, nucleolar targeting and function. A small number of box C/D snoRNAs are involved in rRNA processing; most, however, are known or predicted to serve as guide RNAs in ribose methylation of rRNA. Targeting involves direct base pairing of the snoRNA at the rRNA site to be modified and selection of a rRNA nucleotide a fixed distance from box D or D'.","direct_ancestors":[{"relation_name":"derives_from","term_name":"C_D_box_snoRNA_primary_transcript","termid":"SO:0000595"},{"relation_name":"is_a","term_name":"snoRNA","termid":"SO:0000275"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C_D_box_snoRNA","synonyms":[{"name":"C D box snoRNA","type":"exact"},{"name":"C/D box snoRNA","type":"exact"},{"name":"SNORD","type":"exact"},{"name":"box C/D snoRNA","type":"exact"}],"termid":"SO:0000593"}


id: PBO:0070493
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L5 pseudogene 28","termid":"PBO:0070493"}


id: PBO:0050704
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock protein family B (small) member 1 pseudogene 2","termid":"PBO:0050704"}


id: MONDO:1012092
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"gastric dilatation volvulus syndrome, non-human animal","termid":"MONDO:1011659"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gastric dilatation volvulus syndrome, lesser panda","secondary_identifiers":["OMIA:000404-9649"],"termid":"MONDO:1012092","xrefs":{"Monarch":{"xref_id":"1012092"}}}


id: PBO:0061991
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 2 subfamily C member 1","termid":"PBO:0061991"}


id: PBO:0062952
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PABIR family member 3","termid":"PBO:0062952"}


id: GO:0016560
data:
  {"annotated_genes":["SJAG_00891","SJAG_02693","SJAG_00702"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[96459,102577,111301],"is_not":false,"summary":null,"term":"GO:0016560"}]},"cv_name":"biological_process","definition":"The process in which a complex formed of a peroxisome targeting sequence (PTS) receptor bound to a PTS-bearing protein docks with translocation machinery in the peroxisomal membrane.","definition_xrefs":["PMID:11687502","PMID:11988772","PMID:14754507"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization","termid":"GO:0008104"},{"relation_name":"part_of","term_name":"protein import into peroxisome matrix","termid":"GO:0016558"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00702":null,"SJAG_00891":null,"SJAG_02693":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0007031"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0007031","GO:0006810","GO:0055085"],"is_obsolete":false,"name":"protein import into peroxisome matrix, docking","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"peroxisome matrix protein import, docking","type":"exact"},{"name":"peroxisome receptor docking","type":"related"},{"name":"protein docking during peroxisome matrix protein import","type":"exact"},{"name":"protein docking during protein import into peroxisome matrix","type":"exact"},{"name":"protein docking during protein transport into peroxisome matrix","type":"exact"},{"name":"protein transport into peroxisome matrix, docking","type":"exact"}],"termid":"GO:0016560","terms_by_termid":{"GO:0016560":null}}


id: PR:Q9UT19
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A 5-methyltetrahydropteroyltriglutamate--homocysteine methyltransferase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO00595"],"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":"5-methyltetrahydropteroyltriglutamate--homocysteine methyltransferase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC9.09","secondary_identifiers":["UniProtKB:Q9UT19"],"synonyms":[{"name":"Spom972h-metE","type":"exact"},{"name":"cobalamin-independent methionine synthase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"methionine synthase, vitamin-B12 independent isozyme (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9UT19"}


id: GO:0009550
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A plasmodesma that consists of a simple, single channel; found predominantly in young tissue and formed as a function of cell plate formation during cytokinesis.","definition_xrefs":["PMID:15012255"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasmodesma","termid":"GO:0009506"}],"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":"primary plasmodesma","synonyms":[{"name":"simple plasmodesma","type":"exact"}],"termid":"GO:0009550"}


id: PBO:0059992
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND4L pseudogene 12","termid":"PBO:0059992"}


id: GO:0046380
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of N-acetylneuraminate, the anion of 5-(acetylamino)-3,5-dideoxy-D-glycero-D-galacto-non-3-ulosonic acid.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-acetylneuraminate metabolic process","termid":"GO:0006054"},{"relation_name":"is_a","term_name":"amide biosynthetic process","termid":"GO:0043604"},{"relation_name":"is_a","term_name":"amino sugar biosynthetic process","termid":"GO:0046349"},{"relation_name":"is_a","term_name":"carboxylic acid biosynthetic process","termid":"GO:0046394"}],"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":"N-acetylneuraminate biosynthetic process","synonyms":[{"name":"N-acetylneuraminate anabolism","type":"exact"},{"name":"N-acetylneuraminate biosynthesis","type":"exact"},{"name":"N-acetylneuraminate formation","type":"exact"},{"name":"N-acetylneuraminate synthesis","type":"exact"}],"termid":"GO:0046380"}


id: PATO:0001413
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A physical quality inhering in a bearer by virtue of the rate of the bearer's angular movement about an axis; the angle rotated in a given time.","definition_xrefs":["Wikipedia:http://en.wikipedia.org/wiki/Angular_velocity"],"direct_ancestors":[{"relation_name":"is_a","term_name":"velocity","termid":"PATO:0002242"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"angular velocity","termid":"PATO:0001413"}


id: PBO:0065175
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prominin 1","termid":"PBO:0065175"}


id: FYPO:0005255
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of a carboxypeptidase activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal peptidase activity","termid":"FYPO:0000666"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0001985","FYPO:0000707","FYPO:0000652","FYPO:0000654"],"is_obsolete":false,"name":"abnormal carboxypeptidase activity","termid":"FYPO:0005255"}


id: PBO:0072003
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S7 pseudogene 5","termid":"PBO:0072003"}


id: PBO:0066238
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA binding motif protein 45","termid":"PBO:0066238"}


id: MONDO:0002146
data:
  {"annotated_genes":["SJAG_04110","SJAG_03051","SJAG_04148","SJAG_02829","SJAG_00301","SJAG_03077","SJAG_04398","SJAG_04950"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85352],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:8000015"},{"annotations":[85851],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012794"},{"annotations":[86393],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008980"},{"annotations":[85026],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009514"},{"annotations":[84735],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010961"},{"annotations":[86481],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030736"},{"annotations":[85167],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013689"},{"annotations":[85926],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054850"},{"annotations":[86226],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014497"}]},"cv_name":"mondo","definition":"A disorder characterized by decreased function of the gonads. Clinical manifestations in both males and females include poor libido, infertility, and osteoporosis. Additional signs in males include erectile dysfunction, muscle atrophy, gynecomastia and increased abdominal fat. In females, additional signs include shrinking of the breasts and loss of, or failure to develop menstruation.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gonadal disorder","termid":"MONDO:0002259"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00301":null,"SJAG_02829":null,"SJAG_03051":null,"SJAG_03077":null,"SJAG_04110":null,"SJAG_04148":null,"SJAG_04398":null,"SJAG_04950":null},"genotype_count":0,"is_obsolete":false,"name":"hypogonadism","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:5711","DOID:1924","ICD9:253.4","NCIT:C9227","MESH:D007006","SCTID:48130008","UMLS:C0020619"],"synonyms":[{"name":"gonadotropin deficiency","type":"exact"},{"name":"hypogonadotropism","type":"exact"}],"termid":"MONDO:0002146","terms_by_termid":{"MONDO:0008980":null,"MONDO:0009514":null,"MONDO:0010961":null,"MONDO:0012794":null,"MONDO:0013689":null,"MONDO:0014497":null,"MONDO:0030736":null,"MONDO:0054850":null,"MONDO:8000015":null},"xrefs":{"Monarch":{"xref_id":"0002146"}}}


id: PBO:0065853
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB11 family interacting protein 4","termid":"PBO:0065853"}


id: MONDO:0018798
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete other genetic dermis disorder (obsolete MONDO:0018798)","secondary_identifiers":["Orphanet:477808"],"termid":"MONDO:0018798","xrefs":{"Monarch":{"xref_id":"0018798"}}}


id: GO:1990645
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of phosphorylases by removal of phosphate groups.","definition_xrefs":["PMID:8602837"],"gene_count":0,"genotype_count":0,"name":"obsolete phosphorylase dephosphorylation (obsolete GO:1990645)","synonyms":[{"name":"phosphorylase dephosphorylation","type":"exact"}],"termid":"GO:1990645"}


id: GO:1901038
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving cyanidin 3-O-beta-D-glucoside.","definition_xrefs":["GOC:TermGenie","PMID:21899608"],"direct_ancestors":[{"relation_name":"is_a","term_name":"flavonoid metabolic process","termid":"GO:0009812"},{"relation_name":"is_a","term_name":"beta-glucoside metabolic process","termid":"GO:1901804"}],"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":"cyanidin 3-O-glucoside metabolic process","synonyms":[{"name":"cyanidin 3-O-beta-D-glucoside metabolic process","type":"exact"},{"name":"cyanidin 3-O-beta-D-glucoside metabolism","type":"exact"}],"termid":"GO:1901038"}


id: MONDO:1010044
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Microvillus inclusion disease that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"digestive system disorder, non-human animal","termid":"MONDO:1011311"},{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microvillus inclusion disease, non-human animal","secondary_identifiers":["OMIA:002247"],"termid":"MONDO:1010044","xrefs":{"Monarch":{"xref_id":"1010044"}}}


id: PBO:0077229
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane channel like 5","termid":"PBO:0077229"}


id: FYPO:0007442
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 membrane is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to endoplasmic reticulum during vegetative growth","termid":"FYPO:0006378"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0001320","FYPO:0000002","FYPO:0000138","FYPO:0000257"],"is_obsolete":false,"name":"normal protein localization to endoplasmic reticulum membrane","synonyms":[{"name":"normal protein localization to ER membrane","type":"exact"},{"name":"normal protein localization to endoplasmic reticulum membrane during mitotic cell cycle","type":"related"},{"name":"normal protein localization to endoplasmic reticulum membrane during vegetative growth","type":"exact"}],"termid":"FYPO:0007442"}


id: GO:0180004
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: RNA polymerase II large subunit CTD heptapeptide repeat--phospho-L-tyrosine (consensus YSPTSPS)(position 1) + H2O = RNA polymerase II large subunit + phosphate.","definition_xrefs":["PMID:22622228"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA polymerase II CTD heptapeptide repeat phosphatase activity","termid":"GO:0008420"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0004721"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016788","GO:0003674","GO:0004721","GO:0003824","GO:0016787","GO:0140096"],"is_obsolete":false,"name":"RNA polymerase II CTD heptapeptide repeat Y1 phosphatase activity","synonyms":[{"name":"RNA polymerase II C-terminal domain Y1 phosphatase activity","type":"exact"}],"termid":"GO:0180004"}


id: GO:2000531
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of the biosynthesis of fatty acids, by modulating the frequency, rate or extent of transcription from an RNA polymerase II promoter.","definition_xrefs":["GOC:vw"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of fatty acid biosynthetic process by regulation of transcription from RNA polymerase II promoter (obsolete GO:2000531)","termid":"GO:2000531"}


id: PBO:0038468
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP binding cassette subfamily A member 7","termid":"PBO:0038468"}


id: PBO:0067322
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 413, pseudogene","termid":"PBO:0067322"}


id: GO:0014824
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which force is generated within smooth muscle tissue, resulting in a change in muscle geometry. This process occurs in the artery. Force generation involves a chemo-mechanical energy conversion step that is carried out by the actin/myosin complex activity, which generates force through ATP hydrolysis. The artery is a vessel carrying blood away from the heart.","definition_xrefs":["MA:0000708","MSH:D001158","GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tonic smooth muscle contraction","termid":"GO:0014820"},{"relation_name":"is_a","term_name":"vascular associated smooth muscle contraction","termid":"GO:0014829"}],"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":"artery smooth muscle contraction","termid":"GO:0014824"}


id: PBO:0086786
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; the authentic, non-tagged protein is detected in highly purified mitochondria in high-throughput studies; analysis of HA-tagged protein suggests a membrane localization","termid":"PBO:0086786"}


id: GO:1904440
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of iron ions import across plasma membrane.","definition_xrefs":["PMID:18353247","GO_REF:0000058","GOC:kom","GOC:BHF","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of iron ion transmembrane transport","termid":"GO:0034761"},{"relation_name":"is_a","term_name":"regulation of iron ion import across plasma membrane","termid":"GO:1904438"},{"relation_name":"positively_regulates","term_name":"iron ion import across plasma membrane","termid":"GO:0098711"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0055085"},{"rel_name":"regulates","termid":"GO:0098771"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"positively_regulates","termid":"GO:0098771"}],"interesting_parent_ids":["GO:0098771","GO:0008150","GO:0006810","GO:0055085"],"is_obsolete":false,"name":"positive regulation of iron ion import across plasma membrane","secondary_identifiers":["GO:1903991"],"synonyms":[{"name":"activation of ferrous ion import into cell","type":"narrow"},{"name":"activation of ferrous iron import across plasma membrane","type":"narrow"},{"name":"positive regulation of ferrous ion import into cell","type":"related"},{"name":"positive regulation of ferrous iron import across plasma membrane","type":"related"},{"name":"positive regulation of ferrous iron import into cell","type":"related"},{"name":"up regulation of ferrous ion import into cell","type":"related"},{"name":"up regulation of ferrous iron import across plasma membrane","type":"related"},{"name":"up-regulation of ferrous ion import into cell","type":"related"},{"name":"up-regulation of ferrous iron import across plasma membrane","type":"related"},{"name":"upregulation of ferrous ion import into cell","type":"related"},{"name":"upregulation of ferrous iron import across plasma membrane","type":"related"}],"termid":"GO:1904440"}


id: GO:0009745
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals mediated by the detection of sucrose.","definition_xrefs":["GOC:sm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sugar mediated signaling pathway","termid":"GO:0010182"},{"relation_name":"part_of","term_name":"cellular response to sucrose stimulus","termid":"GO:0071329"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"sucrose mediated signaling","synonyms":[{"name":"sucrose mediated signalling","type":"exact"}],"termid":"GO:0009745"}


id: PBO:0086655
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; haploid deletion mutant exhibits synthetic phenotype with alpha-synuclein; SWAT-GFP fusion protein localizes to the endoplasmic reticulum while mCherry fusion protein localizes to both the endoplasmic reticulum and vacuole","termid":"PBO:0086655"}


id: PR:Q09923
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An uncharacterized oxidoreductase YdjG that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO01759","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":"aldo-keto reductase yakc [NADP(+)] (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1F7.12","secondary_identifiers":["UniProtKB:Q09923"],"synonyms":[{"name":"Spom972h-ydjG","type":"exact"}],"termid":"PR:Q09923"}


id: GO:0050120
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: N-acetyl-D-glucosamine + H2O + NAD+ = N-acetyl-D-glucosaminate + 2 H+ + NADH.","definition_xrefs":["RHEA:23144","EC:1.1.1.240"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"N-acetylhexosamine 1-dehydrogenase activity","secondary_identifiers":["MetaCyc:N-ACETYLHEXOSAMINE-1-DEHYDROGENASE-RXN","KEGG_REACTION:R01202"],"synonyms":[{"name":"N-acetyl-D-hexosamine dehydrogenase activity","type":"related"},{"name":"N-acetyl-D-hexosamine:NAD+ 1-oxidoreductase activity","type":"related"},{"name":"N-acetylhexosamine dehydrogenase activity","type":"related"}],"termid":"GO:0050120"}


id: RO:0002607
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"c is marker for d iff the presence or occurrence of d is correlated with the presence of occurrence of c, and the observation of c is used to infer the presence or occurrence of d. Note that this does not imply that c and d are in a direct causal relationship, as it may be the case that there is a third entity e that stands in a direct causal relationship with c and d.","direct_ancestors":[{"relation_name":"is_a","term_name":"correlated_with","termid":"RO:0002610"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"is_marker_for","termid":"RO:0002607"}


id: PBO:0067899
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 201","termid":"PBO:0067899"}


id: GO:0038154
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by the binding of interleukin-11 to its receptor on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["GOC:signaling","GOC:nhn"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine-mediated signaling pathway","termid":"GO:0019221"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"interleukin-11-mediated signaling pathway","synonyms":[{"name":"IL-11-mediated signaling pathway","type":"exact"},{"name":"interleukin-11-mediated signalling pathway","type":"exact"}],"termid":"GO:0038154"}


id: GO:0090693
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A plant organ developmental process during which a plant dismantles cellular components to reclaim the cellular building blocks and nutrients that have been deposited in the plant organs during growth.","definition_xrefs":["PMID:34938309","GOC:tb","PMID:17177638"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process","termid":"GO:0032502"},{"relation_name":"part_of","term_name":"plant organ development","termid":"GO:0099402"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"plant organ senescence","termid":"GO:0090693"}


id: FYPO:0002009
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 amount of oxygen consumed by cells in a given time is lower than in wild type.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular metabolism phenotype during vegetative growth","termid":"FYPO:0001348"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"decreased oxygen consumption during vegetative growth","synonyms":[{"name":"decreased oxygen consumption during mitotic cell cycle","type":"related"},{"name":"decreased oxygen uptake during vegetative growth","type":"related"},{"name":"reduced oxygen consumption during vegetative growth","type":"exact"}],"termid":"FYPO:0002009"}


id: PBO:0090783
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial carrier, serine Fsf1","termid":"PBO:0090783"}


id: PBO:0065411
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome 20S subunit alpha 8","termid":"PBO:0065411"}


id: PBO:0031303
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_sensitivity_to_chemical_during_vegetative_growth","termid":"PBO:0031303"}


id: GO:0047886
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-trans,6-trans-farnesol + NADP+ = 2-trans,6-trans-farnesal + H+ + NADPH.","definition_xrefs":["EC:1.1.1.216","RHEA:14697"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"farnesol dehydrogenase activity","secondary_identifiers":["MetaCyc:FARNESOL-DEHYDROGENASE-RXN","KEGG_REACTION:R03264"],"synonyms":[{"name":"2-trans,6-trans-farnesol:NADP+ 1-oxidoreductase activity","type":"related"},{"name":"NADP-farnesol dehydrogenase activity","type":"related"},{"name":"farnesol (nicotinamide adenine dinucleotide phosphate) dehydrogenase activity","type":"related"}],"termid":"GO:0047886"}


id: PBO:0050375
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein A2/B1","termid":"PBO:0050375"}


id: PBO:0052602
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KPNB1 divergent transcript","termid":"PBO:0052602"}


id: GO:0006286
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Excision of the sugar phosphate residue at an AP site, i.e. a deoxyribose sugar with a missing base, by a phosphodiesterase enzyme.","definition_xrefs":["ISBN:0815316194"],"gene_count":0,"genotype_count":0,"name":"obsolete base-excision repair, base-free sugar-phosphate removal (obsolete GO:0006286)","termid":"GO:0006286"}


id: FYPO:0000286
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell population phenotype observed in the vegetative growth phase of the life cycle in which a population of cells grow poorly in medium that has a low concentration of manganese (Mn2+).","definition_xrefs":["PMID:14723709","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal vegetative cell population growth","termid":"FYPO:0001356"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0000139","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"sensitive to manganese depletion","synonyms":[{"name":"hypersensitive to manganese depletion","type":"exact"},{"name":"sensitive to manganese depletion during mitotic cell cycle","type":"related"},{"name":"sensitive to manganese depletion during vegetative growth","type":"exact"}],"termid":"FYPO:0000286"}


id: PBO:0062424
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 7 subfamily E member 85B pseudogene","termid":"PBO:0062424"}


id: PBO:0027106
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_termination_of_RNA_polymerase_II_transcription","termid":"PBO:0027106"}


id: GO:0032811
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the regulated release of epinephrine.","definition_xrefs":["GOC:vk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of epinephrine secretion","termid":"GO:0014060"},{"relation_name":"is_a","term_name":"negative regulation of catecholamine secretion","termid":"GO:0033604"},{"relation_name":"negatively_regulates","term_name":"epinephrine secretion","termid":"GO:0048242"}],"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 epinephrine secretion","synonyms":[{"name":"down regulation of epinephrine secretion","type":"exact"},{"name":"down-regulation of epinephrine secretion","type":"exact"},{"name":"downregulation of epinephrine secretion","type":"exact"},{"name":"inhibition of epinephrine secretion","type":"narrow"},{"name":"negative regulation of adrenaline secretion","type":"exact"}],"termid":"GO:0032811"}


id: GO:0102238
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (2E)-geraniol + ATP = (2E)-geranyl phosphate + ADP + H+.","definition_xrefs":["RHEA:61660"],"direct_ancestors":[{"relation_name":"is_a","term_name":"geraniol kinase activity","termid":"GO:0052670"}],"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"}],"interesting_parent_ids":["GO:0003824","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"ATP:geraniol kinase activity","secondary_identifiers":["MetaCyc:RXN-12307"],"synonyms":[{"name":"geraniol kinase activity (ATP-dependent) activity","type":"exact"}],"termid":"GO:0102238"}


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


id: MONDO:0100010
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease involving the tendon.","definition_xrefs":["PMID:19188560","MONDO:patterns/location_top"],"direct_ancestors":[{"relation_name":"is_a","term_name":"musculoskeletal system disorder","termid":"MONDO:0002081"},{"relation_name":"is_a","term_name":"connective tissue disorder","termid":"MONDO:0003900"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"disease of the tendon","secondary_identifiers":["SCTID:68172002","MESH:D052256","EFO:1001434","UMLS:C0151936","MEDGEN:508839"],"synonyms":[{"name":"disease of tendon","type":"exact"},{"name":"disease or disorder of tendon","type":"exact"},{"name":"disorder of tendon","type":"exact"},{"name":"tendinopathy","type":"exact"},{"name":"tendon disease","type":"exact"},{"name":"tendon disease or disorder","type":"exact"}],"termid":"MONDO:0100010","xrefs":{"Monarch":{"xref_id":"0100010"}}}


id: PBO:0066574
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rh blood group D antigen","termid":"PBO:0066574"}


id: GO:1903476
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any protein localization to cell division site that is involved in mitotic actomyosin contractile ring assembly.","definition_xrefs":["GO_REF:0000060","GOC:mtg_cell_cycle","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization to cell division site involved in cytokinesis, actomyosin contractile ring assembly","termid":"GO:1902575"},{"relation_name":"is_a","term_name":"mitotic cell cycle process","termid":"GO:1903047"},{"relation_name":"part_of","term_name":"mitotic actomyosin contractile ring assembly","termid":"GO:1903475"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0030036"},{"rel_name":"part_of","termid":"GO:0000281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0007010"}],"interesting_parent_ids":["GO:0007049","GO:0030036","GO:0051179","GO:0000281","GO:0008150","GO:0044085","GO:0007010"],"is_obsolete":false,"name":"protein localization to cell division site involved in mitotic actomyosin contractile ring assembly","synonyms":[{"name":"protein localisation to cell division site involved in mitotic actomyosin contractile ring assembly","type":"exact"},{"name":"protein localization to cell division site involved in actomyosin contractile ring assembly involved in cytokinesis after mitosis","type":"exact"},{"name":"protein localization to cell division site involved in contractile ring assembly involved in mitotic cytokinesis","type":"exact"}],"termid":"GO:1903476"}


id: GO:1903299
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of hexokinase activity.","definition_xrefs":["GO_REF:0000059","GOC:TermGenie","GOC:mr","PMID:15804508"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of hexokinase activity (obsolete GO:1903299)","synonyms":[{"name":"regulation of ATP-dependent hexokinase activity","type":"exact"},{"name":"regulation of ATP:D-hexose 6-phosphotransferase activity","type":"exact"},{"name":"regulation of glucose ATP phosphotransferase activity","type":"exact"},{"name":"regulation of hexokinase (phosphorylating)","type":"exact"},{"name":"regulation of hexokinase D","type":"related"},{"name":"regulation of hexokinase type I activity","type":"narrow"},{"name":"regulation of hexokinase type II activity","type":"narrow"},{"name":"regulation of hexokinase type III activity","type":"narrow"},{"name":"regulation of hexokinase type IV","type":"related"},{"name":"regulation of hexokinase type IV (glucokinase) activity","type":"narrow"},{"name":"regulation of hexokinase type IV glucokinase activity","type":"exact"}],"termid":"GO:1903299"}


id: MONDO:0100554
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An instance of narcolepsy that is caused by an inherited genomic modification in an individual.","definition_xrefs":["MONDO:patterns/hereditary"],"direct_ancestors":[{"relation_name":"is_a","term_name":"narcolepsy","termid":"MONDO:0021107"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hereditary narcolepsy","secondary_identifiers":["OMIMPS:161400"],"termid":"MONDO:0100554","xrefs":{"Monarch":{"xref_id":"0100554"}}}


id: PATO:0000147
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000147 absolute temperature (obsolete PATO:0000147)","termid":"PATO:0000147"}


id: PBO:0063580
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pescadillo ribosomal biogenesis factor 1","termid":"PBO:0063580"}


id: MONDO:0021203
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"non-suppurative otitis media","termid":"MONDO:0001212"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serous otitis media","secondary_identifiers":["SCTID:80327007","UMLS:C0271453","MEDGEN:75752"],"synonyms":[{"name":"SOM","type":"exact"},{"name":"otitis media with effusion","type":"related"},{"name":"secretory otitis media","type":"exact"}],"termid":"MONDO:0021203","xrefs":{"Monarch":{"xref_id":"0021203"}}}


id: PBO:0090969
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA-binding and 3'-end processing protein Seb1","termid":"PBO:0090969"}


id: PBO:0034289
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-in_plerology_relationship_with","termid":"PBO:0034289"}


id: GO:0072258
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which relatively unspecialized cells acquire specialized structural and/or functional features that characterize the interstitial fibroblasts of the metanephros as it progresses from its formation to the mature state.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kidney interstitial fibroblast differentiation","termid":"GO:0072071"},{"relation_name":"is_a","term_name":"cell differentiation involved in metanephros development","termid":"GO:0072202"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"metanephric interstitial fibroblast differentiation","synonyms":[{"name":"metanephros interstitial cell differentiation","type":"exact"}],"termid":"GO:0072258"}


id: PBO:0090817
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial processing peptidase (MPP) complex alpha subunit Mas2","termid":"PBO:0090817"}


id: PBO:0017738
data:
  {"annotation_feature_type":"gene","cv_name":"subunit_composition","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heteromeric(6)","termid":"PBO:0017738"}


id: PBO:0053345
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 226","termid":"PBO:0053345"}


id: MONDO:0010816
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Qazi-Markouizos syndrome is characterized principally by non-progressive central hypotonia, chronic constipation, severe psychomotor retardation, abnormal dermatoglyphics, dysharmonic skeletal maturation and disproportionate muscle fibers. Seizures or an abnormal electroencephalograph were also reported. To date, the syndrome has been reported in three unrelated Puerto Rican boys.","definition_xrefs":["Orphanet:3010"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Qazi Markouizos syndrome","secondary_identifiers":["DOID:0050740","GARD:371","MEDGEN:443987","MESH:C536259","OMIM:600096","SCTID:721887007","UMLS:C2931142"],"synonyms":[{"name":"Dysharmonic skeletal maturation - muscular fiber disproportion","type":"exact"},{"name":"Dysharmonic skeletal maturation - muscular fibre disproportion","type":"exact"},{"name":"Dysharmonic skeletal maturation muscular fiber disproportion","type":"related"},{"name":"Dysharmonic skeletal maturation muscular fibre disproportion","type":"related"},{"name":"Dysharmonic skeletal maturation-muscular fiber disproportion syndrome","type":"exact"},{"name":"Dysharmonic skeletal maturation-muscular fibre disproportion syndrome","type":"exact"},{"name":"PUERTO RICAN infant hypotonia syndrome","type":"related"},{"name":"Puertorican infant hypotonia syndrome","type":"related"},{"name":"Qazi-Markouizos syndrome","type":"exact"},{"name":"hypotonia, psychomotor retardation, seizures, delayed and Dysharmonic skeletal maturation, and congenital fiber type disproportion","type":"related"},{"name":"hypotonia, psychomotor retardation, seizures, delayed and Dysharmonic skeletal maturation, and congenital fibre type disproportion","type":"related"}],"termid":"MONDO:0010816","xrefs":{"Monarch":{"xref_id":"0010816"}}}


id: GO:0006415
data:
  {"annotated_genes":["SJAG_03658","SJAG_05265","SJAG_04862","SJAG_04283","SJAG_02812","SJAG_02704","SJAG_00338","SJAG_01696","SJAG_01518","SJAG_02189","SJAG_05221","SJAG_02601","SJAG_00642","SJAG_00308","SJAG_03232","SJAG_03949","SJAG_00286"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[61599,102884],"is_not":false,"summary":null,"term":"GO:0006415"},{"annotations":[95982,90605,115472,116937,94622,108621,94309,106642,94623,108620],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002184"},{"annotations":[101558,95002,98155,104182,95441,110974],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070126"},{"annotations":[108625,94310,108624],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0045905"},{"annotations":[111165],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0006449"}]},"cv_name":"biological_process","definition":"The process resulting in the release of a polypeptide chain from the ribosome, usually in response to a termination codon (UAA, UAG, or UGA in the universal genetic code).","definition_xrefs":["GOC:hjd","ISBN:019879276X"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex disassembly","termid":"GO:0032984"},{"relation_name":"part_of","term_name":"translation","termid":"GO:0006412"}],"gene_count":17,"genes_by_uniquename":{"SJAG_00286":null,"SJAG_00308":null,"SJAG_00338":null,"SJAG_00642":null,"SJAG_01518":null,"SJAG_01696":null,"SJAG_02189":null,"SJAG_02601":null,"SJAG_02704":null,"SJAG_02812":null,"SJAG_03232":null,"SJAG_03658":null,"SJAG_03949":null,"SJAG_04283":null,"SJAG_04862":null,"SJAG_05221":null,"SJAG_05265":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"translational termination","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000108":null},"secondary_identifiers":["GO:0006456","GO:0006443","Reactome:R-HSA-72764"],"synonyms":[{"name":"protein synthesis termination","type":"broad"},{"name":"translation termination","type":"exact"},{"name":"translational complex disassembly","type":"exact"}],"termid":"GO:0006415","terms_by_termid":{"GO:0002184":null,"GO:0006415":null,"GO:0006449":null,"GO:0045905":null,"GO:0070126":null}}


id: MONDO:0020739
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hypercalcemia, infantile","termid":"MONDO:0000212"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005066"],"is_obsolete":false,"name":"hypercalcemia, infantile, 1","secondary_identifiers":["GARD:18434","OMIM:143880","MEDGEN:934200","UMLS:C4310232"],"synonyms":[{"name":"HCINF1","type":"exact"},{"name":"autosomal recessive infantile hypercalcemia 1","type":"exact"},{"name":"hypercalcemia, infantile, 1","type":"exact"}],"termid":"MONDO:0020739","xrefs":{"Monarch":{"xref_id":"0020739"}}}


id: MOD:01736
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a hydrogen atom of a residue with the Proteome Sciences TMT6plex-128 reporter+balance group.","definition_xrefs":["Unimod:737"],"direct_ancestors":[{"relation_name":"is_a","term_name":"TMT6plex reporter+balance reagent acylated residue","termid":"MOD:01715"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TMT6plex-128 reporter+balance reagent acylated residue","synonyms":[{"name":"3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl","type":"exact"},{"name":"Sixplex Tandem Mass Tag(TM)","type":"related"},{"name":"TMT6plex","type":"related"}],"termid":"MOD:01736"}


id: GO:0048520
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of behavior, the internally coordinated responses (actions or inactions) of whole living organisms (individuals or groups) to internal or external stimuli.","definition_xrefs":["GOC:pr","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of behavior","termid":"GO:0050795"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"positively_regulates","term_name":"behavior","termid":"GO:0007610"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of behavior","synonyms":[{"name":"activation of behavior","type":"narrow"},{"name":"stimulation of behavior","type":"narrow"},{"name":"up regulation of behavior","type":"exact"},{"name":"up-regulation of behavior","type":"exact"},{"name":"upregulation of behavior","type":"exact"}],"termid":"GO:0048520"}


id: MONDO:0024529
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial mitral valve prolapse","termid":"MONDO:0008004"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"MVP1","secondary_identifiers":["OMIM:157700","GARD:3688","MEDGEN:320443","UMLS:C1834819"],"synonyms":[{"name":"MVP1","type":"exact"},{"name":"PMV","type":"related"},{"name":"barlow syndrome","type":"related"},{"name":"click-murmur syndrome","type":"related"},{"name":"floppy mitral valve","type":"related"},{"name":"mitral regurgitation, familial","type":"related"},{"name":"mitral valve prolapse 1","type":"related"},{"name":"mitral valve prolapse, familial","type":"related"},{"name":"mitral valve prolapse, familial, X-linked","type":"related"},{"name":"mitral valve prolapse, myxomatous 1","type":"related"},{"name":"myxomatous mitral valve prolapse 1","type":"related"},{"name":"myxomatous valvular disease, familial","type":"related"},{"name":"prolapsed mitral valve","type":"related"}],"termid":"MONDO:0024529","xrefs":{"Monarch":{"xref_id":"0024529"}}}


id: GO:0045296
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to cadherin, a type I membrane protein involved in cell adhesion.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell adhesion molecule binding","termid":"GO:0050839"}],"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:0003674","GO:0005515","GO:0005488"],"is_obsolete":false,"name":"cadherin binding","termid":"GO:0045296"}


id: PBO:0006187
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_upstream_target","termid":"PBO:0006187"}


id: MONDO:0021296
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A in situ carcinoma that involves the renal pelvis.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kidney carcinoma in situ","termid":"MONDO:0004732"},{"relation_name":"is_a","term_name":"renal pelvis carcinoma","termid":"MONDO:0005519"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005240"],"is_obsolete":false,"name":"carcinoma in situ of renal pelvis","secondary_identifiers":["NCIT:C4597","UMLS:C0347184","SCTID:92697000","MEDGEN:83855","ICD9:233.9"],"synonyms":[{"name":"carcinoma in situ of kidney pelvis","type":"exact"},{"name":"carcinoma in situ of renal pelvis","type":"exact"},{"name":"carcinoma in situ of the kidney pelvis","type":"exact"},{"name":"carcinoma in situ of the renal pelvis","type":"exact"},{"name":"kidney pelvis carcinoma in situ","type":"exact"},{"name":"renal pelvis carcinoma in situ","type":"exact"},{"name":"renal pelvis in situ carcinoma","type":"exact"},{"name":"stage 0 renal pelvis carcinoma","type":"exact"},{"name":"stage 0is carcinoma of kidney pelvis","type":"exact"},{"name":"stage 0is carcinoma of renal pelvis","type":"exact"},{"name":"stage 0is carcinoma of the kidney pelvis","type":"exact"},{"name":"stage 0is carcinoma of the renal pelvis","type":"exact"},{"name":"stage 0is kidney pelvis carcinoma","type":"exact"},{"name":"stage 0is kidney renal pelvis urothelial cancer","type":"exact"},{"name":"stage 0is renal pelvis cancer","type":"exact"},{"name":"stage 0is renal pelvis cancer aJCC v7","type":"exact"},{"name":"stage 0is renal pelvis urothelial carcinoma","type":"exact"},{"name":"stage 0is renal pelvis urothelial carcinoma aJCC v7","type":"exact"}],"termid":"MONDO:0021296","xrefs":{"Monarch":{"xref_id":"0021296"}}}


id: MONDO:0010251
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"non-syndromic X-linked intellectual disability","termid":"MONDO:0019181"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intellectual disability, X-linked 50","secondary_identifiers":["MESH:C564713","OMIM:300115","UMLS:C1848087","DOID:0112029","GARD:22668","MEDGEN:376278"],"synonyms":[{"name":"MRX50","type":"exact"},{"name":"intellectual developmental disorder, X-linked 50","type":"exact"},{"name":"intellectual disability, X-linked 50","type":"exact"},{"name":"mental retardation, X-linked 50","type":"related"}],"termid":"MONDO:0010251","xrefs":{"Monarch":{"xref_id":"0010251"}}}


id: PBO:0075466
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPATA17 antisense RNA 1","termid":"PBO:0075466"}


id: GO:2001031
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of cellular glucuronidation.","definition_xrefs":["GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of cellular glucuronidation (obsolete GO:2001031)","synonyms":[{"name":"positive regulation of cellular glucuronide biosynthesis","type":"exact"},{"name":"positive regulation of cellular glucuronide biosynthetic process","type":"exact"},{"name":"positive regulation of cellular glucuronoside biosynthesis","type":"exact"},{"name":"positive regulation of cellular glucuronoside biosynthetic process","type":"exact"}],"termid":"GO:2001031"}


id: GO:0031442
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of mRNA 3'-end processing.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mRNA 3'-end processing","termid":"GO:0031440"},{"relation_name":"is_a","term_name":"positive regulation of mRNA processing","termid":"GO:0050685"},{"relation_name":"positively_regulates","term_name":"mRNA 3'-end processing","termid":"GO:0031124"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0016071"},{"rel_name":"positively_regulates","termid":"GO:0016071"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0016071","GO:0008150"],"is_obsolete":false,"name":"positive regulation of mRNA 3'-end processing","synonyms":[{"name":"activation of mRNA 3'-end processing","type":"narrow"},{"name":"stimulation of mRNA 3'-end processing","type":"narrow"},{"name":"up regulation of mRNA 3'-end processing","type":"exact"},{"name":"up-regulation of mRNA 3'-end processing","type":"exact"},{"name":"upregulation of mRNA 3'-end processing","type":"exact"}],"termid":"GO:0031442"}


id: GO:1905871
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of protein localization to cell leading edge.","definition_xrefs":["GO_REF:0000058","PMID:26324884","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein localization","termid":"GO:0032880"},{"relation_name":"regulates","term_name":"protein localization to cell leading edge","termid":"GO:1902463"}],"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 protein localization to cell leading edge","synonyms":[{"name":"regulation of protein localisation in cell leading edge","type":"exact"},{"name":"regulation of protein localisation to cell leading edge","type":"exact"},{"name":"regulation of protein localization in cell leading edge","type":"exact"}],"termid":"GO:1905871"}


id: MONDO:0957787
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":"Fliedner-Zweier syndrome","secondary_identifiers":["OMIM:620511","UMLS:C5882693","MEDGEN:1845438"],"termid":"MONDO:0957787","xrefs":{"Monarch":{"xref_id":"0957787"}}}


id: MONDO:0007989
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital microcoria is a rare autosomal dominant ophthalmological disease caused by maldevelopment of the dilator muscle of the pupil that is characterized by small pupils (<2 mm in diameter) from birth, peripheral iris hypopigmentation and transillumination defects leading to errors of refraction (myopia, astigmatism) and sometimes juvenile open angle glaucoma.","definition_xrefs":["Orphanet:566"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iridogoniodysgenesis","termid":"MONDO:0011119"}],"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":"congenital microcoria","secondary_identifiers":["GARD:3635","OMIM:156600","MEDGEN:227002","MESH:C537550","UMLS:C1303009","SCTID:400962005"],"synonyms":[{"name":"Mcor","type":"related"},{"name":"chromosome 13Q32 deletion syndrome","type":"related"},{"name":"congenital miosis","type":"exact"},{"name":"microcoria, congenital","type":"related"},{"name":"miosis, congenital","type":"related"},{"name":"pinhole pupils","type":"related"}],"termid":"MONDO:0007989","xrefs":{"Monarch":{"xref_id":"0007989"}}}


id: PBO:0083989
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Glutathione-dependent disulfide oxidoreductase; hydroperoxide and superoxide-radical responsive, heat-stable, with active site cysteine pair; protects cells from oxidative damage; GRX1 has a paralog, GRX2, that arose from the whole genome duplication; protein abundance increases in response to DNA replication stress","termid":"PBO:0083989"}


id: PBO:0048218
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gastric cancer associated transcript 2","termid":"PBO:0048218"}


id: GO:0008234
data:
  {"annotated_genes":["SJAG_04538","SJAG_02542","SJAG_01312","SJAG_00546","SJAG_03752","SJAG_05977","SJAG_03672","SJAG_04497","SJAG_00764","SJAG_00135","SJAG_03292","SJAG_01768","SJAG_02341","SJAG_00742","SJAG_16454","SJAG_00776","SJAG_03429","SJAG_00644","SJAG_02244","SJAG_00966","SJAG_04215","SJAG_02214","SJAG_03686","SJAG_00087","SJAG_01283","SJAG_01481","SJAG_00573","SJAG_01528","SJAG_02419","SJAG_02774","SJAG_04651","SJAG_00795"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[104763,108454],"is_not":false,"summary":null,"term":"GO:0008234"},{"annotations":[96044,93645,90914,97517,111152,114611,114258,109790,115397,111211,113750,114684,94003,113065,92911,105107,87880,104094,110589,88008,99366,94800,105273],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004843"},{"annotations":[91132,115279,117019],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004197"},{"annotations":[105599,89781],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016929"},{"annotations":[86957,113383],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003923"},{"annotations":[105600,89782],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070139"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of peptide bonds in a polypeptide chain by a mechanism in which the sulfhydryl group of a cysteine residue at the active center acts as a nucleophile.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidase activity","termid":"GO:0008233"}],"gene_count":32,"genes_by_uniquename":{"SJAG_00087":null,"SJAG_00135":null,"SJAG_00546":null,"SJAG_00573":null,"SJAG_00644":null,"SJAG_00742":null,"SJAG_00764":null,"SJAG_00776":null,"SJAG_00795":null,"SJAG_00966":null,"SJAG_01283":null,"SJAG_01312":null,"SJAG_01481":null,"SJAG_01528":null,"SJAG_01768":null,"SJAG_02214":null,"SJAG_02244":null,"SJAG_02341":null,"SJAG_02419":null,"SJAG_02542":null,"SJAG_02774":null,"SJAG_03292":null,"SJAG_03429":null,"SJAG_03672":null,"SJAG_03686":null,"SJAG_03752":null,"SJAG_04215":null,"SJAG_04497":null,"SJAG_04538":null,"SJAG_04651":null,"SJAG_05977":null,"SJAG_16454":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0008233"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0140096","GO:0016787","GO:0008233","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"cysteine-type peptidase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-5660752","Reactome:R-HSA-2467775","Reactome:R-HSA-9757951","Reactome:R-HSA-2467809","GO:0004220","Reactome:R-HSA-2022381"],"synonyms":[{"name":"cysteine protease activity","type":"narrow"},{"name":"thiol protease activity","type":"narrow"}],"termid":"GO:0008234","terms_by_termid":{"GO:0003923":null,"GO:0004197":null,"GO:0004843":null,"GO:0008234":null,"GO:0016929":null,"GO:0070139":null}}


id: GO:0035980
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The growth of colonies in filamentous chains of cells as a result of a reduced availability of nitrogen.","definition_xrefs":["GOC:vw"],"gene_count":0,"genotype_count":0,"name":"obsolete invasive growth in response to nitrogen limitation (obsolete GO:0035980)","synonyms":[{"name":"invasive growth in response to nitrogen limitation","type":"exact"}],"termid":"GO:0035980"}


id: PBO:0065699
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"purine rich element binding protein A","termid":"PBO:0065699"}


id: GO:0048202
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The addition of clathrin and adaptor proteins to Golgi membranes during the formation of transport vesicles, forming a vesicle coat.","definition_xrefs":["GOC:mah","ISBN:0716731363","GOC:jid","PMID:10219233"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Golgi transport vesicle coating","termid":"GO:0048200"},{"relation_name":"is_a","term_name":"clathrin coat assembly","termid":"GO:0048268"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0061024"},{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0065003","GO:0016192","GO:0006810","GO:0044085","GO:0061024"],"is_obsolete":false,"name":"clathrin coating of Golgi vesicle","synonyms":[{"name":"clathrin coating of Golgi-derived vesicle","type":"exact"}],"termid":"GO:0048202"}


id: PBO:0031326
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_cycloheximide","termid":"PBO:0031326"}


id: PBO:0030546
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-altered_cellular_cAMP_level","termid":"PBO:0030546"}


id: PBO:0060878
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NEMP2 divergent transcript","termid":"PBO:0060878"}


id: GO:0051717
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 1D-myo-inositol 1,3,4,5-tetrakisphosphate + H2O = 1D-myo-inositol 1,4,5-trisphosphate + phosphate.","definition_xrefs":["RHEA:77155"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inositol tetrakisphosphate phosphatase activity","termid":"GO:0052743"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016788"}],"interesting_parent_ids":["GO:0016788","GO:0003824","GO:0016787","GO:0003674"],"is_obsolete":false,"name":"inositol-1,3,4,5-tetrakisphosphate 3-phosphatase activity","secondary_identifiers":["Reactome:R-HSA-1855200","Reactome:R-HSA-1855205","MetaCyc:3.1.3.62-RXN"],"synonyms":[{"name":"inositol (1,3,4,5)-tetrakisphosphate 3-phosphatase activity","type":"related"},{"name":"inositol 1,3,4,5-tetrakisphosphate 3-phosphomonoesterase activity","type":"related"},{"name":"inositol 1,3,4,5-tetrakisphosphate-5-phosphomonoesterase activity","type":"related"}],"termid":"GO:0051717"}


id: MONDO:0016434
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. An instance of dermis elastic tissue disorder that is acquired during the lifetime of the individual.","definition_xrefs":["MONDO:patterns/acquired"],"gene_count":0,"genotype_count":0,"name":"obsolete acquired dermis elastic tissue disorder (obsolete MONDO:0016434)","secondary_identifiers":["Orphanet:228218"],"synonyms":[{"name":"acquired dermis elastic tissue disorder","type":"exact"}],"termid":"MONDO:0016434","xrefs":{"Monarch":{"xref_id":"0016434"}}}


id: GO:0032645
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of granulocyte macrophage colony-stimulating factor production.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytokine production","termid":"GO:0001817"},{"relation_name":"is_a","term_name":"regulation of protein metabolic process","termid":"GO:0051246"},{"relation_name":"regulates","term_name":"granulocyte macrophage colony-stimulating factor production","termid":"GO:0032604"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"regulation of granulocyte macrophage colony-stimulating factor production","secondary_identifiers":["GO:0045423"],"synonyms":[{"name":"regulation of GM-CSF production","type":"exact"},{"name":"regulation of granulocyte macrophage colony stimulating factor production","type":"exact"},{"name":"regulation of granulocyte macrophage colony-stimulating factor biosynthetic process","type":"narrow"}],"termid":"GO:0032645"}


id: SOFP:qseq_type
data:
  {"annotation_feature_type":"gene","cv_name":"feature_property","direct_ancestors":[{"relation_name":"is_a","term_name":"feature_property","termid":"SOFP:feature_property"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"qseq_type","termid":"SOFP:qseq_type"}


id: PBO:0027812
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-short_mitotic_spindle_during_metaphase","termid":"PBO:0027812"}


id: PBO:0055436
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 2866","termid":"PBO:0055436"}


id: GO:1901829
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of zeaxanthin bis(beta-D-glucoside).","definition_xrefs":["UniPathway:UPA00798","MetaCyc:PWY-6288","GOC:yaf","PMID:20075616","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carotenoid catabolic process","termid":"GO:0016118"},{"relation_name":"is_a","term_name":"beta-glucoside catabolic process","termid":"GO:1901805"},{"relation_name":"is_a","term_name":"zeaxanthin bis(beta-D-glucoside) metabolic process","termid":"GO:1901828"}],"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":"zeaxanthin bis(beta-D-glucoside) catabolic process","synonyms":[{"name":"zeaxanthin bis(beta-D-glucoside) breakdown","type":"exact"},{"name":"zeaxanthin bis(beta-D-glucoside) catabolism","type":"exact"},{"name":"zeaxanthin bis(beta-D-glucoside) degradation","type":"exact"},{"name":"zeaxanthin diglucoside breakdown","type":"exact"},{"name":"zeaxanthin diglucoside catabolism","type":"exact"},{"name":"zeaxanthin diglucoside degradation","type":"exact"}],"termid":"GO:1901829"}


id: GO:0006839
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{"annotated_genes":["SJAG_02473","SJAG_03334","SJAG_02797","SJAG_04260","SJAG_00275","SJAG_01924","SJAG_00196","SJAG_03399","SJAG_01649","SJAG_04515","SJAG_01560","SJAG_04737","SJAG_02016","SJAG_03503","SJAG_00543","SJAG_01615","SJAG_03515","SJAG_02917","SJAG_01120","SJAG_00671","SJAG_03358","SJAG_04996","SJAG_02077","SJAG_04218","SJAG_03650","SJAG_00687","SJAG_03873","SJAG_00404","SJAG_00626","SJAG_02050","SJAG_02524","SJAG_02484","SJAG_01597","SJAG_02457","SJAG_00612","SJAG_03415","SJAG_02602","SJAG_00835","SJAG_03416","SJAG_01684","SJAG_00522","SJAG_01639","SJAG_04984","SJAG_01589","SJAG_04208","SJAG_01879","SJAG_03577","SJAG_04432","SJAG_03452","SJAG_01872","SJAG_04593","SJAG_00373","SJAG_04014","SJAG_01949","SJAG_00569","SJAG_01951","SJAG_02034","SJAG_00547","SJAG_01442","SJAG_00564","SJAG_00048","SJAG_03560","SJAG_02398","SJAG_01647","SJAG_04336","SJAG_02355","SJAG_04328","SJAG_01640","SJAG_02445","SJAG_01780","SJAG_01890","SJAG_05259","SJAG_04588","SJAG_03502","SJAG_00760","SJAG_00154","SJAG_02361"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[95135,96857],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036444"},{"annotations":[112579],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0160007"},{"annotations":[99731,97729],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904983"},{"annotations":[76312],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0170036"},{"annotations":[97580,113231,99982],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048250"},{"annotations":[88787],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140466"},{"annotations":[99732],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0170046"},{"annotations":[97730],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110141"},{"annotations":[114076],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990616"},{"annotations":[96063],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990551"},{"annotations":[100846],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990554"},{"annotations":[100847],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990553"},{"annotations":[110346],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140021"},{"annotations":[96064],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990550"},{"annotations":[102342,110347],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990544"},{"annotations":[91289,111711],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006843"},{"annotations":[90343],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990559"},{"annotations":[94554,96638,97996],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0160203"},{"annotations":[107027],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990548"},{"annotations":[114593],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140140"},{"annotations":[87927],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990556"},{"annotations":[107372],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990575"},{"annotations":[106781],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045016"},{"annotations":[92409],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990549"},{"annotations":[87928],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990555"},{"annotations":[104099],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990547"},{"annotations":[93727],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140141"},{"annotations":[93900,113603],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006850"},{"annotations":[102094,87783],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990543"},{"annotations":[87929],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990557"},{"annotations":[103123],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990545"},{"annotations":[89009,96620,100584],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990542"},{"annotations":[75090],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090374"},{"annotations":[87846,109224],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045041"},{"annotations":[98743,99040,90407,104657,96386,98926,106975,102766,102185,87847,107032,116689,105644,114673,99810,111249,89051,109338,116224,94023,107054],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030150"},{"annotations":[98927,89904,92292,102409,106761,107033,107055,112639,115713,88173,106976],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045039"},{"annotations":[90417,98088,111243,109862,89883,97737,109505,109852,107034],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045040"},{"annotations":[98799],"is_not":false,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id: PBO:0058880
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 10396b","termid":"PBO:0058880"}


id: PBO:0067804
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 106","termid":"PBO:0067804"}


id: PBO:0027297
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-fragmented_septum","termid":"PBO:0027297"}


id: PBO:0091719
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ATP-dependent RNA helicase Mss116","termid":"PBO:0091719"}


id: PBO:0067077
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 108, pseudogene","termid":"PBO:0067077"}


id: FYPO:0007728
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of a protein kinase activity is normal (i.e. indistinguishable from wild type) during a cellular response to osmotic stress.","definition_xrefs":["PomBase:mah","PMID:33137119"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein kinase activity","termid":"FYPO:0003075"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000257","FYPO:0000654"],"is_obsolete":false,"name":"normal protein kinase activity during cellular response to osmotic stress","termid":"FYPO:0007728"}


id: PBO:0033832
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S6 kinase Psk1","termid":"PBO:0033832"}


id: MONDO:0015140
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A progressive dementia with reduction of cognitive functions. It presents the same phenotype as sporadic Alzheimer disease (AD) but has an early age of onset, usually before 60 years old.","definition_xrefs":["Orphanet:1020"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"familial Alzheimer disease","termid":"MONDO:0100087"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0002039","MONDO:0005559","MONDO:0000426"],"is_obsolete":false,"name":"early-onset autosomal dominant Alzheimer disease","secondary_identifiers":["GARD:12798"],"synonyms":[{"name":"EOFAD","type":"exact"},{"name":"early-onset familial autosomal dominant Alzheimer disease","type":"exact"},{"name":"early-onset, autosomal dominant Alzheimer disease","type":"related"}],"termid":"MONDO:0015140","xrefs":{"Monarch":{"xref_id":"0015140"}}}


id: PR:P0CT40
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- Tf2-9 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P0CT40"],"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":"transposon Tf2-9 polyprotein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC9B6.02c","synonyms":[{"name":"Spom972h-Tf2-9","type":"exact"},{"name":"retrotransposable element Tf2 155 kDa protein (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P0CT40"}


id: FYPO:0007498
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which occurrence of chromatin binding by a gene product (usually a protein) at one or more cohesin-associated regions (CARs) in a mutant is decreased. The affected gene product may be encoded by the mutated gene, or by a different gene, and may normally bind DNA, protein, or both in chromatin.","definition_xrefs":["PMID:31895039","PomBase:mah","PMID:27226485"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased chromatin binding","termid":"FYPO:0002577"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000702"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000702","FYPO:0000652","FYPO:0000707","FYPO:0001985"],"is_obsolete":false,"name":"decreased chromatin binding at cohesin associated regions","synonyms":[{"name":"decreased chromatin binding at CARs","type":"exact"},{"name":"decreased chromatin binding at cohesin associated regions during mitotic cell cycle","type":"related"},{"name":"decreased chromatin binding at cohesin associated regions during vegetative growth","type":"exact"},{"name":"reduced chromatin binding at cohesin associated regions","type":"exact"}],"termid":"FYPO:0007498"}


id: GO:0033501
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A homeostatic process involved in the maintenance of an internal steady state of galactose within an organism or cell.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete galactose homeostasis (obsolete GO:0033501)","termid":"GO:0033501"}


id: MONDO:0008161
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Otodental syndrome is a very rare inherited condition characterized by grossly enlarged canine and molar teeth (globodontia) associated with sensorineural hearing loss.","definition_xrefs":["Orphanet:2791"],"direct_ancestors":[{"relation_name":"is_a","term_name":"partial deletion of the long arm of chromosome 11","termid":"MONDO:0016910"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"otodental syndrome","secondary_identifiers":["MEDGEN:318937","GARD:4168","OMIM:166750","SCTID:707310009","UMLS:C1833693"],"synonyms":[{"name":"chromosome 11q13 deletion syndrome","type":"related"},{"name":"globodontia","type":"exact"},{"name":"oculootodental syndrome","type":"related"},{"name":"otodental dysplasia","type":"exact"},{"name":"otodental dysplasia chromosome deletion syndrome","type":"exact"},{"name":"otodental syndrome","type":"exact"},{"name":"otodental syndrome with coloboma","type":"related"}],"termid":"MONDO:0008161","xrefs":{"Monarch":{"xref_id":"0008161"}}}


id: MONDO:0019591
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Insufficient production of all the anterior pituitary hormones.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"combined pituitary hormone deficiencies, genetic form","termid":"MONDO:0013099"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"panhypopituitarism","secondary_identifiers":["NCIT:C110940","SCTID:32390006","ICD9:253.2","GARD:15020","MedDRA:10033662","Orphanet:90695","UMLS:C0242343","DOID:9410","MEDGEN:69171","icd11.foundation:1576287890"],"synonyms":[{"name":"Simmond's disease","type":"exact"},{"name":"Simmonds' disease","type":"exact"},{"name":"complete hypopituitarism","type":"exact"}],"termid":"MONDO:0019591","xrefs":{"Monarch":{"xref_id":"0019591"}}}


id: FYPO:0000626
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  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the initiation of premeiotic DNA replication is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal DNA replication initiation","termid":"FYPO:0000176"},{"relation_name":"is_a","term_name":"abnormal premeiotic DNA replication","termid":"FYPO:0000625"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000293","FYPO:0000631","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"abnormal initiation of premeiotic DNA replication","synonyms":[{"name":"abnormal initiation of meiotic DNA synthesis","type":"related"},{"name":"abnormal initiation of premeiotic DNA synthesis","type":"related"},{"name":"abnormal meiotic DNA replication initiation","type":"related"},{"name":"abnormal premeiotic DNA replication initiation","type":"exact"}],"termid":"FYPO:0000626"}


id: MONDO:0001440
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"keratoconjunctivitis","termid":"MONDO:0004768"}],"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":"neurotrophic keratoconjunctivitis","secondary_identifiers":["UMLS:C0155084","MEDGEN:509777","DOID:12125","ICD9:370.35","SCTID:77080005"],"termid":"MONDO:0001440","xrefs":{"Monarch":{"xref_id":"0001440"}}}


id: PBO:0076006
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"STIM activating enhancer","termid":"PBO:0076006"}


id: GO:0002929
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A highly stable complex composed of the ATAC complex and the mediator complex (also called TRAP or MED). MECO binds and regulates the transcription of a subset of non-coding RNAs transcribed by RNA polymerase II.","definition_xrefs":["GOC:hjd","PMID:20508642"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"MECO complex","synonyms":[{"name":"meta-coactivator complex","type":"exact"}],"termid":"GO:0002929"}


id: GO:1903831
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any signal transduction that is involved in cellular response to ammonium ion.","definition_xrefs":["GO_REF:0000060","GOC:TermGenie","PMID:16297994"],"direct_ancestors":[{"relation_name":"is_a","term_name":"signal transduction","termid":"GO:0007165"},{"relation_name":"part_of","term_name":"cellular response to ammonium ion","termid":"GO:0071242"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"signal transduction involved in cellular response to ammonium ion","synonyms":[{"name":"signaling cascade involved in cellular response to ammonium ion","type":"narrow"},{"name":"signaling pathway involved in cellular response to ammonium ion","type":"related"},{"name":"signalling cascade involved in cellular response to ammonium ion","type":"narrow"},{"name":"signalling pathway involved in cellular response to ammonium ion","type":"related"}],"termid":"GO:1903831"}


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: MONDO:0700186
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Histiocytic sarcoma occurring in a cat.","definition_xrefs":["NCIT:C157503"],"direct_ancestors":[{"relation_name":"is_a","term_name":"feline neoplasm","termid":"MONDO:0700175"},{"relation_name":"is_a","term_name":"hematologic disorder, non-human animal","termid":"MONDO:1011319"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"feline histiocytic sarcoma","termid":"MONDO:0700186","xrefs":{"Monarch":{"xref_id":"0700186"}}}


id: MONDO:0001099
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Single or multiple, milk-containing nodules in the breast. It is caused by obstruction of the breast ducts during lactation. Needle aspiration of the milk is the treatment of choice.","definition_xrefs":["NCIT:C3515"],"direct_ancestors":[{"relation_name":"is_a","term_name":"breast cyst","termid":"MONDO:0001011"},{"relation_name":"is_a","term_name":"lactation disease","termid":"MONDO:0045019"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lactocele","secondary_identifiers":["icd11.foundation:1987155556","MESH:C535998","DOID:10686","UMLS:C0152243","ICD9:611.5","MEDGEN:101829","SCTID:42385006"],"synonyms":[{"name":"Galactocoele","type":"related"},{"name":"galactocele","type":"exact"},{"name":"lacteal cyst","type":"related"}],"termid":"MONDO:0001099","xrefs":{"Monarch":{"xref_id":"0001099"}}}


id: PBO:0050921
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IFITM3 pseudogene 4","termid":"PBO:0050921"}


id: PR:Q9UT25
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC9.02c gene.","definition_xrefs":["UniProtKB:Q9UT25","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 N-acetyltransferase C9.02c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC9.02c","synonyms":[{"name":"Spom972h-SPAC9.02c","type":"exact"}],"termid":"PR:Q9UT25"}


id: MONDO:0100069
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A syndromic genetic deafness characterized by segregation of nonsyndromic hearing loss in females and hearing loss with infertility in males. Affected males have been reported to have low count to absent sperm, immobile sperm, and/or sperm with abnormal morphology.","definition_xrefs":["PMID:29293958"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hearing impairment and infertile male syndrome","synonyms":[{"name":"HIIMS","type":"exact"},{"name":"hearing impairment and infertile male syndrome","type":"exact"}],"termid":"MONDO:0100069","xrefs":{"Monarch":{"xref_id":"0100069"}}}


id: MONDO:0007547
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The most common type of cutaneous cyst. It results from the proliferation of epidermal cells in a circumscribed space within the dermis. It is usually asymptomatic and presents as a firm, round nodule.","definition_xrefs":["NCIT:C3134"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"epidermoid cysts","secondary_identifiers":["UMLS:C0014511","MEDGEN:41829","MESH:D004814","OMIM:131600","SCTID:419893006"],"synonyms":[{"name":"Epidermal cyst","type":"exact"},{"name":"Follicular infundibular cyst","type":"exact"},{"name":"epidermal inclusion cyst","type":"exact"},{"name":"epidermoid cyst","type":"exact"},{"name":"epidermoid cysts","type":"exact"},{"name":"epithelial cyst","type":"exact"},{"name":"horn cyst","type":"exact"},{"name":"inclusion cyst","type":"exact"},{"name":"infundibular cyst","type":"exact"},{"name":"keratin cyst","type":"exact"},{"name":"keratinizing cyst","type":"exact"},{"name":"keratinous cyst","type":"exact"},{"name":"squamous cyst","type":"exact"}],"termid":"MONDO:0007547","xrefs":{"Monarch":{"xref_id":"0007547"}}}


id: PBO:0071651
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L36 pseudogene 15","termid":"PBO:0071651"}


id: PBO:0076258
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"supervillin","termid":"PBO:0076258"}


id: GO:0098825
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The guanylylation of peptidyl-histidine to form (phospho-5'-guanosine)-L-histidine.","definition_xrefs":["RESID:AA0325"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-histidine guanylation (obsolete GO:0098825)","termid":"GO:0098825"}


id: PBO:0110401
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piezo type mechanosensitive ion channel component 1 (Er blood group)","termid":"PBO:0110401"}


id: GO:0010034
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an acetate stimulus.","definition_xrefs":["GOC:sm"],"direct_ancestors":[{"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 acetate","termid":"GO:0010034"}


id: GO:1901303
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of cargo loading into a COPII-coated vesicle.","definition_xrefs":["GOC:lb","GOC:TermGenie","PMID:15899885"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of intracellular transport","termid":"GO:0032387"},{"relation_name":"is_a","term_name":"regulation of cargo loading into COPII-coated vesicle","termid":"GO:1901301"},{"relation_name":"negatively_regulates","term_name":"COPII-coated vesicle cargo loading","termid":"GO:0090110"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"negative regulation of cargo loading into COPII-coated vesicle","synonyms":[{"name":"down regulation of COPII coat-cargo complex assembly","type":"related"},{"name":"down regulation of cargo loading into COPII vesicle","type":"exact"},{"name":"down regulation of cargo loading into COPII-coated vesicle","type":"exact"},{"name":"down regulation of cargo selection into COPII-coated vesicle","type":"exact"},{"name":"down-regulation of COPII coat-cargo complex assembly","type":"related"},{"name":"down-regulation of cargo loading into COPII vesicle","type":"exact"},{"name":"down-regulation of cargo loading into COPII-coated vesicle","type":"exact"},{"name":"down-regulation of cargo selection into COPII-coated vesicle","type":"exact"},{"name":"downregulation of COPII coat-cargo complex assembly","type":"related"},{"name":"downregulation of cargo loading into COPII vesicle","type":"exact"},{"name":"downregulation of cargo loading into COPII-coated vesicle","type":"exact"},{"name":"downregulation of cargo selection into COPII-coated vesicle","type":"exact"},{"name":"inhibition of COPII coat-cargo complex assembly","type":"related"},{"name":"inhibition of COPII vesicle protein binding","type":"narrow"},{"name":"inhibition of cargo loading into COPII vesicle","type":"exact"},{"name":"inhibition of cargo loading into COPII-coated vesicle","type":"narrow"},{"name":"inhibition of cargo selection into COPII-coated vesicle","type":"exact"},{"name":"inhibition of protein sorting into COPII-coated vesicles","type":"exact"},{"name":"negative regulation of COPII coat-cargo complex assembly","type":"related"},{"name":"negative regulation of cargo loading into COPII vesicle","type":"exact"},{"name":"negative regulation of cargo selection into COPII-coated vesicle","type":"exact"}],"termid":"GO:1901303"}


id: GO:0034325
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of a decyl group to an oxygen atom on the acceptor molecule.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-acyltransferase activity","termid":"GO:0008374"},{"relation_name":"is_a","term_name":"decanoyltransferase activity","termid":"GO:0034328"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016746"}],"interesting_parent_ids":["GO:0016746","GO:0003674","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"O-decanoyltransferase activity","termid":"GO:0034325"}


id: MONDO:0014094
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"STEAP3/TSAP6-related sideroblastic anemia is a very rare severe non-syndromic hypochromic anemia, which is characterized by transfusion-dependent hypochromic, poorly regenerative anemia, iron overload, resembling non-syndromic sideroblastic anemia except for increased erythrocyte protoporphyrin levels.","definition_xrefs":["Orphanet:300298"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anemia, hypochromic microcytic with iron overload","termid":"MONDO:0000104"},{"relation_name":"is_a","term_name":"congenital anemia","termid":"MONDO:0000577"},{"relation_name":"is_a","term_name":"inherited deficiency anemia","termid":"MONDO:0016624"},{"relation_name":"is_a","term_name":"inherited sideroblastic anemia","termid":"MONDO:0020099"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0002280","MONDO:0005570"],"is_obsolete":false,"name":"severe congenital hypochromic anemia with ringed sideroblasts","secondary_identifiers":["SCTID:725463007","MEDGEN:815250","UMLS:C3808920","GARD:17364","OMIM:615234"],"synonyms":[{"name":"AHMIO2","type":"related"},{"name":"anemia, hypochromic microcytic, with iron overload 2","type":"related"},{"name":"anemia, hypochromic microcytic, with iron overload type 2","type":"exact"},{"name":"severe congenital hypochromic sideroblastic anaemia","type":"exact"},{"name":"severe congenital hypochromic sideroblastic anemia","type":"exact"}],"termid":"MONDO:0014094","xrefs":{"Monarch":{"xref_id":"0014094"}}}


id: GO:0006615
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which an SRP-bound ribosome forms a complex with the SRP receptor in the ER membrane, allowing the ribosome to bind to the membrane, during cotranslational membrane targeting.","definition_xrefs":["ISBN:0815316194"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein to membrane docking","termid":"GO:0022615"},{"relation_name":"part_of","term_name":"SRP-dependent cotranslational protein targeting to membrane","termid":"GO:0006614"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006605"}],"interesting_parent_ids":["GO:0008150","GO:0006605"],"is_obsolete":false,"name":"SRP-dependent cotranslational protein targeting to membrane, docking","synonyms":[{"name":"SRP-dependent cotranslational membrane targeting, docking","type":"exact"},{"name":"SRP-dependent cotranslational protein-membrane targeting, docking","type":"exact"},{"name":"protein docking during SRP-dependent cotranslational protein targeting to membrane","type":"exact"}],"termid":"GO:0006615"}


id: GO:0042890
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Enables the transfer of 3-phenylpropionic acid from one side of a membrane to the other.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete 3-phenylpropionic acid transmembrane transporter activity (obsolete GO:0042890)","synonyms":[{"name":"3-phenylpropionate acid transporter activity","type":"exact"},{"name":"HCA transporter activity","type":"exact"},{"name":"hydrocinnamic acid transporter activity","type":"exact"}],"termid":"GO:0042890"}


id: GO:0102831
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 raffinose = stachyose + sucrose.","definition_xrefs":["PMID:12060258","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hexosyltransferase activity","termid":"GO:0016758"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016740","GO:0016757","GO:0003674"],"is_obsolete":false,"name":"stachyose synthase activity","secondary_identifiers":["MetaCyc:RXN-8287"],"termid":"GO:0102831"}


id: MONDO:0004880
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any disease in which the causes of the disease is a perturbation of the lower digestive tract leading to its dysfunction.","definition_xrefs":["MONDO:patterns/disease_by_dysfunctional_structure"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intestinal disorder","termid":"MONDO:0005020"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"bowel dysfunction","secondary_identifiers":["ICD9:564.9","UMLS:C2004461","SCTID:235594008","MEDGEN:384468","DOID:9779"],"synonyms":[{"name":"disease of lower digestive tract","type":"exact"},{"name":"lower digestive tract disease","type":"exact"}],"termid":"MONDO:0004880","xrefs":{"Monarch":{"xref_id":"0004880"}}}


id: GO:0035379
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of carbon dioxide (CO2) from one side of a membrane to the other.","definition_xrefs":["GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane transporter activity","termid":"GO:0022857"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"carbon dioxide transmembrane transporter activity","secondary_identifiers":["Reactome:R-HSA-1237042","Reactome:R-HSA-1237069","Reactome:R-HSA-1247649","Reactome:R-HSA-1247645"],"termid":"GO:0035379"}


id: PR:Q9Y7R9
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC306.11 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9Y7R9"],"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 C306.11 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC306.11","synonyms":[{"name":"Spom972h-SPCC306.11","type":"exact"}],"termid":"PR:Q9Y7R9"}


id: PBO:0084481
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Medium chain fatty acyl-CoA synthetase; activates imported fatty acids; accepts a wide range of fatty acid chain lengths with a preference for medium chains, C9:0-C13:0; localized to the peroxisome; comparative analysis suggests that a mitochondrially targeted form may result from translation starting at a non-canonical codon upstream of the annotated start codon","termid":"PBO:0084481"}


id: GO:0005630
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The outermost layer of the spore wall, as described in Saccharomyces.","definition_xrefs":["ISBN:0879693568"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"ascospore wall","termid":"GO:0005619"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005618"}],"interesting_parent_ids":["GO:0005618","GO:0005575"],"is_obsolete":false,"name":"dityrosine layer of spore wall","termid":"GO:0005630"}


id: PBO:0003733
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial outer membrane protein Mdm34 (predicted)","termid":"PBO:0003733"}


id: PBO:0051349
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin kappa variable 2D-38 (pseudogene)","termid":"PBO:0051349"}


id: PBO:0085391
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Plasma membrane metalloid/H+ antiporter; member of bile/arsenite/riboflavin transporter (BART) superfamily; transports arsenite and antimonite; required for resistance to arsenic compounds; transcription is activated by Arr1p in the presence of arsenite; protein displays 10 transmembrane segments with cytoplasmically oriented N- and C-terminal domains","termid":"PBO:0085391"}


id: PBO:0085605
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in control of cell wall structure and stress response; direct inhibitor of the nuclear Dbf2 related (NDR) kinase Cbk1p-Mob2p; overproduction confers resistance to cell-wall degrading enzymes; exhibits genetic interactions with genes involved in the cell wall integrity pathway; LRE1 has a paralog, HLR1, that arose from the whole genome duplication","termid":"PBO:0085605"}


id: PBO:0034489
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_reverse_centromeric_outer_repeat_transcript_level","termid":"PBO:0034489"}


id: PBO:0065669
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein tyrosine phosphatase receptor type R","termid":"PBO:0065669"}


id: GO:0072549
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: monocoumaroyl dicaffeoyl spermidine + NADPH + O2 = tricaffeoyl spermidine + NADP+ + H2O.","definition_xrefs":["GOC:kad","PMID:19779199"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tri-(coumaroyl or caffeoyl) spermidine meta-hydroxylase activity","termid":"GO:0072533"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"monocoumaroyl dicaffeoyl spermidine meta-hydroxylase activity","termid":"GO:0072549"}


id: PBO:0046762
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exosome component 3 pseudogene 1","termid":"PBO:0046762"}


id: MONDO:0015875
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare non-malformative uterine adnexal disease (obsolete MONDO:0015875)","secondary_identifiers":["Orphanet:180303"],"termid":"MONDO:0015875","xrefs":{"Monarch":{"xref_id":"0015875"}}}


id: PBO:0090107
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rho GDP dissociation inhibitor Rdi1","termid":"PBO:0090107"}


id: GO:0003296
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any apoptotic process that contributes to the reorganization of tissue resulting in the maturation of the atrial ventricular junction.","definition_xrefs":["GOC:mtg_apoptosis","GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"apoptotic process involved in heart morphogenesis","termid":"GO:0003278"},{"relation_name":"part_of","term_name":"atrial ventricular junction remodeling","termid":"GO:0003294"}],"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":"apoptotic process involved in atrial ventricular junction remodeling","synonyms":[{"name":"apoptosis involved in atrial ventricular junction remodelling","type":"exact"},{"name":"apoptosis involved in atrio-ventricular junction remodeling","type":"exact"},{"name":"apoptosis involved in atrio-ventricular junction remodelling","type":"exact"},{"name":"apoptosis involved in atrioventricular junction remodeling","type":"exact"},{"name":"apoptosis involved in atrioventricular junction remodelling","type":"exact"}],"termid":"GO:0003296"}


id: GO:0031510
data:
  {"annotated_genes":["SJAG_00604","SJAG_05032"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[97254,103957],"is_not":false,"summary":null,"term":"GO:0031510"}]},"cv_name":"cellular_component","definition":"A conserved heterodimeric complex with SUMO activating enzyme activity.","definition_xrefs":["PMID:15601841"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"},{"relation_name":"is_a","term_name":"catalytic complex","termid":"GO:1902494"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00604":null,"SJAG_05032":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005634"],"is_obsolete":false,"name":"SUMO activating enzyme complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"SAE","type":"exact"},{"name":"SUMO E1 activator enzyme complex","type":"exact"}],"termid":"GO:0031510","terms_by_termid":{"GO:0031510":null}}


id: PBO:0055057
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 2473","termid":"PBO:0055057"}


id: MONDO:0013173
data:
  {"annotated_genes":["SJAG_04358"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86017],"is_not":false,"summary":null,"term":"MONDO:0013173"}]},"cv_name":"mondo","definition":"Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the TRAPPC9 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_04358":null},"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:0037792"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0037792","MONDO:0006025"],"is_obsolete":false,"name":"intellectual disability, autosomal recessive 13","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0081098","GARD:22548","MEDGEN:442564","MESH:C567714","UMLS:C2750791","OMIM:613192"],"synonyms":[{"name":"MRT13","type":"related"},{"name":"TRAPPC9 autosomal recessive non-syndromic intellectual disability","type":"exact"},{"name":"autosomal recessive non-syndromic intellectual disability caused by mutation in TRAPPC9","type":"exact"},{"name":"intellectual disability, autosomal recessive 13","type":"exact"},{"name":"intellectual disability, autosomal recessive type 13","type":"exact"},{"name":"mental retardation, autosomal recessive 13","type":"related"},{"name":"mental retardation, autosomal recessive type 13","type":"exact"}],"termid":"MONDO:0013173","terms_by_termid":{"MONDO:0013173":null},"xrefs":{"Monarch":{"xref_id":"0013173"}}}


id: MONDO:0015338
data:
  {"annotated_genes":["SJAG_02165","SJAG_04270","SJAG_03249","SJAG_02200","SJAG_04995"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85140],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008726"},{"annotations":[84614],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0020667"},{"annotations":[84963],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014558"},{"annotations":[85070,85069],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009039"},{"annotations":[86142],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013740"}]},"cv_name":"mondo","definition":"A craniosynostosis that is part of a larger syndrome.","definition_xrefs":["MONDO:patterns/syndromic"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"craniosynostosis","termid":"MONDO:0015469"},{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"gene_count":5,"genes_by_uniquename":{"SJAG_02165":null,"SJAG_02200":null,"SJAG_03249":null,"SJAG_04270":null,"SJAG_04995":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"syndromic craniosynostosis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1842203","GARD:19911","UMLS:C5680624","Orphanet:139393"],"synonyms":[{"name":"syndrome associated with craniosynostosis","type":"exact"},{"name":"syndromic craniosynostosis","type":"exact"}],"termid":"MONDO:0015338","terms_by_termid":{"MONDO:0008726":null,"MONDO:0009039":null,"MONDO:0013740":null,"MONDO:0014558":null,"MONDO:0020667":null},"xrefs":{"Monarch":{"xref_id":"0015338"}}}


id: GO:0050826
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 freezing stimulus, temperatures below 0 degrees Celsius.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to cold","termid":"GO:0009409"}],"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 freezing","synonyms":[{"name":"antifreeze activity","type":"related"},{"name":"ice nucleation inhibitor activity","type":"related"}],"termid":"GO:0050826"}


id: GO:0102083
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 7,8-dihydromonapterin = glycolaldehyde + 2-amino-6-(hydroxymethyl)-7,8-dihydropteridin-4-ol.","definition_xrefs":["GOC:pz","PMID:15107504"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aldehyde-lyase activity","termid":"GO:0016832"}],"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:0003824","GO:0016829","GO:0003674"],"is_obsolete":false,"name":"7,8-dihydromonapterin aldolase activity","secondary_identifiers":["MetaCyc:RXN-10857"],"termid":"GO:0102083"}


id: PBO:0043279
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 C","termid":"PBO:0043279"}


id: MONDO:1012168
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"lower motor neuron disease, non-human animal","termid":"MONDO:1011848"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lower motor neuron disease, horse","secondary_identifiers":["OMIA:000662-9796"],"termid":"MONDO:1012168","xrefs":{"Monarch":{"xref_id":"1012168"}}}


id: GO:0009008
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of a methyl group to a DNA molecule.","definition_xrefs":["GOC:jl","ISBN:0198506732","PMID:7862522"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methyltransferase activity","termid":"GO:0008168"},{"relation_name":"is_a","term_name":"catalytic activity, acting on DNA","termid":"GO:0140097"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0140097"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0016741","GO:0003824","GO:0016740","GO:0140097"],"is_obsolete":false,"name":"DNA-methyltransferase activity","secondary_identifiers":["Reactome:R-HSA-5227490"],"synonyms":[{"name":"DNA methylase","type":"broad"},{"name":"DNA methyltransferase activity","type":"exact"},{"name":"DNA transmethylase activity","type":"exact"},{"name":"Type II DNA methylase","type":"related"},{"name":"deoxyribonucleate methylase activity","type":"exact"},{"name":"deoxyribonucleate methyltransferase activity","type":"exact"},{"name":"deoxyribonucleic acid methylase activity","type":"exact"},{"name":"deoxyribonucleic acid methyltransferase activity","type":"exact"},{"name":"deoxyribonucleic acid modification methylase activity","type":"related"}],"termid":"GO:0009008"}


id: PBO:0079690
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin like 4A","termid":"PBO:0079690"}


id: MONDO:0018989
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Recurrent acute pancreatitis (RAP) is characterized by repeated attacks of acute pancreatitis (AP), which is defined as an acute inflammatory process of the pancreas with variable involvement of other regional tissues or remote organ systems.","definition_xrefs":["Orphanet:64740"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pancreas disorder","termid":"MONDO:0002356"},{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"recurrent acute pancreatitis","secondary_identifiers":["icd11.foundation:300900170","UMLS:C0267937","MedDRA:10033657","MEDGEN:489943","SCTID:197458008","NCIT:C184324"],"termid":"MONDO:0018989","xrefs":{"Monarch":{"xref_id":"0018989"}}}


id: GO:0006513
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Addition of a single ubiquitin group to a protein.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein ubiquitination","termid":"GO:0016567"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0070647"}],"interesting_parent_ids":["GO:0070647","GO:0008150"],"is_obsolete":false,"name":"protein monoubiquitination","synonyms":[{"name":"protein monoubiquitinylation","type":"exact"},{"name":"protein monoubiquitylation","type":"exact"}],"termid":"GO:0006513"}


id: GO:0106250
data:
  {"annotated_genes":["SJAG_02898"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[95894],"is_not":false,"summary":null,"term":"GO:0106250"}]},"cv_name":"molecular_function","definition":"A DNA-binding transcription factor activity that represses or decreases the transcription of specific genes sets transcribed by RNA polymerase III.","definition_xrefs":["PMID:31833215","GOC:txnOH-2018","PMID:15590667"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA-binding transcription repressor activity","termid":"GO:0001217"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02898":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140110"},{"rel_name":"is_a","termid":"GO:0003700"},{"rel_name":"is_a","termid":"GO:0001217"}],"interesting_parent_ids":["GO:0003700","GO:0001217","GO:0003674","GO:0140110"],"is_obsolete":false,"name":"DNA-binding transcription repressor activity, RNA polymerase III-specific","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0106250","terms_by_termid":{"GO:0106250":null}}


id: PBO:0053074
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ladybird homeobox 1","termid":"PBO:0053074"}


id: MONDO:1012357
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hypochondroplastic dwarfism, non-human animal","termid":"MONDO:1011957"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypochondroplastic dwarfism, dog","secondary_identifiers":["OMIA:001296-9615"],"termid":"MONDO:1012357","xrefs":{"Monarch":{"xref_id":"1012357"}}}


id: PBO:0057429
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 550a-2","termid":"PBO:0057429"}


id: PBO:0058978
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mutL homolog 3","termid":"PBO:0058978"}


id: PBO:0081283
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 66","termid":"PBO:0081283"}


id: MONDO:0024305
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An instance of hyperprolactinemia (disease) that is acquired during the lifetime of the individual.","definition_xrefs":["MONDO:patterns/acquired"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hyperprolactinemia","termid":"MONDO:0005804"},{"relation_name":"is_a","term_name":"acquired metabolic disease","termid":"MONDO:0006504"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"acquired hyperprolactinemia","secondary_identifiers":["MESH:D006966","DOID:12700","ICD10CM:E22.1","MESH:D002640"],"synonyms":[{"name":"Chiari-Frommel syndrome","type":"related"},{"name":"acquired hyperprolactinemia (disease)","type":"exact"},{"name":"hyperprolactinemia","type":"related"},{"name":"pregnancy-related A-G syndrome","type":"exact"}],"termid":"MONDO:0024305","xrefs":{"Monarch":{"xref_id":"0024305"}}}


id: GO:1903486
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any establishment of actomyosin contractile ring localization that is involved in mitotic cell cycle.","definition_xrefs":["GOC:mtg_cell_cycle","GO_REF:0000060","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete establishment of mitotic actomyosin contractile ring localization (obsolete GO:1903486)","termid":"GO:1903486"}


id: GO:0070120
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by the binding of a ciliary neurotrophic factor (CNTF) to its receptor on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["GOC:BHF","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine-mediated signaling pathway","termid":"GO:0019221"}],"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":"ciliary neurotrophic factor-mediated signaling pathway","synonyms":[{"name":"CNTF-mediated signaling pathway","type":"exact"},{"name":"ciliary neurotrophic factor-mediated signalling pathway","type":"exact"}],"termid":"GO:0070120"}


id: PBO:0062639
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 11 subfamily K member 1B pseudogene","termid":"PBO:0062639"}


id: PBO:0084259
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Inositol polyphosphate multikinase (IPMK); sequentially phosphorylates Ins(1,4,5)P3 to form Ins(1,3,4,5,6)P5; also has diphosphoinositol polyphosphate synthase activity; regulates genes responsive to arginine, phosphate, and nitrogen; needed by most [PSI+] variants for prion propagation","termid":"PBO:0084259"}


id: PBO:0031610
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_vacuolar_transport","termid":"PBO:0031610"}


id: PBO:0028131
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_histone_deacetylase_activity","termid":"PBO:0028131"}


id: PBO:0044580
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DBI pseudogene 2","termid":"PBO:0044580"}


id: PBO:0034147
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-is_mutualism","termid":"PBO:0034147"}


id: PBO:0056479
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MATN1 antisense RNA 1","termid":"PBO:0056479"}


id: PBO:0005856
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"complexed with Cdc5 protein Cwf18","termid":"PBO:0005856"}


id: GO:0006306
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The covalent transfer of a methyl group to either N-6 of adenine or C-5 or N-4 of cytosine.","definition_xrefs":["GOC:ems","ISBN:0198506732"],"gene_count":0,"genotype_count":0,"name":"obsolete DNA methylation (obsolete GO:0006306)","secondary_identifiers":["Wikipedia:DNA_methylation"],"termid":"GO:0006306"}


id: GO:1990522
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the nematode tail spike is generated and organized. An example of this process is seen in C. elegans, where the tapered tail spike is formed during embryogenesis by a filamentous process that passes posteriorly through hyp10, the tail ventral hypodermis; the filamentous process is formed by a binucleate cell, the tail-spike cell, that subsequently undergoes programmed cell death.","definition_xrefs":["PMID:6684600","PMID:17329362","GOC:kmv"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"}],"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":"tail spike morphogenesis","secondary_identifiers":["WBbt:0006979","WBbt:0008072"],"termid":"GO:1990522"}


id: GO:0031924
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of any of the vitamin B6 compounds, pyridoxal, pyridoxamine and pyridoxine and the active form, pyridoxal phosphate, from one side of a membrane to the other.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vitamin transmembrane transporter activity","termid":"GO:0090482"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0022857","GO:0005215"],"is_obsolete":false,"name":"vitamin B6 transmembrane transporter activity","synonyms":[{"name":"vitamin B6 transporter activity","type":"related"}],"termid":"GO:0031924"}


id: GO:0015305
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: (lactose or galactose)(out) + H+(out) = (lactose or galactose)(in) + H+(in).","definition_xrefs":["TC:2.A.1.1.9"],"gene_count":0,"genotype_count":0,"name":"obsolete lactose, galactose:proton symporter activity (obsolete GO:0015305)","synonyms":[{"name":"lactose, galactose:hydrogen symporter activity","type":"exact"},{"name":"lactose, galactose:proton symporter activity","type":"exact"},{"name":"lactose,galactose:proton symporter activity","type":"exact"}],"termid":"GO:0015305"}


id: PBO:0003130
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotically upregulated gene Mug184","termid":"PBO:0003130"}


id: PBO:0044039
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chondroitin sulfate proteoglycan 4 pseudogene 11","termid":"PBO:0044039"}


id: MONDO:0043895
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Harm or hurt to the ankle or ankle joint usually inflicted by an external source.","definition_xrefs":["MESH:D016512"],"direct_ancestors":[{"relation_name":"is_a","term_name":"injury","termid":"MONDO:0021178"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankle injury","secondary_identifiers":["SCTID:125603006"],"synonyms":[{"name":"Injuries, ankle","type":"related"},{"name":"Injuries, syndesmotic","type":"related"},{"name":"Sprains, ankle","type":"related"},{"name":"ankle Sprains","type":"related"},{"name":"ankle injury","type":"exact"},{"name":"ankle sprain","type":"related"},{"name":"injury of ankle","type":"exact"},{"name":"injury of tarsal region","type":"exact"},{"name":"injury, ankle","type":"related"},{"name":"injury, syndesmotic","type":"related"},{"name":"sprain, ankle","type":"related"},{"name":"syndesmotic Injuries","type":"related"},{"name":"syndesmotic injury","type":"related"},{"name":"tarsal region injury","type":"exact"}],"termid":"MONDO:0043895","xrefs":{"Monarch":{"xref_id":"0043895"}}}


id: PBO:0068366
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring finger protein 149","termid":"PBO:0068366"}


id: GO:0014734
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The enlargement or overgrowth of all or part of an organ due to an increase in size (not length) of individual muscle fibers without cell division. In the case of skeletal muscle cells this happens due to the additional synthesis of sarcomeric proteins and assembly of myofibrils.","definition_xrefs":["GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"striated muscle hypertrophy","termid":"GO:0014897"},{"relation_name":"is_a","term_name":"skeletal muscle adaptation","termid":"GO:0043501"}],"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 hypertrophy","termid":"GO:0014734"}


id: GO:0052773
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + N,N'-diacetylchitobiose = acetate + beta-D-glucosaminyl-(1->4)-N-acetyl-D-glucosamine.","definition_xrefs":["RHEA:62168","PMID:15136574","PMID:16232910","PMID:16736587"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides","termid":"GO:0016811"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016787","GO:0003824","GO:0016810","GO:0003674"],"is_obsolete":false,"name":"diacetylchitobiose deacetylase activity","secondary_identifiers":["MetaCyc:RXN-12543","EC:3.5.1.136"],"synonyms":[{"name":"N,N'-diacetylchitobiose deacetylase (nonreducing end)","type":"exact"}],"termid":"GO:0052773"}


id: GO:2000106
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of leukocyte apoptotic process.","definition_xrefs":["GOC:mtg_apoptosis","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of apoptotic process","termid":"GO:0042981"},{"relation_name":"regulates","term_name":"leukocyte apoptotic process","termid":"GO:0071887"}],"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 leukocyte apoptotic process","synonyms":[{"name":"regulation of leukocyte apoptosis","type":"narrow"}],"termid":"GO:2000106"}


id: PR:Q6BDR8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- nse4 gene.","definition_xrefs":["UniProtKB:Q6BDR8","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":"non-structural maintenance of chromosome element 4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC20F10.04c","synonyms":[{"name":"DNA repair protein rad62 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-nse4","type":"exact"},{"name":"non-SMC element 4 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q6BDR8"}


id: PBO:0041460
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C10orf88B (pseudogene)","termid":"PBO:0041460"}


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


id: PR:Q09810
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An adenylyltransferase and sulfurtransferase MOCS3 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO00323"],"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":"adenylyltransferase and sulfurtransferase uba4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC2G11.10c","secondary_identifiers":["UniProtKB:Q09810"],"synonyms":[{"name":"Spom972h-MOCS3","type":"exact"},{"name":"ubiquitin-like protein activator 4 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q09810"}


id: GO:0051427
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a receptor for a hormone.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"signaling receptor binding","termid":"GO:0005102"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005515","GO:0005488"],"is_obsolete":false,"name":"hormone receptor binding","termid":"GO:0051427"}


id: MONDO:0035562
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"human prion disease","termid":"MONDO:0018926"}],"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":"acquired human prion disease","secondary_identifiers":["MEDGEN:1842786","UMLS:C5680357","Orphanet:576360","GARD:22328"],"synonyms":[{"name":"infectious human prion disease","type":"exact"}],"termid":"MONDO:0035562","xrefs":{"Monarch":{"xref_id":"0035562"}}}


id: PBO:0086705
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; mCherry fusion protein localizes to the cytosol","termid":"PBO:0086705"}


id: PBO:0068969
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 213, pseudogene","termid":"PBO:0068969"}


id: GO:0012510
data:
  {"annotated_genes":["SJAG_04565","SJAG_04609","SJAG_00379","SJAG_04517","SJAG_01809","SJAG_02282"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[112439,112224,100616,118315],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030121"},{"annotations":[112348,94394],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030130"}]},"cv_name":"cellular_component","definition":"The lipid bilayer surrounding a vesicle transporting substances between the trans-Golgi network and other parts of the cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transport vesicle membrane","termid":"GO:0030658"},{"relation_name":"is_a","term_name":"Golgi-associated vesicle membrane","termid":"GO:0030660"},{"relation_name":"is_a","term_name":"clathrin-coated vesicle membrane","termid":"GO:0030665"},{"relation_name":"part_of","term_name":"trans-Golgi network transport vesicle","termid":"GO:0030140"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00379":null,"SJAG_01809":null,"SJAG_02282":null,"SJAG_04517":null,"SJAG_04565":null,"SJAG_04609":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0031410"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0031410","GO:0005737","GO:0005575"],"is_obsolete":false,"name":"trans-Golgi network transport vesicle membrane","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"TGN transport vesicle membrane","type":"exact"},{"name":"trans-Golgi network constitutive secretory pathway transport vesicle membrane","type":"exact"}],"termid":"GO:0012510","terms_by_termid":{"GO:0030121":null,"GO:0030130":null}}


id: GO:0006998
data:
  {"annotated_genes":["SJAG_05207","SJAG_04578","SJAG_03592","SJAG_03073","SJAG_03449","SJAG_02763","SJAG_04883","SJAG_01356","SJAG_03892","SJAG_01906","SJAG_01242","SJAG_01460","SJAG_00810","SJAG_01745","SJAG_01467","SJAG_00416","SJAG_00680","SJAG_04271","SJAG_01422","SJAG_00900","SJAG_00840","SJAG_04509","SJAG_01050","SJAG_04319","SJAG_03219","SJAG_03313","SJAG_03491","SJAG_04972","SJAG_03891","SJAG_03783","SJAG_04489","SJAG_03940","SJAG_04464"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[91241,100093,103218,109779,109915,112189,118952],"is_not":false,"summary":null,"term":"GO:0006998"},{"annotations":[93338,100926],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0140515"},{"annotations":[109778,92561,97184,87409,109374,97863],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0101026"},{"annotations":[109914],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0007077"},{"annotations":[118745,118821,110461,118947],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0101024"},{"annotations":[103217,90853,100382,118887,106028,118884,118886,87471,95467,97458,102629,118885],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0007084"},{"annotations":[103150],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0140516"},{"annotations":[90854,117607],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071765"},{"annotations":[88042],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0048288"},{"annotations":[102947,90855,118674,107187,109191,91451,90971,88589],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071763"},{"annotations":[96140],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031468"}]},"cv_name":"biological_process","definition":"A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of the nuclear envelope.","definition_xrefs":["GOC:mah","GOC:ems","GOC:dph","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane organization","termid":"GO:0061024"},{"relation_name":"part_of","term_name":"nucleus organization","termid":"GO:0006997"},{"relation_name":"part_of","term_name":"endomembrane system organization","termid":"GO:0010256"}],"gene_count":33,"genes_by_uniquename":{"SJAG_00416":null,"SJAG_00680":null,"SJAG_00810":null,"SJAG_00840":null,"SJAG_00900":null,"SJAG_01050":null,"SJAG_01242":null,"SJAG_01356":null,"SJAG_01422":null,"SJAG_01460":null,"SJAG_01467":null,"SJAG_01745":null,"SJAG_01906":null,"SJAG_02763":null,"SJAG_03073":null,"SJAG_03219":null,"SJAG_03313":null,"SJAG_03449":null,"SJAG_03491":null,"SJAG_03592":null,"SJAG_03783":null,"SJAG_03891":null,"SJAG_03892":null,"SJAG_03940":null,"SJAG_04271":null,"SJAG_04319":null,"SJAG_04464":null,"SJAG_04489":null,"SJAG_04509":null,"SJAG_04578":null,"SJAG_04883":null,"SJAG_04972":null,"SJAG_05207":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0061024"}],"interesting_parent_ids":["GO:0061024","GO:0008150"],"is_obsolete":false,"name":"nuclear envelope organization","references_by_uniquename":{"GO_REF:0000107":null,"PMID:21802294":null,"PMID:24184107":null,"PMID:26774782":null,"PMID:28954740":null,"PMID:32243490":null},"synonyms":[{"name":"nuclear envelope organisation","type":"exact"},{"name":"nuclear envelope organization and biogenesis","type":"related"}],"termid":"GO:0006998","terms_by_termid":{"GO:0006998":null,"GO:0007077":null,"GO:0007084":null,"GO:0031468":null,"GO:0048288":null,"GO:0071763":null,"GO:0071765":null,"GO:0101024":null,"GO:0101026":null,"GO:0140515":null,"GO:0140516":null}}


id: MOD:00685
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-glutamine residue to L-glutamic acid.","definition_xrefs":["PubMed:4922541","PubMed:4565668","RESID:AA0006#GLN","PubMed:1881881","PubMed:9192900","PubMed:957425","Unimod:7#Q","PubMed:6692818"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-glutamic acid residue","termid":"MOD:00015"},{"relation_name":"is_a","term_name":"deamidated residue","termid":"MOD:00400"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deamidated L-glutamine","synonyms":[{"name":"(2S)-2-aminopentanedioic acid","type":"exact"},{"name":"1-aminopropane-1,3-dicarboxylic acid","type":"exact"},{"name":"2-aminoglutaric acid","type":"exact"},{"name":"2-azanylpentanedioic acid","type":"exact"},{"name":"L-glutamic acid","type":"exact"},{"name":"MOD_RES Deamidated glutamine","type":"exact"},{"name":"alpha-aminoglutaric acid","type":"exact"},{"name":"dNGln","type":"exact"},{"name":"glutaminic acid","type":"exact"}],"termid":"MOD:00685"}


id: PBO:0024806
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-enabled_by","termid":"PBO:0024806"}


id: MONDO:0010346
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete MRX52 (obsolete MONDO:0010346)","secondary_identifiers":["OMIM:300504"],"termid":"MONDO:0010346","xrefs":{"Monarch":{"xref_id":"0010346"}}}


id: GO:0097403
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 raffinose stimulus.","definition_xrefs":["GOC:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to carbohydrate stimulus","termid":"GO:0071322"},{"relation_name":"is_a","term_name":"response to raffinose","termid":"GO:1901545"}],"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 raffinose","termid":"GO:0097403"}


id: SO:0000703
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region of sequence implicated in an experimental result.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"remark","termid":"SO:0000700"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"experimental_result_region","synonyms":[{"name":"experimental result region","type":"exact"}],"termid":"SO:0000703"}


id: MONDO:0001788
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hepatic vascular disorder","termid":"MONDO:0002405"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0002515"],"is_obsolete":false,"name":"nutmeg liver","secondary_identifiers":["ICD9:573.0","DOID:13739","MEDGEN:510207","SCTID:34736002","UMLS:C0156195"],"synonyms":[{"name":"chronic passive congestion of liver","type":"exact"}],"termid":"MONDO:0001788","xrefs":{"Monarch":{"xref_id":"0001788"}}}


id: GO:0008125
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the hydrolysis of proteins, including elastin. Preferential cleavage: Ala-Xaa.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete pancreatic elastase I activity (obsolete GO:0008125)","synonyms":[{"name":"elaszym","type":"related"},{"name":"pancreatic elastase I activity","type":"exact"},{"name":"pancreatopeptidase E activity","type":"related"},{"name":"serine elastase","type":"broad"}],"termid":"GO:0008125"}


id: GO:0044873
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a lipoprotein is transported to, or maintained in, a specific location in a membrane.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipoprotein localization","termid":"GO:0044872"},{"relation_name":"is_a","term_name":"protein localization to membrane","termid":"GO:0072657"}],"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":"lipoprotein localization to membrane","termid":"GO:0044873"}


id: MONDO:0017861
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ethylene glycol poisoning is a rare poisoning resulting in elevated anion gap metabolic acidosis, due to the production of glycolic acid, glyoxylic acid, and oxalic acid by alcohol dehydrogenase (ADH) in the liver when ethylene glycol is metabolized, characterized initially by euphoria, slurred speech, encephalopathy, coma and seizures, and followed by late manifestations such as tachycardia, arrhythmias, myocardial depression, hemodynamic imbalance and, finally, acute renal failure.","definition_xrefs":["Orphanet:31826"],"direct_ancestors":[{"relation_name":"is_a","term_name":"poisoning","termid":"MONDO:0029000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ethylene glycol poisoning","secondary_identifiers":["SCTID:426692001","GARD:18805","ICD9:982.8"],"termid":"MONDO:0017861","xrefs":{"Monarch":{"xref_id":"0017861"}}}


id: GO:0071039
data:
  {"annotated_genes":["SJAG_01830","SJAG_01064","SJAG_02622","SJAG_00701","SJAG_03745","SJAG_03939","SJAG_04360","SJAG_03984"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[91756,99271,102475,111307,112197,112706,114820,117552],"is_not":false,"summary":null,"term":"GO:0071039"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways occurring in the nucleus and resulting in the breakdown of a cryptic unstable transcript (CUT), initiated by the enzymatic addition of a sequence of adenylyl residues (polyadenylation) at the 3' end the target CUT.","definition_xrefs":["PMID:15935759","GOC:krc","PMID:16973436","PMID:16973437","PMID:18007593","GOC:dgf","PMID:18591258"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear RNA surveillance","termid":"GO:0071027"},{"relation_name":"is_a","term_name":"CUT catabolic process","termid":"GO:0071034"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00701":null,"SJAG_01064":null,"SJAG_01830":null,"SJAG_02622":null,"SJAG_03745":null,"SJAG_03939":null,"SJAG_03984":null,"SJAG_04360":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"nuclear polyadenylation-dependent CUT catabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"nuclear poly(A)-dependent CUT catabolic process","type":"related"}],"termid":"GO:0071039","terms_by_termid":{"GO:0071039":null}}


id: GO:0120536
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: sn-glycerol 1-phosphate + all-trans-heptaprenyl diphosphate = 3-heptaprenyl-sn-glycero-1-phosphate + diphosphate.","definition_xrefs":["PMID:21761520","RHEA:33495"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prenyltransferase activity","termid":"GO:0004659"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016765"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016740","GO:0016765","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"heptaprenylglyceryl phosphate synthase activity","secondary_identifiers":["EC:2.5.1.n9"],"synonyms":[{"name":"HepGP synthase activity","type":"exact"},{"name":"glycerol-1-phosphate heptaprenyltransferase activity","type":"exact"}],"termid":"GO:0120536"}


id: FYPO:0002093
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which cohesion between sister chromatids is decreased during meiosis.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal meiotic sister chromatid cohesion","termid":"FYPO:0002092"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000631","FYPO:0000641","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"decreased meiotic sister chromatid cohesion","synonyms":[{"name":"decreased sister chromatid cohesion during meiosis","type":"exact"},{"name":"reduced meiotic sister chromatid cohesion","type":"exact"}],"termid":"FYPO:0002093"}


id: MONDO:0023581
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":"cleft lip","termid":"MONDO:0004747"},{"relation_name":"is_a","term_name":"cleft palate","termid":"MONDO:0016064"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Kuster syndrome","secondary_identifiers":["MEDGEN:419150","MESH:C538126","UMLS:C2931741","GARD:3152"],"synonyms":[{"name":"cleft lip and palate, lower lip pits, and limb deficiency defects","type":"related"},{"name":"cleft lip palate lip pits limb deficiency","type":"related"}],"termid":"MONDO:0023581","xrefs":{"Monarch":{"xref_id":"0023581"}}}


id: PBO:0059850
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase pseudogene 3","termid":"PBO:0059850"}


id: GO:0140785
data:
  {"annotated_genes":["SJAG_03405"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[112307],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140786"}]},"cv_name":"molecular_function","definition":"Binding to and responding, e.g. by conformational change, to changes in the cellular level of an amino acid.","definition_xrefs":["GOC:pg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"molecular sensor activity","termid":"GO:0140299"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03405":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0140299"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0098772","GO:0140299"],"is_obsolete":false,"name":"amino acid sensor activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"amino acid sensing activity","type":"exact"}],"termid":"GO:0140785","terms_by_termid":{"GO:0140786":null}}


id: PBO:0045841
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 31","termid":"PBO:0045841"}


id: MONDO:0024861
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mixed germ cell tumor","termid":"MONDO:0015864"}],"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":"mixed teratoma and seminoma","secondary_identifiers":["UMLS:C5848073","MEDGEN:1844722","NCIT:C9010"],"synonyms":[{"name":"mixed teratoma and seminoma","type":"exact"}],"termid":"MONDO:0024861","xrefs":{"Monarch":{"xref_id":"0024861"}}}


id: PBO:0027477
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-single_cell_division_prior_to_G0_entry","termid":"PBO:0027477"}


id: GO:0036457
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A cytoplasmic, non-membrane bound granule of, at least, keratinocyte. Associated to keratin intermediate filaments and partially crosslinked to the cell envelope.","definition_xrefs":["GOC:krc","PMID:15854042"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"cytoplasm","termid":"GO:0005737"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005737","GO:0005575"],"is_obsolete":false,"name":"keratohyalin granule","termid":"GO:0036457"}


id: MONDO:0013723
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any bacteremia, susceptibility in which the cause of the disease is a mutation in the TIRAP gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bacteremia, susceptibility","termid":"MONDO:0000108"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bacteremia, susceptibility to, 1","secondary_identifiers":["UMLS:C3280645","OMIM:614382","MEDGEN:482275"],"synonyms":[{"name":"BACTS1","type":"related"},{"name":"TIRAP bacteremia, susceptibility","type":"exact"},{"name":"bacteremia, protection against","type":"exact"},{"name":"bacteremia, resistance to","type":"related"},{"name":"bacteremia, susceptibility caused by mutation in TIRAP","type":"exact"},{"name":"bacteremia, susceptibility to, 1","type":"exact"},{"name":"bacteremia, susceptibility to, type 1","type":"exact"}],"termid":"MONDO:0013723","xrefs":{"Monarch":{"xref_id":"0013723"}}}


id: PBO:0043216
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytoplasmic linker associated protein 1","termid":"PBO:0043216"}


id: PBO:0051327
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin kappa variable 2-18 (pseudogene)","termid":"PBO:0051327"}


id: FYPO:0002531
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 nucleoplasm is abolished.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to nucleus during vegetative growth","termid":"FYPO:0001424"},{"relation_name":"is_a","term_name":"abnormal protein localization to nucleoplasm","termid":"FYPO:0002529"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320","FYPO:0005447","FYPO:0000138"],"is_obsolete":false,"name":"abolished protein localization to nucleoplasm","synonyms":[{"name":"abolished protein localisation to nucleoplasm","type":"exact"},{"name":"abolished protein localization to nucleoplasm during mitotic cell cycle","type":"related"},{"name":"abolished protein localization to nucleoplasm during vegetative growth","type":"exact"},{"name":"protein localization to nucleoplasm abolished","type":"exact"}],"termid":"FYPO:0002531"}


id: PBO:0067225
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 294, pseudogene","termid":"PBO:0067225"}


id: PBO:0051653
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inosine monophosphate dehydrogenase 1 pseudogene 8","termid":"PBO:0051653"}


id: PR:Q09827
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein transport protein Sec61 subunit gamma that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO00296"],"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 transport protein Sec61 subunit gamma (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4G8.02c","secondary_identifiers":["UniProtKB:Q09827"],"synonyms":[{"name":"Spom972h-SEC61G","type":"exact"}],"termid":"PR:Q09827"}


id: PBO:0050284
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H6 family homeobox 1","termid":"PBO:0050284"}


id: MONDO:0032725
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"developmental and epileptic encephalopathy","termid":"MONDO:0100062"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"},{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0700092","MONDO:0005027"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy, 74","secondary_identifiers":["MEDGEN:1680535","OMIM:618396","UMLS:C5193074","DOID:0112210","GARD:16349"],"synonyms":[{"name":"DEE74","type":"exact"},{"name":"EIEE74","type":"exact"},{"name":"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 74","type":"exact"},{"name":"developmental and epileptic encephalopathy 74","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 74","type":"exact"}],"termid":"MONDO:0032725","xrefs":{"Monarch":{"xref_id":"0032725"}}}


id: FYPO:0000513
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which karyogamy involved in conjugation with cellular fusion begins later than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal nuclear fusion during mating","termid":"FYPO:0000510"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000301"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0000301","FYPO:0001985"],"is_obsolete":false,"name":"delayed onset of nuclear fusion during mating","synonyms":[{"name":"delayed nuclear fusion during mating","type":"exact"},{"name":"delayed onset of karyogamy","type":"exact"},{"name":"delayed onset of karyogamy involved in conjugation with cellular fusion","type":"exact"},{"name":"nuclear fusion during mating: delayed","type":"related"}],"termid":"FYPO:0000513"}


id: GO:0034759
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the directed movement of iron ions (Fe) from one side of a membrane to the other by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of iron ion transport","termid":"GO:0034756"},{"relation_name":"is_a","term_name":"regulation of monoatomic cation transmembrane transport","termid":"GO:1904062"},{"relation_name":"regulates","term_name":"iron ion transmembrane transport","termid":"GO:0034755"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0006810","GO:0055085","GO:0008150"],"is_obsolete":false,"name":"regulation of iron ion transmembrane transport","synonyms":[{"name":"regulation of iron ion membrane transport","type":"exact"},{"name":"regulation of transmembrane Fe transport","type":"exact"},{"name":"regulation of transmembrane iron ion transport","type":"exact"},{"name":"regulation of transmembrane iron transport","type":"exact"}],"termid":"GO:0034759"}


id: GO:0072267
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regionalization process in which the identity of the metanephric capsule is specified. Identity is considered to be the aggregate of characteristics by which a structure is recognized.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"renal capsule specification","termid":"GO:0072130"},{"relation_name":"is_a","term_name":"pattern specification involved in metanephros development","termid":"GO:0072268"},{"relation_name":"part_of","term_name":"metanephric capsule formation","termid":"GO:0072266"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"metanephric capsule specification","termid":"GO:0072267"}


id: GO:1903977
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of glial cell migration.","definition_xrefs":["PMID:19100238","GOC:BHF","GOC:TermGenie","GO_REF:0000058","GOC:nc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell migration","termid":"GO:0030335"},{"relation_name":"is_a","term_name":"regulation of glial cell migration","termid":"GO:1903975"},{"relation_name":"positively_regulates","term_name":"glial cell migration","termid":"GO:0008347"}],"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 glial cell migration","synonyms":[{"name":"activation of glia cell migration","type":"narrow"},{"name":"activation of glial cell migration","type":"narrow"},{"name":"positive regulation of glia cell migration","type":"exact"},{"name":"up regulation of glia cell migration","type":"exact"},{"name":"up regulation of glial cell migration","type":"exact"},{"name":"up-regulation of glia cell migration","type":"exact"},{"name":"up-regulation of glial cell migration","type":"exact"},{"name":"upregulation of glia cell migration","type":"exact"},{"name":"upregulation of glial cell migration","type":"exact"}],"termid":"GO:1903977"}


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


id: MONDO:0971130
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"benign neoplasm of choroid","termid":"MONDO:0021487"}],"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":"choroidal osteoma","secondary_identifiers":["Orphanet:674965"],"termid":"MONDO:0971130","xrefs":{"Monarch":{"xref_id":"0971130"}}}


id: MONDO:0017233
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"prion disease","termid":"MONDO:0005429"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"familial Alzheimer-like prion disease","secondary_identifiers":["UMLS:C4303482","Orphanet:280397","GARD:21084","icd11.foundation:1297025427","MEDGEN:929151","SCTID:721219005"],"termid":"MONDO:0017233","xrefs":{"Monarch":{"xref_id":"0017233"}}}


id: GO:0008973
data:
  {"annotated_genes":["SJAG_00134"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[115286],"is_not":false,"summary":null,"term":"GO:0008973"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: D-ribose 1-phosphate = D-ribose 5-phosphate. Also converts 2-deoxy-alpha-D-ribose 1-phosphate into 2-deoxy-D-ribose 5-phosphate.","definition_xrefs":["EC:5.4.2.7"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular phosphotransferase activity","termid":"GO:0016868"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00134":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016853","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"phosphopentomutase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-6787329","Reactome:R-HSA-8982667","MetaCyc:PPENTOMUT-RXN"],"synonyms":[{"name":"D-ribose 1,5-phosphomutase activity","type":"related"},{"name":"alpha-D-glucose-1,6-bisphosphate:deoxy-D-ribose-1-phosphate phosphotransferase activity","type":"related"},{"name":"alpha-D-ribose 1,5-phosphomutase activity","type":"related"},{"name":"deoxyribomutase activity","type":"related"},{"name":"deoxyribose phosphomutase activity","type":"related"},{"name":"phosphodeoxyribomutase activity","type":"related"},{"name":"phosphoribomutase activity","type":"related"}],"termid":"GO:0008973","terms_by_termid":{"GO:0008973":null}}


id: PBO:0083391
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps ORF AIM9/YER080W","termid":"PBO:0083391"}


id: GO:0051055
data:
  {"annotated_genes":["SJAG_03940","SJAG_02104","SJAG_01187","SJAG_01906","SJAG_00053","SJAG_02380","SJAG_03130","SJAG_03170"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[103860,89923],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902647"},{"annotations":[93383],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010895"},{"annotations":[110714],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045717"},{"annotations":[110824,114923],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001211"},{"annotations":[112188,109190],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071072"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of lipids.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of biosynthetic process","termid":"GO:0009890"},{"relation_name":"is_a","term_name":"negative regulation of lipid metabolic process","termid":"GO:0045833"},{"relation_name":"is_a","term_name":"regulation of lipid biosynthetic process","termid":"GO:0046890"},{"relation_name":"negatively_regulates","term_name":"lipid biosynthetic process","termid":"GO:0008610"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00053":null,"SJAG_01187":null,"SJAG_01906":null,"SJAG_02104":null,"SJAG_02380":null,"SJAG_03130":null,"SJAG_03170":null,"SJAG_03940":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"negatively_regulates","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"negative regulation of lipid biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of lipid biosynthetic process","type":"exact"},{"name":"down-regulation of lipid biosynthetic process","type":"exact"},{"name":"downregulation of lipid biosynthetic process","type":"exact"},{"name":"inhibition of lipid biosynthetic process","type":"narrow"},{"name":"negative regulation of lipid anabolism","type":"exact"},{"name":"negative regulation of lipid biosynthesis","type":"exact"},{"name":"negative regulation of lipid formation","type":"exact"},{"name":"negative regulation of lipid synthesis","type":"exact"},{"name":"negative regulation of lipogenesis","type":"exact"}],"termid":"GO:0051055","terms_by_termid":{"GO:0010895":null,"GO:0045717":null,"GO:0071072":null,"GO:1902647":null,"GO:2001211":null}}


id: MONDO:0011884
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome is an extremely rare ectodermal dysplasia syndrome characterized by hypotrichosis universalis with mild to severe scarring alopecia, acro-osteolysis, onychogryphosis, thin and tapered fingertips, periodontitis and caries leading to premature teeth loss, linear or reticular palmoplantar keratoderma and erythematous, scaling, psoriasis-like skin lesions on arms and legs. Lingua plicata and ventricular tachycardia have also been observed.","definition_xrefs":["Orphanet:307936"],"direct_ancestors":[{"relation_name":"is_a","term_name":"focal palmoplantar keratoderma","termid":"MONDO:0017672"},{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"}],"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":"hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome","secondary_identifiers":["GARD:17384","OMIM:607658","UMLS:C1843285","MESH:C564357","SCTID:763658004","MEDGEN:375146"],"synonyms":[{"name":"HOPP syndrome","type":"exact"},{"name":"Hopp syndrome","type":"related"},{"name":"hypotrichosis-osteolysis-periodontitis-palmoplantar hyperkeratosis syndrome","type":"exact"},{"name":"hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome","type":"exact"},{"name":"hypotrichosis-striate palmoplantar hyperkeratosis-acroosteolysis-periodontitis syndrome","type":"exact"},{"name":"hypotrichosis-striate palmoplantar keratoderma-acroosteolysis-periodontitis syndrome","type":"exact"}],"termid":"MONDO:0011884","xrefs":{"Monarch":{"xref_id":"0011884"}}}


id: PBO:0062833
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oligosaccharyltransferase complex subunit 4, non-catalytic","termid":"PBO:0062833"}


id: PATO:0002290
data:
  {"annotation_feature_type":"gene","cv_name":"quality","direct_ancestors":[{"relation_name":"is_a","term_name":"physical object quality","termid":"PATO:0001241"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aplastic/hypoplastic","termid":"PATO:0002290"}


id: MONDO:0003686
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign or malignant sweat gland neoplasm with apocrine differentiation. Representative examples include apocrine adenoma, ceruminous adenocarcinoma, and apocrine breast carcinoma.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sweat gland neoplasm","termid":"MONDO:0002381"},{"relation_name":"is_a","term_name":"apocrine sweat gland disorder","termid":"MONDO:0024467"}],"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":"apocrine sweat gland neoplasm","secondary_identifiers":["DOID:5876","UMLS:C1332318","MEDGEN:272320","NCIT:C6798"],"synonyms":[{"name":"apocrine neoplasm","type":"exact"},{"name":"apocrine neoplasm of skin","type":"exact"},{"name":"apocrine neoplasm of the skin","type":"exact"},{"name":"apocrine skin neoplasm","type":"exact"},{"name":"apocrine skin tumor","type":"exact"},{"name":"apocrine skin tumour","type":"exact"},{"name":"apocrine sweat gland neoplasm (disease)","type":"exact"},{"name":"apocrine sweat gland tumor","type":"exact"},{"name":"apocrine sweat gland tumour","type":"exact"},{"name":"apocrine tumor","type":"exact"},{"name":"apocrine tumor of skin","type":"exact"},{"name":"apocrine tumor of the skin","type":"exact"},{"name":"apocrine tumour","type":"exact"},{"name":"apocrine tumour of skin","type":"exact"},{"name":"apocrine tumour of the skin","type":"exact"},{"name":"neoplasm of apocrine sweat gland","type":"exact"},{"name":"tumor of apocrine sweat gland","type":"exact"},{"name":"tumour of apocrine sweat gland","type":"exact"}],"termid":"MONDO:0003686","xrefs":{"Monarch":{"xref_id":"0003686"}}}


id: GO:0180020
data:
  {"annotated_genes":["SJAG_05289","SJAG_01848","SJAG_04644","SJAG_03010","SJAG_02177","SJAG_03795"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[108026,108103,114327,115638,117936,118024],"is_not":false,"summary":null,"term":"GO:0180020"}]},"cv_name":"molecular_function","definition":"The activity of bending or deforming a membrane. This activity can occur by multiple mechanisms including the insertion amphipathic domains into one or both leaflets.","definition_xrefs":["PMID:19780639"],"direct_ancestors":[{"relation_name":"is_a","term_name":"molecular_function","termid":"GO:0003674"}],"gene_count":6,"genes_by_uniquename":{"SJAG_01848":null,"SJAG_02177":null,"SJAG_03010":null,"SJAG_03795":null,"SJAG_04644":null,"SJAG_05289":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674"],"is_obsolete":false,"name":"membrane bending activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"membrane curving","type":"related"}],"termid":"GO:0180020","terms_by_termid":{"GO:0180020":null}}


id: PBO:0046836
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fatty acid binding protein 5 pseudogene 9","termid":"PBO:0046836"}


id: FYPO:0005214
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A gene expression phenotype observed in the vegetative growth phase of the life cycle in which regulation of translation in response to osmotic stress is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PMID:26493332","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal regulation of translation in response to stress during vegetative growth","termid":"FYPO:0005213"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000298"}],"interesting_parent_ids":["FYPO:0000298","FYPO:0000257","FYPO:0000002","FYPO:0001320","FYPO:0001312"],"is_obsolete":false,"name":"normal regulation of translation in response to osmotic stress","synonyms":[{"name":"normal regulation of translation in response to osmotic stress during mitotic cell cycle","type":"related"},{"name":"normal regulation of translation in response to osmotic stress during vegetative growth","type":"exact"}],"termid":"FYPO:0005214"}


id: PBO:0034258
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-in_equivalogy_relationship_with","termid":"PBO:0034258"}


id: GO:0000738
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of DNA, involving the hydrolysis of terminal 3',5'-phosphodiester bonds in one or two strands of deoxyribonucleotides.","definition_xrefs":["GOC:elh","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete DNA catabolic process, exonucleolytic (obsolete GO:0000738)","synonyms":[{"name":"DNA breakdown, exonucleolytic","type":"exact"},{"name":"DNA degradation, exonucleolytic","type":"exact"},{"name":"exonucleolytic degradation of DNA","type":"exact"}],"termid":"GO:0000738"}


id: PBO:0056427
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microtubule affinity regulating kinase 2","termid":"PBO:0056427"}


id: PBO:0053594
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 621","termid":"PBO:0053594"}


id: PBO:0043035
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"charged multivesicular body protein 5","termid":"PBO:0043035"}


id: PBO:0057900
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3202-1","termid":"PBO:0057900"}


id: GO:0072216
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency or extent of metanephros development. Metanephros development is the process whose specific outcome is the progression of the metanephros over time, from its formation to the mature structure. The metanephros is an organ that filters the blood and excretes the end products of body metabolism in the form of urine.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of metanephros development","termid":"GO:0072215"},{"relation_name":"is_a","term_name":"positive regulation of kidney development","termid":"GO:0090184"},{"relation_name":"positively_regulates","term_name":"metanephros development","termid":"GO:0001656"}],"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 metanephros development","termid":"GO:0072216"}


id: PBO:0045201
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DnaJ heat shock protein family (Hsp40) member B12","termid":"PBO:0045201"}


id: MONDO:0032802
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant nonsyndromic hearing loss","termid":"MONDO:0019587"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0019497","MONDO:0000426"],"is_obsolete":false,"name":"hearing loss, autosomal dominant 37","secondary_identifiers":["MEDGEN:1676950","OMIM:618533","UMLS:C4760307"],"synonyms":[{"name":"DEAFNESS, AUTOSOMAL DOMINANT 37","type":"narrow"},{"name":"DFNA37","type":"narrow"},{"name":"deafness, autosomal dominant 37","type":"narrow"}],"termid":"MONDO:0032802","xrefs":{"Monarch":{"xref_id":"0032802"}}}


id: PBO:0038967
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADNP homeobox 2","termid":"PBO:0038967"}


id: PBO:0083667
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Endoplasmic reticulum packaging chaperone; required for incorporation of amino acid permeases into COPII coated vesicles for transport to the cell surface","termid":"PBO:0083667"}


id: PBO:0004993
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA-binding protein that suppresses calcineurin deletion Rnc1","termid":"PBO:0004993"}


id: MONDO:0006192
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A primary endometrial adenocarcinoma composed of neoplastic cells that form complex glandular patterns associated with budding and branching of the neoplastic glands. The neoplastic glands resemble those of the normal endometrium and may or may not be associated with sheet-like proliferation of malignant cells. Endometrioid adenocarcinoma is the most commonly seen morphologic variant of endometrial adenocarcinoma.","definition_xrefs":["NCIT:C6287"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endometrioid adenocarcinoma","termid":"MONDO:0005026"}],"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":"endometrial endometrioid adenocarcinoma","secondary_identifiers":["MEDGEN:234467","EFO:1000233","icd11.foundation:671511103","ONCOTREE:UEC","UMLS:C1336905"],"synonyms":[{"name":"endometrial endometrioid adenocarcinoma","type":"exact"},{"name":"endometrioid adenocarcinoma of endometrium","type":"exact"},{"name":"endometrioid adenocarcinoma of the endometrium","type":"exact"},{"name":"endometrioid carcinoma of endometrium","type":"exact"},{"name":"endometrioid carcinoma of the endometrium","type":"exact"},{"name":"endometrioid endomet. adenocar.","type":"exact"},{"name":"endometrioid endometrial adenocarcinoma","type":"exact"},{"name":"uterine corpus endometrioid adenocarcinoma","type":"exact"},{"name":"uterine corpus endometrioid carcinoma","type":"exact"},{"name":"uterine endometrioid carcinoma","type":"related"}],"termid":"MONDO:0006192","xrefs":{"Monarch":{"xref_id":"0006192"}}}


id: PBO:0065212
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peripherin 2","termid":"PBO:0065212"}


id: GO:1903431
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of cell maturation.","definition_xrefs":["GOC:TermGenie","PMID:17459944","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell development","termid":"GO:0010720"},{"relation_name":"is_a","term_name":"regulation of cell maturation","termid":"GO:1903429"},{"relation_name":"positively_regulates","term_name":"cell maturation","termid":"GO:0048469"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of cell maturation","synonyms":[{"name":"activation of cell maturation","type":"narrow"},{"name":"activation of functional differentiation","type":"related"},{"name":"positive regulation of functional differentiation","type":"related"},{"name":"up regulation of cell maturation","type":"exact"},{"name":"up regulation of functional differentiation","type":"related"},{"name":"up-regulation of cell maturation","type":"exact"},{"name":"up-regulation of functional differentiation","type":"related"},{"name":"upregulation of cell maturation","type":"exact"},{"name":"upregulation of functional differentiation","type":"related"}],"termid":"GO:1903431"}


id: PATO:0000971
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000971 absolute permeability (obsolete PATO:0000971)","termid":"PATO:0000971"}


id: PBO:0051573
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 17B","termid":"PBO:0051573"}


id: FYPO:0004026
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the increase in gross chromosomal rearrangements that normally results from synthesis template switching during processing of arrested replication forks is diminished or abolished.","definition_xrefs":["PomBase:mah","PMID:25313826"],"direct_ancestors":[{"relation_name":"is_a","term_name":"loss of gross chromosomal rearrangement during replication fork processing","termid":"FYPO:0003587"}],"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:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000293"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985","FYPO:0005447","FYPO:0000293"],"is_obsolete":false,"name":"loss of template switch-mediated chromosomal rearrangement during replication fork processing","termid":"FYPO:0004026"}


id: GO:2001127
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of a methane from a formic acid.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"formate metabolic process","termid":"GO:0015942"},{"relation_name":"is_a","term_name":"methanogenesis","termid":"GO:0015948"}],"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:0006091"}],"interesting_parent_ids":["GO:0006091","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"methane biosynthetic process from formic acid","termid":"GO:2001127"}


id: PBO:0048601
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ghrelin opposite strand/antisense RNA","termid":"PBO:0048601"}


id: GO:0055082
data:
  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homeostatic process involved in the maintenance of a steady state level of a chemical within a cell.","definition_xrefs":["GOC:isa_complete","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular homeostasis","termid":"GO:0019725"},{"relation_name":"is_a","term_name":"chemical 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chemical homeostasis","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000108":null},"synonyms":[{"name":"cellular chemical homeostasis","type":"exact"}],"termid":"GO:0055082","terms_by_termid":{"GO:0001678":null,"GO:0006808":null,"GO:0006874":null,"GO:0006878":null,"GO:0006879":null,"GO:0006882":null,"GO:0007035":null,"GO:0009992":null,"GO:0010106":null,"GO:0010619":null,"GO:0010961":null,"GO:0019676":null,"GO:0019740":null,"GO:0030007":null,"GO:0030026":null,"GO:0030641":null,"GO:0030643":null,"GO:0032468":null,"GO:0033214":null,"GO:0033215":null,"GO:0051453":null,"GO:0090156":null,"GO:0090463":null,"GO:0090464":null,"GO:0090465":null}}


id: MONDO:0011332
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":"Dyserythropoiesis, congenital, with ultrastructurally normal erythroblast heterochromatin","secondary_identifiers":["OMIM:603529","MEDGEN:813565","UMLS:C3807235"],"synonyms":[{"name":"Dyserythropoiesis, congenital, with ultrastructurally normal erythroblast heterochromatin","type":"exact"}],"termid":"MONDO:0011332","xrefs":{"Monarch":{"xref_id":"0011332"}}}


id: GO:0007555
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the regulated release of ecdysteroid from a cell.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of steroid hormone secretion","termid":"GO:2000831"},{"relation_name":"regulates","term_name":"ecdysteroid secretion","termid":"GO:0045457"}],"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:0008150","GO:0006810","GO:0023052"],"is_obsolete":false,"name":"regulation of ecdysteroid secretion","termid":"GO:0007555"}


id: PBO:0113098
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dihydrouridine synthase; member of a widespread family of conserved proteins including Smm1p, Dus1p, and Dus4p; modifies pre-tRNAs at U47 of the variable arm; contains a consensus oleate response element (ORE) in its promoter region; forms nuclear foci upon DNA replication stress","termid":"PBO:0113098"}


id: GO:1902787
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 dodecane stimulus.","definition_xrefs":["GO_REF:0000071","GOC:mengo_curators","GOC:TermGenie","PMID:23826995"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to alkane","termid":"GO:1902779"},{"relation_name":"is_a","term_name":"response to dodecane","termid":"GO:1902786"}],"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 dodecane","termid":"GO:1902787"}


id: PATO:0000286
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000286 cytoplasmic male sterility (obsolete PATO:0000286)","termid":"PATO:0000286"}


id: GO:0048283
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of determinate inflorescences are generated and organized. A determinate inflorescence is one that can produce an undefined number of floral meristems.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inflorescence morphogenesis","termid":"GO:0048281"}],"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":"indeterminate inflorescence morphogenesis","termid":"GO:0048283"}


id: PBO:0040970
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BCL2 interacting protein 3 pseudogene 41","termid":"PBO:0040970"}


id: GO:0070028
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process involving carbon monoxide that modulates the frequency, rate or extent of transcription.","definition_xrefs":["GOC:ecd"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of transcription by carbon monoxide (obsolete GO:0070028)","synonyms":[{"name":"regulation of transcription by CO","type":"exact"}],"termid":"GO:0070028"}


id: SO:0001692
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A site where restriction enzymes can cleave that will produce an overhang or 'sticky end'.","direct_ancestors":[{"relation_name":"is_a","term_name":"restriction_enzyme_recognition_site","termid":"SO:0001687"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sticky_end_restriction_enzyme_cleavage_site","synonyms":[{"name":"sticky end restriction enzyme cleavage site","type":"related"}],"termid":"SO:0001692"}


id: GO:0008459
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 3'-phosphoadenosine 5'-phosphosulfate + chondroitin = adenosine 3',5'-bisphosphate + chondroitin 6'-sulfate.","definition_xrefs":["EC:2.8.2.17"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chondroitin sulfotransferase activity","termid":"GO:0034481"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016782"}],"interesting_parent_ids":["GO:0003824","GO:0016740","GO:0003674","GO:0016782"],"is_obsolete":false,"name":"chondroitin 6-sulfotransferase activity","secondary_identifiers":["KEGG_REACTION:R02181","Reactome:R-HSA-3595175","RHEA:11108","Reactome:R-HSA-2018682","MetaCyc:CHONDROITIN-6-SULFOTRANSFERASE-RXN"],"synonyms":[{"name":"3'-phosphoadenosine 5'-phosphosulfate (PAPS):chondroitin sulfate sulfotransferase activity","type":"related"},{"name":"3'-phosphoadenylyl-sulfate:chondroitin 6'-sulfotransferase activity","type":"related"},{"name":"chondroitin 6-O-sulfotransferase activity","type":"related"},{"name":"chondroitin 6-sulphotransferase activity","type":"exact"},{"name":"terminal 6-sulfotransferase activity","type":"related"}],"termid":"GO:0008459"}


id: FYPO:0001386
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which non-sporulating diploid cells become haploid, without undergoing meiosis, at a higher frequency than normal.","definition_xrefs":["PomBase:al","PMID:9914167","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal vegetative cell phenotype","termid":"FYPO:0003755"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"increased haploidization","secondary_identifiers":["FYPO:0001781"],"synonyms":[{"name":"increased haploidisation","type":"exact"},{"name":"unstable diploid","type":"exact"}],"termid":"FYPO:0001386"}


id: PBO:0003235
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Diamond Blackfan Anemia","termid":"PBO:0003235"}


id: MONDO:0958006
data:
  {"annotated_genes":["SJAG_04369"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85612],"is_not":false,"summary":null,"term":"MONDO:0958006"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spondyloepimetaphyseal dysplasia","termid":"MONDO:0100510"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04369":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"spondyloepimetaphyseal dysplasia, Guo-Campeau type","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5882737","MEDGEN:1844202","OMIM:620663"],"termid":"MONDO:0958006","terms_by_termid":{"MONDO:0958006":null},"xrefs":{"Monarch":{"xref_id":"0958006"}}}


id: PBO:0067094
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 131, pseudogene","termid":"PBO:0067094"}


id: MONDO:0012118
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"COG7-CDG is a congenital disorder of glycosylation characterized by dysmorphism, skeletal dysplasia, hypotonia, hepatosplenomegaly, jaundice, cardiac insufficiency, recurrent infections and epilepsy. To date, it has been described in two infants, both of whom died within the first three months of life. The syndrome is caused by a mutation in the gene encoding COG-7 (chromosome 16), a subunit of the oligomeric Golgi complex.","definition_xrefs":["Orphanet:79333"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"skin disorder","termid":"MONDO:0005093"},{"relation_name":"excluded_subClassOf","term_name":"heart disorder","termid":"MONDO:0005267"},{"relation_name":"excluded_subClassOf","term_name":"congenital disorder of glycosylation","termid":"MONDO:0015286"},{"relation_name":"is_a","term_name":"congenital disorder of glycosylation type II","termid":"MONDO:0005501"},{"relation_name":"is_a","term_name":"developmental anomaly of metabolic origin","termid":"MONDO:0015327"},{"relation_name":"is_a","term_name":"defect in conserved oligomeric Golgi complex","termid":"MONDO:0017750"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0024322","MONDO:0005066"],"is_obsolete":false,"name":"COG7-congenital disorder of glycosylation","secondary_identifiers":["UMLS:C2931010","GARD:9842","SCTID:717773005","MEDGEN:419311","DOID:0070257","OMIM:608779","MESH:C535754"],"synonyms":[{"name":"CDG 2E","type":"related"},{"name":"CDG IIe","type":"related"},{"name":"CDG syndrome type IIe","type":"exact"},{"name":"CDG-IIe","type":"exact"},{"name":"CDG2E","type":"exact"},{"name":"COG7-CDG","type":"exact"},{"name":"COG7-CDG (CDG-IIe)","type":"related"},{"name":"COG7-congenital disorder of glycosylation","type":"exact"},{"name":"carbohydrate deficient glycoprotein syndrome type IIe","type":"exact"},{"name":"congenital disorder of glycosylation type 2e","type":"exact"},{"name":"congenital disorder of glycosylation type IIe","type":"exact"},{"name":"congenital disorder of glycosylation, type IIe","type":"related"}],"termid":"MONDO:0012118","xrefs":{"Monarch":{"xref_id":"0012118"}}}


id: PR:O14230
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A farnesyl pyrophosphate synthase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00542","PRO:DNx","PANTHER:PTHR11525:SF0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"farnesyl pyrophosphate synthase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC6F12.13c","secondary_identifiers":["UniProtKB:O14230"],"synonyms":[{"name":"(2E,6E)-farnesyl diphosphate synthase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Dimethylallyltranstransferase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"FPP synthase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"FPS (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Geranyltranstransferase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-FDPS","type":"exact"},{"name":"farnesyl diphosphate synthase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14230"}


id: MONDO:0016844
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Trisomy 20p is a chromosomal disorder resulting from duplication of all or part of the short arm of chromosome 20. It is mostly characterized by normal growth, mild to moderate intellectual disability, speech delay, poor coordination and evocative facial features.","definition_xrefs":["Orphanet:261318"],"direct_ancestors":[{"relation_name":"is_a","term_name":"partial trisomy of chromosome 20","termid":"MONDO:0016938"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trisomy 20p","secondary_identifiers":["GARD:5333","MEDGEN:418939","MESH:C535371","ICD9:758.5","SCTID:111311004","UMLS:C2930888"],"synonyms":[{"name":"20p duplication","type":"related"},{"name":"20p trisomy","type":"related"},{"name":"Duplication 20p","type":"related"},{"name":"Duplication of 20p","type":"exact"},{"name":"chromosome 20p duplication","type":"related"},{"name":"dup(20p)","type":"exact"},{"name":"partial duplication of chromosome 20p","type":"exact"},{"name":"partial duplication of the short arm of chromosome 20","type":"exact"},{"name":"partial trisomy 20p","type":"related"},{"name":"partial trisomy of chromosome 20p","type":"exact"},{"name":"partial trisomy of the short arm of chromosome 20","type":"exact"},{"name":"trisomy 20p","type":"exact"},{"name":"trisomy type 20p","type":"exact"}],"termid":"MONDO:0016844","xrefs":{"Monarch":{"xref_id":"0016844"}}}


id: GO:1990914
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the plasma membrane consisting of the gene products that penetrate only the periplasmic side of the membrane.","definition_xrefs":["PMID:15919996","GOC:bhm"],"gene_count":0,"genotype_count":0,"name":"obsolete integral component of periplasmic side of plasma membrane (obsolete GO:1990914)","termid":"GO:1990914"}


id: PBO:0111534
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"flocculin-like protein","termid":"PBO:0111534"}


id: FYPO:0001106
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of glutathione-disulfide reductase activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular process","termid":"FYPO:0000628"},{"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:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0000707","FYPO:0005447","FYPO:0000002","FYPO:0000652","FYPO:0001985","FYPO:0000654"],"is_obsolete":false,"name":"abnormal glutathione-disulfide reductase activity","synonyms":[{"name":"abnormal glutathione-disulphide reductase activity","type":"exact"}],"termid":"FYPO:0001106"}


id: GO:0120264
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, extent or location of chromosome attachment to the nuclear envelope.","definition_xrefs":["GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell cycle process","termid":"GO:0010564"},{"relation_name":"is_a","term_name":"regulation of localization","termid":"GO:0032879"},{"relation_name":"regulates","term_name":"chromosome attachment to the nuclear envelope","termid":"GO:0097240"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"regulation of chromosome attachment to the nuclear envelope","termid":"GO:0120264"}


id: PBO:0034298
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-proper_distributary_of","termid":"PBO:0034298"}


id: MONDO:0016615
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"oligoarticular juvenile idiopathic arthritis","termid":"MONDO:0019433"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies","secondary_identifiers":["Orphanet:247839","ICD10CM:M08.4"],"synonyms":[{"name":"oligoarticular JIA with anti-nuclear antibodies","type":"exact"},{"name":"pauciarticular chronic arthritis with anti-nuclear antibodies","type":"exact"}],"termid":"MONDO:0016615","xrefs":{"Monarch":{"xref_id":"0016615"}}}


id: PBO:0046006
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation initiation factor 1 pseudogene 1","termid":"PBO:0046006"}


id: PBO:0047991
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FSHD region gene 2 family member H, pseudogene","termid":"PBO:0047991"}


id: PATO:0001964
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A curled quality inhering in a bearer by virtue of the bearer's edges of its surface being rolled spirally downwards.","definition_xrefs":["ISBN:0881923214"],"direct_ancestors":[{"relation_name":"is_a","term_name":"curled","termid":"PATO:0000405"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"circinate","termid":"PATO:0001964"}


id: PBO:0029064
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-small_vacuoles","termid":"PBO:0029064"}


id: MONDO:0020155
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete eyelid border anomaly (obsolete MONDO:0020155)","secondary_identifiers":["Orphanet:98564"],"termid":"MONDO:0020155","xrefs":{"Monarch":{"xref_id":"0020155"}}}


id: PBO:0067110
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 152, pseudogene","termid":"PBO:0067110"}


id: GO:0097064
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of a non-coding RNA transcript (ncRNA) from the nucleus to the cytoplasm.","definition_xrefs":["PMID:11352936","GOC:dgf"],"gene_count":0,"genotype_count":0,"name":"obsolete ncRNA export from nucleus (obsolete GO:0097064)","termid":"GO:0097064"}


id: MONDO:0006109
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm arising from mesothelial cells in the pleura. It is characterized by the presence of neoplastic epithelioid cells and sarcomatoid features.","definition_xrefs":["NCIT:C4282"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malignant mesothelioma","termid":"MONDO:0006292"}],"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":"malignant biphasic mesothelioma","secondary_identifiers":["MEDGEN:137775","DOID:4486","EFO:1000124","ICDO:9053/3","UMLS:C0334515"],"synonyms":[{"name":"biphasic mesothelioma","type":"exact"},{"name":"malignant biphasic mesothelioma","type":"exact"},{"name":"malignant biphasic mesothelioma, malignant","type":"exact"},{"name":"malignant mixed mesothelioma","type":"exact"},{"name":"mesothelioma, biphasic, malignant","type":"exact"},{"name":"mesothelioma, biphasic, malignant (morphologic abnormality)","type":"exact"},{"name":"mixed mesothelioma","type":"exact"}],"termid":"MONDO:0006109","xrefs":{"Monarch":{"xref_id":"0006109"}}}


id: PBO:0050236
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group nucleosomal binding domain 2 pseudogene14","termid":"PBO:0050236"}


id: GO:0033401
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A triplet codon-amino acid adaptor activity that recognizes a UUU codon.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"triplet codon-amino acid adaptor activity","termid":"GO:0030533"}],"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"},{"rel_name":"is_a","termid":"GO:0060090"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0003723","GO:0060090"],"is_obsolete":false,"name":"UUU codon-amino acid adaptor activity","synonyms":[{"name":"TTT codon-amino acid adaptor activity","type":"exact"},{"name":"phenylalanine tRNA","type":"related"}],"termid":"GO:0033401"}


id: PBO:0087742
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the SWI/SNF chromatin remodeling complex; involved in transcriptional regulation; functions interdependently in transcriptional activation with Snf2p and Snf6p; relocates to the cytosol under hypoxic conditions","termid":"PBO:0087742"}


id: MONDO:0001598
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign lesion that involves the salivary glands, usually the parotid gland. It affects females more often than males and it may be a manifestation of autoimmune diseases such as Sjogren syndrome. There is an increased incidence of benign lymphoepithelial lesions in HIV-positive patients. It is characterized by the presence of a marked lymphocytic infiltrate and epi-myoepithelial islands in the affected salivary gland. Patients usually present with firm and painless swelling of the affected salivary gland. There is an increased risk for development of lymphoma.","definition_xrefs":["NCIT:C3949"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune disorder of exocrine system","termid":"MONDO:0000586"},{"relation_name":"is_a","term_name":"salivary gland disorder","termid":"MONDO:0001142"}],"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":"benign lymphoepithelial lesion of salivary gland","secondary_identifiers":["SCTID:45517002","MEDGEN:120595","DOID:12899","ICD9:527.8","UMLS:C0266995","icd11.foundation:1330363110"],"synonyms":[{"name":"Godwin tumor","type":"exact"},{"name":"Godwin tumour","type":"exact"},{"name":"benign lymphoepithelial lesion of salivary gland","type":"exact"},{"name":"benign lymphoepithelial lesion of the salivary gland","type":"related"},{"name":"benign salivary gland lymphoepithelial lesion","type":"related"}],"termid":"MONDO:0001598","xrefs":{"Monarch":{"xref_id":"0001598"}}}


id: PBO:0036180
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_histone_H4-K20_trimethylation_during_vegetative_growth","termid":"PBO:0036180"}


id: PR:Q9UUC1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rpl2101 gene.","definition_xrefs":["UniProtKB:Q9UUC1","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":"60S ribosomal protein L21-A (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC365.03c","synonyms":[{"name":"Spom972h-rpl2101","type":"exact"}],"termid":"PR:Q9UUC1"}


id: MONDO:0006894
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A syndrome characterized by retropatellar or peripatellar pain resulting from physical and biochemical changes in the patellofemoral joint. The pain is most prominent when ascending or descending stairs, squatting, or sitting with flexed knees. There is a lack of consensus on the etiology and treatment. The syndrome is often confused with (or accompanied by) chondromalacia patellae, the latter describing a pathological condition of the cartilage and not a syndrome.","definition_xrefs":["MESH:D046788"],"direct_ancestors":[{"relation_name":"is_a","term_name":"arthropathy","termid":"MONDO:0006816"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"patellofemoral pain syndrome","secondary_identifiers":["SCTID:430725003","MedDRA:10049143","MEDGEN:164080","EFO:1001092","UMLS:C0877149","DOID:14284"],"termid":"MONDO:0006894","xrefs":{"Monarch":{"xref_id":"0006894"}}}


id: MONDO:0018540
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An auto inflammatory syndrome characterized by recurrent febrile episodes associated with aphthous stomatitis, pharyngitis and cervical adenitis.","definition_xrefs":["Orphanet:42642"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"autoimmune disease","termid":"MONDO:0007179"},{"relation_name":"excluded_subClassOf","term_name":"unexplained periodic fever syndrome","termid":"MONDO:0015158"},{"relation_name":"is_a","term_name":"autoinflammatory syndrome","termid":"MONDO:0019751"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PFAPA syndrome","secondary_identifiers":["GARD:5657","SCTID:717231003","MEDGEN:909507","UMLS:C4082167","DOID:0081451","NCIT:C116917"],"synonyms":[{"name":"Marshall syndrome","type":"related"},{"name":"Marshall syndrome with periodic fever","type":"exact"},{"name":"PFAPA","type":"exact"},{"name":"periodic fever, aphthous stomatitis, pharyngitis and adenitis","type":"exact"},{"name":"periodic fever, aphthous stomatitis, pharyngitis, adenitis syndrome","type":"exact"},{"name":"periodic fever-aphtous stomatitis-pharyngitis-adenopathy syndrome","type":"exact"}],"termid":"MONDO:0018540","xrefs":{"Monarch":{"xref_id":"0018540"}}}


id: PBO:0045742
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EBF family member 4","termid":"PBO:0045742"}


id: PBO:0002794
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit L25 (predicted)","termid":"PBO:0002794"}


id: GO:0016877
data:
  {"annotated_genes":["SJAG_01524","SJAG_02082","SJAG_02084","SJAG_00878","SJAG_03471","SJAG_00853","SJAG_03896","SJAG_00947","SJAG_03813","SJAG_00645","SJAG_02741","SJAG_03909","SJAG_05032","SJAG_00604","SJAG_03950"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[115541],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003987"},{"annotations":[111145],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019778"},{"annotations":[111146],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019779"},{"annotations":[115209],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031956"},{"annotations":[112865,105067],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090432"},{"annotations":[95990,94105],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019781"},{"annotations":[105068],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090434"},{"annotations":[115210],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050203"},{"annotations":[105069],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090433"},{"annotations":[114417,89428],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004775"},{"annotations":[95711,97258,103961],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019948"},{"annotations":[103247],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004839"},{"annotations":[91419],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008641"},{"annotations":[95498],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042292"}]},"cv_name":"molecular_function","definition":"Catalysis of the joining of two molecules via a carbon-sulfur bond, with the concomitant hydrolysis of the diphosphate bond in ATP or a similar triphosphate.","definition_xrefs":["EC:6.2.-.-"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ligase activity","termid":"GO:0016874"}],"gene_count":15,"genes_by_uniquename":{"SJAG_00604":null,"SJAG_00645":null,"SJAG_00853":null,"SJAG_00878":null,"SJAG_00947":null,"SJAG_01524":null,"SJAG_02082":null,"SJAG_02084":null,"SJAG_02741":null,"SJAG_03471":null,"SJAG_03813":null,"SJAG_03896":null,"SJAG_03909":null,"SJAG_03950":null,"SJAG_05032":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016874"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016874"],"is_obsolete":false,"name":"ligase activity, forming carbon-sulfur bonds","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"ligase activity, forming carbon-sulphur bonds","type":"exact"}],"termid":"GO:0016877","terms_by_termid":{"GO:0003987":null,"GO:0004775":null,"GO:0004839":null,"GO:0008641":null,"GO:0019778":null,"GO:0019779":null,"GO:0019781":null,"GO:0019948":null,"GO:0031956":null,"GO:0042292":null,"GO:0050203":null,"GO:0090432":null,"GO:0090433":null,"GO:0090434":null}}


id: FYPO:0003852
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which vegetative cell population growth is normal (i.e. indistinguishable from wild type) in a medium containing FR901464.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal vegetative cell population growth","termid":"FYPO:0001357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0002057","FYPO:0002058","FYPO:0000257","FYPO:0002060","FYPO:0000003","FYPO:0000139"],"is_obsolete":false,"name":"normal growth on FR901464","synonyms":[{"name":"normal cell population growth in presence of FR901464","type":"exact"},{"name":"normal cell population growth on FR901464","type":"exact"},{"name":"normal cellular response to FR901464","type":"related"},{"name":"normal vegetative cell population growth on FR901464","type":"exact"}],"termid":"FYPO:0003852"}


id: PBO:0058187
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4480","termid":"PBO:0058187"}


id: PBO:0064676
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl isomerase A pseudogene 11","termid":"PBO:0064676"}


id: GO:1904001
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A positive regulation of transcription from RNA polymerase II promoter that results in positive regulation of pyrimidine-containing compound salvage.","definition_xrefs":["PMID:23695302","GO_REF:0000063","GOC:TermGenie","GOC:al"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of pyrimidine-containing compound salvage by positive regulation of transcription from RNA polymerase II promoter (obsolete GO:1904001)","synonyms":[{"name":"activation of pyrimidine salvage by positive regulation of transcription from RNA polymerase II promoter","type":"related"},{"name":"activation of pyrimidine-containing compound salvage by positive regulation of transcription from RNA polymerase II promoter","type":"narrow"},{"name":"positive regulation of pyrimidine salvage by positive regulation of transcription from RNA polymerase II promoter","type":"related"},{"name":"up regulation of pyrimidine salvage by positive regulation of transcription from RNA polymerase II promoter","type":"related"},{"name":"up regulation of pyrimidine-containing compound salvage by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"up-regulation of pyrimidine salvage by positive regulation of transcription from RNA polymerase II promoter","type":"related"},{"name":"up-regulation of pyrimidine-containing compound salvage by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"upregulation of pyrimidine salvage by positive regulation of transcription from RNA polymerase II promoter","type":"related"},{"name":"upregulation of pyrimidine-containing compound salvage by positive regulation of transcription from RNA polymerase II promoter","type":"exact"}],"termid":"GO:1904001"}


id: PBO:0051495
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IGSF11 antisense RNA 1","termid":"PBO:0051495"}


id: MONDO:0018714
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An intermediate, rarely metastasizing blood vessel neoplasm. It is characterized by the presence of lymphatic-like vascular channels and papillary endothelial proliferation.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hemangioendothelioma","termid":"MONDO:0021121"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primary intralymphatic angioendothelioma","secondary_identifiers":["GARD:21909","ICDO:9135/1","MEDGEN:138037","Orphanet:458768","UMLS:C0346087","NCIT:C7526"],"synonyms":[{"name":"Dabska tumor","type":"exact"},{"name":"Dabska tumour","type":"exact"},{"name":"PILA","type":"exact"},{"name":"malignant endothelial papillary angioendothelioma","type":"exact"},{"name":"papillary Endovascular angioendothelioma","type":"exact"},{"name":"papillary intralymphatic angioendothelioma","type":"exact"},{"name":"pila","type":"exact"}],"termid":"MONDO:0018714","xrefs":{"Monarch":{"xref_id":"0018714"}}}


id: GO:0102895
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 9(S)-HPODE = colneleate + H2O.","definition_xrefs":["EC:4.2.1.121","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydro-lyase activity","termid":"GO:0016836"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016829","GO:0003674"],"is_obsolete":false,"name":"colneleate synthase activity","secondary_identifiers":["MetaCyc:RXN-8496","RHEA:28174"],"termid":"GO:0102895"}


id: GO:1990444
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to an F-box domain of a protein.","definition_xrefs":["GOC:bf","PMID:12628165","GOC:PARL","InterPro:IPR001810"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein domain specific binding","termid":"GO:0019904"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"F-box domain binding","termid":"GO:1990444"}


id: PR:Q10659
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- spo14 gene.","definition_xrefs":["UniProtKB:Q10659","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":"membrane glycoprotein spo14 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC3H7.01","synonyms":[{"name":"SEC12-like protein (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-spo14","type":"exact"},{"name":"sporulation-specific protein 14 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q10659"}


id: PBO:0003602
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial protein, ribosomal subunit L35 (predicted)","termid":"PBO:0003602"}


id: PBO:0018142
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein carboxyl methyltransferase, implicated in DNA damage response","termid":"PBO:0018142"}


id: GO:0002541
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process activating plasma proteins by proteolysis as part of an acute inflammatory response.","definition_xrefs":["ISBN:0781735149","GOC:jal"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein processing","termid":"GO:0016485"},{"relation_name":"part_of","term_name":"acute inflammatory response","termid":"GO:0002526"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051604"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0051604"],"is_obsolete":false,"name":"activation of plasma proteins involved in acute inflammatory response","termid":"GO:0002541"}


id: GO:0021641
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that contributes to the act of creating the structural organization of the trochlear nerve. This process pertains to the physical shaping of a rudimentary structure. The trochlear nerve is a motor nerve and is the only cranial nerve to exit the brain dorsally. The trochlear nerve innervates the superior oblique muscle.","definition_xrefs":["GOC:dph","GOC:jid","GOC:cls","GOC:dgh","ISBN:0838580343","GO_REF:0000021"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cranial nerve structural organization","termid":"GO:0021604"},{"relation_name":"part_of","term_name":"trochlear nerve morphogenesis","termid":"GO:0021639"}],"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":"trochlear nerve structural organization","synonyms":[{"name":"CN IV structural organization","type":"related"},{"name":"trochlear nerve structural organisation","type":"exact"}],"termid":"GO:0021641"}


id: PBO:0070228
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 164 pseudogene","termid":"PBO:0070228"}


id: PBO:0047802
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"forkhead box J2","termid":"PBO:0047802"}


id: GO:0044439
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. Any constituent part of a peroxisome, a small, membrane-bounded organelle that uses dioxygen (O2) to oxidize organic molecules; contains some enzymes that produce and others that degrade hydrogen peroxide (H2O2).","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete peroxisomal part (obsolete GO:0044439)","synonyms":[{"name":"peroxisome component","type":"exact"}],"termid":"GO:0044439"}


id: PR:O42849
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A phenylalanine--tRNA ligase beta subunit that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR10947:SF0","PRO:DNx","OMA:SCHPO01700"],"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":"phenylalanine--tRNA ligase beta subunit (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC23A1.12c","secondary_identifiers":["UniProtKB:O42849"],"synonyms":[{"name":"PheRS (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-FARSB","type":"exact"},{"name":"phenylalanyl-tRNA synthetase beta subunit (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O42849"}


id: PBO:0089044
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diphthamide biosynthesis protein Dph3","termid":"PBO:0089044"}


id: PBO:0083046
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Deoxyhypusine synthase; catalyzes formation of deoxyhypusine, the first step in hypusine biosynthesis; triggers posttranslational hypusination of translation elongation factor eIF-5A and regulates its intracellular levels; tetrameric; human homolog DHPS allows growth of yeast haploid dys1 null mutant after sporulation of heterozygous diploid","termid":"PBO:0083046"}


id: GO:0018313
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The formation of a protein active site cross-link from the alpha-carboxyl carbon of residue N, an alanine, to the alpha-amino nitrogen of residue N+2, a glycine, coupled with the formation of a double bond to the alpha-amino nitrogen of residue N+1 which loses one hydrogen, and the loss of a molecule of water.","definition_xrefs":["RESID:AA0187"],"gene_count":0,"genotype_count":0,"name":"obsolete peptide cross-linking via L-alanyl-5-imidazolinone glycine (obsolete GO:0018313)","termid":"GO:0018313"}


id: GO:0016785
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of a selenium-containing group from one compound (donor) to another (acceptor).","definition_xrefs":["GOC:jl","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity","termid":"GO:0016740"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"selenotransferase activity","secondary_identifiers":["EC:2.9.1.-","GO:0016786"],"synonyms":[{"name":"transferase activity, transferring selenium-containing groups","type":"exact"}],"termid":"GO:0016785"}


id: MONDO:1010589
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Familial goiter that occurs in goat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial goiter, non-human animal","termid":"MONDO:1010053"},{"relation_name":"is_a","term_name":"congenital hypothyroidism, goat","termid":"MONDO:1010605"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"familial goiter, goat","secondary_identifiers":["OMIA:000424-9925"],"termid":"MONDO:1010589","xrefs":{"Monarch":{"xref_id":"1010589"}}}


id: GO:0021998
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that regulates the coordinated growth and differentiation that establishes the non-random mediolateral spatial arrangement of the neural plate.","definition_xrefs":["GOC:dgh","GOC:cls","GOC:dph","GOC:jid","GO_REF:0000021"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neural plate regionalization","termid":"GO:0060897"}],"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":"neural plate mediolateral regionalization","synonyms":[{"name":"neural plate mediolateral pattern formation","type":"related"}],"termid":"GO:0021998"}


id: PBO:0076680
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription elongation factor A2","termid":"PBO:0076680"}


id: PBO:0085692
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in regulation of sterol biosynthesis; specifically stabilizes Hmg2p, one of two HMG-CoA isoenzymes that catalyze the rate-limiting step in sterol biosynthesis; forms foci at the nuclear periphery upon DNA replication stress; relocalizes to the cytosol in response to hypoxia; homolog of mammalian INSIG proteins; NSG1 has a paralog, NSG2, that arose from the whole genome duplication","termid":"PBO:0085692"}


id: PBO:0069775
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1059, pseudogene","termid":"PBO:0069775"}


id: PBO:0088074
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ubiquitin-specific protease involved in protein deubiquitination; forms a complex with AAA peroxins Pex1p and Pex6p; deubiquitinates mono- and polyubiquitinated forms of Pex5p; deubiquitinates Clb5p, counteracting APC activity, and facilitating both Clb5p accumulation and S phase entry; physically interacts with anaphase-promoting complex/cyclosome (APC/C) activator, Cdh1p; catalytic activity regulated by an N-terminal TRAF-like domain and and C-terminal sequences","termid":"PBO:0088074"}


id: MONDO:0021742
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An infection occurring in puerperium, the period of 6-8 weeks after giving birth.","definition_xrefs":["MESH:D011645"],"direct_ancestors":[{"relation_name":"is_a","term_name":"infectious disease","termid":"MONDO:0005550"},{"relation_name":"is_a","term_name":"puerperal disorder","termid":"MONDO:0044013"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"puerperal infection","secondary_identifiers":["UMLS:C0034041","MEDGEN:11022","EFO:1001407"],"synonyms":[{"name":"Infection, Puerperal","type":"related"},{"name":"Infections, Puerperal","type":"related"},{"name":"Puerperal Infection","type":"related"},{"name":"Puerperal Infections","type":"related"}],"termid":"MONDO:0021742","xrefs":{"Monarch":{"xref_id":"0021742"}}}


id: PBO:0004036
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin-protein ligase E/phosphatidylinositol(3)-phosphate binding protein (predicted)","termid":"PBO:0004036"}


id: PBO:0005150
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1.1.1.95","termid":"PBO:0005150"}


id: GO:0002274
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A change in the morphology or behavior of a myeloid leukocyte resulting from exposure to an activating factor such as a cellular or soluble ligand.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukocyte activation","termid":"GO:0045321"}],"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":"myeloid leukocyte activation","synonyms":[{"name":"myeloid leucocyte activation","type":"exact"}],"termid":"GO:0002274"}


id: GO:1900951
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of 18-methylnonadec-1-ene biosynthetic process.","definition_xrefs":["GOC:TermGenie","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of olefin biosynthetic process","termid":"GO:1900912"},{"relation_name":"is_a","term_name":"regulation of 18-methylnonadec-1-ene biosynthetic process","termid":"GO:1900950"},{"relation_name":"is_a","term_name":"negative regulation of 18-methylnonadec-1-ene metabolic process","termid":"GO:1900954"},{"relation_name":"negatively_regulates","term_name":"18-methylnonadec-1-ene biosynthetic process","termid":"GO:1900881"}],"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 18-methylnonadec-1-ene biosynthetic process","synonyms":[{"name":"down regulation of 18-methylnonadec-1-ene anabolism","type":"exact"},{"name":"down regulation of 18-methylnonadec-1-ene biosynthesis","type":"exact"},{"name":"down regulation of 18-methylnonadec-1-ene biosynthetic process","type":"exact"},{"name":"down regulation of 18-methylnonadec-1-ene formation","type":"exact"},{"name":"down regulation of 18-methylnonadec-1-ene synthesis","type":"exact"},{"name":"down-regulation of 18-methylnonadec-1-ene anabolism","type":"exact"},{"name":"down-regulation of 18-methylnonadec-1-ene biosynthesis","type":"exact"},{"name":"down-regulation of 18-methylnonadec-1-ene biosynthetic process","type":"exact"},{"name":"down-regulation of 18-methylnonadec-1-ene formation","type":"exact"},{"name":"down-regulation of 18-methylnonadec-1-ene synthesis","type":"exact"},{"name":"downregulation of 18-methylnonadec-1-ene anabolism","type":"exact"},{"name":"downregulation of 18-methylnonadec-1-ene biosynthesis","type":"exact"},{"name":"downregulation of 18-methylnonadec-1-ene biosynthetic process","type":"exact"},{"name":"downregulation of 18-methylnonadec-1-ene formation","type":"exact"},{"name":"downregulation of 18-methylnonadec-1-ene synthesis","type":"exact"},{"name":"inhibition of 18-methylnonadec-1-ene anabolism","type":"exact"},{"name":"inhibition of 18-methylnonadec-1-ene biosynthesis","type":"exact"},{"name":"inhibition of 18-methylnonadec-1-ene biosynthetic process","type":"narrow"},{"name":"inhibition of 18-methylnonadec-1-ene formation","type":"exact"},{"name":"inhibition of 18-methylnonadec-1-ene synthesis","type":"exact"},{"name":"negative regulation of 18-methylnonadec-1-ene anabolism","type":"exact"},{"name":"negative regulation of 18-methylnonadec-1-ene biosynthesis","type":"exact"},{"name":"negative regulation of 18-methylnonadec-1-ene formation","type":"exact"},{"name":"negative regulation of 18-methylnonadec-1-ene synthesis","type":"exact"}],"termid":"GO:1900951"}


id: PR:Q9UTS7
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC977.12 gene.","definition_xrefs":["UniProtKB:Q9UTS7","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":"L-asparaginase 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC977.12","synonyms":[{"name":"L-asparagine amidohydrolase 2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-SPAC977.12","type":"exact"}],"termid":"PR:Q9UTS7"}


id: GO:0047166
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 1-alkenylglycerophosphoethanolamine + acyl-CoA = 1-alkenyl-2-acyl-glycerophosphoethanolamine + CoA.","definition_xrefs":["MetaCyc:2.3.1.121-RXN","EC:2.3.1.121"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-acyltransferase activity","termid":"GO:0008374"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0016746","GO:0003824"],"is_obsolete":false,"name":"1-alkenylglycerophosphoethanolamine O-acyltransferase activity","secondary_identifiers":["RHEA:16245"],"synonyms":[{"name":"acyl-CoA:1-alkenylglycerophosphoethanolamine O-acyltransferase activity","type":"related"}],"termid":"GO:0047166"}


id: MONDO:1012389
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"exercise-induced collapse, non-human animal","termid":"MONDO:1011877"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exercise-induced collapse, dog","secondary_identifiers":["OMIA:001466-9615"],"termid":"MONDO:1012389","xrefs":{"Monarch":{"xref_id":"1012389"}}}


id: FYPO:0000190
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 actin cortical patch localization is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal actin cytoskeleton organization during vegetative growth","termid":"FYPO:0000801"},{"relation_name":"is_a","term_name":"localization phenotype during vegetative growth","termid":"FYPO:0001337"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0004803"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0001320","FYPO:0000002","FYPO:0004803","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"abnormal actin cortical patch localization during vegetative growth","synonyms":[{"name":"abnormal F-actin patch localization during vegetative growth","type":"exact"},{"name":"abnormal actin cortical patch localisation during vegetative growth","type":"exact"},{"name":"abnormal actin cortical patch localization during mitotic cell cycle","type":"related"},{"name":"abnormal actin cortical patch location during vegetative growth","type":"related"},{"name":"abnormal actin patch localization during vegetative growth","type":"exact"}],"termid":"FYPO:0000190"}


id: PBO:0080061
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"USP30 antisense RNA 1","termid":"PBO:0080061"}


id: MONDO:0022510
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"atlanto-axial fusion","secondary_identifiers":["MESH:C538196"],"synonyms":[{"name":"atlantoaxial fusion","type":"related"},{"name":"atlantoaxial joint fusion","type":"related"}],"termid":"MONDO:0022510","xrefs":{"Monarch":{"xref_id":"0022510"}}}


id: PBO:0052990
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"laminin subunit alpha 2","termid":"PBO:0052990"}


id: MONDO:0031697
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete genetic intractable diarrhea of infancy (obsolete MONDO:0031697)","secondary_identifiers":["Orphanet:363300"],"termid":"MONDO:0031697","xrefs":{"Monarch":{"xref_id":"0031697"}}}


id: PBO:0041583
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 22 open reading frame 39","termid":"PBO:0041583"}


id: GO:0090412
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any positive regulation of transcription from RNA polymerase II promoter that is involved in fatty acid biosynthetic process.","definition_xrefs":["GOC:vw"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of transcription from RNA polymerase II promoter involved in fatty acid biosynthetic process (obsolete GO:0090412)","synonyms":[{"name":"positive regulation of transcription from RNA polymerase II promoter involved in fatty acid biosynthetic process","type":"exact"}],"termid":"GO:0090412"}


id: MONDO:0007965
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial melanoma","termid":"MONDO:0018961"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"melanoma, malignant familial intraocular","secondary_identifiers":["MESH:C563596","GARD:18576","OMIM:155700","UMLS:C1835043","MEDGEN:322559"],"synonyms":[{"name":"melanoma, malignant familial intraocular","type":"exact"}],"termid":"MONDO:0007965","xrefs":{"Monarch":{"xref_id":"0007965"}}}


id: GO:1902379
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Any chemoattractant activity that is involved in axon guidance.","definition_xrefs":["GOC:BHF","GOC:rl","GOC:TermGenie","PMID:21658587"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chemoattractant activity","termid":"GO:0042056"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0140677"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005515","GO:0140677","GO:0003674","GO:0098772","GO:0005488"],"is_obsolete":false,"name":"chemoattractant activity involved in axon guidance","synonyms":[{"name":"chemoattractant activity involved in axon chemotaxis","type":"related"},{"name":"chemoattractant activity involved in axon growth cone guidance","type":"narrow"},{"name":"chemoattractant activity involved in axon pathfinding","type":"exact"}],"termid":"GO:1902379"}


id: PBO:0041052
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bromodomain containing 7 pseudogene 3","termid":"PBO:0041052"}


id: PBO:0070125
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 39 pseudogene","termid":"PBO:0070125"}


id: GO:0015277
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"An ionotropic glutamate receptor activity that exhibits fast gating by glutamate, acts by opening a cation channel permeable to sodium and potassium, and for which kainate is an agonist.","definition_xrefs":["PMID:10049997","GOC:mah","PMID:8804111"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glutamate-gated receptor activity","termid":"GO:0004970"},{"relation_name":"is_a","term_name":"potassium channel activity","termid":"GO:0005267"},{"relation_name":"is_a","term_name":"ligand-gated sodium channel activity","termid":"GO:0015280"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0038023"},{"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:0038023","GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"kainate selective glutamate receptor activity","termid":"GO:0015277"}


id: GO:0072315
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the developmental fate of a cell becomes restricted such that it will develop into a metanephric glomerular epithelial cell. Metanephric glomerular epithelial cells are specialized epithelial cells that form part of the metanephric glomerulus; there are two types, metanephric glomerular parietal epithelial cells and metanephric glomerular visceral epithelial cells.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glomerular epithelial cell fate commitment","termid":"GO:0072314"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"metanephric glomerular epithelial cell fate commitment","termid":"GO:0072315"}


id: PBO:0067028
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 41, pseudogene","termid":"PBO:0067028"}


id: GO:0035846
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the oviduct epithelium over time from its initial formation to the mature structure. An oviduct is a tube through which an ova passes from the ovary to the uterus, or from the ovary to the outside of the organism. The oviduct epithelium is the specialized epithelium that lines the oviduct.","definition_xrefs":["PMID:34496237","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"is_a","term_name":"epithelium development","termid":"GO:0060429"},{"relation_name":"part_of","term_name":"oviduct development","termid":"GO:0060066"}],"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":"oviduct epithelium development","synonyms":[{"name":"fallopian tube epithelium development","type":"narrow"}],"termid":"GO:0035846"}


id: MONDO:0012532
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary hemorrhagic telangiectasia","termid":"MONDO:0019180"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"hereditary hemorrhagic telangiectasia type 4","secondary_identifiers":["MEDGEN:341824","UMLS:C1857688","OMIM:610655","GARD:10615","MESH:C565691"],"synonyms":[{"name":"HHT4","type":"related"},{"name":"telangiectasia, hereditary hemorrhagic, type 4","type":"related"}],"termid":"MONDO:0012532","xrefs":{"Monarch":{"xref_id":"0012532"}}}


id: GO:0046664
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The changes that occur during dorsal closure of the shape and structure of the amnioserosa, an epithelium that occupies the dorsal side of the embryo.","definition_xrefs":["PMID:12147138"],"direct_ancestors":[{"relation_name":"is_a","term_name":"embryonic morphogenesis","termid":"GO:0048598"},{"relation_name":"is_a","term_name":"tissue morphogenesis","termid":"GO:0048729"},{"relation_name":"part_of","term_name":"dorsal closure","termid":"GO:0007391"}],"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":"dorsal closure, amnioserosa morphology change","termid":"GO:0046664"}


id: PR:000027705
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A kinesin-like motor protein klp9/SPBC15D4.01c unmodified form in Schizosaccharomyces pombe.","definition_xrefs":["PMID:18257517","PomBase:MAH","PMID:19686686"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinesin-like motor protein klp9/SPBC15D4.01c","termid":"PR:000027702"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"klp9/UnMod","pombase_gene_id":"SPBC15D4.01c","synonyms":[{"name":"PomBase_original_PRO_term_name: kinesin-like motor protein klp9/SPBC15D4.01c unmodified form (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-klp9/UnMod","type":"exact"},{"name":"klp9/UnMod","type":"exact"}],"termid":"PR:000027705"}


id: GO:0030403
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 collagenase 4 activity (obsolete GO:0030403)","synonyms":[{"name":"MMP-18","type":"narrow"},{"name":"collagenase 4 activity","type":"exact"},{"name":"matrix metalloproteinase 18","type":"exact"}],"termid":"GO:0030403"}


id: PBO:0078008
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TNF receptor associated factor 7","termid":"PBO:0078008"}


id: PR:O59945
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A plastin-3 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03567","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":"fimbrin (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1778.06c","secondary_identifiers":["UniProtKB:O59945"],"synonyms":[{"name":"Spom972h-PLS3","type":"exact"}],"termid":"PR:O59945"}


id: PBO:0079721
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin domain containing 1","termid":"PBO:0079721"}


id: PBO:0043535
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"component of oligomeric golgi complex 3","termid":"PBO:0043535"}


id: PBO:0052291
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KHDC1 antisense RNA 1","termid":"PBO:0052291"}


id: PBO:0055004
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 2419","termid":"PBO:0055004"}


id: PBO:0082016
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZW10 interacting kinetochore protein","termid":"PBO:0082016"}


id: GO:0008945
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the hydrolysis of Arg-Xaa and Lys-Xaa bonds in oligopeptides, even when P1' residue is proline.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete oligopeptidase B activity (obsolete GO:0008945)","synonyms":[{"name":"Escherichia coli alkaline proteinase II","type":"related"},{"name":"oligopeptidase B activity","type":"exact"},{"name":"protease II activity","type":"related"}],"termid":"GO:0008945"}


id: MONDO:0009691
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Classical mycosis fungoides is the most common type of mycosis fungoides (MF), a form of cutaneous T-cell lymphoma, and is characterized by slow progression from patches to more infiltrated plaques and eventually to tumors.","definition_xrefs":["Orphanet:2584"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary cutaneous T-cell non-Hodgkin lymphoma","termid":"MONDO:0000607"},{"relation_name":"is_a","term_name":"mycosis fungoides and variants","termid":"MONDO:0015821"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005093","MONDO:0004992"],"is_obsolete":false,"name":"mycosis fungoides","secondary_identifiers":["EFO:1001051","ICD9:202.1","MEDGEN:7771","MESH:D009182","NCIT:C3246","MedDRA:10028483","NORD:1479","UMLS:C0026948","OMIM:254400","ONCOTREE:MYCF","ICDO:9700/3","icd11.foundation:901411509","SCTID:118618005","GARD:3863","DOID:8691","ICD10CM:C84.0"],"synonyms":[{"name":"Alibert-Bazin syndrome","type":"related"},{"name":"CTCL/ mycosis fungoides","type":"exact"},{"name":"MF","type":"exact"},{"name":"classic mycosis fungoides","type":"related"},{"name":"cutaneous T-cell lymphoma/mycosis fungoides","type":"exact"},{"name":"granuloma fungoides","type":"related"},{"name":"mycosis fungoides","type":"exact"},{"name":"mycosis fungoides (morphologic abnormality)","type":"exact"},{"name":"mycosis fungoides NOS (morphologic abnormality)","type":"exact"},{"name":"mycosis fungoides lymphoma","type":"exact"},{"name":"mycosis fungoides of unspecified site","type":"exact"},{"name":"mycosis fungoides, Alibert-Bazin type","type":"exact"},{"name":"mycosis fungoides, unspecified site, extranodal and solid organ sites","type":"exact"}],"termid":"MONDO:0009691","xrefs":{"Monarch":{"xref_id":"0009691"}}}


id: PBO:0076357
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"synaptotagmin like 4","termid":"PBO:0076357"}


id: GO:0019122
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation of peptidyl-D-alanine, by either racemization or from peptidyl-L-serine.","definition_xrefs":["RESID:AA0191"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidyl-L-amino acid racemization","termid":"GO:0018085"},{"relation_name":"is_a","term_name":"peptidyl-alanine modification","termid":"GO:0018194"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006520","GO:0008150"],"is_obsolete":false,"name":"peptidyl-D-alanine racemization","synonyms":[{"name":"alanine racemization","type":"broad"}],"termid":"GO:0019122"}


id: MONDO:0024287
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A congenital abnormality of the arteries and veins, lymph vessels or veins and lymph vessels.","definition_xrefs":["NCIT:C112117"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vascular malformation","termid":"MONDO:0024291"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital vascular malformation","secondary_identifiers":["MEDGEN:743837","UMLS:C1961121"],"synonyms":[{"name":"congenital vascular malformation","type":"exact"},{"name":"vascular malformation","type":"broad"}],"termid":"MONDO:0024287","xrefs":{"Monarch":{"xref_id":"0024287"}}}


id: GO:0002105
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Endonucleolytic cleavage between the LSU-rRNA and the 4.5S rRNA of an rRNA molecule originally produced as a tetracistronic rRNA transcript that contains the Small Subunit (SSU) rRNA, Large Subunit (LSU) the 4.5S rRNA, and the 5S rRNA in that order from 5' to 3' along the primary transcript. Note that the use of the word tetracistronic refers only to the number of mature rRNA molecules which will be produced from the primary transcript and ignores tRNAs that may also be present within the primary transcript.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endonucleolytic cleavage of tetracistronic rRNA transcript (SSU-rRNA, LSU-rRNA, 4.5S-rRNA, 5S-rRNA)","termid":"GO:0002103"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0042254"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0044085","GO:0042254","GO:0010467"],"is_obsolete":false,"name":"endonucleolytic cleaveage between LSU-rRNA and 4.5S rRNA of tetracistronic rRNA transcript (SSU-rRNA, LSU-rRNA, 4.5S-rRNA, 5S-rRNA)","termid":"GO:0002105"}


id: MONDO:0007852
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Palmoplantar keratoderma-deafness syndrome is a keratinization disorder characterized by focal or diffuse palmoplantar keratoderma. A patchy distribution is observed with accentuation on the thenars, hypothenars and the arches of the feet. The disease becomes apparent in infancy and is associated with sensorineural hearing loss that shows a variable age of onset. Due to genetic and clinical similarities, it has been proposed that palmoplantar keratoderma-deafness syndrome, knuckle pads-leukonychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome and keratoderma hereditarium mutilans may represent variants of one broad disorder of syndromic deafness with heterogeneous phenotype. The disease is transmitted in an autosomal dominant manner with incomplete penetrance.","definition_xrefs":["Orphanet:2202"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diffuse palmoplantar keratoderma","termid":"MONDO:0017666"}],"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":"palmoplantar keratoderma-deafness syndrome","secondary_identifiers":["MEDGEN:332030","MESH:C536152","OMIM:148350","DOID:0111505","GARD:3094","UMLS:C1835672"],"synonyms":[{"name":"PPK-deafness syndrome","type":"exact"},{"name":"diffuse palmoplantar keratoderma with deafness (subtype)","type":"related"},{"name":"focal palmoplantar keratoderma with sensorineural deafness (subtype)","type":"related"},{"name":"hereditary palmoplantar keratoderma with deafness (subtype)","type":"related"},{"name":"keratoderma palmoplantar deafness","type":"related"},{"name":"keratoderma palmoplantar, with deafness","type":"related"},{"name":"keratoderma, palmoplantar, with deafness","type":"related"},{"name":"palmoplantar hyperkeratosis-deafness syndrome","type":"exact"},{"name":"palmoplantar hyperkeratosis-hearing loss syndrome","type":"exact"},{"name":"palmoplantar keratoderma and sensorineural deafness","type":"related"},{"name":"palmoplantar keratoderma-hearing loss syndrome","type":"exact"}],"termid":"MONDO:0007852","xrefs":{"Monarch":{"xref_id":"0007852"}}}


id: GO:0030512
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of any TGF-beta receptor signaling pathway.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transforming growth factor beta receptor signaling pathway","termid":"GO:0017015"},{"relation_name":"is_a","term_name":"negative regulation of transmembrane receptor protein serine/threonine kinase signaling pathway","termid":"GO:0090101"},{"relation_name":"negatively_regulates","term_name":"transforming growth factor beta receptor signaling pathway","termid":"GO:0007179"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"negative regulation of transforming growth factor beta receptor signaling pathway","secondary_identifiers":["Reactome:R-HSA-2173788"],"synonyms":[{"name":"down regulation of transforming growth factor beta receptor signaling pathway","type":"exact"},{"name":"down-regulation of transforming growth factor beta receptor signaling pathway","type":"exact"},{"name":"downregulation of transforming growth factor beta receptor signaling pathway","type":"exact"},{"name":"inhibition of transforming growth factor beta receptor signaling pathway","type":"narrow"},{"name":"negative regulation of TGF-beta receptor signaling pathway","type":"exact"},{"name":"negative regulation of TGFbeta receptor signaling pathway","type":"exact"},{"name":"negative regulation of transforming growth factor beta receptor signalling pathway","type":"exact"}],"termid":"GO:0030512"}


id: FYPO:0007892
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which histone exchange at subtelomeric heterochromatin is increased. Histone exchange is replacement, within chromatin, of resident histones or histone subunits with alternative, sometimes variant, histones or subunits.","definition_xrefs":["PMID:34731638","PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone turnover","termid":"FYPO:0007472"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0005447","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"increased histone turnover at subtelomeric heterochromatin","termid":"FYPO:0007892"}


id: PR:000085737
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A DNA-directed RNA polymerase II subunit rpb1 CTD-phosphorylated form (Schizosaccharomyces pombe) that has been post-translationally modified to include phosphoserine at the fifth and seventh positions of one or more of the C-terminal heptad repeats (YSPTSPS).","definition_xrefs":["PMID:26264592","PomBase:VW","PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rpb1/Phos(CTD-S2,S5,S7)","termid":"PR:000050494"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rpb1/Phos(CTD-S5,S7)","pombase_gene_id":"SPBC28F2.12","synonyms":[{"name":"PomBase_original_PRO_term_name: DNA-directed RNA polymerase II subunit rpb1 phosphorylated 4 (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-rpb1/Phos:4","type":"exact"},{"name":"rpb1/Phos(CTD-S5,S7)","type":"exact"}],"termid":"PR:000085737"}


id: PBO:0048412
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GATA binding protein 2","termid":"PBO:0048412"}


id: PBO:0026938
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_onset_of_meiosis_I","termid":"PBO:0026938"}


id: PBO:0071182
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23a pseudogene 23","termid":"PBO:0071182"}


id: GO:0003719
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete transcription factor binding, cytoplasmic sequestering (obsolete GO:0003719)","synonyms":[{"name":"transcription factor binding, cytoplasmic sequestering","type":"exact"}],"termid":"GO:0003719"}


id: GO:0010125
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of mycothiol, which consists of N-acetyl-L-cysteine linked to a pseudodisaccharide, D-glucosamine and myo-inositol. Mycothiol is produced in actinomycetes like mycobacteria and serves similar functions to glutathione.","definition_xrefs":["GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mycothiol metabolic process","termid":"GO:0010126"},{"relation_name":"is_a","term_name":"glycoside biosynthetic process","termid":"GO:0016138"},{"relation_name":"is_a","term_name":"sulfur compound biosynthetic process","termid":"GO:0044272"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006790"}],"interesting_parent_ids":["GO:0006790","GO:0008150"],"is_obsolete":false,"name":"mycothiol biosynthetic process","secondary_identifiers":["MetaCyc:PWY1G-0"],"synonyms":[{"name":"mycothiol anabolism","type":"exact"},{"name":"mycothiol biosynthesis","type":"exact"},{"name":"mycothiol formation","type":"exact"},{"name":"mycothiol synthesis","type":"exact"}],"termid":"GO:0010125"}


id: GO:1990501
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Component of the core exon-exon-junction complex (EJC). Fairly conserved in eukaryotes; in Drosophila, consists of the Mago and Y14 (tsunagi) gene products. Important for coupling nuclear and cytoplasmic events in gene expression. Inhibits the ATPase activity of eIF4AIII (Q9VHS8) to ensure a stable association of the EJC core with the mRNA.","definition_xrefs":["GOC:bhm","PMID:12730685"],"direct_ancestors":[{"relation_name":"is_a","term_name":"exon-exon junction complex","termid":"GO:0035145"},{"relation_name":"is_a","term_name":"ATPase inhibitor complex","termid":"GO:1903503"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0005634","GO:0032991"],"is_obsolete":false,"name":"exon-exon junction subcomplex mago-y14","synonyms":[{"name":"MGN-RBM8A complex","type":"exact"},{"name":"exon junction subcomplex MAGOH-Y14","type":"exact"},{"name":"mago-y14 complex","type":"related"}],"termid":"GO:1990501"}


id: GO:0032986
data:
  {"annotated_genes":["SJAG_02314","SJAG_04038","SJAG_01653"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89579,96587,116347],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006337"}]},"cv_name":"biological_process","definition":"The disaggregation of a protein-DNA complex into its constituent components.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex disassembly","termid":"GO:0032984"},{"relation_name":"is_a","term_name":"protein-DNA complex organization","termid":"GO:0071824"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01653":null,"SJAG_02314":null,"SJAG_04038":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"protein-DNA complex disassembly","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"DNA-protein complex disassembly","type":"exact"}],"termid":"GO:0032986","terms_by_termid":{"GO:0006337":null}}


id: MONDO:0034142
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"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":"pancreatic agenesis-holoprosencephaly syndrome","secondary_identifiers":["UMLS:C5681334","MEDGEN:1808942","Orphanet:556955","GARD:17992"],"termid":"MONDO:0034142","xrefs":{"Monarch":{"xref_id":"0034142"}}}


id: PR:O13964
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC24C9.04 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O13964"],"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 C24C9.04 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC24C9.04","synonyms":[{"name":"Spom972h-SPAC24C9.04","type":"exact"}],"termid":"PR:O13964"}


id: GO:0010766
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the frequency, rate or extent of the directed movement of sodium ions (Na+) into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of sodium ion transport","termid":"GO:0002028"},{"relation_name":"is_a","term_name":"negative regulation of monoatomic ion transport","termid":"GO:0043271"},{"relation_name":"negatively_regulates","term_name":"sodium ion transport","termid":"GO:0006814"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"negative regulation of sodium ion transport","termid":"GO:0010766"}


id: PBO:0038596
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acyl-CoA dehydrogenase short chain","termid":"PBO:0038596"}


id: FYPO:0003796
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 from an RNA polymerase II promoter does not occur. All genes, or a specific subset of genes, may be affected.","definition_xrefs":["PomBase:mah","PMID:16874521"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished transcription during vegetative growth","termid":"FYPO:0001443"},{"relation_name":"is_a","term_name":"decreased transcription from RNA polymerase II promoter during vegetative growth","termid":"FYPO:0005229"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000294","FYPO:0006551","FYPO:0005447","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"abolished transcription from RNA polymerase II promoter","synonyms":[{"name":"abolished transcription from RNA polymerase II promoter during mitotic cell cycle","type":"related"},{"name":"abolished transcription from RNA polymerase II promoter during vegetative growth","type":"exact"},{"name":"transcription from RNA polymerase II promoter abolished","type":"exact"}],"termid":"FYPO:0003796"}


id: MONDO:0002809
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-metastasizing cystic epithelial neoplasm arising from the exocrine pancreas.","definition_xrefs":["NCIT:C4374"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cystadenoma","termid":"MONDO:0002369"},{"relation_name":"is_a","term_name":"pancreatic exocrine neoplasm","termid":"MONDO:0021076"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"pancreatic cystadenoma","secondary_identifiers":["UMLS:C0341486","SCTID:235967003","DOID:3918","MEDGEN:90963"],"synonyms":[{"name":"cystadenoma of pancreas","type":"exact"},{"name":"cystadenoma of the pancreas","type":"exact"},{"name":"exocrine pancreas cystadenoma","type":"exact"},{"name":"pancreatic cystadenoma","type":"exact"}],"termid":"MONDO:0002809","xrefs":{"Monarch":{"xref_id":"0002809"}}}


id: MONDO:0018513
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A squamous cell carcinoma that involves the colon.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"colon carcinoma","termid":"MONDO:0002032"},{"relation_name":"is_a","term_name":"colorectal squamous cell carcinoma","termid":"MONDO:0006165"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"squamous cell carcinoma of colon","secondary_identifiers":["DOID:5519","GARD:21768","MEDGEN:272494","NCIT:C5490","Orphanet:423994","SCTID:766981007","UMLS:C1333100"],"synonyms":[{"name":"colon epidermoid carcinoma","type":"exact"},{"name":"colon squamous cell cancer","type":"exact"},{"name":"colon squamous cell carcinoma","type":"exact"},{"name":"colonic epidermoid carcinoma","type":"exact"},{"name":"colonic squamous cell carcinoma","type":"exact"},{"name":"epidermoid carcinoma of colon","type":"exact"},{"name":"epidermoid carcinoma of the colon","type":"exact"},{"name":"squamous cell carcinoma of colon","type":"exact"},{"name":"squamous cell carcinoma of the colon","type":"exact"},{"name":"squamous cell colon carcinoma","type":"exact"}],"termid":"MONDO:0018513","xrefs":{"Monarch":{"xref_id":"0018513"}}}


id: PBO:0051698
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inositol polyphosphate-1-phosphatase","termid":"PBO:0051698"}


id: PATO:0000816
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000816 relative odor acuity value (obsolete PATO:0000816)","termid":"PATO:0000816"}


id: PBO:0074784
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 5","termid":"PBO:0074784"}


id: PBO:0113178
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Killer toxin defense factor; key polymorphic factor in the defense against K28 toxin; localizes mainly to vacuolar membrane; most likely acts against K28 during its trafficking after endocytosis; member of DUP240 gene family","termid":"PBO:0113178"}


id: PBO:0044485
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome P450 family 27 subfamily A member 1","termid":"PBO:0044485"}


id: MONDO:0010353
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A syndrome characterized by severe bilateral deafness, intellectual deficit, umbilical hernia and abnormal dermatoglyphics. It has been described in three males from three generations of one family. Mild facial dysmorphism (telangiectasias, hypertelorism, dental anomalies and a wide nasal root) was also present. Short stature, pancytopaenia, microcephaly, and renal and genitourinary anomalies were present in some of the patients. The mode of transmission is X-linked recessive and the causative gene has been localized to the q1-21 region of the X chromosome.","definition_xrefs":["Orphanet:85321"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"excluded_subClassOf","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deafness-intellectual disability, Martin-Probst type syndrome","secondary_identifiers":["OMIM:300519","SCTID:721087008","GARD:16750","UMLS:C1845285","MESH:C564495","MEDGEN:375620","DOID:0060830"],"synonyms":[{"name":"MRXSMP","type":"related"},{"name":"Martin-Probst deafness-intellectual disability syndrome","type":"related"},{"name":"Martin-Probst deafness-mental retardation syndrome","type":"related"},{"name":"Martin-Probst syndrome","type":"exact"},{"name":"X-linked deafness-intellectual disability syndrome syndrome","type":"exact"},{"name":"deafness-intellectual disability syndrome, Martin-Probst type","type":"related"},{"name":"intellectual disability, X-linked, syndromic, MARTIN-Probst type","type":"related"},{"name":"intellectual disability, X-linked, syndromic, Martin-Probst type","type":"exact"},{"name":"martin-probst syndrome, X-linked recessive","type":"exact"},{"name":"mental retardation, X-linked, syndromic, MARTIN-Probst type","type":"related"},{"name":"mental retardation, X-linked, syndromic, Martin-Probst type","type":"exact"}],"termid":"MONDO:0010353","xrefs":{"Monarch":{"xref_id":"0010353"}}}


id: MONDO:0013221
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Miyoshi myopathy","termid":"MONDO:0009685"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"Miyoshi muscular dystrophy 2","secondary_identifiers":["DOID:0070200","MESH:C567646","UMLS:C2750077","GARD:15648","MEDGEN:413751","OMIM:613318"],"synonyms":[{"name":"MIYOSHI muscular dystrophy 2","type":"related"},{"name":"MMD2","type":"exact"},{"name":"Miyoshi muscular dystrophy 2","type":"exact"},{"name":"Miyoshi myopathy 2","type":"related"}],"termid":"MONDO:0013221","xrefs":{"Monarch":{"xref_id":"0013221"}}}


id: MONDO:0016422
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, endocrine disease characterized by autoimmune thyroid disease associated with at least one other autoimmune disease, such as type I diabetes mellitus, chronic atrophic gastritis, pernicious anemia, vitiligo, alopecia, or myasthenia gravis, but excluding Addison disease.","definition_xrefs":["Orphanet:227982"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"type 1 diabetes mellitus","termid":"MONDO:0005147"},{"relation_name":"is_a","term_name":"autoimmune polyendocrinopathy","termid":"MONDO:0017278"}],"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":"autoimmune polyendocrinopathy type 3","secondary_identifiers":["UMLS:C1535942","icd11.foundation:1361747293","ICD9:258.1","MEDGEN:453060","SCTID:449731009","GARD:10980"],"synonyms":[{"name":"APS type 3","type":"exact"},{"name":"APS3","type":"exact"},{"name":"PAS3","type":"related"},{"name":"autoimmune polyendocrine syndrome type 3","type":"exact"},{"name":"autoimmune polyglandular syndrome type 3","type":"exact"},{"name":"polyglandular autoimmune syndrome type 3","type":"related"}],"termid":"MONDO:0016422","xrefs":{"Monarch":{"xref_id":"0016422"}}}


id: FYPO:0001445
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of trehalose measured in a cell is higher than normal when the cell is subject to heat shock.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased cellular trehalose level during vegetative growth","termid":"FYPO:0001444"}],"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:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"increased cellular trehalose level during heat shock","synonyms":[{"name":"increased cellular trehalose level during heat shock during mitotic cell cycle","type":"related"},{"name":"increased cellular trehalose level during vegetative growth and during heat shock","type":"exact"},{"name":"increased trehalose accumulation during heat shock","type":"related"}],"termid":"FYPO:0001445"}


id: PBO:0086845
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative pyridoxal kinase; a key enzyme involved in pyridoxal 5'-phosphate synthesis, the active form of vitamin B6; required for genome integrity; involved in bud-site selection; similarity to yeast BUD17 and human pyridoxal kinase (PDXK)","termid":"PBO:0086845"}


id: GO:0102742
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: H+ + 3,4-dihydroxyphenylpyruvate + NADPH = (2R)-3-(3,4-dihydroxyphenyl)lactate + NADP.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete R(+)-3,4-dihydroxyphenyllactate:NADP+ oxidoreductase activity (obsolete GO:0102742)","termid":"GO:0102742"}


id: PBO:0059324
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein L57 pseudogene 9","termid":"PBO:0059324"}


id: PBO:0003796
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Chediak-Higashi syndrome","termid":"PBO:0003796"}


id: PBO:0061434
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear receptor subfamily 1 group I member 3","termid":"PBO:0061434"}


id: MONDO:0000244
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A dermatophyte infection of the hair that nvade the hair shaft and internalize into the hair cell.","definition_xrefs":["Wikipedia:Endothrix"],"direct_ancestors":[{"relation_name":"is_a","term_name":"piedra","termid":"MONDO:0000253"},{"relation_name":"is_a","term_name":"dermatophytosis","termid":"MONDO:0004678"}],"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":"endothrix infectious disease","secondary_identifiers":["DOID:0050105"],"termid":"MONDO:0000244","xrefs":{"Monarch":{"xref_id":"0000244"}}}


id: FYPO:0007962
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A biological process phenotype in which the observed mating efficiency, as determined by counting zygotes, asci, and sometimes spores, is lower than normal after nitrogen removal.","definition_xrefs":["PomBase:val"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased mating efficiency","termid":"FYPO:0000708"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000003"],"is_obsolete":false,"name":"decreased mating efficiency during nitrogen starvation","termid":"FYPO:0007962"}


id: PBO:0076706
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor 7","termid":"PBO:0076706"}


id: PBO:0002514
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA dihydrouridine synthase Dus3 (predicted)","termid":"PBO:0002514"}


id: MONDO:0012900
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any familial isolated restrictive cardiomyopathy in which the cause of the disease is a mutation in the TNNT2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial restrictive cardiomyopathy","termid":"MONDO:0016340"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"cardiomyopathy, familial restrictive, 3","secondary_identifiers":["DOID:0111427","MEDGEN:382807","MESH:C567316","OMIM:612422","UMLS:C2676271","GARD:18072"],"synonyms":[{"name":"RCM3","type":"related"},{"name":"TNNT2 familial isolated restrictive cardiomyopathy","type":"exact"},{"name":"cardiomyopathy, familial restrictive, 3","type":"exact"},{"name":"cardiomyopathy, familial restrictive, type 3","type":"exact"},{"name":"familial isolated restrictive cardiomyopathy caused by mutation in TNNT2","type":"exact"}],"termid":"MONDO:0012900","xrefs":{"Monarch":{"xref_id":"0012900"}}}


id: GO:1905334
data:
  {"annotated_genes":["SJAG_02267","SJAG_01410"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[98579,100049],"is_not":false,"summary":null,"term":"GO:1905334"}]},"cv_name":"molecular_function","definition":"Binding to a Swi5-Sfr1 complex.","definition_xrefs":["PMID:16921379","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex binding","termid":"GO:0044877"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01410":null,"SJAG_02267":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"Swi5-Sfr1 complex binding","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"Sae3-Mei5 complex binding","type":"exact"}],"termid":"GO:1905334","terms_by_termid":{"GO:1905334":null}}


id: PBO:0047384
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box protein 21","termid":"PBO:0047384"}


id: GO:1990042
data:
  {"annotated_genes":["SJAG_04048"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[88124],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008888"}]},"cv_name":"molecular_function","definition":"Catalysis of an oxidation-reduction (redox) reaction in which glycerol is converted into glycerone and NAD+ or NADP is reduced.","definition_xrefs":["PMID:22979944"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04048":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"glycerol dehydrogenase [NAD(P)+] activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"glycerol dehydrogenase activity, NAD or NADP as acceptor","type":"exact"}],"termid":"GO:1990042","terms_by_termid":{"GO:0008888":null}}


id: PBO:0087402
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Stretch-activated Ca2+-permeable cation channel; required for Ca2+ influx stimulated by mating pheromones and some abiotic stresses; sensor of compressive mechanical stress; N-glycosylated membrane protein of the ER and plasma membrane; interacts with Cch1p; oligomerizes; is an alpha2/delta-like protein and participates in the generation of stretch-activated Ca2+-permeable cation channel activity when expressed in mammalian cells","termid":"PBO:0087402"}


id: PBO:0047764
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FosB proto-oncogene, AP-1 transcription factor subunit","termid":"PBO:0047764"}


id: GO:0046089
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of cytosine, 4-amino-2-hydroxypyrimidine, a pyrimidine derivative that is one of the five main bases found in nucleic acids; it occurs widely in cytidine derivatives.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine nucleobase biosynthetic process","termid":"GO:0019856"},{"relation_name":"is_a","term_name":"cytosine metabolic process","termid":"GO:0019858"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"cytosine biosynthetic process","synonyms":[{"name":"cytosine anabolism","type":"exact"},{"name":"cytosine biosynthesis","type":"exact"},{"name":"cytosine formation","type":"exact"},{"name":"cytosine synthesis","type":"exact"}],"termid":"GO:0046089"}


id: MONDO:0010689
data:
  {"annotated_genes":["SJAG_02016"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85007],"is_not":false,"summary":null,"term":"MONDO:0010689"}]},"cv_name":"mondo","definition":"X-linked Charcot-Marie-Tooth disease type 4 is a rare, genetic, axonal, peripheral sensorimotor neuropathy characterized by an X-linked recessive inheritance pattern and the neonatal- to early childhood-onset of severe, slowly progressive, distal muscle weakness and atrophy (in particular of the peroneal group), as well as sensory impairment (with the lower extremities being more affected than the upper extremities), pes cavus, areflexia and hammertoes. Sensorineural hearing loss and cognitive impairment may also be associated. Females are asymptomatic and do not display the phenotype.","definition_xrefs":["Orphanet:101078"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Charcot-Marie-Tooth disease type X","termid":"MONDO:0018994"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02016":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 X-linked recessive 4","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:1240","UMLS:C0795910","MEDGEN:162891","SCTID:763400005","DOID:0110212","OMIM:310490"],"synonyms":[{"name":"CMT4X","type":"exact"},{"name":"CMTX 4","type":"exact"},{"name":"CMTX4","type":"exact"},{"name":"COWCK","type":"exact"},{"name":"Charcot-Marie-Tooth disease X-linked recessive type 4","type":"exact"},{"name":"Charcot-Marie-Tooth disease with deafness and intellectual disability","type":"exact"},{"name":"Charcot-Marie-Tooth disease with deafness and mental retardation","type":"exact"},{"name":"Charcot-Marie-Tooth disease, X-linked recessive, 4","type":"exact"},{"name":"Cowchock syndrome, X-linked recessive","type":"exact"},{"name":"NADMR","type":"exact"},{"name":"NAMSD","type":"exact"},{"name":"X-linked Charcot-Marie-Tooth disease type 4","type":"exact"},{"name":"axonal motor sensory neuropathy with deafness and intellectual disability","type":"exact"},{"name":"axonal motor sensory neuropathy with deafness and mental retardation","type":"exact"},{"name":"cowchock syndrome","type":"exact"},{"name":"neuropathy, axonal motor-sensory with deafness and intellectual disability","type":"related"},{"name":"neuropathy, axonal motor-sensory with deafness and mental retardation","type":"related"},{"name":"neuropathy, axonal motor-sensory, with deafness and intellectual disability","type":"related"},{"name":"neuropathy, axonal motor-sensory, with deafness and mental retardation","type":"related"}],"termid":"MONDO:0010689","terms_by_termid":{"MONDO:0010689":null},"xrefs":{"Monarch":{"xref_id":"0010689"}}}


id: PBO:0090151
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial carrier, coenzyme A, Leu5","termid":"PBO:0090151"}


id: PBO:0027927
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_RNA_level_during_cellular_response_to_pheromone_and_nitrogen_starvation","termid":"PBO:0027927"}


id: MONDO:1012547
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"vitreous degeneration, non-human animal","termid":"MONDO:1012002"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vitreous degeneration, dog","secondary_identifiers":["OMIA:002409-9615"],"termid":"MONDO:1012547","xrefs":{"Monarch":{"xref_id":"1012547"}}}


id: PBO:0047883
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fragile site, aphidicolin type, common, fra(5)(q15)","termid":"PBO:0047883"}


id: MONDO:0009190
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":"epiphyseal dysplasia of femoral head, myopia, and deafness","secondary_identifiers":["OMIM:226950","MESH:C565585","UMLS:C1856918","MEDGEN:346470"],"synonyms":[{"name":"epiphyseal dysplasia of femoral head, myopia, and deafness","type":"exact"}],"termid":"MONDO:0009190","xrefs":{"Monarch":{"xref_id":"0009190"}}}


id: PBO:0060810
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase core subunit V2 pseudogene 1","termid":"PBO:0060810"}


id: PBO:0116190
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5-oxoprolinase (ATP-hydrolizing), Oxp2","termid":"PBO:0116190"}


id: FYPO:0006840
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which LinE complex assembly is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein-containing complex assembly","termid":"FYPO:0006839"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal LinE complex assembly","synonyms":[{"name":"normal linear element protein complex assembly","type":"exact"}],"termid":"FYPO:0006840"}


id: PR:O94505
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- tol1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94505"],"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":"3'(2'),5'-bisphosphate nucleotidase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1753.04","synonyms":[{"name":"3'(2'),5-bisphosphonucleoside 3'(2')-phosphohydrolase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"DPNPase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-tol1","type":"exact"},{"name":"halotolerance protein tol1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"target of lithium protein 1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94505"}


id: PR:000035574
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A MAD2:MAD3 complex whose components are encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PMID:12676091","PRO:KER"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein","termid":"PR:000000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAD2:MAD3 complex (Schizosaccharomyces pombe 972h-)","synonyms":[{"name":"Spom972h-(MAD2:MAD3)","type":"exact"}],"termid":"PR:000035574"}


id: MONDO:0100026
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"This group of epilepsies are typically is characterized by onset of seizures from day 1 of life to 5 years (peak 12 months). Both sexes are affected, however the male to female ratio is 1:2. Antecedent (including birth) history, head size, neurological and developmental findings reflect the underlying cause (if known). Myoclonic status epilepticus is often the initial presenting seizure type, however other initial seizure types may also occur. Prognosis is unfavorable with severe neurological and developmental impairments typically seen.","direct_ancestors":[{"relation_name":"is_a","term_name":"neonatal/infantile epilepsy syndrome","termid":"MONDO:0100022"}],"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":"myoclonic encephalopathy in non-progressive disorder","termid":"MONDO:0100026","xrefs":{"Monarch":{"xref_id":"0100026"}}}


id: PBO:0059408
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein S34","termid":"PBO:0059408"}


id: PBO:0088531
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uridine kinase Yfh7","termid":"PBO:0088531"}


id: GO:1905254
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any positive regulation of epidermal growth factor receptor signaling pathway that is involved in heart process.","definition_xrefs":["GO_REF:0000060","PMID:23069713","GOC:bc","GOC:TermGenie","GOC:BHF_miRNA","GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of epidermal growth factor receptor signaling pathway involved in heart process (obsolete GO:1905254)","synonyms":[{"name":"activation of epidermal growth factor receptor signaling pathway involved in cardiac process","type":"related"},{"name":"activation of epidermal growth factor receptor signaling pathway involved in heart process","type":"narrow"},{"name":"positive regulation of EGF receptor signaling pathway involved in cardiac process","type":"related"},{"name":"positive regulation of EGF receptor signaling pathway involved in heart process","type":"exact"},{"name":"positive regulation of EGF receptor signalling pathway involved in cardiac process","type":"related"},{"name":"positive regulation of EGF receptor signalling pathway involved in heart process","type":"exact"},{"name":"positive regulation of EGFR signaling pathway involved in cardiac process","type":"related"},{"name":"positive regulation of EGFR signaling pathway involved in heart process","type":"exact"},{"name":"positive regulation of epidermal growth factor receptor signaling pathway involved in cardiac process","type":"related"},{"name":"stimulation of epidermal growth factor receptor signaling pathway involved in cardiac process","type":"related"},{"name":"stimulation of epidermal growth factor receptor signaling pathway involved in heart process","type":"narrow"},{"name":"up regulation of epidermal growth factor receptor signaling pathway involved in cardiac process","type":"related"},{"name":"up regulation of epidermal growth factor receptor signaling pathway involved in heart process","type":"exact"},{"name":"up-regulation of epidermal growth factor receptor signaling pathway involved in cardiac process","type":"related"},{"name":"up-regulation of epidermal growth factor receptor signaling pathway involved in heart process","type":"exact"},{"name":"upregulation of epidermal growth factor receptor signaling pathway involved in cardiac process","type":"related"},{"name":"upregulation of epidermal growth factor receptor signaling pathway involved in heart process","type":"exact"}],"termid":"GO:1905254"}


id: MOD:00447
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively results from forming an adduct with a glucuronic acid either through a carboxyl group amide or ester bond, or through C1-glycosylation.","definition_xrefs":["PubMed:7398618","DeltaMass:0","Unimod:54#N-term"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycoconjugated residue","termid":"MOD:00764"}],"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":"N-glucuronylated residue","synonyms":[{"name":"Glucuronyl","type":"related"},{"name":"N-Glucuronyl (N terminus)","type":"exact"},{"name":"N-glucuronylation","type":"related"}],"termid":"MOD:00447"}


id: GO:0160211
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Any of the lipid bilayers that surround an apicoplast and form the apicoplast envelope.","definition_xrefs":["PMID:20124342","PMID:38865262"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plastid membrane","termid":"GO:0042170"},{"relation_name":"part_of","term_name":"apicoplast","termid":"GO:0020011"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005737","GO:0005575"],"is_obsolete":false,"name":"apicoplast membrane","termid":"GO:0160211"}


id: GO:0009949
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process resulting in the establishment of polarity along the anterior/posterior axis.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"specification of axis polarity","termid":"GO:0065001"},{"relation_name":"part_of","term_name":"anterior/posterior axis specification","termid":"GO:0009948"}],"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":"polarity specification of anterior/posterior axis","termid":"GO:0009949"}


id: PR:O94390
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- atp7 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94390"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP synthase subunit d, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC29A10.13","synonyms":[{"name":"Spom972h-atp7","type":"exact"}],"termid":"PR:O94390"}


id: GO:0120203
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The volume enclosed by the membrane of a rod photoreceptor cell disc membrane.","definition_xrefs":["GOC:pde","PMID:19501669","PMID:26574505","GOC:krc","PMID:6771304"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organelle lumen","termid":"GO:0043233"},{"relation_name":"part_of","term_name":"rod photoreceptor outer segment","termid":"GO:0120200"}],"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":"rod photoreceptor disc lumen","termid":"GO:0120203"}


id: GO:0099147
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The component of the postsynaptic density membrane consisting of gene products and protein complexes that are loosely bound to one of its surfaces, but not integrated into the hydrophobic region.","definition_xrefs":["GOC:mf","GOC:autophagy"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extrinsic component of postsynaptic specialization membrane","termid":"GO:0098892"},{"relation_name":"part_of","term_name":"postsynaptic density membrane","termid":"GO:0098839"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005575","GO:0005886"],"is_obsolete":false,"name":"extrinsic component of postsynaptic density membrane","termid":"GO:0099147"}


id: PBO:0002049
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U5 snRNP-associated protein Aar2 (predicted)","termid":"PBO:0002049"}


id: PBO:0080202
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vascular endothelial zinc finger 1","termid":"PBO:0080202"}


id: PBO:0048590
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gamma-glutamyltransferase light chain 4 pseudogene","termid":"PBO:0048590"}


id: PR:O74832
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pet127 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74832"],"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":"mRNA degradation protein pet127, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1183.04c","synonyms":[{"name":"Spom972h-pet127","type":"exact"}],"termid":"PR:O74832"}


id: PBO:0050969
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interferon omega 1 pseudogene 4","termid":"PBO:0050969"}


id: GO:0007358
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Specification of the borders of central gap gene expression mediated largely by the effects of other gap genes; in insects this is exemplified by knirps repression of Kruppel.","definition_xrefs":["ISBN:0879694238"],"gene_count":0,"genotype_count":0,"name":"obsolete establishment of central gap gene boundaries (obsolete GO:0007358)","termid":"GO:0007358"}


id: PBO:0043658
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coenzyme Q3, methyltransferase","termid":"PBO:0043658"}


id: PBO:0057806
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3128","termid":"PBO:0057806"}


id: PR:P06652
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An M-phase inducer phosphatase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PomBase:MAH","PMID:9774107"],"direct_ancestors":[{"relation_name":"is_a","term_name":"M-phase inducer phosphatase","termid":"PR:000027506"},{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"M-phase inducer phosphatase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC24H6.05","secondary_identifiers":["PR:000027507","UniProtKB:P06652"],"synonyms":[{"name":"SPAC24H6.05","type":"related"},{"name":"Spom972h-cdc25","type":"exact"}],"termid":"PR:P06652"}


id: PR:Q9Y816
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC1105.13c gene.","definition_xrefs":["UniProtKB:Q9Y816","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 C1105.13c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1105.13c","synonyms":[{"name":"Spom972h-SPBC1105.13c","type":"exact"}],"termid":"PR:Q9Y816"}


id: PBO:0048465
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamate-cysteine ligase catalytic subunit","termid":"PBO:0048465"}


id: GO:0021950
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The creation and reception of signals that repel a precerebellar neuron as a component of the process of tangential migration.","definition_xrefs":["GOC:jid","PMID:15157725","GOC:dgh","GO_REF:0000021","GOC:cls","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative chemotaxis","termid":"GO:0050919"},{"relation_name":"part_of","term_name":"brainstem precerebellar neuron precursor migration","termid":"GO:0021949"}],"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":"chemorepulsion involved in precerebellar neuron migration","synonyms":[{"name":"negative chemotaxis involved in precerebellar neuron migration","type":"exact"}],"termid":"GO:0021950"}


id: MONDO:0010639
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Laryngeal abductor paralysis-intellectual disability syndrome is characterized by congenital and permanent laryngeal abductor paralysis, associated, in the majority of cases, with intellectual deficit. It has been described in several families. X-linked inheritance is likely.","definition_xrefs":["Orphanet:2375"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"respiratory system disorder","termid":"MONDO:0005087"},{"relation_name":"excluded_subClassOf","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"laryngeal abductor paralysis-intellectual disability syndrome","secondary_identifiers":["MEDGEN:1378465","OMIM:308850","SCTID:724178000","UMLS:C4319572","GARD:16597"],"synonyms":[{"name":"Plott syndrome","type":"exact"},{"name":"laryngeal abductor paralysis","type":"related"},{"name":"vocal cord dysfunction, familial","type":"related"}],"termid":"MONDO:0010639","xrefs":{"Monarch":{"xref_id":"0010639"}}}


id: MONDO:1011955
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"musculoskeletal system disorder, non-human animal","termid":"MONDO:1011335"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spondylosis deformans, non-human animal","secondary_identifiers":["OMIA:001132"],"termid":"MONDO:1011955","xrefs":{"Monarch":{"xref_id":"1011955"}}}


id: GO:0007576
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The cell aging process that results in the nucleolus breaking down into fragments.","definition_xrefs":["PMID:9271578","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete nucleolar fragmentation (obsolete GO:0007576)","synonyms":[{"name":"nucleolar size increase","type":"related"}],"termid":"GO:0007576"}


id: PBO:0030155
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_segregation","termid":"PBO:0030155"}


id: MONDO:0014883
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the FLNC gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial hypertrophic cardiomyopathy","termid":"MONDO:0024573"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"hypertrophic cardiomyopathy 26","secondary_identifiers":["DOID:0110327","OMIM:617047","MEDGEN:934716","UMLS:C4310749"],"synonyms":[{"name":"CMH26","type":"exact"},{"name":"FLNC hypertrophic cardiomyopathy","type":"exact"},{"name":"cardiomyopathy familial hypertrophic 26","type":"exact"},{"name":"cardiomyopathy, familial hypertrophic, 26","type":"exact"},{"name":"cardiomyopathy, familial hypertrophic, type 26","type":"exact"},{"name":"cardiomyopathy, familial restrictive 5","type":"exact"},{"name":"cardiomyopathy, familial restrictive, 5","type":"related"},{"name":"hypertrophic cardiomyopathy caused by mutation in FLNC","type":"exact"},{"name":"hypertrophic cardiomyopathy type 26","type":"exact"}],"termid":"MONDO:0014883","xrefs":{"Monarch":{"xref_id":"0014883"}}}


id: PBO:0086184
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein required for uridine thiolation of Lys(UUU) and Glu(UUC) tRNAs; required for the thiolation of uridine at the wobble position of Lys(UUU) and Glu(UUC) tRNAs; has a role in urmylation and in invasive and pseudohyphal growth; inhibits replication of Brome mosaic virus in S. cerevisiae","termid":"PBO:0086184"}


id: GO:0018590
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: methylsilanetriol + O2 + 2 H+ + 2 e- = H2O + hydroxymethylsilanetriol.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete methylsilanetriol hydroxylase activity (obsolete GO:0018590)","termid":"GO:0018590"}


id: MONDO:0002169
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An adenocarcinoma arising from the rectum. It is more frequently seen in populations with a Western type diet and in patients with a history of chronic inflammatory bowel disease. Signs and symptoms include intestinal bleeding, anemia, and change in bowel habits. According to the degree of cellular differentiation, rectal adenocarcinomas are divided into well, moderately, and poorly differentiated. Histologic variants include mucinous adenocarcinoma, signet ring cell carcinoma, medullary carcinoma, serrated adenocarcinoma, cribriform comedo-type adenocarcinoma, and micropapillary adenocarcinoma.","definition_xrefs":["NCIT:C9383"],"direct_ancestors":[{"relation_name":"is_a","term_name":"colorectal adenocarcinoma","termid":"MONDO:0005008"},{"relation_name":"is_a","term_name":"rectal carcinoma","termid":"MONDO:0044937"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"rectum adenocarcinoma","secondary_identifiers":["DOID:1996","ONCOTREE:READ","EFO:0005631","MEDGEN:56214","UMLS:C0149978","SCTID:254582000"],"synonyms":[{"name":"adenocarcinoma - rectum","type":"exact"},{"name":"adenocarcinoma of rectum","type":"exact"},{"name":"adenocarcinoma of the rectum","type":"exact"},{"name":"read","type":"related"},{"name":"rectal adenocarcinoma","type":"exact"},{"name":"rectum adenocarcinoma","type":"exact"}],"termid":"MONDO:0002169","xrefs":{"Monarch":{"xref_id":"0002169"}}}


id: MONDO:0044098
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An abnormal pregnancy in which the conception is implanted on the ovary.","definition_xrefs":["NCIT:C92945"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ectopic pregnancy","termid":"MONDO:0000755"},{"relation_name":"is_a","term_name":"ovarian disorder","termid":"MONDO:0005558"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ovarian ectopic pregnancy","secondary_identifiers":["MEDGEN:46073","SCTID:9899009","MESH:D065172","UMLS:C0032991"],"synonyms":[{"name":"Pregnancies, ovarian","type":"related"},{"name":"ectopic pregnancy of ovary","type":"exact"},{"name":"ovarian Pregnancies","type":"related"},{"name":"ovarian pregnancy","type":"exact"},{"name":"ovary ectopic pregnancy","type":"exact"}],"termid":"MONDO:0044098","xrefs":{"Monarch":{"xref_id":"0044098"}}}


id: GO:0018139
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of a peptidyl cysteine-peptidyl phenylalanine cross-link by the condensation of a cysteine thiol with the carbonyl of the preceding residue and alpha-beta dehydrogenation.","definition_xrefs":["RESID:AA0243"],"gene_count":0,"genotype_count":0,"name":"obsolete peptide cross-linking via L-phenylalanine thiazolecarboxylic acid (obsolete GO:0018139)","termid":"GO:0018139"}


id: PBO:0111926
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mating-type m-specific polypeptide matMc","termid":"PBO:0111926"}


id: MONDO:0001237
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A lymphoma arising from the appendix. The majority of lymphomas affecting the appendix represent disease extension from the intestinal wall; primary lymphomas of the appendix are rare.","definition_xrefs":["NCIT:C5513"],"direct_ancestors":[{"relation_name":"is_a","term_name":"appendix cancer","termid":"MONDO:0001235"},{"relation_name":"is_a","term_name":"cecum lymphoma","termid":"MONDO:0002034"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0004335","MONDO:0004992"],"is_obsolete":false,"name":"appendix lymphoma","secondary_identifiers":["MEDGEN:231078","UMLS:C1332328","DOID:11241"],"synonyms":[{"name":"appendiceal lymphoma","type":"exact"},{"name":"appendix lymphoma","type":"exact"},{"name":"lymphoma of appendix","type":"exact"},{"name":"lymphoma of the appendix","type":"exact"},{"name":"lymphoma of vermiform appendix","type":"exact"},{"name":"primary appendix lymphoma","type":"exact"},{"name":"vermiform appendix lymphoma","type":"exact"}],"termid":"MONDO:0001237","xrefs":{"Monarch":{"xref_id":"0001237"}}}


id: PBO:0053109
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine carboxyl methyltransferase 1","termid":"PBO:0053109"}


