# terms

id: PBO:0066073
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retinoic acid receptor responder 2 pseudogene 1","termid":"PBO:0066073"}


id: PBO:0054829
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 2242","termid":"PBO:0054829"}


id: GO:0004159
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a 5,6-dihydropyrimidine (5,6-dihydrouracil or 5,6-dihydrothymine) + NAD+ = a pyrimidine (uracil or thymine) + NADH + H+.","definition_xrefs":["PMID:23150645"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor","termid":"GO:0016628"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"dihydropyrimidine dehydrogenase (NAD+) activity","secondary_identifiers":["EC:1.3.1.1","MetaCyc:DIHYDROURACIL-DEHYDROGENASE-NAD+-RXN"],"synonyms":[{"name":"5,6-dihydrouracil:NAD+ oxidoreductase activity","type":"related"},{"name":"dihydrothymine dehydrogenase (NAD+) activity","type":"narrow"},{"name":"dihydrouracil dehydrogenase (NAD+) activity","type":"narrow"},{"name":"pyrimidine reductase activity","type":"related"},{"name":"thymine reductase activity","type":"narrow"},{"name":"uracil reductase activity","type":"narrow"}],"termid":"GO:0004159"}


id: PBO:0045065
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"discs large MAGUK scaffold protein 4","termid":"PBO:0045065"}


id: MONDO:0004121
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete prostate small cell carcinoma (obsolete MONDO:0004121)","termid":"MONDO:0004121","xrefs":{"Monarch":{"xref_id":"0004121"}}}


id: GO:0030004
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process involved in the maintenance of an internal steady state of monovalent inorganic cations at the level of a cell.","definition_xrefs":["GOC:ai","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete cellular monovalent inorganic cation homeostasis (obsolete GO:0030004)","termid":"GO:0030004"}


id: GO:0036133
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: thromboxane B2 + NAD+ = 11-dehydro-thromboxane B2 + NADH + H+.","definition_xrefs":["PMID:3823488","PMID:3461463","KEGG_REACTION:R05060","GOC:mw","PMID:8200461"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor","termid":"GO:0016628"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"11-hydroxythromboxane B2 dehydrogenase activity","secondary_identifiers":["RHEA:52312","Reactome:R-HSA-2161732"],"synonyms":[{"name":"NAD dependent 11-hydroxythromboxane B2 dehydrogenase activity","type":"exact"}],"termid":"GO:0036133"}


id: PBO:0108984
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sperm microtubule inner protein 8","termid":"PBO:0108984"}


id: MONDO:0002780
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete MONDO:0002780 (obsolete MONDO:0002780)","termid":"MONDO:0002780","xrefs":{"Monarch":{"xref_id":"0002780"}}}


id: _global:results_in_disappearance_of
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","direct_ancestors":[{"relation_name":"is_a","term_name":"results_in_ending_of","termid":"RO:0002552"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"results_in_disappearance_of","termid":"_global:results_in_disappearance_of"}


id: PBO:0056279
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mannosidase alpha class 2B member 1","termid":"PBO:0056279"}


id: MONDO:0008579
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":"toes, relative length of first and second","secondary_identifiers":["UMLS:C1861059","OMIM:189200","MEDGEN:396051"],"synonyms":[{"name":"toes, relative length of first and second","type":"exact"}],"termid":"MONDO:0008579","xrefs":{"Monarch":{"xref_id":"0008579"}}}


id: GO:0030266
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (-)-quinate + NAD+ = (-)-3-dehydroquinate + NADH + H+.","definition_xrefs":["EC:1.1.1.24"],"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:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"quinate 3-dehydrogenase (NAD+) activity","secondary_identifiers":["MetaCyc:QUINATE-5-DEHYDROGENASE-RXN","RHEA:22364","KEGG_REACTION:R01872"],"synonyms":[{"name":"quinate:NAD 3-oxidoreductase activity","type":"exact"},{"name":"quinate:NAD 5-oxidoreductase activity","type":"related"},{"name":"quinate:NAD(+) 3-oxidoreductase activity","type":"exact"},{"name":"quinate:NAD(+) 5-oxidoreductase activity","type":"related"},{"name":"quinic dehydrogenase activity","type":"broad"}],"termid":"GO:0030266"}


id: GO:0045890
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of transcription of homeotic genes of the trithorax group.","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of transcription of homeotic gene (trithorax group) (obsolete GO:0045890)","synonyms":[{"name":"regulation of transcription of homeotic gene (trithorax group)","type":"exact"}],"termid":"GO:0045890"}


id: MONDO:0012612
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive non-syndromic intellectual disability","termid":"MONDO:0019502"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0006025","MONDO:0037792"],"is_obsolete":false,"name":"intellectual disability, autosomal recessive 12","secondary_identifiers":["UMLS:C1970200","GARD:22540","MESH:C567019","OMIM:611090","MEDGEN:370850","DOID:0081180"],"synonyms":[{"name":"MRT12","type":"related"},{"name":"intellectual developmental disorder, autosomal recessive 12","type":"exact"},{"name":"intellectual disability, autosomal recessive 12","type":"exact"},{"name":"intellectual disability, autosomal recessive type 12","type":"exact"},{"name":"mental retardation, autosomal recessive 12","type":"related"},{"name":"mental retardation, autosomal recessive type 12","type":"exact"}],"termid":"MONDO:0012612","xrefs":{"Monarch":{"xref_id":"0012612"}}}


id: PBO:0052648
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 8 pseudogene 16","termid":"PBO:0052648"}


id: PBO:0036466
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Hrd1 complex ubiquitin-protein ligase E3 subunit, Hrd1","termid":"PBO:0036466"}


id: GO:0090291
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate, frequency, or extent of the multiplication or reproduction of osteoclasts, resulting in the expansion of an osteoclast cell population.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of leukocyte proliferation","termid":"GO:0070664"},{"relation_name":"is_a","term_name":"regulation of osteoclast proliferation","termid":"GO:0090289"},{"relation_name":"negatively_regulates","term_name":"osteoclast proliferation","termid":"GO:0002158"}],"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 osteoclast proliferation","termid":"GO:0090291"}


id: PBO:0052917
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin associated protein 17-1","termid":"PBO:0052917"}


id: PR:Q9UTC4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- reg1 gene.","definition_xrefs":["UniProtKB:Q9UTC4","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 C227.15 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC227.15","synonyms":[{"name":"Spom972h-reg1","type":"exact"}],"termid":"PR:Q9UTC4"}


id: PBO:0070491
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L5 pseudogene 26","termid":"PBO:0070491"}


id: PR:Q10212
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein MEMO1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR11060:SF0","OMA:SCHPO01586","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":"MEMO1 family protein C4H3.04c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4H3.04c","secondary_identifiers":["UniProtKB:Q10212"],"synonyms":[{"name":"Spom972h-MEMO1","type":"exact"}],"termid":"PR:Q10212"}


id: GO:0038078
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: a phosphorylated MAP kinase + H2O = a MAP kinase + phosphate, where the MAP kinase (MAPK) is part of a MAPK signaling cascade that contributes to an innate immune response.","definition_xrefs":["GOC:signaling"],"gene_count":0,"genotype_count":0,"name":"obsolete MAP kinase phosphatase activity involved in regulation of innate immune response (obsolete GO:0038078)","synonyms":[{"name":"MAPK phosphatase activity involved in regulation of innate immune response","type":"exact"}],"termid":"GO:0038078"}


id: PBO:0043294
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CLEC12A antisense RNA 1","termid":"PBO:0043294"}


id: PBO:0069575
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 848, pseudogene","termid":"PBO:0069575"}


id: PBO:0045590
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"double homeobox 4 like 1 (pseudogene)","termid":"PBO:0045590"}


id: _global:biotically_interacts_with
data:
  {"annotation_feature_type":"gene","cv_name":"external","definition":"An interaction relationship in which at least one of the partners is an organism and the other is either an organism or an abiotic entity with which the organism interacts.","direct_ancestors":[{"relation_name":"is_a","term_name":"ecologically_related_to","termid":"_global:ecologically_related_to"},{"relation_name":"is_a","term_name":"interacts_with","termid":"_global:interacts_with"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"biotically_interacts_with","secondary_identifiers":["RO:0002437"],"termid":"_global:biotically_interacts_with"}


id: PBO:0072328
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S26 pseudogene 14","termid":"PBO:0072328"}


id: MOD:01585
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively crosslinks an L-serine residue and a glycine residue by an ester bond to form O-glycyl-L-serine.","definition_xrefs":["RESID:AA0495","PubMed:17502423"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ester crosslinked residues","termid":"MOD:00885"},{"relation_name":"is_a","term_name":"crosslinked residues with loss of water","termid":"MOD:00954"},{"relation_name":"is_a","term_name":"crosslinked glycine residue","termid":"MOD:02047"},{"relation_name":"is_a","term_name":"crosslinked L-serine residue","termid":"MOD:02055"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"O-glycyl-L-serine","synonyms":[{"name":"(2S)-2-amino-3-[(aminoacetyl)oxy]propanoic acid","type":"exact"},{"name":"CROSSLNK Glycyl serine ester (Gly-Ser) (interchain with S-...)","type":"exact"},{"name":"CROSSLNK Glycyl serine ester (Ser-Gly) (interchain with G-...)","type":"exact"},{"name":"O-(glycyl)-L-serine","type":"exact"},{"name":"O3-(aminoacetyl)serine","type":"exact"},{"name":"serine glycinate ester","type":"exact"}],"termid":"MOD:01585"}


id: FYPO:0000931
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 microtubule cytoskeleton is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization during vegetative growth","termid":"FYPO:0000443"},{"relation_name":"is_a","term_name":"abnormal cellular process during vegetative growth","termid":"FYPO:0001362"},{"relation_name":"is_a","term_name":"abnormal protein localization to microtubule cytoskeleton","termid":"FYPO:0004090"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985","FYPO:0005447","FYPO:0000138"],"is_obsolete":false,"name":"abnormal protein localization to microtubule cytoskeleton during vegetative growth","synonyms":[{"name":"abnormal protein localisation to microtubule cytoskeleton during vegetative growth","type":"exact"},{"name":"abnormal protein localization to microtubule cytoskeleton during mitotic cell cycle","type":"related"}],"termid":"FYPO:0000931"}


id: MONDO:0013003
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Isolated aglossia and hypoglossia are terms covering the spectrum from partial to total absence of the tongue. These congenital malformations have been classified as part of the group of oromandibular-limb hypogenesis syndromes (OLHS).","definition_xrefs":["Orphanet:141152"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tongue disorder","termid":"MONDO:0001165"},{"relation_name":"is_a","term_name":"oromandibular-limb hypogenesis syndrome","termid":"MONDO:0017139"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"isolated congenital hypoglossia/aglossia","secondary_identifiers":["OMIM:612776","UMLS:C2748587","GARD:16972","MEDGEN:411249"],"synonyms":[{"name":"hypoglossia with situs inversus","type":"related"},{"name":"hypoglossia, isolated","type":"related"}],"termid":"MONDO:0013003","xrefs":{"Monarch":{"xref_id":"0013003"}}}


id: PBO:0044126
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CTAGE family member 12, pseudogene","termid":"PBO:0044126"}


id: GO:0040019
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of embryonic development.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of embryonic development","termid":"GO:0045995"},{"relation_name":"is_a","term_name":"positive regulation of developmental process","termid":"GO:0051094"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"positively_regulates","term_name":"embryo development","termid":"GO:0009790"}],"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 embryonic development","synonyms":[{"name":"activation of embryonic development","type":"narrow"},{"name":"stimulation of embryonic development","type":"narrow"},{"name":"up regulation of embryonic development","type":"exact"},{"name":"up-regulation of embryonic development","type":"exact"},{"name":"upregulation of embryonic development","type":"exact"}],"termid":"GO:0040019"}


id: GO:1905746
data:
  {"annotated_genes":["SJAG_01040"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[117910],"is_not":false,"summary":null,"term":"GO:1905746"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of mRNA cis splicing, via spliceosome.","definition_xrefs":["GOC:TermGenie","PMID:2880558","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of mRNA splicing, via spliceosome","termid":"GO:0048026"},{"relation_name":"is_a","term_name":"regulation of mRNA cis splicing, via spliceosome","termid":"GO:1905744"},{"relation_name":"positively_regulates","term_name":"mRNA cis splicing, via spliceosome","termid":"GO:0045292"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01040":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0016071"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0016071"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"positively_regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150","GO:0016071"],"is_obsolete":false,"name":"positive regulation of mRNA cis splicing, via spliceosome","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1905746","terms_by_termid":{"GO:1905746":null}}


id: PBO:0045344
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"docking protein 4","termid":"PBO:0045344"}


id: MONDO:0014292
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"leukodystrophy","termid":"MONDO:0019046"}],"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":"leukoencephalopathy with mild cerebellar ataxia and white matter edema","secondary_identifiers":["Orphanet:363540","SCTID:768663003","OMIM:615651","UMLS:C4554120","GARD:17565","NCIT:C171603","MEDGEN:1638681"],"synonyms":[{"name":"LKPAT","type":"related"},{"name":"leukoencephalopathy with ataxia","type":"related"}],"termid":"MONDO:0014292","xrefs":{"Monarch":{"xref_id":"0014292"}}}


id: GO:0033089
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of T cell differentiation in the thymus.","definition_xrefs":["GOC:mah","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of T cell differentiation in thymus","termid":"GO:0033081"},{"relation_name":"is_a","term_name":"positive regulation of T cell differentiation","termid":"GO:0045582"},{"relation_name":"positively_regulates","term_name":"T cell differentiation in thymus","termid":"GO:0033077"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"positive regulation of T cell differentiation in thymus","synonyms":[{"name":"positive regulation of T cell development in thymus","type":"related"},{"name":"positive regulation of thymic T cell differentiation","type":"exact"},{"name":"positive regulation of thymocyte cell differentiation","type":"exact"},{"name":"positive regulation of thymocyte differentiation","type":"exact"}],"termid":"GO:0033089"}


id: SO:0000135
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The maternal copy of the gene is modified, rendering it transcriptionally silent.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"genomically_imprinted","termid":"SO:0000134"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"maternally_imprinted","synonyms":[{"name":"maternally imprinted","type":"exact"}],"termid":"SO:0000135"}


id: GO:0044382
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process by which a CLRC complex is transported to, or maintained in, heterochromatin. CLRC complex is an active cullin-dependent E3 ubiquitin ligase complex essential for heterochromatin assembly by RNAi and histone H3K9 methylation.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex localization","termid":"GO:0031503"},{"relation_name":"is_a","term_name":"protein localization to heterochromatin","termid":"GO:0097355"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"CLRC complex localization to heterochromatin","synonyms":[{"name":"CLRC ubiquitin ligase complex localisation to heterochromatin","type":"exact"},{"name":"CLRC ubiquitin ligase complex localization to heterochromatin","type":"exact"}],"termid":"GO:0044382"}


id: GO:0000459
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Exonucleolytic digestion of a pre-rRNA molecule in the process to generate a mature rRNA molecule.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete exonucleolytic trimming involved in rRNA processing (obsolete GO:0000459)","synonyms":[{"name":"exonucleolytic trimming during rRNA processing","type":"related"}],"termid":"GO:0000459"}


id: GO:0075109
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process by which a symbiont alters or subverts a receptor-mediated signal transduction pathway in its host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host signal transduction pathway","termid":"GO:0052027"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated perturbation of host receptor-mediated signal transduction","synonyms":[{"name":"perturbation of host receptor-mediated signal transduction","type":"exact"}],"termid":"GO:0075109"}


id: PBO:0074975
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 114-17","termid":"PBO:0074975"}


id: PBO:0005329
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"xrcc4 like factor, cernunnon","termid":"PBO:0005329"}


id: PBO:0080571
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WDFY family member 4","termid":"PBO:0080571"}


id: GO:0010999
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency, or extent of eIF2 alpha phosphorylation as a result of heme levels.","definition_xrefs":["GOC:dph","GOC:BHF","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein phosphorylation","termid":"GO:0001932"},{"relation_name":"is_a","term_name":"regulation of translational initiation","termid":"GO:0006446"},{"relation_name":"is_a","term_name":"regulation of cellular response to stress","termid":"GO:0080135"},{"relation_name":"regulates","term_name":"regulation of translational initiation by eIF2 alpha phosphorylation","termid":"GO:0010998"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"regulation of eIF2 alpha phosphorylation by heme","secondary_identifiers":["Reactome:R-HSA-9648895"],"termid":"GO:0010999"}


id: PBO:0071846
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S2 pseudogene 41","termid":"PBO:0071846"}


id: PBO:0073763
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 3 member 1","termid":"PBO:0073763"}


id: MONDO:1012037
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cerebellar Purkinje cell degeneration, non-human animal","termid":"MONDO:1011833"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cerebellar Purkinje cell degeneration, dog","secondary_identifiers":["OMIA:000174-9615"],"termid":"MONDO:1012037","xrefs":{"Monarch":{"xref_id":"1012037"}}}


id: PBO:0005500
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Jmj4 protein (predicted)","termid":"PBO:0005500"}


id: MONDO:0004914
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A vascular compression syndrome attributed to celiac trunk compression by the median arcuate ligament of the diaphragm, with presentations ranging from completely asymptomatic to myriad gastrointestinal symptoms, including chronic abdominal pain (CAP), post-prandial pain, nausea and vomiting, anorexia, early satiety, and subsequently weight loss.","definition_xrefs":["PMID:34729265"],"direct_ancestors":[{"relation_name":"is_a","term_name":"arterial disorder","termid":"MONDO:0000473"},{"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":"celiac artery stenosis from compression by median arcuate ligament of diaphragm","secondary_identifiers":["ICD9:447.4","MESH:C566151","UMLS:C1861783","MEDGEN:349361","SCTID:9250002","DOID:9892","OMIM:116870"],"synonyms":[{"name":"Harjola-Marable syndrome","type":"exact"},{"name":"Marable's syndrome","type":"exact"},{"name":"celiac access syndrome","type":"related"},{"name":"celiac artery compression syndrome","type":"exact"},{"name":"celiac artery stenosis from compression by median arcuate ligament of diaphragm","type":"exact"},{"name":"coeliac access syndrome","type":"related"},{"name":"coeliac artery compression syndrome","type":"exact"},{"name":"median arcuate ligament syndrome","type":"exact"},{"name":"median arcuate ligament syndromic disease","type":"exact"},{"name":"syndromic disease of median arcuate ligament","type":"exact"}],"termid":"MONDO:0004914","xrefs":{"Monarch":{"xref_id":"0004914"}}}


id: MONDO:0014199
data:
  {"annotated_genes":["SJAG_02233"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85325],"is_not":false,"summary":null,"term":"MONDO:0014199"}]},"cv_name":"mondo","definition":"Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the GNAO1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental and epileptic encephalopathy","termid":"MONDO:0100062"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02233":null},"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, 17","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C3809606","GARD:13378","DOID:0080450","OMIM:615473","MEDGEN:815936"],"synonyms":[{"name":"DEE17","type":"exact"},{"name":"EIEE17","type":"exact"},{"name":"GNAO1 early infantile epileptic encephalopathy","type":"exact"},{"name":"GNAO1 encephalopathy","type":"related"},{"name":"developmental and epileptic encephalopathy 17","type":"exact"},{"name":"early infantile epileptic encephalopathy caused by mutation in GNAO1","type":"exact"},{"name":"early infantile epileptic encephalopathy-17","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 17","type":"exact"},{"name":"epileptic encephalopathy, early infantile, type 17","type":"exact"}],"termid":"MONDO:0014199","terms_by_termid":{"MONDO:0014199":null},"xrefs":{"Monarch":{"xref_id":"0014199"}}}


id: PBO:0080053
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin specific peptidase 24 pseudogene 1","termid":"PBO:0080053"}


id: PBO:0069883
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1171, pseudogene","termid":"PBO:0069883"}


id: PBO:0075810
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"single stranded DNA binding protein 3","termid":"PBO:0075810"}


id: PBO:0055915
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat containing 37 member A3","termid":"PBO:0055915"}


id: GO:0036222
data:
  {"annotated_genes":["SJAG_03797"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[118103],"is_not":false,"summary":null,"term":"GO:0036222"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: XTP + H2O = XMP + H+ + diphosphate.","definition_xrefs":["PMID:16216582","PMID:22531138","GOC:pz","RHEA:28610"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside triphosphate diphosphatase activity","termid":"GO:0047429"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03797":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0047429"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016787","GO:0047429","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"XTP diphosphatase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["KEGG_REACTION:R02720","MetaCyc:RXN0-1603","GO:0103024","Reactome:R-HSA-2509831"],"synonyms":[{"name":"XTP pyrophosphohydrolase activity","type":"exact"},{"name":"XTP/dITP diphosphatase","type":"related"},{"name":"XTPase activity","type":"exact"},{"name":"hypoxanthine/xanthine dNTP pyrophosphatase","type":"related"}],"termid":"GO:0036222","terms_by_termid":{"GO:0036222":null}}


id: GO:0008960
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: phosphatidylglycerol + membrane-derived-oligosaccharide D-glucose = 1,2-diacyl-sn-glycerol + membrane-derived-oligosaccharide 6-(glycerophospho)-D-glucose.","definition_xrefs":["EC:2.7.8.20"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphotransferase activity, for other substituted phosphate groups","termid":"GO:0016780"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016780"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016780","GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"phosphatidylglycerol-membrane-oligosaccharide glycerophosphotransferase activity","secondary_identifiers":["MetaCyc:PGLYCEROLTRANSI-RXN"],"synonyms":[{"name":"oligosaccharide glycerophosphotransferase activity","type":"related"},{"name":"phosphatidylglycerol:membrane-derived-oligosaccharide-D-glucose glycerophosphotransferase activity","type":"related"},{"name":"phosphoglycerol transferase I","type":"related"},{"name":"phosphoglycerol transferase activity","type":"related"}],"termid":"GO:0008960"}


id: GO:0005586
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A collagen homotrimer of alpha1(III) chains; type III collagen triple helices associate to form fibrils.","definition_xrefs":["ISBN:0721639976"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fibrillar collagen trimer","termid":"GO:0005583"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"collagen type III trimer","termid":"GO:0005586"}


id: GO:0071622
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency or extent of granulocyte chemotaxis. Granulocyte chemotaxis is the movement of a granulocyte in response to an external stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of leukocyte chemotaxis","termid":"GO:0002688"},{"relation_name":"regulates","term_name":"granulocyte chemotaxis","termid":"GO:0071621"}],"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 granulocyte chemotaxis","termid":"GO:0071622"}


id: PBO:0071469
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L32 pseudogene 10","termid":"PBO:0071469"}


id: PBO:0041410
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 6 open reading frame 226","termid":"PBO:0041410"}


id: MONDO:0006684
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Increased intracellular or extracellular fluid in brain tissue. Cytotoxic brain edema (swelling due to increased intracellular fluid) is indicative of a disturbance in cell metabolism, and is commonly associated with hypoxic or ischemic injuries (see hypoxia, brain). An increase in extracellular fluid may be caused by increased brain capillary permeability (vasogenic edema), an osmotic gradient, local blockages in interstitial fluid pathways, or by obstruction of csf flow (e.g., obstructive hydrocephalus). (From Childs Nerv Syst 1992 Sep; 8(6):301-6)","definition_xrefs":["MESH:D001929"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brain disorder","termid":"MONDO:0005560"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"brain edema","secondary_identifiers":["ICD9:348.5","MEDGEN:2337","MedDRA:10006121","SCTID:2032001","UMLS:C0006114","DOID:4724","EFO:1000845"],"synonyms":[{"name":"intracranial swelling","type":"exact"},{"name":"wet brain","type":"exact"}],"termid":"MONDO:0006684","xrefs":{"Monarch":{"xref_id":"0006684"}}}


id: FYECO:0000387
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which tebuconazole was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ tebuconazole","termid":"FYECO:0000387"}


id: GO:0072375
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The memory process that deals with the storage, retrieval and modification of information received at a time ago that is intermediate between that of short and long term memory (30min - 7hrs in Drosophila melanogaster).","definition_xrefs":["GOC:sart","PMID:14659098","PMID:7923375"],"direct_ancestors":[{"relation_name":"is_a","term_name":"memory","termid":"GO:0007613"}],"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":"medium-term memory","synonyms":[{"name":"MTM","type":"narrow"},{"name":"middle-term memory","type":"exact"}],"termid":"GO:0072375"}


id: PBO:0052661
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 8 pseudogene 29","termid":"PBO:0052661"}


id: GO:1904765
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that increases the frequency, rate or extent of transcription from an RNA polymerase II promoter as a result of a maltose stimulus.","definition_xrefs":["PMID:24224056","GO_REF:0000060","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of transcription from RNA polymerase II promoter in response to maltose (obsolete GO:1904765)","synonyms":[{"name":"activation of global transcription from RNA polymerase II promoter involved in cellular response to maltose stimulus","type":"related"},{"name":"activation of transcription from RNA polymerase II promoter involved in cellular response to maltose stimulus","type":"exact"},{"name":"positive regulation of gene-specific transcription from RNA polymerase II promoter involved in cellular response to maltose stimulus","type":"related"},{"name":"positive regulation of global transcription from Pol II promoter involved in cellular response to maltose stimulus","type":"related"},{"name":"positive regulation of transcription from Pol II promoter involved in cellular response to maltose stimulus","type":"exact"},{"name":"positive regulation of transcription from RNA polymerase II promoter involved in cellular response to maltose stimulus","type":"exact"},{"name":"positive regulation of transcription from RNA polymerase II promoter, global involved in cellular response to maltose stimulus","type":"related"},{"name":"stimulation of global transcription from RNA polymerase II promoter involved in cellular response to maltose stimulus","type":"narrow"},{"name":"stimulation of transcription from RNA polymerase II promoter involved in cellular response to maltose stimulus","type":"exact"},{"name":"up regulation of global transcription from RNA polymerase II promoter involved in cellular response to maltose stimulus","type":"related"},{"name":"up regulation of transcription from RNA polymerase II promoter involved in cellular response to maltose stimulus","type":"exact"},{"name":"up-regulation of global transcription from RNA polymerase II promoter involved in cellular response to maltose stimulus","type":"related"},{"name":"up-regulation of transcription from RNA polymerase II promoter involved in cellular response to maltose stimulus","type":"exact"},{"name":"upregulation of global transcription from RNA polymerase II promoter involved in cellular response to maltose stimulus","type":"related"},{"name":"upregulation of transcription from RNA polymerase II promoter involved in cellular response to maltose stimulus","type":"exact"}],"termid":"GO:1904765"}


id: SO:0000819
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A chromosome originating in a mitochondria.","definition_xrefs":["SO:xp"],"direct_ancestors":[{"relation_name":"has_origin","term_name":"mitochondrial_sequence","termid":"SO:0000737"},{"relation_name":"is_a","term_name":"chromosome","termid":"SO:0000340"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial_chromosome","synonyms":[{"name":"mitochondrial chromosome","type":"exact"}],"termid":"SO:0000819"}


id: GO:0102747
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: H+ + chlorophyllide a(1-) + 2-trans,6-trans,10-trans-geranylgeranyl diphosphate(3-) = geranylgeranyl-chlorophyll a + diphosphoric acid.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete chlorophyllide-a:geranyl-geranyl diphosphate geranyl-geranyl transferase activity (obsolete GO:0102747)","termid":"GO:0102747"}


id: GO:0034948
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2,6-dihydroxypseudooxynicotine + H2O = 2,6-dihydroxypyridine + 4-methylaminobutyrate.","definition_xrefs":["UM-BBD_reactionID:r0482"],"gene_count":0,"genotype_count":0,"name":"obsolete 2,6-dihydroxypseudooxynicotine hydrolase activity (obsolete GO:0034948)","termid":"GO:0034948"}


id: PBO:0075343
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SORL1 antisense RNA 1","termid":"PBO:0075343"}


id: PR:Q8J1M8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC1952.04c gene.","definition_xrefs":["UniProtKB:Q8J1M8","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":"UPF0768 protein C1952.04c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1952.04c","synonyms":[{"name":"Spom972h-SPAC1952.04c","type":"exact"}],"termid":"PR:Q8J1M8"}


id: PBO:0067058
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 79, pseudogene","termid":"PBO:0067058"}


id: PBO:0041232
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 1 open reading frame 54","termid":"PBO:0041232"}


id: GO:1904456
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of neuronal action potential.","definition_xrefs":["PMID:25126967","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of action potential","termid":"GO:0045759"},{"relation_name":"is_a","term_name":"negative regulation of transmission of nerve impulse","termid":"GO:0051970"},{"relation_name":"is_a","term_name":"regulation of neuronal action potential","termid":"GO:0098908"},{"relation_name":"negatively_regulates","term_name":"neuronal action potential","termid":"GO:0019228"}],"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 neuronal action potential","synonyms":[{"name":"down regulation of generation of action potential","type":"related"},{"name":"down regulation of neuronal action potential","type":"exact"},{"name":"down-regulation of generation of action potential","type":"related"},{"name":"down-regulation of neuronal action potential","type":"exact"},{"name":"downregulation of generation of action potential","type":"related"},{"name":"downregulation of neuronal action potential","type":"exact"},{"name":"inhibition of generation of action potential","type":"related"},{"name":"inhibition of neuronal action potential","type":"narrow"},{"name":"negative regulation of generation of action potential","type":"related"}],"termid":"GO:1904456"}


id: PATO:0000511
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000511 absolute disease sensitivity value (obsolete PATO:0000511)","termid":"PATO:0000511"}


id: PBO:0029120
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-mononucleate","termid":"PBO:0029120"}


id: PBO:0069305
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 561, pseudogene","termid":"PBO:0069305"}


id: MONDO:0005768
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Tuberculosis that involves any region of the gastrointestinal tract, mostly in the distal ileum and the cecum. In most cases, mycobacterium tuberculosis is the pathogen. Clinical features include abdominal pain; fever; and palpable mass in the ileocecal area.","definition_xrefs":["MESH:D014385"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"abdominal tuberculosis","termid":"MONDO:0000369"},{"relation_name":"is_a","term_name":"extrapulmonary tuberculosis","termid":"MONDO:0000368"},{"relation_name":"is_a","term_name":"digestive system infectious disorder","termid":"MONDO:0043424"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"gastrointestinal tuberculosis","secondary_identifiers":["UMLS:C0041312","SCTID:186225008","EFO:0007280","ICD9:014.86","DOID:404","ICD9:014.81","MEDGEN:52885","ICD9:014.80"],"synonyms":[{"name":"tuberculosis of gastrointestinal tract","type":"exact"},{"name":"tuberculosis of intestines, peritoneum and mesenteric glands","type":"exact"},{"name":"tuberculosis of intestines, peritoneum, and mesenteric glands","type":"exact"}],"termid":"MONDO:0005768","xrefs":{"Monarch":{"xref_id":"0005768"}}}


id: PR:O13696
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An isocitrate dehydrogenase [NAD] subunit gamma, mitochondrial that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:CNA"],"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":"isocitrate dehydrogenase [NAD] subunit 1, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC11G7.03","secondary_identifiers":["UniProtKB:O13696"],"synonyms":[{"name":"NAD(+)-specific ICDH (Schizosaccharomyces pombe 972h-)","type":"broad"},{"name":"SPAC11G7.03","type":"related"},{"name":"Spom972h-IDH3G","type":"exact"},{"name":"isocitric dehydrogenase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O13696"}


id: PBO:0048719
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutaredoxin pseudogene 2","termid":"PBO:0048719"}


id: PBO:0052976
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"laccase domain containing 1","termid":"PBO:0052976"}


id: PBO:0075696
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sterol regulatory element binding transcription factor 1","termid":"PBO:0075696"}


id: MONDO:0006695
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete cervical rib syndrome (obsolete MONDO:0006695)","termid":"MONDO:0006695","xrefs":{"Monarch":{"xref_id":"0006695"}}}


id: PBO:0079818
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin interaction motif containing 1","termid":"PBO:0079818"}


id: GO:0070775
data:
  {"annotated_genes":["SJAG_04815","SJAG_00411","SJAG_01385","SJAG_02165","SJAG_02629","SJAG_01009","SJAG_00545"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[99172,90232,103933,104801],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036410"},{"annotations":[104802,93434,107410,106002],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033100"},{"annotations":[90233],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990467"}]},"cv_name":"cellular_component","definition":"A multisubunit complex that catalyzes the acetylation of histone H3.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone acetyltransferase complex","termid":"GO:0000123"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00411":null,"SJAG_00545":null,"SJAG_01009":null,"SJAG_01385":null,"SJAG_02165":null,"SJAG_02629":null,"SJAG_04815":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005694","GO:0032991"],"is_obsolete":false,"name":"H3 histone acetyltransferase complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"H3 HAT complex","type":"exact"}],"termid":"GO:0070775","terms_by_termid":{"GO:0033100":null,"GO:0036410":null,"GO:1990467":null}}


id: GO:0002513
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Tolerance induction directed at self antigens.","definition_xrefs":["GO_REF:0000022","GOC:jal","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tolerance induction","termid":"GO:0002507"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"tolerance induction to self antigen","termid":"GO:0002513"}


id: GO:2000059
data:
  {"annotated_genes":["SJAG_00475","SJAG_00052","SJAG_03048"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[101863],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905785"},{"annotations":[106438,89880],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032435"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of ubiquitin-dependent protein catabolic process.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of catabolic process","termid":"GO:0009895"},{"relation_name":"is_a","term_name":"negative regulation of proteolysis involved in protein catabolic process","termid":"GO:1903051"},{"relation_name":"is_a","term_name":"regulation of ubiquitin-dependent protein catabolic process","termid":"GO:2000058"},{"relation_name":"negatively_regulates","term_name":"ubiquitin-dependent protein catabolic process","termid":"GO:0006511"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00052":null,"SJAG_00475":null,"SJAG_03048":null},"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 ubiquitin-dependent protein catabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"negative regulation of protein degradation tagging activity","type":"broad"},{"name":"negative regulation of protein ubiquitination during ubiquitin-dependent protein breakdown","type":"narrow"},{"name":"negative regulation of protein ubiquitination during ubiquitin-dependent protein catabolic process","type":"narrow"},{"name":"negative regulation of protein ubiquitination during ubiquitin-dependent protein catabolism","type":"narrow"},{"name":"negative regulation of protein ubiquitination during ubiquitin-dependent protein degradation","type":"narrow"},{"name":"negative regulation of protein ubiquitination involved in ubiquitin-dependent protein catabolic process","type":"narrow"},{"name":"negative regulation of protein ubiquitinylation during ubiquitin-dependent protein catabolic process","type":"narrow"},{"name":"negative regulation of protein ubiquitinylation during ubiquitin-dependent protein catabolism","type":"narrow"},{"name":"negative regulation of protein ubiquitylation during ubiquitin-dependent protein catabolic process","type":"narrow"},{"name":"negative regulation of protein ubiquitylation during ubiquitin-dependent protein catabolism","type":"narrow"}],"termid":"GO:2000059","terms_by_termid":{"GO:0032435":null,"GO:1905785":null}}


id: PATO:0002282
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A mobility which is relative high.","definition_xrefs":["PATO:GVG"],"direct_ancestors":[{"relation_name":"increased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"mobile","termid":"PATO:0000299"},{"relation_name":"is_a","term_name":"increased object quality","termid":"PATO:0002305"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased mobility","termid":"PATO:0002282"}


id: PBO:0051146
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable 3-25 (pseudogene)","termid":"PBO:0051146"}


id: PATO:0002157
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A positional quality inhering in a bearer by virtue of the bearer's being slightly out of its usual or proper place, or position.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dislocated","termid":"PATO:0001852"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partially dislocated","secondary_identifiers":["PATO:0002160"],"synonyms":[{"name":"partial dislocated towards","type":"exact"},{"name":"subluxation","type":"exact"},{"name":"suluxated towards","type":"exact"}],"termid":"PATO:0002157"}


id: PBO:0057418
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 548t","termid":"PBO:0057418"}


id: GO:0043756
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: adenosylcobinamide + H2O = (R)-1-aminopropan-2-ol + adenosylcobyrate.","definition_xrefs":["RHEA:23504","EC:3.5.1.90"],"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:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016810","GO:0003674","GO:0016787","GO:0003824"],"is_obsolete":false,"name":"adenosylcobinamide hydrolase activity","secondary_identifiers":["KEGG_REACTION:R05226","MetaCyc:R346-RXN"],"synonyms":[{"name":"AdoCbi amidohydrolase activity","type":"related"},{"name":"AdoCbi hydrolase activity","type":"related"},{"name":"CbiZ","type":"related"},{"name":"adenosylcobinamide amidohydrolase activity","type":"related"}],"termid":"GO:0043756"}


id: PBO:0084527
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Member of the FLO family of cell wall flocculation proteins; not expressed in most lab strains; overproduction induces flocculation that can be inhibited by mannose, sucrose, or glucose; overproduction also promotes haploid invasive growth and diploid filamentous growth","termid":"PBO:0084527"}


id: GO:0051848
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any mechanism of active immune avoidance which works by regulating symbiont cytokine networks, e.g. by secreting proteins that mimic cytokine receptors that act to sequester symbiont cytokines and inhibit action. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","gene_count":0,"genotype_count":0,"name":"obsolete active evasion of symbiont immune response via regulation of symbiont cytokine network (obsolete GO:0051848)","synonyms":[{"name":"active evasion of symbiont immune response via regulation of symbiont cytokine network","type":"exact"},{"name":"active immune evasion via modulation of symbiont cytokine network","type":"exact"},{"name":"active immune evasion via regulation of symbiont cytokine network","type":"exact"}],"termid":"GO:0051848"}


id: PBO:0059751
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO3 pseudogene 25","termid":"PBO:0059751"}


id: MONDO:0016976
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"thymic neuroendocrine carcinoma","termid":"MONDO:0020516"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"well-differentiated thymic neuroendocrine carcinoma","secondary_identifiers":["Orphanet:263331","icd11.foundation:2004515128","MEDGEN:931134","UMLS:C4305465","GARD:20895","SCTID:717922007"],"termid":"MONDO:0016976","xrefs":{"Monarch":{"xref_id":"0016976"}}}


id: PBO:0063043
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"palladin, cytoskeletal associated protein","termid":"PBO:0063043"}


id: GO:1990023
data:
  {"annotated_genes":["SJAG_01371","SJAG_02266","SJAG_02336","SJAG_00723","SJAG_04464","SJAG_00082","SJAG_01805","SJAG_02542","SJAG_04745","SJAG_00930","SJAG_00697","SJAG_01297","SJAG_00762","SJAG_03345","SJAG_01429","SJAG_04140","SJAG_03959","SJAG_01837","SJAG_03048","SJAG_00840","SJAG_01909","SJAG_04412","SJAG_02045","SJAG_04841","SJAG_03073"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[88732,89096,89463,90460,90863,91407,93272,94251,95243,96769,100029,100546,100922,101852,103040,103158,103389,107734,110498,110679,111382,114649,116159,117070,118186],"is_not":false,"summary":null,"term":"GO:1990023"}]},"cv_name":"cellular_component","definition":"The area in the center of the anaphase spindle consisting of microtubules, microtubule bundling factors and kinesin motors where the spindle microtubules from opposite poles overlap in an antiparallel manner.","definition_xrefs":["GOC:mtg_cell_cycle","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spindle midzone","termid":"GO:0051233"},{"relation_name":"part_of","term_name":"mitotic spindle","termid":"GO:0072686"}],"gene_count":25,"genes_by_uniquename":{"SJAG_00082":null,"SJAG_00697":null,"SJAG_00723":null,"SJAG_00762":null,"SJAG_00840":null,"SJAG_00930":null,"SJAG_01297":null,"SJAG_01371":null,"SJAG_01429":null,"SJAG_01805":null,"SJAG_01837":null,"SJAG_01909":null,"SJAG_02045":null,"SJAG_02266":null,"SJAG_02336":null,"SJAG_02542":null,"SJAG_03048":null,"SJAG_03073":null,"SJAG_03345":null,"SJAG_03959":null,"SJAG_04140":null,"SJAG_04412":null,"SJAG_04464":null,"SJAG_04745":null,"SJAG_04841":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0015630"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0072686"}],"interesting_parent_ids":["GO:0005575","GO:0015630","GO:0072686"],"is_obsolete":false,"name":"mitotic spindle midzone","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1990023","terms_by_termid":{"GO:1990023":null}}


id: MONDO:1012450
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"leukoencephalomyelopathy, non-human animal","termid":"MONDO:1011890"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leukoencephalomyelopathy, dog","secondary_identifiers":["OMIA:001788-9615"],"termid":"MONDO:1012450","xrefs":{"Monarch":{"xref_id":"1012450"}}}


id: PBO:0054619
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 2024","termid":"PBO:0054619"}


id: PBO:0082827
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Conserved protein involved in autophagy; interacts with Atg12p-Atg5p conjugates to form Atg12p-Atg5p-Atg16p multimers, which binds to membranes and localizes to the pre-autophagosomal structure and are required for autophagy; relocalizes from nucleus to cytoplasmic foci upon DNA replication stress","termid":"PBO:0082827"}


id: GO:0071218
data:
  {"annotated_genes":["SJAG_00219","SJAG_00552","SJAG_05022","SJAG_03345","SJAG_01160","SJAG_04567","SJAG_02341","SJAG_00054","SJAG_00270","SJAG_03657","SJAG_00173","SJAG_01556","SJAG_01737","SJAG_04187","SJAG_02419","SJAG_04612","SJAG_03815"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[87550,103710,104705,109498,109499,111780],"is_not":false,"summary":null,"term":"GO:0071218"},{"annotations":[113117,109825,109134,109237,107492],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071629"},{"annotations":[112477,102909,88737,87269],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0180027"},{"annotations":[89902,110345],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071630"}]},"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 misfolded protein stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to topologically incorrect protein","termid":"GO:0035967"},{"relation_name":"is_a","term_name":"response to misfolded protein","termid":"GO:0051788"}],"gene_count":17,"genes_by_uniquename":{"SJAG_00054":null,"SJAG_00173":null,"SJAG_00219":null,"SJAG_00270":null,"SJAG_00552":null,"SJAG_01160":null,"SJAG_01556":null,"SJAG_01737":null,"SJAG_02341":null,"SJAG_02419":null,"SJAG_03345":null,"SJAG_03657":null,"SJAG_03815":null,"SJAG_04187":null,"SJAG_04567":null,"SJAG_04612":null,"SJAG_05022":null},"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 misfolded protein","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0071218","terms_by_termid":{"GO:0071218":null,"GO:0071629":null,"GO:0071630":null,"GO:0180027":null}}


id: PBO:0084093
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Guanine nucleotide exchange factor (GEF) for Cdc42p; activates Cdc42p in early G1, accounting for the first stage of biphasic activation, with Cdc24p accounting for the second stage in late G1; involved in the Cdc42p-mediated assembly of the axial landmark that dictates the site for the next round of budding, resulting in the axial budding pattern observed in haploids; localizes with septins to the bud neck contractile ring in mitosis","termid":"PBO:0084093"}


id: PBO:0013439
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transcription factor Overexpression Elongated","termid":"PBO:0013439"}


id: PBO:0058731
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6859-1","termid":"PBO:0058731"}


id: GO:0001530
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a lipopolysaccharide.","definition_xrefs":["PMID:11079463"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipid binding","termid":"GO:0008289"},{"relation_name":"is_a","term_name":"carbohydrate derivative binding","termid":"GO:0097367"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0008289"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0008289","GO:0005488"],"is_obsolete":false,"name":"lipopolysaccharide binding","synonyms":[{"name":"LPS binding","type":"exact"},{"name":"endotoxin binding","type":"broad"}],"termid":"GO:0001530"}


id: PR:Q10307
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["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 C6C3.02c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC6C3.02c","secondary_identifiers":["UniProtKB:Q10307"],"synonyms":[{"name":"Spom972h-CHCHD10","type":"exact"}],"termid":"PR:Q10307"}


id: GO:1902383
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of 11-oxo-beta-amyrin.","definition_xrefs":["PMID:22128119","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pentacyclic triterpenoid biosynthetic process","termid":"GO:0019745"},{"relation_name":"is_a","term_name":"ketone biosynthetic process","termid":"GO:0042181"},{"relation_name":"is_a","term_name":"11-oxo-beta-amyrin metabolic process","termid":"GO:1902381"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006629","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"11-oxo-beta-amyrin biosynthetic process","synonyms":[{"name":"11-oxo-beta-amyrin anabolism","type":"exact"},{"name":"11-oxo-beta-amyrin biosynthesis","type":"exact"},{"name":"11-oxo-beta-amyrin formation","type":"exact"},{"name":"11-oxo-beta-amyrin synthesis","type":"exact"}],"termid":"GO:1902383"}


id: GO:0014738
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of muscle hyperplasia.","definition_xrefs":["GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of muscle adaptation","termid":"GO:0043502"},{"relation_name":"regulates","term_name":"muscle hyperplasia","termid":"GO:0014900"}],"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 muscle hyperplasia","termid":"GO:0014738"}


id: PBO:0087612
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the condensin complex; condensin reorganizes chromosomes during both mitosis and meiosis; essential SMC chromosomal ATPase family member that forms a subcomplex with Smc2p that has ATP-hydrolyzing and DNA-binding activity, but other condensin subunits are required for chromatin binding; required for clustering of tRNA genes at the nucleolus","termid":"PBO:0087612"}


id: RO:HOM0000032
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Paedomorphosis that is produced by a retardation of somatic development.","definition_xrefs":["ISBN:978-0674639416"],"direct_ancestors":[{"relation_name":"is_a","term_name":"in_paedomorphorsis_relationship_with","termid":"RO:HOM0000029"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"in_neoteny_relationship_with","synonyms":[{"name":"juvenilization","type":"exact"},{"name":"neotenous to","type":"exact"}],"termid":"RO:HOM0000032"}


id: PBO:0009082
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chitin synthase regulatory factor Cfh4 (predicted)","termid":"PBO:0009082"}


id: GO:0047929
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-gluconate = 2-dehydro-3-deoxy-D-gluconate + H2O.","definition_xrefs":["RHEA:21612","EC:4.2.1.39"],"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:0016829"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016829","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"gluconate dehydratase activity","secondary_identifiers":["KEGG_REACTION:R01538","MetaCyc:GLUCONATE-DEHYDRATASE-RXN"],"synonyms":[{"name":"D-gluconate dehydratase activity","type":"related"},{"name":"D-gluconate hydro-lyase (2-dehydro-3-deoxy-D-gluconate-forming)","type":"related"},{"name":"D-gluconate hydro-lyase activity","type":"related"}],"termid":"GO:0047929"}


id: PBO:0041290
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C1RL antisense RNA 1","termid":"PBO:0041290"}


id: PBO:0058563
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6505","termid":"PBO:0058563"}


id: GO:0098813
data:
  {"annotated_genes":["SJAG_01224","SJAG_00418","SJAG_01613","SJAG_01538","SJAG_04076","SJAG_00244","SJAG_03540","SJAG_01278","SJAG_04573","SJAG_02045","SJAG_03681","SJAG_02609","SJAG_02380","SJAG_03942","SJAG_01546","SJAG_03575","SJAG_05260","SJAG_01956","SJAG_00697","SJAG_00794","SJAG_03353","SJAG_04950","SJAG_00727","SJAG_00768","SJAG_00600","SJAG_00145","SJAG_05321","SJAG_03835","SJAG_00666","SJAG_00335","SJAG_04884","SJAG_00871","SJAG_04699","SJAG_04177","SJAG_04259","SJAG_00883","SJAG_03073","SJAG_02498","SJAG_00930","SJAG_03116","SJAG_00302","SJAG_05196","SJAG_01371","SJAG_00684","SJAG_04140","SJAG_03685","SJAG_01370","SJAG_00646","SJAG_03680","SJAG_02513","SJAG_05226","SJAG_03327","SJAG_07018","SJAG_02246","SJAG_04623","SJAG_05266","SJAG_03161","SJAG_05290","SJAG_02624","SJAG_01067","SJAG_00773","SJAG_02169","SJAG_03682","SJAG_00918","SJAG_01601","SJAG_04661","SJAG_03989","SJAG_03567","SJAG_04999","SJAG_02606","SJAG_01228","SJAG_00460","SJAG_00207","SJAG_04968","SJAG_01837","SJAG_03832","SJAG_03220","SJAG_04853","SJAG_03698","SJAG_03287","SJAG_00146","SJAG_04126","SJAG_01805","SJAG_01263","SJAG_00678","SJAG_04508","SJAG_03543","SJAG_03926","SJAG_04745","SJAG_04040","SJAG_04581","SJAG_01330","SJAG_02346","SJAG_01515","SJAG_04901","SJAG_05032","SJAG_03217","SJAG_00756","SJAG_03092","SJAG_00082","SJAG_05295","SJAG_01777","SJAG_02731","SJAG_01211","SJAG_04003","SJAG_03048","SJAG_01873","SJAG_04457","SJAG_04255","SJAG_02761","SJAG_03619","SJAG_04280","SJAG_03683","SJAG_00796","SJAG_04412","SJAG_01297","SJAG_02814","SJAG_03437","SJAG_07002","SJAG_05329","SJAG_02104","SJAG_02664","SJAG_01215","SJAG_02286","SJAG_02336","SJAG_03126","SJAG_00229","SJAG_01775","SJAG_02186","SJAG_04597","SJAG_04841","SJAG_00350","SJAG_03062","SJAG_05193","SJAG_02542","SJAG_01082","SJAG_02451","SJAG_05319","SJAG_05220","SJAG_01928","SJAG_01679","SJAG_05019","SJAG_04143","SJAG_02807"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[116162],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051316"},{"annotations":[93312,87343],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051456"},{"annotations":[111175,98120,109851,118157,87230,99876,104968,113274,116023,94791,95045,117642,89516,97396,109401,87478,90475,100830,101938,109806,90868],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051315"},{"annotations":[111448],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0008608"},{"annotations":[117643],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051305"},{"annotations":[103394,111451,115397,106723,99089,90204,113763,107739,113275],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1902426"},{"annotations":[113276,93276,115033,100831,107309,89764,87286,98121,116556],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031619"},{"annotations":[87233,92358,110042,110716,107310],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0007129"},{"annotations":[93362,93277,112720,116362,117209,109674,91275,113992,88837],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045143"},{"annotations":[75191,94793,94255],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000073"},{"annotations":[107740],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0099607"},{"annotations":[89070,116557],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030999"},{"annotations":[105807,113993],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1905318"},{"annotations":[89239,105443],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070197"},{"annotations":[99420,102319,86878,89240,104596],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032121"},{"annotations":[117645,99878,108631,118160,101939,94795,98722,115421,93279],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990571"},{"annotations":[93280,113277,113994,98627,104000,112721,101294,115398,100772,107311],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990813"},{"annotations":[115440],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045132"},{"annotations":[117075],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051307"},{"annotations":[93363,109675],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051755"},{"annotations":[87479,111176,112722],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045144"},{"annotations":[98723,94256,96258],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0090306"},{"annotations":[116164,101295,105808],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0033316"},{"annotations":[100930],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051232"},{"annotations":[98724,100931],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0140642"},{"annotations":[86879,117197,96205,105444,117058,115441],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0045141"},{"annotations":[113481,105445],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0044821"},{"annotations":[99633,98194],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1990949"},{"annotations":[101791,99634],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1990950"},{"annotations":[112619,89823,101335],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0007091"},{"annotations":[96259,102549,98725,108514],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990810"},{"annotations":[94257,109402],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0099606"},{"annotations":[111177,87480],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990893"},{"annotations":[105684,112878,117210,116024,97247,91276,104127,111541,115409,102677],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0007076"},{"annotations":[107743,103396,99880],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0007079"},{"annotations":[107744,103397,93683,98729,98123],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990942"},{"annotations":[101514,112111,118189,109386,103045,113278,112723,116165,88838,98628,100017,103398,113995,116411,101940,101513,112109,101515,106993,98125,90463,107745,108371,113591,98124,93684,93314,112110,88618,89222],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990758"},{"annotations":[116166,115422,104970,90261,108632,102550,89165,100832,107746,98768,113048,118190,95730,105854,113630,96261,94183,105041,111385,89517,114060,103399,111675,89824,93787,108515,87481,116364,109808,108702],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000070"},{"annotations":[100294,117077,101336,91239,94650,89825],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051306"},{"annotations":[99881,96778,110075,100487,96262,96360,114544,118162,109104],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0090307"},{"annotations":[101296,98933,109403,113279,90206,113996,115052,105809,116167],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0007094"},{"annotations":[98730,106917,103046,103400,107747,100935,117649,118163],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000022"},{"annotations":[94258,99882,103047],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061805"},{"annotations":[94259,96779,98126,99883,107748,99356,100936,103401],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061804"},{"annotations":[100937,98731],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0140641"},{"annotations":[108342,94260,98732,96780,100938],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051256"},{"annotations":[101864],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1902424"},{"annotations":[98195],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1902103"},{"annotations":[105810,115053],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0045841"},{"annotations":[102780],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:2000816"},{"annotations":[93685],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0140499"},{"annotations":[115506,111452,104672],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1902425"},{"annotations":[113280],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1905326"},{"annotations":[94642],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1905191"},{"annotations":[116171],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0090267"},{"annotations":[101610,99635,93287,101883,110866,111454,113764,114265,97188],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0045842"},{"annotations":[93288,116174,89476,110693,101884],"is_not":false,"rel_names":["regulates","part_of"],"summary":null,"term":"GO:0140429"},{"annotations":[89477,93898],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1902846"},{"annotations":[93368,109678],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0090006"},{"annotations":[101894],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0062123"},{"annotations":[100834],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1905325"},{"annotations":[93686],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0090266"},{"annotations":[116176],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0033047"},{"annotations":[116177],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1904967"},{"annotations":[116178],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0140273"},{"annotations":[108633],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031134"},{"annotations":[93293,97397,107313,100019,98129,95046,109388,109852,88620,100835,104971,106995,109809,113593,115423,116413,108634,89224,90465,94796,112724,101941,108373],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051455"}]},"cv_name":"biological_process","definition":"The process in which genetic material, in the form of nuclear chromosomes, is organized into specific structures and then physically separated and apportioned to two or more sets. Nuclear chromosome segregation begins with the condensation of chromosomes, includes chromosome separation, and ends when chromosomes have completed movement to the spindle poles.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome segregation","termid":"GO:0007059"}],"gene_count":144,"genes_by_uniquename":{"SJAG_00082":null,"SJAG_00145":null,"SJAG_00146":null,"SJAG_00207":null,"SJAG_00229":null,"SJAG_00244":null,"SJAG_00302":null,"SJAG_00335":null,"SJAG_00350":null,"SJAG_00418":null,"SJAG_00460":null,"SJAG_00600":null,"SJAG_00646":null,"SJAG_00666":null,"SJAG_00678":null,"SJAG_00684":null,"SJAG_00697":null,"SJAG_00727":null,"SJAG_00756":null,"SJAG_00768":null,"SJAG_00773":null,"SJAG_00794":null,"SJAG_00796":null,"SJAG_00871":null,"SJAG_00883":null,"SJAG_00918":null,"SJAG_00930":null,"SJAG_01067":null,"SJAG_01082":null,"SJAG_01211":null,"SJAG_01215":null,"SJAG_01224":null,"SJAG_01228":null,"SJAG_01263":null,"SJAG_01278":null,"SJAG_01297":null,"SJAG_01330":null,"SJAG_01370":null,"SJAG_01371":null,"SJAG_01515":null,"SJAG_01538":null,"SJAG_01546":null,"SJAG_01601":null,"SJAG_01613":null,"SJAG_01679":null,"SJAG_01775":null,"SJAG_01777":null,"SJAG_01805":null,"SJAG_01837":null,"SJAG_01873":null,"SJAG_01928":null,"SJAG_01956":null,"SJAG_02045":null,"SJAG_02104":null,"SJAG_02169":null,"SJAG_02186":null,"SJAG_02246":null,"SJAG_02286":null,"SJAG_02336":null,"SJAG_02346":null,"SJAG_02380":null,"SJAG_02451":null,"SJAG_02498":null,"SJAG_02513":null,"SJAG_02542":null,"SJAG_02606":null,"SJAG_02609":null,"SJAG_02624":null,"SJAG_02664":null,"SJAG_02731":null,"SJAG_02761":null,"SJAG_02807":null,"SJAG_02814":null,"SJAG_03048":null,"SJAG_03062":null,"SJAG_03073":null,"SJAG_03092":null,"SJAG_03116":null,"SJAG_03126":null,"SJAG_03161":null,"SJAG_03217":null,"SJAG_03220":null,"SJAG_03287":null,"SJAG_03327":null,"SJAG_03353":null,"SJAG_03437":null,"SJAG_03540":null,"SJAG_03543":null,"SJAG_03567":null,"SJAG_03575":null,"SJAG_03619":null,"SJAG_03680":null,"SJAG_03681":null,"SJAG_03682":null,"SJAG_03683":null,"SJAG_03685":null,"SJAG_03698":null,"SJAG_03832":null,"SJAG_03835":null,"SJAG_03926":null,"SJAG_03942":null,"SJAG_03989":null,"SJAG_04003":null,"SJAG_04040":null,"SJAG_04076":null,"SJAG_04126":null,"SJAG_04140":null,"SJAG_04143":null,"SJAG_04177":null,"SJAG_04255":null,"SJAG_04259":null,"SJAG_04280":null,"SJAG_04412":null,"SJAG_04457":null,"SJAG_04508":null,"SJAG_04573":null,"SJAG_04581":null,"SJAG_04597":null,"SJAG_04623":null,"SJAG_04661":null,"SJAG_04699":null,"SJAG_04745":null,"SJAG_04841":null,"SJAG_04853":null,"SJAG_04884":null,"SJAG_04901":null,"SJAG_04950":null,"SJAG_04968":null,"SJAG_04999":null,"SJAG_05019":null,"SJAG_05032":null,"SJAG_05193":null,"SJAG_05196":null,"SJAG_05220":null,"SJAG_05226":null,"SJAG_05260":null,"SJAG_05266":null,"SJAG_05290":null,"SJAG_05295":null,"SJAG_05319":null,"SJAG_05321":null,"SJAG_05329":null,"SJAG_07002":null,"SJAG_07018":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"nuclear chromosome segregation","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0098813","terms_by_termid":{"GO:0000022":null,"GO:0000070":null,"GO:0000073":null,"GO:0007076":null,"GO:0007079":null,"GO:0007091":null,"GO:0007094":null,"GO:0007129":null,"GO:0008608":null,"GO:0030999":null,"GO:0031134":null,"GO:0031619":null,"GO:0032121":null,"GO:0033047":null,"GO:0033316":null,"GO:0044821":null,"GO:0045132":null,"GO:0045141":null,"GO:0045143":null,"GO:0045144":null,"GO:0045841":null,"GO:0045842":null,"GO:0051232":null,"GO:0051256":null,"GO:0051305":null,"GO:0051306":null,"GO:0051307":null,"GO:0051315":null,"GO:0051316":null,"GO:0051455":null,"GO:0051456":null,"GO:0051755":null,"GO:0061804":null,"GO:0061805":null,"GO:0062123":null,"GO:0070197":null,"GO:0090006":null,"GO:0090266":null,"GO:0090267":null,"GO:0090306":null,"GO:0090307":null,"GO:0099606":null,"GO:0099607":null,"GO:0140273":null,"GO:0140429":null,"GO:0140499":null,"GO:0140641":null,"GO:0140642":null,"GO:1902103":null,"GO:1902424":null,"GO:1902425":null,"GO:1902426":null,"GO:1902846":null,"GO:1904967":null,"GO:1905191":null,"GO:1905318":null,"GO:1905325":null,"GO:1905326":null,"GO:1990571":null,"GO:1990758":null,"GO:1990810":null,"GO:1990813":null,"GO:1990893":null,"GO:1990942":null,"GO:1990949":null,"GO:1990950":null,"GO:2000816":null}}


id: GO:0046074
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of dTMP, deoxyribosylthymine monophosphate.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine deoxyribonucleoside monophosphate catabolic process","termid":"GO:0009178"},{"relation_name":"is_a","term_name":"pyrimidine deoxyribonucleotide catabolic process","termid":"GO:0009223"},{"relation_name":"is_a","term_name":"dTMP metabolic process","termid":"GO:0046073"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"dTMP catabolic process","synonyms":[{"name":"dTMP breakdown","type":"exact"},{"name":"dTMP catabolism","type":"exact"},{"name":"dTMP degradation","type":"exact"}],"termid":"GO:0046074"}


id: PBO:0060541
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NAV2 antisense RNA 1","termid":"PBO:0060541"}


id: PBO:0065444
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome 26S subunit, ATPase 3","termid":"PBO:0065444"}


id: MONDO:0011267
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":"intellectual disability, severe, with spasticity and pigmentary tapetoretinal degeneration","secondary_identifiers":["UMLS:C1864549","MEDGEN:351159","MESH:C566429","OMIM:602685"],"synonyms":[{"name":"Mrst","type":"related"},{"name":"intellectual disability, severe, with spasticity and pigmentary tapetoretinal degeneration","type":"exact"},{"name":"mental retardation, severe, with spasticity and pigmentary tapetoretinal degeneration","type":"related"},{"name":"mental retardation, severe, with spasticity and tapetoretinal degeneration","type":"exact"}],"termid":"MONDO:0011267","xrefs":{"Monarch":{"xref_id":"0011267"}}}


id: MONDO:0003006
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Bartter disease (obsolete MONDO:0003006)","termid":"MONDO:0003006","xrefs":{"Monarch":{"xref_id":"0003006"}}}


id: GO:1902834
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of proline import into cell.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:24344203"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of amino acid import across plasma membrane","termid":"GO:0010958"},{"relation_name":"is_a","term_name":"regulation of organic acid transport","termid":"GO:0032890"},{"relation_name":"regulates","term_name":"proline import across plasma membrane","termid":"GO:1905647"}],"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:0008150","GO:0055085"],"is_obsolete":false,"name":"regulation of proline import across plasma membrane","synonyms":[{"name":"regulation of proline import into cell","type":"exact"}],"termid":"GO:1902834"}


id: PBO:0043231
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chloride voltage-gated channel 3","termid":"PBO:0043231"}


id: GO:1905337
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of aggrephagy.","definition_xrefs":["GOC:pad","GOC:PARL","GO_REF:0000058","GOC:TermGenie","PMID:25686248"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of macroautophagy","termid":"GO:0016239"},{"relation_name":"is_a","term_name":"regulation of aggrephagy","termid":"GO:1905335"},{"relation_name":"positively_regulates","term_name":"aggrephagy","termid":"GO:0035973"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006914"},{"rel_name":"positively_regulates","termid":"GO:0006914"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006914","GO:0008150"],"is_obsolete":false,"name":"positive regulation of aggrephagy","synonyms":[{"name":"activation of aggrephagy","type":"narrow"},{"name":"up regulation of aggrephagy","type":"exact"},{"name":"up-regulation of aggrephagy","type":"exact"},{"name":"upregulation of aggrephagy","type":"exact"}],"termid":"GO:1905337"}


id: PBO:0005632
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase subunit VIb (predicted)","termid":"PBO:0005632"}


id: PBO:0073947
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLC20A1 divergent transcript","termid":"PBO:0073947"}


id: GO:0006974
data:
  {"annotated_genes":["SJAG_02069","SJAG_02616","SJAG_03680","SJAG_04816","SJAG_03720","SJAG_02918","SJAG_03048","SJAG_04011","SJAG_02439","SJAG_02724","SJAG_02079","SJAG_02339","SJAG_00213","SJAG_00335","SJAG_02990","SJAG_00327","SJAG_01429","SJAG_01605","SJAG_04039","SJAG_02465","SJAG_03618","SJAG_02026","SJAG_02556","SJAG_02521","SJAG_01221","SJAG_03724","SJAG_02294","SJAG_00863","SJAG_04183","SJAG_00783","SJAG_05020","SJAG_03454","SJAG_00623","SJAG_02187","SJAG_00429","SJAG_04457","SJAG_00796","SJAG_00111","SJAG_03734","SJAG_04332","SJAG_01480","SJAG_03325","SJAG_05373","SJAG_04199","SJAG_04190","SJAG_01205","SJAG_00250","SJAG_01354","SJAG_01855","SJAG_00486","SJAG_05173","SJAG_04508","SJAG_02460","SJAG_05282","SJAG_00293","SJAG_00757","SJAG_00758","SJAG_04995","SJAG_01010","SJAG_03665","SJAG_04114","SJAG_05180","SJAG_00823","SJAG_03941","SJAG_01807","SJAG_00500","SJAG_02708","SJAG_02082","SJAG_03628","SJAG_00512","SJAG_01938","SJAG_02680","SJAG_05232","SJAG_01873","SJAG_01385","SJAG_03612","SJAG_04210","SJAG_01611","SJAG_02116","SJAG_02528","SJAG_03695","SJAG_01540","SJAG_05280","SJAG_01572","SJAG_02701","SJAG_00369","SJAG_00618","SJAG_03106","SJAG_06597","SJAG_04242","SJAG_00177","SJAG_02031","SJAG_04843","SJAG_02822","SJAG_02872","SJAG_02348","SJAG_03097","SJAG_01620","SJAG_02500","SJAG_16460","SJAG_02223","SJAG_04368","SJAG_02503","SJAG_04877","SJAG_01644","SJAG_01044","SJAG_00349","SJAG_00729","SJAG_00941","SJAG_04418","SJAG_00221","SJAG_03722","SJAG_02098","SJAG_02261","SJAG_01076","SJAG_02542","SJAG_05372","SJAG_01067","SJAG_02908","SJAG_03702","SJAG_03780","SJAG_02039","SJAG_05295","SJAG_01084","SJAG_00857","SJAG_01419","SJAG_00169","SJAG_02198","SJAG_01146","SJAG_02690","SJAG_04671","SJAG_03728","SJAG_05105","SJAG_00441","SJAG_03613","SJAG_04512","SJAG_03926","SJAG_05012","SJAG_03994","SJAG_03906","SJAG_02818","SJAG_02563","SJAG_02334","SJAG_04410","SJAG_05257","SJAG_02200","SJAG_00045","SJAG_00634","SJAG_01776","SJAG_01878","SJAG_04932","SJAG_00995","SJAG_00082","SJAG_01262","SJAG_00640","SJAG_01832","SJAG_04879","SJAG_04793","SJAG_03026","SJAG_01332","SJAG_02181","SJAG_00853","SJAG_04142","SJAG_03792","SJAG_03436","SJAG_01049","SJAG_00364","SJAG_02226","SJAG_03675","SJAG_03855","SJAG_00727","SJAG_00819","SJAG_00901","SJAG_04778","SJAG_01648","SJAG_00208","SJAG_00696","SJAG_01799","SJAG_04791","SJAG_01624","SJAG_02748","SJAG_02262","SJAG_00884","SJAG_01573","SJAG_00805","SJAG_02104","SJAG_02837","SJAG_00406","SJAG_03160","SJAG_02199","SJAG_03797","SJAG_02576","SJAG_00475","SJAG_01016","SJAG_03942","SJAG_01762","SJAG_04971","SJAG_02416","SJAG_00153","SJAG_02575","SJAG_04089","SJAG_03898","SJAG_02169","SJAG_02182","SJAG_00814","SJAG_00302","SJAG_02866","SJAG_06642","SJAG_05239","SJAG_05353","SJAG_04272","SJAG_02237","SJAG_04280","SJAG_00312","SJAG_00198","SJAG_02667","SJAG_02790","SJAG_04530","SJAG_01680","SJAG_03840","SJAG_02267","SJAG_04989","SJAG_05197","SJAG_00611","SJAG_03221","SJAG_02266","SJAG_04287","SJAG_03051","SJAG_00573","SJAG_05323","SJAG_02527","SJAG_01971","SJAG_03092","SJAG_04097","SJAG_03417","SJAG_02545","SJAG_01677","SJAG_04353","SJAG_03543","SJAG_00272","SJAG_02698","SJAG_04372","SJAG_03230","SJAG_04140","SJAG_01979","SJAG_02303","SJAG_01777","SJAG_02298","SJAG_01652","SJAG_03145","SJAG_02771","SJAG_01410","SJAG_00460","SJAG_00935","SJAG_02828","SJAG_01887","SJAG_03206","SJAG_01204","SJAG_00980","SJAG_01708","SJAG_04147","SJAG_01698","SJAG_00119","SJAG_00187","SJAG_03579","SJAG_04150","SJAG_03529","SJAG_04540","SJAG_01173","SJAG_05237","SJAG_03068","SJAG_01207","SJAG_01119"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[87517,89469,90205,93221,94350,95495,96404,98874,99550,100569,100719,100812,100998,101504,101505,101506,102778,102847,103257,105981,108001,108812,109064,109438,110979,112100,112101,112102,114096,116360,116816,117074,118099],"is_not":false,"summary":null,"term":"GO:0006974"},{"annotations":[96612,95361,92039,93184,113393,115748,117265,109446,110910,118436,105429,94347,95627],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006284"},{"annotations":[106556,101074,94348,95628,73629],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006285"},{"annotations":[113394],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0097510"},{"annotations":[106834,108594],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006287"},{"annotations":[94349],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0045007"},{"annotations":[103110,101075,74070],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006307"},{"annotations":[108803],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000077"},{"annotations":[92085,94091,111216,116292,107237,88015,95496,88637,113613],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000729"},{"annotations":[101693,92154,100041,107147,95659,98556,109789],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000730"},{"annotations":[98689,88595,106436,106103,92041,97671,87344,112433,59416,65730,88372,92208,111039,58563,114142,68077,111932,118209,92206,87604,112437,112434,96175,91698,96916,110710,112435,92479,116736,95692,112436,100999,87277,94958,106121,71185,115093,109447,90720,92209,90913,111217,92207,91020],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006281"},{"annotations":[98464,106364,94310,99175,115094,90175,108554,92273,98643,93494,103724,88348,112643,98404,98891,103538,118061,89525,91857,94553,114212,104216,93791,94092,107218,96715],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0140861"},{"annotations":[106838,108595],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045004"},{"annotations":[94540],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000731"},{"annotations":[102327,104423,108597,94719],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1904161"},{"annotations":[91273,115729,111218,116595,101019,110711,115239,116361,98644,116793,78877,115822,117207,110980,88016,87518],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006302"},{"annotations":[107150,98559,116293,88638,88017],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990918"},{"annotations":[111392,112978,89924,111524,109713,91445,98921,114603,116596,114774,98781,105914,106735],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000727"},{"annotations":[113385,115823],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097680"},{"annotations":[87519,103367,105229,100107,98805,116737,107238,117363,117220,94360,89228,106437,92156,70386,102695,92008,105794,117088,88018,116294,105915,98560,90349,107151,87869,118257,100668,89680,92729,88529,95497,96586,109792,95660,116597,96172,111040,111219,101694,106894,95793,103654,88639,115021,98875,96406,108569,110981,115750],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000724"},{"annotations":[95362,115824,110436,88640,116295,99438,113777,88019,111220,104520],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006303"},{"annotations":[110310,101695,95661,118258],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045002"},{"annotations":[118259],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000736"},{"annotations":[92131,88768,116943,100142,107634],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045003"},{"annotations":[103487,103726,116817,98806,102398,102378],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0070987"},{"annotations":[102379,98807,102399,103488,116818,95363,103727,113063],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0042276"},{"annotations":[95364],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061674"},{"annotations":[87649],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070911"},{"annotations":[102696,104449,108040,92132,96644],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036297"},{"annotations":[116297,89766,107240],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000706"},{"annotations":[96407],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000707"},{"annotations":[109795,107152],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0010772"},{"annotations":[107241,91244],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000710"},{"annotations":[100143],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1902346"},{"annotations":[115751,87763,94351,100079,107242,115937,115179,105559,88069,103728,116639,104072,91245,105430],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006298"},{"annotations":[97612],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070716"},{"annotations":[113395,108041,95629,98808,88070,102400,112006,102380,105431],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043504"},{"annotations":[88021],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097552"},{"annotations":[91277,98690,115502,106106,101860,93423,108804,115730,79513,93045,113754,113964,77494,117211,110689],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044773"},{"annotations":[90791,109165],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031571"},{"annotations":[100549,116513,100035,113755,93425,117212,90916,88597,91278,88022,108806,98860,111221,89690,106108],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007095"},{"annotations":[115559,101862,94026,98692,116600,90917,88598,98861,88023,95499,107155,111527,115560,88643,101021,92011,106109,89926,100355,111222],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031573"},{"annotations":[101867],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:2001033"},{"annotations":[111251],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1904332"},{"annotations":[89071],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036299"},{"annotations":[107598,92043,111043,116206,116186,118262,116187,91658,109527,88107,110734,107971,110911,114635,102653,87764,105432,93143,61698,116640,115022,89365,111574,92012,115753,95630],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006289"},{"annotations":[118263,109528,92480,93144,110912],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:1901255"},{"annotations":[113386,108599,104426,106843],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006297"},{"annotations":[108469],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006294"},{"annotations":[116772,111528],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0045739"},{"annotations":[109676,93366],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:2000781"},{"annotations":[106896],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:2001034"},{"annotations":[88108,97747,103731,104450,116601,95501,103928,87486,116280],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006301"},{"annotations":[89242,104598],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031848"},{"annotations":[105580,97811],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106300"},{"annotations":[105433],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006290"},{"annotations":[116188,116189],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000720"},{"annotations":[98565,100146,102697,111077],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036298"},{"annotations":[108042,95502,97748,101832,103370,96989,90288],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000725"},{"annotations":[93367,109677],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0006282"},{"annotations":[106070,90393],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:2000779"},{"annotations":[108807],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0010569"},{"annotations":[95731,116366,89529,74741],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990414"},{"annotations":[97614],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990516"},{"annotations":[93185,115180],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000012"},{"annotations":[87650,101275,110641,89738,90352,91461,87837,96223,108870,118419],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006283"},{"annotations":[116819,97812,103492],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0019985"},{"annotations":[96615,103732,93145,94542,106473,110913,111767,105434,95505,110313,87487,89053,94754,112323,93447],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070914"}]},"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 stimulus indicating damage to its DNA from environmental insults or errors during metabolism.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to stress","termid":"GO:0033554"}],"gene_count":273,"genes_by_uniquename":{"SJAG_00045":null,"SJAG_00082":null,"SJAG_00111":null,"SJAG_00119":null,"SJAG_00153":null,"SJAG_00169":null,"SJAG_00177":null,"SJAG_00187":null,"SJAG_00198":null,"SJAG_00208":null,"SJAG_00213":null,"SJAG_00221":null,"SJAG_00250":null,"SJAG_00272":null,"SJAG_00293":null,"SJAG_00302":null,"SJAG_00312":null,"SJAG_00327":null,"SJAG_00335":null,"SJAG_00349":null,"SJAG_00364":null,"SJAG_00369":null,"SJAG_00406":null,"SJAG_00429":null,"SJAG_00441":null,"SJAG_00460":null,"SJAG_00475":null,"SJAG_00486":null,"SJAG_00500":null,"SJAG_00512":null,"SJAG_00573":null,"SJAG_00611":null,"SJAG_00618":null,"SJAG_00623":null,"SJAG_00634":null,"SJAG_00640":null,"SJAG_00696":null,"SJAG_00727":null,"SJAG_00729":null,"SJAG_00757":null,"SJAG_00758":null,"SJAG_00783":null,"SJAG_00796":null,"SJAG_00805":null,"SJAG_00814":null,"SJAG_00819":null,"SJAG_00823":null,"SJAG_00853":null,"SJAG_00857":null,"SJAG_00863":null,"SJAG_00884":null,"SJAG_00901":null,"SJAG_00935":null,"SJAG_00941":null,"SJAG_00980":null,"SJAG_00995":null,"SJAG_01010":null,"SJAG_01016":null,"SJAG_01044":null,"SJAG_01049":null,"SJAG_01067":null,"SJAG_01076":null,"SJAG_01084":null,"SJAG_01119":null,"SJAG_01146":null,"SJAG_01173":null,"SJAG_01204":null,"SJAG_01205":null,"SJAG_01207":null,"SJAG_01221":null,"SJAG_01262":null,"SJAG_01332":null,"SJAG_01354":null,"SJAG_01385":null,"SJAG_01410":null,"SJAG_01419":null,"SJAG_01429":null,"SJAG_01480":null,"SJAG_01540":null,"SJAG_01572":null,"SJAG_01573":null,"SJAG_01605":null,"SJAG_01611":null,"SJAG_01620":null,"SJAG_01624":null,"SJAG_01644":null,"SJAG_01648":null,"SJAG_01652":null,"SJAG_01677":null,"SJAG_01680":null,"SJAG_01698":null,"SJAG_01708":null,"SJAG_01762":null,"SJAG_01776":null,"SJAG_01777":null,"SJAG_01799":null,"SJAG_01807":null,"SJAG_01832":null,"SJAG_01855":null,"SJAG_01873":null,"SJAG_01878":null,"SJAG_01887":null,"SJAG_01938":null,"SJAG_01971":null,"SJAG_01979":null,"SJAG_02026":null,"SJAG_02031":null,"SJAG_02039":null,"SJAG_02069":null,"SJAG_02079":null,"SJAG_02082":null,"SJAG_02098":null,"SJAG_02104":null,"SJAG_02116":null,"SJAG_02169":null,"SJAG_02181":null,"SJAG_02182":null,"SJAG_02187":null,"SJAG_02198":null,"SJAG_02199":null,"SJAG_02200":null,"SJAG_02223":null,"SJAG_02226":null,"SJAG_02237":null,"SJAG_02261":null,"SJAG_02262":null,"SJAG_02266":null,"SJAG_02267":null,"SJAG_02294":null,"SJAG_02298":null,"SJAG_02303":null,"SJAG_02334":null,"SJAG_02339":null,"SJAG_02348":null,"SJAG_02416":null,"SJAG_02439":null,"SJAG_02460":null,"SJAG_02465":null,"SJAG_02500":null,"SJAG_02503":null,"SJAG_02521":null,"SJAG_02527":null,"SJAG_02528":null,"SJAG_02542":null,"SJAG_02545":null,"SJAG_02556":null,"SJAG_02563":null,"SJAG_02575":null,"SJAG_02576":null,"SJAG_02616":null,"SJAG_02667":null,"SJAG_02680":null,"SJAG_02690":null,"SJAG_02698":null,"SJAG_02701":null,"SJAG_02708":null,"SJAG_02724":null,"SJAG_02748":null,"SJAG_02771":null,"SJAG_02790":null,"SJAG_02818":null,"SJAG_02822":null,"SJAG_02828":null,"SJAG_02837":null,"SJAG_02866":null,"SJAG_02872":null,"SJAG_02908":null,"SJAG_02918":null,"SJAG_02990":null,"SJAG_03026":null,"SJAG_03048":null,"SJAG_03051":null,"SJAG_03068":null,"SJAG_03092":null,"SJAG_03097":null,"SJAG_03106":null,"SJAG_03145":null,"SJAG_03160":null,"SJAG_03206":null,"SJAG_03221":null,"SJAG_03230":null,"SJAG_03325":null,"SJAG_03417":null,"SJAG_03436":null,"SJAG_03454":null,"SJAG_03529":null,"SJAG_03543":null,"SJAG_03579":null,"SJAG_03612":null,"SJAG_03613":null,"SJAG_03618":null,"SJAG_03628":null,"SJAG_03665":null,"SJAG_03675":null,"SJAG_03680":null,"SJAG_03695":null,"SJAG_03702":null,"SJAG_03720":null,"SJAG_03722":null,"SJAG_03724":null,"SJAG_03728":null,"SJAG_03734":null,"SJAG_03780":null,"SJAG_03792":null,"SJAG_03797":null,"SJAG_03840":null,"SJAG_03855":null,"SJAG_03898":null,"SJAG_03906":null,"SJAG_03926":null,"SJAG_03941":null,"SJAG_03942":null,"SJAG_03994":null,"SJAG_04011":null,"SJAG_04039":null,"SJAG_04089":null,"SJAG_04097":null,"SJAG_04114":null,"SJAG_04140":null,"SJAG_04142":null,"SJAG_04147":null,"SJAG_04150":null,"SJAG_04183":null,"SJAG_04190":null,"SJAG_04199":null,"SJAG_04210":null,"SJAG_04242":null,"SJAG_04272":null,"SJAG_04280":null,"SJAG_04287":null,"SJAG_04332":null,"SJAG_04353":null,"SJAG_04368":null,"SJAG_04372":null,"SJAG_04410":null,"SJAG_04418":null,"SJAG_04457":null,"SJAG_04508":null,"SJAG_04512":null,"SJAG_04530":null,"SJAG_04540":null,"SJAG_04671":null,"SJAG_04778":null,"SJAG_04791":null,"SJAG_04793":null,"SJAG_04816":null,"SJAG_04843":null,"SJAG_04877":null,"SJAG_04879":null,"SJAG_04932":null,"SJAG_04971":null,"SJAG_04989":null,"SJAG_04995":null,"SJAG_05012":null,"SJAG_05020":null,"SJAG_05105":null,"SJAG_05173":null,"SJAG_05180":null,"SJAG_05197":null,"SJAG_05232":null,"SJAG_05237":null,"SJAG_05239":null,"SJAG_05257":null,"SJAG_05280":null,"SJAG_05282":null,"SJAG_05295":null,"SJAG_05323":null,"SJAG_05353":null,"SJAG_05372":null,"SJAG_05373":null,"SJAG_06597":null,"SJAG_06642":null,"SJAG_16460":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"DNA damage response","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["GO:0034984"],"synonyms":[{"name":"cellular DNA damage response","type":"exact"},{"name":"cellular response to DNA damage stimulus","type":"exact"},{"name":"response to DNA damage stimulus","type":"broad"},{"name":"response to genotoxic stress","type":"exact"}],"termid":"GO:0006974","terms_by_termid":{"GO:0000012":null,"GO:0000077":null,"GO:0000706":null,"GO:0000707":null,"GO:0000710":null,"GO:0000720":null,"GO:0000724":null,"GO:0000725":null,"GO:0000727":null,"GO:0000729":null,"GO:0000730":null,"GO:0000731":null,"GO:0000736":null,"GO:0006281":null,"GO:0006282":null,"GO:0006283":null,"GO:0006284":null,"GO:0006285":null,"GO:0006287":null,"GO:0006289":null,"GO:0006290":null,"GO:0006294":null,"GO:0006297":null,"GO:0006298":null,"GO:0006301":null,"GO:0006302":null,"GO:0006303":null,"GO:0006307":null,"GO:0006974":null,"GO:0007095":null,"GO:0010569":null,"GO:0010772":null,"GO:0019985":null,"GO:0031571":null,"GO:0031573":null,"GO:0031848":null,"GO:0036297":null,"GO:0036298":null,"GO:0036299":null,"GO:0042276":null,"GO:0043504":null,"GO:0044773":null,"GO:0045002":null,"GO:0045003":null,"GO:0045004":null,"GO:0045007":null,"GO:0045739":null,"GO:0061674":null,"GO:0070716":null,"GO:0070911":null,"GO:0070914":null,"GO:0070987":null,"GO:0097510":null,"GO:0097552":null,"GO:0097680":null,"GO:0106300":null,"GO:0140861":null,"GO:1901255":null,"GO:1902346":null,"GO:1904161":null,"GO:1904332":null,"GO:1990414":null,"GO:1990516":null,"GO:1990918":null,"GO:2000779":null,"GO:2000781":null,"GO:2001033":null,"GO:2001034":null}}


id: GO:0004370
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + glycerol = sn-glycerol 3-phosphate + ADP + 2 H+.","definition_xrefs":["EC:2.7.1.30","RHEA:21644"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinase activity","termid":"GO:0016301"},{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016301"},{"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:0016301","GO:0003674"],"is_obsolete":false,"name":"glycerol kinase activity","secondary_identifiers":["KEGG_REACTION:R00847","MetaCyc:GLYCEROL-KIN-RXN","Reactome:R-HSA-75887"],"synonyms":[{"name":"ATP:glycerol 3-phosphotransferase activity","type":"related"},{"name":"ATP:glycerol-3-phosphotransferase activity","type":"related"},{"name":"GK","type":"related"},{"name":"glyceric kinase activity","type":"related"},{"name":"glycerokinase activity","type":"related"},{"name":"glycerol kinase (phosphorylating)","type":"related"}],"termid":"GO:0004370"}


id: PBO:0087732
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the signal peptidase complex (SPC); SPC cleaves the signal sequence from proteins targeted to the endoplasmic reticulum (ER); homolog of the SPC12 subunit of mammalian signal peptidase complex; protein abundance increases in response to DNA replication stress","termid":"PBO:0087732"}


id: FYPO:0002383
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cellular process phenotype observed in the vegetative growth phase of the life cycle in which acetylation of lysine at positions 9 and 14 of histone H3 in regions of the genome that are actively transcribed occurs to a greater extent than normal.","definition_xrefs":["PomBase:mah","PMID:23851719"],"gene_count":0,"genotype_count":0,"name":"obsolete increased histone H3-K9 and H3-K14 acetylation at centromere outer repeat during vegetative growth (obsolete FYPO:0002383)","synonyms":[{"name":"increased histone H3 acetylation (K9 and K14) at centromere outer repeat during vegetative growth","type":"exact"},{"name":"increased histone H3-K9 and H3-K14 acetylation at centromere otr during vegetative growth","type":"exact"},{"name":"increased histone H3-K9 and H3-K14 acetylation at centromere outer repeat during mitotic cell cycle","type":"related"},{"name":"increased histone H3-K9 and H3-K14 acetylation at centromeric outer repeat region during vegetative growth","type":"exact"},{"name":"increased histone H3-K9 and H3-K14 acetylation at pericentric region during vegetative growth","type":"related"},{"name":"increased histone H3-K9 and H3-K14 acetylation at pericentromeric region during vegetative growth","type":"related"},{"name":"increased histone H3K9 and H3K14 acetylation at centromere outer repeat during vegetative growth","type":"exact"}],"termid":"FYPO:0002383"}


id: PBO:0059539
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrially encoded transcription factor binding site Y","termid":"PBO:0059539"}


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


id: MONDO:0000134
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia (obsolete MONDO:0000134)","termid":"MONDO:0000134","xrefs":{"Monarch":{"xref_id":"0000134"}}}


id: PATO:0001453
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An attachment quality inhering in a bearer by virtue of the bearer's lacking connection or association with another entity.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"attachment quality","termid":"PATO:0001435"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"detached from","synonyms":[{"name":"detached","type":"exact"}],"termid":"PATO:0001453"}


id: MONDO:0006770
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare tumor-like lesion of the hands and feet characterized by the presence of hemorrhagic fibrous tissue, hemosiderin deposition, osteoclast-like giant cells which are irregularly distributed, and reactive bone formation. Pain and swelling are the most frequent symptoms. It may recur following curettage, but is usually cured after a second procedure.","definition_xrefs":["NCIT:C121893"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bone giant cell tumor","termid":"MONDO:0005674"}],"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":"giant cell reparative granuloma","secondary_identifiers":["SCTID:15350006","EFO:1000950","DOID:1866","ICD9:526.3","MEDGEN:102385","UMLS:C0162375","MESH:D006101"],"synonyms":[{"name":"GCLSB","type":"exact"},{"name":"central giant cell (reparative) granuloma","type":"exact"},{"name":"central giant cell granuloma","type":"exact"},{"name":"central giant cell reparative granuloma of jaw","type":"exact"},{"name":"giant cell lesion of small bones","type":"exact"}],"termid":"MONDO:0006770","xrefs":{"Monarch":{"xref_id":"0006770"}}}


id: PBO:0089270
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial inner membrane i-AAA protease complex subunit Yme1","termid":"PBO:0089270"}


id: PBO:0070162
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 76 pseudogene","termid":"PBO:0070162"}


id: PBO:0110035
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IDH1 pseudogene 1","termid":"PBO:0110035"}


id: PBO:0040468
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP synthase mitochondrial F1 complex assembly factor 2","termid":"PBO:0040468"}


id: SO:0001228
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A modified RNA base in which the 5,6-dihydrouracil is bound to the ribose ring.","definition_xrefs":["RSC:cb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified_uridine","termid":"SO:0001277"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dihydrouridine","secondary_identifiers":["http://en.wikipedia.org/wiki/Dihydrouridine","RNAMOD:051"],"synonyms":[{"name":" D","type":"exact"}],"termid":"SO:0001228"}


id: PBO:0057461
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 580","termid":"PBO:0057461"}


id: PBO:0087056
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribosomal 60S subunit protein L27A; homologous to mammalian ribosomal protein L27, no bacterial homolog; RPL27A has a paralog, RPL27B, that arose from the whole genome duplication","termid":"PBO:0087056"}


id: PBO:0079127
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"teashirt zinc finger homeobox 3","termid":"PBO:0079127"}


id: PBO:0079098
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Tyr (anticodon GTA) 11-1","termid":"PBO:0079098"}


id: MONDO:0020743
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An acute leukemia of ambiguous lineage. It is characterized by the presence of either separate populations of blasts of more than one lineage, or one population of blasts co-expressing markers of more than one lineage.","definition_xrefs":["NCIT:C82179"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute leukemia of ambiguous lineage","termid":"MONDO:0019460"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0004992","MONDO:0005570"],"is_obsolete":false,"name":"mixed phenotype acute leukemia","secondary_identifiers":["UMLS:C2826025","MedDRA:10067399","MEDGEN:417342","Orphanet:530995","NANDO:2200018","GARD:17972"],"synonyms":[{"name":"MPAL","type":"exact"},{"name":"mixed phenotype acute leukemia","type":"exact"}],"termid":"MONDO:0020743","xrefs":{"Monarch":{"xref_id":"0020743"}}}


id: PBO:0005064
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UTP-glucose-1-phosphate uridylyltransferase (predicted)","termid":"PBO:0005064"}


id: GO:0036362
data:
  {"annotated_genes":["SJAG_04236","SJAG_02626"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[117289,117652],"is_not":false,"summary":null,"term":"GO:0036362"}]},"cv_name":"cellular_component","definition":"A double layer of lipid molecules that surrounds an ascus, a capsule containing the sexual spores in some fungi.","definition_xrefs":["PMID:21900489","GOC:mcc","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane","termid":"GO:0016020"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02626":null,"SJAG_04236":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"ascus membrane","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0036362","terms_by_termid":{"GO:0036362":null}}


id: FYPO:0003892
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 error-prone translesion synthesis is abnormal. Error-prone translesion synthesis a DNA repair process that results in the conversion of DNA-damage induced single-stranded gaps into large molecular weight DNA after replication.","definition_xrefs":["PomBase:mah","GO:0042276"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal DNA repair during vegetative growth","termid":"FYPO:0000188"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000298","FYPO:0005447","FYPO:0000293","FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"abnormal error-prone translesion synthesis","synonyms":[{"name":"abnormal error-prone translesion synthesis during mitotic cell cycle","type":"related"},{"name":"abnormal error-prone translesion synthesis during vegetative growth","type":"exact"}],"termid":"FYPO:0003892"}


id: PBO:0048021
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibroblast growth factor receptor substrate 2","termid":"PBO:0048021"}


id: FYPO:0003941
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of m7G(5')pppN diphosphatase activity is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased catalytic activity","termid":"FYPO:0000663"},{"relation_name":"is_a","term_name":"abnormal m7G(5')pppN diphosphatase activity","termid":"FYPO:0003939"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0000652","FYPO:0000654","FYPO:0001985","FYPO:0000707"],"is_obsolete":false,"name":"decreased m7G(5')pppN diphosphatase activity","synonyms":[{"name":"decreased mRNA decapping activity","type":"related"},{"name":"reduced m7G(5')pppN diphosphatase activity","type":"exact"}],"termid":"FYPO:0003941"}


id: PR:O74755
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pst3 gene.","definition_xrefs":["UniProtKB:O74755","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":"paired amphipathic helix protein pst3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1734.16c","synonyms":[{"name":"SIN3 homolog 3 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-pst3","type":"exact"}],"termid":"PR:O74755"}


id: GO:0045831
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents, or reduces the frequency, rate or extent of light-activated channel activity.","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of light-activated channel activity (obsolete GO:0045831)","synonyms":[{"name":"down regulation of light-activated channel activity","type":"exact"},{"name":"down-regulation of light-activated channel activity","type":"exact"},{"name":"downregulation of light-activated channel activity","type":"exact"},{"name":"inhibition of light-activated channel activity","type":"narrow"}],"termid":"GO:0045831"}


id: GO:0048778
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of erythrophore differentiation.","definition_xrefs":["GOC:mh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of pigment cell differentiation","termid":"GO:0050932"},{"relation_name":"regulates","term_name":"erythrophore differentiation","termid":"GO:0048773"}],"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 erythrophore differentiation","termid":"GO:0048778"}


id: PBO:0000310
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Meiotically Upregulated Gene","termid":"PBO:0000310"}


id: PBO:0086206
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein that associates with ribosomes; homolog of translationally controlled tumor protein; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm and relocates to the mitochondrial outer surface upon oxidative stress; homolog of human TPT1","termid":"PBO:0086206"}


id: PBO:0067987
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 289","termid":"PBO:0067987"}


id: MONDO:0016882
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndrome caused by partial chromosomal deletion","termid":"MONDO:0000761"},{"relation_name":"is_a","term_name":"chromosome 20 disorder","termid":"MONDO:0700025"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partial deletion of chromosome 20","secondary_identifiers":["MEDGEN:1825964","UMLS:C5679662","Orphanet:261846","GARD:20805"],"synonyms":[{"name":"partial deletion of chromosome type 20","type":"exact"},{"name":"partial monosomy of chromosome 20","type":"exact"}],"termid":"MONDO:0016882","xrefs":{"Monarch":{"xref_id":"0016882"}}}


id: MONDO:0007521
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete egasyn (obsolete MONDO:0007521)","secondary_identifiers":["OMIM:129905"],"synonyms":[{"name":"egasyn","type":"exact"},{"name":"esterase 22","type":"related"}],"termid":"MONDO:0007521","xrefs":{"Monarch":{"xref_id":"0007521"}}}


id: PBO:0064877
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase 1 regulatory subunit 36","termid":"PBO:0064877"}


id: GO:1904672
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of somatic stem cell population maintenance.","definition_xrefs":["GOC:rph","GOC:TermGenie","GOC:BHF_miRNA","PMID:19409607","GO_REF:0000058","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of stem cell population maintenance","termid":"GO:2000036"},{"relation_name":"regulates","term_name":"somatic stem cell population maintenance","termid":"GO:0035019"}],"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 somatic stem cell population maintenance","termid":"GO:1904672"}


id: PBO:0013790
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fumerate reductase Osm1 (predicted)","termid":"PBO:0013790"}


id: PBO:0074652
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, H/ACA box 40C","termid":"PBO:0074652"}


id: MONDO:0001055
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"conjunctival degeneration","termid":"MONDO:0000949"},{"relation_name":"is_a","term_name":"pterygium","termid":"MONDO:0005085"}],"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":"conjunctival pterygium","secondary_identifiers":["MEDGEN:1625284","UMLS:C4520843","DOID:10526"],"synonyms":[{"name":"web eye","type":"exact"}],"termid":"MONDO:0001055","xrefs":{"Monarch":{"xref_id":"0001055"}}}


id: PBO:0031560
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_catalytic_activity","termid":"PBO:0031560"}


id: PBO:0082150
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Acyltransferase; enzyme mainly responsible for the introduction of saturated very long chain fatty acids into neo-synthesized molecules of phosphatidylinositol; required for incorporation of stearic acid into phosphatidylinositol; affects chromosome stability when overexpressed; CST26 has a paralog, YDR018C, that arose from the whole genome duplication","termid":"PBO:0082150"}


id: PBO:0001083
data:
  {"annotation_feature_type":"gene","cv_name":"cat_act","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"active site mapping","termid":"PBO:0001083"}


id: PR:O94369
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC1604.03c gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94369"],"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 C1604.03c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1604.03c","synonyms":[{"name":"Spom972h-SPBC1604.03c","type":"exact"}],"termid":"PR:O94369"}


id: MONDO:1011338
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Nutritional disorder that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-human animal disease","termid":"MONDO:0005583"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nutritional disorder, non-human animal","termid":"MONDO:1011338","xrefs":{"Monarch":{"xref_id":"1011338"}}}


id: FYPO:0004729
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 cytoplasmic microtubules are formed by the extension of existing nuclear microtubules arising from fragmentation of the mitotic spindle. Normally, cytoplasmic microtubules are nucleated from microtubule organizing centers in the cytoplasm.","definition_xrefs":["PomBase:mah","PMID:15772152"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoplasmic microtubule formation from nuclear microtubules","termid":"FYPO:0004727"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000054"}],"interesting_parent_ids":["FYPO:0000054","FYPO:0001320","FYPO:0005447","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"cytoplasmic microtubule formation from nuclear microtubules following spindle microtubule fragmentation","synonyms":[{"name":"cytoplasmic microtubule formation from nuclear microtubules following mitotic spindle microtubule fragmentation","type":"exact"},{"name":"cytoplasmic microtubule formation from nuclear microtubules following spindle microtubule fragmentation during mitotic cell cycle","type":"related"},{"name":"cytoplasmic microtubule formation from nuclear microtubules following spindle microtubule fragmentation during vegetative growth","type":"exact"}],"termid":"FYPO:0004729"}


id: GO:0004438
data:
  {"annotated_genes":["SJAG_03248"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[90974],"is_not":false,"summary":null,"term":"GO:0004438"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 1-phosphatidyl-1D-myo-inositol 3-phosphate + H2O = 1-phosphatidyl-1D-myo-inositol + phosphate.","definition_xrefs":["EC:3.1.3.64"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatidylinositol monophosphate phosphatase activity","termid":"GO:0052744"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03248":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016788"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016787","GO:0016788"],"is_obsolete":false,"name":"phosphatidylinositol-3-phosphate phosphatase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-6809325","Reactome:R-HSA-1675795","Reactome:R-HSA-1676141","Reactome:R-HSA-6809720","RHEA:12316","GO:0016315","Reactome:R-HSA-6809777","Reactome:R-HSA-6809975","Reactome:R-HSA-1676114","Reactome:R-HSA-1675994","MetaCyc:PHOSPHATIDYLINOSITOL-3-PHOSPHATASE-RXN"],"synonyms":[{"name":"1-phosphatidyl-1D-myo-inositol-3-phosphate 3-phosphohydrolase activity","type":"related"},{"name":"D-myo-inositol-1,3-bisphosphate 3-phosphohydrolase activity","type":"related"},{"name":"inositol 1,3-bisphosphate phosphatase activity","type":"related"},{"name":"inositol-1,3-bisphosphate 3-phosphatase activity","type":"related"},{"name":"inositol-polyphosphate 3-phosphatase activity","type":"related"},{"name":"phosphatidyl-3-phosphate 3-phosphohydrolase activity","type":"related"},{"name":"phosphatidylinositol-3-phosphatase activity","type":"exact"}],"termid":"GO:0004438","terms_by_termid":{"GO:0004438":null}}


id: PBO:0042074
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil domain containing 144A","termid":"PBO:0042074"}


id: PBO:0048334
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 45","termid":"PBO:0048334"}


id: FYPO:0004314
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 CENP-A containing chromatin is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to centromeric chromatin","termid":"FYPO:0005072"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0000257","FYPO:0000138","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"normal protein localization to CENP-A containing chromatin","synonyms":[{"name":"normal protein localisation to CENP-A containing chromatin","type":"exact"},{"name":"normal protein localization to CENP-A containing chromatin during mitotic cell cycle","type":"related"},{"name":"normal protein localization to CENP-A containing chromatin during vegetative growth","type":"exact"},{"name":"normal protein localization to centromeric core region chromatin","type":"exact"}],"termid":"FYPO:0004314"}


id: MONDO:0006564
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inflammatory skin condition caused by direct contact between the skin and an irritating substance. It is typically manifested by erythema, mild edema, and scaling at the affected site.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"contact dermatitis","termid":"MONDO:0005480"}],"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":"irritant dermatitis","secondary_identifiers":["EFO:1000718","DOID:2772","MESH:D017453","UMLS:C0162823","ICD9:692.9","NCIT:C27151","SCTID:110979008","MEDGEN:56513"],"synonyms":[{"name":"irritant contact dermatitis","type":"exact"},{"name":"primary irritant dermatitis","type":"exact"}],"termid":"MONDO:0006564","xrefs":{"Monarch":{"xref_id":"0006564"}}}


id: GO:0044610
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the directed movement of flavine mononucleotide (FMN) from one side of a membrane to the other.","definition_xrefs":["GOC:ans","PMID:22185573"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic anion transmembrane transporter activity","termid":"GO:0008514"},{"relation_name":"is_a","term_name":"nucleotide transmembrane transporter activity","termid":"GO:0015215"},{"relation_name":"is_a","term_name":"carbohydrate derivative transmembrane transporter activity","termid":"GO:1901505"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"FMN transmembrane transporter activity","synonyms":[{"name":"flavine mononucleotide transmembrane transporter activity","type":"exact"}],"termid":"GO:0044610"}


id: PBO:0017085
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schizosaccharomyces pombe specific protein Mug112","termid":"PBO:0017085"}


id: GO:0051130
data:
  {"annotated_genes":["SJAG_02336","SJAG_00766","SJAG_00666","SJAG_02189","SJAG_01771","SJAG_03851","SJAG_03631","SJAG_01805","SJAG_04509","SJAG_04468","SJAG_01188","SJAG_02433","SJAG_04968","SJAG_02498","SJAG_03421","SJAG_05290","SJAG_02342","SJAG_02812","SJAG_04776","SJAG_05265","SJAG_01837","SJAG_03048","SJAG_03342","SJAG_02451","SJAG_02332","SJAG_01679","SJAG_01297","SJAG_04573","SJAG_03957","SJAG_03812","SJAG_03936","SJAG_02380","SJAG_00823","SJAG_00082","SJAG_01114","SJAG_03704","SJAG_04597","SJAG_03353","SJAG_04666","SJAG_03681","SJAG_00718","SJAG_00142","SJAG_03438","SJAG_00973","SJAG_02169","SJAG_00845","SJAG_01212","SJAG_04259","SJAG_02592","SJAG_03581","SJAG_03624","SJAG_01794","SJAG_03453","SJAG_02379","SJAG_00883","SJAG_00266","SJAG_05289","SJAG_00514","SJAG_03126","SJAG_02990","SJAG_03137","SJAG_04312"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[107457],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010846"},{"annotations":[107739,99089,106723,115397,113763,90204,111451,113275,103394],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902426"},{"annotations":[93685],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140499"},{"annotations":[90209],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903024"},{"annotations":[108142,108052],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000786"},{"annotations":[97114],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901098"},{"annotations":[103200],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045807"},{"annotations":[64194],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903373"},{"annotations":[98465],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031453"},{"annotations":[116170,89126,101878],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905561"},{"annotations":[87370,89344,90329,92959,110856],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902917"},{"annotations":[87690,105184],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001178"},{"annotations":[101349],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031117"},{"annotations":[95233],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090297"},{"annotations":[108366],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090141"},{"annotations":[89474,93896],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903501"},{"annotations":[110014,94066,87012,93897,112855],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903473"},{"annotations":[101882,116172],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903380"},{"annotations":[91902,104673,106535,112856,114967,117392,105874,88717,89345,93286],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140281"},{"annotations":[99635,101883,97188,114265,111454,93287,113764,110866,101610],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045842"},{"annotations":[89477,93898],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902846"},{"annotations":[110927],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110161"},{"annotations":[90668],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090053"},{"annotations":[88538],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010845"},{"annotations":[114683,89185],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045899"},{"annotations":[110015,89478,93290,101888,87014],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031031"},{"annotations":[90669,93858,109837],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090055"},{"annotations":[106897],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045876"},{"annotations":[96677],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032215"},{"annotations":[111455],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904595"},{"annotations":[108656,94291,108655],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045905"},{"annotations":[109759,97115],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061191"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of a process involved in the formation, arrangement of constituent parts, or disassembly of cell structures, including the plasma membrane and any external encapsulating structures such as the cell wall and cell envelope.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cellular process","termid":"GO:0048522"},{"relation_name":"is_a","term_name":"regulation of cellular component organization","termid":"GO:0051128"},{"relation_name":"positively_regulates","term_name":"cellular component organization","termid":"GO:0016043"}],"gene_count":62,"genes_by_uniquename":{"SJAG_00082":null,"SJAG_00142":null,"SJAG_00266":null,"SJAG_00514":null,"SJAG_00666":null,"SJAG_00718":null,"SJAG_00766":null,"SJAG_00823":null,"SJAG_00845":null,"SJAG_00883":null,"SJAG_00973":null,"SJAG_01114":null,"SJAG_01188":null,"SJAG_01212":null,"SJAG_01297":null,"SJAG_01679":null,"SJAG_01771":null,"SJAG_01794":null,"SJAG_01805":null,"SJAG_01837":null,"SJAG_02169":null,"SJAG_02189":null,"SJAG_02332":null,"SJAG_02336":null,"SJAG_02342":null,"SJAG_02379":null,"SJAG_02380":null,"SJAG_02433":null,"SJAG_02451":null,"SJAG_02498":null,"SJAG_02592":null,"SJAG_02812":null,"SJAG_02990":null,"SJAG_03048":null,"SJAG_03126":null,"SJAG_03137":null,"SJAG_03342":null,"SJAG_03353":null,"SJAG_03421":null,"SJAG_03438":null,"SJAG_03453":null,"SJAG_03581":null,"SJAG_03624":null,"SJAG_03631":null,"SJAG_03681":null,"SJAG_03704":null,"SJAG_03812":null,"SJAG_03851":null,"SJAG_03936":null,"SJAG_03957":null,"SJAG_04259":null,"SJAG_04312":null,"SJAG_04468":null,"SJAG_04509":null,"SJAG_04573":null,"SJAG_04597":null,"SJAG_04666":null,"SJAG_04776":null,"SJAG_04968":null,"SJAG_05265":null,"SJAG_05289":null,"SJAG_05290":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of cellular component organization","references_by_uniquename":{"GO_REF:0000104":null,"GO_REF:0000107":null},"synonyms":[{"name":"activation of cell organization","type":"narrow"},{"name":"positive regulation of cell organisation","type":"exact"},{"name":"positive regulation of cellular component organization and biogenesis","type":"related"},{"name":"stimulation of cell organization","type":"narrow"},{"name":"up regulation of cell organization","type":"exact"},{"name":"up-regulation of cell organization","type":"exact"},{"name":"upregulation of cell organization","type":"exact"}],"termid":"GO:0051130","terms_by_termid":{"GO:0010845":null,"GO:0010846":null,"GO:0031031":null,"GO:0031117":null,"GO:0031453":null,"GO:0032215":null,"GO:0045807":null,"GO:0045842":null,"GO:0045876":null,"GO:0045899":null,"GO:0045905":null,"GO:0061191":null,"GO:0090053":null,"GO:0090055":null,"GO:0090141":null,"GO:0090297":null,"GO:0110161":null,"GO:0140281":null,"GO:0140499":null,"GO:1901098":null,"GO:1902426":null,"GO:1902846":null,"GO:1902917":null,"GO:1903024":null,"GO:1903373":null,"GO:1903380":null,"GO:1903473":null,"GO:1903501":null,"GO:1904595":null,"GO:1905561":null,"GO:2000786":null,"GO:2001178":null}}


id: GO:0042761
data:
  {"annotated_genes":["SJAG_02885","SJAG_01356","SJAG_01458","SJAG_02717","SJAG_01300"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[88985,91431,102973,105377,110813],"is_not":false,"summary":null,"term":"GO:0042761"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of a very long-chain fatty acid. A very long-chain fatty acid has an aliphatic tail containing more than 22 carbons.","definition_xrefs":["PMID:7744868"],"direct_ancestors":[{"relation_name":"is_a","term_name":"very long-chain fatty acid metabolic process","termid":"GO:0000038"},{"relation_name":"is_a","term_name":"fatty acid biosynthetic process","termid":"GO:0006633"}],"gene_count":5,"genes_by_uniquename":{"SJAG_01300":null,"SJAG_01356":null,"SJAG_01458":null,"SJAG_02717":null,"SJAG_02885":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006629","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"very long-chain fatty acid biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:PWY-5080"],"synonyms":[{"name":"very-long-chain fatty acid anabolism","type":"exact"},{"name":"very-long-chain fatty acid biosynthesis","type":"exact"},{"name":"very-long-chain fatty acid biosynthetic process","type":"exact"},{"name":"very-long-chain fatty acid formation","type":"exact"},{"name":"very-long-chain fatty acid synthesis","type":"exact"}],"termid":"GO:0042761","terms_by_termid":{"GO:0042761":null}}


id: MONDO:0010233
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"periventricular nodular heterotopia","termid":"MONDO:0020341"}],"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":"heterotopia, periventricular, X-linked dominant","secondary_identifiers":["GARD:7371","ICD9:742.4","OMIM:300049","MEDGEN:376309","SCTID:448227009","UMLS:C1848213"],"synonyms":[{"name":"BPNH","type":"related"},{"name":"NHBP","type":"related"},{"name":"PVNH1","type":"related"},{"name":"X-linked periventricular heterotopia","type":"related"},{"name":"bilateral periventricular nodular heterotopia","type":"related"},{"name":"heterotopia familial nodular","type":"related"},{"name":"heterotopia periventricular X-linked dominant","type":"related"},{"name":"heterotopia, familial nodular","type":"related"},{"name":"heterotopia, periventricular nodular, with Frontometaphyseal dysplasia","type":"related"},{"name":"heterotopia, periventricular, 1, X-linked dominant","type":"exact"},{"name":"heterotopia, periventricular, Ehlers-Danlos variant","type":"exact"},{"name":"heterotopia, periventricular, X-linked dominant","type":"exact"},{"name":"nodular heterotopia bilateral periventricular","type":"related"},{"name":"nodular heterotopia, bilateral periventricular","type":"related"},{"name":"periventricular nodular heterotopia 1","type":"related"},{"name":"periventricular nodular heterotopia 4","type":"related"},{"name":"periventricular nodular heterotopia 4, formerly","type":"related"}],"termid":"MONDO:0010233","xrefs":{"Monarch":{"xref_id":"0010233"}}}


id: MONDO:0003969
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Disorders related or resulting from use of amphetamines.","definition_xrefs":["MESH:D019969"],"direct_ancestors":[{"relation_name":"is_a","term_name":"substance abuse","termid":"MONDO:0002491"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amphetamine abuse","secondary_identifiers":["ICD9:305.70","SCTID:84758004","UMLS:C0236807","icd11.foundation:879494155","ICD9:305.7","MEDGEN:66744","DOID:670"],"termid":"MONDO:0003969","xrefs":{"Monarch":{"xref_id":"0003969"}}}


id: PR:O94354
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An argininosuccinate synthase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO02459"],"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":"argininosuccinate synthase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC428.05c","secondary_identifiers":["UniProtKB:O94354"],"synonyms":[{"name":"Spom972h-ASS1","type":"exact"},{"name":"citrulline--aspartate ligase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94354"}


id: GO:0043036
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Plant storage body for amylose and amylopectin, 1-100um in diameter. Also contains small amounts of enzymes, amino acids, lipids and nucleic acids. The shape of the grain varies widely amongst species, but is often spherical or disk-shaped.","definition_xrefs":["PMID:11217978","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"plastid","termid":"GO:0009536"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0005737"],"is_obsolete":false,"name":"starch grain","synonyms":[{"name":"starch granule","type":"exact"}],"termid":"GO:0043036"}


id: PBO:0068392
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring finger protein 212B","termid":"PBO:0068392"}


id: GO:1904603
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of advanced glycation end-product receptor activity.","definition_xrefs":["PMID:16503878","GO_REF:0000059","GOC:krc","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of advanced glycation end-product receptor activity (obsolete GO:1904603)","synonyms":[{"name":"regulation of AGE receptor activity","type":"exact"},{"name":"regulation of RAGE activity","type":"exact"}],"termid":"GO:1904603"}


id: PBO:0081651
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 576","termid":"PBO:0081651"}


id: PBO:0066236
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA binding motif protein 43 pseudogene 1","termid":"PBO:0066236"}


id: GO:0009223
data:
  {"annotated_genes":["SJAG_04487"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[98492],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046081"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of a pyrimidine deoxyribonucleotide, a compound consisting of nucleoside (a pyrimidine base linked to a deoxyribose sugar) esterified with a phosphate group at either the 3' or 5'-hydroxyl group of the sugar.","definition_xrefs":["ISBN:0198506732","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine nucleotide catabolic process","termid":"GO:0006244"},{"relation_name":"is_a","term_name":"pyrimidine deoxyribonucleotide metabolic process","termid":"GO:0009219"},{"relation_name":"is_a","term_name":"deoxyribonucleotide catabolic process","termid":"GO:0009264"},{"relation_name":"is_a","term_name":"deoxyribose phosphate catabolic process","termid":"GO:0046386"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04487":null},"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:0055086","GO:0044281"],"is_obsolete":false,"name":"pyrimidine deoxyribonucleotide catabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"pyrimidine deoxyribonucleotide breakdown","type":"exact"},{"name":"pyrimidine deoxyribonucleotide catabolism","type":"exact"},{"name":"pyrimidine deoxyribonucleotide degradation","type":"exact"}],"termid":"GO:0009223","terms_by_termid":{"GO:0046081":null}}


id: GO:0032179
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The slender tubular outgrowth first produced by most spores in germination.","definition_xrefs":["ISBN:0877799148"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"}],"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":"germ tube","secondary_identifiers":["Wikipedia:Germ_tube"],"termid":"GO:0032179"}


id: GO:0060754
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency or extent of mast cell chemotaxis. Mast cell chemotaxis is the movement of a mast cell in response to an external stimulus.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of leukocyte chemotaxis","termid":"GO:0002690"},{"relation_name":"is_a","term_name":"regulation of mast cell chemotaxis","termid":"GO:0060753"},{"relation_name":"positively_regulates","term_name":"mast cell chemotaxis","termid":"GO:0002551"}],"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 mast cell chemotaxis","termid":"GO:0060754"}


id: PBO:0062169
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 4 subfamily K member 12 pseudogene","termid":"PBO:0062169"}


id: PBO:0049363
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"general transcription factor IIi pseudogene 22","termid":"PBO:0049363"}


id: PBO:0066565
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rhomboid 5 homolog 1","termid":"PBO:0066565"}


id: GO:0034835
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2-mercaptobenzothiazole + 1/2 O2 = 6-hydroxy-2-mercaptobenzothiazole.","definition_xrefs":["UM-BBD_reactionID:r1178"],"gene_count":0,"genotype_count":0,"name":"obsolete 2-mercaptobenzothiazole monooxygenase activity (obsolete GO:0034835)","termid":"GO:0034835"}


id: PBO:0082600
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Clathrin-coated vesicle component, regulator of endocytosis; copurifies with the DSC ubiquitin ligase complex; UBX (ubiquitin regulatory X) domain-containing protein that interacts with Cdc48p; required for efficient clathrin-mediated endocytosis; ortholog of fission yeast Ucp10","termid":"PBO:0082600"}


id: PBO:0074624
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, H/ACA box 22","termid":"PBO:0074624"}


id: GO:0060019
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which neuroepithelial cells of the neural tube give rise to radial glial cells, specialized bipotential progenitors cells of the brain. Differentiation includes the processes involved in commitment of a cell to a specific fate.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glial cell differentiation","termid":"GO:0010001"}],"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":"radial glial cell differentiation","termid":"GO:0060019"}


id: GO:0106069
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A SUMO-E3 ligase complex capable of promoting synapsis, the meiotic cell cycle process where side by side pairing and physical juxtaposition of homologous chromosomes is created during meiotic prophase.","definition_xrefs":["PMID:16847351"],"direct_ancestors":[{"relation_name":"is_a","term_name":"SUMO ligase complex","termid":"GO:0106068"},{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"},{"relation_name":"part_of","term_name":"condensed nuclear chromosome","termid":"GO:0000794"}],"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":"part_of","termid":"GO:0005694"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005634","GO:0032991","GO:0005575","GO:0005694"],"is_obsolete":false,"name":"synapsis initiation complex","termid":"GO:0106069"}


id: GO:0039723
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in which a symbiont stops, prevents, or reduces a cytoplasmic pattern recognition receptor signaling pathway in a host organism by reducing the activity of a host serine/threonine kinase TBK1.","definition_xrefs":["PMID:34084167","PMID:22171259"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated suppression of cytoplasmic pattern recognition receptor signaling pathway","termid":"GO:0039537"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated suppression of host cytoplasmic pattern recognition receptor signaling pathway via inhibition of TBK1 activity","secondary_identifiers":["VZ:4477"],"synonyms":[{"name":"inhibition of host TBK1 by virus","type":"related"},{"name":"suppression by virus of host TBK1 activity","type":"related"},{"name":"suppression by virus of host viral-induced cytoplasmic pattern recognition receptor signaling pathway via inhibition of TBK1 activity","type":"narrow"},{"name":"symbiont-mediated suppression of host TKB signaling","type":"related"}],"termid":"GO:0039723"}


id: MONDO:1011421
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Complement component 3 deficiency that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune system disorder, non-human animal","termid":"MONDO:0700106"},{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"complement component 3 deficiency, non-human animal","secondary_identifiers":["OMIA:000155"],"synonyms":[{"name":"C3 deficiency","type":"exact"}],"termid":"MONDO:1011421","xrefs":{"Monarch":{"xref_id":"1011421"}}}


id: SO:0000625
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A regulatory region which upon binding of transcription factors, suppress the transcription of the gene or genes they control.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cis_regulatory_module","termid":"SO:0000727"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"silencer","secondary_identifiers":["http://en.wikipedia.org/wiki/Silencer_(DNA)"],"synonyms":[{"name":"INSDC_feature:regulatory","type":"broad"},{"name":"INSDC_qualifier:silencer","type":"exact"}],"termid":"SO:0000625"}


id: GO:1903789
data:
  {"annotated_genes":["SJAG_03970","SJAG_03591","SJAG_02605","SJAG_00991","SJAG_05346"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[87565],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905533"},{"annotations":[92812,91226,110030,98379],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905589"},{"annotations":[92813,91227,98380],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905534"},{"annotations":[92814],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905626"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of amino acid transmembrane transport.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:16115814"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transmembrane transport","termid":"GO:0034762"},{"relation_name":"is_a","term_name":"regulation of amino acid transport","termid":"GO:0051955"},{"relation_name":"regulates","term_name":"amino acid transmembrane transport","termid":"GO:0003333"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00991":null,"SJAG_02605":null,"SJAG_03591":null,"SJAG_03970":null,"SJAG_05346":null},"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:0008150","GO:0006810","GO:0055085"],"is_obsolete":false,"name":"regulation of amino acid transmembrane transport","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"regulation of amino acid membrane transport","type":"exact"}],"termid":"GO:1903789","terms_by_termid":{"GO:1905533":null,"GO:1905534":null,"GO:1905589":null,"GO:1905626":null}}


id: PBO:0076406
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TATA-box binding protein associated factor 4","termid":"PBO:0076406"}


id: MONDO:0000395
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A physical or cognitive mental abnormality caused by maternal alcohol consumption and its toxic effect on the developing embryo during pregnancy.","definition_xrefs":["NCIT:C92727"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fetal alcohol spectrum disorder","termid":"MONDO:0000408"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alcohol-related birth defect","secondary_identifiers":["UMLS:C3146244","MEDGEN:459973","DOID:0050668"],"synonyms":[{"name":"ARBD","type":"exact"},{"name":"alcohol related birth defect","type":"exact"}],"termid":"MONDO:0000395","xrefs":{"Monarch":{"xref_id":"0000395"}}}


id: PBO:0034483
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_spatial_extent_of_histone_H2B-K119_ubiquitination_at_double-strand_break_site","termid":"PBO:0034483"}


id: GO:0034917
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2-methylhex-2-enoyl-CoA + H2O = 3-hydroxy-2-methylhexanoyl-CoA.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete 2-methylhex-2-enoyl-CoA hydratase activity (obsolete GO:0034917)","termid":"GO:0034917"}


id: GO:0046005
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the duration or quality of rapid eye movement (REM) sleep.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of circadian sleep/wake cycle, REM sleep","termid":"GO:0042320"},{"relation_name":"is_a","term_name":"positive regulation of circadian sleep/wake cycle, sleep","termid":"GO:0045938"},{"relation_name":"positively_regulates","term_name":"circadian sleep/wake cycle, REM sleep","termid":"GO:0042747"}],"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 circadian sleep/wake cycle, REM sleep","synonyms":[{"name":"activation of circadian sleep/wake cycle, REM sleep","type":"narrow"},{"name":"positive regulation of REM sleep","type":"exact"},{"name":"stimulation of circadian sleep/wake cycle, REM sleep","type":"narrow"},{"name":"up regulation of circadian sleep/wake cycle, REM sleep","type":"exact"},{"name":"up-regulation of circadian sleep/wake cycle, REM sleep","type":"exact"},{"name":"upregulation of circadian sleep/wake cycle, REM sleep","type":"exact"}],"termid":"GO:0046005"}


id: GO:1900344
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of methane biosynthetic process from dimethyl sulfide.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of sulfur metabolic process","termid":"GO:0051176"},{"relation_name":"is_a","term_name":"regulation of methane biosynthetic process from dimethyl sulfide","termid":"GO:1900342"},{"relation_name":"is_a","term_name":"positive regulation of alkane biosynthetic process","termid":"GO:1901579"},{"relation_name":"is_a","term_name":"positive regulation of cellular respiration","termid":"GO:1901857"},{"relation_name":"positively_regulates","term_name":"methane biosynthetic process from dimethyl sulfide","termid":"GO:2001131"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006790"},{"rel_name":"regulates","termid":"GO:0006091"},{"rel_name":"regulates","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006091"}],"interesting_parent_ids":["GO:0008150","GO:0006790","GO:0006091"],"is_obsolete":false,"name":"positive regulation of methane biosynthetic process from dimethyl sulfide","synonyms":[{"name":"activation of methane biosynthetic process from dimethyl sulfide","type":"narrow"},{"name":"up regulation of methane biosynthetic process from dimethyl sulfide","type":"exact"},{"name":"up-regulation of methane biosynthetic process from dimethyl sulfide","type":"exact"},{"name":"upregulation of methane biosynthetic process from dimethyl sulfide","type":"exact"}],"termid":"GO:1900344"}


id: GO:1905294
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of neural crest cell differentiation.","definition_xrefs":["GO_REF:0000058","GOC:BHF","PMID:15073157","GOC:rl","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"is_a","term_name":"regulation of neural crest cell differentiation","termid":"GO:1905292"},{"relation_name":"is_a","term_name":"positive regulation of stem cell differentiation","termid":"GO:2000738"},{"relation_name":"positively_regulates","term_name":"neural crest cell differentiation","termid":"GO:0014033"}],"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 neural crest cell differentiation","synonyms":[{"name":"activation of neural crest cell differentiation","type":"narrow"},{"name":"up regulation of neural crest cell differentiation","type":"exact"},{"name":"up-regulation of neural crest cell differentiation","type":"exact"},{"name":"upregulation of neural crest cell differentiation","type":"exact"}],"termid":"GO:1905294"}


id: GO:0000793
data:
  {"annotated_genes":["SJAG_03161","SJAG_03619","SJAG_01775","SJAG_05266","SJAG_04076","SJAG_01082","SJAG_02771","SJAG_03437","SJAG_05273","SJAG_02336","SJAG_04255","SJAG_02451","SJAG_04745","SJAG_03438","SJAG_00213","SJAG_00918","SJAG_00666","SJAG_03698","SJAG_03217","SJAG_05019","SJAG_03867","SJAG_03989","SJAG_01546","SJAG_03683","SJAG_03540","SJAG_01297","SJAG_04884","SJAG_02664","SJAG_02652","SJAG_01836","SJAG_02513","SJAG_04412","SJAG_03048","SJAG_01211","SJAG_02346","SJAG_02814","SJAG_04259","SJAG_00646","SJAG_01224","SJAG_02807","SJAG_03436","SJAG_01067","SJAG_03220","SJAG_05220","SJAG_03702","SJAG_01228","SJAG_03418","SJAG_01831","SJAG_05319","SJAG_02545","SJAG_00684","SJAG_04581","SJAG_00697","SJAG_05333","SJAG_04303","SJAG_05323","SJAG_03682","SJAG_03926","SJAG_04950","SJAG_04177","SJAG_00418","SJAG_04699","SJAG_01330","SJAG_01410","SJAG_01613","SJAG_01928","SJAG_01677","SJAG_02731","SJAG_01278","SJAG_00794","SJAG_03026","SJAG_03681","SJAG_01601","SJAG_00082","SJAG_00172","SJAG_01837","SJAG_02624","SJAG_01605","SJAG_04126","SJAG_04748","SJAG_03843","SJAG_04038","SJAG_04932","SJAG_02267","SJAG_02761","SJAG_03832","SJAG_03327","SJAG_01805","SJAG_01371","SJAG_02490","SJAG_04696","SJAG_00307","SJAG_03916","SJAG_04040","SJAG_04623","SJAG_05321","SJAG_07002","SJAG_00207","SJAG_01332","SJAG_01776","SJAG_04841","SJAG_00350"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[115404,116553],"is_not":false,"summary":null,"term":"GO:0000793"},{"annotations":[92001,90907,98682],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030896"},{"annotations":[89214,93783,109847,109800,107267,100009,101565,106984,112605,104964,94177,107303,89159,90397,98111,111670,105035,90456,98762,107223,115416,112713,94786,89540,98614,90747,101933,113270,113625,87280,116352,108626,95041],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000779"},{"annotations":[90398,88634,92354,100038,98552],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000794"},{"annotations":[89216,108369,116409,113589,100011,98113,90458,106986,109384,88616],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0042729"},{"annotations":[113626,116155,105037,89512,109801,115392,111671,98764,89160,112714,113986],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000939"},{"annotations":[88832,96250,111536,111672,112606,113987,118919,113627,116156,112874,107730,97393,90258,112715,101934,111380,101848,117632,118147,115049,118348,103385,94787,105802,104965,100827,113044,108699,89513,109396,93681,90459,114575,94246,93267,118815,89459,98765,96765,109802,87473,98708,95042,98114,108628,101291,115417,118183,105850,89161,113271,99865,114057,99627,100012,109848,94179,106987],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000776"},{"annotations":[113272,100828],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0180019"},{"annotations":[109140,90954,94231,110613,115031,104365,89812,109045,88534],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030998"},{"annotations":[98766,109803,109849,95043],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000444"},{"annotations":[105851,112607,97394,93785,113628,89162,105038,94180,89514,113045,114058],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031511"},{"annotations":[111172,87475],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0033551"},{"annotations":[101935,115418,108629,94789],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031262"},{"annotations":[118154,98119,113273,113991,95044,101937,89220,109805,115420,99872],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000940"},{"annotations":[117362,87516,88528,116735,105793,117087,89227,110978],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030915"}]},"cv_name":"cellular_component","definition":"A highly compacted molecule of DNA and associated proteins resulting in a cytologically distinct structure.","definition_xrefs":["GOC:elh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome","termid":"GO:0005694"}],"gene_count":102,"genes_by_uniquename":{"SJAG_00082":null,"SJAG_00172":null,"SJAG_00207":null,"SJAG_00213":null,"SJAG_00307":null,"SJAG_00350":null,"SJAG_00418":null,"SJAG_00646":null,"SJAG_00666":null,"SJAG_00684":null,"SJAG_00697":null,"SJAG_00794":null,"SJAG_00918":null,"SJAG_01067":null,"SJAG_01082":null,"SJAG_01211":null,"SJAG_01224":null,"SJAG_01228":null,"SJAG_01278":null,"SJAG_01297":null,"SJAG_01330":null,"SJAG_01332":null,"SJAG_01371":null,"SJAG_01410":null,"SJAG_01546":null,"SJAG_01601":null,"SJAG_01605":null,"SJAG_01613":null,"SJAG_01677":null,"SJAG_01775":null,"SJAG_01776":null,"SJAG_01805":null,"SJAG_01831":null,"SJAG_01836":null,"SJAG_01837":null,"SJAG_01928":null,"SJAG_02267":null,"SJAG_02336":null,"SJAG_02346":null,"SJAG_02451":null,"SJAG_02490":null,"SJAG_02513":null,"SJAG_02545":null,"SJAG_02624":null,"SJAG_02652":null,"SJAG_02664":null,"SJAG_02731":null,"SJAG_02761":null,"SJAG_02771":null,"SJAG_02807":null,"SJAG_02814":null,"SJAG_03026":null,"SJAG_03048":null,"SJAG_03161":null,"SJAG_03217":null,"SJAG_03220":null,"SJAG_03327":null,"SJAG_03418":null,"SJAG_03436":null,"SJAG_03437":null,"SJAG_03438":null,"SJAG_03540":null,"SJAG_03619":null,"SJAG_03681":null,"SJAG_03682":null,"SJAG_03683":null,"SJAG_03698":null,"SJAG_03702":null,"SJAG_03832":null,"SJAG_03843":null,"SJAG_03867":null,"SJAG_03916":null,"SJAG_03926":null,"SJAG_03989":null,"SJAG_04038":null,"SJAG_04040":null,"SJAG_04076":null,"SJAG_04126":null,"SJAG_04177":null,"SJAG_04255":null,"SJAG_04259":null,"SJAG_04303":null,"SJAG_04412":null,"SJAG_04581":null,"SJAG_04623":null,"SJAG_04696":null,"SJAG_04699":null,"SJAG_04745":null,"SJAG_04748":null,"SJAG_04841":null,"SJAG_04884":null,"SJAG_04932":null,"SJAG_04950":null,"SJAG_05019":null,"SJAG_05220":null,"SJAG_05266":null,"SJAG_05273":null,"SJAG_05319":null,"SJAG_05321":null,"SJAG_05323":null,"SJAG_05333":null,"SJAG_07002":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0005694"}],"interesting_parent_ids":["GO:0005575","GO:0005694"],"is_obsolete":false,"name":"condensed chromosome","references_by_uniquename":{"GO_REF:0000107":null,"PMID:21802294":null,"PMID:32109380":null},"synonyms":[{"name":"cytoplasmic mitotic chromosome","type":"related"},{"name":"metaphase chromosome","type":"related"},{"name":"mitotic chromosome","type":"related"}],"termid":"GO:0000793","terms_by_termid":{"GO:0000444":null,"GO:0000776":null,"GO:0000779":null,"GO:0000793":null,"GO:0000794":null,"GO:0000939":null,"GO:0000940":null,"GO:0030896":null,"GO:0030915":null,"GO:0030998":null,"GO:0031262":null,"GO:0031511":null,"GO:0033551":null,"GO:0042729":null,"GO:0180019":null}}


id: FYPO:0006104
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the occurrence of retrotransposon integration is decreased.","definition_xrefs":["PomBase:mah","PMID:26358720"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal transposition","termid":"FYPO:0000591"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"decreased retrotransposon integration","synonyms":[{"name":"decreased retrotransposon integration during mitotic cell cycle","type":"related"},{"name":"decreased retrotransposon integration during vegetative growth","type":"exact"},{"name":"decreased transposon integration involved in RNA-mediated transposition","type":"exact"},{"name":"reduced retrotransposon integration","type":"exact"}],"termid":"FYPO:0006104"}


id: GO:0055041
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: cyclopentanol + NAD+ = cyclopentanone + H+ + NADH.","definition_xrefs":["RHEA:11728","EC:1.1.1.163"],"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:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"cyclopentanol dehydrogenase activity","secondary_identifiers":["KEGG_REACTION:R02553","MetaCyc:CYCLOPENTANOL-DEHYDROGENASE-RXN"],"synonyms":[{"name":"cyclopentanol:NAD+ oxidoreductase activity","type":"related"},{"name":"cyclopentanol:NADP+ oxidoreductase activity","type":"related"}],"termid":"GO:0055041"}


id: PBO:0034379
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-lumen_of","termid":"PBO:0034379"}


id: MONDO:1010698
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any glycogen storage disease that occurs in dogs due to a mutation in the G6PC1 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycogen storage disease, non-human animal","termid":"MONDO:1011419"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycogen storage disease, G6PC1-related, dog","secondary_identifiers":["OMIA:000418-9615"],"synonyms":[{"name":"glycogen storage disease Ia, dog","type":"related"}],"termid":"MONDO:1010698","xrefs":{"Monarch":{"xref_id":"1010698"}}}


id: PBO:0055932
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat containing 38","termid":"PBO:0055932"}


id: FYPO:0001225
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which a cell contains a single septum.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"septated vegetative cell","termid":"FYPO:0002342"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"monoseptate","synonyms":[{"name":"monoseptate during mitotic cell cycle","type":"related"},{"name":"monoseptate during vegetative growth","type":"exact"}],"termid":"FYPO:0001225"}


id: PBO:0088525
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mRNA cleavage and polyadenylation specificity factor complex zinc finger subunit Yth1","termid":"PBO:0088525"}


id: PBO:0086131
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein required for initiation of G0 program; prevents degradation of nutrient-regulated mRNAs via the 5'-3' mRNA decay pathway; phosphorylated by Rim15p; GFP protein localizes to the cytoplasm and nucleus; IGO2 has a paralog, IGO1, that arose from the whole genome duplication","termid":"PBO:0086131"}


id: PBO:0076785
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trans-2,3-enoyl-CoA reductase","termid":"PBO:0076785"}


id: PATO:0000294
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000294 process value (obsolete PATO:0000294)","termid":"PATO:0000294"}


id: PBQ:0000003
data:
  {"annotation_feature_type":"gene","cv_name":"pb_quiescence","definition":"Cell quiescence, i.e. a specialized resting state in which the cells do not grow or divide, and the gene expression pattern changes globally, that a cell enters following cell cycle arrest in G1 due to nitrogen limitation. In some cell types or under certain conditions, cellular metabolism may proceed.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell quiescence following G1 arrest","termid":"PBQ:0000002"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell quiescence following G1 arrest due to nitrogen limitation","synonyms":[{"name":"cellular quiescence following G1 arrest due to nitrogen limitation","type":"exact"},{"name":"quiescence following G1 arrest due to nitrogen limitation","type":"broad"}],"termid":"PBQ:0000003"}


id: FYECO:0000056
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which 3'5'-cyclic AMP was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["CHEBI:17489"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ 3,5-cyclic AMP","termid":"FYECO:0000056"}


id: PR:O14043
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- csc4 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14043"],"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 C2C4.10c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC2C4.10c","synonyms":[{"name":"Spom972h-csc4","type":"exact"}],"termid":"PR:O14043"}


id: GO:0005805
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete ER-Golgi transport vesicle (obsolete GO:0005805)","synonyms":[{"name":"ER-Golgi transport vesicle","type":"exact"}],"termid":"GO:0005805"}


id: GO:0097039
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A protein ubiquitination process in which a linear polymer of ubiquitin, formed by the amino-terminal methionine (M1) of one ubiquitin molecule and by the carboxy-terminal glycine (G76) of the next, is added to a protein.","definition_xrefs":["PMID:21455173","PMID:21455180","GOC:jsg","PMID:21455181","PMID:31998699","GOC:sp"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein polyubiquitination","termid":"GO:0000209"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0070647"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0070647","GO:0008150"],"is_obsolete":false,"name":"protein linear polyubiquitination","synonyms":[{"name":"M1 linkage","type":"narrow"}],"termid":"GO:0097039"}


id: PBO:0088685
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein phosphatase PP4 catalytic subunit Pph3","termid":"PBO:0088685"}


id: PBO:0034451
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_transcription_from_CRE_promoter_during_cellular_response_to_miconazole","termid":"PBO:0034451"}


id: MONDO:0018311
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acromelanosis is a congenital hyperpigmentation of the skin usually located on the acral areas of the fingers and toes. It is mostly observed in newborns or during the first years of life.","definition_xrefs":["Orphanet:39"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hyperpigmentation of the skin","termid":"MONDO:0019289"}],"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":"acromelanosis","secondary_identifiers":["MEDGEN:98038","GARD:4500","UMLS:C0406779","SCTID:239089006","ICD9:709.09"],"synonyms":[{"name":"progressive acromelanosis","type":"related"}],"termid":"MONDO:0018311","xrefs":{"Monarch":{"xref_id":"0018311"}}}


id: GO:0019982
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to interleukin-7.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"growth factor binding","termid":"GO:0019838"},{"relation_name":"is_a","term_name":"cytokine binding","termid":"GO:0019955"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"interleukin-7 binding","synonyms":[{"name":"IL-7 binding","type":"exact"}],"termid":"GO:0019982"}


id: MONDO:0032780
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":"hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities","secondary_identifiers":["MEDGEN:1672905","UMLS:C5193124","OMIM:618493","Orphanet:656273"],"synonyms":[{"name":"HIDEA","type":"related"},{"name":"HYPOTONIA, HYPOVENTILATION, IMPAIRED INTELLECTUAL DEVELOPMENT, DYSAUTONOMIA, EPILEPSY, AND EYE ABNORMALITIES","type":"related"}],"termid":"MONDO:0032780","xrefs":{"Monarch":{"xref_id":"0032780"}}}


id: MOD:02074
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that contains an L-lysine residue coordinated to one or more metal atoms or metal clusters.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-lysine residue","termid":"MOD:00912"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metal or metal cluster coordinated L-lysine residue","termid":"MOD:02074"}


id: MONDO:0010317
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, with or without seizures, arx-related","secondary_identifiers":["DOID:0112021","OMIM:300419","GARD:5614","MESH:C563150","MEDGEN:208681","MESH:C564502","UMLS:C0796244"],"synonyms":[{"name":"ARX-related intellectual disability","type":"related"},{"name":"MRX52","type":"related"},{"name":"MRXARX","type":"related"},{"name":"intellectual developmental disorder, X-linked 29, X-linked recessive","type":"exact"},{"name":"intellectual disability, X-linked 29","type":"related"},{"name":"intellectual disability, X-linked 32","type":"related"},{"name":"intellectual disability, X-linked 33","type":"related"},{"name":"intellectual disability, X-linked 38","type":"related"},{"name":"intellectual disability, X-linked 43","type":"related"},{"name":"intellectual disability, X-linked 52","type":"related"},{"name":"intellectual disability, X-linked 54","type":"related"},{"name":"intellectual disability, X-linked 76","type":"related"},{"name":"intellectual disability, X-linked 87","type":"related"},{"name":"intellectual disability, X-linked, with or without seizures, ARX-related","type":"related"},{"name":"intellectual disability, X-linked, with or without seizures, arx-RELATED","type":"related"},{"name":"mental retardation, X-linked 29","type":"related"},{"name":"mental retardation, X-linked 32","type":"related"},{"name":"mental retardation, X-linked 33","type":"related"},{"name":"mental retardation, X-linked 38","type":"related"},{"name":"mental retardation, X-linked 43","type":"related"},{"name":"mental retardation, X-linked 52","type":"related"},{"name":"mental retardation, X-linked 54","type":"related"},{"name":"mental retardation, X-linked 76","type":"related"},{"name":"mental retardation, X-linked 87","type":"related"},{"name":"mental retardation, X-linked, with or without seizures, arx-RELATED","type":"related"},{"name":"mental retardation, X-linked, with or without seizures, arx-related","type":"related"}],"termid":"MONDO:0010317","xrefs":{"Monarch":{"xref_id":"0010317"}}}


id: PBO:0069622
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 899, pseudogene","termid":"PBO:0069622"}


id: PBO:0044173
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"catenin alpha 2","termid":"PBO:0044173"}


id: MONDO:0016038
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare slow-growing benign neoplasm arising from the soft tissues in children. It is a poorly circumscribed tumor characterized by the presence of chondrocyte-like cells, nodular calcification, nuclear palisading, and in some cases osteoclastic giant cells.","definition_xrefs":["NCIT:C4818"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fibroma","termid":"MONDO:0005167"},{"relation_name":"is_a","term_name":"superficial Fibromatosis","termid":"MONDO:0016037"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcified aponeurotic fibroma","secondary_identifiers":["MEDGEN:107818","GARD:20329","Orphanet:199260","UMLS:C0553647","SCTID:703614006"],"synonyms":[{"name":"Juvenile aponeurotic fibroma","type":"exact"},{"name":"Juvenile aponeurotic fibrosis","type":"exact"},{"name":"Keasby tumor","type":"exact"},{"name":"Keasby tumour","type":"exact"},{"name":"calcifying aponeurotic fibroma","type":"related"},{"name":"juvenile aponeurotic fibromatosis","type":"exact"}],"termid":"MONDO:0016038","xrefs":{"Monarch":{"xref_id":"0016038"}}}


id: PBO:0057894
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3198-1","termid":"PBO:0057894"}


id: PBO:0053771
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 1016","termid":"PBO:0053771"}


id: MONDO:0004832
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign smooth muscle neoplasm arising from the lower part of the esophagus. It is the most common mesenchymal neoplasm of the esophagus. Dysphagia is a frequent clinical symptom.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leiomyoma","termid":"MONDO:0001572"},{"relation_name":"is_a","term_name":"benign neoplasm of esophagus","termid":"MONDO:0021459"}],"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":"esophagus leiomyoma","secondary_identifiers":["MEDGEN:65947","UMLS:C0238114","DOID:960","NCIT:C3866","SCTID:276805005"],"synonyms":[{"name":"esophageal leiomyoma","type":"exact"},{"name":"esophagus leiomyoma","type":"exact"},{"name":"leiomyoma of esophagus","type":"exact"},{"name":"leiomyoma of oesophagus","type":"exact"},{"name":"leiomyoma of the esophagus","type":"exact"},{"name":"leiomyoma of the oesophagus","type":"exact"}],"termid":"MONDO:0004832","xrefs":{"Monarch":{"xref_id":"0004832"}}}


id: PBO:0079578
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin conjugating enzyme E2 B","termid":"PBO:0079578"}


id: GO:1903664
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of asexual reproduction.","definition_xrefs":["PMID:24390142","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of reproductive process","termid":"GO:2000241"},{"relation_name":"regulates","term_name":"asexual reproduction","termid":"GO:0019954"}],"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 asexual reproduction","termid":"GO:1903664"}


id: PR:O14260
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC7D4.03c gene.","definition_xrefs":["UniProtKB:O14260","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":"UPF0592 membrane protein C7D4.03c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC7D4.03c","synonyms":[{"name":"Spom972h-SPAC7D4.03c","type":"exact"}],"termid":"PR:O14260"}


id: GO:0033972
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: amidinoproclavaminate + H2O = proclavaminate + urea.","definition_xrefs":["EC:3.5.3.22","RHEA:17001"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amidines","termid":"GO:0016813"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016810","GO:0016787","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"proclavaminate amidinohydrolase activity","secondary_identifiers":["KEGG_REACTION:R05357","MetaCyc:3.5.3.22-RXN"],"synonyms":[{"name":"PAH","type":"related"},{"name":"proclavaminate amidino hydrolase activity","type":"related"},{"name":"proclavaminic acid amidino hydrolase activity","type":"related"}],"termid":"GO:0033972"}


id: PBO:0073683
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sirtuin 5","termid":"PBO:0073683"}


id: GO:0036211
data:
  {"annotated_genes":["SJAG_03656","SJAG_02056","SJAG_03325","SJAG_01418","SJAG_04948","SJAG_03676","SJAG_04363","SJAG_00235","SJAG_05977","SJAG_00924","SJAG_00831","SJAG_02783","SJAG_00747","SJAG_02764","SJAG_01389","SJAG_02163","SJAG_04544","SJAG_00033","SJAG_04127","SJAG_05297","SJAG_03932","SJAG_03733","SJAG_01018","SJAG_00604","SJAG_03555","SJAG_03188","SJAG_00183","SJAG_00776","SJAG_04316","SJAG_03032","SJAG_00720","SJAG_03311","SJAG_01950","SJAG_00554","SJAG_01264","SJAG_01972","SJAG_01021","SJAG_04728","SJAG_00727","SJAG_01776","SJAG_02102","SJAG_04085","SJAG_04770","SJAG_04821","SJAG_04095","SJAG_01006","SJAG_05348","SJAG_03150","SJAG_01276","SJAG_04231","SJAG_03333","SJAG_04952","SJAG_00251","SJAG_02341","SJAG_03950","SJAG_01491","SJAG_03871","SJAG_00598","SJAG_05219","SJAG_03149","SJAG_03764","SJAG_01858","SJAG_00394","SJAG_00437","SJAG_02648","SJAG_00334","SJAG_02519","SJAG_03056","SJAG_04401","SJAG_04090","SJAG_04906","SJAG_02996","SJAG_00816","SJAG_01595","SJAG_04011","SJAG_00878","SJAG_03790","SJAG_01069","SJAG_00615","SJAG_02082","SJAG_02467","SJAG_02503","SJAG_04846","SJAG_03082","SJAG_05032","SJAG_04053","SJAG_03843","SJAG_03330","SJAG_00795","SJAG_04571","SJAG_03616","SJAG_04954","SJAG_03896","SJAG_01302","SJAG_03774","SJAG_01058","SJAG_02903"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[97842,103071,99284,108780,116234,97892,89852,61211,99490,110575,93381,98182,90610,101801,104494,112045],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006488"},{"annotations":[93027],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904380"},{"annotations":[92489,100813,104785,92367,105982,108482,109826,89114,94780,90939],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000338"},{"annotations":[115581,117325,107877,107504,113450,103275,99525,95194,97271,105257,95911,63177,113258],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006486"},{"annotations":[116954,109200,100214,115221,100070,118274,104741,110651],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017183"},{"annotations":[98275,92634,104012,86983,104558,105453,108507,98273,110202,110196,110397,112191,92633,117546,117874,88681,92632,102217,62693,100842,99145,100262,98265,102286,98423,92631,98272,98274],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006487"},{"annotations":[108781,92635,94809,98256,102070,86984,98255,104441,116341,98258,92637,97378,92636,98257,98276,99827,99491,92638,98277,98278,110576,98279,100851,117547],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0018279"},{"annotations":[111809,117889,88724,95972,94082,102371],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045116"},{"annotations":[100263,98266,117548,102218,103584,110197,110203,117875,104013],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006493"},{"annotations":[92516,101040,105454],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035269"},{"annotations":[95693,114143,89072,97248,103977,89229,109049],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016925"},{"annotations":[107899,116692,95476,105350],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032447"}]},"cv_name":"biological_process","definition":"The covalent alteration of one or more amino acids occurring in proteins, peptides and nascent polypeptides (co-translational, post-translational modifications). Includes the modification of charged tRNAs that are destined to occur in a protein (pre-translation modification).","definition_xrefs":["GOC:jl","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein metabolic process","termid":"GO:0019538"},{"relation_name":"is_a","term_name":"macromolecule modification","termid":"GO:0043412"}],"gene_count":97,"genes_by_uniquename":{"SJAG_00033":null,"SJAG_00183":null,"SJAG_00235":null,"SJAG_00251":null,"SJAG_00334":null,"SJAG_00394":null,"SJAG_00437":null,"SJAG_00554":null,"SJAG_00598":null,"SJAG_00604":null,"SJAG_00615":null,"SJAG_00720":null,"SJAG_00727":null,"SJAG_00747":null,"SJAG_00776":null,"SJAG_00795":null,"SJAG_00816":null,"SJAG_00831":null,"SJAG_00878":null,"SJAG_00924":null,"SJAG_01006":null,"SJAG_01018":null,"SJAG_01021":null,"SJAG_01058":null,"SJAG_01069":null,"SJAG_01264":null,"SJAG_01276":null,"SJAG_01302":null,"SJAG_01389":null,"SJAG_01418":null,"SJAG_01491":null,"SJAG_01595":null,"SJAG_01776":null,"SJAG_01858":null,"SJAG_01950":null,"SJAG_01972":null,"SJAG_02056":null,"SJAG_02082":null,"SJAG_02102":null,"SJAG_02163":null,"SJAG_02341":null,"SJAG_02467":null,"SJAG_02503":null,"SJAG_02519":null,"SJAG_02648":null,"SJAG_02764":null,"SJAG_02783":null,"SJAG_02903":null,"SJAG_02996":null,"SJAG_03032":null,"SJAG_03056":null,"SJAG_03082":null,"SJAG_03149":null,"SJAG_03150":null,"SJAG_03188":null,"SJAG_03311":null,"SJAG_03325":null,"SJAG_03330":null,"SJAG_03333":null,"SJAG_03555":null,"SJAG_03616":null,"SJAG_03656":null,"SJAG_03676":null,"SJAG_03733":null,"SJAG_03764":null,"SJAG_03774":null,"SJAG_03790":null,"SJAG_03843":null,"SJAG_03871":null,"SJAG_03896":null,"SJAG_03932":null,"SJAG_03950":null,"SJAG_04011":null,"SJAG_04053":null,"SJAG_04085":null,"SJAG_04090":null,"SJAG_04095":null,"SJAG_04127":null,"SJAG_04231":null,"SJAG_04316":null,"SJAG_04363":null,"SJAG_04401":null,"SJAG_04544":null,"SJAG_04571":null,"SJAG_04728":null,"SJAG_04770":null,"SJAG_04821":null,"SJAG_04846":null,"SJAG_04906":null,"SJAG_04948":null,"SJAG_04952":null,"SJAG_04954":null,"SJAG_05032":null,"SJAG_05219":null,"SJAG_05297":null,"SJAG_05348":null,"SJAG_05977":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"protein modification process","references_by_uniquename":{"GO_REF:0000041":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0006464"],"synonyms":[{"name":"cellular protein modification process","type":"exact"},{"name":"process resulting in protein modification","type":"exact"},{"name":"protein modification","type":"exact"}],"termid":"GO:0036211","terms_by_termid":{"GO:0000338":null,"GO:0006486":null,"GO:0006487":null,"GO:0006488":null,"GO:0006493":null,"GO:0016925":null,"GO:0017183":null,"GO:0018279":null,"GO:0032447":null,"GO:0035269":null,"GO:0045116":null,"GO:1904380":null}}


id: PATO:0000287
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000287 absolute litter size (obsolete PATO:0000287)","termid":"PATO:0000287"}


id: GO:0032177
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Two separate septin rings that are formed from the septin collar at the time of cytokinesis in cells that divide by budding. These two rings are thought to delineate a special compartment in which factors involved in cytokinesis are concentrated.","definition_xrefs":["GOC:krc","PMID:16009555"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular bud neck septin structure","termid":"GO:0000399"},{"relation_name":"is_a","term_name":"cleavage apparatus septin structure","termid":"GO:0032161"},{"relation_name":"is_a","term_name":"split septin rings","termid":"GO:0032176"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005938"}],"interesting_parent_ids":["GO:0005737","GO:0005938","GO:0005575"],"is_obsolete":false,"name":"cellular bud neck split septin rings","termid":"GO:0032177"}


id: GO:0033813
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: acetyl-CoA + deacetylcephalosporin C = cephalosporin C + CoA.","definition_xrefs":["RHEA:23860","EC:2.3.1.175"],"direct_ancestors":[{"relation_name":"is_a","term_name":"C-acyltransferase activity","termid":"GO:0016408"}],"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:0016746"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0016746","GO:0003824"],"is_obsolete":false,"name":"deacetylcephalosporin-C acetyltransferase activity","secondary_identifiers":["KEGG_REACTION:R03064","MetaCyc:2.3.1.175-RXN"],"synonyms":[{"name":"CPC acetylhydrolase activity","type":"related"},{"name":"DAC acetyltransferase activity","type":"related"},{"name":"DAC-AT","type":"related"},{"name":"acetyl coenzyme A:DAC acetyltransferase activity","type":"related"},{"name":"acetyl-CoA:DAC O-acetyltransferase activity","type":"related"},{"name":"acetyl-CoA:DAC acetyltransferase activity","type":"related"},{"name":"acetyl-CoA:deacetylcephalosporin-C O-acetyltransferase activity","type":"related"},{"name":"acetyl-CoA:deacetylcephalosporin-C acetyltransferase activity","type":"related"},{"name":"cefG","type":"related"},{"name":"deacetylcephalosporin C acetyltransferase activity","type":"related"}],"termid":"GO:0033813"}


id: PBO:0076958
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transforming growth factor beta receptor 1","termid":"PBO:0076958"}


id: GO:0102042
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-amino-2,3,7-trideoxy-D-lyxo-hept-6-ulosonic acid + H2O + NAD = 3-dehydroquinate + ammonium + NADH + H+.","definition_xrefs":["RHEA:25956","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-NH2 group of donors, NAD or NADP as acceptor","termid":"GO:0016639"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"dehydroquinate synthase activity","secondary_identifiers":["EC:1.4.1.24","MetaCyc:RXN-10032"],"termid":"GO:0102042"}


id: GO:0070185
data:
  {"annotated_genes":["SJAG_02428"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[97160],"is_not":false,"summary":null,"term":"GO:0070185"}]},"cv_name":"biological_process","definition":"The process of coupling valine to valyl-tRNA in a mitochondrion, catalyzed by valyl-tRNA synthetase. In tRNA aminoacylation, the amino acid is first activated by linkage to AMP and then transferred to either the 2'- or the 3'-hydroxyl group of the 3'-adenosine residue of the tRNA.","definition_xrefs":["GOC:mah","GOC:mcc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"valyl-tRNA aminoacylation","termid":"GO:0006438"},{"relation_name":"is_a","term_name":"tRNA aminoacylation for mitochondrial protein translation","termid":"GO:0070127"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02428":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006399"},{"rel_name":"part_of","termid":"GO:0140053"}],"interesting_parent_ids":["GO:0010467","GO:0006399","GO:0006520","GO:0140053","GO:0008150"],"is_obsolete":false,"name":"mitochondrial valyl-tRNA aminoacylation","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0070185","terms_by_termid":{"GO:0070185":null}}


id: PBO:0071500
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L34 pseudogene 3","termid":"PBO:0071500"}


id: FYPO:0000408
data:
  {"alleles_by_uniquename":{"SJAG_01956:allele-1":{"allele_type":"amino_acid_mutation","description":"E405K ts","gene_uniquename":"SJAG_01956","name":"nuc2-1051","uniquename":"SJAG_01956:allele-1"},"SJAG_03351:allele-1":{"allele_type":"amino_acid_mutation","description":"A186T ts","gene_uniquename":"SJAG_03351","name":"cut23-415","uniquename":"SJAG_03351:allele-1"},"SJAG_03575:allele-1":{"allele_type":"amino_acid_mutation","description":"E548K ts","gene_uniquename":"SJAG_03575","name":"apc2-361","uniquename":"SJAG_03575:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[118656,118655,118654],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000618"}]},"cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the duration of one or more cell cycle phases is longer than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell cycle phase","termid":"FYPO:0002735"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01956":null,"SJAG_03351":null,"SJAG_03575":null},"genotype_count":3,"genotypes_by_uniquename":{"apc2-361-E548K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"apc2-361(E548K ts)","display_uniquename":"apc2-361-E548K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03575:allele-1","expression":"Not assayed or wild type"}]}]},"cut23-415-A186T_ts-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"cut23-415(A186T ts)","display_uniquename":"cut23-415-A186T_ts-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03351:allele-1","expression":"Not assayed or wild type"}]}]},"nuc2-1051-E405K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"nuc2-1051(E405K ts)","display_uniquename":"nuc2-1051-E405K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01956:allele-1","expression":"Not assayed or wild type"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000002","FYPO:0000631"],"is_obsolete":false,"name":"increased duration of cell cycle phase","references_by_uniquename":{"PMID:23786411":null},"single_locus_annotated_genes":["SJAG_01956","SJAG_03575","SJAG_03351"],"single_locus_genotype_uniquenames":["cut23-415-A186T_ts-amino_acid_mutation-expression-not_assayed_or_wild_type","apc2-361-E548K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type","nuc2-1051-E405K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type"],"synonyms":[{"name":"cell cycle progression: decreased rate","type":"related"},{"name":"decreased rate of cell cycle progression","type":"related"},{"name":"prolonged cell cycle phase","type":"exact"},{"name":"reduced rate of cell cycle progression","type":"related"}],"termid":"FYPO:0000408","terms_by_termid":{"FYECO:0000004":null,"FYECO:0000137":null,"FYPO:0000618":null}}


id: PBO:0081833
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger family member 767, pseudogene","termid":"PBO:0081833"}


id: PBO:0059254
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein L20 pseudogene 1","termid":"PBO:0059254"}


id: GO:0004779
data:
  {"annotated_genes":["SJAG_03475"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[107005],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004781"}]},"cv_name":"molecular_function","definition":"Catalysis of the transfer of an adenylyl group from an adenosine nucleotide (ATP or ADP) to sulfate, forming adenylylsulfate.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenylyltransferase activity","termid":"GO:0070566"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03475":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016779"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016740","GO:0016779","GO:0003674"],"is_obsolete":false,"name":"sulfate adenylyltransferase activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"sulphate adenylyltransferase activity","type":"exact"}],"termid":"GO:0004779","terms_by_termid":{"GO:0004781":null}}


id: GO:1990749
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Increases the activity of the enzyme polynucleotide adenylyltransferase.","definition_xrefs":["GOC:kmv","PMID:19460348"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme activator activity","termid":"GO:0008047"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0140677"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0030234","GO:0098772","GO:0140677","GO:0003674"],"is_obsolete":false,"name":"polynucleotide adenylyltransferase activator activity","termid":"GO:1990749"}


id: PBO:0014584
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"electron transfer flavoprotein alpha subunit EtfA (predicted)","termid":"PBO:0014584"}


id: GO:0007629
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The response to external or internal stimuli that results in the locomotory process of flight. Flight is the self-propelled movement of an organism through the air.","definition_xrefs":["GOC:jid","ISBN:0198606907"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adult locomotory behavior","termid":"GO:0008344"}],"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":"flight behavior","synonyms":[{"name":"flight behaviour","type":"exact"}],"termid":"GO:0007629"}


id: GO:0021951
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The creation and reception of signals that guide a precerebellar neuron towards their signals, where this process is involved in tangential migration.","definition_xrefs":["GOC:dgh","PMID:15157725","GO_REF:0000021","GOC:dph","GOC:jid","GOC:cls"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive chemotaxis","termid":"GO:0050918"},{"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":"chemoattraction involved in precerebellar neuron migration","synonyms":[{"name":"positive chemotaxis involved in precerebellar neuron migration","type":"exact"}],"termid":"GO:0021951"}


id: GO:0070648
data:
  {"annotated_genes":["SJAG_00938","SJAG_02864","SJAG_04887"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[94766,97786,107613,119032],"is_not":false,"summary":null,"term":"GO:0070648"}]},"cv_name":"cellular_component","definition":"An actin filament bundle that consists of short filaments organized into bundles of uniform polarity, and is nucleated by formins. In fungal cells, myosin motors transport cargo along actin cables toward sites of polarized cell growth; actin cables may play a similar role in pollen tube growth.","definition_xrefs":["PMID:14671023","PMID:16959963"],"direct_ancestors":[{"relation_name":"is_a","term_name":"parallel actin filament bundle","termid":"GO:0097518"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00938":null,"SJAG_02864":null,"SJAG_04887":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0015629"}],"interesting_parent_ids":["GO:0015629","GO:0005575"],"is_obsolete":false,"name":"formin-nucleated actin cable","references_by_uniquename":{"GO_REF:0000107":null,"PMID:36148799":null},"termid":"GO:0070648","terms_by_termid":{"GO:0070648":null}}


id: MONDO:0007663
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary glaucoma","termid":"MONDO:0018174"}],"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":"glaucoma with elevated episcleral venous pressure","secondary_identifiers":["OMIM:137700","UMLS:C1842030","MESH:C564235","MEDGEN:333975"],"synonyms":[{"name":"glaucoma with elevated episcleral venous pressure","type":"exact"}],"termid":"MONDO:0007663","xrefs":{"Monarch":{"xref_id":"0007663"}}}


id: PBO:0066625
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RIC8 guanine nucleotide exchange factor B","termid":"PBO:0066625"}


id: SO:0001303
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"2_methylthio_N6_cis_hydroxyisopentenyl_adenosine is a modified adenosine.","direct_ancestors":[{"relation_name":"is_a","term_name":"modified_adenosine","termid":"SO:0001273"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"two_methylthio_N6_cis_hydroxyisopentenyl_adenosine","secondary_identifiers":["RNAMOD:009"],"synonyms":[{"name":"2-methylthio-N6-(cis-hydroxyisopentenyl) adenosine","type":"exact"},{"name":"ms2io6A","type":"exact"},{"name":"two methylthio N6 cis hydroxyisopentenyl adenosine","type":"exact"}],"termid":"SO:0001303"}


id: GO:0061307
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a cardiac neural crest cell that will migrate to the heart and contribute to its development. Cardiac neural crest cells are specialized cells that migrate toward the heart from the third, fourth and sixth pharyngeal arches.","definition_xrefs":["GOC:dph","GOC:mtg_heart","PMID:19705442"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neural crest cell differentiation","termid":"GO:0014033"},{"relation_name":"is_a","term_name":"cardiocyte differentiation","termid":"GO:0035051"}],"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":"cardiac neural crest cell differentiation involved in heart development","termid":"GO:0061307"}


id: PBO:0113315
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 diacylglycerol lipids levels; deletion causes sensitivity to unfolded protein response-inducing agents","termid":"PBO:0113315"}


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


id: GO:0060162
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the dopamine receptor, phospholipase C activating pathway.","definition_xrefs":["GOC:dph","GOC:tb","PMID:15016423"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of dopamine receptor signaling pathway","termid":"GO:0060160"},{"relation_name":"is_a","term_name":"negative regulation of phospholipase C-activating G protein-coupled receptor signaling pathway","termid":"GO:1900737"},{"relation_name":"negatively_regulates","term_name":"phospholipase C-activating dopamine receptor signaling pathway","termid":"GO:0060158"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of phospholipase C-activating dopamine receptor signaling pathway","synonyms":[{"name":"negative regulation of dopamine receptor, phospholipase C activating pathway","type":"exact"},{"name":"negative regulation of phospholipase C-activating dopamine receptor signalling pathway","type":"exact"}],"termid":"GO:0060162"}


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


id: MOD:01740
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces an N'-hydrogen atom of a histidine residue with the Proteome Sciences TMT6plex-128 reporter+balance group.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-histidine residue","termid":"MOD:00909"},{"relation_name":"is_a","term_name":"TMT6plex reporter+balance reagent N-acylated residue","termid":"MOD:01717"},{"relation_name":"is_a","term_name":"TMT6plex-128 reporter+balance reagent acylated residue","termid":"MOD:01736"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TMT6plex-128 reporter+balance reagent N'-acylated histidine","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:01740"}


id: GO:0071453
data:
  {"annotated_genes":["SJAG_00642","SJAG_00221","SJAG_01585","SJAG_03345","SJAG_01150","SJAG_04018"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[116480,100718,109344,111203],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071456"},{"annotations":[88739,115890],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1900039"}]},"cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a stimulus reflecting the presence, absence, or concentration of oxygen.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to oxygen levels","termid":"GO:0070482"},{"relation_name":"is_a","term_name":"cellular response to chemical stimulus","termid":"GO:0070887"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00221":null,"SJAG_00642":null,"SJAG_01150":null,"SJAG_01585":null,"SJAG_03345":null,"SJAG_04018":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to oxygen levels","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"cellular response to oxygen","type":"related"}],"termid":"GO:0071453","terms_by_termid":{"GO:0071456":null,"GO:1900039":null}}


id: GO:1905422
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of plant organ morphogenesis.","definition_xrefs":["GO_REF:0000058","GOC:tb","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of developmental process","termid":"GO:0051093"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"is_a","term_name":"regulation of plant organ morphogenesis","termid":"GO:1905421"},{"relation_name":"negatively_regulates","term_name":"plant organ morphogenesis","termid":"GO:1905392"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of plant organ morphogenesis","synonyms":[{"name":"down regulation of plant organ morphogenesis","type":"exact"},{"name":"down-regulation of plant organ morphogenesis","type":"exact"},{"name":"downregulation of plant organ morphogenesis","type":"exact"},{"name":"inhibition of plant organ morphogenesis","type":"narrow"}],"termid":"GO:1905422"}


id: MONDO:0010529
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A form of spinocerebellar degeneration characterized by onset in infancy of hypotonia, ataxia, sensorineural deafness, developmental delay, esotropia, and optic atrophy, and by a progressive course leading to death in childhood. It has been described one family with at least six affected males from five different sibships (connected through carrier females). It is transmitted as an X-linked recessive trait.","definition_xrefs":["Orphanet:85297"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"},{"relation_name":"is_a","term_name":"X-linked cerebellar ataxia","termid":"MONDO:0016612"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"X-linked spinocerebellar ataxia type 3","secondary_identifiers":["SCTID:719817002","OMIM:301790","UMLS:C1844936","MEDGEN:337124","MESH:C537315","GARD:9981","icd11.foundation:261426817","DOID:0111831"],"synonyms":[{"name":"SCAX3","type":"exact"},{"name":"Scax3","type":"related"},{"name":"X-linked ataxia-deafness syndrome","type":"exact"},{"name":"ataxia-deafness syndrome X-linked","type":"related"},{"name":"ataxia-deafness syndrome, X-linked","type":"related"},{"name":"spinocerebellar ataxia X-linked type 3","type":"related"},{"name":"spinocerebellar ataxia, X-linked 3","type":"related"},{"name":"spinocerebellar ataxia, X-linked type 3","type":"exact"}],"termid":"MONDO:0010529","xrefs":{"Monarch":{"xref_id":"0010529"}}}


id: MONDO:0015110
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. An instance of cardiac rhythm disease that is caused by a modification of the individual's genome.","definition_xrefs":["MONDO:patterns/genetic"],"gene_count":0,"genotype_count":0,"name":"obsolete genetic cardiac rhythm disease (obsolete MONDO:0015110)","secondary_identifiers":["Orphanet:101934"],"synonyms":[{"name":"genetic cardiac rhythm disease","type":"exact"}],"termid":"MONDO:0015110","xrefs":{"Monarch":{"xref_id":"0015110"}}}


id: GO:0035286
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Division of a leg into a series of semi-repetitive parts or segments. Most arthropod appendages are visibly segmented; the Drosophila leg for example has nine segments, each separated from the next by a flexible joint.","definition_xrefs":["PMID:10357895"],"gene_count":0,"genotype_count":0,"name":"obsolete leg segmentation (obsolete GO:0035286)","synonyms":[{"name":"leg segmentation","type":"exact"}],"termid":"GO:0035286"}


id: PBO:0034222
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_morphology_of","termid":"PBO:0034222"}


id: GO:0102344
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: (R)-3-hydroxybehenoyl-CoA = trans-2-docosenoyl-CoA + H2O.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 3-hydroxy-behenoyl-CoA dehydratase activity (obsolete GO:0102344)","termid":"GO:0102344"}


id: GO:0002841
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of a T cell mediated immune response to tumor cell.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of T cell mediated immunity","termid":"GO:0002710"},{"relation_name":"is_a","term_name":"negative regulation of immune response to tumor cell","termid":"GO:0002838"},{"relation_name":"is_a","term_name":"regulation of T cell mediated immune response to tumor cell","termid":"GO:0002840"},{"relation_name":"negatively_regulates","term_name":"T cell mediated immune response to tumor cell","termid":"GO:0002424"}],"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 T cell mediated immune response to tumor cell","synonyms":[{"name":"down regulation of T cell mediated immune response to tumor cell","type":"exact"},{"name":"down-regulation of T cell mediated immune response to tumor cell","type":"exact"},{"name":"downregulation of T cell mediated immune response to tumor cell","type":"exact"},{"name":"inhibition of T cell mediated immune response to tumor cell","type":"narrow"},{"name":"negative regulation of T cell mediated immune response to tumour cell","type":"exact"},{"name":"negative regulation of T lymphocyte mediated immune response to tumor cell","type":"exact"},{"name":"negative regulation of T-cell mediated immune response to tumor cell","type":"exact"},{"name":"negative regulation of T-lymphocyte mediated immune response to tumor cell","type":"exact"}],"termid":"GO:0002841"}


id: PBO:0052778
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 19 pseudogene 1","termid":"PBO:0052778"}


id: MONDO:0011354
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"situs inversus","termid":"MONDO:0010029"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"situs inversus totalis with cystic dysplasia of kidneys and pancreas","secondary_identifiers":["UMLS:C1863647","GARD:8567","MEDGEN:400349","MESH:C536666","OMIM:603643"],"synonyms":[{"name":"situs inversus totalis with cystic dysplasia of kidneys and pancreas","type":"exact"},{"name":"situs inversus, cystic dysplastic kidney and pancreas, bowed lower limbs,severe intrauterine growth retardation, and oligohydramnios","type":"related"}],"termid":"MONDO:0011354","xrefs":{"Monarch":{"xref_id":"0011354"}}}


id: GO:0032593
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A small membrane-bounded vesicle that releases its contents by exocytosis in response to insulin stimulation; the contents are enriched in GLUT4, IRAP and VAMP2.","definition_xrefs":["PMID:17644329"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secretory granule","termid":"GO:0030141"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0031410"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0031410","GO:0005737"],"is_obsolete":false,"name":"insulin-responsive compartment","synonyms":[{"name":"GLUT4 storage compartment","type":"exact"},{"name":"GSC","type":"related"},{"name":"IRC","type":"related"}],"termid":"GO:0032593"}


id: GO:1901589
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An arrangement of closely apposed microtubules running parallel to each other in the axon hillock and initial segment.","definition_xrefs":["GOC:TermGenie","NIF_Subcellular:sao707332678"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microtubule bundle","termid":"GO:0097427"},{"relation_name":"part_of","term_name":"axon","termid":"GO:0030424"}],"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":"axon microtubule bundle","synonyms":[{"name":"axon microtubule fascicle","type":"exact"},{"name":"microtubule bundle of axon","type":"exact"},{"name":"microtubule fascicle of axon","type":"exact"}],"termid":"GO:1901589"}


id: GO:1900975
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of tatiopterin biosynthetic process.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of biosynthetic process","termid":"GO:0009890"},{"relation_name":"is_a","term_name":"regulation of tatiopterin biosynthetic process","termid":"GO:1900974"},{"relation_name":"is_a","term_name":"negative regulation of tatiopterin metabolic process","termid":"GO:1900978"},{"relation_name":"negatively_regulates","term_name":"tatiopterin biosynthetic process","termid":"GO:1900870"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0042559"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0042559"},{"rel_name":"negatively_regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0042559","GO:0008150"],"is_obsolete":false,"name":"negative regulation of tatiopterin biosynthetic process","synonyms":[{"name":"down regulation of tatiopterin anabolism","type":"exact"},{"name":"down regulation of tatiopterin biosynthesis","type":"exact"},{"name":"down regulation of tatiopterin biosynthetic process","type":"exact"},{"name":"down regulation of tatiopterin formation","type":"exact"},{"name":"down regulation of tatiopterin synthesis","type":"exact"},{"name":"down-regulation of tatiopterin anabolism","type":"exact"},{"name":"down-regulation of tatiopterin biosynthesis","type":"exact"},{"name":"down-regulation of tatiopterin biosynthetic process","type":"exact"},{"name":"down-regulation of tatiopterin formation","type":"exact"},{"name":"down-regulation of tatiopterin synthesis","type":"exact"},{"name":"downregulation of tatiopterin anabolism","type":"exact"},{"name":"downregulation of tatiopterin biosynthesis","type":"exact"},{"name":"downregulation of tatiopterin biosynthetic process","type":"exact"},{"name":"downregulation of tatiopterin formation","type":"exact"},{"name":"downregulation of tatiopterin synthesis","type":"exact"},{"name":"inhibition of tatiopterin anabolism","type":"exact"},{"name":"inhibition of tatiopterin biosynthesis","type":"exact"},{"name":"inhibition of tatiopterin biosynthetic process","type":"narrow"},{"name":"inhibition of tatiopterin formation","type":"exact"},{"name":"inhibition of tatiopterin synthesis","type":"exact"},{"name":"negative regulation of tatiopterin anabolism","type":"exact"},{"name":"negative regulation of tatiopterin biosynthesis","type":"exact"},{"name":"negative regulation of tatiopterin formation","type":"exact"},{"name":"negative regulation of tatiopterin synthesis","type":"exact"}],"termid":"GO:1900975"}


id: PBO:0084345
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Largest subunit of the Anaphase-Promoting Complex/Cyclosome; APC/C is a ubiquitin-protein ligase required for degradation of anaphase inhibitors, including mitotic cyclins, during the metaphase/anaphase transition; component of the platform domain of the APC/C, based on structural analysis; localizes to nuclear foci that become diffuse upon DNA replication stress","termid":"PBO:0084345"}


id: PBO:0068954
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 198, pseudogene","termid":"PBO:0068954"}


id: MONDO:0030966
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":"neurofacioskeletal syndrome with or without renal agenesis","secondary_identifiers":["OMIM:619194","MEDGEN:1778926","UMLS:C5543070"],"synonyms":[{"name":"NFSRA","type":"exact"},{"name":"Neurodevelopmental Disorder With Corpus Callosum Agenesis, Craniofacial Dysmorphism, and Skeletal Anomalies, With or Without Renal Agenesis","type":"exact"}],"termid":"MONDO:0030966","xrefs":{"Monarch":{"xref_id":"0030966"}}}


id: FYPO:0005063
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 methylation of lysine at position 4 of histone H3 at the mating type locus occurs to a greater extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased histone methylation during vegetative growth","termid":"FYPO:0000869"},{"relation_name":"is_a","term_name":"abnormal histone H3-K4 methylation during vegetative growth","termid":"FYPO:0002330"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0002494","FYPO:0002274","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"increased histone H3-K4 methylation at mating type locus during vegetative growth","synonyms":[{"name":"increased histone H3 K4 methylation at mating type locus during vegetative growth","type":"exact"},{"name":"increased histone H3-K4 methylation at mating type locus during mitotic cell cycle","type":"related"},{"name":"increased histone H3K4 methylation at mating type locus during vegetative growth","type":"exact"},{"name":"increased histone H3K4me at mating type locus during vegetative growth","type":"exact"},{"name":"increased histone lysine H3 K4 methylation at mating type locus during vegetative growth","type":"exact"}],"termid":"FYPO:0005063"}


id: MONDO:0021668
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete disorder involving pain (obsolete MONDO:0021668)","secondary_identifiers":["DOID:0060164","SCTID:373673007"],"synonyms":[{"name":"pain disorder","type":"exact"}],"termid":"MONDO:0021668","xrefs":{"Monarch":{"xref_id":"0021668"}}}


id: FYPO:0000556
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which re-entry into the mitotic cell cycle after pheromone arrest does not occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal re-entry into mitotic cell cycle after pheromone arrest","termid":"FYPO:0000555"},{"relation_name":"is_a","term_name":"abolished cellular process","termid":"FYPO:0005449"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001985","FYPO:0000298","FYPO:0000631"],"is_obsolete":false,"name":"abolished re-entry into mitotic cell cycle after pheromone arrest","synonyms":[{"name":"absent recovery from pheromone-induced cell cycle arrest","type":"exact"},{"name":"re-entry into mitotic cell cycle after pheromone arrest abolished","type":"exact"},{"name":"recovery from pheromone-induced cell cycle arrest abolished","type":"exact"},{"name":"recovery from pheromone-induced cell cycle arrest: absent","type":"related"}],"termid":"FYPO:0000556"}


id: GO:0072360
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the vascular cord over time from its initial formation until its mature state. The vascular cord is the primordial vasculature that will develop into blood vessels by the process of tubulogenesis.","definition_xrefs":["PMID:7084422","ZFA:0005077","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"circulatory system development","termid":"GO:0072359"}],"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":"vascular cord development","termid":"GO:0072360"}


id: PBO:0085471
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pre-ribosomal factor involved in 60S ribosomal protein subunit export; associates with the pre-60S particle; shuttles between the nucleus and cytoplasm","termid":"PBO:0085471"}


id: MONDO:0000809
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A severe, rapidly fatal reaction occurring most commonly in children following an infectious illness. It is characterized by large, rapidly spreading skin hemorrhages, fever, or shock. Purpura fulminans often accompanies or is triggered by disseminated intravascular coagulation.","definition_xrefs":["MESH:D055665"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disseminated intravascular coagulation","termid":"MONDO:0001243"},{"relation_name":"is_a","term_name":"purpura","termid":"MONDO:0002610"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"purpura fulminans","secondary_identifiers":["MEDGEN:88448","DOID:0060538","icd11.foundation:1293848111","UMLS:C0085650","SCTID:13507004"],"synonyms":[{"name":"fibrinolytic purpura","type":"related"},{"name":"purpura gangrenosa","type":"exact"}],"termid":"MONDO:0000809","xrefs":{"Monarch":{"xref_id":"0000809"}}}


id: PBO:0061167
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear-encoded mitochondrial tRNA-Leu (TAA) 5-1","termid":"PBO:0061167"}


id: GO:0042448
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving progesterone, a steroid hormone produced in the ovary which prepares and maintains the uterus for pregnancy. Also found in plants.","definition_xrefs":["GOC:jl","PMID:11392024"],"direct_ancestors":[{"relation_name":"is_a","term_name":"C21-steroid hormone metabolic process","termid":"GO:0008207"},{"relation_name":"is_a","term_name":"ketone metabolic process","termid":"GO:0042180"},{"relation_name":"is_a","term_name":"olefinic compound metabolic process","termid":"GO:0120254"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"progesterone metabolic process","synonyms":[{"name":"progesterone metabolism","type":"exact"}],"termid":"GO:0042448"}


id: GO:0007498
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the mesoderm over time, from its formation to the mature structure. The mesoderm is the middle germ layer that develops into muscle, bone, cartilage, blood and connective tissue.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tissue development","termid":"GO:0009888"}],"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":"mesoderm development","termid":"GO:0007498"}


id: PBO:0079012
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Thr (anticodon TGT) 6-1","termid":"PBO:0079012"}


id: GO:0046899
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: nucleoside triphosphate + AMP = nucleoside diphosphate + ADP.","definition_xrefs":["EC:2.7.4.10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphotransferase activity, phosphate group as acceptor","termid":"GO:0016776"},{"relation_name":"is_a","term_name":"nucleobase-containing compound kinase activity","termid":"GO:0019205"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016301","GO:0016740","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"nucleoside triphosphate adenylate kinase activity","secondary_identifiers":["Reactome:R-HSA-1008248","RHEA:13749","MetaCyc:2.7.4.10-RXN"],"synonyms":[{"name":"GTP:AMP phosphotransferase","type":"narrow"},{"name":"guanosine triphosphate-adenylate kinase","type":"narrow"},{"name":"isozyme 3 of adenylate kinase activity","type":"related"},{"name":"nucleoside triphosphate-adenosine monophosphate transphosphorylase activity","type":"exact"},{"name":"nucleoside-triphosphate-adenylate kinase activity","type":"exact"},{"name":"nucleoside-triphosphate:AMP phosphotransferase activity","type":"related"}],"termid":"GO:0046899"}


id: PBO:0091330
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by A. fumigatus PzhA","termid":"PBO:0091330"}


id: PBO:0050490
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homeobox B cluster","termid":"PBO:0050490"}


id: PBO:0062437
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 101 pseudogene","termid":"PBO:0062437"}


id: PBO:0041361
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"complement component 4 binding protein beta","termid":"PBO:0041361"}


id: PBO:0085525
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein component of the small (40S) ribosomal subunit; homologous to mammalian ribosomal protein S26, no bacterial homolog; RPS26A has a paralog, RPS26B, that arose from the whole genome duplication; human homolog can partially complement an RPS26A, RPS26B double null mutant; mutations in the human gene are associated with Diamond-Blackfan anemia","termid":"PBO:0085525"}


id: MONDO:0034641
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare genetic hyperkinetic movement disorder (obsolete MONDO:0034641)","secondary_identifiers":["Orphanet:496916"],"termid":"MONDO:0034641","xrefs":{"Monarch":{"xref_id":"0034641"}}}


id: GO:0061435
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of transcription from a mobile element promoter.","definition_xrefs":["GOC:dph","PMID:12230120","PMID:9271107"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of DNA-templated transcription","termid":"GO:0045893"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"positively_regulates","termid":"GO:0006351"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006351"},{"rel_name":"is_a","termid":"GO:0006355"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0006351","GO:0006355"],"is_obsolete":false,"name":"positive regulation of transcription from a mobile element promoter","termid":"GO:0061435"}


id: PBO:0060517
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"napsin B aspartic peptidase, pseudogene","termid":"PBO:0060517"}


id: PBO:0067049
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 69, pseudogene","termid":"PBO:0067049"}


id: MOD:00166
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-tyrosine residue to O4'-glucosyl-tyrosine.","definition_xrefs":["PubMed:15279557","PubMed:3181138","RESID:AA0157","Unimod:41#Y"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glucosylated residue","termid":"MOD:00433"},{"relation_name":"is_a","term_name":"monohexosylated (Hex1)","termid":"MOD:00761"},{"relation_name":"is_a","term_name":"O-glycosyl-L-tyrosine","termid":"MOD:01927"}],"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":"O4'-glucosyl-L-tyrosine","synonyms":[{"name":"(2S)-2-amino-3-(4-alpha-D-glucopyranosyloxy)phenylpropanoic acid","type":"exact"},{"name":"CARBOHYD O-linked (Glc) tyrosine","type":"exact"},{"name":"Hex","type":"related"},{"name":"Hexose","type":"related"},{"name":"O4'-glucosyl-L-tyrosine","type":"exact"},{"name":"O4'-glycosyl-L-tyrosine","type":"exact"},{"name":"O4GlcTyr","type":"exact"}],"termid":"MOD:00166"}


id: PBO:0049336
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTF2H2 family member C","termid":"PBO:0049336"}


id: GO:0031568
data:
  {"annotated_genes":["SJAG_03048","SJAG_01401","SJAG_01210","SJAG_00071","SJAG_03681"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[88420,101119,101861,108375,115399],"is_not":false,"summary":null,"term":"GO:0031568"}]},"cv_name":"biological_process","definition":"A signal transduction process that contributes to a cell size control checkpoint during the G1/S transition of the cell cycle.","definition_xrefs":["GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitotic cell size control checkpoint signaling","termid":"GO:0031567"},{"relation_name":"is_a","term_name":"negative regulation of G1/S transition of mitotic cell cycle","termid":"GO:2000134"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00071":null,"SJAG_01210":null,"SJAG_01401":null,"SJAG_03048":null,"SJAG_03681":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044772"},{"rel_name":"negatively_regulates","termid":"GO:0044772"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"negatively_regulates","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0007049","GO:0023052","GO:0008150","GO:0044772"],"is_obsolete":false,"name":"mitotic G1 cell size control checkpoint signaling","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0072450"],"synonyms":[{"name":"G1 cell size control checkpoint","type":"related"},{"name":"G1 cell size control checkpoint signalling","type":"related"},{"name":"mitotic G1 cell size control checkpoint","type":"exact"},{"name":"mitotic cell cycle G1/S transition size control checkpoint","type":"exact"},{"name":"signal transduction involved in G1 cell size control checkpoint","type":"related"},{"name":"signal transduction involved in mitotic cell cycle G1/S transition size control checkpoint","type":"related"}],"termid":"GO:0031568","terms_by_termid":{"GO:0031568":null}}


id: MONDO:0001045
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A congenital malformation characterized by the absence of a normal opening in a part of the intestine. It can occur either in the small or the large intestine.","definition_xrefs":["NCIT:P378"],"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":"intestinal atresia","secondary_identifiers":["HP:0011100","MEDGEN:7129","MESH:D007409","DOID:10486","UMLS:C0021828","NCIT:C84790"],"synonyms":[{"name":"atresia of the intestine","type":"exact"},{"name":"congenital intestinal atresia","type":"exact"},{"name":"intestinal atresia","type":"exact"},{"name":"intestinal atresia (disease)","type":"exact"}],"termid":"MONDO:0001045","xrefs":{"Monarch":{"xref_id":"0001045"}}}


id: PBO:0076146
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"succinate receptor 1","termid":"PBO:0076146"}


id: GO:0097160
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a polychlorinated biphenyl (PCB), a biphenyl compound containing between 2 and 10 chlorine atoms attached to the two benzene rings.","definition_xrefs":["PMID:7583672","GOC:sjw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"binding","termid":"GO:0005488"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"polychlorinated biphenyl binding","synonyms":[{"name":"PCB binding","type":"exact"},{"name":"polychlorobiphenyl binding","type":"exact"}],"termid":"GO:0097160"}


id: PBO:0079026
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-undetermined (NNN) 9-1","termid":"PBO:0079026"}


id: PBO:0004527
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"linear element associated protein Hop1","termid":"PBO:0004527"}


id: GO:0106320
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: (4R)-limonene + NADPH + H+ + O2 = NADP+ + H2O + (4R)-limonene-1,2-epoxide.","definition_xrefs":["RHEA:26097"],"gene_count":0,"genotype_count":0,"name":"obsolete (R)-limonene 1,2-monooxygenase NADPH activity (obsolete GO:0106320)","termid":"GO:0106320"}


id: PBO:0066904
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 205","termid":"PBO:0066904"}


id: MONDO:0008379
data:
  {"annotated_genes":["SJAG_01298"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85813],"is_not":false,"summary":null,"term":"MONDO:0008379"}]},"cv_name":"mondo","definition":"Any retinitis pigmentosa in which the cause of the disease is a mutation in the IMPDH1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinitis pigmentosa","termid":"MONDO:0019200"},{"relation_name":"is_a","term_name":"IMPDH1-related retinopathy","termid":"MONDO:1040051"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01298":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0005328","MONDO:0005066"],"is_obsolete":false,"name":"retinitis pigmentosa 10","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:C566715","DOID:0110388","UMLS:C1867299","ICD10CM:H35.5","OMIM:180105","MEDGEN:357247","GARD:15110"],"synonyms":[{"name":"IMPDH1 retinitis pigmentosa","type":"exact"},{"name":"RP10","type":"exact"},{"name":"retinitis pigmentosa 10","type":"exact"},{"name":"retinitis pigmentosa caused by mutation in IMPDH1","type":"exact"},{"name":"retinitis pigmentosa type 10","type":"exact"}],"termid":"MONDO:0008379","terms_by_termid":{"MONDO:0008379":null},"xrefs":{"Monarch":{"xref_id":"0008379"}}}


id: PBO:0090612
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial isoleucine-tRNA ligase","termid":"PBO:0090612"}


id: MONDO:0017434
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy (obsolete MONDO:0017434)","secondary_identifiers":["icd11.foundation:1911144861","Orphanet:294959"],"termid":"MONDO:0017434","xrefs":{"Monarch":{"xref_id":"0017434"}}}


id: PBO:0039012
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AFG1 like ATPase","termid":"PBO:0039012"}


id: PBO:0055303
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 2730","termid":"PBO:0055303"}


id: FYPO:0002892
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which any process of heterochromatin organization is normal (i.e. indistinguishable from wild type) in the vegetative growth phase of the life cycle. Heterochromatin organization results in the specification, formation or maintenance of the physical structure of eukaryotic heterochromatin, a compact and highly condensed form of chromatin.","definition_xrefs":["GO:0070828","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal chromatin organization during vegetative growth","termid":"FYPO:0002891"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000257","FYPO:0001312","FYPO:0000002"],"is_obsolete":false,"name":"normal heterochromatin organization during vegetative growth","synonyms":[{"name":"normal heterochromatin organisation during vegetative growth","type":"exact"},{"name":"normal heterochromatin organization during mitotic cell cycle","type":"related"}],"termid":"FYPO:0002892"}


id: FYPO:0004448
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which a protein is observed in a particular location where it is not normally found during the meiotic cell cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mislocalized protein","termid":"FYPO:0003452"},{"relation_name":"output_of","term_name":"abolished protein localization during meiotic cell cycle","termid":"FYPO:0005208"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0000138","FYPO:0005447"],"is_obsolete":false,"name":"mislocalized protein during meiotic cell cycle","synonyms":[{"name":"mislocalised protein during meiotic cell cycle","type":"exact"}],"termid":"FYPO:0004448"}


id: FYPO:0006431
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which the mitotic spindle pole body is larger than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic spindle pole body morphology","termid":"FYPO:0001474"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"enlarged mitotic spindle pole body","synonyms":[{"name":"enlarged mitotic SPB","type":"exact"},{"name":"enlarged spindle pole body during mitotic cell cycle","type":"exact"},{"name":"enlarged spindle pole body during vegetative growth","type":"exact"}],"termid":"FYPO:0006431"}


id: GO:0008881
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-glutamate = D-glutamate.","definition_xrefs":["EC:5.1.1.3","RHEA:12813"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino-acid racemase activity","termid":"GO:0047661"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016853"],"is_obsolete":false,"name":"glutamate racemase activity","secondary_identifiers":["KEGG_REACTION:R00260","MetaCyc:GLUTRACE-RXN"],"termid":"GO:0008881"}


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


id: GO:0061272
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the mesonephric connecting tubule over time, from its formation to the mature structure. The mesonephric connecting tubule is a tubular segment of the mesonephric nephron; it connects the distal tubule to the collecting duct in the mesonephros.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mesonephric nephron tubule development","termid":"GO:0061242"},{"relation_name":"is_a","term_name":"connecting tubule development","termid":"GO:0072027"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"mesonephric connecting tubule development","synonyms":[{"name":"mesonephric collecting tubule development","type":"exact"},{"name":"mesonephric connecting duct development","type":"related"}],"termid":"GO:0061272"}


id: GO:0004081
data:
  {"annotated_genes":["SJAG_04169"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[116585],"is_not":false,"summary":null,"term":"GO:0004081"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: P(1),P(4)-bis(5'-nucleosyl)tetraphosphate + H2O = NTP + NMP. Acts on bis(5'-guanosyl)-, bis(5'-xanthosyl)-, bis(5'-adenosyl)- and bis(5'-uridyl)-tetraphosphate.","definition_xrefs":["PMID:4955726","EC:3.6.1.17"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bis(5'-nucleosyl)-tetraphosphatase activity","termid":"GO:0008796"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04169":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016787","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"bis(5'-nucleosyl)-tetraphosphatase (asymmetrical) activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:3.6.1.17-RXN","Reactome:R-HSA-5696197","RHEA:22484"],"synonyms":[{"name":"1-P,4-P-bis(5'-nucleosyl)-tetraphosphate nucleotidohydrolase activity","type":"related"},{"name":"Ap(4)A hydrolase activity","type":"broad"},{"name":"Ap(4)Aase activity","type":"broad"},{"name":"Ap4A hydrolase activity","type":"broad"},{"name":"Ap4Aase activity","type":"broad"},{"name":"P1,P4-bis(5'-nucleosyl)-tetraphosphate nucleotidohydrolase activity","type":"related"},{"name":"bis(5'-adenosyl)-tetraphosphatase activity","type":"narrow"},{"name":"bis(5'-guanosyl)-tetraphosphatase activity","type":"narrow"},{"name":"diadenosine 5',5'''-P(1),P(4)-tetraphosphate asymmetrical hydrolase activity","type":"related"},{"name":"diadenosine 5',5'''-P1,P4-tetraphosphate asymmetrical hydrolase activity","type":"related"},{"name":"diadenosine 5',5'''-P1,P4-tetraphosphate hydrolase","type":"narrow"},{"name":"diadenosine P1,P4-tetraphosphatase activity","type":"related"},{"name":"diadenosinetetraphosphatase (asymmetrical) activity","type":"narrow"},{"name":"diguanosinetetraphosphatase (asymmetrical) activity","type":"narrow"},{"name":"dinucleoside tetraphosphatase activity","type":"related"},{"name":"dinucleosidetetraphosphatase (asymmetrical) activity","type":"related"}],"termid":"GO:0004081","terms_by_termid":{"GO:0004081":null}}


id: MONDO:0034846
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare intestinal disease characterized by congenital partial or complete lack of the collagen mesh network in the intestinal wall, resulting in hypoperistalsis or aperistalsis. The enteric nervous system is normal or near-normal in the affected areas, although hypo- and dysganglionosis may be found in some proximal segments of the colon and/or small bowel. Patients present with chronic intractable slow transit constipation.","definition_xrefs":["Orphanet:565641"],"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":"primary desmosis coli","secondary_identifiers":["GARD:22268","MEDGEN:1812159","UMLS:C5680125"],"termid":"MONDO:0034846","xrefs":{"Monarch":{"xref_id":"0034846"}}}


id: GO:0101031
data:
  {"annotated_genes":["SJAG_00447","SJAG_02926","SJAG_02378","SJAG_01002","SJAG_03320","SJAG_04121","SJAG_00609","SJAG_03570"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[108708,106823,110840,102331,101320,105710,91604,88320],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005832"}]},"cv_name":"cellular_component","definition":"A protein complex required for the non-covalent folding or unfolding, maturation, stabilization or assembly or disassembly of macromolecular structures. Usually active during or immediately after completion of translation. Many chaperone complexes contain heat shock proteins.","definition_xrefs":["GOC:bhm","PMID:21855797"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular protein-containing complex","termid":"GO:0140535"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00447":null,"SJAG_00609":null,"SJAG_01002":null,"SJAG_02378":null,"SJAG_02926":null,"SJAG_03320":null,"SJAG_03570":null,"SJAG_04121":null},"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":"protein folding chaperone complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"chaperone complex","type":"broad"}],"termid":"GO:0101031","terms_by_termid":{"GO:0005832":null}}


id: PBO:0087709
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the RNA polymerase II mediator complex; associates with core polymerase subunits to form the RNA polymerase II holoenzyme; essential for transcriptional regulation; involved in glucose repression","termid":"PBO:0087709"}


id: GO:0021675
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a nerve over time, from its formation to the mature structure.","definition_xrefs":["GOC:dph","GO_REF:0000021","GOC:cls","GOC:dgh","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"nervous system development","termid":"GO:0007399"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"nerve development","termid":"GO:0021675"}


id: PBO:0070190
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 110 pseudogene","termid":"PBO:0070190"}


id: GO:0044239
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of polysaccharides by salivary amylase. Salivary amylase is released by salivary glands, usually in the mouth.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete salivary polysaccharide catabolic process (obsolete GO:0044239)","synonyms":[{"name":"salivary polysaccharide breakdown","type":"exact"},{"name":"salivary polysaccharide catabolism","type":"exact"},{"name":"salivary polysaccharide degradation","type":"exact"}],"termid":"GO:0044239"}


id: GO:0045445
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a myoblast. A myoblast is a mononucleate cell type that, by fusion with other myoblasts, gives rise to the myotubes that eventually develop into striated muscle fibers.","definition_xrefs":["GOC:go_curators","GOC:mtg_muscle","CL:0000056"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"},{"relation_name":"part_of","term_name":"muscle structure development","termid":"GO:0061061"}],"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":"myoblast differentiation","synonyms":[{"name":"myoblast cell differentiation","type":"exact"}],"termid":"GO:0045445"}


id: PR:P04688
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- nda2 gene.","definition_xrefs":["UniProtKB:P04688","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":"tubulin alpha-1 chain (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC16A3.15c","synonyms":[{"name":"Spom972h-nda2","type":"exact"}],"termid":"PR:P04688"}


id: PR:O14224
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A rho GDP-dissociation inhibitor 3 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO00535"],"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":"rho GDP-dissociation inhibitor (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC6F12.06","secondary_identifiers":["UniProtKB:O14224"],"synonyms":[{"name":"Spom972h-ARHGDIG","type":"exact"},{"name":"rho GDI (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14224"}


id: PR:Q09687
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC13C5.05c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q09687"],"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":"phosphoacetylglucosamine mutase 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC13C5.05c","synonyms":[{"name":"N-acetylglucosamine-phosphate mutase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"PAGM (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-SPAC13C5.05c","type":"exact"},{"name":"acetylglucosamine phosphomutase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q09687"}


id: PBO:0051752
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inositol hexakisphosphate kinase 1","termid":"PBO:0051752"}


id: MONDO:0033981
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete krt1-related diffuse nonepidermolytic keratoderma (obsolete MONDO:0033981)","termid":"MONDO:0033981","xrefs":{"Monarch":{"xref_id":"0033981"}}}


id: GO:0016819
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of any acid anhydride which contains a sulfonyl group, -SO2-.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on acid anhydrides","termid":"GO:0016817"}],"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:0016787"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"hydrolase activity, acting on acid anhydrides, in sulfonyl-containing anhydrides","secondary_identifiers":["EC:3.6.2.-"],"synonyms":[{"name":"hydrolase activity, acting on acid anhydrides, in sulphonyl-containing anhydrides","type":"exact"}],"termid":"GO:0016819"}


id: PBO:0110315
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase feature property types","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"insdc_protein_id","termid":"PBO:0110315"}


id: PBO:0080614
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat domain 48","termid":"PBO:0080614"}


id: MONDO:0000242
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A dermatophytosis that involves the beard.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"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":"tinea barbae","secondary_identifiers":["MESH:C000656825","SCTID:399329002","UMLS:C2349994","MEDGEN:748519","DOID:0050096"],"synonyms":[{"name":"beard dermatophytosis","type":"exact"},{"name":"dermatophytosis of beard","type":"exact"}],"termid":"MONDO:0000242","xrefs":{"Monarch":{"xref_id":"0000242"}}}


id: GO:0006962
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An immune response against bacteria, specific to males and mediated through a body fluid.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"antibacterial humoral response","termid":"GO:0019731"},{"relation_name":"is_a","term_name":"male-specific defense response to bacterium","termid":"GO:0050831"}],"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":"male-specific antibacterial humoral response","termid":"GO:0006962"}


id: GO:0008023
data:
  {"annotated_genes":["SJAG_00483","SJAG_03481","SJAG_02209","SJAG_03967","SJAG_03118","SJAG_02097","SJAG_02416","SJAG_01149","SJAG_03211","SJAG_04353","SJAG_00139","SJAG_04670","SJAG_01213","SJAG_02238","SJAG_01610","SJAG_01151","SJAG_02393","SJAG_00540","SJAG_03677","SJAG_03128","SJAG_02057","SJAG_04933","SJAG_03061"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[91459,91861,105654,113464],"is_not":false,"summary":null,"term":"GO:0008023"},{"annotations":[104857,94693,110970,102553,98648],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016593"},{"annotations":[95287,110400,116486],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070692"},{"annotations":[106310,93428],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032044"},{"annotations":[107378,104995],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070449"},{"annotations":[110756,113096],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035101"},{"annotations":[108360,108519],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070691"},{"annotations":[112678,113566,99430],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032783"}]},"cv_name":"cellular_component","definition":"Any protein complex that interacts with RNA polymerase II to increase (positive transcription elongation factor) or reduce (negative transcription elongation factor) the rate of transcription elongation.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"},{"relation_name":"part_of","term_name":"nucleoplasm","termid":"GO:0005654"}],"gene_count":23,"genes_by_uniquename":{"SJAG_00139":null,"SJAG_00483":null,"SJAG_00540":null,"SJAG_01149":null,"SJAG_01151":null,"SJAG_01213":null,"SJAG_01610":null,"SJAG_02057":null,"SJAG_02097":null,"SJAG_02209":null,"SJAG_02238":null,"SJAG_02393":null,"SJAG_02416":null,"SJAG_03061":null,"SJAG_03118":null,"SJAG_03128":null,"SJAG_03211":null,"SJAG_03481":null,"SJAG_03677":null,"SJAG_03967":null,"SJAG_04353":null,"SJAG_04670":null,"SJAG_04933":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005654"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005654","GO:0005634","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"transcription elongation factor complex","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0008023","terms_by_termid":{"GO:0008023":null,"GO:0016593":null,"GO:0032044":null,"GO:0032783":null,"GO:0035101":null,"GO:0070449":null,"GO:0070691":null,"GO:0070692":null}}


id: GO:1901343
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of vasculature development.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of developmental process","termid":"GO:0051093"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"is_a","term_name":"regulation of vasculature development","termid":"GO:1901342"},{"relation_name":"negatively_regulates","term_name":"vasculature development","termid":"GO:0001944"}],"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 vasculature development","synonyms":[{"name":"down regulation of vascular system development","type":"related"},{"name":"down regulation of vasculature development","type":"exact"},{"name":"down-regulation of vascular system development","type":"related"},{"name":"down-regulation of vasculature development","type":"exact"},{"name":"downregulation of vascular system development","type":"related"},{"name":"downregulation of vasculature development","type":"exact"},{"name":"inhibition of vascular system development","type":"related"},{"name":"inhibition of vasculature development","type":"narrow"},{"name":"negative regulation of vascular system development","type":"related"}],"termid":"GO:1901343"}


id: PBO:0089246
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane ThrE amino acid transmembrane transporter family protein","termid":"PBO:0089246"}


id: PBO:0031904
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein kinase Tor1","termid":"PBO:0031904"}


id: PBO:0068232
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 18S ribosomal 3","termid":"PBO:0068232"}


id: GO:0015829
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of valine, 2-amino-3-methylbutanoic acid, into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"branched-chain amino acid transport","termid":"GO:0015803"},{"relation_name":"is_a","term_name":"neutral amino acid transport","termid":"GO:0015804"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"valine transport","synonyms":[{"name":"L-valine transport","type":"narrow"}],"termid":"GO:0015829"}


id: GO:0014804
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The region between the inner and outer lipid bilayers of the terminal cisterna envelope. This space is enriched in calsequestrin.","definition_xrefs":["GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sarcoplasmic reticulum lumen","termid":"GO:0033018"},{"relation_name":"part_of","term_name":"terminal cisterna","termid":"GO:0014802"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005783"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0005783"],"is_obsolete":false,"name":"terminal cisterna lumen","termid":"GO:0014804"}


id: PBO:0076957
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transforming growth factor beta induced","termid":"PBO:0076957"}


id: GO:0042127
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cell proliferation.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cellular process","termid":"GO:0050794"},{"relation_name":"regulates","term_name":"cell population proliferation","termid":"GO:0008283"}],"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 cell population proliferation","synonyms":[{"name":"regulation of cell proliferation","type":"related"}],"termid":"GO:0042127"}


id: PR:O74393
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC4F6.07c gene.","definition_xrefs":["UniProtKB:O74393","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":"ATP-dependent RNA helicase mak5 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC4F6.07c","synonyms":[{"name":"Spom972h-SPBC4F6.07c","type":"exact"}],"termid":"PR:O74393"}


id: PBO:0034758
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Hrd1 ubiquitin ligase complex subunit (predicted)","termid":"PBO:0034758"}


id: MONDO:0021479
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that involves the oropharynx.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"respiratory system benign neoplasm","termid":"MONDO:0000382"},{"relation_name":"is_a","term_name":"benign digestive system neoplasm","termid":"MONDO:0000385"},{"relation_name":"is_a","term_name":"neoplasm of oropharynx","termid":"MONDO:0021364"},{"relation_name":"is_a","term_name":"benign neoplasm of pharynx","termid":"MONDO:0021523"}],"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":"benign neoplasm of oropharynx","secondary_identifiers":["ICD9:210.6","NCIT:C4604","MEDGEN:87572","SCTID:92259008","UMLS:C0347229","icd11.foundation:441557450"],"synonyms":[{"name":"benign neoplasm of the oropharynx","type":"exact"},{"name":"benign oropharyngeal neoplasm","type":"exact"},{"name":"benign oropharyngeal tumor","type":"exact"},{"name":"benign oropharyngeal tumour","type":"exact"},{"name":"benign tumor of oropharynx","type":"exact"},{"name":"benign tumor of the oropharynx","type":"exact"},{"name":"benign tumour of oropharynx","type":"exact"},{"name":"benign tumour of the oropharynx","type":"exact"},{"name":"oropharyngeal neoplasm benign","type":"exact"},{"name":"oropharynx benign neoplasm","type":"exact"}],"termid":"MONDO:0021479","xrefs":{"Monarch":{"xref_id":"0021479"}}}


id: MOD:01022
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-lysine residue to 2-piperidinecarboxylic acid.","definition_xrefs":["DeltaMass:0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cyclized residue","termid":"MOD:00601"},{"relation_name":"is_a","term_name":"modified L-lysine residue","termid":"MOD:00912"},{"relation_name":"is_a","term_name":"deaminated residue","termid":"MOD:01160"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2-piperidinecarboxylic acid","synonyms":[{"name":"Pip","type":"exact"}],"termid":"MOD:01022"}


id: MOD:02041
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that contains an L-arginine residue crosslinked to one or more amino acid residues.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-arginine residue","termid":"MOD:00902"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"crosslinked L-arginine residue","synonyms":[{"name":"XlnkArg","type":"exact"}],"termid":"MOD:02041"}


id: GO:0010753
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency or extent of cGMP-mediated signaling.","definition_xrefs":["GOC:dph","GOC:tb","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cGMP-mediated signaling","termid":"GO:0010752"},{"relation_name":"is_a","term_name":"positive regulation of intracellular signal transduction","termid":"GO:1902533"},{"relation_name":"positively_regulates","term_name":"cGMP-mediated signaling","termid":"GO:0019934"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"positive regulation of cGMP-mediated signaling","synonyms":[{"name":"positive regulation of cGMP-mediated signalling","type":"exact"}],"termid":"GO:0010753"}


id: PBO:0034531
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_elongated_vegetative_cell_with_fragmented_nucleus_and_mitotic_cell_cycle_arrest_in_interphase_during_cellular_response_to_UV","termid":"PBO:0034531"}


id: PBO:0042202
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclin G2","termid":"PBO:0042202"}


id: PBO:0058840
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 8070","termid":"PBO:0058840"}


id: PBO:0044504
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytohesin 1","termid":"PBO:0044504"}


id: PBO:0027739
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_localization_to_cell_tip_during_cellular_response_to_salt_stress","termid":"PBO:0027739"}


id: GO:0010871
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that decreases the frequency or rate of receptor biosynthesis. Receptor biosynthesis is the collection of chemical reactions and pathways resulting in the formation of a receptor molecule, a macromolecule that undergoes combination with a hormone, neurotransmitter, drug or intracellular messenger to initiate a change in cell function.","definition_xrefs":["GOC:BHF","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of receptor biosynthetic process (obsolete GO:0010871)","termid":"GO:0010871"}


id: MONDO:0018801
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital bilateral absence of the vas deferens (CBAVD) is a condition leading to male infertility.","definition_xrefs":["Orphanet:48"],"direct_ancestors":[{"relation_name":"is_a","term_name":"male reproductive system disorder","termid":"MONDO:0003150"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital bilateral absence of vas deferens","secondary_identifiers":["GARD:5461","MEDGEN:400764","UMLS:C1865433","MedDRA:10010670","OMIMPS:277180","DOID:0111862","ICD9:752.89","SCTID:275416002"],"synonyms":[{"name":"congenital bilateral agenesis of vas deferens","type":"exact"},{"name":"congenital bilateral aplasia of vas deferens","type":"exact"}],"termid":"MONDO:0018801","xrefs":{"Monarch":{"xref_id":"0018801"}}}


id: PBO:0070746
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L10 pseudogene 2","termid":"PBO:0070746"}


id: PBO:0050797
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5-hydroxytryptamine receptor 5B, pseudogene","termid":"PBO:0050797"}


id: PBO:0085414
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Plasma membrane sulfite pump involved in sulfite metabolism; required for efficient sulfite efflux; major facilitator superfamily protein","termid":"PBO:0085414"}


id: GO:0004361
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: glutaryl-CoA + 2 H+ + oxidized [electron-transfer flavoprotein] = (2E)-butenoyl-CoA + CO2 + reduced [electron-transfer flavoprotein].","definition_xrefs":["RHEA:13389"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyl-CoA dehydrogenase activity","termid":"GO:0003995"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"glutaryl-CoA dehydrogenase activity","secondary_identifiers":["MetaCyc:GLUTARYL-COA-DEHYDROGENASE-RXN","Reactome:R-HSA-71046","UM-BBD_reactionID:r0198","EC:1.3.8.6"],"synonyms":[{"name":"glutaryl coenzyme A dehydrogenase activity","type":"related"}],"termid":"GO:0004361"}


id: GO:0090497
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The orderly movement of a mesenchymal cell from one site to another, often during the development of a multicellular organism.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ameboidal-type cell migration","termid":"GO:0001667"}],"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":"mesenchymal cell migration","termid":"GO:0090497"}


id: PBO:0011125
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3-oxoacyl-[acyl-carrier-protein]reductase (predicted)","termid":"PBO:0011125"}


id: PBO:0089403
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BTB/POZ family substrate adaptor for cullin 3 ubiquitin ligase Btb3","termid":"PBO:0089403"}


id: GO:1902136
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving (-)-secoisolariciresinol.","definition_xrefs":["GOC:TermGenie","PMID:8910615","PMID:9872995"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lignan metabolic process","termid":"GO:0009806"},{"relation_name":"is_a","term_name":"phenol-containing compound metabolic process","termid":"GO:0018958"},{"relation_name":"is_a","term_name":"diol metabolic process","termid":"GO:0034311"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0044281","GO:0019748","GO:0008150"],"is_obsolete":false,"name":"(-)-secoisolariciresinol metabolic process","synonyms":[{"name":"(-)-secoisolariciresinol metabolism","type":"exact"}],"termid":"GO:1902136"}


id: PBO:0086092
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein phosphatase that regulates the mating response; negatively regulates the MAP kinase signaling cascade during mating; member of the serine/threonine phosphatase PP1 family","termid":"PBO:0086092"}


id: PBO:0058473
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5581","termid":"PBO:0058473"}


id: GO:1901207
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of heart looping.","definition_xrefs":["GOC:TermGenie","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of morphogenesis of an epithelium","termid":"GO:1905330"},{"relation_name":"regulates","term_name":"heart looping","termid":"GO:0001947"}],"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 heart looping","synonyms":[{"name":"regulation of cardiac looping","type":"exact"}],"termid":"GO:1901207"}


id: FYPO:0002737
data:
  {"alleles_by_uniquename":{"SJAG_00118:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00118","name":"mid2delta","uniquename":"SJAG_00118:allele-1"},"SJAG_01143:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01143","name":"mid1delta","uniquename":"SJAG_01143:allele-1"},"SJAG_01330:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01330","name":"mad2delta","uniquename":"SJAG_01330:allele-1"},"SJAG_01956:allele-1":{"allele_type":"amino_acid_mutation","description":"E405K ts","gene_uniquename":"SJAG_01956","name":"nuc2-1051","uniquename":"SJAG_01956:allele-1"},"SJAG_02392:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02392","name":"pom1delta","uniquename":"SJAG_02392:allele-1"},"SJAG_02592:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02592","name":"sty1delta","uniquename":"SJAG_02592:allele-1"},"SJAG_03351:allele-1":{"allele_type":"amino_acid_mutation","description":"A186T ts","gene_uniquename":"SJAG_03351","name":"cut23-415","uniquename":"SJAG_03351:allele-1"},"SJAG_03449:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03449","name":"man1delta","uniquename":"SJAG_03449:allele-1"},"SJAG_03449:allele-2":{"allele_type":"partial_amino_acid_deletion","description":"man1DHEH","gene_uniquename":"SJAG_03449","name":"Man1DHEH","uniquename":"SJAG_03449:allele-2"},"SJAG_03449:allele-3":{"allele_type":"amino_acid_insertion_and_deletion","description":"man1-1-488","gene_uniquename":"SJAG_03449","name":"man1-1-488","uniquename":"SJAG_03449:allele-3"},"SJAG_03575:allele-1":{"allele_type":"amino_acid_mutation","description":"E548K ts","gene_uniquename":"SJAG_03575","name":"apc2-361","uniquename":"SJAG_03575:allele-1"},"SJAG_03596:allele-1":{"allele_type":"amino_acid_mutation","description":"L264P,P442T","gene_uniquename":"SJAG_03596","name":"cdc15-A","uniquename":"SJAG_03596:allele-1"},"SJAG_04280:allele-1":{"allele_type":"amino_acid_mutation","description":"T582G","gene_uniquename":"SJAG_04280","name":"wee1-as8","uniquename":"SJAG_04280:allele-1"},"SJAG_04522:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04522","name":"rga4delta","uniquename":"SJAG_04522:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[118751],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000231"},{"annotations":[118756],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000729"},{"annotations":[118799],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0001369"},{"annotations":[118752],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0000118"}],"single_locus_phenotype":[{"annotations":[118744],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000231"},{"annotations":[118718,118719,118717],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"FYPO:0000671"},{"annotations":[118637,118702],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0002998"},{"annotations":[118832,118928],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0004318"},{"annotations":[118777],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0002026"},{"annotations":[118745,118642],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000729"},{"annotations":[118800],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0001369"},{"annotations":[118650,118649,118648],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000324"},{"annotations":[118741,118742],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0000118"}]},"cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which a cell does not execute a mitotic cell cycle process normally. A mitotic cell cycle process is any of the processes that form part of the mitotic cell cycle, and thereby ensures successive accurate and complete genome replication and chromosome segregation during the vegetative growth phase of the life cycle.","definition_xrefs":["PomBase:mah","GO:0022402"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic cell cycle","termid":"FYPO:0000059"},{"relation_name":"is_a","term_name":"abnormal cell cycle process","termid":"FYPO:0002734"}],"gene_count":12,"genes_by_uniquename":{"SJAG_00118":null,"SJAG_01143":null,"SJAG_01330":null,"SJAG_01956":null,"SJAG_02392":null,"SJAG_02592":null,"SJAG_03351":null,"SJAG_03449":null,"SJAG_03575":null,"SJAG_03596":null,"SJAG_04280":null,"SJAG_04522":null},"genotype_count":17,"genotypes_by_uniquename":{"Man1DHEH-man1DHEH-partial_amino_acid_deletion-expression-not_assayed_or_wild_type":{"display_name":"Man1DHEH(man1DHEH)","display_uniquename":"Man1DHEH-man1DHEH-partial_amino_acid_deletion-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03449:allele-2","expression":"Not assayed or wild type"}]}]},"apc2-361-E548K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"apc2-361(E548K ts)","display_uniquename":"apc2-361-E548K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03575:allele-1","expression":"Not assayed or wild type"}]}]},"cdc15-A-L264P,P442T-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"cdc15-A(L264P,P442T aa)","display_uniquename":"cdc15-A-L264P,P442T-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03596:allele-1","expression":"Not assayed or wild type"}]}]},"cdc15-A-L264P,P442T-amino_acid_mutation-expression-not_assayed_or_wild_type__mid1delta":{"display_name":"cdc15-A(L264P,P442T aa) mid1delta","display_uniquename":"cdc15-A-L264P,P442T-amino_acid_mutation-expression-not_assayed_or_wild_type__mid1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03596:allele-1","expression":"Not assayed or wild type"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-1","expression":"Null"}]}]},"cut23-415-A186T_ts-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"cut23-415(A186T ts)","display_uniquename":"cut23-415-A186T_ts-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03351:allele-1","expression":"Not assayed or wild type"}]}]},"mad2delta":{"display_name":"mad2delta","display_uniquename":"mad2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01330:allele-1","expression":"Null"}]}]},"man1-1-488-man1-1-488-amino_acid_insertion_and_deletion-expression-not_assayed_or_wild_type":{"display_name":"man1-1-488(aa)","display_uniquename":"man1-1-488-man1-1-488-amino_acid_insertion_and_deletion-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03449:allele-3","expression":"Not assayed or wild type"}]}]},"man1delta":{"display_name":"man1delta","display_uniquename":"man1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03449:allele-1","expression":"Null"}]}]},"mid1delta":{"display_name":"mid1delta","display_uniquename":"mid1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-1","expression":"Null"}]}]},"mid1delta__mid2delta":{"display_name":"mid1delta mid2delta","display_uniquename":"mid1delta__mid2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_00118:allele-1","expression":"Null"}]}]},"mid1delta__pom1delta":{"display_name":"mid1delta pom1delta","display_uniquename":"mid1delta__pom1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_02392:allele-1","expression":"Null"}]}]},"mid2delta":{"display_name":"mid2delta","display_uniquename":"mid2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00118:allele-1","expression":"Null"}]}]},"nuc2-1051-E405K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"nuc2-1051(E405K ts)","display_uniquename":"nuc2-1051-E405K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01956:allele-1","expression":"Not assayed or wild type"}]}]},"pom1delta":{"display_name":"pom1delta","display_uniquename":"pom1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02392:allele-1","expression":"Null"}]}]},"rga4delta":{"display_name":"rga4delta","display_uniquename":"rga4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04522:allele-1","expression":"Null"}]}]},"rga4delta__wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"rga4delta wee1-as8(T582G aa)","display_uniquename":"rga4delta__wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04522:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_04280:allele-1","expression":"Not assayed or wild type"}]}]},"sty1delta":{"display_name":"sty1delta","display_uniquename":"sty1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02592:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0000631","FYPO:0005447"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_04280","SJAG_03596","SJAG_01143","SJAG_04522","SJAG_00118","SJAG_02392"],"name":"abnormal mitotic cell cycle process","references_by_uniquename":{"PMID:21802294":null,"PMID:23786411":null,"PMID:24184107":null,"PMID:25866389":null,"PMID:27059155":null,"PMID:30664646":null,"PMID:32109380":null,"PMID:32915139":null,"PMID:33791858":null},"single_locus_annotated_genes":["SJAG_03351","SJAG_01330","SJAG_03575","SJAG_02592","SJAG_01956","SJAG_00118","SJAG_04522","SJAG_03449","SJAG_03596","SJAG_02392","SJAG_01143"],"single_locus_genotype_uniquenames":["Man1DHEH-man1DHEH-partial_amino_acid_deletion-expression-not_assayed_or_wild_type","man1delta","mad2delta","cut23-415-A186T_ts-amino_acid_mutation-expression-not_assayed_or_wild_type","man1-1-488-man1-1-488-amino_acid_insertion_and_deletion-expression-not_assayed_or_wild_type","pom1delta","rga4delta","cdc15-A-L264P,P442T-amino_acid_mutation-expression-not_assayed_or_wild_type","mid1delta","nuc2-1051-E405K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type","apc2-361-E548K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type","sty1delta","mid2delta"],"synonyms":[{"name":"abnormal mitotic cell cycle process during mitotic cell cycle","type":"related"},{"name":"abnormal mitotic cell cycle process during vegetative growth","type":"exact"}],"termid":"FYPO:0002737","terms_by_termid":{"FYECO:0000004":null,"FYECO:0000005":null,"FYECO:0000126":null,"FYECO:0000137":null,"FYECO:0000162":null,"FYECO:0000248":null,"FYECO:0000338":null,"FYPO:0000118":null,"FYPO:0000231":null,"FYPO:0000324":null,"FYPO:0000671":null,"FYPO:0000729":null,"FYPO:0001369":null,"FYPO:0002026":null,"FYPO:0002998":null,"FYPO:0004318":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null}}


id: GO:0061321
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires the specialized structural and/or functional features of a garland nephrocyte. A garland nephrocyte is an insect renal cell that filters hemolymph and forms a ring with other garland nephrocytes around the esophagus. Differentiation includes the processes involved in commitment of a cell to a specific fate and its subsequent development to the mature state.","definition_xrefs":["PMID:19783135","GOC:sart","CL:0000486","GOC:dph","GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nephrocyte differentiation","termid":"GO:0061319"},{"relation_name":"part_of","term_name":"embryonic development via the syncytial blastoderm","termid":"GO:0001700"}],"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":"garland nephrocyte differentiation","secondary_identifiers":["GO:0007514"],"synonyms":[{"name":"garland cell differentiation","type":"exact"}],"termid":"GO:0061321"}


id: PBO:0077684
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TNF superfamily member 13b","termid":"PBO:0077684"}


id: FYPO:0005080
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to chromatin at the centromere inner repeat regions is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PMID:21151114","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to centromeric heterochromatin","termid":"FYPO:0008154"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257","FYPO:0000138","FYPO:0001320","FYPO:0001312"],"is_obsolete":false,"name":"normal protein localization to heterochromatin at centromere inner repeat","synonyms":[{"name":"normal protein localisation to chromatin at centromere inner repeat","type":"exact"},{"name":"normal protein localization to chromatin at centromere imr","type":"exact"},{"name":"normal protein localization to chromatin at centromere inner repeat during mitotic cell cycle","type":"related"},{"name":"normal protein localization to chromatin at centromere inner repeat during vegetative growth","type":"exact"}],"termid":"FYPO:0005080"}


id: MONDO:0021570
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Hauptmann-Thannhauser muscular dystrophy (obsolete MONDO:0021570)","termid":"MONDO:0021570","xrefs":{"Monarch":{"xref_id":"0021570"}}}


id: PBO:0091972
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"wtf antidote-like meiotic drive suppressor Wtf18","termid":"PBO:0091972"}


id: GO:0070611
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + (histone H3)-arginine (position 2) = S-adenosyl-L-homocysteine + (histone H3)-N-methyl-arginine (position 2). This reaction is the addition of a methyl group to the arginine residue at position 2 of histone H3.","definition_xrefs":["PMID:17898714","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-arginine N-methyltransferase activity","termid":"GO:0016274"},{"relation_name":"is_a","term_name":"histone H3 methyltransferase activity","termid":"GO:0140938"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0008276"}],"interesting_parent_ids":["GO:0008276","GO:0016741","GO:0016740","GO:0003674","GO:0003824","GO:0140096"],"is_obsolete":false,"name":"histone H3R2 methyltransferase activity","synonyms":[{"name":"histone H3R2 arginine methyltransferase activity","type":"exact"},{"name":"histone methylase activity (H3-R2 specific)","type":"exact"},{"name":"histone methyltransferase activity (H3-R2 specific)","type":"exact"},{"name":"histone-H3R2 methyltransferase activity","type":"exact"},{"name":"histone-arginine N-methyltransferase activity (H3-R2 specific)","type":"exact"}],"termid":"GO:0070611"}


id: FYPO:0002060
data:
  {"alleles_by_uniquename":{"SJAG_00266:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00266","name":"atf1delta","uniquename":"SJAG_00266:allele-1"},"SJAG_00364:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00364","name":"rad3delta","uniquename":"SJAG_00364:allele-1"},"SJAG_00409:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00409","name":"gpd1delta","uniquename":"SJAG_00409:allele-1"},"SJAG_00426:allele-1":{"allele_type":"amino_acid_mutation","description":"P363S","gene_uniquename":"SJAG_00426","name":"bbl1-P363S","uniquename":"SJAG_00426:allele-1"},"SJAG_00429:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00429","name":"rad26delta","uniquename":"SJAG_00429:allele-1"},"SJAG_00514:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00514","name":"scd1delta","uniquename":"SJAG_00514:allele-1"},"SJAG_00601:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00601","name":"rip1delta","uniquename":"SJAG_00601:allele-1"},"SJAG_01242:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01242","name":"vps32delta","uniquename":"SJAG_01242:allele-1"},"SJAG_01355:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01355","name":"cox6delta","uniquename":"SJAG_01355:allele-1"},"SJAG_01794:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01794","name":"scd2delta","uniquename":"SJAG_01794:allele-1"},"SJAG_01946:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01946","name":"cem1delta","uniquename":"SJAG_01946:allele-1"},"SJAG_02527:allele-1":{"allele_type":"disruption","description":"RNA sequencing revealed that only the 5' end of the disrupted allele showed low RNA expression and coverage","gene_uniquename":"SJAG_02527","name":"lig4::KanMX6","uniquename":"SJAG_02527:allele-1"},"SJAG_02592:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02592","name":"sty1delta","uniquename":"SJAG_02592:allele-1"},"SJAG_02763:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02763","name":"ned1delta","uniquename":"SJAG_02763:allele-1"},"SJAG_03198:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03198","name":"oar2delta","uniquename":"SJAG_03198:allele-1"},"SJAG_03198:allele-2":{"allele_type":"amino_acid_mutation","description":"Y189D cold sensitive","gene_uniquename":"SJAG_03198","name":"oar2-51","uniquename":"SJAG_03198:allele-2"},"SJAG_03198:allele-3":{"allele_type":"amino_acid_mutation","description":"R72A,L75A,R106A,L109A","gene_uniquename":"SJAG_03198","name":"oar2-dm12","synonyms":[{"name":"destruction box mutations","reference":"PMID:23786411","type":"exact"}],"uniquename":"SJAG_03198:allele-3"},"SJAG_03449:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03449","name":"man1delta","uniquename":"SJAG_03449:allele-1"},"SJAG_03453:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03453","name":"ras1delta","uniquename":"SJAG_03453:allele-1"},"SJAG_03575:allele-1":{"allele_type":"amino_acid_mutation","description":"E548K ts","gene_uniquename":"SJAG_03575","name":"apc2-361","uniquename":"SJAG_03575:allele-1"},"SJAG_03720:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03720","name":"tel1delta","uniquename":"SJAG_03720:allele-1"},"SJAG_03892:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03892","name":"vps4delta","uniquename":"SJAG_03892:allele-1"},"SJAG_04464:allele-1":{"allele_type":"amino_acid_mutation","description":"R152C","gene_uniquename":"SJAG_04464","name":"pim1-R152C","synonyms":[{"name":"Inferred CDK-phospho-mimic mutation","reference":"PMID:28954740","type":"exact"}],"uniquename":"SJAG_04464:allele-1"},"SJAG_04697:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04697","name":"gms1delta","uniquename":"SJAG_04697:allele-1"},"SJAG_04703:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04703","name":"for3delta","uniquename":"SJAG_04703:allele-1"},"SJAG_05207:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_05207","name":"cmp7delta","uniquename":"SJAG_05207:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[118660,118658,118659,118662],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000674"}],"single_locus_phenotype":[{"annotations":[118595,118607],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0004481"},{"annotations":[119059,119039],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000082"},{"annotations":[118647,118645,118646,118731,118661],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000080"},{"annotations":[118882,118683,118934,118938,118942],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001355"},{"annotations":[119030],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001690"},{"annotations":[118673,118674,119075,118672],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001357"},{"annotations":[119081],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001408"},{"annotations":[119028,118793,118709,118857,118730,118671,118856,118899,119027,118729],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001234"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell population phenotype in which cells in the population are viable in the vegetative growth phase of the life cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viable cell population","termid":"FYPO:0002058"}],"gene_count":24,"genes_by_uniquename":{"SJAG_00266":null,"SJAG_00364":null,"SJAG_00409":null,"SJAG_00426":null,"SJAG_00429":null,"SJAG_00514":null,"SJAG_00601":null,"SJAG_01242":null,"SJAG_01355":null,"SJAG_01794":null,"SJAG_01946":null,"SJAG_02527":null,"SJAG_02592":null,"SJAG_02763":null,"SJAG_03198":null,"SJAG_03449":null,"SJAG_03453":null,"SJAG_03575":null,"SJAG_03720":null,"SJAG_03892":null,"SJAG_04464":null,"SJAG_04697":null,"SJAG_04703":null,"SJAG_05207":null},"genotype_count":29,"genotypes_by_uniquename":{"apc2-361-E548K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type__cem1delta":{"display_name":"apc2-361(E548K ts) cem1delta","display_uniquename":"apc2-361-E548K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type__cem1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03575:allele-1","expression":"Not assayed or wild type"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_01946:allele-1","expression":"Null"}]}]},"apc2-361-E548K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type__oar2-51-Y189D_cold_sensitive-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"apc2-361(E548K ts) oar2-51(Y189D cold sensitive)","display_uniquename":"apc2-361-E548K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type__oar2-51-Y189D_cold_sensitive-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03575:allele-1","expression":"Not assayed or wild type"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_03198:allele-2","expression":"Not assayed or wild type"}]}]},"apc2-361-E548K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type__oar2-dm12-R72A,L75A,R106A,L109A-amino_acid_mutation-expression-overexpression":{"display_name":"apc2-361(E548K ts) oar2-dm12(R72A,L75A,R106A,L109A aa)[Overexpression]","display_uniquename":"apc2-361-E548K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type__oar2-dm12-R72A,L75A,R106A,L109A-amino_acid_mutation-expression-overexpression","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03575:allele-1","expression":"Not assayed or wild type"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_03198:allele-3","expression":"Overexpression"}]}]},"apc2-361-E548K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type__oar2delta":{"display_name":"apc2-361(E548K ts) oar2delta","display_uniquename":"apc2-361-E548K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type__oar2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03575:allele-1","expression":"Not assayed or wild type"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_03198:allele-1","expression":"Null"}]}]},"atf1delta":{"display_name":"atf1delta","display_uniquename":"atf1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00266:allele-1","expression":"Null"}]}]},"bbl1-P363S-P363S-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"bbl1-P363S(aa)","display_uniquename":"bbl1-P363S-P363S-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00426:allele-1","expression":"Not assayed or wild type"}]}]},"cem1delta":{"display_name":"cem1delta","display_uniquename":"cem1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01946:allele-1","expression":"Null"}]}]},"cmp7delta":{"display_name":"cmp7delta","display_uniquename":"cmp7delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_05207:allele-1","expression":"Null"}]}]},"cox6delta":{"display_name":"cox6delta","display_uniquename":"cox6delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01355:allele-1","expression":"Null"}]}]},"for3delta":{"display_name":"for3delta","display_uniquename":"for3delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04703:allele-1","expression":"Null"}]}]},"gms1delta":{"display_name":"gms1delta","display_uniquename":"gms1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04697:allele-1","expression":"Null"}]}]},"gpd1delta":{"display_name":"gpd1delta","display_uniquename":"gpd1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00409:allele-1","expression":"Null"}]}]},"lig4::KanMX6-RNA_sequencing_revealed_that_only_the_5'_end_of_the_disrupted_allele_showed_low_RNA_expression_and_coverage-disruption-expression-knockdown":{"display_name":"lig4::KanMX6(RNA sequencing revealed that only the 5' end of the disrupted allele showed low RNA expression and coverage)[Knockdown]","display_uniquename":"lig4::KanMX6-RNA_sequencing_revealed_that_only_the_5'_end_of_the_disrupted_allele_showed_low_RNA_expression_and_coverage-disruption-expression-knockdown","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02527:allele-1","expression":"Knockdown"}]}]},"man1delta":{"display_name":"man1delta","display_uniquename":"man1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03449:allele-1","expression":"Null"}]}]},"ned1delta":{"display_name":"ned1delta","display_uniquename":"ned1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02763:allele-1","expression":"Null"}]}]},"oar2-51-Y189D_cold_sensitive-amino_acid_mutation-expression-overexpression":{"display_name":"oar2-51(Y189D cold sensitive)[Overexpression]","display_uniquename":"oar2-51-Y189D_cold_sensitive-amino_acid_mutation-expression-overexpression","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03198:allele-2","expression":"Overexpression"}]}]},"oar2-dm12-R72A,L75A,R106A,L109A-amino_acid_mutation-expression-overexpression":{"display_name":"oar2-dm12(R72A,L75A,R106A,L109A aa)[Overexpression]","display_uniquename":"oar2-dm12-R72A,L75A,R106A,L109A-amino_acid_mutation-expression-overexpression","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03198:allele-3","expression":"Overexpression"}]}]},"oar2delta":{"display_name":"oar2delta","display_uniquename":"oar2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03198:allele-1","expression":"Null"}]}]},"pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"pim1-R152C(aa)","display_uniquename":"pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04464:allele-1","expression":"Not assayed or wild type"}]}]},"rad26delta":{"display_name":"rad26delta","display_uniquename":"rad26delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00429:allele-1","expression":"Null"}]}]},"rad3delta":{"display_name":"rad3delta","display_uniquename":"rad3delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00364:allele-1","expression":"Null"}]}]},"ras1delta":{"display_name":"ras1delta","display_uniquename":"ras1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03453:allele-1","expression":"Null"}]}]},"rip1delta":{"display_name":"rip1delta","display_uniquename":"rip1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00601:allele-1","expression":"Null"}]}]},"scd1delta":{"display_name":"scd1delta","display_uniquename":"scd1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00514:allele-1","expression":"Null"}]}]},"scd2delta":{"display_name":"scd2delta","display_uniquename":"scd2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01794:allele-1","expression":"Null"}]}]},"sty1delta":{"display_name":"sty1delta","display_uniquename":"sty1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02592:allele-1","expression":"Null"}]}]},"tel1delta":{"display_name":"tel1delta","display_uniquename":"tel1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03720:allele-1","expression":"Null"}]}]},"vps32delta":{"display_name":"vps32delta","display_uniquename":"vps32delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01242:allele-1","expression":"Null"}]}]},"vps4delta":{"display_name":"vps4delta","display_uniquename":"vps4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03892:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0002058","FYPO:0002057","FYPO:0000003"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_03575","SJAG_03198","SJAG_01946"],"name":"viable vegetative cell population","references_by_uniquename":{"PMID:23090706":null,"PMID:23786411":null,"PMID:24184107":null,"PMID:25318672":null,"PMID:26774782":null,"PMID:28954740":null,"PMID:29566183":null,"PMID:30664646":null,"PMID:30726171":null,"PMID:31150379":null,"PMID:32109380":null,"PMID:32243490":null,"PMID:36058798":null,"PMID:37164017":null,"PMID:37233261":null},"single_locus_annotated_genes":["SJAG_04703","SJAG_00601","SJAG_01355","SJAG_02527","SJAG_03892","SJAG_03453","SJAG_04464","SJAG_00266","SJAG_04697","SJAG_03198","SJAG_01794","SJAG_05207","SJAG_03449","SJAG_02763","SJAG_00409","SJAG_01946","SJAG_00364","SJAG_02592","SJAG_00514","SJAG_03720","SJAG_00426","SJAG_01242","SJAG_00429"],"single_locus_genotype_uniquenames":["scd1delta","atf1delta","oar2delta","tel1delta","cox6delta","oar2-dm12-R72A,L75A,R106A,L109A-amino_acid_mutation-expression-overexpression","cem1delta","lig4::KanMX6-RNA_sequencing_revealed_that_only_the_5'_end_of_the_disrupted_allele_showed_low_RNA_expression_and_coverage-disruption-expression-knockdown","bbl1-P363S-P363S-amino_acid_mutation-expression-not_assayed_or_wild_type","sty1delta","vps4delta","scd2delta","pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type","rad26delta","ras1delta","rad3delta","gms1delta","cmp7delta","ned1delta","for3delta","gpd1delta","man1delta","vps32delta","rip1delta","oar2-51-Y189D_cold_sensitive-amino_acid_mutation-expression-overexpression"],"synonyms":[{"name":"viable cell population during vegetative growth","type":"exact"},{"name":"viable vegetative cell population during mitotic cell cycle","type":"related"}],"termid":"FYPO:0002060","terms_by_termid":{"FYECO:0000004":null,"FYECO:0000005":null,"FYECO:0000006":null,"FYECO:0000103":null,"FYECO:0000117":null,"FYECO:0000126":null,"FYECO:0000137":null,"FYECO:0000162":null,"FYPO:0000080":null,"FYPO:0000082":null,"FYPO:0000674":null,"FYPO:0001234":null,"FYPO:0001355":null,"FYPO:0001357":null,"FYPO:0001408":null,"FYPO:0001690":null,"FYPO:0004481":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null,"FYPO_EXT:0000003":null}}


id: PBO:0063524
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PDZ domain containing 2","termid":"PBO:0063524"}


id: MONDO:1010788
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Ehlers-Danlos syndrome in horses in which the cause of the disease is a mutation in the PLOD1 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Ehlers-Danlos syndrome, horse","termid":"MONDO:1011495"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ehlers-Danlos syndrome, kyphoscoliotic type, PLOD1-related, horse","secondary_identifiers":["OMIA:001982-9796"],"synonyms":[{"name":"Fragile Foal Syndrome","type":"exact"},{"name":"kEDS","type":"exact"}],"termid":"MONDO:1010788","xrefs":{"Monarch":{"xref_id":"1010788"}}}


id: PBO:0080035
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin specific peptidase 17 like family member 21","termid":"PBO:0080035"}


id: RO:0002242
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"A broad relationship between an exposure event or process and a process by which the exposure stressor comes into contact with the exposure receptor","direct_ancestors":[{"relation_name":"is_a","term_name":"related_via_exposure_to","termid":"RO:0002244"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_exposure_route","termid":"RO:0002242"}


id: GO:0106151
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Interacting selectivity and noncovalently with a cyclic nucleotide mimicking protein motif that is part of the same protein. The CNBHD is a domain on KCNH channels that creates a binding pocket on the KCNH channel that resembles the cyclic nucleotide- binding domain on other ion channels. It binds to a peptide motif that is part of the same protein rather than a cyclic nucleotide.","definition_xrefs":["PMID:29567795","GOC:cvs","PMID:27025590"],"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:0005488"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"CNBH domain intrinsic ligand binding","termid":"GO:0106151"}


id: FYPO:0005634
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which sister kinetochores become separated during the first meiotic nuclear division, and sister chromatids subsequently separate to result in equational segregation. Equational sister chromatid separation is caused by  bi-orientated attachment of sister chromatids.","definition_xrefs":["PMID:21920317","PomBase:vw","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sister kinetochore dissociation in meiotic metaphase I","termid":"FYPO:0005648"},{"relation_name":"is_a","term_name":"equational sister chromatid separation at meiosis I","termid":"FYPO:0008202"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000641","FYPO:0000002","FYPO:0000631"],"is_obsolete":false,"name":"sister kinetochore dissociation in meiotic metaphase I with  equational sister chromatid  segregation in meiosis I","synonyms":[{"name":"abnormal chromosome segregation during meiosis I with premature sister kinetochore separation and equational sister chromatid separation","type":"exact"},{"name":"abolished monopolar kinetochore attachment during meiosis I","type":"related"},{"name":"equational sister chromatid separation during first meiotic nuclear division","type":"exact"},{"name":"equational sister chromatid separation during meiosis I with split kinetochores","type":"related"},{"name":"equational sister chromatid separation in meiosis I","type":"exact"},{"name":"increased bi-orientated attachment of sister chromatids in meiosis I","type":"related"}],"termid":"FYPO:0005634"}


id: PR:O42919
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC16A3.14 gene.","definition_xrefs":["UniProtKB:O42919","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"37S ribosomal protein S26A, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC16A3.14","synonyms":[{"name":"Spom972h-SPBC16A3.14","type":"exact"}],"termid":"PR:O42919"}


id: PBO:0043996
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chorionic somatomammotropin hormone 1","termid":"PBO:0043996"}


id: MONDO:0013185
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any leprosy in which the cause of the disease is a mutation in the TLR1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leprosy, susceptibility to, 5","secondary_identifiers":["OMIM:613223","UMLS:C2750733","MEDGEN:442551"],"synonyms":[{"name":"LPRS5","type":"related"},{"name":"TLR1 leprosy","type":"exact"},{"name":"leprosy caused by mutation in TLR1","type":"exact"},{"name":"leprosy, protection against","type":"related"},{"name":"leprosy, susceptibility to, 5","type":"exact"},{"name":"leprosy, susceptibility to, type 5","type":"exact"},{"name":"susceptibility to leprosy 5","type":"related"}],"termid":"MONDO:0013185","xrefs":{"Monarch":{"xref_id":"0013185"}}}


id: GO:0048498
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that determines the orientation of petals with reference to the central axis.","definition_xrefs":["GOC:tb","PMID:10572040"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment of floral organ orientation","termid":"GO:0048559"},{"relation_name":"part_of","term_name":"petal morphogenesis","termid":"GO:0048446"}],"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":"establishment of petal orientation","termid":"GO:0048498"}


id: GO:2000078
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of pancreatic B cell development.","definition_xrefs":["GOC:yaf","GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell development","termid":"GO:0010720"},{"relation_name":"is_a","term_name":"positive regulation of epithelial cell differentiation","termid":"GO:0030858"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"is_a","term_name":"regulation of type B pancreatic cell development","termid":"GO:2000074"},{"relation_name":"positively_regulates","term_name":"type B pancreatic cell development","termid":"GO:0003323"}],"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 type B pancreatic cell development","synonyms":[{"name":"positive regulation of pancreatic B cell development","type":"exact"},{"name":"positive regulation of pancreatic beta cell development","type":"exact"}],"termid":"GO:2000078"}


id: GO:0035185
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The first nine mitotic division cycles of the insect embryo, during which the dividing nuclei lie deep in the interior of the egg and divide nearly synchronously. This is the first phase of the syncytial period where nuclei divide in a common cytoplasm without cytokinesis.","definition_xrefs":["ISBN:0879694238"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell cycle comprising mitosis without cytokinesis","termid":"GO:0033301"},{"relation_name":"is_a","term_name":"mitotic cell cycle, embryonic","termid":"GO:0045448"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"preblastoderm mitotic cell cycle","termid":"GO:0035185"}


id: GO:0110020
data:
  {"annotated_genes":["SJAG_02795","SJAG_03048","SJAG_00082","SJAG_01805","SJAG_04597","SJAG_02592"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[97778],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000432"},{"annotations":[101869],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903500"},{"annotations":[89474,93896],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903501"},{"annotations":[118639,93862,93292],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903499"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the assembly, arrangement of constituent parts, or disassembly of cytoskeletal structures containing both actin and myosin or paramyosin.","definition_xrefs":["GOC:lf","PMID:22790195"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of actin cytoskeleton organization","termid":"GO:0032956"},{"relation_name":"regulates","term_name":"actomyosin structure organization","termid":"GO:0031032"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00082":null,"SJAG_01805":null,"SJAG_02592":null,"SJAG_02795":null,"SJAG_03048":null,"SJAG_04597":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007010"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0030036"}],"interesting_parent_ids":["GO:0007010","GO:0008150","GO:0030036"],"is_obsolete":false,"name":"regulation of actomyosin structure organization","references_by_uniquename":{"GO_REF:0000107":null,"PMID:32915139":null},"termid":"GO:0110020","terms_by_termid":{"GO:0120306":null,"GO:1903499":null,"GO:1903500":null,"GO:1903501":null,"GO:2000432":null}}


id: PR:O74887
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A peroxiredoxin tpx1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["UniProtKB:O74887","PRO:CNA"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peroxiredoxin tpx1","termid":"PR:000028932"},{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peroxiredoxin tpx1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC576.03c","synonyms":[{"name":"Spom972h-tpx1","type":"exact"}],"termid":"PR:O74887"}


id: GO:0032968
data:
  {"annotated_genes":["SJAG_01149","SJAG_02551","SJAG_03967","SJAG_00150","SJAG_03061","SJAG_01151","SJAG_03118"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[95292,102557,104860,105532,108522,114793,116491],"is_not":false,"summary":null,"term":"GO:0032968"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of transcription elongation, the extension of an RNA molecule after transcription initiation and promoter clearance by the addition of ribonucleotides, catalyzed by RNA polymerase II.","definition_xrefs":["GOC:mah","GOC:txnOH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of DNA-templated transcription, elongation","termid":"GO:0032786"},{"relation_name":"is_a","term_name":"regulation of transcription elongation by RNA polymerase II","termid":"GO:0034243"},{"relation_name":"is_a","term_name":"positive regulation of transcription by RNA polymerase II","termid":"GO:0045944"},{"relation_name":"positively_regulates","term_name":"transcription elongation by RNA polymerase II","termid":"GO:0006368"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00150":null,"SJAG_01149":null,"SJAG_01151":null,"SJAG_02551":null,"SJAG_03061":null,"SJAG_03118":null,"SJAG_03967":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006351"},{"rel_name":"is_a","termid":"GO:0006355"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0006351"}],"interesting_parent_ids":["GO:0010467","GO:0006351","GO:0006355","GO:0008150"],"is_obsolete":false,"name":"positive regulation of transcription elongation by RNA polymerase II","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0090040"],"synonyms":[{"name":"positive regulation of RNA elongation from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of gene-specific transcription elongation from RNA polymerase II promoter","type":"related"},{"name":"positive regulation of transcription elongation from RNA polymerase II promoter","type":"exact"}],"termid":"GO:0032968","terms_by_termid":{"GO:0032968":null}}


id: PBO:0002403
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleotide-sugar phosphatase (predicted)","termid":"PBO:0002403"}


id: MONDO:0030376
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Martsolf syndrome","termid":"MONDO:0023910"}],"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":"Martsolf syndrome 2","secondary_identifiers":["UMLS:C5543626","MEDGEN:1779703","OMIM:619420"],"synonyms":[{"name":"MARTS2","type":"exact"}],"termid":"MONDO:0030376","xrefs":{"Monarch":{"xref_id":"0030376"}}}


id: GO:1900933
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of nonadec-1-ene metabolic process.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of olefin metabolic process","termid":"GO:1900909"},{"relation_name":"is_a","term_name":"regulation of nonadec-1-ene metabolic process","termid":"GO:1900932"},{"relation_name":"negatively_regulates","term_name":"nonadec-1-ene metabolic process","termid":"GO:1900876"}],"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 nonadec-1-ene metabolic process","synonyms":[{"name":"down regulation of nonadec-1-ene metabolic process","type":"exact"},{"name":"down regulation of nonadec-1-ene metabolism","type":"exact"},{"name":"down-regulation of nonadec-1-ene metabolic process","type":"exact"},{"name":"down-regulation of nonadec-1-ene metabolism","type":"exact"},{"name":"downregulation of nonadec-1-ene metabolic process","type":"exact"},{"name":"downregulation of nonadec-1-ene metabolism","type":"exact"},{"name":"inhibition of nonadec-1-ene metabolic process","type":"narrow"},{"name":"inhibition of nonadec-1-ene metabolism","type":"exact"},{"name":"negative regulation of nonadec-1-ene metabolism","type":"exact"}],"termid":"GO:1900933"}


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


id: GO:0032588
data:
  {"annotated_genes":["SJAG_02912","SJAG_00296","SJAG_05330","SJAG_03953","SJAG_02168"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[90217,90699,92702,95216,106858],"is_not":false,"summary":null,"term":"GO:0032588"}]},"cv_name":"cellular_component","definition":"The lipid bilayer surrounding any of the compartments that make up the trans-Golgi network.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organelle membrane","termid":"GO:0031090"},{"relation_name":"part_of","term_name":"trans-Golgi network","termid":"GO:0005802"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00296":null,"SJAG_02168":null,"SJAG_02912":null,"SJAG_03953":null,"SJAG_05330":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005794"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005794","GO:0005737","GO:0005575"],"is_obsolete":false,"name":"trans-Golgi network membrane","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"Golgi trans face membrane","type":"related"},{"name":"trans Golgi network membrane","type":"exact"}],"termid":"GO:0032588","terms_by_termid":{"GO:0032588":null}}


id: GO:0061762
data:
  {"annotated_genes":["SJAG_03802","SJAG_03486","SJAG_03501"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[115639,115977,117724],"is_not":false,"summary":null,"term":"GO:0061762"}]},"cv_name":"biological_process","definition":"The series of molecular signals in which calmodulin-dependent protein kinase activity enabled by a CAMKK directly activates an AMPK. The cascade begins with calmodulin binding calcium which in turn binds CAMKK enabling its calmodulin-dependent protein kinase activity. The cascade ends with AMP-activated protein kinase activity.","definition_xrefs":["GOC:pad","PMID:23010169","GOC:PARL","PMID:24709372","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"calcium-mediated signaling","termid":"GO:0019722"}],"gene_count":3,"genes_by_uniquename":{"SJAG_03486":null,"SJAG_03501":null,"SJAG_03802":null},"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":"CAMKK-AMPK signaling cascade","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"stress-activated AMP-activated protein kinase signaling cascade","type":"related"}],"termid":"GO:0061762","terms_by_termid":{"GO:0061762":null}}


id: PBO:0053049
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"La ribonucleoprotein 7, transcriptional regulator","termid":"PBO:0053049"}


id: GO:0034959
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process leading to the attainment of the full functional capacity of endothelin by conversion of Big-endothelin substrate into mature endothelin.","definition_xrefs":["GOC:BHF","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptide hormone processing","termid":"GO:0016486"},{"relation_name":"part_of","term_name":"regulation of systemic arterial blood pressure by endothelin","termid":"GO:0003100"}],"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:0051604","GO:0010467","GO:0008150"],"is_obsolete":false,"name":"endothelin maturation","termid":"GO:0034959"}


id: PBO:0046665
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"embryonic stem cell related","termid":"PBO:0046665"}


id: GO:0048891
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a lateral line ganglion neuron.","definition_xrefs":["PMID:15018940"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peripheral nervous system neuron differentiation","termid":"GO:0048934"},{"relation_name":"part_of","term_name":"lateral line ganglion development","termid":"GO:0048890"}],"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":"lateral line ganglion neuron differentiation","synonyms":[{"name":"gLL neuron differentiation","type":"exact"}],"termid":"GO:0048891"}


id: MONDO:0700160
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An adenoma arising from the mammary gland of a dog.","definition_xrefs":["NCIT:C147073"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mammary neoplasms, animal","termid":"MONDO:0025483"},{"relation_name":"is_a","term_name":"adenoma, non-human","termid":"MONDO:0700133"},{"relation_name":"is_a","term_name":"canine neoplasm","termid":"MONDO:0700139"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"canine mammary adenoma","termid":"MONDO:0700160","xrefs":{"Monarch":{"xref_id":"0700160"}}}


id: MONDO:0009518
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any leprosy in which the cause of the disease is a mutation in the TLR2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leprosy, susceptibility to, 3","secondary_identifiers":["OMIM:246300","UMLS:C1968668","MEDGEN:368500"],"synonyms":[{"name":"LPRS3","type":"related"},{"name":"TLR2 leprosy","type":"exact"},{"name":"leprosy caused by mutation in TLR2","type":"exact"},{"name":"leprosy, susceptibility to","type":"exact"},{"name":"leprosy, susceptibility to, 3","type":"exact"},{"name":"leprosy, susceptibility to, type 3","type":"exact"},{"name":"susceptibility to leprosy 3","type":"related"}],"termid":"MONDO:0009518","xrefs":{"Monarch":{"xref_id":"0009518"}}}


id: PBO:0046261
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER membrane protein complex subunit 1","termid":"PBO:0046261"}


id: PBO:0066693
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"regulator of microtubule dynamics 3","termid":"PBO:0066693"}


id: PBO:0056406
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"membrane associated ring-CH-type finger 4","termid":"PBO:0056406"}


id: MONDO:0018848
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Retroperitoneal fibrosis (RPF) is characterized by the development of a fibrotic mass surrounding retroperitoneal structures, such as aorta, vena cava, ureters and psoas muscle.","definition_xrefs":["Orphanet:49041"],"direct_ancestors":[{"relation_name":"is_a","term_name":"IgG4-related disease","termid":"MONDO:0017287"}],"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":"IgG4-related retroperitoneal fibrosis","secondary_identifiers":["MESH:D012185","NCIT:C26876","UMLS:C0035357","NORD:1665","ICD9:593.4","GARD:9568","SCTID:197808006","icd11.foundation:900354709","MEDGEN:20554","MedDRA:10038979"],"synonyms":[{"name":"Ormond disease","type":"exact"},{"name":"Ormond's disease","type":"related"},{"name":"Retroperitoneal Fibrosis","type":"exact"},{"name":"idiopathic retroperitoneal fibrosis","type":"exact"},{"name":"retroperitoneal fibrosis","type":"exact"}],"termid":"MONDO:0018848","xrefs":{"Monarch":{"xref_id":"0018848"}}}


id: MONDO:1012872
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Primary ciliary dyskinesia that occurs in sheep due to a mutation in the CCDC65 gene. Homozygous affected lambs suffer from respiratory defects predisposing infectious pneumonia with a fatal ending at a young age.","definition_xrefs":["PMID:35052387","MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary ciliary dyskinesia, non-human animal","termid":"MONDO:1011925"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primary ciliary dyskinesia, CCDC65-related, sheep","secondary_identifiers":["OMIA:002342-9940"],"synonyms":[{"name":"LDHH6","type":"exact"},{"name":"Lacaune deficient homozygous haplotype 6, sheep","type":"related"}],"termid":"MONDO:1012872","xrefs":{"Monarch":{"xref_id":"1012872"}}}


id: GO:0015479
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete outer membrane exporter porin (obsolete GO:0015479)","synonyms":[{"name":"outer membrane exporter porin","type":"exact"}],"termid":"GO:0015479"}


id: PR:O74830
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC1183.02 gene.","definition_xrefs":["UniProtKB:O74830","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":"glutathione S-transferase C1183.02 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1183.02","synonyms":[{"name":"Spom972h-SPCC1183.02","type":"exact"}],"termid":"PR:O74830"}


id: MONDO:0968991
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"primary central precocious puberty in male","termid":"MONDO:0958356"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-genetic central precocious puberty in male","secondary_identifiers":["MEDGEN:1853153","Orphanet:650102","UMLS:C5816759"],"termid":"MONDO:0968991","xrefs":{"Monarch":{"xref_id":"0968991"}}}


id: PBO:0055589
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 3025","termid":"PBO:0055589"}


id: MONDO:0015200
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infection with roundworms of the genus anisakis. Human infection results from the consumption of fish harboring roundworm larvae. The worms may cause acute nausea; vomiting; or penetrate into the wall of the digestive tract where they give rise to eosinophilic granuloma in the stomach; intestines; or the omentum.","definition_xrefs":["MESH:D017129"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Ascaridida infectious disease","termid":"MONDO:0005656"},{"relation_name":"is_a","term_name":"intestinal helminthiasis","termid":"MONDO:0024271"}],"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":"anisakiasis","secondary_identifiers":["icd11.foundation:2005274000","DOID:7033","MEDGEN:102418","NCIT:C128393","Orphanet:1070","SCTID:442652006","UMLS:C0162576","EFO:0007146","GARD:693","ICD9:127.1","MedDRA:10002533","ICD10CM:B81.0"],"synonyms":[{"name":"Anisakiases","type":"related"},{"name":"Anisakis infection","type":"related"},{"name":"Anisakis simplex infection","type":"exact"},{"name":"Pseudoterranova infection","type":"related"},{"name":"infection by Anisakis larva","type":"exact"},{"name":"infections, Anisakis simplex","type":"related"}],"termid":"MONDO:0015200","xrefs":{"Monarch":{"xref_id":"0015200"}}}


id: MONDO:1011316
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Disorder of visual system that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-human animal disease","termid":"MONDO:0005583"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"disorder of visual system, non-human animal","termid":"MONDO:1011316","xrefs":{"Monarch":{"xref_id":"1011316"}}}


id: PBO:0051471
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin lambda variable (I)-70 (pseudogene)","termid":"PBO:0051471"}


id: MONDO:0033570
data:
  {"annotated_genes":["SJAG_05270"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85358],"is_not":false,"summary":null,"term":"MONDO:0033570"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05270":null},"genotype_count":0,"is_obsolete":false,"name":"combined oxidative phosphorylation deficiency 50","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:619025","MEDGEN:1753519","UMLS:C5436623","DOID:0112111"],"synonyms":[{"name":"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 50","type":"related"},{"name":"COXPD50","type":"related"}],"termid":"MONDO:0033570","terms_by_termid":{"MONDO:0033570":null},"xrefs":{"Monarch":{"xref_id":"0033570"}}}


id: GO:0032663
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of interleukin-2 production.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytokine production","termid":"GO:0001817"},{"relation_name":"regulates","term_name":"interleukin-2 production","termid":"GO:0032623"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"regulation of interleukin-2 production","secondary_identifiers":["GO:0045076","GO:1900040"],"synonyms":[{"name":"regulation of IL-2 production","type":"exact"},{"name":"regulation of interleukin-2 biosynthetic process","type":"narrow"},{"name":"regulation of interleukin-2 secretion","type":"narrow"}],"termid":"GO:0032663"}


id: GO:1904296
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of osmolarity-sensing cation channel activity.","definition_xrefs":["GOC:TermGenie","PMID:18279313","GO_REF:0000059"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of osmolarity-sensing cation channel activity (obsolete GO:1904296)","synonyms":[{"name":"down regulation of osmolarity-sensing cation channel activity","type":"exact"},{"name":"down-regulation of osmolarity-sensing cation channel activity","type":"exact"},{"name":"downregulation of osmolarity-sensing cation channel activity","type":"exact"},{"name":"inhibition of osmolarity-sensing cation channel activity","type":"narrow"}],"termid":"GO:1904296"}


id: SO:0000824
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A chromosome originating in a macronucleus.","definition_xrefs":["SO:xp"],"direct_ancestors":[{"relation_name":"has_origin","term_name":"macronuclear_sequence","termid":"SO:0000083"},{"relation_name":"is_a","term_name":"chromosome","termid":"SO:0000340"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"macronuclear_chromosome","synonyms":[{"name":"macronuclear chromosome","type":"exact"}],"termid":"SO:0000824"}


id: PBO:0080621
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat domain 62","termid":"PBO:0080621"}


id: PBO:0047800
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"forkhead box I3","termid":"PBO:0047800"}


id: GO:0019431
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of acetyl-CoA from ethanol via acetaldehyde.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ethanol metabolic process","termid":"GO:0006067"},{"relation_name":"is_a","term_name":"acetyl-CoA biosynthetic process","termid":"GO:0006085"},{"relation_name":"is_a","term_name":"generation of precursor metabolites and energy","termid":"GO:0006091"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006091"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0006091","GO:0055086","GO:0044281","GO:0006790"],"is_obsolete":false,"name":"acetyl-CoA biosynthetic process from ethanol","synonyms":[{"name":"acetyl-CoA anabolism from ethanol","type":"exact"},{"name":"acetyl-CoA formation from ethanol","type":"exact"},{"name":"acetyl-CoA synthesis from ethanol","type":"exact"}],"termid":"GO:0019431"}


id: FYPO:0004471
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 a protein that is not normally found in the nucleolus is observed there during telophase of mitosis.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein mislocalized to nucleus during vegetative growth","termid":"FYPO:0000784"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000138","FYPO:0000002","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"protein mislocalized to nucleolus during mitotic telophase","synonyms":[{"name":"ectopic protein localization to nucleolus during mitotic telophase","type":"exact"},{"name":"protein mislocalised to nucleolus during mitotic telophase","type":"exact"},{"name":"protein mislocalised to nucleolus during telophase during vegetative growth","type":"exact"},{"name":"protein mislocalized to nucleolus during mitotic telophase during vegetative growth","type":"exact"},{"name":"protein mislocalized to nucleolus during telophase of mitosis","type":"exact"}],"termid":"FYPO:0004471"}


id: MONDO:0009044
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Crigler-Najjar syndrome (CNS) is a hereditary disorder of bilirubin metabolism characterized by unconjugated hyperbilirubinemia due to a hepatic deficit of bilirubin glucuronosyltransferase (GT) activity. Two types have been described, CNS types 1 and 2. CNS1 is characterized by a complete deficit of the enzyme and is unaffected by phenobarbital induction therapy, whereas the enzymatic deficit is partial and responds to phenobarbital in CNS2.","definition_xrefs":["Orphanet:205"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary hyperbilirubinemia","termid":"MONDO:0002408"}],"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":"Crigler-Najjar syndrome","secondary_identifiers":["MEDGEN:1789261","NANDO:2200941","MESH:D003414","SCTID:28259009","UMLS:C5551003","DOID:3803","NORD:1016","GARD:16526","ICD10CM:E80.5","icd11.foundation:291439191","MedDRA:10011386","NANDO:2100272","NCIT:C84656"],"synonyms":[{"name":"Crigler Najjar Syndrome","type":"exact"},{"name":"Crigler Najjar syndrome","type":"exact"},{"name":"Crigler-Najjar syndrome","type":"exact"},{"name":"UGT deficiency","type":"exact"},{"name":"bilirubin UDP glucuronyl transferase deficiency","type":"exact"},{"name":"bilirubin uridinediphosphate glucuronosyltransferase deficiency","type":"exact"},{"name":"bilirubin-UGT deficiency","type":"exact"},{"name":"hereditary unconjugated hyperbilirubinemia","type":"exact"}],"termid":"MONDO:0009044","xrefs":{"Monarch":{"xref_id":"0009044"}}}


id: GO:0046944
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The addition of a carbamoyl group to a protein amino acid. A carbamoyl group is the acyl group -CO-NH2.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein modification process","termid":"GO:0036211"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"protein carbamoylation","synonyms":[{"name":"protein amino acid carbamoylation","type":"exact"}],"termid":"GO:0046944"}


id: PBO:0063139
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PAS domain containing repressor 1","termid":"PBO:0063139"}


id: PBO:0039327
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arachidonate 15-lipoxygenase type B","termid":"PBO:0039327"}


id: MONDO:0022196
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"gastritis","termid":"MONDO:0004966"}],"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":"chronic erosive gastritis","secondary_identifiers":["SCTID:63137003","MEDGEN:78626","UMLS:C0267145","ICD9:535.40"],"synonyms":[{"name":"ceg - chronic erosive gastritis","type":"related"},{"name":"chronic erosive gastritis","type":"exact"},{"name":"diffuse varioliform gastritis","type":"related"},{"name":"idiopathic chronic, erosive gastritis","type":"related"},{"name":"varioliform gastritis","type":"related"}],"termid":"MONDO:0022196","xrefs":{"Monarch":{"xref_id":"0022196"}}}


id: PBO:0045560
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dual specificity phosphatase 9","termid":"PBO:0045560"}


id: MONDO:0006086
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign soft tissue neoplasm characterized by the presence of neoplastic spindle and stellate cells, and vascular proliferation in a myxoid stroma.","definition_xrefs":["NCIT:C3254"],"direct_ancestors":[{"relation_name":"is_a","term_name":"connective tissue neoplasm","termid":"MONDO:0021581"},{"relation_name":"is_a","term_name":"benign soft tissue neoplasm","termid":"MONDO:0044335"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"angiomyxoma","secondary_identifiers":["MEDGEN:1790210","UMLS:C5551004","ICD9:215.9","ICDO:8841/0","SCTID:404083008","ICDO:8841/1","EFO:1000087"],"termid":"MONDO:0006086","xrefs":{"Monarch":{"xref_id":"0006086"}}}


id: PBO:0046055
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation initiation factor 3 subunit F pseudogene 3","termid":"PBO:0046055"}


id: PBO:0043080
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cholinergic receptor nicotinic alpha 10 subunit","termid":"PBO:0043080"}


id: PBO:0073908
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 16 member 1","termid":"PBO:0073908"}


id: GO:1902313
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of copper ion transmembrane transport.","definition_xrefs":["GOC:di","GOC:TermGenie","PMID:21489137"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of copper ion transmembrane transport","termid":"GO:1902311"},{"relation_name":"is_a","term_name":"positive regulation of cation transmembrane transport","termid":"GO:1904064"},{"relation_name":"positively_regulates","term_name":"copper ion transmembrane transport","termid":"GO:0035434"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0055085"},{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0055085","GO:0006810"],"is_obsolete":false,"name":"positive regulation of copper ion transmembrane transport","synonyms":[{"name":"activation of copper cation transmembrane transport","type":"narrow"},{"name":"activation of copper ion membrane transport","type":"narrow"},{"name":"activation of copper ion transmembrane transport","type":"narrow"},{"name":"positive regulation of copper cation transmembrane transport","type":"exact"},{"name":"positive regulation of copper ion membrane transport","type":"exact"},{"name":"up regulation of copper cation transmembrane transport","type":"exact"},{"name":"up regulation of copper ion membrane transport","type":"exact"},{"name":"up regulation of copper ion transmembrane transport","type":"exact"},{"name":"up-regulation of copper cation transmembrane transport","type":"exact"},{"name":"up-regulation of copper ion membrane transport","type":"exact"},{"name":"up-regulation of copper ion transmembrane transport","type":"exact"},{"name":"upregulation of copper cation transmembrane transport","type":"exact"},{"name":"upregulation of copper ion membrane transport","type":"exact"},{"name":"upregulation of copper ion transmembrane transport","type":"exact"}],"termid":"GO:1902313"}


id: GO:0090396
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A plant cell papilla that is part of a leaf papilla cell.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plant cell papilla","termid":"GO:0090395"}],"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":"leaf papilla","termid":"GO:0090396"}


id: RO:0002597
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Holds between c and p if and only if c is capable of some activity a, and a negatively regulates p.","direct_ancestors":[{"relation_name":"is_a","term_name":"capable_of_regulating","termid":"RO:0002596"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"capable_of_negatively_regulating","termid":"RO:0002597"}


id: GO:0002893
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of type II hypersensitivity.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of hypersensitivity","termid":"GO:0002884"},{"relation_name":"is_a","term_name":"negative regulation of myeloid leukocyte mediated immunity","termid":"GO:0002887"},{"relation_name":"is_a","term_name":"negative regulation of immunoglobulin mediated immune response","termid":"GO:0002890"},{"relation_name":"is_a","term_name":"regulation of type II hypersensitivity","termid":"GO:0002892"},{"relation_name":"negatively_regulates","term_name":"type II hypersensitivity","termid":"GO:0002445"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of type II hypersensitivity","synonyms":[{"name":"down regulation of type II hypersensitivity","type":"exact"},{"name":"down-regulation of type II hypersensitivity","type":"exact"},{"name":"downregulation of type II hypersensitivity","type":"exact"},{"name":"inhibition of type II hypersensitivity","type":"narrow"}],"termid":"GO:0002893"}


id: MONDO:0019219
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inborn disorder of biogenic amine metabolism and transport","termid":"MONDO:0019250"}],"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":"inborn disorder of neurotransmitter metabolism and transport","secondary_identifiers":["GARD:18950","MEDGEN:1842206","Orphanet:79169","UMLS:C5681289"],"synonyms":[{"name":"disorder of neurotransmitter metabolism and transport","type":"related"}],"termid":"MONDO:0019219","xrefs":{"Monarch":{"xref_id":"0019219"}}}


id: PBO:0066549
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"regulator of G protein signaling 12","termid":"PBO:0066549"}


id: PBO:0017552
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EF hand family protein, centrin-like","termid":"PBO:0017552"}


id: PBO:0075248
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sorting nexin 18","termid":"PBO:0075248"}


id: PBO:0000946
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"expression induced by UV","termid":"PBO:0000946"}


id: PBO:0082765
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the SMC5-SMC6 complex; this complex plays a key role in the removal of X-shaped DNA structures that arise between sister chromatids during DNA replication and repair","termid":"PBO:0082765"}


id: GO:0048047
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The behavior of individuals for the purpose of discriminating between the sexes, for the purpose of finding a suitable mating partner.","definition_xrefs":["PMID:12486700","GOC:pr","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mating behavior","termid":"GO:0007617"}],"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":"mating behavior, sex discrimination","synonyms":[{"name":"mating behaviour, sex discrimination","type":"exact"}],"termid":"GO:0048047"}


id: GO:0016063
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of rhodopsin, a brilliant purplish-red, light-sensitive visual pigment found in the rod cells of the retinas.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eye pigment biosynthetic process","termid":"GO:0006726"},{"relation_name":"is_a","term_name":"macromolecule biosynthetic process","termid":"GO:0009059"},{"relation_name":"is_a","term_name":"rhodopsin metabolic process","termid":"GO:0046154"}],"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":"rhodopsin biosynthetic process","synonyms":[{"name":"rhodopsin anabolism","type":"exact"},{"name":"rhodopsin biosynthesis","type":"exact"},{"name":"rhodopsin formation","type":"exact"},{"name":"rhodopsin synthesis","type":"exact"}],"termid":"GO:0016063"}


id: MONDO:0022693
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":"cerebral calcification cerebellar hypoplasia","termid":"MONDO:0022693","xrefs":{"Monarch":{"xref_id":"0022693"}}}


id: GO:0140247
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of a protein at a presynapse.","definition_xrefs":["PMID:27764673"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein catabolic process at synapse","termid":"GO:0140246"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0030163"}],"interesting_parent_ids":["GO:0030163","GO:0008150"],"is_obsolete":false,"name":"protein catabolic process at presynapse","termid":"GO:0140247"}


id: PBO:0066975
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 278","termid":"PBO:0066975"}


id: GO:0048719
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the epistomal sclerite are generated and organized.","definition_xrefs":["GOC:rc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"post-embryonic animal morphogenesis","termid":"GO:0009886"},{"relation_name":"part_of","term_name":"clypeo-labral disc morphogenesis","termid":"GO:0007453"},{"relation_name":"part_of","term_name":"epistomal sclerite development","termid":"GO:0048724"}],"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":"epistomal sclerite morphogenesis","termid":"GO:0048719"}


id: PBO:0061019
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleolar protein interacting with the FHA domain of MKI67 pseudogene 2","termid":"PBO:0061019"}


id: GO:0141212
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An intracellular signaling cassette that starts with activation of phospholipase C (PLC) activity and ends with the activation of protein kinase C (PKC). PLC produces inositol 1,4,5-trisphosphate (IP3) and diacylglycerol (DAG). IP3 regulates the opening of calcium channels in intracellular calcium store, leading to the release of calcium into the cytosol. Calcium and DAG activate protein kinase C (PKC), which in turn activates downstream effectors. This cassette is often part of the phospholipase C-activating G protein-coupled receptor signaling pathway.","definition_xrefs":["PMID:26605346"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular signaling cassette","termid":"GO:0141124"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"phospholipase C/protein kinase C signal transduction","synonyms":[{"name":"PLC/PKC signaling","type":"exact"},{"name":"PLC/PKC/PKD signaling","type":"exact"}],"termid":"GO:0141212"}


id: PBO:0059184
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Morf4 family associated protein 1","termid":"PBO:0059184"}


id: MONDO:0009547
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Macrosomia-microphthalmia-cleft palate syndrome is a rare, genetic, multiple congenital anomalies/dysmorphic syndrome characterized by early macrosomia, bilateral severe microphthalmia and a protuberant abdomen with hepatomegaly. Additional reported features include brachycephaly, large fontanelles, prominent forehead, upturned nose and median cleft palate. Cyanotic apneic spells and overwhelming infection lead to death within the first 6 months of life. There have been no further descriptions in the literature since 1989.","definition_xrefs":["Orphanet:2432"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"macrosomia-microphthalmia-cleft palate syndrome","secondary_identifiers":["UMLS:C1855467","MEDGEN:340874","OMIM:248110","GARD:177","MESH:C537830"],"synonyms":[{"name":"Teebi Al-Saleh Hassoon syndrome","type":"related"},{"name":"Teebi-Al Saleh-Hassoon syndrome","type":"exact"},{"name":"macrosomia microphthalmia cleft palate","type":"related"},{"name":"macrosomia with lethal microphthalmia","type":"related"},{"name":"macrosomia with microphthalmia, lethal","type":"related"}],"termid":"MONDO:0009547","xrefs":{"Monarch":{"xref_id":"0009547"}}}


id: PR:Q9UTK1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- cox16 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9UTK1"],"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":"cytochrome c oxidase assembly protein cox16, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1486.08","synonyms":[{"name":"Spom972h-cox16","type":"exact"}],"termid":"PR:Q9UTK1"}


id: GO:0090147
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of the directed movement of mitochondria to the correct region of the cell that contributes to the process of mitochondrial fission.","definition_xrefs":["GOC:dph","GOC:tb","GOC:ascb_2009"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of establishment of mitochondrion localization involved in mitochondrial fission (obsolete GO:0090147)","synonyms":[{"name":"regulation of establishment of mitochondrion localisation involved in mitochondrial fission","type":"exact"},{"name":"regulation of mitochondrial localization involved in mitochondrial fission","type":"related"}],"termid":"GO:0090147"}


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


id: PBO:0090042
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphatidylinositol-3-phosphatase, myotubularin family","termid":"PBO:0090042"}


id: MONDO:1012351
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"progressive neuronopathy, non-human animal","termid":"MONDO:1011871"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"progressive neuronopathy, dog","secondary_identifiers":["OMIA:001282-9615"],"termid":"MONDO:1012351","xrefs":{"Monarch":{"xref_id":"1012351"}}}


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


id: FYPO:0003590
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which vacuoles are smaller than normal during sporulation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"small vacuoles","termid":"FYPO:0002787"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"small vacuoles during sporulation","synonyms":[{"name":"vacuoles present in increased numbers, with decreased vacuole size, during sporulation","type":"exact"}],"termid":"FYPO:0003590"}


id: GO:0043935
data:
  {"annotated_genes":["SJAG_05309","SJAG_02248","SJAG_01017","SJAG_02712","SJAG_03250","SJAG_04010","SJAG_00826","SJAG_00486","SJAG_03557","SJAG_04853","SJAG_04868","SJAG_04859","SJAG_04184","SJAG_00663","SJAG_04922","SJAG_01321","SJAG_01483","SJAG_00974","SJAG_02320","SJAG_02169","SJAG_02736","SJAG_03013","SJAG_04615","SJAG_02241","SJAG_04271","SJAG_00114","SJAG_00405","SJAG_03090","SJAG_04236","SJAG_00971","SJAG_03746","SJAG_04238","SJAG_04901","SJAG_00821","SJAG_01531","SJAG_03483","SJAG_04080","SJAG_02529","SJAG_03057","SJAG_04140","SJAG_04470","SJAG_02718","SJAG_03915","SJAG_03688","SJAG_03536","SJAG_01769","SJAG_04781","SJAG_01662","SJAG_00993","SJAG_04275","SJAG_04483","SJAG_03587"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[118030,96008,94854,112200,111002,96426,100224,103629,104615,107206,109605,96358,113422],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030437"},{"annotations":[93502,110806],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071998"},{"annotations":[93948],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034413"},{"annotations":[89726,88179,91254,87686],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030476"},{"annotations":[108790],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034412"},{"annotations":[117290,103672,117282,113577,108561],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070591"},{"annotations":[97079,104465,108791,90984,109606],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031321"},{"annotations":[104781,118031,109607,90774,98329,101208,106874,99332,116422,118332,97041,113423,118513,99333,94855,97080,99402],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032120"},{"annotations":[103630,107207,99335,97042,96359,91777,106320,113424,99334,102419],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031322"},{"annotations":[110690],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0075297"},{"annotations":[101792],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0075296"},{"annotations":[90209],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1903024"},{"annotations":[91673],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0034307"},{"annotations":[105501,115468,93990,99336,99337,99614],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070583"}]},"cv_name":"biological_process","definition":"The formation of spores derived from the products of meiosis. A cellular spore is a cell form that can be used for dissemination, for survival of adverse conditions because of its heat and desiccation resistance, and/or for reproduction.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sporulation resulting in formation of a cellular spore","termid":"GO:0030435"},{"relation_name":"is_a","term_name":"sexual sporulation","termid":"GO:0034293"}],"gene_count":52,"genes_by_uniquename":{"SJAG_00114":null,"SJAG_00405":null,"SJAG_00486":null,"SJAG_00663":null,"SJAG_00821":null,"SJAG_00826":null,"SJAG_00971":null,"SJAG_00974":null,"SJAG_00993":null,"SJAG_01017":null,"SJAG_01321":null,"SJAG_01483":null,"SJAG_01531":null,"SJAG_01662":null,"SJAG_01769":null,"SJAG_02169":null,"SJAG_02241":null,"SJAG_02248":null,"SJAG_02320":null,"SJAG_02529":null,"SJAG_02712":null,"SJAG_02718":null,"SJAG_02736":null,"SJAG_03013":null,"SJAG_03057":null,"SJAG_03090":null,"SJAG_03250":null,"SJAG_03483":null,"SJAG_03536":null,"SJAG_03557":null,"SJAG_03587":null,"SJAG_03688":null,"SJAG_03746":null,"SJAG_03915":null,"SJAG_04010":null,"SJAG_04080":null,"SJAG_04140":null,"SJAG_04184":null,"SJAG_04236":null,"SJAG_04238":null,"SJAG_04271":null,"SJAG_04275":null,"SJAG_04470":null,"SJAG_04483":null,"SJAG_04615":null,"SJAG_04781":null,"SJAG_04853":null,"SJAG_04859":null,"SJAG_04868":null,"SJAG_04901":null,"SJAG_04922":null,"SJAG_05309":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"sexual sporulation resulting in formation of a cellular spore","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0043935","terms_by_termid":{"GO:0030437":null,"GO:0030476":null,"GO:0031321":null,"GO:0031322":null,"GO:0032120":null,"GO:0034307":null,"GO:0034412":null,"GO:0034413":null,"GO:0070583":null,"GO:0070591":null,"GO:0071998":null,"GO:0075296":null,"GO:0075297":null,"GO:1903024":null}}


