# terms

id: GO:0071314
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a cocaine stimulus. Cocaine is a crystalline alkaloid obtained from the leaves of the coca plant.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to cocaine","termid":"GO:0042220"},{"relation_name":"is_a","term_name":"cellular response to alkaloid","termid":"GO:0071312"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to cocaine","termid":"GO:0071314"}


id: GO:0046406
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: Mg-protoporphyrin IX + S-adenosyl-L-methionine = Mg-protoporphyrin IX 13-monomethyl ester + S-adenosyl-L-homocysteine.","definition_xrefs":["RHEA:17809"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-methyltransferase activity","termid":"GO:0008171"},{"relation_name":"is_a","term_name":"S-adenosylmethionine-dependent methyltransferase activity","termid":"GO:0008757"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016741"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0016741","GO:0003824"],"is_obsolete":false,"name":"magnesium protoporphyrin IX methyltransferase activity","secondary_identifiers":["MetaCyc:RXN-MG-PROTOPORPHYRIN-METHYLESTER-SYN","EC:2.1.1.11","KEGG_REACTION:R04237"],"synonyms":[{"name":"(-)-S-adenosyl-L-methionine:magnesium-protoporphyrin IX methyltransferase activity","type":"related"},{"name":"Mg-protoporphyrin IX methyltransferase activity","type":"related"},{"name":"S-adenosyl-L-methionine:Mg protoporphyrin methyltransferase activity","type":"related"},{"name":"S-adenosyl-L-methionine:magnesium-protoporphyrin O-methyltransferase activity","type":"related"},{"name":"S-adenosyl-L-methionine:magnesium-protoporphyrin-IX O-methyltransferase activity","type":"related"},{"name":"S-adenosylmethionine-magnesium protoporphyrin methyltransferase activity","type":"related"},{"name":"S-adenosylmethioninemagnesium protoporphyrin methyltransferase activity","type":"related"},{"name":"magnesium-protoporphyrin O-methyltransferase activity","type":"exact"}],"termid":"GO:0046406"}


id: MONDO:0002787
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A craniopharyngioma consisting of broad strands, cords and bridges of a multistratified squamous epithelium with peripheral palisading of nuclei. Diagnostic features include nodules of compact 'wet' keratin and dystrophic calcification. (Adapted from WHO)","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"craniopharyngioma","termid":"MONDO:0018907"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adamantinous craniopharyngioma","secondary_identifiers":["NCIT:C4726","DOID:3846","UMLS:C0431129","ICDO:9351/1","MEDGEN:98126"],"synonyms":[{"name":"adamantinomatous craniopharyngioma","type":"exact"},{"name":"adamantinous Rathke's pouch neoplasm","type":"exact"},{"name":"adamantinous Rathke's pouch tumor","type":"exact"},{"name":"adamantinous Rathke's pouch tumour","type":"exact"},{"name":"adamantinous craniopharyngioma (morphologic abnormality)","type":"exact"},{"name":"adamantinous neoplasm of Rathke's pouch","type":"exact"},{"name":"adamantinous tumor of Rathke's pouch","type":"exact"},{"name":"adamantinous tumour of Rathke's pouch","type":"exact"},{"name":"craniopharyngioma, adamantinomatous","type":"exact"}],"termid":"MONDO:0002787","xrefs":{"Monarch":{"xref_id":"0002787"}}}


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: GO:0045964
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the chemical reactions and pathways involving dopamine.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of dopamine metabolic process","termid":"GO:0042053"},{"relation_name":"is_a","term_name":"positive regulation of catecholamine metabolic process","termid":"GO:0045915"},{"relation_name":"positively_regulates","term_name":"dopamine metabolic process","termid":"GO:0042417"}],"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 dopamine metabolic process","synonyms":[{"name":"activation of dopamine metabolic process","type":"narrow"},{"name":"positive regulation of dopamine metabolism","type":"exact"},{"name":"stimulation of dopamine metabolic process","type":"narrow"},{"name":"up regulation of dopamine metabolic process","type":"exact"},{"name":"up-regulation of dopamine metabolic process","type":"exact"},{"name":"upregulation of dopamine metabolic process","type":"exact"}],"termid":"GO:0045964"}


id: PBO:0051617
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin like domain containing receptor 2","termid":"PBO:0051617"}


id: GO:0120255
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of an olefinic compound, any compound which contains a carbon-carbon double bond (aka C=C).","definition_xrefs":["GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biosynthetic process","termid":"GO:0009058"},{"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"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"olefinic compound biosynthetic process","synonyms":[{"name":"alkene substituted compound anabolic process","type":"exact"},{"name":"alkene substituted compound anabolism","type":"exact"},{"name":"alkene substituted compound biosynthesis","type":"exact"},{"name":"alkene substituted compound biosynthetic process","type":"exact"},{"name":"alkene substituted compound synthesis","type":"exact"}],"termid":"GO:0120255"}


id: MONDO:0010696
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"omphalocele","termid":"MONDO:0019015"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"omphalocele, X-linked","secondary_identifiers":["OMIM:310980","GARD:18587","UMLS:C3275625","MEDGEN:477256"],"synonyms":[{"name":"omphalocele, X-linked","type":"exact"}],"termid":"MONDO:0010696","xrefs":{"Monarch":{"xref_id":"0010696"}}}


id: PBO:0059568
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metallothionein 1L, pseudogene","termid":"PBO:0059568"}


id: PBO:0040952
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BCL2 interacting protein 3 pseudogene 23","termid":"PBO:0040952"}


id: GO:0099611
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that regulates the potential at which an axon potential is triggered.","definition_xrefs":["ISBN:978-0071390118"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of action potential","termid":"GO:0098900"}],"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 action potential firing threshold","termid":"GO:0099611"}


id: PBO:0014589
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitosis Inhibitory Kinase","termid":"PBO:0014589"}


id: PBO:0036340
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"allantoicase Dal2","termid":"PBO:0036340"}


id: MONDO:0017110
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Dandy-Walker syndrome","termid":"MONDO:0009072"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0020022"}],"interesting_parent_ids":["MONDO:0020022"],"is_obsolete":false,"name":"isolated Dandy-Walker malformation with hydrocephalus","secondary_identifiers":["GARD:20993","UMLS:C5680779","MEDGEN:1842616","Orphanet:269212"],"termid":"MONDO:0017110","xrefs":{"Monarch":{"xref_id":"0017110"}}}


id: PBO:0077365
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 106A","termid":"PBO:0077365"}


id: MONDO:0500018
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare pulmonary disease with histological pattern of interstitial pneumonitis characterized by the deposit of intra-alveolar fibrin and diffuse organizing pneumonia within the alveolar ducts and bronchioles, with large etiological spectra.","definition_xrefs":["PMID:31076239"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pneumonia","termid":"MONDO:0005249"},{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acute fibrinous and organizing pneumonia","synonyms":[{"name":"AFOP","type":"exact"}],"termid":"MONDO:0500018","xrefs":{"Monarch":{"xref_id":"0500018"}}}


id: PBO:0051701
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inositol polyphosphate-5-phosphatase A","termid":"PBO:0051701"}


id: IAO:0000412
data:
  {"annotation_feature_type":"gene","cv_name":"iao","definition":"For external terms/classes, the ontology from which the term was imported","definition_xrefs":["OBI:mc","OBI:ar"],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"imported from","termid":"IAO:0000412"}


id: PR:O59744
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC530.08 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O59744"],"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 transcriptional regulatory protein C530.08 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC530.08","synonyms":[{"name":"Spom972h-SPBC530.08","type":"exact"}],"termid":"PR:O59744"}


id: PBO:0042981
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromodomain helicase DNA binding protein 7","termid":"PBO:0042981"}


id: GO:0070082
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The volume enclosed by the membrane of the clathrin-sculpted monoamine transport vesicle.","definition_xrefs":["GOC:mg2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoplasmic vesicle lumen","termid":"GO:0060205"},{"relation_name":"part_of","term_name":"clathrin-sculpted monoamine transport vesicle","termid":"GO:0070081"}],"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:0031410"}],"interesting_parent_ids":["GO:0031410","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"clathrin-sculpted monoamine transport vesicle lumen","synonyms":[{"name":"clathrin sculpted monoamine constitutive secretory pathway transport vesicle lumen","type":"exact"},{"name":"clathrin sculpted monoamine transport vesicle lumen","type":"exact"}],"termid":"GO:0070082"}


id: PBO:0063755
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PHB1 pseudogene 20","termid":"PBO:0063755"}


id: GO:0030466
data:
  {"annotated_genes":["SJAG_02311","SJAG_00160","SJAG_03997","SJAG_00266","SJAG_02621","SJAG_03128","SJAG_01601","SJAG_00142","SJAG_02778","SJAG_03689","SJAG_03916","SJAG_04574","SJAG_02592","SJAG_02401","SJAG_03844","SJAG_00934","SJAG_03680","SJAG_02342","SJAG_01579","SJAG_03982","SJAG_03356","SJAG_04186","SJAG_04141","SJAG_01540","SJAG_02409","SJAG_00756","SJAG_02119","SJAG_03042"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[71407,91028,92511,93840,95281,96501,98915,99352,103017,103882,103978,107775,107960,110284,111006,111069,111906,112008,113101,113475,113794,115794,117510,117905,118626],"is_not":false,"summary":null,"term":"GO:0030466"},{"annotations":[90941,94132,110143],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0090055"}]},"cv_name":"biological_process","definition":"Repression of transcription at silent mating-type loci by alteration of the structure of chromatin.","definition_xrefs":["GOC:mcc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"constitutive heterochromatin formation","termid":"GO:0140719"}],"gene_count":28,"genes_by_uniquename":{"SJAG_00142":null,"SJAG_00160":null,"SJAG_00266":null,"SJAG_00756":null,"SJAG_00934":null,"SJAG_01540":null,"SJAG_01579":null,"SJAG_01601":null,"SJAG_02119":null,"SJAG_02311":null,"SJAG_02342":null,"SJAG_02401":null,"SJAG_02409":null,"SJAG_02592":null,"SJAG_02621":null,"SJAG_02778":null,"SJAG_03042":null,"SJAG_03128":null,"SJAG_03356":null,"SJAG_03680":null,"SJAG_03689":null,"SJAG_03844":null,"SJAG_03916":null,"SJAG_03982":null,"SJAG_03997":null,"SJAG_04141":null,"SJAG_04186":null,"SJAG_04574":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0006325"}],"interesting_parent_ids":["GO:0010467","GO:0008150","GO:0006325"],"is_obsolete":false,"name":"silent mating-type cassette heterochromatin formation","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0035389","GO:0006347"],"synonyms":[{"name":"aging-dependent sterility","type":"narrow"},{"name":"chromatin silencing at HML and HMR","type":"narrow"},{"name":"chromatin silencing at silent mating-type cassette","type":"exact"},{"name":"establishment of chromatin silencing at silent mating-type cassette","type":"related"},{"name":"heterochromatic silencing at silent mating-type cassette","type":"exact"},{"name":"silent mating-type cassette chromatin silencing","type":"exact"},{"name":"silent mating-type cassette heterochromatin assembly","type":"exact"}],"termid":"GO:0030466","terms_by_termid":{"GO:0030466":null,"GO:0090055":null}}


id: PBO:0088386
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER protein disulfide isomerase","termid":"PBO:0088386"}


id: PBO:0075002
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 115-13","termid":"PBO:0075002"}


id: PBO:0062503
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 8 subfamily G member 3 pseudogene","termid":"PBO:0062503"}


id: GO:1903842
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an arsenite ion stimulus.","definition_xrefs":["PMID:12106899","GO_REF:0000071","GOC:mr","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to arsenic-containing substance","termid":"GO:0046685"},{"relation_name":"is_a","term_name":"response to oxygen-containing compound","termid":"GO:1901700"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to arsenite ion","termid":"GO:1903842"}


id: PBO:0068299
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring finger protein 5 pseudogene 1","termid":"PBO:0068299"}


id: MONDO:0018237
data:
  {"annotated_genes":["SJAG_00504","SJAG_00414","SJAG_03144","SJAG_00197"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84877],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014651"},{"annotations":[85730],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012516"},{"annotations":[84934],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007943"},{"annotations":[85158],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009903"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"dysostosis","termid":"MONDO:0018234"},{"relation_name":"is_a","term_name":"congenital limb malformation","termid":"MONDO:0019054"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00197":null,"SJAG_00414":null,"SJAG_00504":null,"SJAG_03144":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"acrofacial dysostosis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:364574","UMLS:C1332140","NCIT:C35795","GARD:21574","DOID:0060379","icd11.foundation:1702160042","MEDGEN:272278"],"termid":"MONDO:0018237","terms_by_termid":{"MONDO:0007943":null,"MONDO:0009903":null,"MONDO:0012516":null,"MONDO:0014651":null},"xrefs":{"Monarch":{"xref_id":"0018237"}}}


id: GO:0052907
data:
  {"annotated_genes":["SJAG_01958"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[94950],"is_not":false,"summary":null,"term":"GO:0052907"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + adenine(1618) in 23S rRNA = S-adenosyl-L-homocysteine + rRNA containing N(6)-methyladenine(1618) in 23S rRNA.","definition_xrefs":["RHEA:16497"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rRNA (adenine-N6-)-methyltransferase activity","termid":"GO:0008988"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01958":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016740","GO:0003824","GO:0140098","GO:0016741","GO:0003674"],"is_obsolete":false,"name":"23S rRNA (adenine(1618)-N(6))-methyltransferase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["EC:2.1.1.181","MetaCyc:RXN-11596","KEGG_REACTION:R07232"],"synonyms":[{"name":"M(6)A(1618) activity","type":"broad"},{"name":"rRNA large subunit methyltransferase F activity","type":"related"}],"termid":"GO:0052907","terms_by_termid":{"GO:0052907":null}}


id: GO:0061042
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Blood vessel formation when new vessels emerge from the proliferation of pre-existing blood vessels and contribute to the series of events that restore integrity to damaged vasculature.","definition_xrefs":["GOC:BHF","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"angiogenesis involved in wound healing","termid":"GO:0060055"}],"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 wound healing","termid":"GO:0061042"}


id: PBO:0051596
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 22","termid":"PBO:0051596"}


id: PBO:0087205
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S-adenosylmethionine-dependent lysine methyltransferase; involved in the trimethylation of eEF1A (Tef1p/Tef2p) at lysine 79; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm; required for replication of Brome mosaic virus in budding yeast; expresses a circular RNA; originally misclassified as a N-6-adenine specific DNA methyltransferase based on sequence similarity; both Efm5p and human ortholog N6AMT2 can methylate eEF1a from either species in vitro","termid":"PBO:0087205"}


id: PBO:0041443
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C9orf78 pseudogene 2","termid":"PBO:0041443"}


id: GO:0015556
data:
  {"annotated_genes":["SJAG_02140","SJAG_01406","SJAG_00671","SJAG_00522"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[96331],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015183"},{"annotations":[67123],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015140"},{"annotations":[101447],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015366"},{"annotations":[88162],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015131"},{"annotations":[101450],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097434"}]},"cv_name":"molecular_function","definition":"Enables the transfer of C4-dicarboxylate from one side of a membrane to the other.","definition_xrefs":["GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxylic acid transmembrane transporter activity","termid":"GO:0046943"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00522":null,"SJAG_00671":null,"SJAG_01406":null,"SJAG_02140":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"C4-dicarboxylate transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000107":null},"termid":"GO:0015556","terms_by_termid":{"GO:0015131":null,"GO:0015140":null,"GO:0015183":null,"GO:0015366":null,"GO:0097434":null}}


id: GO:2000983
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of ATP citrate synthase activity.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transferase activity","termid":"GO:0051338"}],"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 ATP citrate synthase activity","synonyms":[{"name":"regulation of ATP citrate (pro-S)-lyase activity","type":"exact"},{"name":"regulation of ATP-citrate (pro-S)-lyase activity","type":"exact"},{"name":"regulation of ATP-citrate (pro-S-)-lyase activity","type":"exact"},{"name":"regulation of ATP-citric lyase activity","type":"exact"},{"name":"regulation of ATP:citrate oxaloacetate-lyase ((pro-S)-CH(2)COO(-)->acetyl-CoA) (ATP- dephosphorylating) activity","type":"exact"},{"name":"regulation of ATP:citrate oxaloacetate-lyase [(pro-S)-CH2COO-rightacetyl-CoA] (ATP-dephosphorylating)","type":"related"},{"name":"regulation of acetyl-CoA:oxaloacetate C-acetyltransferase [(pro-S)-carboxymethyl-forming, ADP-phosphorylating]","type":"related"},{"name":"regulation of acetyl-CoA:oxaloacetate acetyltransferase (isomerizing; ADP- phosphorylating) activity","type":"exact"},{"name":"regulation of acetyl-CoA:oxaloacetate acetyltransferase (isomerizing; ADP-phosphorylating)","type":"exact"},{"name":"regulation of adenosine triphosphate citrate lyase activity","type":"exact"},{"name":"regulation of citrate cleavage enzyme activity","type":"related"},{"name":"regulation of citrate-ATP lyase activity","type":"exact"},{"name":"regulation of citric cleavage enzyme activity","type":"related"}],"termid":"GO:2000983"}


id: MOD:01270
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Chemical derivative -","definition_xrefs":["PubMed:14670044","PubMed:15549660","Unimod:271#S"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleophilic addition to cytopiloyne+H2O","termid":"MOD:00591"},{"relation_name":"is_a","term_name":"modified L-serine residue","termid":"MOD:00916"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleophilic addition to cytopiloyne+H2O - site S","synonyms":[{"name":"Cytopiloyne+water","type":"related"},{"name":"nucleophilic addition to cytopiloyne+H2O","type":"related"}],"termid":"MOD:01270"}


id: PR:O13770
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- erp2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O13770"],"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 membrane protein C17A5.08 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC17A5.08","synonyms":[{"name":"Spom972h-erp2","type":"exact"}],"termid":"PR:O13770"}


id: GO:0070748
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to an interleukin-35 receptor.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine receptor binding","termid":"GO:0005126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"interleukin-35 receptor binding","synonyms":[{"name":"IL-35","type":"narrow"},{"name":"interleukin-35 receptor ligand","type":"narrow"}],"termid":"GO:0070748"}


id: PBO:0077472
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 191C","termid":"PBO:0077472"}


id: PBO:0080292
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vomeronasal 1 receptor 56 pseudogene","termid":"PBO:0080292"}


id: GO:0009998
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that restricts, stops or prevents a cell from specifying into a retinal cone cell.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell fate specification","termid":"GO:0009996"},{"relation_name":"is_a","term_name":"regulation of retinal cone cell fate specification","termid":"GO:0042673"},{"relation_name":"is_a","term_name":"negative regulation of retinal cone cell fate commitment","termid":"GO:0060226"},{"relation_name":"negatively_regulates","term_name":"retinal cone cell fate specification","termid":"GO:0042672"}],"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 retinal cone cell fate specification","synonyms":[{"name":"down regulation of retinal cone cell fate specification","type":"exact"},{"name":"down-regulation of retinal cone cell fate specification","type":"exact"},{"name":"downregulation of retinal cone cell fate specification","type":"exact"},{"name":"inhibition of retinal cone cell fate specification","type":"narrow"},{"name":"negative regulation of retina cone cell fate specification","type":"exact"},{"name":"suppression of retina cone cell fate","type":"exact"},{"name":"suppression of retinal cone cell fate","type":"exact"}],"termid":"GO:0009998"}


id: PBO:0044047
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cysteine and glycine rich protein 1","termid":"PBO:0044047"}


id: GO:0002306
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a precursor cell type acquires the specialized features of a CD4-positive, gamma-delta intraepithelial T cell. Intraepithelial T cells are found among epithelial cells in mucosal areas and have distinct phenotypes and developmental pathways.","definition_xrefs":["ISBN:0781735149","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gamma-delta intraepithelial T cell differentiation","termid":"GO:0002304"}],"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":"CD4-positive gamma-delta intraepithelial T cell differentiation","synonyms":[{"name":"CD4-positive, gamma-delta intraepithelial T cell development","type":"related"},{"name":"CD4-positive, gamma-delta intraepithelial T lymphocyte differentiation","type":"exact"},{"name":"CD4-positive, gamma-delta intraepithelial T-cell differentiation","type":"exact"},{"name":"CD4-positive, gamma-delta intraepithelial T-lymphocyte differentiation","type":"exact"}],"termid":"GO:0002306"}


id: PBO:0074829
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 25","termid":"PBO:0074829"}


id: GO:0010374
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the stomatal complex over time from its formation to the mature structure. The stomatal complex is the stomatal guard cells and their associated epidermal cells.","definition_xrefs":["PMID:17259259"],"direct_ancestors":[{"relation_name":"is_a","term_name":"post-embryonic development","termid":"GO:0009791"},{"relation_name":"is_a","term_name":"plant epidermis development","termid":"GO:0090558"}],"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":"stomatal complex development","termid":"GO:0010374"}


id: PBO:0043133
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"capicua transcriptional repressor pseudogene 1","termid":"PBO:0043133"}


id: PBO:0073462
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"surfactant protein C","termid":"PBO:0073462"}


id: GO:0045292
data:
  {"annotated_genes":["SJAG_02078","SJAG_03291","SJAG_00888","SJAG_00911","SJAG_03369","SJAG_04529","SJAG_05208","SJAG_04230","SJAG_02905","SJAG_00083","SJAG_01452","SJAG_05211","SJAG_01654","SJAG_01200","SJAG_01504","SJAG_03210","SJAG_03711","SJAG_04163","SJAG_00643","SJAG_01152","SJAG_04898","SJAG_02304","SJAG_01008","SJAG_02862","SJAG_03687","SJAG_00531","SJAG_05926","SJAG_01064","SJAG_00249","SJAG_02688","SJAG_01547","SJAG_00147","SJAG_16453","SJAG_02018","SJAG_00639","SJAG_01958","SJAG_03849","SJAG_01557","SJAG_00322","SJAG_01015","SJAG_03993","SJAG_04949","SJAG_03966","SJAG_04214","SJAG_04914","SJAG_03410","SJAG_00571","SJAG_04318","SJAG_02879","SJAG_01440","SJAG_02844","SJAG_04222","SJAG_02686","SJAG_02279","SJAG_04863","SJAG_05009","SJAG_01144","SJAG_01301","SJAG_05349","SJAG_01810","SJAG_02455","SJAG_03427","SJAG_03469","SJAG_04293","SJAG_04589","SJAG_00225","SJAG_05240","SJAG_01040","SJAG_01852","SJAG_02772","SJAG_05025","SJAG_01511","SJAG_00539","SJAG_01634","SJAG_03890","SJAG_02185","SJAG_00313","SJAG_02396","SJAG_00998","SJAG_05212","SJAG_00363","SJAG_03301","SJAG_00577","SJAG_01327","SJAG_05235","SJAG_04405","SJAG_03937","SJAG_04071","SJAG_04497","SJAG_00597","SJAG_04783","SJAG_02227","SJAG_04911","SJAG_01308","SJAG_01214","SJAG_00809","SJAG_01433","SJAG_00859","SJAG_00058","SJAG_00818","SJAG_03894","SJAG_03983","SJAG_03430","SJAG_01629","SJAG_01870","SJAG_00498","SJAG_04117","SJAG_00504","SJAG_03601","SJAG_02469","SJAG_02687","SJAG_02722","SJAG_02317","SJAG_03460","SJAG_03245","SJAG_03214","SJAG_00076","SJAG_04079","SJAG_03995","SJAG_03279","SJAG_03547","SJAG_03498","SJAG_02843","SJAG_01408","SJAG_02083","SJAG_00414","SJAG_03954","SJAG_03070","SJAG_04433","SJAG_04025","SJAG_02558","SJAG_03238","SJAG_02295","SJAG_00989","SJAG_00446","SJAG_04694","SJAG_05224","SJAG_01819","SJAG_03112","SJAG_00094"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[59466,74747,78069,79006,87177,87522,88265,88737,91178,91557,91860,92424,92445,92647,92873,93347,94490,95097,95559,95713,95740,95975,96207,96610,97175,97451,100420,102202,102264,102495,102811,102995,104305,104469,104751,105290,106562,107445,107688,108672,109586,110310,111081,111327,112454,112973,113262,113644,114158,114164,114667,116687,116835,117030,117787,118359,118705,56781,57371,57890,58970,58980,61702,64148,64182,64270,64909,64988,66085,66883,67138,67593,70019,70057,70326,70805,71172,71449,71461,71825,71851,72391,72535,72929,73000,73657,73699,73728,73754,73934,74210,74369,74371,74782,75083,75117,75279,75506,75509,75668,75695,75700,76009,76342,76758,77100,77112,77179,77204,77476,77654,78088,78533,78986,79185,79576,79786,80050,91911,94947],"is_not":false,"summary":null,"term":"GO:0045292"},{"annotations":[117642],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000354"},{"annotations":[91322,94687,94941,102337,79296,95364,105678,110425,110439,102499,112165,93759,97611,113082,115055,109866],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000395"},{"annotations":[118223,89221],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1905746"},{"annotations":[98353],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1905744"}]},"cv_name":"biological_process","definition":"The joining together, after removal of an intervening sequence composed of one or more introns, of two segments of the same RNA molecule via spliceosomal catalysis to produce an mRNA composed only of exon sequences that all came from the same primary transcript.","definition_xrefs":["ISBN:0879695897","GOC:krc","PMID:18458335"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mRNA splicing, via spliceosome","termid":"GO:0000398"}],"gene_count":140,"genes_by_uniquename":{"SJAG_00058":null,"SJAG_00076":null,"SJAG_00083":null,"SJAG_00094":null,"SJAG_00147":null,"SJAG_00225":null,"SJAG_00249":null,"SJAG_00313":null,"SJAG_00322":null,"SJAG_00363":null,"SJAG_00414":null,"SJAG_00446":null,"SJAG_00498":null,"SJAG_00504":null,"SJAG_00531":null,"SJAG_00539":null,"SJAG_00571":null,"SJAG_00577":null,"SJAG_00597":null,"SJAG_00639":null,"SJAG_00643":null,"SJAG_00809":null,"SJAG_00818":null,"SJAG_00859":null,"SJAG_00888":null,"SJAG_00911":null,"SJAG_00989":null,"SJAG_00998":null,"SJAG_01008":null,"SJAG_01015":null,"SJAG_01040":null,"SJAG_01064":null,"SJAG_01144":null,"SJAG_01152":null,"SJAG_01200":null,"SJAG_01214":null,"SJAG_01301":null,"SJAG_01308":null,"SJAG_01327":null,"SJAG_01408":null,"SJAG_01433":null,"SJAG_01440":null,"SJAG_01452":null,"SJAG_01504":null,"SJAG_01511":null,"SJAG_01547":null,"SJAG_01557":null,"SJAG_01629":null,"SJAG_01634":null,"SJAG_01654":null,"SJAG_01810":null,"SJAG_01819":null,"SJAG_01852":null,"SJAG_01870":null,"SJAG_01958":null,"SJAG_02018":null,"SJAG_02078":null,"SJAG_02083":null,"SJAG_02185":null,"SJAG_02227":null,"SJAG_02279":null,"SJAG_02295":null,"SJAG_02304":null,"SJAG_02317":null,"SJAG_02396":null,"SJAG_02455":null,"SJAG_02469":null,"SJAG_02558":null,"SJAG_02686":null,"SJAG_02687":null,"SJAG_02688":null,"SJAG_02722":null,"SJAG_02772":null,"SJAG_02843":null,"SJAG_02844":null,"SJAG_02862":null,"SJAG_02879":null,"SJAG_02905":null,"SJAG_03070":null,"SJAG_03112":null,"SJAG_03210":null,"SJAG_03214":null,"SJAG_03238":null,"SJAG_03245":null,"SJAG_03279":null,"SJAG_03291":null,"SJAG_03301":null,"SJAG_03369":null,"SJAG_03410":null,"SJAG_03427":null,"SJAG_03430":null,"SJAG_03460":null,"SJAG_03469":null,"SJAG_03498":null,"SJAG_03547":null,"SJAG_03601":null,"SJAG_03687":null,"SJAG_03711":null,"SJAG_03849":null,"SJAG_03890":null,"SJAG_03894":null,"SJAG_03937":null,"SJAG_03954":null,"SJAG_03966":null,"SJAG_03983":null,"SJAG_03993":null,"SJAG_03995":null,"SJAG_04025":null,"SJAG_04071":null,"SJAG_04079":null,"SJAG_04117":null,"SJAG_04163":null,"SJAG_04214":null,"SJAG_04222":null,"SJAG_04230":null,"SJAG_04293":null,"SJAG_04318":null,"SJAG_04405":null,"SJAG_04433":null,"SJAG_04497":null,"SJAG_04529":null,"SJAG_04589":null,"SJAG_04694":null,"SJAG_04783":null,"SJAG_04863":null,"SJAG_04898":null,"SJAG_04911":null,"SJAG_04914":null,"SJAG_04949":null,"SJAG_05009":null,"SJAG_05025":null,"SJAG_05208":null,"SJAG_05211":null,"SJAG_05212":null,"SJAG_05224":null,"SJAG_05235":null,"SJAG_05240":null,"SJAG_05349":null,"SJAG_05926":null,"SJAG_16453":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0016071"}],"interesting_parent_ids":["GO:0010467","GO:0008150","GO:0016071"],"is_obsolete":false,"name":"mRNA cis splicing, via spliceosome","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"synonyms":[{"name":"nuclear mRNA cis splicing, via U2-type spliceosome","type":"narrow"},{"name":"nuclear mRNA cis splicing, via spliceosome","type":"exact"},{"name":"splicing","type":"broad"}],"termid":"GO:0045292","terms_by_termid":{"GO:0000354":null,"GO:0000395":null,"GO:0045292":null,"GO:1905744":null,"GO:1905746":null}}


id: PBO:0039369
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AMMECR nuclear protein 1","termid":"PBO:0039369"}


id: MONDO:0011384
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"essential hypertension","termid":"MONDO:0001134"},{"relation_name":"excluded_subClassOf","term_name":"essential hypertension, genetic","termid":"MONDO:0007781"},{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypertension, essential, susceptibility to, 1","secondary_identifiers":["UMLS:C1858967","MEDGEN:395143","OMIM:603918"],"synonyms":[{"name":"Hyt1","type":"related"},{"name":"hypertension, essential, susceptibility to, 1","type":"exact"},{"name":"hypertension, essential, susceptibility to, type 1","type":"exact"}],"termid":"MONDO:0011384","xrefs":{"Monarch":{"xref_id":"0011384"}}}


id: PBO:0064552
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"POM121 transmembrane nucleoporin like 14, pseudogene","termid":"PBO:0064552"}


id: PBO:0111495
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EJC auxiliary factor, pinin ortholog Pnn1","termid":"PBO:0111495"}


id: PBO:0028310
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_RNA_level_during_cellular_response_to_methylglyoxal","termid":"PBO:0028310"}


id: PBO:0036387
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by Rhodotorula minuta DPS1","termid":"PBO:0036387"}


id: PBO:0045575
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dual specificity phosphatase 28","termid":"PBO:0045575"}


id: GO:0051962
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates, maintains or increases the frequency, rate or extent of nervous system development, the origin and formation of nervous tissue.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of developmental process","termid":"GO:0051094"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"is_a","term_name":"regulation of nervous system development","termid":"GO:0051960"},{"relation_name":"positively_regulates","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":"positive regulation of nervous system development","synonyms":[{"name":"activation of nervous system development","type":"narrow"},{"name":"stimulation of nervous system development","type":"narrow"},{"name":"up regulation of nervous system development","type":"exact"},{"name":"up-regulation of nervous system development","type":"exact"},{"name":"upregulation of nervous system development","type":"exact"}],"termid":"GO:0051962"}


id: GO:0002149
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of hypochlorous acid.","definition_xrefs":["PMID:10085024","PMID:176150","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypochlorous acid metabolic process","termid":"GO:0002148"},{"relation_name":"is_a","term_name":"small molecule biosynthetic process","termid":"GO:0044283"},{"relation_name":"is_a","term_name":"reactive oxygen species biosynthetic process","termid":"GO:1903409"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"hypochlorous acid biosynthetic process","synonyms":[{"name":"HClO biosynthetic process","type":"exact"},{"name":"HOCl biosynthetic process","type":"exact"},{"name":"hypochlorite biosynthetic process","type":"related"},{"name":"hypochlorous acid biosynthesis","type":"exact"}],"termid":"GO:0002149"}


id: PBO:0065993
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retinoic acid induced 2","termid":"PBO:0065993"}


id: MONDO:0016775
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lichen planus (LP) pemphigoides is a rare cross-over syndrome between lichen planus and bullous pemphigoid.","definition_xrefs":["Orphanet:254478"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lichen planus","termid":"MONDO:0006572"}],"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":"lichen planus pemphigoides","secondary_identifiers":["MEDGEN:590352","SCTID:238653005","UMLS:C0406369","GARD:12677","icd11.foundation:1373932539"],"synonyms":[{"name":"LP pemphigoides","type":"exact"}],"termid":"MONDO:0016775","xrefs":{"Monarch":{"xref_id":"0016775"}}}


id: PBO:0059580
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metastasis associated 1 family member 2","termid":"PBO:0059580"}


id: MONDO:0024265
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Duane syndrome type 1 is the most common type of Duane syndrome, an eye movement disorder that is present at birth. People with Duane syndrome have restricted ability to move the affected eye(s) outward toward the ear (abduction) and/or inward toward the nose (adduction). The different types are distinguished by the eye movements that are most restricted. Duane syndrome type 1 is characterized by absent to very restricted abduction and normal to mildly restricted adduction. The eye opening (palpebral fissure) narrows and the eyeball retracts into the orbit with adduction. With abduction, the reverse occurs. One or both eyes may be affected. The majority of cases are sporadic (not inherited), while about 10% are familial. 70% of affected people do not have any other abnormalities at birth (isolated Duane syndrome). Treatment is mainly supportive and may include glasses or contact lenses for vision correction, eye patches, or surgery.","definition_xrefs":["GARD:0010763"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Duane retraction syndrome","termid":"MONDO:0007473"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Duane syndrome type 1","secondary_identifiers":["OMIM:126800","UMLS:C0994516","GARD:10763","SCTID:128082002","MEDGEN:201329"],"synonyms":[{"name":"DURS1","type":"exact"},{"name":"Drs","type":"related"},{"name":"Duane anomaly","type":"related"},{"name":"Duane retraction syndrome 1","type":"exact"},{"name":"Duane syndrome","type":"related"},{"name":"retraction syndrome","type":"related"}],"termid":"MONDO:0024265","xrefs":{"Monarch":{"xref_id":"0024265"}}}


id: MONDO:0012781
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"celiac disease","termid":"MONDO:0005130"},{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"celiac disease, susceptibility to, 12","secondary_identifiers":["MEDGEN:436989","OMIM:612010","UMLS:C2677602"],"synonyms":[{"name":"CELIAC12","type":"exact"},{"name":"celiac disease, susceptibility to, 12","type":"exact"},{"name":"gluten-sensitive enteropathy, susceptibility to, 12","type":"related"}],"termid":"MONDO:0012781","xrefs":{"Monarch":{"xref_id":"0012781"}}}


id: GO:0045595
data:
  {"annotated_genes":["SJAG_02392","SJAG_04140","SJAG_00993","SJAG_04853","SJAG_00514","SJAG_02169","SJAG_03581"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[95608,89611,94337],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051519"},{"annotations":[110996],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0075297"},{"annotations":[90480],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051517"},{"annotations":[102079],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0075296"},{"annotations":[90482],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903024"},{"annotations":[91946],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034307"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cell differentiation, the process in which relatively unspecialized cells acquire specialized structural and functional features.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of developmental process","termid":"GO:0050793"},{"relation_name":"is_a","term_name":"regulation of cellular process","termid":"GO:0050794"},{"relation_name":"regulates","term_name":"cell differentiation","termid":"GO:0030154"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00514":null,"SJAG_00993":null,"SJAG_02169":null,"SJAG_02392":null,"SJAG_03581":null,"SJAG_04140":null,"SJAG_04853":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of cell differentiation","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0045595","terms_by_termid":{"GO:0034307":null,"GO:0051517":null,"GO:0051519":null,"GO:0075296":null,"GO:0075297":null,"GO:1903024":null}}


id: MONDO:0021962
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":"baetz-greenwalt syndrome","secondary_identifiers":["MEDGEN:444099","MESH:C537795","UMLS:C2931615"],"synonyms":[{"name":"hypoplastic right-sided heart complex","type":"related"}],"termid":"MONDO:0021962","xrefs":{"Monarch":{"xref_id":"0021962"}}}


id: MONDO:0004536
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete villoglandular variant cervical mucinous adenocarcinoma (obsolete MONDO:0004536)","termid":"MONDO:0004536","xrefs":{"Monarch":{"xref_id":"0004536"}}}


id: FYPO:0003447
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of glycosylated protein measured the cell is lower than normal when the cell is in the vegetative growth phase of the life cycle. Total protein or a specific protein may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein level during vegetative growth","termid":"FYPO:0001324"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0006551","FYPO:0001985","FYPO:0001320","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"decreased level of glycosylated protein in cell","synonyms":[{"name":"decreased accumulation of glycosylated protein in cell","type":"related"},{"name":"decreased cellular glycoprotein level","type":"exact"},{"name":"decreased glycosylated protein level during vegetative growth","type":"exact"},{"name":"decreased level of glycosylated protein in cell during mitotic cell cycle","type":"related"},{"name":"decreased level of glycosylated protein in cell during vegetative growth","type":"exact"},{"name":"reduced level of glycosylated protein in cell","type":"exact"}],"termid":"FYPO:0003447"}


id: FYPO:0002567
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of RNAs transcribed from the centromere outer repeat region measured in a cell is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal centromeric RNA level during vegetative growth","termid":"FYPO:0008177"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0001312","FYPO:0000257"],"is_obsolete":false,"name":"normal centromeric outer repeat transcript level","synonyms":[{"name":"normal accumulation of centromeric outer repeat transcripts","type":"related"},{"name":"normal accumulation of centromeric outer repeat transcripts during vegetative growth","type":"exact"},{"name":"normal accumulation of non-coding outer repeat transcripts","type":"exact"},{"name":"normal centromeric outer repeat transcript accumulation","type":"related"},{"name":"normal centromeric outer repeat transcript level during mitotic cell cycle","type":"related"},{"name":"normal centromeric outer repeat transcript level during vegetative growth","type":"exact"},{"name":"normal level of centromeric outer repeat transcripts","type":"exact"}],"termid":"FYPO:0002567"}


id: PBO:0082094
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"6-phosphogluconate dehydrogenase (decarboxylating); catalyzes an NADPH regenerating reaction in the pentose phosphate pathway; required for growth on D-glucono-delta-lactone; GND2 has a paralog, GND1, that arose from the whole genome duplication","termid":"PBO:0082094"}


id: PBO:0058032
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4253","termid":"PBO:0058032"}


id: GO:0033751
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: linoleate + O2 = (9Z,12Z)-(7S,8S)-dihydroxyoctadeca-9,12-dienoate.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete linoleate 8R-lipoxygenase (obsolete GO:0033751)","synonyms":[{"name":"5,8-linoleate diol synthase (bifunctional enzyme)","type":"related"},{"name":"7,8-linoleate diol synthase (bifunctional enzyme)","type":"related"},{"name":"linoleate diol synthase activity","type":"related"}],"termid":"GO:0033751"}


id: GO:0032544
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of a protein in a plastid. This is a ribosome-mediated process in which the information in messenger RNA (mRNA) is used to specify the sequence of amino acids in the protein; the plastid has its own ribosomes and transfer RNAs, and uses a genetic code that differs from the nuclear code.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"translation","termid":"GO:0006412"},{"relation_name":"is_a","term_name":"plastid organization","termid":"GO:0009657"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"plastid translation","synonyms":[{"name":"plastid protein anabolism","type":"exact"},{"name":"plastid protein biosynthesis","type":"exact"},{"name":"plastid protein formation","type":"exact"},{"name":"plastid protein synthesis","type":"exact"},{"name":"plastid protein translation","type":"exact"}],"termid":"GO:0032544"}


id: PBO:0072730
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sphingosine-1-phosphate receptor 1","termid":"PBO:0072730"}


id: PBO:0058205
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4498","termid":"PBO:0058205"}


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


id: PBO:0043278
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-type lectin domain family 4 member A","termid":"PBO:0043278"}


id: GO:0021909
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of transcription from an RNA polymerase II promoter that results in the spatial identity of regions along the anterior-posterior axis of the spinal cord.","definition_xrefs":["GOC:cls","PMID:11262869","GOC:dph","GOC:jid","GO_REF:0000021","GOC:dgh"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of transcription from RNA polymerase II promoter involved in spinal cord anterior-posterior patterning (obsolete GO:0021909)","termid":"GO:0021909"}


id: GO:0035781
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of CD86, a CD marker that occurs on antigen presenting cells that provides co-stimulatory signals necessary for T cell activation and survival.","definition_xrefs":["GOC:ebc","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycoprotein biosynthetic process","termid":"GO:0009101"}],"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":"CD86 biosynthetic process","synonyms":[{"name":"CD86 anabolism","type":"exact"},{"name":"CD86 biosynthesis","type":"exact"},{"name":"CD86 formation","type":"exact"},{"name":"CD86 synthesis","type":"exact"}],"termid":"GO:0035781"}


id: MONDO:1011118
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypogonadism that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypogonadism, non-human animal","termid":"MONDO:1010276"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypogonadism, dog","secondary_identifiers":["OMIA:000522-9615"],"termid":"MONDO:1011118","xrefs":{"Monarch":{"xref_id":"1011118"}}}


id: FYPO:0002704
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which autophagic vacuole docking is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular component organization","termid":"FYPO:0006003"},{"relation_name":"part_of","term_name":"normal macroautophagy","termid":"FYPO:0000385"}],"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":"part_of","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal autophagic vacuole docking","termid":"FYPO:0002704"}


id: GO:0046660
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The establishment of the sex of a female organism by physical differentiation.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sex differentiation","termid":"GO:0007548"},{"relation_name":"part_of","term_name":"multicellular organism development","termid":"GO:0007275"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"female sex differentiation","termid":"GO:0046660"}


id: MONDO:0012584
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any systemic lupus erythematosus in which the cause of the disease is a mutation in the CR2 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":"systemic lupus erythematosus, susceptibility to, 9","secondary_identifiers":["OMIM:610927","MEDGEN:369736","NANDO:2200801","UMLS:C1970455"],"synonyms":[{"name":"CR2 systemic lupus erythematosus (disease)","type":"exact"},{"name":"SLEB9","type":"related"},{"name":"susceptibility to systemic lupus erythematosus 9","type":"related"},{"name":"systemic lupus erythematosus (disease) caused by mutation in CR2","type":"exact"},{"name":"systemic lupus erythematosus, susceptibility to, 9","type":"exact"},{"name":"systemic lupus erythematosus, susceptibility to, type 9","type":"exact"}],"termid":"MONDO:0012584","xrefs":{"Monarch":{"xref_id":"0012584"}}}


id: PBO:0058234
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4523","termid":"PBO:0058234"}


id: GO:0003908
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: DNA (containing 6-O-methylguanine) + (protein)-L-cysteine = DNA (without 6-O-methylguanine) + protein S-methyl-L-cysteine.","definition_xrefs":["EC:2.1.1.63"],"direct_ancestors":[{"relation_name":"is_a","term_name":"S-methyltransferase activity","termid":"GO:0008172"},{"relation_name":"is_a","term_name":"protein methyltransferase activity","termid":"GO:0008276"}],"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:0003824"},{"rel_name":"is_a","termid":"GO:0008276"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0140096","GO:0016741","GO:0008276","GO:0003824","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"methylated-DNA-[protein]-cysteine S-methyltransferase activity","secondary_identifiers":["MetaCyc:2.1.1.63-RXN","Reactome:R-HSA-73892","RHEA:24000"],"synonyms":[{"name":"6-O-methylguanine-DNA methyltransferase activity","type":"related"},{"name":"DNA-6-O-methylguanine:[protein]-L-cysteine S-methyltransferase activity","type":"exact"},{"name":"DNA-6-O-methylguanine:protein-L-cysteine S-methyltransferase activity","type":"related"},{"name":"MGMT","type":"exact"},{"name":"O-6-methylguanine-DNA-alkyltransferase activity","type":"related"},{"name":"O6-alkylguanine-DNA alkyltransferase","type":"broad"},{"name":"methylated-DNA-protein-cysteine S-methyltransferase activity","type":"related"}],"termid":"GO:0003908"}


id: PBO:0043238
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chloride voltage-gated channel Kb","termid":"PBO:0043238"}


id: MONDO:0012009
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"excluded_subClassOf","term_name":"coronary artery disorder","termid":"MONDO:0005010"},{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coronary heart disease, susceptibility to, 2","secondary_identifiers":["MEDGEN:330807","OMIM:608316","UMLS:C1842260"],"synonyms":[{"name":"Chds2","type":"related"},{"name":"coronary heart disease, susceptibility to, 2","type":"exact"},{"name":"coronary heart disease, susceptibility to, type 2","type":"exact"}],"termid":"MONDO:0012009","xrefs":{"Monarch":{"xref_id":"0012009"}}}


id: GO:0042221
data:
  {"annotated_genes":["SJAG_00903","SJAG_04036","SJAG_04404","SJAG_02247","SJAG_00984","SJAG_01978","SJAG_01404","SJAG_00365","SJAG_02599","SJAG_01162","SJAG_00948","SJAG_02774","SJAG_04608","SJAG_04516","SJAG_00627","SJAG_02091","SJAG_04429","SJAG_00668","SJAG_02010","SJAG_03166","SJAG_01345","SJAG_03330","SJAG_00614","SJAG_03799","SJAG_04674","SJAG_01699","SJAG_00993","SJAG_03316","SJAG_01854","SJAG_00221","SJAG_02135","SJAG_01995","SJAG_00990","SJAG_00126","SJAG_00931","SJAG_01145","SJAG_02044","SJAG_03903","SJAG_02592","SJAG_03879","SJAG_03828","SJAG_00403","SJAG_01612","SJAG_00219","SJAG_02495","SJAG_00661","SJAG_01457","SJAG_00409","SJAG_03209","SJAG_04311","SJAG_00419","SJAG_02433","SJAG_02858","SJAG_04345","SJAG_04612","SJAG_01768","SJAG_01584","SJAG_04063","SJAG_04205","SJAG_02249","SJAG_04125","SJAG_06611","SJAG_04823","SJAG_01351","SJAG_01233","SJAG_02883","SJAG_00489","SJAG_03185","SJAG_04726","SJAG_00472","SJAG_02988","SJAG_03363","SJAG_00996","SJAG_03414","SJAG_04454","SJAG_05022","SJAG_02539","SJAG_02960","SJAG_01656","SJAG_01754","SJAG_02106","SJAG_05256","SJAG_01651","SJAG_05181","SJAG_03896","SJAG_03108","SJAG_00790","SJAG_01626","SJAG_03653","SJAG_04026","SJAG_00988","SJAG_00766","SJAG_01254","SJAG_00642","SJAG_03476","SJAG_05274","SJAG_02694","SJAG_04583","SJAG_04632","SJAG_03032","SJAG_02276","SJAG_03288","SJAG_01084","SJAG_01134","SJAG_02444","SJAG_02907","SJAG_00141","SJAG_01216","SJAG_02485","SJAG_00027","SJAG_01051","SJAG_02573","SJAG_00530","SJAG_01292","SJAG_04312","SJAG_02973","SJAG_03497","SJAG_01150","SJAG_01803","SJAG_04242","SJAG_00596","SJAG_06621","SJAG_00941","SJAG_03340","SJAG_02244","SJAG_02685","SJAG_04384","SJAG_00681","SJAG_01734","SJAG_00574","SJAG_03623","SJAG_01528","SJAG_00044","SJAG_03893","SJAG_04668","SJAG_02945","SJAG_01199","SJAG_07000","SJAG_01709","SJAG_03081","SJAG_03951","SJAG_03657","SJAG_01585","SJAG_03631","SJAG_03303","SJAG_04399","SJAG_01858","SJAG_00179","SJAG_01596","SJAG_00131","SJAG_03227","SJAG_02515","SJAG_03924","SJAG_04018","SJAG_04904","SJAG_02630","SJAG_04953","SJAG_03841","SJAG_02342","SJAG_01855","SJAG_01718","SJAG_04788","SJAG_03797","SJAG_01628","SJAG_04403","SJAG_06622","SJAG_01078","SJAG_01973","SJAG_01344","SJAG_03153","SJAG_00270","SJAG_02923","SJAG_03494","SJAG_03345"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[116370,106644,115338,93987,109321,105704,101636,106292,108814],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0010619"},{"annotations":[117988,96873,87723,92884,102579,94442,113304,87820,112085,118551,92202,114405,87718,98153,92883,98800,114506,94712,102652,89863,106401,98989,99632,108519,100110,103406,112813,118409,113266],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990748"},{"annotations":[112531],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0110095"},{"annotations":[70508,93066,108234,96784,96822,118013],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0098849"},{"annotations":[113544],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0140114"},{"annotations":[117178,118100,104841,94954,108636,99787],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061692"},{"annotations":[104844],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0140041"},{"annotations":[102008,87151],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070458"},{"annotations":[92160],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071474"},{"annotations":[63293,57336,67791,65076,68336,106594],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0098869"},{"annotations":[88628],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071276"},{"annotations":[109959,100780,97887,113162,114483,115936],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071277"},{"annotations":[77341],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071244"},{"annotations":[89259],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071473"},{"annotations":[109651,116793,101008,111509],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071456"},{"annotations":[105022],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036245"},{"annotations":[92892],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071248"},{"annotations":[102009],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071500"},{"annotations":[116886,104317,91645,94124,95732,110140,114271,102580,106297,116092],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071470"},{"annotations":[74739,90643,77339,74896,89844,95749,73386,108734,69921,76643,88308,95323,97397,114272,107603,108738,76560,67860,93322,63742,108737,108740,75345,78806,108739,91916,89943,66778,108736,101646,108735,73032],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034599"},{"annotations":[114484],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035865"},{"annotations":[99959],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071472"},{"annotations":[70507],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0010273"},{"annotations":[93525,93526],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0010312"},{"annotations":[78236,73004,74568,78484,111777,116964,70705,70894,115666,70291,78422,100556,94745,75989,89294,70318,97615,104611,87539,70379,71874,98006,107973,91159,107473,104527,78465,102714,78264,94478,79210,74065,107908,93329,116402],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036503"},{"annotations":[77889,95294],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0046294"},{"annotations":[72857],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031990"},{"annotations":[77307,77808],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1904293"},{"annotations":[106077,96816,93084,88980,96142,91945],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071507"},{"annotations":[70568],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000750"},{"annotations":[89009,116201],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1900039"},{"annotations":[92894,68274,57879,89150,74019,60664,88728,64774,99061],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0019430"},{"annotations":[105322],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000749"},{"annotations":[78791,75240],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030970"},{"annotations":[93306,95469],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097466"},{"annotations":[58290,63380,117765],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990961"}]},"cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a chemical stimulus.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to stimulus","termid":"GO:0050896"}],"gene_count":174,"genes_by_uniquename":{"SJAG_00027":null,"SJAG_00044":null,"SJAG_00126":null,"SJAG_00131":null,"SJAG_00141":null,"SJAG_00179":null,"SJAG_00219":null,"SJAG_00221":null,"SJAG_00270":null,"SJAG_00365":null,"SJAG_00403":null,"SJAG_00409":null,"SJAG_00419":null,"SJAG_00472":null,"SJAG_00489":null,"SJAG_00530":null,"SJAG_00574":null,"SJAG_00596":null,"SJAG_00614":null,"SJAG_00627":null,"SJAG_00642":null,"SJAG_00661":null,"SJAG_00668":null,"SJAG_00681":null,"SJAG_00766":null,"SJAG_00790":null,"SJAG_00903":null,"SJAG_00931":null,"SJAG_00941":null,"SJAG_00948":null,"SJAG_00984":null,"SJAG_00988":null,"SJAG_00990":null,"SJAG_00993":null,"SJAG_00996":null,"SJAG_01051":null,"SJAG_01078":null,"SJAG_01084":null,"SJAG_01134":null,"SJAG_01145":null,"SJAG_01150":null,"SJAG_01162":null,"SJAG_01199":null,"SJAG_01216":null,"SJAG_01233":null,"SJAG_01254":null,"SJAG_01292":null,"SJAG_01344":null,"SJAG_01345":null,"SJAG_01351":null,"SJAG_01404":null,"SJAG_01457":null,"SJAG_01528":null,"SJAG_01584":null,"SJAG_01585":null,"SJAG_01596":null,"SJAG_01612":null,"SJAG_01626":null,"SJAG_01628":null,"SJAG_01651":null,"SJAG_01656":null,"SJAG_01699":null,"SJAG_01709":null,"SJAG_01718":null,"SJAG_01734":null,"SJAG_01754":null,"SJAG_01768":null,"SJAG_01803":null,"SJAG_01854":null,"SJAG_01855":null,"SJAG_01858":null,"SJAG_01973":null,"SJAG_01978":null,"SJAG_01995":null,"SJAG_02010":null,"SJAG_02044":null,"SJAG_02091":null,"SJAG_02106":null,"SJAG_02135":null,"SJAG_02244":null,"SJAG_02247":null,"SJAG_02249":null,"SJAG_02276":null,"SJAG_02342":null,"SJAG_02433":null,"SJAG_02444":null,"SJAG_02485":null,"SJAG_02495":null,"SJAG_02515":null,"SJAG_02539":null,"SJAG_02573":null,"SJAG_02592":null,"SJAG_02599":null,"SJAG_02630":null,"SJAG_02685":null,"SJAG_02694":null,"SJAG_02774":null,"SJAG_02858":null,"SJAG_02883":null,"SJAG_02907":null,"SJAG_02923":null,"SJAG_02945":null,"SJAG_02960":null,"SJAG_02973":null,"SJAG_02988":null,"SJAG_03032":null,"SJAG_03081":null,"SJAG_03108":null,"SJAG_03153":null,"SJAG_03166":null,"SJAG_03185":null,"SJAG_03209":null,"SJAG_03227":null,"SJAG_03288":null,"SJAG_03303":null,"SJAG_03316":null,"SJAG_03330":null,"SJAG_03340":null,"SJAG_03345":null,"SJAG_03363":null,"SJAG_03414":null,"SJAG_03476":null,"SJAG_03494":null,"SJAG_03497":null,"SJAG_03623":null,"SJAG_03631":null,"SJAG_03653":null,"SJAG_03657":null,"SJAG_03797":null,"SJAG_03799":null,"SJAG_03828":null,"SJAG_03841":null,"SJAG_03879":null,"SJAG_03893":null,"SJAG_03896":null,"SJAG_03903":null,"SJAG_03924":null,"SJAG_03951":null,"SJAG_04018":null,"SJAG_04026":null,"SJAG_04036":null,"SJAG_04063":null,"SJAG_04125":null,"SJAG_04205":null,"SJAG_04242":null,"SJAG_04311":null,"SJAG_04312":null,"SJAG_04345":null,"SJAG_04384":null,"SJAG_04399":null,"SJAG_04403":null,"SJAG_04404":null,"SJAG_04429":null,"SJAG_04454":null,"SJAG_04516":null,"SJAG_04583":null,"SJAG_04608":null,"SJAG_04612":null,"SJAG_04632":null,"SJAG_04668":null,"SJAG_04674":null,"SJAG_04726":null,"SJAG_04788":null,"SJAG_04823":null,"SJAG_04904":null,"SJAG_04953":null,"SJAG_05022":null,"SJAG_05181":null,"SJAG_05256":null,"SJAG_05274":null,"SJAG_06611":null,"SJAG_06621":null,"SJAG_06622":null,"SJAG_07000":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to chemical","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000108":null},"synonyms":[{"name":"response to chemical stimulus","type":"exact"},{"name":"response to chemical substance","type":"exact"}],"termid":"GO:0042221","terms_by_termid":{"GO:0000749":null,"GO:0000750":null,"GO:0010273":null,"GO:0010312":null,"GO:0010619":null,"GO:0019430":null,"GO:0030970":null,"GO:0031990":null,"GO:0034599":null,"GO:0035865":null,"GO:0036245":null,"GO:0036503":null,"GO:0046294":null,"GO:0061692":null,"GO:0070458":null,"GO:0071244":null,"GO:0071248":null,"GO:0071276":null,"GO:0071277":null,"GO:0071456":null,"GO:0071470":null,"GO:0071472":null,"GO:0071473":null,"GO:0071474":null,"GO:0071500":null,"GO:0071507":null,"GO:0097466":null,"GO:0098849":null,"GO:0098869":null,"GO:0110095":null,"GO:0140041":null,"GO:0140114":null,"GO:1900039":null,"GO:1904293":null,"GO:1990748":null,"GO:1990961":null}}


id: GO:0044205
data:
  {"annotated_genes":["SJAG_00197","SJAG_00964","SJAG_03164","SJAG_00694","SJAG_00444"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[57041,58901,59216,60888,61603],"is_not":false,"summary":null,"term":"GO:0044205"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of UMP, uridine monophosphate, starting with the synthesis of (S)-dihydroorotate from bicarbonate; UMP biosynthesis may either occur via reduction by quinone, NAD+ or oxygen.","definition_xrefs":["GOC:ecd","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UMP biosynthetic process","termid":"GO:0006222"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00197":null,"SJAG_00444":null,"SJAG_00694":null,"SJAG_00964":null,"SJAG_03164":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"'de novo' UMP biosynthetic process","references_by_uniquename":{"GO_REF:0000041":null},"synonyms":[{"name":"'de novo' UMP biosynthesis","type":"exact"}],"termid":"GO:0044205","terms_by_termid":{"GO:0044205":null}}


id: PBO:0038719
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actin gamma 1 pseudogene 14","termid":"PBO:0038719"}


id: PR:Q9HFF2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC683.02c gene.","definition_xrefs":["UniProtKB:Q9HFF2","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 C683.02c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC683.02c","synonyms":[{"name":"Spom972h-SPAC683.02c","type":"exact"}],"termid":"PR:Q9HFF2"}


id: PBO:0088314
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bromodomain protein Bdc1","termid":"PBO:0088314"}


id: MONDO:0019265
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Diazoxide-resistant focal hyperinsulism (DRFH) is a form of diazoxide-resistant hyperinsulinism characterized by recurrent episodes of profound hypoglycemia caused by an excessive/ uncontrolled insulin secretion (inappropriate for the level of glycemia) due to a focal adenomatous hyperplasia of pancreas, that is unresponsive to medical treatment with diazoxide, necessitating complete excision of the focal lesion.","definition_xrefs":["Orphanet:79298"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diazoxide-resistant hyperinsulinism","termid":"MONDO:0017186"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0037792","MONDO:0004335","MONDO:0005066"],"is_obsolete":false,"name":"diazoxide-resistant focal hyperinsulinism","secondary_identifiers":["UMLS:C5680204","GARD:18983","MEDGEN:1843436"],"synonyms":[{"name":"hyperinsulinemic hypoglycemia, diazoxide-resistant focal form","type":"exact"}],"termid":"MONDO:0019265","xrefs":{"Monarch":{"xref_id":"0019265"}}}


id: PBO:0017965
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine-type peptidase activity","termid":"PBO:0017965"}


id: GO:0000208
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of a MAP kinase to the nucleus during osmolarity sensing.","definition_xrefs":["PMID:9561267"],"gene_count":0,"genotype_count":0,"name":"obsolete MAPK import into nucleus involved in osmosensory signaling pathway (obsolete GO:0000208)","synonyms":[{"name":"MAPK import into nucleus during osmolarity sensing","type":"exact"},{"name":"MAPK import into nucleus involved in osmosensory signalling pathway","type":"exact"},{"name":"nuclear translocation of MAPK during osmolarity sensing","type":"exact"},{"name":"nuclear translocation of MAPK involved in osmosensory signaling pathway","type":"narrow"},{"name":"nuclear translocation of MAPK involved in osmosensory signalling pathway","type":"narrow"},{"name":"osmolarity sensing, MAPK import into nucleus","type":"exact"},{"name":"osmolarity sensing, nuclear translocation of MAPK","type":"narrow"}],"termid":"GO:0000208"}


id: PBO:0062458
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 136 pseudogene","termid":"PBO:0062458"}


id: GO:0005250
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transmembrane transfer of a potassium ion by an outwardly-rectifying voltage-gated channel that produces a transient outward current upon a step change in membrane potential.","definition_xrefs":["PMID:5575340","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"outward rectifier potassium channel activity","termid":"GO:0015271"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"A-type (transient outward) potassium channel activity","secondary_identifiers":["Reactome:R-HSA-5577234"],"termid":"GO:0005250"}


id: GO:0032267
data:
  {"annotated_genes":["SJAG_05249"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[64944],"is_not":false,"summary":null,"term":"GO:0032267"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + cytidine(34) in tRNA(Ile2) + L-lysine = AMP + diphosphate + H+ + lysidine(34) in tRNA(Ile2). This modification converts both the codon specificity of tRNA(Ile) from AUG to AUA and its amino acid specificity from methionine to isoleucine.","definition_xrefs":["RHEA:43744","PMID:14527414"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ligase activity, forming carbon-nitrogen bonds","termid":"GO:0016879"},{"relation_name":"is_a","term_name":"catalytic activity, acting on a tRNA","termid":"GO:0140101"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05249":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140101"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0140098"}],"interesting_parent_ids":["GO:0140101","GO:0003674","GO:0016874","GO:0140098","GO:0003824"],"is_obsolete":false,"name":"tRNA(Ile)-lysidine synthase activity","references_by_uniquename":{"GO_REF:0000003":null},"secondary_identifiers":["EC:6.3.4.19"],"synonyms":[{"name":"tRNA(Ile)-2-lysyl-cytidine synthase activity","type":"exact"},{"name":"tRNA(Ile)-lysidine synthetase activity","type":"exact"}],"termid":"GO:0032267","terms_by_termid":{"GO:0032267":null}}


id: FYPO:0003050
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which homologous chromosome pairing during meiosis (synapsis) is normal (i.e. indistinguishable from wild type). Synapsis is the process in which the side by side pairing and physical juxtaposition of homologous chromosomes is established and maintained. Pairing may be assayed globally or at one or more specific loci.","definition_xrefs":["GO:0007129","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular component organization","termid":"FYPO:0006003"},{"relation_name":"is_a","term_name":"normal meiotic cell cycle process","termid":"FYPO:0007078"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal homologous chromosome pairing","synonyms":[{"name":"normal homologous chromosome pairing at meiosis","type":"exact"},{"name":"normal synapsis","type":"exact"}],"termid":"FYPO:0003050"}


id: MONDO:0019064
data:
  {"annotated_genes":["SJAG_01848","SJAG_05289","SJAG_00773","SJAG_04292","SJAG_01854","SJAG_03866","SJAG_02306","SJAG_01857","SJAG_04566","SJAG_01159","SJAG_04757","SJAG_00564","SJAG_03895","SJAG_00199","SJAG_04145","SJAG_01530","SJAG_04110","SJAG_04123","SJAG_02615","SJAG_03457","SJAG_00660","SJAG_00308","SJAG_01537","SJAG_04913","SJAG_04537","SJAG_03320","SJAG_04325","SJAG_02322","SJAG_04628","SJAG_04506"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84773,84772],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014702"},{"annotations":[86744,86745],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014975"},{"annotations":[87011],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030669"},{"annotations":[85192],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014567"},{"annotations":[85407],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009748"},{"annotations":[85460],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011489"},{"annotations":[86813],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011532"},{"annotations":[84932],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010043"},{"annotations":[84936,84937,84935],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012256"},{"annotations":[84822],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012476"},{"annotations":[84942],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012453"},{"annotations":[86796],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012866"},{"annotations":[86066],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012787"},{"annotations":[86255,86254],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008438"},{"annotations":[86514],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012928"},{"annotations":[85040,85039,85038],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014018"},{"annotations":[85037],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014020"},{"annotations":[85399],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014305"},{"annotations":[85383],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014282"},{"annotations":[84869],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014644"},{"annotations":[85874],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014882"},{"annotations":[86245,86246],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011006"},{"annotations":[84853],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014679"},{"annotations":[86499],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012651"},{"annotations":[86285],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957221"},{"annotations":[85795],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957958"},{"annotations":[86453],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032906"},{"annotations":[85797],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030482"},{"annotations":[85841],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030512"},{"annotations":[86592,86593],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0031019"},{"annotations":[86090],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957308"},{"annotations":[86091],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957309"}]},"cv_name":"mondo","definition":"Hereditary spastic paraplegias (HSP) comprise a genetically and clinically heterogeneous group of neurodegenerative disorders characterized by progressive spasticity and hyperreflexia of the lower limbs.","definition_xrefs":["Orphanet:685"],"direct_ancestors":[{"relation_name":"is_a","term_name":"paraplegia","termid":"MONDO:0003757"},{"relation_name":"is_a","term_name":"inherited neurodegenerative disorder","termid":"MONDO:0024237"},{"relation_name":"is_a","term_name":"hereditary neuromuscular disease","termid":"MONDO:0100546"}],"gene_count":30,"genes_by_uniquename":{"SJAG_00199":null,"SJAG_00308":null,"SJAG_00564":null,"SJAG_00660":null,"SJAG_00773":null,"SJAG_01159":null,"SJAG_01530":null,"SJAG_01537":null,"SJAG_01848":null,"SJAG_01854":null,"SJAG_01857":null,"SJAG_02306":null,"SJAG_02322":null,"SJAG_02615":null,"SJAG_03320":null,"SJAG_03457":null,"SJAG_03866":null,"SJAG_03895":null,"SJAG_04110":null,"SJAG_04123":null,"SJAG_04145":null,"SJAG_04292":null,"SJAG_04325":null,"SJAG_04506":null,"SJAG_04537":null,"SJAG_04566":null,"SJAG_04628":null,"SJAG_04757":null,"SJAG_04913":null,"SJAG_05289":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"hereditary spastic paraplegia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:D015419","NANDO:1200052","SCTID:39912006","NCIT:C140267","GARD:6637","NORD:1238","OMIMPS:303350","UMLS:C0037773","ICD10CM:G11.4","DOID:2476","icd11.foundation:810807375","ICD9:334.1","MedDRA:10019903","MEDGEN:20844"],"synonyms":[{"name":"FSP","type":"related"},{"name":"French settlement disease","type":"exact"},{"name":"HSP","type":"exact"},{"name":"SPG","type":"exact"},{"name":"Strumpell-Lorrain disease","type":"exact"},{"name":"Strümpell-Lorrain disease","type":"exact"},{"name":"familial spastic paraparesis","type":"related"},{"name":"familial spastic paraplegia","type":"exact"},{"name":"hereditary spastic paraparesis","type":"exact"},{"name":"spastic paraplegia","type":"broad"}],"termid":"MONDO:0019064","terms_by_termid":{"MONDO:0008438":null,"MONDO:0009748":null,"MONDO:0010043":null,"MONDO:0011006":null,"MONDO:0011489":null,"MONDO:0011532":null,"MONDO:0012256":null,"MONDO:0012453":null,"MONDO:0012476":null,"MONDO:0012651":null,"MONDO:0012787":null,"MONDO:0012866":null,"MONDO:0012928":null,"MONDO:0014018":null,"MONDO:0014020":null,"MONDO:0014282":null,"MONDO:0014305":null,"MONDO:0014567":null,"MONDO:0014644":null,"MONDO:0014679":null,"MONDO:0014702":null,"MONDO:0014882":null,"MONDO:0014975":null,"MONDO:0030482":null,"MONDO:0030512":null,"MONDO:0030669":null,"MONDO:0031019":null,"MONDO:0032906":null,"MONDO:0957221":null,"MONDO:0957308":null,"MONDO:0957309":null,"MONDO:0957958":null},"xrefs":{"Monarch":{"xref_id":"0019064"}}}


id: MONDO:1010013
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cor triatriatum dexter that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiovascular disorder, non-human animal","termid":"MONDO:1011306"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis, non-human animal","termid":"MONDO:1011313"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cor triatriatum dexter, non-human animal","secondary_identifiers":["OMIA:000227"],"termid":"MONDO:1010013","xrefs":{"Monarch":{"xref_id":"1010013"}}}


id: PBO:0080898
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein beta pseudogene 1","termid":"PBO:0080898"}


id: MONDO:0006244
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A biologic subset of breast carcinoma defined by high expression of HER2, GRB7, and TRAP100, and by lack of expression of estrogen receptor (ER).","definition_xrefs":["NCIT:C53556"],"direct_ancestors":[{"relation_name":"is_a","term_name":"breast carcinoma by gene expression profile","termid":"MONDO:0006116"}],"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":"HER2 positive breast carcinoma","secondary_identifiers":["UMLS:C1960398","SCTID:427685000","MEDGEN:743175","EFO:1000294","DOID:0060079"],"synonyms":[{"name":"ERBB2 Overexpressing subtype of breast carcinoma","type":"exact"},{"name":"HER2 Overexpressing breast carcinoma","type":"exact"},{"name":"HER2 Overexpressing subtype of breast carcinoma","type":"exact"},{"name":"HER2 Positive breast cancer","type":"exact"},{"name":"HER2 positive breast carcinoma","type":"exact"},{"name":"Her2-receptor positive breast cancer","type":"exact"}],"termid":"MONDO:0006244","xrefs":{"Monarch":{"xref_id":"0006244"}}}


id: GO:0019474
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of L-lysine into other compounds, including acetyl-CoA.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acetyl-CoA metabolic process","termid":"GO:0006084"},{"relation_name":"is_a","term_name":"L-lysine catabolic process","termid":"GO:0019477"},{"relation_name":"is_a","term_name":"amide catabolic process","termid":"GO:0043605"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0044248"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006790","GO:0044248","GO:0008150","GO:0006520","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"L-lysine catabolic process to acetyl-CoA","synonyms":[{"name":"L-lysine breakdown to acetyl-CoA","type":"exact"},{"name":"L-lysine degradation to acetyl-CoA","type":"exact"}],"termid":"GO:0019474"}


id: PBO:0076021
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine kinase 17a","termid":"PBO:0076021"}


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


id: GO:0060971
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The pattern specification process that results in the subdivision of the left/right axis of the embryonic heart tube in space to define an area or volume in which specific patterns of cell differentiation will take place.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"left/right pattern formation","termid":"GO:0060972"},{"relation_name":"part_of","term_name":"embryonic heart tube development","termid":"GO:0035050"}],"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":"embryonic heart tube left/right pattern formation","termid":"GO:0060971"}


id: PATO:0002478
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A shape quality inhering in a bearer by virtue of the bearer's being marked by narrow lines or grooves, usually parallel, that are oriented transversely relative to the long axis of the bearer.","definition_xrefs":["PATOC:DS"],"direct_ancestors":[{"relation_name":"is_a","term_name":"striated","termid":"PATO:0001410"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transversely striated","termid":"PATO:0002478"}


id: PR:Q09895
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC24B11.08c gene.","definition_xrefs":["UniProtKB:Q09895","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 C24B11.08c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC24B11.08c","synonyms":[{"name":"Spom972h-SPAC24B11.08c","type":"exact"}],"termid":"PR:Q09895"}


id: GO:0000514
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: 3-sulfino-L-alanine (cysteinesulfinate) (out) + H+(in) + L-glutamate(in) = 3-sulfino-L-alanine(in) + H+(out) + L-glutamate(out).","definition_xrefs":["PMID:11566871","RHEA:70967"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfur amino acid transmembrane transporter activity","termid":"GO:0000099"},{"relation_name":"is_a","term_name":"proton transmembrane transporter activity","termid":"GO:0015078"},{"relation_name":"is_a","term_name":"neutral L-amino acid transmembrane transporter activity","termid":"GO:0015175"},{"relation_name":"is_a","term_name":"L-amino acid transmembrane transporter activity","termid":"GO:0015179"},{"relation_name":"is_a","term_name":"modified amino acid transmembrane transporter activity","termid":"GO:0072349"},{"relation_name":"is_a","term_name":"amino acid:monoatomic cation antiporter activity","termid":"GO:0140848"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"3-sulfino-L-alanine: proton, glutamate antiporter activity","termid":"GO:0000514"}


id: PBO:0084186
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Histone E3 ligase, component of CORVET membrane tethering complex; peripheral vacuolar membrane protein required for protein trafficking and vacuole biogenesis; interacts with Pep7p; involved in ubiquitination and degradation of excess histones","termid":"PBO:0084186"}


id: PBO:0047353
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box and leucine rich repeat protein 6","termid":"PBO:0047353"}


id: GO:0140714
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that assists early maturation of nascent 60S ribosomal subunits. The complex interacts with the large ribosomal subunit rRNA via one of the components (Urb2 in S. cerevisiae) and requires a RNA helicase (Dbp6 in S. cerevisiae).","definition_xrefs":["PMID:9528757","GOC:lnp","PMID:17145778"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein folding chaperone complex","termid":"GO:0101031"}],"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":"large ribosomal subunit pre-assembly complex","termid":"GO:0140714"}


id: PBO:0046869
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"focally amplified long non-coding RNA in epithelial cancer","termid":"PBO:0046869"}


id: PBO:0034297
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-is_symbiosis","termid":"PBO:0034297"}


id: PBO:0066734
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 31","termid":"PBO:0066734"}


id: PBO:0077743
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transducer of ERBB2, 2 pseudogene 1","termid":"PBO:0077743"}


id: FYPO:0002598
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which histone H2A phosphorylation occurs to a lower extent than normal. All histone H2A phosphorylation may be affected, or phosphorylation of specific sites on histone H2A may be decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone phosphorylation during vegetative growth","termid":"FYPO:0002591"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0002274","FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0002494"],"is_obsolete":false,"name":"decreased histone H2A phosphorylation during vegetative growth","synonyms":[{"name":"decreased histone H2A phosphorylation during mitotic cell cycle","type":"related"},{"name":"reduced histone H2A phosphorylation","type":"exact"}],"termid":"FYPO:0002598"}


id: MONDO:0008514
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Syndactyly type 3 (SD3) is a rare congenital distal limb malformation characterized by complete and bilateral syndactyly between the 4th and 5th fingers.","definition_xrefs":["Orphanet:93404"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-syndromic syndactyly","termid":"MONDO:0019530"},{"relation_name":"is_a","term_name":"polydactyly-syndactyly-triphalangism","termid":"MONDO:0800066"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"syndactyly type 3","secondary_identifiers":["GARD:5088","OMIM:186100","DOID:0111817","SCTID:715725001","UMLS:C1861366","icd11.foundation:144846004","MESH:C538154","MEDGEN:396117"],"synonyms":[{"name":"GJA1 non-syndromic syndactyly","type":"exact"},{"name":"Ring and Little finger syndactyly","type":"related"},{"name":"SD3","type":"exact"},{"name":"Sdty3","type":"related"},{"name":"non-syndromic syndactyly caused by mutation in GJA1","type":"exact"},{"name":"syndactyly of fingers 4 and 5","type":"exact"},{"name":"syndactyly of fingers four and five","type":"related"},{"name":"syndactyly of the ring and little finger","type":"related"},{"name":"syndactyly, type 3","type":"related"},{"name":"syndactyly, type III","type":"related"}],"termid":"MONDO:0008514","xrefs":{"Monarch":{"xref_id":"0008514"}}}


id: PBO:0048340
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 51","termid":"PBO:0048340"}


id: GO:0015629
data:
  {"annotated_genes":["SJAG_00845","SJAG_03581","SJAG_03455","SJAG_03681","SJAG_00268","SJAG_03086","SJAG_01739","SJAG_04465","SJAG_02737","SJAG_03887","SJAG_04052","SJAG_03465","SJAG_02831","SJAG_01017","SJAG_04624","SJAG_02169","SJAG_00677","SJAG_01665","SJAG_04724","SJAG_04886","SJAG_02864","SJAG_01268","SJAG_04982","SJAG_02392","SJAG_01894","SJAG_00229","SJAG_03631","SJAG_03025","SJAG_04509","SJAG_04001","SJAG_01171","SJAG_04461","SJAG_01732","SJAG_02245","SJAG_04077","SJAG_00807","SJAG_03379","SJAG_02320","SJAG_01993","SJAG_00140","SJAG_01889","SJAG_00938","SJAG_04498","SJAG_02838","SJAG_02278","SJAG_04375","SJAG_01964","SJAG_04621","SJAG_00700","SJAG_03374","SJAG_04887","SJAG_03704","SJAG_02700","SJAG_04703","SJAG_00397","SJAG_02566","SJAG_01943","SJAG_04100","SJAG_05001","SJAG_02718","SJAG_02266","SJAG_01888","SJAG_00663","SJAG_02075","SJAG_04479","SJAG_03044","SJAG_00920","SJAG_03673","SJAG_03119","SJAG_03088","SJAG_03453","SJAG_01114","SJAG_05185","SJAG_03625","SJAG_03646","SJAG_00152","SJAG_02431","SJAG_03444","SJAG_03380","SJAG_01143","SJAG_03011","SJAG_04517","SJAG_03564","SJAG_01384","SJAG_04597","SJAG_04644","SJAG_04901","SJAG_02228","SJAG_03357","SJAG_02282","SJAG_03145","SJAG_01748","SJAG_02177","SJAG_00228","SJAG_00082","SJAG_01787","SJAG_02511","SJAG_02486","SJAG_00750","SJAG_01277","SJAG_03596","SJAG_00279","SJAG_00185","SJAG_02869","SJAG_05285","SJAG_00649","SJAG_04781","SJAG_00521","SJAG_03375","SJAG_03703","SJAG_00907","SJAG_03146","SJAG_00970","SJAG_00667","SJAG_02202"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[80155],"is_not":false,"summary":null,"term":"GO:0015629"},{"annotations":[104934,98673,101532],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0099079"},{"annotations":[89110],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030478"},{"annotations":[106831,114684,68778,74178,77410,95038,99463,118664,108852,68774,71731,102525,90422,105146,102847,65606,105818,97492,100734,111463,74514,79313,110813,112704,114117,78958,110479,67719,69627,76602,111984,74935,111958,92334,87891,64658,78899,93409,73637,104935,118300,101533,115974,79803,97690,100703,75773,104953,106646,93576,76635],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030479"},{"annotations":[108853,95039,75369,71076,76479],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005884"},{"annotations":[76937,119370,71074],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032432"},{"annotations":[119167,119171,119369,119120,119169,119170,119168],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005826"},{"annotations":[77600,79666,76251,74516,79492,77901,78638],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005885"},{"annotations":[80189,94961,76365,110843,67318],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005869"},{"annotations":[78901,79804],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0008290"},{"annotations":[98069,107924,118904],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070648"},{"annotations":[93775,88838,118906,95124,92265,99932,99336,93579,90595,107925,101731,115981,101730,107864,111111,114427,88020],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990819"},{"annotations":[74543,90473,87633,92293,119046,119039,94336,98070,106687,115706,118643,89071,93580,101049,105150,115622,117450,119044,101056,118905,119041,119048,110553,76165,89559],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0110085"},{"annotations":[100484,104940,108858,100317,117685],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0120106"},{"annotations":[108859,117703,89733,94164,88017,103482,106001,90520,100717,113160,110593,117686,95605,112098,96972,94696,96082],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0120105"},{"annotations":[97421,77991,97671,79494,107929,108860,117687,99899,103706,97804,116839,100745,116745,92080,106840],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0120104"},{"annotations":[62017,57000],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0016459"},{"annotations":[96636,103040,95127],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0045160"},{"annotations":[72200,71398,79609,97423,117689],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0016460"},{"annotations":[65677],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0001725"}]},"cv_name":"cellular_component","definition":"The part of the cytoskeleton (the internal framework of a cell) composed of actin and associated proteins. Includes actin cytoskeleton-associated complexes.","definition_xrefs":["ISBN:0395825172","GOC:jl","ISBN:0815316194"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoskeleton","termid":"GO:0005856"}],"gene_count":115,"genes_by_uniquename":{"SJAG_00082":null,"SJAG_00140":null,"SJAG_00152":null,"SJAG_00185":null,"SJAG_00228":null,"SJAG_00229":null,"SJAG_00268":null,"SJAG_00279":null,"SJAG_00397":null,"SJAG_00521":null,"SJAG_00649":null,"SJAG_00663":null,"SJAG_00667":null,"SJAG_00677":null,"SJAG_00700":null,"SJAG_00750":null,"SJAG_00807":null,"SJAG_00845":null,"SJAG_00907":null,"SJAG_00920":null,"SJAG_00938":null,"SJAG_00970":null,"SJAG_01017":null,"SJAG_01114":null,"SJAG_01143":null,"SJAG_01171":null,"SJAG_01268":null,"SJAG_01277":null,"SJAG_01384":null,"SJAG_01665":null,"SJAG_01732":null,"SJAG_01739":null,"SJAG_01748":null,"SJAG_01787":null,"SJAG_01888":null,"SJAG_01889":null,"SJAG_01894":null,"SJAG_01943":null,"SJAG_01964":null,"SJAG_01993":null,"SJAG_02075":null,"SJAG_02169":null,"SJAG_02177":null,"SJAG_02202":null,"SJAG_02228":null,"SJAG_02245":null,"SJAG_02266":null,"SJAG_02278":null,"SJAG_02282":null,"SJAG_02320":null,"SJAG_02392":null,"SJAG_02431":null,"SJAG_02486":null,"SJAG_02511":null,"SJAG_02566":null,"SJAG_02700":null,"SJAG_02718":null,"SJAG_02737":null,"SJAG_02831":null,"SJAG_02838":null,"SJAG_02864":null,"SJAG_02869":null,"SJAG_03011":null,"SJAG_03025":null,"SJAG_03044":null,"SJAG_03086":null,"SJAG_03088":null,"SJAG_03119":null,"SJAG_03145":null,"SJAG_03146":null,"SJAG_03357":null,"SJAG_03374":null,"SJAG_03375":null,"SJAG_03379":null,"SJAG_03380":null,"SJAG_03444":null,"SJAG_03453":null,"SJAG_03455":null,"SJAG_03465":null,"SJAG_03564":null,"SJAG_03581":null,"SJAG_03596":null,"SJAG_03625":null,"SJAG_03631":null,"SJAG_03646":null,"SJAG_03673":null,"SJAG_03681":null,"SJAG_03703":null,"SJAG_03704":null,"SJAG_03887":null,"SJAG_04001":null,"SJAG_04052":null,"SJAG_04077":null,"SJAG_04100":null,"SJAG_04375":null,"SJAG_04461":null,"SJAG_04465":null,"SJAG_04479":null,"SJAG_04498":null,"SJAG_04509":null,"SJAG_04517":null,"SJAG_04597":null,"SJAG_04621":null,"SJAG_04624":null,"SJAG_04644":null,"SJAG_04703":null,"SJAG_04724":null,"SJAG_04781":null,"SJAG_04886":null,"SJAG_04887":null,"SJAG_04901":null,"SJAG_04982":null,"SJAG_05001":null,"SJAG_05185":null,"SJAG_05285":null},"genotype_count":0,"in_subsets":["cc_goslim_japonicus"],"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"actin cytoskeleton","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000024":null,"GO_REF:0000033":null,"GO_REF:0000044":null,"GO_REF:0000107":null,"PMID:25866389":null,"PMID:27059155":null,"PMID:27734801":null,"PMID:28655757":null,"PMID:36148799":null},"termid":"GO:0015629","terms_by_termid":{"GO:0001725":null,"GO:0005826":null,"GO:0005869":null,"GO:0005884":null,"GO:0005885":null,"GO:0008290":null,"GO:0015629":null,"GO:0016459":null,"GO:0016460":null,"GO:0030478":null,"GO:0030479":null,"GO:0032432":null,"GO:0045160":null,"GO:0070648":null,"GO:0099079":null,"GO:0110085":null,"GO:0120104":null,"GO:0120105":null,"GO:0120106":null,"GO:1990819":null}}


id: PBO:0030117
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_protein_level_during_cellular_response_to_zinc_ion_starvation","termid":"PBO:0030117"}


id: GO:0043511
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Heterodimeric hormone composed of an inhibin alpha subunit complexed with either an inhibin beta-A subunit, to form inhibin A, or an inhibin beta-B subunit, to form inhibin B.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"extracellular space","termid":"GO:0005615"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005576"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005576"],"is_obsolete":false,"name":"inhibin complex","termid":"GO:0043511"}


id: PBO:0087796
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Swi2/Snf2-related translocase, SUMO-Targeted Ubiquitin Ligase (STUbL); required for maintenance of NHEJ inhibition at telomeres; functions at telomeres to translocate and ubiquitinylate poly-sumoylated Rap1p for proteosomal degradation; plays role in antagonizing silencing during mating-type switching; only known STUbL with a translocase activity; contains RING finger domain; relocalizes from nucleus to cytoplasm upon DNA replication stress","termid":"PBO:0087796"}


id: PBO:0054771
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 2183","termid":"PBO:0054771"}


id: SO:0000039
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A part of a match, for example an hsp from blast is a match_part.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"experimental_feature","termid":"SO:0001410"},{"relation_name":"part_of","term_name":"match","termid":"SO:0000343"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"match_part","synonyms":[{"name":"match part","type":"exact"}],"termid":"SO:0000039"}


id: MONDO:0023273
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A morphologic variant of dermatofibrosarcoma protuberans characterized by the presence of melanin-pigmented dendritic cells.","definition_xrefs":["NCIT:C9430"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dermatofibrosarcoma protuberans","termid":"MONDO:0011934"}],"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":"pigmented dermatofibrosarcoma protuberans","secondary_identifiers":["MEDGEN:90786","SCTID:398670003","UMLS:C0334464"],"synonyms":[{"name":"Bednar Tumor","type":"related"},{"name":"Bednar Tumour","type":"related"},{"name":"Bednar's Tumor","type":"related"},{"name":"Bednar's Tumour","type":"related"},{"name":"Bednars Tumor","type":"related"},{"name":"Bednars Tumour","type":"related"},{"name":"DFSP, Pigmented","type":"related"},{"name":"DFSPs, Pigmented","type":"related"},{"name":"Dermatofibrosarcoma Protuberan, Pigmented","type":"related"},{"name":"Dermatofibrosarcoma Protuberans, Pigmented","type":"related"},{"name":"Pigmented DFSP","type":"related"},{"name":"Pigmented DFSPs","type":"related"},{"name":"Pigmented Dermatofibrosarcoma Protuberan","type":"related"},{"name":"Pigmented Dermatofibrosarcoma Protuberans","type":"related"},{"name":"Pigmented Dermatofibrosarcoma Protuberans (Bednar Tumor)","type":"related"},{"name":"Pigmented dermatofibrosarcoma","type":"related"},{"name":"Pigmented dermatofibrosarcoma protuberans","type":"related"},{"name":"Pigmented dermatofibrosarcoma protuberans of skin","type":"related"},{"name":"Pigmented storiform neurofibroma","type":"related"},{"name":"Protuberan, Pigmented Dermatofibrosarcoma","type":"related"},{"name":"Protuberans, Pigmented Dermatofibrosarcoma","type":"related"},{"name":"Tumor, Bednar","type":"related"},{"name":"Tumor, Bednar's","type":"related"},{"name":"bednar tumor","type":"exact"},{"name":"bednar tumour","type":"exact"},{"name":"pigmented dermatofibrosarcoma protuberans","type":"exact"},{"name":"pigmented dermatofibrosarcoma protuberans (bednar tumor)","type":"exact"}],"termid":"MONDO:0023273","xrefs":{"Monarch":{"xref_id":"0023273"}}}


id: GO:0046548
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Development of a rod cell, one of the sensory cells in the eye that reacts to the presence of light. Rod cells contain the photopigment rhodopsin or porphyropsin and are responsible for vision in dim light.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eye photoreceptor cell development","termid":"GO:0042462"},{"relation_name":"part_of","term_name":"retinal rod cell differentiation","termid":"GO:0060221"}],"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":"retinal rod cell development","termid":"GO:0046548"}


id: SO:0000059
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A binding site that, of a nucleotide molecule, that interacts selectively and non-covalently with polypeptide residues of a nuclease.","definition_xrefs":["SO:cb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide_to_protein_binding_site","termid":"SO:0001654"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclease_binding_site","synonyms":[{"name":"nuclease binding site","type":"exact"}],"termid":"SO:0000059"}


id: PBO:0038949
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adipogenin","termid":"PBO:0038949"}


id: PBO:0028601
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_level_during_cellular_response_to_nitrosative_stress","termid":"PBO:0028601"}


id: MONDO:0012923
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any congenital generalized lipodystrophy in which the cause of the disease is a mutation in the CAV1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital generalized lipodystrophy","termid":"MONDO:0006536"},{"relation_name":"is_a","term_name":"Berardinelli-Seip congenital lipodystrophy","termid":"MONDO:0018883"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005093"],"is_obsolete":false,"name":"congenital generalized lipodystrophy type 3","secondary_identifiers":["OMIM:612526","UMLS:C2675861","GARD:13389","MESH:C567282","DOID:0111137","MEDGEN:436541"],"synonyms":[{"name":"BSCL3","type":"exact"},{"name":"Berardinelli-Seip congenital lipodystrophy type 3","type":"exact"},{"name":"Berardinelli-Seip congenital lipodystrophy, type 3","type":"related"},{"name":"CAV1 congenital generalised lipodystrophy (disease)","type":"exact"},{"name":"CAV1 congenital generalized lipodystrophy (disease)","type":"exact"},{"name":"CGL3","type":"exact"},{"name":"congenital generalised lipodystrophy (disease) caused by mutation in CAV1","type":"exact"},{"name":"congenital generalized lipodystrophy (disease) caused by mutation in CAV1","type":"exact"},{"name":"lipodystrophy, Berardinelli-Seip congenital, type 3","type":"related"},{"name":"lipodystrophy, congenital generalized, type 3","type":"related"},{"name":"type 3 Berardinelli-Seip congenital lipodystrophy","type":"related"}],"termid":"MONDO:0012923","xrefs":{"Monarch":{"xref_id":"0012923"}}}


id: GO:0052643
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving chlorophyllides, any chlorophyll lacking the terpenoid side chain such as phytyl or farnesyl.","definition_xrefs":["PMID:7724548"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chlorophyll metabolic process","termid":"GO:0015994"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0033013"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0033013"],"is_obsolete":false,"name":"chlorophyllide metabolic process","synonyms":[{"name":"chlorophyllide metabolism","type":"exact"}],"termid":"GO:0052643"}


id: PBO:0041645
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcium voltage-gated channel auxiliary subunit alpha2delta 1","termid":"PBO:0041645"}


id: SO:0001719
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A kind of histone modification, whereby the 23rd residue (a lysine), from the start of the H3 histone protein is acetylated.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone_3_acetylation_site","termid":"SO:0001973"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"SO:0000839"}],"interesting_parent_ids":["SO:0000839"],"is_obsolete":false,"name":"H3K23_acetylation_site","synonyms":[{"name":"H3K23 acetylation site","type":"exact"},{"name":"H3K23ac","type":"exact"}],"termid":"SO:0001719"}


id: PBO:0017823
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"26S proteasome regulatory particle assembly protein Nas2 (predicted)","termid":"PBO:0017823"}


id: GO:0038046
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with an enkephalin, and transmitting the signal across the membrane by activating an associated G-protein. A enkephalin is a pentapeptide (Tyr-Gly-Gly-Phe-Met or Tyr-Gly-Gly-Phe-Leu) involved in regulating nociception in the body.","definition_xrefs":["GOC:bf","Wikipedia:Enkephalin"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled opioid receptor activity","termid":"GO:0004985"},{"relation_name":"is_a","term_name":"G protein-coupled peptide receptor activity","termid":"GO:0008528"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"G protein-coupled enkephalin receptor activity","synonyms":[{"name":"delta-opioid receptor activity","type":"related"},{"name":"enkephalin receptor activity","type":"broad"}],"termid":"GO:0038046"}


id: GO:0051874
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of sphinganine-1-phosphate, the phosphorylated derivative of D-erythro-2-amino-1,3-octadecanediol.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sphinganine-1-phosphate metabolic process","termid":"GO:0006668"},{"relation_name":"is_a","term_name":"phospholipid catabolic process","termid":"GO:0009395"},{"relation_name":"is_a","term_name":"sphingolipid catabolic process","termid":"GO:0030149"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"sphinganine-1-phosphate catabolic process","synonyms":[{"name":"dihydrosphingosine-1-phosphate catabolic process","type":"exact"},{"name":"dihydrosphingosine-1-phosphate catabolism","type":"exact"}],"termid":"GO:0051874"}


id: GO:0102303
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 S-adenosyl-L-methionine + trans-resveratrol = 2 S-adenosyl-L-homocysteine + pterostilbene + 2 H+.","definition_xrefs":["GOC:pz","EC:2.1.1.240"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methyltransferase activity","termid":"GO:0008168"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0003824","GO:0016741"],"is_obsolete":false,"name":"resveratrol 3,5-O-dimethyltransferase activity","secondary_identifiers":["MetaCyc:RXN-12805","RHEA:32103"],"termid":"GO:0102303"}


id: GO:1990818
data:
  {"annotated_genes":["SJAG_03400"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[97129],"is_not":false,"summary":null,"term":"GO:1990818"}]},"cv_name":"biological_process","definition":"The directed movement of L-arginine out of the vacuole, across the vacuolar membrane.","definition_xrefs":["PMID:26083598"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic cation transport","termid":"GO:0015695"},{"relation_name":"is_a","term_name":"amino acid transmembrane export from vacuole","termid":"GO:0032974"},{"relation_name":"is_a","term_name":"L-alpha-amino acid transmembrane transport","termid":"GO:1902475"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03400":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150","GO:0055085"],"is_obsolete":false,"name":"L-arginine transmembrane export from vacuole","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1990818","terms_by_termid":{"GO:1990818":null}}


id: MONDO:0005978
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infection of cattle, sheep, or goats with protozoa of the genus theileria. This infection results in an acute or chronic febrile condition.","definition_xrefs":["MESH:D013801"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protozoa infectious disease","termid":"MONDO:0002428"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"theileriasis","secondary_identifiers":["UMLS:C0039753","SCTID:68771000","MEDGEN:11763","EFO:0007506","DOID:3733","ICD9:136.8"],"synonyms":[{"name":"infection by Theileria","type":"exact"},{"name":"theileriosis","type":"exact"}],"termid":"MONDO:0005978","xrefs":{"Monarch":{"xref_id":"0005978"}}}


id: GO:0031525
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of menthol, the monoterpene 2-isopropyl-5-methylcyclohexanol.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monoterpenoid biosynthetic process","termid":"GO:0016099"},{"relation_name":"is_a","term_name":"menthol metabolic process","termid":"GO:0031524"},{"relation_name":"is_a","term_name":"secondary alcohol biosynthetic process","termid":"GO:1902653"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"menthol biosynthetic process","synonyms":[{"name":"menthol anabolism","type":"exact"},{"name":"menthol biosynthesis","type":"exact"},{"name":"menthol formation","type":"exact"},{"name":"menthol synthesis","type":"exact"}],"termid":"GO:0031525"}


id: PBO:0065755
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycogen phosphorylase, muscle associated","termid":"PBO:0065755"}


id: PBO:0087561
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of Slx5-Slx8 SUMO-targeted ubiquitin ligase (STUbL) complex; role in proteolysis of spindle positioning protein Kar9, DNA repair proteins Rad52p and Rad57p; stimulated by SUMO-modified substrates; contains a C-terminal RING domain; forms nuclear foci upon DNA replication stress; required for maintenance of genome integrity like human ortholog RNF","termid":"PBO:0087561"}


id: FYPO:0007691
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the activity of a DNA strand exchange activator is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah","PMID:33493431"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal molecular function","termid":"FYPO:0000706"},{"relation_name":"is_a","term_name":"catalytic activity regulator phenotype","termid":"FYPO:0007690"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000257"],"is_obsolete":false,"name":"normal DNA strand exchange activator activity","synonyms":[{"name":"normal RecA-family recombinase activator activity","type":"exact"},{"name":"normal positive regulation of RecA-family recombinase activity","type":"related"}],"termid":"FYPO:0007691"}


id: PBO:0087345
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sphinganine C4-hydroxylase; catalyses the conversion of sphinganine to phytosphingosine in sphingolipid biosyntheis","termid":"PBO:0087345"}


id: GO:0021845
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The response of migrating interneurons to neurotransmitters that alter electrical activity in cells in calcium dependent manner.","definition_xrefs":["GOC:dph","GO_REF:0000021","GOC:dgh","PMID:12626695","GOC:cls","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell migration","termid":"GO:0030334"},{"relation_name":"part_of","term_name":"substrate-independent telencephalic tangential interneuron migration","termid":"GO:0021843"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"neurotransmitter-mediated guidance of interneurons involved in substrate-independent cerebral cortex tangential migration","termid":"GO:0021845"}


id: PBO:0017587
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MFS myo-inositol transmembrane transporter","termid":"PBO:0017587"}


id: PBO:0040761
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"beclin 1 pseudogene 2","termid":"PBO:0040761"}


id: SO:0000328
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A DNA sequence used experimentally to detect the presence or absence of a complementary nucleic acid.","direct_ancestors":[{"relation_name":"is_a","term_name":"probe","termid":"SO:0000051"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microarray_oligo","synonyms":[{"name":"microarray oligo","type":"exact"},{"name":"microarray oligonucleotide","type":"exact"}],"termid":"SO:0000328"}


id: PBO:0062778
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 56 subfamily A member 7 pseudogene","termid":"PBO:0062778"}


id: GO:0043150
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The synthesis of DNA that contributes to the process of double-strand break repair via homologous recombination.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA synthesis involved in DNA repair","termid":"GO:0000731"},{"relation_name":"part_of","term_name":"double-strand break repair via homologous recombination","termid":"GO:0000724"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"part_of","termid":"GO:0006310"},{"rel_name":"part_of","termid":"GO:0006281"},{"rel_name":"part_of","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006281","GO:0008150","GO:0006259","GO:0006310"],"is_obsolete":false,"name":"DNA synthesis involved in double-strand break repair via homologous recombination","synonyms":[{"name":"DNA synthesis during double-strand break repair via homologous recombination","type":"related"}],"termid":"GO:0043150"}


id: GO:0003873
data:
  {"annotated_genes":["SJAG_00039","SJAG_03336","SJAG_02596","SJAG_02713"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[73107,74696,78665,79968],"is_not":false,"summary":null,"term":"GO:0003873"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: beta-D-fructose 6-phosphate + ATP = beta-D-fructose 2,6-bisphosphate + ADP + 2 H+.","definition_xrefs":["EC:2.7.1.105","RHEA:15653"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphofructokinase activity","termid":"GO:0008443"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00039":null,"SJAG_02596":null,"SJAG_02713":null,"SJAG_03336":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016301","GO:0016740"],"is_obsolete":false,"name":"6-phosphofructo-2-kinase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-71802","KEGG_REACTION:R02732","MetaCyc:6-PHOSPHOFRUCTO-2-KINASE-RXN"],"synonyms":[{"name":"6-phosphofructo-2-kinase (phosphorylating)","type":"related"},{"name":"6-phosphofructose 2-kinase activity","type":"related"},{"name":"ATP:D-fructose-6-phosphate 2-phosphotransferase activity","type":"related"},{"name":"ATP:beta-D-fructose-6-phosphate 2-phosphotransferase activity","type":"related"},{"name":"fructose 6-phosphate 2-kinase activity","type":"related"},{"name":"phosphofructokinase 2 activity","type":"related"}],"termid":"GO:0003873","terms_by_termid":{"GO:0003873":null}}


id: GO:0051370
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Binding to Z-band alternatively spliced PDZ motif protein (ZASP). ZASP is a Z-band protein specifically expressed in heart and skeletal muscle. This protein contains N-terminal PDZ domain and C-terminal LIM domain.","definition_xrefs":["PMID:11699871","PMID:10427098"],"gene_count":0,"genotype_count":0,"name":"obsolete ZASP binding (obsolete GO:0051370)","synonyms":[{"name":"Z-band alternatively spliced PDZ-motif protein binding","type":"exact"},{"name":"ZASP binding","type":"exact"}],"termid":"GO:0051370"}


id: PBO:0029678
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-dispersed_actin_cortical_patch_localization","termid":"PBO:0029678"}


id: PBO:0079490
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thioredoxin domain containing 11","termid":"PBO:0079490"}


id: PBO:0004911
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sorting receptor for vacuolar proteins, Vps10","termid":"PBO:0004911"}


id: PBO:0003113
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G2/M transition checkpoint protein Sum2","termid":"PBO:0003113"}


id: PBO:0082911
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cysteinyl-tRNA synthetase; CRS1 has two in-frame start codons resulting in a shorter isoform that is retained in the cytosol and a longer form that is mitochondrial; may interact with ribosomes, based on co-purification experiments; human gene CARS allows growth of the yeast haploid null mutant after sporulation of a heterozygous diploid","termid":"PBO:0082911"}


id: PBO:0061353
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleophosmin 1 pseudogene 11","termid":"PBO:0061353"}


id: GO:0061153
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of a trachea gland over time, from its formation to the mature structure. Trachea glands are found under the mucus of the trachea and secrete mucus, and agents that help protect the lung from injury and infection.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gland development","termid":"GO:0048732"},{"relation_name":"part_of","term_name":"trachea submucosa development","termid":"GO:0061152"}],"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":"trachea gland development","termid":"GO:0061153"}


id: MONDO:0859257
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant dopa-responsive dystonia","termid":"MONDO:0971063"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0003441"}],"interesting_parent_ids":["MONDO:0003441","MONDO:0005066"],"is_obsolete":false,"name":"intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism","secondary_identifiers":["MEDGEN:1805453","Orphanet:660017","UMLS:C5677001","OMIM:619911"],"termid":"MONDO:0859257","xrefs":{"Monarch":{"xref_id":"0859257"}}}


id: MONDO:0021285
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A in situ carcinoma that involves the urethra.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"in situ carcinoma","termid":"MONDO:0004647"},{"relation_name":"is_a","term_name":"carcinoma of urethra","termid":"MONDO:0021327"}],"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":"carcinoma in situ of urethra","secondary_identifiers":["ICD9:233.9","SCTID:92784007","UMLS:C4721449","MEDGEN:1661236","NCIT:C4531"],"synonyms":[{"name":"carcinoma in situ of the urethra","type":"exact"},{"name":"carcinoma in situ of urethra","type":"exact"},{"name":"stage 0 urethra carcinoma","type":"exact"},{"name":"stage 0is carcinoma of the urethra","type":"exact"},{"name":"stage 0is carcinoma of urethra","type":"exact"},{"name":"stage 0is urethra carcinoma","type":"exact"},{"name":"stage 0is urethral cancer","type":"exact"},{"name":"stage 0is urethral cancer aJCC v7","type":"exact"},{"name":"stage 0is urethral carcinoma","type":"exact"},{"name":"urethra carcinoma in situ","type":"exact"},{"name":"urethra in situ carcinoma","type":"exact"},{"name":"urethral carcinoma in situ","type":"exact"}],"termid":"MONDO:0021285","xrefs":{"Monarch":{"xref_id":"0021285"}}}


id: PBO:0041024
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BPI fold containing family B member 9, pseudogene","termid":"PBO:0041024"}


id: GO:0022015
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The division of a radial glial cell in the pallium. A radial glial cell is a precursor cell that gives rise to neurons and astrocytes.","definition_xrefs":["GOC:dph","GOC:jid","GOC:dgh","GOC:cls","GO_REF:0000021"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell division","termid":"GO:0051301"},{"relation_name":"part_of","term_name":"pallium cell proliferation in forebrain","termid":"GO:0022013"}],"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 division in pallium","termid":"GO:0022015"}


id: GO:0071635
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of production of transforming growth factor-beta.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cytokine production","termid":"GO:0001818"},{"relation_name":"is_a","term_name":"regulation of transforming growth factor beta production","termid":"GO:0071634"},{"relation_name":"negatively_regulates","term_name":"transforming growth factor beta production","termid":"GO:0071604"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"negative regulation of transforming growth factor beta production","secondary_identifiers":["GO:2001202"],"synonyms":[{"name":"negative regulation of TGF-B production","type":"exact"},{"name":"negative regulation of TGF-beta production","type":"exact"},{"name":"negative regulation of TGFB production","type":"exact"},{"name":"negative regulation of TGFbeta production","type":"exact"},{"name":"negative regulation of transforming growth factor-beta production","type":"exact"},{"name":"negative regulation of transforming growth factor-beta secretion","type":"narrow"}],"termid":"GO:0071635"}


id: PBO:0038498
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP binding cassette subfamily C member 6 pseudogene 2","termid":"PBO:0038498"}


id: GO:0047889
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: nitrite + H2O + 2 oxidized ferredoxin = nitrate + 2 reduced ferredoxin.","definition_xrefs":["RHEA:21828"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nitrate reductase activity","termid":"GO:0008940"},{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on other nitrogenous compounds as donors, iron-sulfur protein as acceptor","termid":"GO:0016664"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"ferredoxin-nitrate reductase activity","secondary_identifiers":["MetaCyc:1.7.7.2-RXN","EC:1.7.7.2"],"synonyms":[{"name":"assimilatory ferredoxin-nitrate reductase activity","type":"related"},{"name":"assimilatory nitrate reductase activity","type":"broad"},{"name":"nitrate (ferredoxin) reductase activity","type":"related"},{"name":"nitrite:ferredoxin oxidoreductase activity","type":"related"}],"termid":"GO:0047889"}


id: SO:0000976
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A feature_attribute describing a feature that is not manifest under normal conditions.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"feature_attribute","termid":"SO:0000733"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cryptic","termid":"SO:0000976"}


id: GO:1902440
data:
  {"annotated_genes":["SJAG_02514","SJAG_01546","SJAG_00918","SJAG_02731","SJAG_00883","SJAG_06270","SJAG_01775","SJAG_00082","SJAG_03508","SJAG_03437","SJAG_05319","SJAG_00229","SJAG_01790","SJAG_01224","SJAG_01211","SJAG_05220","SJAG_05266","SJAG_04455","SJAG_01371"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89751],"is_not":false,"summary":null,"term":"GO:1902440"},{"annotations":[101060,104836,107340,95399,109966,74344],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061509"},{"annotations":[107033],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1902543"},{"annotations":[90737,100308,98411,108688,88889,107305,116725,113901,109694,89494,96546],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990976"}]},"cv_name":"biological_process","definition":"A process in which a protein is transported to, or maintained in, a location within a mitotic spindle pole body.","definition_xrefs":["PMID:22438582","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization to spindle pole body","termid":"GO:0071988"}],"gene_count":19,"genes_by_uniquename":{"SJAG_00082":null,"SJAG_00229":null,"SJAG_00883":null,"SJAG_00918":null,"SJAG_01211":null,"SJAG_01224":null,"SJAG_01371":null,"SJAG_01546":null,"SJAG_01775":null,"SJAG_01790":null,"SJAG_02514":null,"SJAG_02731":null,"SJAG_03437":null,"SJAG_03508":null,"SJAG_04455":null,"SJAG_05220":null,"SJAG_05266":null,"SJAG_05319":null,"SJAG_06270":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"protein localization to mitotic spindle pole body","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:1990975"],"synonyms":[{"name":"establishment of protein localization to mitotic spindle pole body","type":"narrow"},{"name":"protein localisation in mitotic spindle pole body","type":"exact"},{"name":"protein localisation to mitotic spindle pole body","type":"exact"},{"name":"protein localization in mitotic spindle pole body","type":"exact"}],"termid":"GO:1902440","terms_by_termid":{"GO:0061509":null,"GO:1902440":null,"GO:1902543":null,"GO:1990976":null}}


id: PBO:0091286
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"does not complement S. cerevisiae NRD1","termid":"PBO:0091286"}


id: GO:0180048
data:
  {"annotated_genes":["SJAG_04537"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[110926],"is_not":false,"summary":null,"term":"GO:0180048"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of phosphatidylinositol 4-phosphate.","definition_xrefs":["PMID:39239853"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biosynthetic process","termid":"GO:0009058"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04537":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"phosphatidylinositol 4-phosphate biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"1-phosphatidyl-1D-myo-inositol 4-phosphate biosynthesis","type":"exact"},{"name":"1-phosphatidyl-1D-myo-inositol biosynthetic process","type":"exact"},{"name":"PI4P biosynthesis","type":"exact"},{"name":"phosphatidylinositol (PI)-4- phosphate biosynthetic process","type":"exact"},{"name":"phosphatidylinositol-4-phosphate synthesis","type":"exact"}],"termid":"GO:0180048","terms_by_termid":{"GO:0180048":null}}


id: MONDO:0013625
data:
  {"annotated_genes":["SJAG_01039"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87052],"is_not":false,"summary":null,"term":"MONDO:0013625"}]},"cv_name":"mondo","definition":"Any Parkinson disease in which the cause of the disease is a mutation in the VPS35 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"late-onset Parkinson disease","termid":"MONDO:0008199"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01039":null},"genotype_count":0,"is_obsolete":false,"name":"Parkinson disease 17","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:481763","UMLS:C3280133","DOID:0060897","GARD:18478","OMIM:614203"],"synonyms":[{"name":"PARK17","type":"related"},{"name":"Parkinson disease 17","type":"exact"},{"name":"Parkinson disease caused by mutation in VPS35","type":"exact"},{"name":"Parkinson disease type 17","type":"exact"},{"name":"Parkinson's disease 17","type":"related"},{"name":"VPS35 Parkinson disease","type":"exact"},{"name":"autosomal dominant Parkinson disease 17","type":"exact"}],"termid":"MONDO:0013625","terms_by_termid":{"MONDO:0013625":null},"xrefs":{"Monarch":{"xref_id":"0013625"}}}


id: FYPO:0003377
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of RNA measured in a cell during a cellular response to nitrosative stress is lower than normal. Total RNA or a specific RNA may be affected. Nitrosative stress often results from exposure to high levels of nitric oxide (NO) or the highly reactive oxidant peroxynitrite, which is produced following interaction of NO with superoxide anions.","definition_xrefs":["PomBase:mah","PMID:20204527","GO:0071500"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased RNA level during vegetative growth","termid":"FYPO:0001117"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0006551","FYPO:0005447","FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"decreased RNA level during cellular response to nitrosative stress","synonyms":[{"name":"decreased RNA accumulation during cellular response to nitrosative stress","type":"related"},{"name":"decreased RNA level during cellular response to nitrosative stress during mitotic cell cycle","type":"related"},{"name":"decreased RNA level during cellular response to nitrosative stress during vegetative growth","type":"exact"},{"name":"decreased mRNA level during cellular response to nitrosative stress","type":"narrow"},{"name":"decreased transcript level during cellular response to nitrosative stress","type":"exact"},{"name":"reduced RNA level during cellular response to nitrosative stress","type":"exact"}],"termid":"FYPO:0003377"}


id: GO:1903828
data:
  {"annotated_genes":["SJAG_03970","SJAG_04597","SJAG_00883","SJAG_02392","SJAG_01084","SJAG_01311","SJAG_01373"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[87835],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042997"},{"annotations":[105613],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042308"},{"annotations":[90718,95614],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903067"},{"annotations":[94168],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140325"},{"annotations":[107033],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902543"},{"annotations":[114276],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1900181"},{"annotations":[95615],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903077"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of a protein localization.","definition_xrefs":["GOC:TermGenie","GOC:vw","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein localization","termid":"GO:0032880"},{"relation_name":"is_a","term_name":"negative regulation of cellular process","termid":"GO:0048523"},{"relation_name":"negatively_regulates","term_name":"protein localization","termid":"GO:0008104"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00883":null,"SJAG_01084":null,"SJAG_01311":null,"SJAG_01373":null,"SJAG_02392":null,"SJAG_03970":null,"SJAG_04597":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 protein localization","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of cellular protein localisation","type":"exact"},{"name":"down regulation of cellular protein localization","type":"exact"},{"name":"down-regulation of cellular protein localisation","type":"exact"},{"name":"down-regulation of cellular protein localization","type":"exact"},{"name":"downregulation of cellular protein localisation","type":"exact"},{"name":"downregulation of cellular protein localization","type":"exact"},{"name":"inhibition of cellular protein localisation","type":"narrow"},{"name":"inhibition of cellular protein localization","type":"narrow"},{"name":"negative regulation of cellular protein localisation","type":"exact"},{"name":"negative regulation of cellular protein localization","type":"exact"}],"termid":"GO:1903828","terms_by_termid":{"GO:0042308":null,"GO:0042997":null,"GO:0140325":null,"GO:1900181":null,"GO:1902543":null,"GO:1903067":null,"GO:1903077":null}}


id: GO:0097714
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a viscosity stimulus.","definition_xrefs":["PMID:7061416","GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to abiotic stimulus","termid":"GO:0009628"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to viscosity","termid":"GO:0097714"}


id: PBO:0053260
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LIF antisense RNA 1","termid":"PBO:0053260"}


id: PBO:0055731
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LIM domain 7","termid":"PBO:0055731"}


id: PBO:0052611
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KRBOX1 antisense RNA 1","termid":"PBO:0052611"}


id: MOD:00657
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-glutamine residue to L-glutamate 5-methyl ester.","definition_xrefs":["Unimod:528","PubMed:6300110","RESID:AA0072#GLN","PubMed:16888"],"direct_ancestors":[{"relation_name":"has_functional_parent","term_name":"methylated glutamine","termid":"MOD:00659"},{"relation_name":"is_a","term_name":"deamidated and methyl esterified residue","termid":"MOD:01369"},{"relation_name":"is_a","term_name":"L-glutamic acid 5-methyl ester","termid":"MOD:01453"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00427"}],"interesting_parent_ids":["MOD:00427"],"is_obsolete":false,"name":"L-glutamic acid 5-methyl ester (Gln)","synonyms":[{"name":"(2S)-2-amino-5-methoxy-5-oxopentanoic acid","type":"exact"},{"name":"(5)-methyl L-hydrogen glutamate","type":"exact"},{"name":"2-aminopentanedioic acid 5-methyl ester","type":"exact"},{"name":"5-methyl L-2-aminoglutarate","type":"exact"},{"name":"5-methyl L-glutamate","type":"exact"},{"name":"Deamidation followed by a methylation","type":"related"},{"name":"L-glutamic acid 5-methyl ester","type":"exact"},{"name":"MOD_RES Glutamate methyl ester (Gln)","type":"exact"},{"name":"Methyl+Deamidated","type":"related"},{"name":"O5MeGlu(Gln)","type":"exact"},{"name":"deamidated 5-methyl esterified glutamine","type":"exact"},{"name":"glutamic acid 5-methyl ester","type":"exact"},{"name":"glutamic acid gamma-methyl ester","type":"exact"}],"termid":"MOD:00657"}


id: PR:Q10308
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC6C3.05 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q10308"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotically up-regulated gene 43 protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC6C3.05","synonyms":[{"name":"Spom972h-SPAC6C3.05","type":"exact"}],"termid":"PR:Q10308"}


id: MONDO:0002329
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-neoplastic or neoplastic disorder affecting the testis. Representative examples include torsion, infarction, germ cell tumor, sex cord-stromal tumor, lymphoma, and leukemia.","definition_xrefs":["NCIT:C26890"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gonadal disorder","termid":"MONDO:0002259"},{"relation_name":"is_a","term_name":"male reproductive system disorder","termid":"MONDO:0003150"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testicular disorder","secondary_identifiers":["MESH:D013733","UMLS:C0039584","ICD9:608.89","MEDGEN:11743","EFO:0009601","DOID:2519","SCTID:64910008"],"synonyms":[{"name":"disease of testis","type":"exact"},{"name":"disease or disorder of testis","type":"exact"},{"name":"disorder of testis","type":"exact"},{"name":"testicular disease","type":"exact"},{"name":"testicular disorder","type":"exact"},{"name":"testis disease","type":"exact"},{"name":"testis disease or disorder","type":"exact"},{"name":"testis disorder","type":"exact"}],"termid":"MONDO:0002329","xrefs":{"Monarch":{"xref_id":"0002329"}}}


id: PBO:0028286
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_mitotic_G2_DNA_damage_checkpoint","termid":"PBO:0028286"}


id: PR:000027619
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A transcription factor zip1 phosphorylated form in Schizosaccharomyces pombe. Example: UniProtKB:Q10424-1, MOD:00696.","definition_xrefs":["PomBase:MAH","PMID:15660136"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcription factor zip1","termid":"PR:000027614"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zip1/PhosRes+","pombase_gene_id":"SPAC25G10.03","synonyms":[{"name":"PomBase_original_PRO_term_name: transcription factor zip1 phosphorylated form (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-zip1/PhosRes+","type":"exact"},{"name":"zip1/PhosRes+","type":"exact"}],"termid":"PR:000027619"}


id: GO:0014863
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events in which a inactivity stimulus is received by a cell or organism and converted into a molecular signal.","definition_xrefs":["GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to inactivity","termid":"GO:0014854"},{"relation_name":"is_a","term_name":"detection of stimulus","termid":"GO:0051606"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"detection of inactivity","termid":"GO:0014863"}


id: GO:0018784
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (S)-2-haloacid + H2O = (R)-2-hydroxyacid + halide.","definition_xrefs":["EC:3.8.1.2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on acid halide bonds, in C-halide compounds","termid":"GO:0019120"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"(S)-2-haloacid dehalogenase activity","secondary_identifiers":["RHEA:11192","UM-BBD_reactionID:r0090"],"synonyms":[{"name":"(S)-2-haloacid halidohydrolase activity","type":"related"},{"name":"2-haloacid dehalogenase activity","type":"exact"},{"name":"2-haloacid halidohydrolase activity","type":"related"},{"name":"2-haloalkanoic acid dehalogenase activity","type":"related"},{"name":"2-haloalkanoid acid halidohydrolase activity","type":"related"},{"name":"2-halocarboxylic acid dehalogenase II activity","type":"related"},{"name":"DL-2-haloacid dehalogenase activity","type":"related"},{"name":"L-2-haloacid dehalogenase activity","type":"related"},{"name":"L-DEX activity","type":"related"},{"name":"halocarboxylic acid halidohydrolase activity","type":"related"}],"termid":"GO:0018784"}


id: GO:0015748
data:
  {"annotated_genes":["SJAG_02050","SJAG_01305","SJAG_03746","SJAG_03851","SJAG_03338","SJAG_03050","SJAG_03644","SJAG_04697","SJAG_02943","SJAG_01229","SJAG_03334","SJAG_01960","SJAG_00835","SJAG_02897","SJAG_00339","SJAG_06440","SJAG_00760","SJAG_05209","SJAG_01470","SJAG_00434","SJAG_04370","SJAG_03172","SJAG_02581","SJAG_03721","SJAG_03710","SJAG_01731","SJAG_00612","SJAG_02957","SJAG_00587","SJAG_04734","SJAG_01177","SJAG_05325","SJAG_02132","SJAG_00018","SJAG_05268","SJAG_02114","SJAG_03741","SJAG_00589","SJAG_01095","SJAG_00154","SJAG_03452","SJAG_00276","SJAG_03209","SJAG_16459","SJAG_04328","SJAG_01225","SJAG_00576","SJAG_01945","SJAG_00230","SJAG_04325","SJAG_00669","SJAG_03503","SJAG_02516","SJAG_04162","SJAG_04406","SJAG_03416","SJAG_00232"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[59390],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035348"},{"annotations":[74300],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015866"},{"annotations":[68302],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140331"},{"annotations":[74374],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015917"},{"annotations":[93098],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036085"},{"annotations":[71440],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990570"},{"annotations":[102381,102380,102382],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001407"},{"annotations":[63497],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903790"},{"annotations":[116051,90657,100312,107321,105647,97327,88975,103831,108453,101071,97266,107447,98415,106538,109327],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120010"},{"annotations":[101144],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990554"},{"annotations":[101145],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990553"},{"annotations":[58733],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140021"},{"annotations":[58732,102643],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990544"},{"annotations":[70153],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990559"},{"annotations":[107362],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990548"},{"annotations":[92661],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990549"},{"annotations":[103424],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990545"},{"annotations":[93099,76331],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990536"},{"annotations":[71650,90273,90277,90272,74202,90278,90270,72577,90274,90275,109313,72606,59704,102005,62403,74383,90276,90271,99261,101073],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045332"},{"annotations":[72858],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017121"},{"annotations":[78974],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990519"},{"annotations":[92867,112056],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035436"},{"annotations":[74597,88113],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097624"},{"annotations":[75640],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072334"},{"annotations":[74864],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015786"},{"annotations":[112171],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120112"},{"annotations":[77381],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990569"},{"annotations":[66030],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015790"}]},"cv_name":"biological_process","definition":"The directed movement of organophosphate esters into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. Organophosphate esters are small organic molecules containing phosphate ester bonds.","definition_xrefs":["GOC:mcc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transport","termid":"GO:0006810"}],"gene_count":57,"genes_by_uniquename":{"SJAG_00018":null,"SJAG_00154":null,"SJAG_00230":null,"SJAG_00232":null,"SJAG_00276":null,"SJAG_00339":null,"SJAG_00434":null,"SJAG_00576":null,"SJAG_00587":null,"SJAG_00589":null,"SJAG_00612":null,"SJAG_00669":null,"SJAG_00760":null,"SJAG_00835":null,"SJAG_01095":null,"SJAG_01177":null,"SJAG_01225":null,"SJAG_01229":null,"SJAG_01305":null,"SJAG_01470":null,"SJAG_01731":null,"SJAG_01945":null,"SJAG_01960":null,"SJAG_02050":null,"SJAG_02114":null,"SJAG_02132":null,"SJAG_02516":null,"SJAG_02581":null,"SJAG_02897":null,"SJAG_02943":null,"SJAG_02957":null,"SJAG_03050":null,"SJAG_03172":null,"SJAG_03209":null,"SJAG_03334":null,"SJAG_03338":null,"SJAG_03416":null,"SJAG_03452":null,"SJAG_03503":null,"SJAG_03644":null,"SJAG_03710":null,"SJAG_03721":null,"SJAG_03741":null,"SJAG_03746":null,"SJAG_03851":null,"SJAG_04162":null,"SJAG_04325":null,"SJAG_04328":null,"SJAG_04370":null,"SJAG_04406":null,"SJAG_04697":null,"SJAG_04734":null,"SJAG_05209":null,"SJAG_05268":null,"SJAG_05325":null,"SJAG_06440":null,"SJAG_16459":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"organophosphate ester transport","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000108":null},"termid":"GO:0015748","terms_by_termid":{"GO:0001407":null,"GO:0015786":null,"GO:0015790":null,"GO:0015866":null,"GO:0015917":null,"GO:0017121":null,"GO:0035348":null,"GO:0035436":null,"GO:0036085":null,"GO:0045332":null,"GO:0072334":null,"GO:0097624":null,"GO:0120010":null,"GO:0120112":null,"GO:0140021":null,"GO:0140331":null,"GO:1903790":null,"GO:1990519":null,"GO:1990536":null,"GO:1990544":null,"GO:1990545":null,"GO:1990548":null,"GO:1990549":null,"GO:1990553":null,"GO:1990554":null,"GO:1990559":null,"GO:1990569":null,"GO:1990570":null}}


id: PBO:0048730
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamate dehydrogenase 1","termid":"PBO:0048730"}


id: PBO:0063125
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"poly(ADP-ribose) polymerase family member 10","termid":"PBO:0063125"}


id: PBO:0079221
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TTBK2 antisense RNA 1","termid":"PBO:0079221"}


id: GO:0071330
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a trehalose-6-phosphate stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to disaccharide stimulus","termid":"GO:0071324"},{"relation_name":"is_a","term_name":"response to trehalose-6-phosphate","termid":"GO:0080094"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to trehalose-6-phosphate stimulus","termid":"GO:0071330"}


id: PBO:0090893
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Golgi alpha-1,6-mannosyltransferase Och1","termid":"PBO:0090893"}


id: MONDO:0017519
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"symbrachydactyly of hands and feet","termid":"MONDO:0015516"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"symbrachydactyly of hand and foot, unilateral","secondary_identifiers":["Orphanet:295136"],"termid":"MONDO:0017519","xrefs":{"Monarch":{"xref_id":"0017519"}}}


id: GO:0018180
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The removal of a sulfur group from a protein amino acid.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete protein desulfurization (obsolete GO:0018180)","synonyms":[{"name":"protein amino acid desulfurisation","type":"exact"},{"name":"protein amino acid desulfurization","type":"exact"},{"name":"protein amino acid desulphurisation","type":"exact"},{"name":"protein amino acid desulphurization","type":"exact"}],"termid":"GO:0018180"}


id: PBO:0036411
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"R3H and G-patch domain protein Sqs1 (predicted)","termid":"PBO:0036411"}


id: PBO:0038485
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP binding cassette subfamily B member 10","termid":"PBO:0038485"}


id: PATO:0001542
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A phase which starts later than natural start point.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phase","termid":"PATO:0000083"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"delayed phase","termid":"PATO:0001542"}


id: PBO:0081485
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 367","termid":"PBO:0081485"}


id: PBO:0013829
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pescadillo-family BRCT domain protein Ppp1 (predicted)","termid":"PBO:0013829"}


id: PR:Q10409
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- tsr3 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q10409"],"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":"ribosome biogenesis protein tsr3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1F3.04c","synonyms":[{"name":"Spom972h-tsr3","type":"exact"}],"termid":"PR:Q10409"}


id: PBO:0011953
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-component_or_sequence","termid":"PBO:0011953"}


id: GO:0009448
data:
  {"annotated_genes":["SJAG_03293","SJAG_03434","SJAG_00674"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[56788],"is_not":false,"summary":null,"term":"GO:0009448"},{"annotations":[88167,87186],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009450"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving gamma-aminobutyric acid (GABA, 4-aminobutyrate), an amino acid which acts as a neurotransmitter in some organisms.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monocarboxylic acid metabolic process","termid":"GO:0032787"},{"relation_name":"is_a","term_name":"non-proteinogenic amino acid metabolic process","termid":"GO:0170041"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00674":null,"SJAG_03293":null,"SJAG_03434":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006520","GO:0044281"],"is_obsolete":false,"name":"gamma-aminobutyric acid metabolic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000107":null},"synonyms":[{"name":"4-aminobutanoate metabolic process","type":"exact"},{"name":"4-aminobutanoate metabolism","type":"exact"},{"name":"4-aminobutyrate metabolic process","type":"exact"},{"name":"4-aminobutyrate metabolism","type":"exact"},{"name":"GABA metabolic process","type":"exact"},{"name":"GABA metabolism","type":"exact"},{"name":"gamma-aminobutyric acid metabolism","type":"exact"}],"termid":"GO:0009448","terms_by_termid":{"GO:0009448":null,"GO:0009450":null}}


id: GO:0085016
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Exit from dormant state, also known as resuscitation, of the symbiont within the host organism.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dormancy process","termid":"GO:0022611"},{"relation_name":"is_a","term_name":"development of symbiont in host","termid":"GO:0044114"}],"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":"dormancy exit of symbiont in host","synonyms":[{"name":"resuscitation of symbiont","type":"exact"}],"termid":"GO:0085016"}


id: MONDO:0002920
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm that arises from the ovary and is characterized by the presence of an invasive malignant transitional cell component and nests of benign transitional cells in a fibrotic stroma. When the neoplasm is confined to the ovary, the prognosis is good.","definition_xrefs":["NCIT:C4270"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ovarian Brenner tumor","termid":"MONDO:0002370"},{"relation_name":"is_a","term_name":"malignant epithelial tumor of ovary","termid":"MONDO:0018364"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"malignant ovarian Brenner tumor","secondary_identifiers":["MEDGEN:90793","UMLS:C0334495","ICDO:9000/3","DOID:4217"],"synonyms":[{"name":"malignant Brenner tumor of ovary","type":"exact"},{"name":"malignant Brenner tumor of the ovary","type":"exact"},{"name":"malignant Brenner tumour of ovary","type":"exact"},{"name":"malignant Brenner tumour of the ovary","type":"exact"},{"name":"malignant ovarian Brenner tumor","type":"exact"},{"name":"ovarian Brenner tumor, malignant","type":"exact"}],"termid":"MONDO:0002920","xrefs":{"Monarch":{"xref_id":"0002920"}}}


id: GO:1902890
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of root hair elongation.","definition_xrefs":["GOC:als","PMID:22329353","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell growth","termid":"GO:0001558"},{"relation_name":"is_a","term_name":"regulation of developmental growth","termid":"GO:0048638"},{"relation_name":"regulates","term_name":"root hair elongation","termid":"GO:0048767"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of root hair elongation","termid":"GO:1902890"}


id: GO:0036114
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of medium-chain fatty-acyl-CoAs, any derivative of coenzyme A in which the sulfhydryl group is in a thioester linkage with a medium-chain fatty-acyl group. A medium-chain fatty acid has an aliphatic tail containing 6 to 12 carbons.","definition_xrefs":["GOC:pm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"medium-chain fatty-acyl-CoA metabolic process","termid":"GO:0036112"},{"relation_name":"is_a","term_name":"fatty-acyl-CoA catabolic process","termid":"GO:0036115"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0044248"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006790"}],"interesting_parent_ids":["GO:0008150","GO:0006790","GO:0006629","GO:0044281","GO:0044248","GO:0055086"],"is_obsolete":false,"name":"medium-chain fatty-acyl-CoA catabolic process","synonyms":[{"name":"medium-chain fatty-acyl-CoA breakdown","type":"exact"},{"name":"medium-chain fatty-acyl-CoA catabolism","type":"exact"},{"name":"medium-chain fatty-acyl-CoA degradation","type":"exact"}],"termid":"GO:0036114"}


id: MONDO:0004787
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, benign, papillary neoplasm that arises from the cervix. It is characterized by the presence of a fibrovascular core covered by mucinous epithelial cells.","definition_xrefs":["NCIT:C40215"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cervical benign neoplasm","termid":"MONDO:0000644"},{"relation_name":"is_a","term_name":"papilloma","termid":"MONDO:0002363"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cervical mullerian papilloma","secondary_identifiers":["DOID:9442","UMLS:C1516427","MEDGEN:273910"],"synonyms":[{"name":"cervical Muellerian papilloma","type":"exact"},{"name":"cervical Mullerian papilloma","type":"exact"},{"name":"cervical Müllerian papilloma","type":"exact"}],"termid":"MONDO:0004787","xrefs":{"Monarch":{"xref_id":"0004787"}}}


id: GO:0060464
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The developmental process pertaining to the initial formation of a lung lobe from unspecified parts. This process begins with the specific processes that contribute to the appearance of the lobe and ends when the structural rudiment is recognizable. A lung lobe is a projection that extends from the lung.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure formation involved in morphogenesis","termid":"GO:0048646"},{"relation_name":"part_of","term_name":"lung lobe morphogenesis","termid":"GO:0060463"}],"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":"lung lobe formation","termid":"GO:0060464"}


id: PBO:0030473
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_vacuolar_glutamine_level","termid":"PBO:0030473"}


id: MONDO:0007571
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Primary erythermalgia is characterized by intermittent attacks of red, warm, painful burning extremities. It spontaneously arises during early childhood and adolescence in the absence of any detectable underlying disorder.","definition_xrefs":["Orphanet:90026"],"direct_ancestors":[{"relation_name":"is_a","term_name":"erythromelalgia","termid":"MONDO:0016028"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primary erythermalgia","secondary_identifiers":["UMLS:C0014805","SCTID:709489006","NCIT:C125383","GARD:6377","MEDGEN:8688","OMIM:133020"],"synonyms":[{"name":"Mitchell disease (formerly)","type":"related"},{"name":"PERYTHM","type":"exact"},{"name":"erythermalgia, primary","type":"related"},{"name":"erythromelalgia, familial","type":"related"},{"name":"erythromelalgia, primary","type":"related"},{"name":"neuropathy, small fiber","type":"related"},{"name":"neuropathy, small fibre","type":"related"},{"name":"primary erythromelalgia","type":"exact"},{"name":"small fiber neuropathy","type":"related"},{"name":"small fibre neuropathy","type":"related"}],"termid":"MONDO:0007571","xrefs":{"Monarch":{"xref_id":"0007571"}}}


id: PR:Q9UUC9
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mdm34 gene.","definition_xrefs":["UniProtKB:Q9UUC9","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":"mitochondrial distribution and morphology protein 34 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC19C2.11c","synonyms":[{"name":"Spom972h-mdm34","type":"exact"}],"termid":"PR:Q9UUC9"}


id: PBO:0072622
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"radial spoke head component 9","termid":"PBO:0072622"}


id: SO:0000508
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Genomic DNA of immunoglobulin/T-cell receptor gene in rearranged configuration including at least one D-gene, one DJ-gene, and one J-gene.","direct_ancestors":[{"relation_name":"has_part","term_name":"D_gene_segment","termid":"SO:0000458"},{"relation_name":"has_part","term_name":"J_gene_segment","termid":"SO:0000470"},{"relation_name":"has_part","term_name":"DJ_gene_segment","termid":"SO:0000572"},{"relation_name":"is_a","term_name":"vertebrate_immunoglobulin_T_cell_receptor_rearranged_gene_cluster","termid":"SO:0000938"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"D_DJ_J_cluster","synonyms":[{"name":"D DJ J cluster","type":"exact"},{"name":"D-(DJ)-J-CLUSTER","type":"exact"}],"termid":"SO:0000508"}


id: PBO:0030879
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_cellular_component_assembly_during_vegetative_growth","termid":"PBO:0030879"}


id: GO:0009537
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The precursor of other plastids.","definition_xrefs":["ISBN:0943088399"],"direct_ancestors":[{"relation_name":"is_a","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:0005737","GO:0005575"],"is_obsolete":false,"name":"proplastid","termid":"GO:0009537"}


id: PBO:0071668
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L37a pseudogene 9","termid":"PBO:0071668"}


id: MONDO:0008219
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pemphigus is a group of chronic autoimmune skin diseases characterized by blister formations on the outer layer of the skin and the mucous membranes. Three clinical forms have been characterized, of which pemphigus vulgaris is the most frequent (75%).","definition_xrefs":["Orphanet:704"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pemphigus","termid":"MONDO:0006594"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005093"],"is_obsolete":false,"name":"pemphigus vulgaris","secondary_identifiers":["GARD:7355","DOID:0060851","SCTID:49420001","ICD10CM:L10.0","icd11.foundation:278358681","MedDRA:10052802","MESH:C536645","NCIT:C34910","OMIM:169610","EFO:0004719","NANDO:1200229","MEDGEN:10621","UMLS:C0030809"],"synonyms":[{"name":"familial pemphigus vulgaris","type":"exact"},{"name":"pemphigus vulgaris, familial","type":"related"}],"termid":"MONDO:0008219","xrefs":{"Monarch":{"xref_id":"0008219"}}}


id: PBO:0080844
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Y-box binding protein 1 pseudogene 8","termid":"PBO:0080844"}


id: MONDO:0003650
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hepatoblastoma characterized by the presence of fetal and embryonal epithelial components and a mesenchymal component.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hepatoblastoma","termid":"MONDO:0018666"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"}],"interesting_parent_ids":["MONDO:0002515","MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"mixed hepatoblastoma","secondary_identifiers":["DOID:5789","NCIT:C7097","UMLS:C1334784","MEDGEN:233194","ICDO:8970/3"],"synonyms":[{"name":"mixed epithelial and mesenchymal hepatoblastoma","type":"exact"}],"termid":"MONDO:0003650","xrefs":{"Monarch":{"xref_id":"0003650"}}}


id: MONDO:0010339
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An epilepsy, X-linked, with or without impaired intellectual development and dysmorphic features characterized by epilepsy, learning difficulties, macrocephaly, and aggressive behavior. It has been described in males from a four-generation kindred. It is transmitted as an X-linked recessive trait and is likely to be caused by mutations in the gene encoding synapsin I (Xp11.3-q12).","definition_xrefs":["Orphanet:85294"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"excluded_subClassOf","term_name":"monogenic epilepsy","termid":"MONDO:0015653"},{"relation_name":"excluded_subClassOf","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"},{"relation_name":"is_a","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"},{"relation_name":"is_a","term_name":"epilepsy, X-linked, with or without impaired intellectual development and dysmorphic features","termid":"MONDO:0859390"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"epilepsy, X-linked 1, with variable learning disabilities and behavior disorders","secondary_identifiers":["UMLS:C5774177","GARD:16748","MESH:C564505","DOID:0112122","MEDGEN:1823951","OMIM:300491"],"synonyms":[{"name":"X-linked epilepsy-learning disabilities-behavior disorders syndrome","type":"exact"},{"name":"epilepsy, X-linked, with variable learning disabilities and behavior disorders","type":"related"},{"name":"epilepsy, X-linked, with variable learning disabilities and behavior disorders, X-linked recessive, X-linked dominant","type":"exact"},{"name":"epilepsy, X-linked, with variable learning disabilities and behaviour disorders","type":"related"},{"name":"epilepsy, X-linked, with variable learning disabilities and behaviour disorders, X-linked recessive, X-linked dominant","type":"exact"}],"termid":"MONDO:0010339","xrefs":{"Monarch":{"xref_id":"0010339"}}}


id: PBO:0076059
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"STON1-GTF2A1L readthrough","termid":"PBO:0076059"}


id: GO:0061521
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 hepatic stellate cell.","definition_xrefs":["PMID:9407545","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"}],"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":"hepatic stellate cell differentiation","termid":"GO:0061521"}


id: FYPO:0003611
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of protein measured in a cell during one or both meiotic nuclear divisions is higher than normal. Total protein or a specific protein may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein level","termid":"FYPO:0000836"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0006551","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"increased protein level during meiosis","synonyms":[{"name":"increased protein accumulation during meiosis","type":"related"},{"name":"increased protein level during meiotic nuclear division","type":"exact"}],"termid":"FYPO:0003611"}


id: PBO:0038297
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase feature property types","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_throughput_type","termid":"PBO:0038297"}


id: GO:0008911
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (S)-lactaldehyde + NAD+ + H2O = (S)-lactate + NADH + H+.","definition_xrefs":["RHEA:14277"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aldehyde dehydrogenase (NAD+) activity","termid":"GO:0004029"}],"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:0003824","GO:0016491"],"is_obsolete":false,"name":"lactaldehyde dehydrogenase (NAD+) activity","secondary_identifiers":["MetaCyc:LACTALDDEHYDROG-RXN","EC:1.2.1.22"],"synonyms":[{"name":"(S)-lactaldehyde:NAD+ oxidoreductase activity","type":"related"},{"name":"L-lactaldehyde:NAD oxidoreductase activity","type":"related"},{"name":"nicotinamide adenine dinucleotide (NAD)-linked dehydrogenase activity","type":"related"}],"termid":"GO:0008911"}


id: PBO:0058868
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 9901","termid":"PBO:0058868"}


id: PBO:0059965
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND3 pseudogene 10","termid":"PBO:0059965"}


id: FYPO:0002903
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype in which a cell is viable and shaped in the form of a pear in the vegetative growth phase of the life cycle. One end is rounded, while the other resembles an end of a normal rod-shaped cell. The normally shaped end has the same diameter as a wild-type cell.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"pear-shaped cell","termid":"FYPO:0000020"},{"relation_name":"is_a","term_name":"pear-shaped vegetative cell","termid":"FYPO:0001120"},{"relation_name":"is_a","term_name":"viable vegetative cell with abnormal cell shape","termid":"FYPO:0002197"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000005","FYPO:0001985","FYPO:0001320","FYPO:0000004","FYPO:0000002"],"is_obsolete":false,"name":"viable pear-shaped vegetative cell","synonyms":[{"name":"viable ice cream cone-shaped cell during vegetative growth","type":"exact"},{"name":"viable pear-shaped cell during vegetative growth","type":"exact"},{"name":"viable pear-shaped vegetative cell during mitotic cell cycle","type":"related"}],"termid":"FYPO:0002903"}


id: PBO:0087885
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transcriptional repressor, activator; role in cellular adjustment to osmotic stress including modulation of mating efficiency; involved in repression of subset of hypoxic genes by Rox1p, repression of several DAN/TIR genes during aerobic growth, ergosterol biosynthetic genes in response to hyperosmotic stress; contributes to recruitment of Tup1p-Cyc8p general repressor to promoters; relocalizes to cytosol under hypoxia; forms [MOT3+] prion under anaerobic conditions","termid":"PBO:0087885"}


id: PBO:0005758
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Swr1 complex subunit Swc5","termid":"PBO:0005758"}


id: PBO:0088958
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DUF866 family protein, human C1orf123 ortholog","termid":"PBO:0088958"}


id: PBO:0040643
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BCL2 associated X, apoptosis regulator","termid":"PBO:0040643"}


id: GO:1900818
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of ochratoxin A.","definition_xrefs":["GOC:TermGenie","GOC:di"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified amino acid biosynthetic process","termid":"GO:0042398"},{"relation_name":"is_a","term_name":"amide biosynthetic process","termid":"GO:0043604"},{"relation_name":"is_a","term_name":"secondary metabolite biosynthetic process","termid":"GO:0044550"},{"relation_name":"is_a","term_name":"monocarboxylic acid biosynthetic process","termid":"GO:0072330"},{"relation_name":"is_a","term_name":"ochratoxin A metabolic process","termid":"GO:1900816"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0019748","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"ochratoxin A biosynthetic process","synonyms":[{"name":"Ochratoxin A anabolism","type":"exact"},{"name":"Ochratoxin A biosynthesis","type":"exact"},{"name":"Ochratoxin A formation","type":"exact"},{"name":"Ochratoxin A synthesis","type":"exact"}],"termid":"GO:1900818"}


id: MONDO:1011488
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Complement component 3 deficiency that occurs in domestic guinea pig.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"complement component 3 deficiency, non-human animal","termid":"MONDO:1011421"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"complement component 3 deficiency, domestic guinea pig","secondary_identifiers":["OMIA:000155-10141"],"synonyms":[{"name":"C3 deficiency, domestic guinea pig","type":"exact"}],"termid":"MONDO:1011488","xrefs":{"Monarch":{"xref_id":"1011488"}}}


id: PBO:0030621
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_maltase_activity","termid":"PBO:0030621"}


id: PBO:0082175
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADP-ribosylation factor; GTPase of the Ras superfamily involved in regulation of coated vesicle formation in intracellular trafficking within the Golgi; involved in mitochondrial morphology; ARF1 has a paralog, ARF2, that arose from the whole genome duplication; arf1 arf2 double null mutation is complemented by human ARF1, ARF4, ARF5, or ARF6","termid":"PBO:0082175"}


id: FYPO:0001051
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. An inviable phenotype in which a cell undergoes mitotic catastrophe (i.e. enters mitosis prematurely and with defective chromosome segregation), entering mitosis when longer than wild type.","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete mitotic catastrophe, elongated cell (obsolete FYPO:0001051)","synonyms":[{"name":"mitotic catastrophe, elongated cell during mitotic cell cycle","type":"related"},{"name":"mitotic catastrophe, elongated cell during vegetative growth","type":"exact"},{"name":"mitotic catastrophe, long cell","type":"exact"}],"termid":"FYPO:0001051"}


id: GO:0102718
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: TRIBOA-beta-D-glucoside + S-adenosyl-L-methionine = (2R)-DIMBOA glucoside + S-adenosyl-L-homocysteine + H+.","definition_xrefs":["EC:2.1.1.241","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methyltransferase activity","termid":"GO:0008168"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016741"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016740","GO:0016741"],"is_obsolete":false,"name":"TRIBOA-glucoside methyltransferase activity","secondary_identifiers":["MetaCyc:RXN-6687","RHEA:32099"],"termid":"GO:0102718"}


id: MOD:00795
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod","definition_xrefs":["PubMed:11743741","Unimod:371"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-cysteine residue","termid":"MOD:00905"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"Michael addition of hydroxymethylvinyl ketone to cysteine","synonyms":[{"name":"HMVK","type":"related"},{"name":"Michael addition of hydroxymethylvinyl ketone to cysteine","type":"related"}],"termid":"MOD:00795"}


id: GO:0120166
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of producing fruiting body precursors, called protoperithecia. Protoperitheicium is a spherical structure that is formed in the sexual phase of ascomycetous fungi such as Neurospora crassa and Sordaria macrospora. Protoperithecium is formed by the enveloping of ascogonia cells by sterile hyphae and it develops into perithecium.","definition_xrefs":["PMID:20739093","PMID:25311923","PMID:125266","PMID:6235211","PMID:6235212","PMID:4410944","DOI:10.1007/978-3-642-00286-1_2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reproductive fruiting body development","termid":"GO:0030582"}],"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":"protoperithecium formation","termid":"GO:0120166"}


id: GO:0006967
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of antifungal peptide biosynthesis.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of antifungal peptide production","termid":"GO:0002804"},{"relation_name":"is_a","term_name":"positive regulation of antimicrobial peptide biosynthetic process","termid":"GO:0002807"},{"relation_name":"is_a","term_name":"regulation of antifungal peptide biosynthetic process","termid":"GO:0002810"},{"relation_name":"positively_regulates","term_name":"antifungal peptide biosynthetic process","termid":"GO:0002783"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"positive regulation of antifungal peptide biosynthetic process","synonyms":[{"name":"activation of antifungal peptide biosynthetic process","type":"narrow"},{"name":"antifungal peptide induction","type":"exact"},{"name":"antifungal polypeptide induction","type":"exact"},{"name":"stimulation of antifungal peptide biosynthetic process","type":"narrow"},{"name":"up regulation of antifungal peptide biosynthetic process","type":"exact"},{"name":"up-regulation of antifungal peptide biosynthetic process","type":"exact"},{"name":"upregulation of antifungal peptide biosynthetic process","type":"exact"}],"termid":"GO:0006967"}


id: PBO:0003071
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fizzy-related protein Mfr1","termid":"PBO:0003071"}


id: MONDO:0014020
data:
  {"annotated_genes":["SJAG_00308"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85037],"is_not":false,"summary":null,"term":"MONDO:0014020"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"complex hereditary spastic paraplegia","termid":"MONDO:0015150"},{"relation_name":"is_a","term_name":"mitochondrial oxidative phosphorylation disorder","termid":"MONDO:0016387"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00308":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004069","MONDO:0005559"],"is_obsolete":false,"name":"hereditary spastic paraplegia 55","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:320375","SCTID:723825006","UMLS:C3539506","DOID:0110807","MEDGEN:761342","GARD:17474","OMIM:615035"],"synonyms":[{"name":"SPG55","type":"exact"},{"name":"autosomal recessive spastic paraplegia 55","type":"exact"},{"name":"autosomal recessive spastic paraplegia type 55","type":"exact"},{"name":"hereditary spastic paraplegia type 55","type":"exact"},{"name":"spastic paraplegia 55, autosomal recessive","type":"related"}],"termid":"MONDO:0014020","terms_by_termid":{"MONDO:0014020":null},"xrefs":{"Monarch":{"xref_id":"0014020"}}}


id: SO:0002344
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Mitochondrial SSU rRNA is an RNA component of the small subunit of mitochondrial ribosomes.","definition_xrefs":["PMID:3044395"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mt_rRNA","termid":"SO:0002128"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mt_SSU_rRNA","synonyms":[{"name":"MT SSU rRNA","type":"exact"},{"name":"mitochondrial SSU rRNA","type":"exact"},{"name":"mitochondrial small subunit rRNA","type":"exact"}],"termid":"SO:0002344"}


id: GO:0090205
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency, or extent of cholesterol metabolism, the chemical reactions and pathways involving cholesterol, cholest-5-en-3 beta-ol, the principal sterol of vertebrates and the precursor of many steroids, including bile acids and steroid hormones.","definition_xrefs":["GOC:dph","GOC:sl","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of steroid metabolic process","termid":"GO:0045940"},{"relation_name":"is_a","term_name":"positive regulation of small molecule metabolic process","termid":"GO:0062013"},{"relation_name":"is_a","term_name":"regulation of cholesterol metabolic process","termid":"GO:0090181"},{"relation_name":"positively_regulates","term_name":"cholesterol metabolic process","termid":"GO:0008203"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006629"},{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"positively_regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006629","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"positive regulation of cholesterol metabolic process","termid":"GO:0090205"}


id: FYPO:0005621
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 cell contains more adducts formed between a topoisomerase and DNA than normal.","definition_xrefs":["PMID:22730331","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal vegetative cell phenotype","termid":"FYPO:0003755"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"increased topoisomerase-DNA adduct level","synonyms":[{"name":"increased Top1-DNA adduct level","type":"narrow"},{"name":"increased Top1cc level","type":"narrow"},{"name":"increased topoisomerase I-DNA adduct level","type":"narrow"},{"name":"increased topoisomerase-DNA adduct level during mitotic cell cycle","type":"related"},{"name":"increased topoisomerase-DNA adduct level during vegetative growth","type":"exact"}],"termid":"FYPO:0005621"}


id: PBO:0085569
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein homologous to Chediak-Higashi syndrome and Beige proteins; both of which are implicated in disease syndromes in human and mouse, respectively, due to defective lysosomal trafficking; mutant phenotype and genetic interactions suggest a role in protein sorting","termid":"PBO:0085569"}


id: GO:1905016
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of isoleucine-tRNA ligase activity.","definition_xrefs":["GOC:TermGenie","GO_REF:0000059","PMID:1665486"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of isoleucine-tRNA ligase activity (obsolete GO:1905016)","synonyms":[{"name":"down regulation of L-isoleucine:tRNAIle ligase (AMP-forming)","type":"exact"},{"name":"down regulation of isoleucine translase activity","type":"exact"},{"name":"down regulation of isoleucine-tRNA ligase activity","type":"exact"},{"name":"down regulation of isoleucine-tRNA synthetase activity","type":"exact"},{"name":"down regulation of isoleucine-transfer RNA ligase activity","type":"exact"},{"name":"down regulation of isoleucyl-tRNA synthetase activity","type":"exact"},{"name":"down regulation of isoleucyl-transfer RNA synthetase activity","type":"exact"},{"name":"down regulation of isoleucyl-transfer ribonucleate synthetase activity","type":"exact"},{"name":"down-regulation of L-isoleucine:tRNAIle ligase (AMP-forming)","type":"exact"},{"name":"down-regulation of isoleucine translase activity","type":"exact"},{"name":"down-regulation of isoleucine-tRNA ligase activity","type":"exact"},{"name":"down-regulation of isoleucine-tRNA synthetase activity","type":"exact"},{"name":"down-regulation of isoleucine-transfer RNA ligase activity","type":"exact"},{"name":"down-regulation of isoleucyl-tRNA synthetase activity","type":"exact"},{"name":"down-regulation of isoleucyl-transfer RNA synthetase activity","type":"exact"},{"name":"down-regulation of isoleucyl-transfer ribonucleate synthetase activity","type":"exact"},{"name":"downregulation of L-isoleucine:tRNAIle ligase (AMP-forming)","type":"exact"},{"name":"downregulation of isoleucine translase activity","type":"exact"},{"name":"downregulation of isoleucine-tRNA ligase activity","type":"exact"},{"name":"downregulation of isoleucine-tRNA synthetase activity","type":"exact"},{"name":"downregulation of isoleucine-transfer RNA ligase activity","type":"exact"},{"name":"downregulation of isoleucyl-tRNA synthetase activity","type":"exact"},{"name":"downregulation of isoleucyl-transfer RNA synthetase activity","type":"exact"},{"name":"downregulation of isoleucyl-transfer ribonucleate synthetase activity","type":"exact"},{"name":"inhibition of L-isoleucine:tRNAIle ligase (AMP-forming)","type":"narrow"},{"name":"inhibition of isoleucine translase activity","type":"narrow"},{"name":"inhibition of isoleucine-tRNA ligase activity","type":"narrow"},{"name":"inhibition of isoleucine-tRNA synthetase activity","type":"narrow"},{"name":"inhibition of isoleucine-transfer RNA ligase activity","type":"narrow"},{"name":"inhibition of isoleucyl-tRNA synthetase activity","type":"narrow"},{"name":"inhibition of isoleucyl-transfer RNA synthetase activity","type":"narrow"},{"name":"inhibition of isoleucyl-transfer ribonucleate synthetase activity","type":"narrow"},{"name":"negative regulation of L-isoleucine:tRNAIle ligase (AMP-forming)","type":"exact"},{"name":"negative regulation of isoleucine translase activity","type":"exact"},{"name":"negative regulation of isoleucine-tRNA synthetase activity","type":"exact"},{"name":"negative regulation of isoleucine-transfer RNA ligase activity","type":"exact"},{"name":"negative regulation of isoleucyl-tRNA synthetase activity","type":"exact"},{"name":"negative regulation of isoleucyl-transfer RNA synthetase activity","type":"exact"},{"name":"negative regulation of isoleucyl-transfer ribonucleate synthetase activity","type":"exact"}],"termid":"GO:1905016"}


id: FYPO:0008122
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which mitochondrion fusion is increased.","direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitochondrial fusion","termid":"FYPO:0008089"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"increased mitochondrial fusion","termid":"FYPO:0008122"}


id: PBO:0043293
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-type lectin domain family 12 member A","termid":"PBO:0043293"}


id: PBO:0029891
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_chromatin_silencing_at_centromere_outer_repeat","termid":"PBO:0029891"}


id: MONDO:1012395
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"rupture of the cranial cruciate ligament, non-human animal","termid":"MONDO:1011960"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rupture of the cranial cruciate ligament, dog","secondary_identifiers":["OMIA:001474-9615"],"termid":"MONDO:1012395","xrefs":{"Monarch":{"xref_id":"1012395"}}}


id: MONDO:0021345
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma that involves the pharynx.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"digestive system carcinoma","termid":"MONDO:0006181"},{"relation_name":"is_a","term_name":"pharynx neoplasm","termid":"MONDO:0021246"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"carcinoma of pharynx","secondary_identifiers":["MEDGEN:757152","SCTID:449254004","UMLS:C3164746","NCIT:C9466"],"synonyms":[{"name":"cancer of the pharynx","type":"exact"},{"name":"carcinoma of pharynx","type":"exact"},{"name":"carcinoma of the pharynx","type":"exact"},{"name":"pharyngeal carcinoma","type":"exact"},{"name":"pharyngeal throat cancer","type":"exact"},{"name":"pharynx carcinoma","type":"exact"}],"termid":"MONDO:0021345","xrefs":{"Monarch":{"xref_id":"0021345"}}}


id: PBO:0055846
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat, Ig-like and transmembrane domains 2","termid":"PBO:0055846"}


id: PBO:0062919
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyrimidinergic receptor P2Y4","termid":"PBO:0062919"}


id: MONDO:0012343
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial abdominal aortic aneurysm","termid":"MONDO:0007031"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aortic aneurysm, familial abdominal, 2","secondary_identifiers":["GARD:16492","MEDGEN:339960","MESH:C565229","UMLS:C1853364","OMIM:609782"],"synonyms":[{"name":"AAA2","type":"exact"},{"name":"aortic aneurysm, familial abdominal 2","type":"exact"},{"name":"aortic aneurysm, familial abdominal, 2","type":"exact"}],"termid":"MONDO:0012343","xrefs":{"Monarch":{"xref_id":"0012343"}}}


id: GO:0061696
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that is a protein hormone secreted by gonadotrope cells of the anterior pituitary of vertebrates. capable of regulating normal growth, sexual development, and reproductive function.","definition_xrefs":["PMID:11420129","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"extracellular region","termid":"GO:0005576"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005576"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005576"],"is_obsolete":false,"name":"pituitary gonadotropin complex","termid":"GO:0061696"}


id: PBO:0045526
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DTWD1 pseudogene 2","termid":"PBO:0045526"}


id: GO:0046860
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The lipid bilayer surrounding a glycosome.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peroxisomal membrane","termid":"GO:0005778"},{"relation_name":"part_of","term_name":"glycosome","termid":"GO:0020015"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005777"}],"interesting_parent_ids":["GO:0005777","GO:0005737","GO:0005575"],"is_obsolete":false,"name":"glycosome membrane","termid":"GO:0046860"}


id: PBO:0027335
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_pre-replicative_complex_assembly","termid":"PBO:0027335"}


id: GO:0005788
data:
  {"annotated_genes":["SJAG_00288","SJAG_01180","SJAG_00790","SJAG_00530","SJAG_03535","SJAG_02875","SJAG_02413","SJAG_00403","SJAG_04046","SJAG_04571"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[78790,88358,92067,92093,102712,110781,113458,113565,118324],"is_not":false,"summary":null,"term":"GO:0005788"},{"annotations":[92847],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0099021"},{"annotations":[92853],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0099020"}]},"cv_name":"cellular_component","definition":"The volume enclosed by the membranes of the endoplasmic reticulum.","definition_xrefs":["ISBN:0198547684"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular organelle lumen","termid":"GO:0070013"},{"relation_name":"part_of","term_name":"endoplasmic reticulum","termid":"GO:0005783"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00288":null,"SJAG_00403":null,"SJAG_00530":null,"SJAG_00790":null,"SJAG_01180":null,"SJAG_02413":null,"SJAG_02875":null,"SJAG_03535":null,"SJAG_04046":null,"SJAG_04571":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005783"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0005783"],"is_obsolete":false,"name":"endoplasmic reticulum lumen","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0016022"],"synonyms":[{"name":"ER cisterna","type":"exact"},{"name":"ER lumen","type":"exact"},{"name":"cisternal lumen","type":"exact"},{"name":"endoplasmic reticulum cisterna","type":"exact"}],"termid":"GO:0005788","terms_by_termid":{"GO:0005788":null,"GO:0099020":null,"GO:0099021":null}}


id: PBO:0034309
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-eats","termid":"PBO:0034309"}


id: GO:1902466
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of histone H3-K27 trimethylation.","definition_xrefs":["GOC:TermGenie","PMID:19270745"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of histone H3-K27 trimethylation (obsolete GO:1902466)","synonyms":[{"name":"activation of histone H3-K27 trimethylation","type":"narrow"},{"name":"up regulation of histone H3-K27 trimethylation","type":"exact"},{"name":"up-regulation of histone H3-K27 trimethylation","type":"exact"},{"name":"upregulation of histone H3-K27 trimethylation","type":"exact"}],"termid":"GO:1902466"}


id: MONDO:0008089
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":"neutropenia, chronic familial","secondary_identifiers":["OMIM:162700","MESH:C535815","MEDGEN:777137","SCTID:234576008","ICD9:288.09","UMLS:C3665676"],"synonyms":[{"name":"chronic familial neutropenia","type":"related"},{"name":"leukopenia benign familial","type":"related"},{"name":"leukopenia, benign familial","type":"related"},{"name":"neutropenia chronic familial","type":"related"},{"name":"neutropenia, chronic familial","type":"exact"}],"termid":"MONDO:0008089","xrefs":{"Monarch":{"xref_id":"0008089"}}}


id: MONDO:0859169
data:
  {"annotated_genes":["SJAG_03454"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86092],"is_not":false,"summary":null,"term":"MONDO:0859169"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03454":null},"genotype_count":0,"is_obsolete":false,"name":"White-Kernohan syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1785087","OMIM:619426","UMLS:C5543635"],"termid":"MONDO:0859169","terms_by_termid":{"MONDO:0859169":null},"xrefs":{"Monarch":{"xref_id":"0859169"}}}


id: PR:O94502
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A solute carrier family 25 member 41 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO03222"],"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 mitochondrial carrier C12D12.05c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC12D12.05c","secondary_identifiers":["UniProtKB:O94502"],"synonyms":[{"name":"Spom972h-SLC25A41","type":"exact"}],"termid":"PR:O94502"}


id: MONDO:0009036
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pfeiffer-type cardiocranial syndrome is an extremely rare disorder recognized in less than ten patients worldwide and characterized by a congenital heart defect, sagittal craniosynostosis and severe developmental delay (growth retardation and intellectual deficit).","definition_xrefs":["Orphanet:2872"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"syndromic craniosynostosis","termid":"MONDO:0015338"}],"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":"cardiocranial syndrome, Pfeiffer type","secondary_identifiers":["MEDGEN:346598","icd11.foundation:629231429","OMIM:218450","MESH:C535578","GARD:8586","SCTID:720606005","UMLS:C1857495"],"synonyms":[{"name":"Cardiocranial syndrome","type":"related"},{"name":"Pfeiffer Cardiocranial syndrome","type":"related"},{"name":"Pfeiffer Singer Zschiesche syndrome","type":"related"},{"name":"Pfeiffer-Singer-Zschiesche syndrome","type":"exact"},{"name":"Pfeiffer-type cardiocranial syndrome","type":"related"},{"name":"craniostenosis, sagittal, with congenital heart disease, mental deficiency, and mandibular ankylosis","type":"related"},{"name":"craniosynostosis-congenital heart disease-intellectual disability syndrome","type":"exact"},{"name":"sagittal craniostenosis with congenital heart disease, mental deficiency and mandibular ankylosis","type":"exact"}],"termid":"MONDO:0009036","xrefs":{"Monarch":{"xref_id":"0009036"}}}


id: PBO:0070392
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"receptor tyrosine kinase like orphan receptor 2","termid":"PBO:0070392"}


id: PBO:0034664
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_mitotic_cohesin_loading","termid":"PBO:0034664"}


id: PATO:0000837
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000837 auditory threshold value (obsolete PATO:0000837)","termid":"PATO:0000837"}


id: MONDO:0957228
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"intellectual disability, autosomal dominant","termid":"MONDO:0100172"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities","secondary_identifiers":["UMLS:C5830437","OMIM:620330","MEDGEN:1841073"],"termid":"MONDO:0957228","xrefs":{"Monarch":{"xref_id":"0957228"}}}


id: GO:0044128
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which the symbiont activates, maintains or increases its size or mass within the cells or tissues of the host organism. The host is defined as the larger of the organisms involved in the symbiotic interaction.","definition_xrefs":["GOC:jl","GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of growth of symbiont in host (obsolete GO:0044128)","termid":"GO:0044128"}


id: PBO:0060608
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NCBP2 antisense 2 (head to head)","termid":"PBO:0060608"}


id: FYPO:0001735
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 movement of an assembled iron-sulfur cluster from a scaffold protein to an acceptor protein is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal metabolic process during vegetative growth","termid":"FYPO:0001363"},{"relation_name":"is_a","term_name":"abnormal gene expression","termid":"FYPO:0006551"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0001320","FYPO:0000002","FYPO:0006551"],"is_obsolete":false,"name":"abnormal iron-sulfur cluster transfer","synonyms":[{"name":"abnormal iron-sulfur cluster transfer during mitotic cell cycle","type":"related"},{"name":"abnormal iron-sulfur cluster transfer during vegetative growth","type":"exact"},{"name":"abnormal iron-sulphur cluster transfer","type":"exact"}],"termid":"FYPO:0001735"}


id: GO:2000267
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of blood coagulation, intrinsic pathway.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of blood coagulation","termid":"GO:0030195"},{"relation_name":"is_a","term_name":"negative regulation of protein activation cascade","termid":"GO:2000258"},{"relation_name":"is_a","term_name":"regulation of blood coagulation, intrinsic pathway","termid":"GO:2000266"},{"relation_name":"negatively_regulates","term_name":"blood coagulation, intrinsic pathway","termid":"GO:0007597"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"negatively_regulates","termid":"GO:0051604"},{"rel_name":"regulates","termid":"GO:0051604"}],"interesting_parent_ids":["GO:0008150","GO:0051604","GO:0010467"],"is_obsolete":false,"name":"negative regulation of blood coagulation, intrinsic pathway","termid":"GO:2000267"}


id: GO:0001587
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with serotonin and transmitting the signal across the membrane by activation of the Gq/11 subunit of an associated cytoplasmic heterotrimeric G protein complex. The Gq/11 subunit subsequently activates phospholipase C and results in an increase in inositol triphosphate (IP3) levels.","definition_xrefs":["PMID:18703043","GOC:bf","PMID:18571247","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled serotonin receptor activity","termid":"GO:0004993"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0038023","GO:0003674"],"is_obsolete":false,"name":"Gq/11-coupled serotonin receptor activity","synonyms":[{"name":"5-HT2 receptor activity","type":"broad"},{"name":"serotonin receptor activity, coupled via Gq/11","type":"exact"}],"termid":"GO:0001587"}


id: PBO:0077912
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TPT1 pseudogene 3","termid":"PBO:0077912"}


id: PBO:0029123
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_swollen_elongated_cell_with_enlarged_nucleus_upon_entry_into_stationary_phase","termid":"PBO:0029123"}


id: GO:0019450
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of L-cysteine into other compounds, including pyruvate.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyruvate metabolic process","termid":"GO:0006090"},{"relation_name":"is_a","term_name":"L-cysteine catabolic process","termid":"GO:0019448"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0044248"}],"interesting_parent_ids":["GO:0044281","GO:0006790","GO:0008150","GO:0006520","GO:0044248"],"is_obsolete":false,"name":"L-cysteine catabolic process to pyruvate","secondary_identifiers":["MetaCyc:LCYSDEG-PWY"],"synonyms":[{"name":"L-cysteine breakdown to pyruvate","type":"exact"},{"name":"L-cysteine degradation to pyruvate","type":"exact"}],"termid":"GO:0019450"}


id: GO:0005227
data:
  {"annotated_genes":["SJAG_02322","SJAG_03895"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[72717,79585],"is_not":false,"summary":null,"term":"GO:0005227"}]},"cv_name":"molecular_function","definition":"Enables the transmembrane transfer of an inorganic cation by a channel that opens when a calcium cation has been bound by the channel complex or one of its constituent parts.","definition_xrefs":["GOC:dph","GOC:mtg_transport"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monoatomic ion-gated channel activity","termid":"GO:0022839"},{"relation_name":"is_a","term_name":"ligand-gated monoatomic cation channel activity","termid":"GO:0099094"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02322":null,"SJAG_03895":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"calcium-activated cation channel activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-9717383"],"synonyms":[{"name":"calcium activated cation channel activity","type":"exact"},{"name":"intracellular calcium-activated potassium channel","type":"narrow"},{"name":"polycystin","type":"narrow"}],"termid":"GO:0005227","terms_by_termid":{"GO:0005227":null}}


id: PBO:0050127
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group box 1 pseudogene 37","termid":"PBO:0050127"}


id: PBO:0068620
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U2 small nuclear 72, pseudogene","termid":"PBO:0068620"}


id: PBO:0110191
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial MIB complex subunit, human DNAJC11 ortholog Mib1","termid":"PBO:0110191"}


id: PBO:0040916
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BMS1 pseudogene 20","termid":"PBO:0040916"}


id: PBO:0065723
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PWP2 small subunit processome component","termid":"PBO:0065723"}


id: PBO:0054172
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 1545","termid":"PBO:0054172"}


id: FYPO:0008160
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 acetylation of lysine at position 56 of histone H3 is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PMID:18344406"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal histone acetylation during vegetative growth","termid":"FYPO:0003221"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0000257","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"normal histone H3-K56 acetylation during vegetative growth","termid":"FYPO:0008160"}


id: PBO:0059733
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO3 pseudogene 7","termid":"PBO:0059733"}


id: PBO:0080289
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vomeronasal 1 receptor 53 pseudogene","termid":"PBO:0080289"}


id: PBO:0027544
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_growth_on_latrunculin_A","termid":"PBO:0027544"}


id: MONDO:0001527
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"strabismus","termid":"MONDO:0003432"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conjugate gaze palsy","secondary_identifiers":["UMLS:C0702143","DOID:12445","SCTID:1534008","ICD9:378.81","MEDGEN:675273"],"synonyms":[{"name":"palsy of conjugate gaze","type":"exact"}],"termid":"MONDO:0001527","xrefs":{"Monarch":{"xref_id":"0001527"}}}


id: GO:0060632
data:
  {"annotated_genes":["SJAG_03073","SJAG_04597"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[101229],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0062168"},{"annotations":[94173],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902854"}]},"cv_name":"biological_process","definition":"Any process that modulates the rate, frequency, or extent of microtubule-based movement, the movement of organelles, other microtubules and other particles along microtubules, mediated by motor proteins.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of microtubule-based process","termid":"GO:0032886"},{"relation_name":"regulates","term_name":"microtubule-based movement","termid":"GO:0007018"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03073":null,"SJAG_04597":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of microtubule-based movement","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0060632","terms_by_termid":{"GO:0062168":null,"GO:1902854":null}}


id: PBO:0076065
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"STPG2 antisense RNA 1","termid":"PBO:0076065"}


id: GO:0035146
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The joining of specific branches of a tubular system to form a continuous network.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tube morphogenesis","termid":"GO:0035239"},{"relation_name":"part_of","term_name":"branching morphogenesis of an epithelial tube","termid":"GO:0048754"}],"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":"tube fusion","termid":"GO:0035146"}


id: GO:0035120
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process, occurring after embryonic development, by which the anatomical structures of an appendage are generated and organized. An appendage is an organ or part that is attached to the trunk of an organism, such as a limb or a branch.","definition_xrefs":["ISBN:0582227089"],"direct_ancestors":[{"relation_name":"is_a","term_name":"post-embryonic animal morphogenesis","termid":"GO:0009886"},{"relation_name":"is_a","term_name":"appendage morphogenesis","termid":"GO:0035107"}],"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":"post-embryonic appendage morphogenesis","termid":"GO:0035120"}


id: MONDO:0021977
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A type of pilosebaceous hamartoma characterized by basal cell epitheliomata, epidermoid cysts and comedones, and epidermal atrophy.","definition_xrefs":["NCIT:C4749"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hamartoma","termid":"MONDO:0006499"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"basaloid follicular hamartoma","secondary_identifiers":["UMLS:C0474964","SCTID:254705003","icd11.foundation:648125144","ICD9:706.1","MEDGEN:96887"],"synonyms":[{"name":"basal cell nevus with comedones","type":"exact"},{"name":"basaloid follicular hamartoma","type":"exact"}],"termid":"MONDO:0021977","xrefs":{"Monarch":{"xref_id":"0021977"}}}


id: GO:0044192
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The inner, i.e. lumen-facing, lipid bilayer of the host cell mitochondrial envelope. It is highly folded to form cristae.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host cell mitochondrial membrane","termid":"GO:0044191"}],"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":"host cell mitochondrial inner membrane","termid":"GO:0044192"}


id: PBO:0070765
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L11 pseudogene 1","termid":"PBO:0070765"}


id: GO:0046843
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Establishment of the dorsal filaments, elaborate specializations of the chorion that protrude from the anterior end of the egg and facilitate embryonic respiration.","definition_xrefs":["ISBN:0879694238"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"is_a","term_name":"anatomical structure formation involved in morphogenesis","termid":"GO:0048646"},{"relation_name":"part_of","term_name":"egg chorion assembly","termid":"GO:0007306"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"dorsal appendage formation","termid":"GO:0046843"}


id: PBO:0018271
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SUMO activating enzyme E1-type Uba2 (predicted)","termid":"PBO:0018271"}


id: MONDO:0018813
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"aggressive B-cell non-Hodgkin lymphoma","termid":"MONDO:0017595"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"high grade B-cell lymphoma with MYC and/ or BCL2 and/or BCL6 rearrangement","secondary_identifiers":["GARD:21980","MEDGEN:1617477","Orphanet:480541","UMLS:C4524190"],"termid":"MONDO:0018813","xrefs":{"Monarch":{"xref_id":"0018813"}}}


id: MONDO:0021354
data:
  {"annotated_genes":["SJAG_00031"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86440],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007908"}]},"cv_name":"mondo","definition":"A neoplasm (disease) that involves the adipose tissue.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mesenchymal cell neoplasm","termid":"MONDO:0002616"},{"relation_name":"is_a","term_name":"connective tissue neoplasm","termid":"MONDO:0021581"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00031":null},"genotype_count":0,"is_obsolete":false,"name":"tumor of adipose tissue","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0206631","MEDGEN:61646","SCTID:254831005","ICD9:239.2","NCIT:C4248"],"synonyms":[{"name":"adipose tissue neoplasm","type":"exact"},{"name":"adipose tissue neoplasm (disease)","type":"exact"},{"name":"adipose tissue tumor","type":"exact"},{"name":"adipose tissue tumour","type":"exact"},{"name":"lipomatous neoplasm","type":"exact"},{"name":"lipomatous tumor","type":"exact"},{"name":"lipomatous tumour","type":"exact"},{"name":"neoplasm of adipose tissue","type":"exact"},{"name":"neoplasm of the adipose tissue","type":"exact"},{"name":"tumor of adipose tissue","type":"exact"},{"name":"tumor of the adipose tissue","type":"exact"},{"name":"tumour of the adipose tissue","type":"exact"}],"termid":"MONDO:0021354","terms_by_termid":{"MONDO:0007908":null},"xrefs":{"Monarch":{"xref_id":"0021354"}}}


id: MONDO:0859168
data:
  {"annotated_genes":["SJAG_01665"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86089],"is_not":false,"summary":null,"term":"MONDO:0859168"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"myofibrillar myopathy","termid":"MONDO:0018943"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01665":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:619424","MEDGEN:1794147","UMLS:C5561937"],"termid":"MONDO:0859168","terms_by_termid":{"MONDO:0859168":null},"xrefs":{"Monarch":{"xref_id":"0859168"}}}


id: GO:0140010
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of D-aspartate from one side of a membrane to the other.","definition_xrefs":["PMID:7914198","GO_REF:0000070"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dicarboxylic acid transmembrane transporter activity","termid":"GO:0005310"},{"relation_name":"is_a","term_name":"C4-dicarboxylate transmembrane transporter activity","termid":"GO:0015556"},{"relation_name":"is_a","term_name":"D-amino acid transmembrane transporter activity","termid":"GO:0042943"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"D-aspartate transmembrane transporter activity","termid":"GO:0140010"}


id: PBO:0060547
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuron navigator 3","termid":"PBO:0060547"}


id: MONDO:0012413
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Syndromic microphthalmia, type 5 is characterized by the association of a range of ocular anomalies (anophthalmia, microphthalmia and retinal abnormalities) with variable developmental delay and central nervous system malformations.","definition_xrefs":["Orphanet:178364"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic microphthalmia","termid":"MONDO:0016073"}],"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":"syndromic microphthalmia type 5","secondary_identifiers":["UMLS:C1864690","SCTID:718761007","OMIM:610125","MEDGEN:350491","MESH:C566441","GARD:3692","DOID:0111806"],"synonyms":[{"name":"MCOPS5","type":"exact"},{"name":"OTX2 syndromic microphthalmia","type":"exact"},{"name":"OTX2-related eye disorders","type":"related"},{"name":"microphthalmia syndromic 5","type":"related"},{"name":"microphthalmia, syndromic 5","type":"related"},{"name":"microphthalmia, syndromic type 5","type":"exact"},{"name":"retinal dystrophy, early-onset, with or without pituitary dysfunction","type":"related"},{"name":"syndromic microphthalmia caused by mutation in OTX2","type":"exact"},{"name":"syndromic microphthalmia type 5","type":"exact"},{"name":"syndromic microphthalmia/anophthalmia due to OTX2 mutation","type":"exact"}],"termid":"MONDO:0012413","xrefs":{"Monarch":{"xref_id":"0012413"}}}


id: MONDO:0004136
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm of the ovary characterized by the presence of cystic structures lined by endometrial-type well-differentiated cells.","definition_xrefs":["NCIT:C40075"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ovarian cystadenoma","termid":"MONDO:0005183"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ovarian endometrioid cystadenoma","secondary_identifiers":["DOID:7191","MEDGEN:309509","UMLS:C1518713"],"synonyms":[{"name":"ovarian endometrioid cystadenoma","type":"exact"}],"termid":"MONDO:0004136","xrefs":{"Monarch":{"xref_id":"0004136"}}}


id: PBO:0062868
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"OTU deubiquitinase 5","termid":"PBO:0062868"}


id: SO:0000041
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An operation that can be applied to a sequence, that results in a change.","definition_xrefs":["SO:ke"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:0000041 sequence_operation (obsolete SO:0000041)","synonyms":[{"name":"sequence operation","type":"exact"}],"termid":"SO:0000041"}


id: PBO:0110198
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial tRNA (guanine-N2-)-methyltransferase Trm1.1","termid":"PBO:0110198"}


id: PBO:0055311
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 2739","termid":"PBO:0055311"}


id: GO:0014847
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which force is generated within smooth muscle tissue, resulting in a change in muscle geometry. This process occurs in the proximal stomach. Force generation involves a chemo-mechanical energy conversion step that is carried out by the actin/myosin complex activity, which generates force through ATP hydrolysis. The proximal stomach, composed of the fundus and upper body, shows low frequency, sustained tonic contractions that are responsible for generating a basal pressure within the stomach.","definition_xrefs":["GOC:mtg_muscle","PMID:30252381"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tonic smooth muscle contraction","termid":"GO:0014820"},{"relation_name":"is_a","term_name":"stomach smooth muscle contraction","termid":"GO:0120063"}],"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":"proximal stomach smooth muscle contraction","termid":"GO:0014847"}


id: PBO:0055605
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 3043","termid":"PBO:0055605"}


id: FYPO:0001599
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 asparagine import into the cell is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal amino acid import","termid":"FYPO:0001596"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0001312","FYPO:0000257","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"normal asparagine import","synonyms":[{"name":"normal L-asparagine import","type":"exact"},{"name":"normal L-asparagine import across plasma membrane","type":"exact"},{"name":"normal asparagine import during mitotic cell cycle","type":"related"},{"name":"normal asparagine import during vegetative growth","type":"exact"},{"name":"normal asparagine import into cell","type":"exact"},{"name":"normal asparagine uptake","type":"exact"}],"termid":"FYPO:0001599"}


id: PBO:0072450
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S29 pseudogene 14","termid":"PBO:0072450"}


id: PBO:0061382
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleophosmin 1 pseudogene 42","termid":"PBO:0061382"}


id: PBO:0039371
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AMMECR1 like","termid":"PBO:0039371"}


id: PBO:0086130
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; IGO1 has a paralog, IGO2, that arose from the whole genome duplication","termid":"PBO:0086130"}


id: MONDO:0002381
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign or malignant neoplasm arising from the sweat glands.","definition_xrefs":["NCIT:C3398"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epidermal appendage tumor","termid":"MONDO:0002297"},{"relation_name":"is_a","term_name":"sweat gland disorder","termid":"MONDO:0006615"}],"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":"sweat gland neoplasm","secondary_identifiers":["UMLS:C0038987","MESH:D013544","MEDGEN:21039","DOID:2664","ICDO:8400/1","MONDO:0021219","EFO:1001204","ICD9:239.2","SCTID:126490003"],"synonyms":[{"name":"neoplasm of sweat gland","type":"exact"},{"name":"neoplasm of the sweat gland","type":"exact"},{"name":"sweat gland neoplasm","type":"exact"},{"name":"sweat gland neoplasm (disease)","type":"exact"},{"name":"sweat gland neoplasms","type":"exact"},{"name":"sweat gland tumor","type":"exact"},{"name":"sweat gland tumor (morphologic abnormality)","type":"exact"},{"name":"sweat gland tumor NOS (morphologic abnormality)","type":"exact"},{"name":"sweat gland tumour","type":"exact"},{"name":"sweat gland tumour (morphologic abnormality)","type":"exact"},{"name":"sweat gland tumour NOS (morphologic abnormality)","type":"exact"},{"name":"tumor of sweat gland","type":"exact"},{"name":"tumor of the sweat gland","type":"exact"},{"name":"tumour of sweat gland","type":"exact"},{"name":"tumour of the sweat gland","type":"exact"}],"termid":"MONDO:0002381","xrefs":{"Monarch":{"xref_id":"0002381"}}}


id: MONDO:0022930
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Dandy-Walker syndrome","termid":"MONDO:0009072"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0020022"}],"interesting_parent_ids":["MONDO:0020022"],"is_obsolete":false,"name":"Dandy-Walker malformation with nasopharyngeal teratoma and diaphragmatic hernia","secondary_identifiers":["MESH:C538340","UMLS:C2931823","GARD:137","MEDGEN:419910"],"synonyms":[{"name":"Aughton sloan Milad syndrome","type":"exact"}],"termid":"MONDO:0022930","xrefs":{"Monarch":{"xref_id":"0022930"}}}


id: PBO:0053788
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 1039","termid":"PBO:0053788"}


id: PBO:0039820
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADP ribosylation factor guanine nucleotide exchange factor 1","termid":"PBO:0039820"}


id: MONDO:0015451
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Univentricular heart (UVH) is a severe congenital cardiac malformation characterized by both atria related entirely or almost entirely to one functionally single ventricular chamber. The clinical manifestations include congestive heart failure, failure to thrive, cyanosis, hypoxemia and neurodevelopmental disabilities.","definition_xrefs":["Orphanet:1464"],"direct_ancestors":[{"relation_name":"is_a","term_name":"univentricular cardiopathy","termid":"MONDO:0019820"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"univentricular heart","secondary_identifiers":["SCTID:253283000","NANDO:2200250","icd11.foundation:1786413029","MESH:D000080039","MEDGEN:488862","MedDRA:10045545","NANDO:1200704","GARD:18725","UMLS:C0344622","ICD9:746.89"],"synonyms":[{"name":"Double inlet left ventricle","type":"exact"}],"termid":"MONDO:0015451","xrefs":{"Monarch":{"xref_id":"0015451"}}}


id: PBO:0030772
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_growth_on_thiabendazole","termid":"PBO:0030772"}


id: MONDO:0015674
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A genetically heterogeneous group of neuronal ceroid lipofuscinoses (NCLs) typically characterized by onset during infancy or early childhood with decline of mental and motor capacities, epilepsy, and vision loss through retinal degeneration.","definition_xrefs":["Orphanet:168491"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"infantile neuronal ceroid lipofuscinosis","termid":"MONDO:0019261"},{"relation_name":"excluded_subClassOf","term_name":"progressive myoclonus epilepsy","termid":"MONDO:0020074"},{"relation_name":"is_a","term_name":"lysosomal storage disease","termid":"MONDO:0002561"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002561"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0002561"],"is_obsolete":false,"name":"late infantile neuronal ceroid lipofuscinosis","secondary_identifiers":["NANDO:2201242","SCTID:14637005","UMLS:C0022340","GARD:17032","icd11.foundation:1923920542","MEDGEN:9589","NANDO:1200153"],"synonyms":[{"name":"Bielschowsky-jansky disease","type":"related"},{"name":"Bielschowsky-jansky type neuronal ceroid lipofuscinosis","type":"related"},{"name":"Jansky-Bielschowsky disease","type":"exact"},{"name":"LINCL","type":"exact"},{"name":"amaurotic idiocy early juvenile type","type":"related"},{"name":"amaurotic idiocy late infantile type","type":"related"},{"name":"amaurotic idiocy, early juvenile type","type":"related"},{"name":"amaurotic idiocy, late infantile type","type":"related"},{"name":"dollinger-Bielschowsky syndrome","type":"related"},{"name":"dollinger-Bielschowsky type neuronal ceroid lipofuscinosis","type":"related"},{"name":"late infantile NCL","type":"exact"},{"name":"late-infantile neuronal ceroid lipofuscinosis","type":"exact"}],"termid":"MONDO:0015674","xrefs":{"Monarch":{"xref_id":"0015674"}}}


id: PBO:0030173
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_small_tapered_vegetative_cell","termid":"PBO:0030173"}


id: MONDO:0004097
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete lipid-rich breast carcinoma (obsolete MONDO:0004097)","termid":"MONDO:0004097","xrefs":{"Monarch":{"xref_id":"0004097"}}}


id: PBO:0013131
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae PUS1","termid":"PBO:0013131"}


id: PBO:0051969
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"involucrin","termid":"PBO:0051969"}


id: FYPO:0005661
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which transcription occurs to a greater extent than normal when the cell is subject to nitrogen starvation. All genes, or a specific subset of genes, may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased transcription","termid":"FYPO:0002875"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000294"}],"interesting_parent_ids":["FYPO:0000294","FYPO:0005447","FYPO:0001985","FYPO:0006551","FYPO:0000002"],"is_obsolete":false,"name":"increased transcription during nitrogen starvation","synonyms":[{"name":"increased transcription during cellular response to nitrogen starvation","type":"exact"},{"name":"increased transcription during nitrogen depletion","type":"exact"},{"name":"increased transcription during nitrogen deprivation","type":"exact"},{"name":"increased transcription during nitrogen limitation","type":"exact"},{"name":"increased transcription in response to nitrogen starvation","type":"exact"},{"name":"increased transcriptional response to nitrogen starvation","type":"exact"}],"termid":"FYPO:0005661"}


id: PBO:0080210
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vestigial like family member 4","termid":"PBO:0080210"}


id: PBO:0004893
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial PPR repeat protein Ppr7","termid":"PBO:0004893"}


id: MONDO:0005307
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Prolonged shortening of the muscle or other soft tissue around a joint, preventing movement of the joint.","definition_xrefs":["MESH:D003286"],"gene_count":0,"genotype_count":0,"name":"obsolete contracture (obsolete MONDO:0005307)","synonyms":[{"name":"muscle contracture","type":"narrow"}],"termid":"MONDO:0005307","xrefs":{"Monarch":{"xref_id":"0005307"}}}


id: PBO:0070678
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7 pseudogene 49","termid":"PBO:0070678"}


id: GO:0017042
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: glycosyl-N-acylsphingosine + H2O = a sugar + N-acylsphingosine.","definition_xrefs":["PMID:9762914","PMID:10692580","EC:3.2.1.62"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, hydrolyzing O-glycosyl compounds","termid":"GO:0004553"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016798"}],"interesting_parent_ids":["GO:0016787","GO:0016798","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"glycosylceramidase activity","secondary_identifiers":["MetaCyc:GLYCOSYLCERAMIDASE-RXN"],"synonyms":[{"name":"cerebrosidase activity","type":"related"},{"name":"glycosyl ceramide glycosylhydrolase activity","type":"related"},{"name":"glycosyl-N-acylsphingosine glycohydrolase activity","type":"related"}],"termid":"GO:0017042"}


id: GO:0047590
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + 5-dehydro-2-deoxy-D-gluconate = ADP + 6-phospho-5-dehydro-2-deoxy-D-gluconate.","definition_xrefs":["MetaCyc:5-DEHYDRO-2-DEOXYGLUCONOKINASE-RXN","EC:2.7.1.92"],"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:0016740","GO:0003824","GO:0003674","GO:0016301"],"is_obsolete":false,"name":"5-dehydro-2-deoxygluconokinase activity","secondary_identifiers":["RHEA:13497"],"synonyms":[{"name":"5-keto-2-deoxyglucono kinase (phosphorylating)","type":"related"},{"name":"5-keto-2-deoxygluconokinase activity","type":"related"},{"name":"ATP:5-dehydro-2-deoxy-D-gluconate 6-phosphotransferase activity","type":"related"},{"name":"DKH kinase activity","type":"related"}],"termid":"GO:0047590"}


id: PBO:0041463
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C10orf95 antisense RNA 1","termid":"PBO:0041463"}


id: PBO:0073552
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SH3 and multiple ankyrin repeat domains 3","termid":"PBO:0073552"}


id: PBO:0002784
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DUF1716 family protein","termid":"PBO:0002784"}


id: PBO:0041439
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 9 open reading frame 57","termid":"PBO:0041439"}


id: PBO:0045149
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynein axonemal heavy chain 7","termid":"PBO:0045149"}


id: PBO:0091996
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"promoter located -692--679","termid":"PBO:0091996"}


id: GO:0018564
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 9H-carbazole + H+ + NAD(P)H + O2 = 2'-aminobiphenyl-2,3-diol + NAD(P)+.","definition_xrefs":["EC:1.14.12.22"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of two atoms of oxygen into one donor","termid":"GO:0016708"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"carbazole 1,9a-dioxygenase [NAD(P)H] activity","secondary_identifiers":["UM-BBD_reactionID:r0456"],"synonyms":[{"name":"CARDO","type":"exact"},{"name":"carbazole 1,9alpha-dioxygenase activity","type":"exact"}],"termid":"GO:0018564"}


id: PBO:0028034
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_post-anaphase_microtubule_array_organization","termid":"PBO:0028034"}


id: GO:1903556
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of tumor necrosis factor superfamily cytokine production.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:24187568"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cytokine production","termid":"GO:0001818"},{"relation_name":"is_a","term_name":"regulation of tumor necrosis factor superfamily cytokine production","termid":"GO:1903555"},{"relation_name":"negatively_regulates","term_name":"tumor necrosis factor superfamily cytokine production","termid":"GO:0071706"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"negative regulation of tumor necrosis factor superfamily cytokine production","synonyms":[{"name":"down regulation of TNF superfamily production","type":"related"},{"name":"down regulation of TNFSF cytokine production","type":"exact"},{"name":"down regulation of tumor necrosis factor superfamily cytokine production","type":"exact"},{"name":"down-regulation of TNF superfamily production","type":"related"},{"name":"down-regulation of TNFSF cytokine production","type":"exact"},{"name":"down-regulation of tumor necrosis factor superfamily cytokine production","type":"exact"},{"name":"downregulation of TNF superfamily production","type":"related"},{"name":"downregulation of TNFSF cytokine production","type":"exact"},{"name":"downregulation of tumor necrosis factor superfamily cytokine production","type":"exact"},{"name":"inhibition of TNF superfamily production","type":"related"},{"name":"inhibition of TNFSF cytokine production","type":"narrow"},{"name":"inhibition of tumor necrosis factor superfamily cytokine production","type":"narrow"},{"name":"negative regulation of TNF superfamily production","type":"related"},{"name":"negative regulation of TNFSF cytokine production","type":"exact"}],"termid":"GO:1903556"}


id: PBO:0030287
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-altered_cellular_sulfide_level","termid":"PBO:0030287"}


id: GO:0090635
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The desmosomal part containing the desmosomal cadherins, desmogleins and desmocollins, that establish contact and adhere to neighboring cells in a Ca2+-dependent manner.","definition_xrefs":["PMID:20066089"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"desmosome","termid":"GO:0030057"}],"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":"extracellular core region of desmosome","synonyms":[{"name":"desmoglea","type":"exact"}],"termid":"GO:0090635"}


id: GO:0102745
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: H+ + dihydrogeranylgeranyl-PP + NADPH = tetrahydrogeranylgeranyl-PP + NADP.","definition_xrefs":["GOC:pz","EC:1.3.1.-"],"gene_count":0,"genotype_count":0,"name":"obsolete dihydrogeranylgeranyl-PP reductase activity (obsolete GO:0102745)","termid":"GO:0102745"}


id: PBO:0063846
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidase inhibitor 16","termid":"PBO:0063846"}


id: GO:0080189
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Growth of a plant structure from the time of its initiation by an apical meristem until its expansion is completed.","definition_xrefs":["ISBN:0471245208"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multicellular organismal process","termid":"GO:0032501"},{"relation_name":"is_a","term_name":"growth","termid":"GO:0040007"}],"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":"primary growth","termid":"GO:0080189"}


id: GO:0042628
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The deposition of a plug of sperm or other gelatinous material into the opening of the vulva by a male at the termination of copulation. Probably acts to prevent subsequent matings by other males.","definition_xrefs":["GOC:jl","PMID:11267893"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reproductive process","termid":"GO:0022414"},{"relation_name":"part_of","term_name":"insemination","termid":"GO:0007320"}],"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 plug formation","synonyms":[{"name":"copulatory plug biosynthesis","type":"exact"},{"name":"copulatory plug deposition","type":"exact"},{"name":"copulatory plug formation","type":"exact"},{"name":"mating plug deposition","type":"exact"}],"termid":"GO:0042628"}


id: PBO:0075069
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 118","termid":"PBO:0075069"}


id: PBO:0086033
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function, contains a putative zinc-binding domain; expressed during sporulation; SPS18 has a paralog, GCS1, that arose from the whole genome duplication","termid":"PBO:0086033"}


id: PBO:0049132
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GPRIN family member 3","termid":"PBO:0049132"}


id: PBO:0003134
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arginosuccinicaciduria","termid":"PBO:0003134"}


id: PBO:0030050
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_ferric-chelate_reductase_activity","termid":"PBO:0030050"}


id: PBO:0084126
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Hexameric ring ATPase that remodels chromosome axis protein Hop1p; nucleolar component of the pachytene checkpoint, which prevents chromosome segregation when recombination and chromosome synapsis are defective; also represses meiotic interhomolog recombination in rDNA; required for meiotic double-stranded break formation","termid":"PBO:0084126"}


id: GO:0048928
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a neuron of the posterior lateral line ganglion.","definition_xrefs":["PMID:15018940"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lateral line ganglion neuron differentiation","termid":"GO:0048891"},{"relation_name":"part_of","term_name":"posterior lateral line ganglion development","termid":"GO:0048917"}],"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":"posterior lateral line ganglion neuron differentiation","termid":"GO:0048928"}


id: PBO:0040800
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BHLHE22 antisense RNA 1","termid":"PBO:0040800"}


id: PBO:0041018
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BPI fold containing family B member 1","termid":"PBO:0041018"}


id: MONDO:0013561
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with multiple joint dislocations (obsolete MONDO:0019700)","termid":"MONDO:0019700"},{"relation_name":"is_a","term_name":"mineral metabolism disease","termid":"MONDO:0000226"},{"relation_name":"is_a","term_name":"musculoskeletal system disorder","termid":"MONDO:0002081"},{"relation_name":"is_a","term_name":"inborn errors of metabolism","termid":"MONDO:0019052"}],"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":"chondrodysplasia with joint dislocations, gPAPP type","secondary_identifiers":["Orphanet:280586","MEDGEN:481387","OMIM:614078","UMLS:C3279757","GARD:11009","DOID:0112224"],"synonyms":[{"name":"chondrodysplasia with joint dislocations, gPAPP type","type":"exact"},{"name":"gPAPP deficiency","type":"exact"}],"termid":"MONDO:0013561","xrefs":{"Monarch":{"xref_id":"0013561"}}}


id: PBO:0072029
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S10","termid":"PBO:0072029"}


id: PBO:0047655
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FKBP prolyl isomerase 7","termid":"PBO:0047655"}


id: GO:0007559
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The breakdown of tissues; usually, if not always, accompanied by cell death, followed by the complete dissolution of dead tissue.","definition_xrefs":["GOC:dph","GOC:ma"],"gene_count":0,"genotype_count":0,"name":"obsolete histolysis (obsolete GO:0007559)","secondary_identifiers":["Wikipedia:Histolysis"],"termid":"GO:0007559"}


id: PR:Q9P782
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An activator of 90 kDa heat shock protein ATPase homolog 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO03151","PANTHER:PTHR13009:SF0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C1711.08 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1711.08","secondary_identifiers":["UniProtKB:Q9P782"],"synonyms":[{"name":"Spom972h-AHSA1","type":"exact"}],"termid":"PR:Q9P782"}


id: GO:1990844
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A mitochondrion that occurs in between fibrils of striated muscle cells and responds in distinct ways to physiological triggers.","definition_xrefs":["PMID:23297307","PMID:26039174"],"gene_count":0,"genotype_count":0,"name":"obsolete interfibrillar mitochondrion (obsolete GO:1990844)","synonyms":[{"name":"IFM","type":"exact"},{"name":"IMF mitochondrion","type":"exact"},{"name":"intermyofibrillar mitochondrion","type":"exact"}],"termid":"GO:1990844"}


id: GO:1905279
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of retrograde transport, endosome to Golgi.","definition_xrefs":["GOC:bf","GOC:PARL","GOC:TermGenie","GO_REF:0000058","PMID:23395371"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of intracellular transport","termid":"GO:0032386"},{"relation_name":"is_a","term_name":"regulation of vesicle-mediated transport","termid":"GO:0060627"},{"relation_name":"regulates","term_name":"retrograde transport, endosome to Golgi","termid":"GO:0042147"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0016192"],"is_obsolete":false,"name":"regulation of retrograde transport, endosome to Golgi","synonyms":[{"name":"regulation of retrograde (endosome to Golgi) transport","type":"exact"}],"termid":"GO:1905279"}


id: PBO:0046652
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"esterase activator","termid":"PBO:0046652"}


id: PBO:0044621
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dermcidin","termid":"PBO:0044621"}


id: PBO:0056240
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAGOH divergent transcript","termid":"PBO:0056240"}


id: MONDO:0850001
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital neuronal ceroid lipofuscinosis (CNCL) is a severe form of neuronal ceroid lipofuscinosis (NCL; see this term) with onset at birth characterized by primary microcephaly, neonatal epilepsy, and death in early infancy.","definition_xrefs":["Orphanet:168486"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuronal ceroid lipofuscinosis","termid":"MONDO:0016295"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0002561"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0002525","MONDO:0002561","MONDO:0005066"],"is_obsolete":false,"name":"congenital neuronal ceroid lipofuscinosis","secondary_identifiers":["icd11.foundation:641209188","GARD:17031","MEDGEN:351189","UMLS:C1864670"],"termid":"MONDO:0850001","xrefs":{"Monarch":{"xref_id":"0850001"}}}


id: MONDO:0030714
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"osteogenesis imperfecta","termid":"MONDO:0019019"}],"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":"osteogenesis imperfecta, IIA 22","secondary_identifiers":["UMLS:C5676943","MEDGEN:1801631","OMIM:619795"],"synonyms":[{"name":"OI22","type":"exact"},{"name":"osteogenesis imperfecta, IIA 22","type":"exact"}],"termid":"MONDO:0030714","xrefs":{"Monarch":{"xref_id":"0030714"}}}


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


id: PBO:0046879
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 8 member A4, pseudogene","termid":"PBO:0046879"}


id: PBO:0055240
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 2667","termid":"PBO:0055240"}


id: PBO:0089287
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane transporter","termid":"PBO:0089287"}


id: PBO:0051839
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"insulin receptor substrate 1","termid":"PBO:0051839"}


id: GO:0048390
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the intermediate mesoderm are generated and organized.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mesoderm morphogenesis","termid":"GO:0048332"},{"relation_name":"part_of","term_name":"intermediate mesoderm development","termid":"GO:0048389"}],"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":"intermediate mesoderm morphogenesis","termid":"GO:0048390"}


id: MONDO:1011979
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"vision disorder, non-human animal","termid":"MONDO:1011367"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retinal dysplasia, non-human animal","secondary_identifiers":["OMIA:000868"],"termid":"MONDO:1011979","xrefs":{"Monarch":{"xref_id":"1011979"}}}


id: PBO:0071454
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L31 pseudogene 60","termid":"PBO:0071454"}


id: MONDO:0009087
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":"deafness, neural, congenital moderate","secondary_identifiers":["MEDGEN:347425","MESH:C565640","OMIM:221500","UMLS:C1857337"],"synonyms":[{"name":"deafness, neural, congenital moderate","type":"exact"}],"termid":"MONDO:0009087","xrefs":{"Monarch":{"xref_id":"0009087"}}}


id: SO:0001324
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"1_methylguanosine is a modified guanosine base feature.","direct_ancestors":[{"relation_name":"is_a","term_name":"modified_guanosine","termid":"SO:0001276"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"one_methylguanosine","secondary_identifiers":["RNAMOD:029"],"synonyms":[{"name":"1-methylguanosine","type":"exact"},{"name":"m1G","type":"exact"},{"name":"one methylguanosine","type":"exact"}],"termid":"SO:0001324"}


id: GO:0015387
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: K+(out) + H+(out) = K+(in) + H+(in).","definition_xrefs":["TC:2.A.38.-.-"],"direct_ancestors":[{"relation_name":"is_a","term_name":"potassium ion transmembrane transporter activity","termid":"GO:0015079"},{"relation_name":"is_a","term_name":"solute:proton symporter activity","termid":"GO:0015295"}],"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:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"potassium:proton symporter activity","secondary_identifiers":["RHEA:28490","MetaCyc:TRANS-RXN-3"],"synonyms":[{"name":"potassium:hydrogen symporter activity","type":"exact"}],"termid":"GO:0015387"}


id: FYPO:0007510
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which progression through the mitotic cell cycle is abnormally arrested at the mitotic G2/M phase transition in the absence of the mitotic DNA replication checkpoint. The previous S phase is completed, no replication intermediates can be observed, and cells do not undergo rereplication.","definition_xrefs":["PomBase:jh","PMID:17690116","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell cycle arrest at mitotic G2/M phase transition","termid":"FYPO:0000400"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0005447","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"cell cycle arrest at mitotic G2/M phase transition in absence of mitotic DNA replication checkpoint","synonyms":[{"name":"cell cycle arrest at G2/M phase transition in absence of mitotic DNA replication checkpoint during mitotic cell cycle","type":"exact"},{"name":"cell cycle arrest at mitotic G2/M phase transition in absence of mitotic DNA replication checkpoint during vegetative growth","type":"exact"},{"name":"mitotic cell cycle arrest at the G2/M transition with completed S phase","type":"related"}],"termid":"FYPO:0007510"}


id: GO:0048361
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving mucilage that occur in the root epithelium; mucilage is normally synthesized during root growth.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mucilage metabolic process","termid":"GO:0010191"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"root epithelial mucilage metabolic process","synonyms":[{"name":"root epithelial mucilage metabolism","type":"exact"}],"termid":"GO:0048361"}


id: GO:0071621
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The movement of a granulocyte in response to an external stimulus.","definition_xrefs":["GOC:rph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukocyte chemotaxis","termid":"GO:0030595"},{"relation_name":"is_a","term_name":"granulocyte migration","termid":"GO:0097530"}],"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":"granulocyte chemotaxis","termid":"GO:0071621"}


id: PBO:0083860
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Farnesyl cysteine-carboxyl methyltransferase; mediates the carboxyl methylation step during C-terminal CAAX motif processing of a-factor and RAS proteins in the endoplasmic reticulum, localizes to the ER membrane","termid":"PBO:0083860"}


id: GO:0015316
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 nitrite/nitrate porter activity (obsolete GO:0015316)","synonyms":[{"name":"nitrite/nitrate porter activity","type":"exact"}],"termid":"GO:0015316"}


id: PBO:0066500
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"raftlin, lipid raft linker 1 pseudogene 1","termid":"PBO:0066500"}


id: GO:0032928
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of enzymatic generation of superoxide by a cell.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of superoxide metabolic process","termid":"GO:0090322"},{"relation_name":"regulates","term_name":"superoxide anion generation","termid":"GO:0042554"}],"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 superoxide anion generation","synonyms":[{"name":"regulation of superoxide release","type":"exact"}],"termid":"GO:0032928"}


id: GO:0050898
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving nitriles, an organic compound containing trivalent nitrogen attached to one carbon atom. The nitriles are named with reference to the acids produced by their decomposition; for example, hydrocyanic acid is formic nitrile, and methyl cyanide is acetic nitrile.","definition_xrefs":["PMID:18987211"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metabolic process","termid":"GO:0008152"}],"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":"nitrile metabolic process","synonyms":[{"name":"nitrile metabolism","type":"exact"}],"termid":"GO:0050898"}


id: PBO:0089235
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial nuclease Lcl3, implicated in DNA repair","termid":"PBO:0089235"}


id: MONDO:0007295
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A childhood-onset epilepsy syndrome that is characterized by onset of seizures between 3 and 14 years (peak 8-9 years) that usually resolve by age 13 years, but can occasionally occur up to age 18 years of age. Both sexes are affected. Antecedent, birth and neonatal history is normal. A history of febrile seizure (in 5-15%) may be seen. A history of Panayiotopoulos syndrome may be present in a very small number of cases. Neurological exam and head size is normal. Development and cognition prior to onset of seizures is normal. During the course of the active epilepsy, behavioral and neuropsychological deficits may be found, particularly in language and executive functioning. These deficits improve when seizures remit.","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"excluded_subClassOf","term_name":"epilepsy","termid":"MONDO:0005027"},{"relation_name":"excluded_subClassOf","term_name":"Landau-Kleffner syndrome","termid":"MONDO:0009509"},{"relation_name":"is_a","term_name":"childhood electroclinical syndrome","termid":"MONDO:0000414"},{"relation_name":"is_a","term_name":"familial partial epilepsy","termid":"MONDO:0017704"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"childhood epilepsy with centrotemporal spikes","secondary_identifiers":["MEDGEN:138210","SCTID:44145005","UMLS:C0376532","icd11.foundation:1046279423","DOID:3329","ICD9:345.80","NCIT:C116538","OMIM:117100","Orphanet:1945","GARD:10287"],"synonyms":[{"name":"BCECTS","type":"exact"},{"name":"BECRS","type":"exact"},{"name":"BECTS","type":"exact"},{"name":"BRE","type":"exact"},{"name":"Rolandic epilepsy","type":"exact"},{"name":"benign Rolandic epilepsy","type":"exact"},{"name":"benign Rolandic epilepsy (BRE)","type":"exact"},{"name":"benign Rolandic epilepsy of childhood (BREC)","type":"exact"},{"name":"benign childhood epilepsy with centrotemporal spike","type":"exact"},{"name":"benign childhood epilepsy with centrotemporal spikes","type":"exact"},{"name":"benign epilepsy of childhood with centrotemporal spikes","type":"exact"},{"name":"benign epilepsy of childhood with centrotemporal spikes (BECCT)","type":"related"},{"name":"benign epilepsy with centro-temporal spikes (BECTS)","type":"related"},{"name":"benign epilepsy with centrotemporal spikes","type":"exact"},{"name":"benign familial epilepsy of childhood with rolandic spikes","type":"exact"},{"name":"centralopathic epilepsy","type":"exact"},{"name":"centrotemporal epilepsy","type":"exact"},{"name":"centrotemporal epilepsy, isolated cases","type":"exact"},{"name":"sylvan seizures","type":"exact"},{"name":"temporal-central focal epilepsy","type":"exact"}],"termid":"MONDO:0007295","xrefs":{"Monarch":{"xref_id":"0007295"}}}


id: GO:0048149
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in the behavior of an organism as a result of an ethanol stimulus.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adult behavior","termid":"GO:0030534"},{"relation_name":"part_of","term_name":"response to ethanol","termid":"GO:0045471"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"behavioral response to ethanol","synonyms":[{"name":"behavioural response to ethanol","type":"exact"}],"termid":"GO:0048149"}


id: GO:0034468
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The volume enclosed by the membrane of a glycosome.","definition_xrefs":["GOC:rph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peroxisomal matrix","termid":"GO:0005782"},{"relation_name":"part_of","term_name":"glycosome","termid":"GO:0020015"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005777"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005777","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"glycosome lumen","termid":"GO:0034468"}


id: MONDO:0004766
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An acute exacerbation of asthma, characterized by inadequate response to initial bronchodilators.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"asthma","termid":"MONDO:0004979"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"status asthmaticus","secondary_identifiers":["NCIT:C122577","EFO:0008590","SCTID:708090002","ICD9:493.91","UMLS:C0038218","DOID:9362","MEDGEN:11584","MESH:D013224"],"synonyms":[{"name":"asthma with status asthmaticus","type":"exact"},{"name":"severe asthma attack","type":"exact"}],"termid":"MONDO:0004766","xrefs":{"Monarch":{"xref_id":"0004766"}}}


id: PBO:0004965
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleotide-sugar 4,6-dehydratase (predicted)","termid":"PBO:0004965"}


id: PBO:0079443
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TUB like protein 1","termid":"PBO:0079443"}


id: MONDO:0032783
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any aortic valve disease characterized by aortic stenosis and/or bicuspid aortic valve in which the cause of the disease is a mutation in the ROBO4 gene.","definition_xrefs":["OMIM:618496"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial bicuspid aortic valve","termid":"MONDO:0007194"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"aortic valve disease 3","secondary_identifiers":["UMLS:C5193127","MEDGEN:1681142","DOID:0080977"],"synonyms":[{"name":"AORTIC VALVE DISEASE 3","type":"related"},{"name":"AOVD3","type":"related"}],"termid":"MONDO:0032783","xrefs":{"Monarch":{"xref_id":"0032783"}}}


id: GO:0045707
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of salivary gland determination in an adult organism.","definition_xrefs":["GOC:go_curators","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of salivary gland boundary specification","termid":"GO:0045704"},{"relation_name":"regulates","term_name":"adult salivary gland boundary specification","termid":"GO:0007434"}],"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 adult salivary gland boundary specification","synonyms":[{"name":"regulation of adult salivary gland determination","type":"exact"}],"termid":"GO:0045707"}


id: PBO:0078222
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor beta variable 10-3","termid":"PBO:0078222"}


id: GO:0000001
data:
  {"annotated_genes":["SJAG_02848"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[102553],"is_not":false,"summary":null,"term":"GO:0000001"}]},"cv_name":"biological_process","definition":"The distribution of mitochondria, including the mitochondrial genome, into daughter cells after mitosis or meiosis, mediated by interactions between mitochondria and the cytoskeleton.","definition_xrefs":["GOC:mcc","PMID:10873824","PMID:11389764"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organelle inheritance","termid":"GO:0048308"},{"relation_name":"is_a","term_name":"mitochondrion distribution","termid":"GO:0048311"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02848":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"mitochondrion inheritance","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"mitochondrial inheritance","type":"exact"}],"termid":"GO:0000001","terms_by_termid":{"GO:0000001":null}}


id: PBO:0030664
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_leucine_import","termid":"PBO:0030664"}


id: GO:1900620
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of an acetate esteran acetate ester, any carboxylic ester where the carboxylic acid component is acetic acid.","definition_xrefs":["PMID:15042596","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biosynthetic process","termid":"GO:0009058"},{"relation_name":"is_a","term_name":"acetate ester metabolic process","termid":"GO:1900619"}],"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":"acetate ester biosynthetic process","synonyms":[{"name":"acetate ester anabolism","type":"exact"},{"name":"acetate ester biosynthesis","type":"exact"},{"name":"acetate ester formation","type":"exact"},{"name":"acetate ester synthesis","type":"exact"},{"name":"acetyl ester biosynthesis","type":"exact"},{"name":"acetyl ester biosynthetic process","type":"exact"}],"termid":"GO:1900620"}


id: GO:0031553
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of brain-derived neurotrophic factor-activated receptor activity.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of brain-derived neurotrophic factor-activated receptor activity (obsolete GO:0031553)","synonyms":[{"name":"activation of brain-derived neurotrophic factor receptor activity","type":"narrow"},{"name":"positive regulation of BDNF receptor activity","type":"exact"},{"name":"positive regulation of brain-derived neurotrophic factor receptor activity","type":"exact"},{"name":"stimulation of brain-derived neurotrophic factor receptor activity","type":"narrow"},{"name":"up regulation of brain-derived neurotrophic factor receptor activity","type":"exact"},{"name":"up-regulation of brain-derived neurotrophic factor receptor activity","type":"exact"},{"name":"upregulation of brain-derived neurotrophic factor receptor activity","type":"exact"}],"termid":"GO:0031553"}


id: MONDO:0002784
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete craniopharyngioma (obsolete MONDO:0002784)","termid":"MONDO:0002784","xrefs":{"Monarch":{"xref_id":"0002784"}}}


id: PBO:0005875
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"15S rRNA","termid":"PBO:0005875"}


id: PBO:0052507
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kelch like family member 21","termid":"PBO:0052507"}


id: PBO:0043498
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"contactin 5","termid":"PBO:0043498"}


id: MONDO:0000373
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma in situ involving a gall bladder.","definition_xrefs":["MONDO:patterns/carcinoma_in_situ"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gallbladder carcinoma","termid":"MONDO:0003220"},{"relation_name":"is_a","term_name":"in situ carcinoma","termid":"MONDO:0004647"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992","MONDO:0002515"],"is_obsolete":false,"name":"gall bladder carcinoma in situ","secondary_identifiers":["MEDGEN:87523","DOID:0050612","UMLS:C0345911"],"synonyms":[{"name":"carcinoma in situ of gall bladder","type":"exact"},{"name":"gall bladder in situ carcinoma","type":"exact"},{"name":"stage 0 gall bladder carcinoma","type":"exact"}],"termid":"MONDO:0000373","xrefs":{"Monarch":{"xref_id":"0000373"}}}


id: PBO:0049455
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycogenin 1","termid":"PBO:0049455"}


id: PBO:0030379
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_growth_on_staurosporine","termid":"PBO:0030379"}


id: MONDO:0016034
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete cleft lip with or without cleft palate (obsolete MONDO:0016034)","secondary_identifiers":["Orphanet:1991"],"synonyms":[{"name":"Tessier cleft number 1,2","type":"exact"}],"termid":"MONDO:0016034","xrefs":{"Monarch":{"xref_id":"0016034"}}}


id: PBO:0083124
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dolichyl-phosphoglucose-dependent alpha-1,2-glucosyltransferase; located in the ER; functions in pathway that synthesizes the dolichol-linked oligosaccharide precursor for N-linked protein glycosylation; has a role in regulation of ITR1 and INO1; human homolog ALG10B can complement yeast die2 null mutant","termid":"PBO:0083124"}


id: PBO:0051720
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"INSM transcriptional repressor 1","termid":"PBO:0051720"}


id: PATO:0000676
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000676 relative temperature value (obsolete PATO:0000676)","termid":"PATO:0000676"}


id: MONDO:0007018
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the vulva. It is characterized by pruritus and painful urination.","definition_xrefs":["MESH:D014847"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vulvar disease","termid":"MONDO:0002187"},{"relation_name":"is_a","term_name":"inflammatory disease","termid":"MONDO:0021166"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vulvitis","secondary_identifiers":["DOID:3901","MEDGEN:22690","EFO:1001239","MedDRA:10047780","SCTID:63144007","UMLS:C0042996","icd11.foundation:727252860"],"synonyms":[{"name":"inflammation of mammalian vulva","type":"exact"},{"name":"mammalian vulva inflammation","type":"exact"}],"termid":"MONDO:0007018","xrefs":{"Monarch":{"xref_id":"0007018"}}}


id: PBO:0027864
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_histone_H3-K4_acetylation","termid":"PBO:0027864"}


id: GO:1900667
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of endocrocin biosynthetic process.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of ketone biosynthetic process","termid":"GO:0010566"},{"relation_name":"is_a","term_name":"regulation of secondary metabolite biosynthetic process","termid":"GO:1900376"},{"relation_name":"regulates","term_name":"endocrocin biosynthetic process","termid":"GO:1900602"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0019748","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"regulation of endocrocin biosynthetic process","synonyms":[{"name":"regulation of endocrocin anabolism","type":"exact"},{"name":"regulation of endocrocin biosynthesis","type":"exact"},{"name":"regulation of endocrocin formation","type":"exact"},{"name":"regulation of endocrocin synthesis","type":"exact"}],"termid":"GO:1900667"}


id: PBO:0069452
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 717, pseudogene","termid":"PBO:0069452"}


id: FYPO:0004328
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which cellular protein localization is normal (i.e. indistinguishable from wild type) during mitosis.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization during vegetative growth","termid":"FYPO:0000644"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001312","FYPO:0000257","FYPO:0001320","FYPO:0000138"],"is_obsolete":false,"name":"normal protein localization during mitosis","synonyms":[{"name":"normal cellular protein localization during mitosis","type":"exact"},{"name":"normal protein localisation during mitosis during vegetative growth","type":"exact"},{"name":"normal protein localization during mitotic M phase","type":"related"},{"name":"normal protein localization during mitotic nuclear division","type":"exact"}],"termid":"FYPO:0004328"}


id: GO:0010739
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency, or extent of protein kinase A signaling. PKA signaling is the series of reactions, mediated by the intracellular serine/threonine kinase protein kinase A, which occurs as a result of a single trigger reaction or compound.","definition_xrefs":["GOC:BHF","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein kinase A signaling","termid":"GO:0010738"},{"relation_name":"is_a","term_name":"positive regulation of intracellular signal transduction","termid":"GO:1902533"},{"relation_name":"positively_regulates","term_name":"protein kinase A signaling","termid":"GO:0010737"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"positively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"positive regulation of protein kinase A signaling","synonyms":[{"name":"positive regulation of PKA signaling cascade","type":"related"},{"name":"positive regulation of protein kinase A signaling cascade","type":"related"},{"name":"positive regulation of protein kinase A signalling cascade","type":"related"}],"termid":"GO:0010739"}


id: PBO:0046213
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"elongin C pseudogene 6","termid":"PBO:0046213"}


id: PBO:0017593
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Golgi phosphoprotein 3 family Vps74 (predicted)","termid":"PBO:0017593"}


id: PBO:0057517
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 635","termid":"PBO:0057517"}


id: MONDO:0007264
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. An unexpected natural death from a cardiac cause within a short time period from the onset of symptoms.","definition_xrefs":["NCIT:C50911"],"gene_count":0,"genotype_count":0,"name":"obsolete sudden cardiac death (obsolete MONDO:0007264)","secondary_identifiers":["SCTID:95281009"],"synonyms":[{"name":"sudden cardiac death","type":"exact"}],"termid":"MONDO:0007264","xrefs":{"Monarch":{"xref_id":"0007264"}}}


id: PBO:0081840
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 775","termid":"PBO:0081840"}


id: PBO:0028527
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_chromatin_silencing_at_centromere_central_core","termid":"PBO:0028527"}


id: PBO:0004604
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CENP-H homolog Fta3","termid":"PBO:0004604"}


id: PBO:0080475
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vault RNA 1-1","termid":"PBO:0080475"}


id: PBO:0059230
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein L2","termid":"PBO:0059230"}


id: PBO:0066357
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"REST corepressor 1","termid":"PBO:0066357"}


id: PBO:0005519
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kinetochore protein Spc25","termid":"PBO:0005519"}


id: GO:0031059
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The removal of acetyl groups from histones in centromeric DNA.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete histone deacetylation at centromere (obsolete GO:0031059)","termid":"GO:0031059"}


id: GO:0102187
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 4alpha-carboxy,4beta,14alpha-dimethyl-9beta,19-cyclo-5alpha-cholest-24-en-3beta-ol + NAD(1-) = 4alpha,14alpha-dimethyl-9beta,19-cyclo-5alpha-cholest-24-en-3-one + NADH(2-) + carbon dioxide.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 4alpha-carboxy,4beta,14alpha-dimethyl-9beta,19-cyclo-5alpha-cholest-24-en-3beta-ol dehydrogenase/C4-decarboxylase activity (obsolete GO:0102187)","termid":"GO:0102187"}


id: PBO:0072270
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S21 pseudogene 8","termid":"PBO:0072270"}


id: MONDO:0021244
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplasm (disease) that involves the submandibular gland.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"submandibular gland disorder","termid":"MONDO:0001597"},{"relation_name":"is_a","term_name":"neoplasm of major salivary gland","termid":"MONDO:0021368"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"submandibular gland neoplasm","secondary_identifiers":["NCIT:C3393","SCTID:254464000","MESH:D013365","EFO:1001853","MEDGEN:20986","UMLS:C0038558"],"synonyms":[{"name":"neoplasm of submandibular gland","type":"exact"},{"name":"neoplasm of the submandibular gland","type":"exact"},{"name":"submandibular gland neoplasm (disease)","type":"exact"},{"name":"submandibular gland tumor","type":"exact"},{"name":"submandibular gland tumour","type":"exact"},{"name":"tumor of submandibular gland","type":"exact"},{"name":"tumor of the submandibular gland","type":"exact"},{"name":"tumour of submandibular gland","type":"exact"},{"name":"tumour of the submandibular gland","type":"exact"}],"termid":"MONDO:0021244","xrefs":{"Monarch":{"xref_id":"0021244"}}}


id: MONDO:0011534
data:
  {"annotated_genes":["SJAG_04495","SJAG_04334"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86816,86817],"is_not":false,"summary":null,"term":"MONDO:0011534"}]},"cv_name":"mondo","definition":"Charcot-Marie-Tooth disease type 4G (CMT4G) is a subtype of Charcot-Marie-Tooth disease type 4 characterized by early childhood onset of progressive distal muscle weakness and atrophy, delayed motor development, prominent distal sensory impairment, areflexia, moderately reduced nerve conduction velocities, and foot and hand deformities in Balkan (Russe) Gypsies.","definition_xrefs":["Orphanet:99953"],"direct_ancestors":[{"relation_name":"is_a","term_name":"motor peripheral neuropathy","termid":"MONDO:0002316"},{"relation_name":"is_a","term_name":"disorder of glycolysis","termid":"MONDO:0017688"},{"relation_name":"is_a","term_name":"Charcot-Marie-Tooth disease type 4","termid":"MONDO:0018995"}],"gene_count":2,"genes_by_uniquename":{"SJAG_04334":null,"SJAG_04495":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0019254"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0019254","MONDO:0005244","MONDO:0037792"],"is_obsolete":false,"name":"Charcot-Marie-Tooth disease type 4G","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:715799004","GARD:10132","icd11.foundation:995395080","DOID:0110196","MESH:C535813","OMIM:605285","UMLS:C1854449","MEDGEN:343122"],"synonyms":[{"name":"CMT4G","type":"exact"},{"name":"Charcot-Marie-Tooth disease type 4 caused by mutation in HK1","type":"exact"},{"name":"Charcot-Marie-Tooth disease, autosomal recessive, type 4G","type":"related"},{"name":"Charcot-Marie-Tooth disease, type 4G","type":"related"},{"name":"Charcot-Marie-Tooth neuropathy type 4G","type":"exact"},{"name":"Charcot-Marie-Tooth neuropathy, type 4G","type":"related"},{"name":"HK1 Charcot-Marie-Tooth disease type 4","type":"exact"},{"name":"HMSNR","type":"exact"},{"name":"autosomal recessive Charcot-Marie-Tooth disease type 4G","type":"exact"},{"name":"hereditary motor and sensory neuropathy Russe type","type":"exact"},{"name":"hereditary motor and sensory neuropathy, Russe type","type":"exact"},{"name":"neuropathy, hereditary motor and sensory, Russe type","type":"related"}],"termid":"MONDO:0011534","terms_by_termid":{"MONDO:0011534":null},"xrefs":{"Monarch":{"xref_id":"0011534"}}}


id: PBO:0059119
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial pyruvate carrier 1","termid":"PBO:0059119"}


id: PBO:0075175
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SNRPE pseudogene 5","termid":"PBO:0075175"}


id: PBO:0050166
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group box 3 pseudogene 22","termid":"PBO:0050166"}


id: PBO:0065923
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB, member of RAS oncogene family like 2B","termid":"PBO:0065923"}


id: GO:0075527
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process by which bases in viral mRNA are chemically altered during viral transcription. This is usually the incorporation of 1 - 6 additional nucleotides, which shifts the reading frame, allowing the generation of different protein products or through a specific nucleotide change that eliminates the termination codon.","definition_xrefs":["VZ:857","PMID:1629949"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral process","termid":"GO:0016032"},{"relation_name":"part_of","term_name":"viral transcription","termid":"GO:0019083"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"viral RNA editing","synonyms":[{"name":"RNA editing involved in viral mRNA transcription","type":"exact"}],"termid":"GO:0075527"}


id: GO:0004526
data:
  {"annotated_genes":["SJAG_06613","SJAG_03234","SJAG_04916","SJAG_00306","SJAG_02553","SJAG_03796","SJAG_01623","SJAG_00955","SJAG_04582"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[60306,63327,68089,70871,94472,96563,101848,104351,115119],"is_not":false,"summary":null,"term":"GO:0004526"}]},"cv_name":"molecular_function","definition":"Catalysis of the endonucleolytic cleavage of RNA, removing 5' extra nucleotides from tRNA precursor.","definition_xrefs":["EC:3.1.26.5"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA-specific ribonuclease activity","termid":"GO:0004549"},{"relation_name":"is_a","term_name":"RNA endonuclease activity, producing 5'-phosphomonoesters","termid":"GO:0016891"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00306":null,"SJAG_00955":null,"SJAG_01623":null,"SJAG_02553":null,"SJAG_03234":null,"SJAG_03796":null,"SJAG_04582":null,"SJAG_04916":null,"SJAG_06613":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140101"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016788","GO:0140098","GO:0003824","GO:0016787","GO:0003674","GO:0140101"],"is_obsolete":false,"name":"ribonuclease P activity","references_by_uniquename":{"GO_REF:0000003":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:3.1.26.5-RXN","Reactome:R-HSA-5696810","Wikipedia:RNase_P"],"synonyms":[{"name":"RNase P","type":"exact"},{"name":"tRNA 5' leader endonuclease activity","type":"exact"}],"termid":"GO:0004526","terms_by_termid":{"GO:0004526":null}}


id: PBO:0044339
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CYCS pseudogene 23","termid":"PBO:0044339"}


id: MONDO:0019000
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Perineural (or Tarlov) cysts are cerebrospinal fluid-filled nerve root cysts most commonly found at the sacral level of the spine, although they can be found in any section of the spine, which can cause progressively painful radiculopathy.","definition_xrefs":["Orphanet:65250"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder","termid":"MONDO:0005071"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"perineural cyst","secondary_identifiers":["GARD:9258","SCTID:81634008","MEDGEN:105457","MESH:D052958","UMLS:C0520720","icd11.foundation:881909739"],"synonyms":[{"name":"Tarlov cyst","type":"exact"},{"name":"Tarlov cysts","type":"related"},{"name":"perineural cysts","type":"related"},{"name":"sacral Tarlov cysts","type":"related"},{"name":"sacral neural cysts","type":"related"},{"name":"sacral perineural cysts","type":"related"}],"termid":"MONDO:0019000","xrefs":{"Monarch":{"xref_id":"0019000"}}}


id: PBO:0029088
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_tRNA_(guanine(9)-N(1))-methyltransferase_activity","termid":"PBO:0029088"}


id: PBO:0028634
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_growth_on_aculeacin_A","termid":"PBO:0028634"}


id: GO:1900757
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of D-amino-acid oxidase activity.","definition_xrefs":["GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of D-amino-acid oxidase activity (obsolete GO:1900757)","synonyms":[{"name":"regulation of D-amino-acid:oxygen oxidoreductase (deaminating)","type":"exact"},{"name":"regulation of L-amino acid:O2 oxidoreductase activity","type":"exact"},{"name":"regulation of new yellow enzyme","type":"related"}],"termid":"GO:1900757"}


id: PR:Q09705
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rsm24 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q09705"],"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 S24, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC2F7.15","synonyms":[{"name":"Spom972h-rsm24","type":"exact"}],"termid":"PR:Q09705"}


id: PBO:0076870
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis expressed 16, pseudogene","termid":"PBO:0076870"}


id: GO:0090369
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binds to and stops, prevents, or reduces the activity of ornithine carbamoyltransferase.","definition_xrefs":["GOC:dph","GOC:tb","GOC:jp"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme inhibitor activity","termid":"GO:0004857"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0004857"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140678"},{"rel_name":"is_a","termid":"GO:0030234"}],"interesting_parent_ids":["GO:0004857","GO:0098772","GO:0140678","GO:0030234","GO:0003674"],"is_obsolete":false,"name":"ornithine carbamoyltransferase inhibitor activity","termid":"GO:0090369"}


id: PBO:0070495
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L5 pseudogene 30","termid":"PBO:0070495"}


id: GO:0089706
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of L-ornithine out of the vacuole, across the vacuolar membrane.","definition_xrefs":["PMID:21307582"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid transmembrane export from vacuole","termid":"GO:0032974"},{"relation_name":"is_a","term_name":"L-ornithine transmembrane transport","termid":"GO:1903352"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0055085","GO:0008150","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"L-ornithine transmembrane export from vacuole","termid":"GO:0089706"}


id: FYPO:0002204
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cell population phenotype in which a cell undergoes one or a few rounds of cell division before cells die, resulting in the formation a colony that contains only a few inviable cells that each contain one or more septa, and in which the cell diameter is larger than normal and the cell length is shorter than normal. Up to 6 rounds of cell division (generating 64 cells) may be observed, but 3 divisions or fewer is more typical.","definition_xrefs":["PomBase:mah","PomBase:vw"],"gene_count":0,"genotype_count":0,"name":"obsolete inviable microcolony, stubby septated cells (obsolete FYPO:0002204)","synonyms":[{"name":"inviable microcolony, stubby septated vegetative cells","type":"exact"}],"termid":"FYPO:0002204"}


id: PBO:0005333
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"triosephosphate isomerase","termid":"PBO:0005333"}


id: PBO:0000782
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP-dependent RNA helicase Ddx27/Drs1 (predicted)","termid":"PBO:0000782"}


id: GO:0006859
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed extracellular movement of carbohydrates.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete extracellular carbohydrate transport (obsolete GO:0006859)","termid":"GO:0006859"}


id: PBO:0030373
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_RNA_level_during_cellular_response_to_thiamine_starvation","termid":"PBO:0030373"}


id: PBO:0058489
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5683","termid":"PBO:0058489"}


id: FYECO:0000038
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which magnesium ions were added to the assay buffer in excess compared to standard assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"+ ions","termid":"FYECO:0000030"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ Mg ions","synonyms":[{"name":"magnesium ions added","type":"exact"}],"termid":"FYECO:0000038"}


id: GO:0045862
data:
  {"annotated_genes":["SJAG_01489","SJAG_01210","SJAG_01131","SJAG_02723","SJAG_03048","SJAG_00642","SJAG_00766","SJAG_03699","SJAG_00071","SJAG_00077","SJAG_04477","SJAG_00712","SJAG_01544"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89707],"is_not":false,"summary":null,"term":"GO:0045862"},{"annotations":[88692],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905786"},{"annotations":[66655,65385,61267,66879,67909,68254],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901800"},{"annotations":[116881,106456,111511,108696,102171],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032436"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the hydrolysis of a peptide bond or bonds within a protein.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of proteolysis","termid":"GO:0030162"},{"relation_name":"is_a","term_name":"positive regulation of protein metabolic process","termid":"GO:0051247"},{"relation_name":"positively_regulates","term_name":"proteolysis","termid":"GO:0006508"}],"gene_count":13,"genes_by_uniquename":{"SJAG_00071":null,"SJAG_00077":null,"SJAG_00642":null,"SJAG_00712":null,"SJAG_00766":null,"SJAG_01131":null,"SJAG_01210":null,"SJAG_01489":null,"SJAG_01544":null,"SJAG_02723":null,"SJAG_03048":null,"SJAG_03699":null,"SJAG_04477":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of proteolysis","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000108":null},"synonyms":[{"name":"activation of proteolysis","type":"narrow"},{"name":"positive regulation of peptidolysis","type":"exact"},{"name":"stimulation of proteolysis","type":"narrow"},{"name":"up regulation of proteolysis","type":"exact"},{"name":"up-regulation of proteolysis","type":"exact"},{"name":"upregulation of proteolysis","type":"exact"}],"termid":"GO:0045862","terms_by_termid":{"GO:0032436":null,"GO:0045862":null,"GO:1901800":null,"GO:1905786":null}}


id: GO:0070498
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by interleukin-1 binding to its receptor on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["GOC:signaling","GOC:mah","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine-mediated signaling pathway","termid":"GO:0019221"},{"relation_name":"part_of","term_name":"cellular response to interleukin-1","termid":"GO:0071347"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"interleukin-1-mediated signaling pathway","secondary_identifiers":["Reactome:R-HSA-9020702"],"synonyms":[{"name":"IL-1 alpha-mediated signaling pathway","type":"narrow"},{"name":"IL-1 beta-mediated signaling pathway","type":"narrow"},{"name":"IL-1-mediated signaling pathway","type":"exact"},{"name":"interleukin-1 alpha-mediated signaling pathway","type":"narrow"},{"name":"interleukin-1 beta-mediated signaling pathway","type":"narrow"},{"name":"interleukin-1-mediated signalling pathway","type":"exact"}],"termid":"GO:0070498"}


id: GO:0033554
data:
  {"annotated_genes":["SJAG_01787","SJAG_02116","SJAG_02724","SJAG_01620","SJAG_03263","SJAG_04082","SJAG_01410","SJAG_05000","SJAG_02339","SJAG_00403","SJAG_01385","SJAG_02818","SJAG_00781","SJAG_04205","SJAG_04262","SJAG_05323","SJAG_02785","SJAG_02685","SJAG_00054","SJAG_03695","SJAG_02342","SJAG_03092","SJAG_05020","SJAG_00618","SJAG_02385","SJAG_04063","SJAG_02031","SJAG_00327","SJAG_01709","SJAG_00111","SJAG_02601","SJAG_05274","SJAG_04429","SJAG_00213","SJAG_03221","SJAG_01292","SJAG_02474","SJAG_04280","SJAG_01605","SJAG_04272","SJAG_00272","SJAG_04283","SJAG_04311","SJAG_00126","SJAG_04372","SJAG_04345","SJAG_01680","SJAG_04114","SJAG_00634","SJAG_01429","SJAG_01205","SJAG_04089","SJAG_16460","SJAG_02699","SJAG_01114","SJAG_05239","SJAG_05022","SJAG_02698","SJAG_03303","SJAG_03414","SJAG_00329","SJAG_01979","SJAG_00486","SJAG_03256","SJAG_01146","SJAG_02503","SJAG_03302","SJAG_02079","SJAG_02244","SJAG_01150","SJAG_03675","SJAG_01527","SJAG_01657","SJAG_04125","SJAG_00209","SJAG_03602","SJAG_01199","SJAG_03869","SJAG_04632","SJAG_04150","SJAG_01873","SJAG_00984","SJAG_04435","SJAG_02667","SJAG_05012","SJAG_04551","SJAG_02542","SJAG_03330","SJAG_01585","SJAG_02990","SJAG_02223","SJAG_04613","SJAG_00805","SJAG_01887","SJAG_00623","SJAG_02822","SJAG_02181","SJAG_05280","SJAG_05180","SJAG_03855","SJAG_01044","SJAG_02433","SJAG_02267","SJAG_01354","SJAG_01652","SJAG_04147","SJAG_00500","SJAG_00460","SJAG_04183","SJAG_02521","SJAG_03166","SJAG_03325","SJAG_01160","SJAG_01051","SJAG_04036","SJAG_04287","SJAG_04791","SJAG_00668","SJAG_02592","SJAG_02918","SJAG_00814","SJAG_04018","SJAG_04097","SJAG_03185","SJAG_01181","SJAG_06642","SJAG_05197","SJAG_03097","SJAG_04778","SJAG_04210","SJAG_00931","SJAG_00153","SJAG_02341","SJAG_02774","SJAG_03529","SJAG_03653","SJAG_04031","SJAG_04668","SJAG_00335","SJAG_02266","SJAG_00233","SJAG_04512","SJAG_04788","SJAG_03032","SJAG_01855","SJAG_04677","SJAG_01624","SJAG_04388","SJAG_01119","SJAG_00729","SJAG_02616","SJAG_02303","SJAG_04067","SJAG_02866","SJAG_01419","SJAG_03613","SJAG_04877","SJAG_03815","SJAG_02858","SJAG_02091","SJAG_00564","SJAG_00790","SJAG_00045","SJAG_02169","SJAG_02098","SJAG_00293","SJAG_01216","SJAG_04118","SJAG_02576","SJAG_04242","SJAG_03319","SJAG_03519","SJAG_00475","SJAG_03501","SJAG_01307","SJAG_03722","SJAG_03665","SJAG_05173","SJAG_03949","SJAG_02837","SJAG_02527","SJAG_03543","SJAG_00406","SJAG_00718","SJAG_02575","SJAG_04989","SJAG_00941","SJAG_02945","SJAG_02381","SJAG_00758","SJAG_00819","SJAG_04332","SJAG_00786","SJAG_00696","SJAG_04522","SJAG_02424","SJAG_02771","SJAG_07000","SJAG_04726","SJAG_04457","SJAG_02298","SJAG_01832","SJAG_02200","SJAG_00364","SJAG_03486","SJAG_03841","SJAG_02573","SJAG_01938","SJAG_04471","SJAG_03724","SJAG_02026","SJAG_04904","SJAG_00429","SJAG_05286","SJAG_00642","SJAG_03702","SJAG_00365","SJAG_00027","SJAG_00823","SJAG_02883","SJAG_00853","SJAG_00250","SJAG_02226","SJAG_00681","SJAG_04793","SJAG_01067","SJAG_01807","SJAG_00380","SJAG_02237","SJAG_00690","SJAG_06611","SJAG_01162","SJAG_04384","SJAG_01854","SJAG_04567","SJAG_00863","SJAG_06622","SJAG_00082","SJAG_01528","SJAG_00349","SJAG_00441","SJAG_01262","SJAG_00419","SJAG_02465","SJAG_01184","SJAG_04353","SJAG_02973","SJAG_02439","SJAG_01204","SJAG_06597","SJAG_00141","SJAG_04190","SJAG_01084","SJAG_02187","SJAG_00256","SJAG_04046","SJAG_01799","SJAG_01737","SJAG_02182","SJAG_01626","SJAG_03048","SJAG_00573","SJAG_01134","SJAG_02545","SJAG_00640","SJAG_02460","SJAG_05181","SJAG_01186","SJAG_02878","SJAG_03227","SJAG_01777","SJAG_01584","SJAG_03206","SJAG_01173","SJAG_02485","SJAG_01942","SJAG_03780","SJAG_00727","SJAG_00884","SJAG_03068","SJAG_02500","SJAG_03051","SJAG_00534","SJAG_00845","SJAG_02690","SJAG_02515","SJAG_02563","SJAG_03160","SJAG_02392","SJAG_03309","SJAG_01648","SJAG_02334","SJAG_03893","SJAG_01572","SJAG_03753","SJAG_00552","SJAG_00436","SJAG_05373","SJAG_05282","SJAG_00409","SJAG_00226","SJAG_03345","SJAG_02708","SJAG_03728","SJAG_03926","SJAG_01245","SJAG_01573","SJAG_04612","SJAG_00208","SJAG_00288","SJAG_04508","SJAG_03417","SJAG_03611","SJAG_05105","SJAG_03903","SJAG_01644","SJAG_02039","SJAG_03153","SJAG_05257","SJAG_02198","SJAG_02528","SJAG_02680","SJAG_03657","SJAG_03371","SJAG_02199","SJAG_04140","SJAG_04151","SJAG_00796","SJAG_00857","SJAG_02135","SJAG_02069","SJAG_04932","SJAG_03612","SJAG_04368","SJAG_04666","SJAG_03436","SJAG_05372","SJAG_01038","SJAG_01480","SJAG_03579","SJAG_01677","SJAG_02872","SJAG_01049","SJAG_02495","SJAG_04540","SJAG_00935","SJAG_04199","SJAG_00596","SJAG_04011","SJAG_04103","SJAG_05295","SJAG_04039","SJAG_00627","SJAG_02082","SJAG_04873","SJAG_00270","SJAG_02348","SJAG_02294","SJAG_01556","SJAG_03145","SJAG_01253","SJAG_01734","SJAG_01768","SJAG_01858","SJAG_04142","SJAG_01878","SJAG_00119","SJAG_05237","SJAG_04971","SJAG_02416","SJAG_00948","SJAG_03886","SJAG_02262","SJAG_04671","SJAG_01971","SJAG_02426","SJAG_02701","SJAG_01776","SJAG_02748","SJAG_01698","SJAG_02419","SJAG_03792","SJAG_01762","SJAG_03527","SJAG_02104","SJAG_04583","SJAG_02694","SJAG_03969","SJAG_04825","SJAG_04953","SJAG_03828","SJAG_05353","SJAG_03628","SJAG_05232","SJAG_04399","SJAG_00131","SJAG_03026","SJAG_01509","SJAG_01332","SJAG_00512","SJAG_00198","SJAG_00610","SJAG_03482","SJAG_00611","SJAG_04995","SJAG_00187","SJAG_04816","SJAG_02556","SJAG_00757","SJAG_00996","SJAG_00221","SJAG_00661","SJAG_00424","SJAG_04879","SJAG_01611","SJAG_04743","SJAG_03797","SJAG_03230","SJAG_01076","SJAG_04725","SJAG_02703","SJAG_02908","SJAG_02261","SJAG_03942","SJAG_00302","SJAG_03941","SJAG_02380","SJAG_05014","SJAG_00530","SJAG_03680","SJAG_03720","SJAG_03994","SJAG_03288","SJAG_03924","SJAG_01656","SJAG_02249","SJAG_03454","SJAG_04843","SJAG_00901","SJAG_01516","SJAG_04403","SJAG_04032","SJAG_04530","SJAG_04410","SJAG_00766","SJAG_04383","SJAG_00995","SJAG_04418","SJAG_02044","SJAG_04573","SJAG_00312","SJAG_03618","SJAG_00457","SJAG_01708","SJAG_03906","SJAG_02539","SJAG_02828","SJAG_03237","SJAG_05304","SJAG_04055","SJAG_01540","SJAG_03734","SJAG_04187","SJAG_01010","SJAG_03896","SJAG_01970","SJAG_00783","SJAG_06621","SJAG_02072","SJAG_00177","SJAG_00369","SJAG_03898","SJAG_00173","SJAG_00169","SJAG_01221","SJAG_00219","SJAG_01207","SJAG_01885","SJAG_00980","SJAG_04823"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[72836,79680,93459,62309,92314,118747,95635,105738,116059,69771],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006284"},{"annotations":[73825,69763,76624,74268],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006285"},{"annotations":[78006],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0097510"},{"annotations":[74838,73918],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006287"},{"annotations":[92021,110773,101931],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000196"},{"annotations":[94954,118100,99787,104841,108636,117178],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061692"},{"annotations":[87151,102008],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070458"},{"annotations":[78732,104108],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070370"},{"annotations":[92160],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071474"},{"annotations":[71904,73271,94438,71277,73756,75600,94981],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034198"},{"annotations":[89259],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071473"},{"annotations":[75716,69730,98212,100225,116290,75710],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042149"},{"annotations":[96243,95451,91843,104792,109801,88587,105078,100322,109802,115306,90565,115305],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034605"},{"annotations":[101008,111509,116793,109651],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071456"},{"annotations":[93870,93862,103573,100271,77257],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010106"},{"annotations":[70618,109804,109803,112086,87821,103996],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071218"},{"annotations":[102009],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071500"},{"annotations":[102580,106297,116092,114271,91645,116886,94124,104317,110140,95732],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071470"},{"annotations":[95323,114272,74739,75345,89844,108739,66778,101646,107603,73386,95749,76560,93322,73032,74896,97397,108734,108737,91916,77339,108738,76643,88308,63742,108735,67860,89943,90643,78806,69921,108736,108740],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034599"},{"annotations":[107376,113142,113143,71819],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016036"},{"annotations":[99959],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071472"},{"annotations":[94387,74448,80187,76924,71311,72179,78097,76152],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009267"},{"annotations":[109805,109806,102713],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034620"},{"annotations":[107803,109544,110131,113425,109440],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071629"},{"annotations":[94623],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0045007"},{"annotations":[69764,74269],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006307"},{"annotations":[73772,74407,112410,101102,69975,72243,106289,112408,66035,103066,103135,73588,69297,89741,100858,112409,118411,117388,90478],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006974"},{"annotations":[95770,88907,111522,71840,72521,88285,79886],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000729"},{"annotations":[65249,75462,74780,71946,64598],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000730"},{"annotations":[87548,112742,77129,71353,61296,88643,72057,87875,97196,59423,68208,96455,112240,71178,95968,70163,91293,70761,73573,77953,112744,112743,112745,118521,77854,114452,58561,72612,65834,97955,71053],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006281"},{"annotations":[107529,103824,99178,104513,92550,94828,98688,99462,89797,94065,96997,92131,104010,88619,90448,94366,94584,98926,106675,108866,98748,112952,114522,115405,118373,73448],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0140861"},{"annotations":[74834,73912],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045004"},{"annotations":[78317],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000731"},{"annotations":[76678,94995,108909,102614],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1904161"},{"annotations":[71422,91546,79135,75662,115551,71390,78926,117519,117107],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006302"},{"annotations":[88287,88908,107461,116606,98843],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990918"},{"annotations":[79748,69588,99068,80057,71744,73169,70586,77135,74327,111830,74042,72972,77932],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000727"},{"annotations":[116134,113695],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097680"},{"annotations":[77475,77505,100397,76901,94634,103940,106102,116607,117675,70537,74063,102983,74985,72127,88909,78591,70296,79171,77863,105539,96452,71001,87790,69819,111287,117532,88139,80008,107549,116061,76761,103654,111525,79041,96868,100958,74610,90622,73968,79161],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000724"},{"annotations":[99728,104827,111526,110742,116608,114086,88289,88910],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006303"},{"annotations":[110616,76718,76198],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045002"},{"annotations":[74611],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000736"},{"annotations":[70697,107945,117256,77704],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045003"},{"annotations":[70895,70319,67766,113609,114012,116586,98500,115838,75990,117036,76948,101025,106976,113880],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0030968"},{"annotations":[111777,93329,70318,74065,78465,74568,116402,78236,78484,97615,116964,107973,79210,94745,91159,73004,104611,98006,71874,89294,102714,87539,115666,70894,100556,70379,70705,107908,94478,78264,78422,70291,104527,75989,107473],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036503"},{"annotations":[102665,104012,60759,99093,70070,66444],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0070987"},{"annotations":[74735,102666,104013,70068,95637,72961,77503,77710],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0042276"},{"annotations":[95638],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061674"},{"annotations":[69655,109470,79926,99226],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140469"},{"annotations":[87920],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070911"},{"annotations":[115393],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031142"},{"annotations":[87540,103197,112786,89007],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0180027"},{"annotations":[77705,104755,75192,96926],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036297"},{"annotations":[92855,77624],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0036498"},{"annotations":[103619],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1901481"},{"annotations":[102589,103622],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1901482"},{"annotations":[79028,116610,107551],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000706"},{"annotations":[78292],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000707"},{"annotations":[107463,110101],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0010772"},{"annotations":[91517,107552],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000710"},{"annotations":[100433],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1902346"},{"annotations":[71992,69409,72271,71044,64433,105739,72231,115491,73379,116062,73111,70848],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006298"},{"annotations":[99095,102667,76051,70856,102687,108356,95905,112314,113705],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043504"},{"annotations":[79039],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097552"},{"annotations":[77345],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034514"},{"annotations":[110995,114273,77735,93323,79772,115814,116041],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044773"},{"annotations":[91063,109471],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031571"},{"annotations":[100325,100838,91188,71911,89962,117524,79037,74944,99147,109119,91551,88867,111527,106417,116826],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007095"},{"annotations":[88913,73574,91189,99148,107466,94300,102148,74043,78928,100645,106418,78593,111528,115872,88868,79042,90199,111833,95773],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031573"},{"annotations":[72857],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031990"},{"annotations":[99227,106845,107411,103589,95612,118126],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1903138"},{"annotations":[115423,74920,99122,109473,69580,94126],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990625"},{"annotations":[102153],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:2001033"},{"annotations":[77307,77808],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1904293"},{"annotations":[111557],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1904332"},{"annotations":[111510,105696,90994],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:2000639"},{"annotations":[89341],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036299"},{"annotations":[76184,110651],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071630"},{"annotations":[61748,69679,80010,65765,67266,63609,68243,78592,116519,58410,76903,111040,76625,75982,71991,116064,74046,88377,92319,72270],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006289"},{"annotations":[92757,93422,109833,69770,74612],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:1901255"},{"annotations":[74839,73919,79902,76677],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006297"},{"annotations":[108783],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006294"},{"annotations":[87830,92176,90522,102631,89184],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1903139"},{"annotations":[116201,89009],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1900039"},{"annotations":[111834,117086],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0045739"},{"annotations":[109981,93642],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:2000781"},{"annotations":[107206],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:2001034"},{"annotations":[101173,87595],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1905287"},{"annotations":[78126],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:2000640"},{"annotations":[104214,88378,87757,116914,76712,116593,95775,98031],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006301"},{"annotations":[89513,79538],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031848"},{"annotations":[98094,105891],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106300"},{"annotations":[105742],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006290"},{"annotations":[116501,116502],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000720"},{"annotations":[98849,111383,100436,102985],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036298"},{"annotations":[102119,90561,77263,75194,97273],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000725"},{"annotations":[102176],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1904547"},{"annotations":[103750,103118,94983],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990611"},{"annotations":[90666,72369],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:2000779"},{"annotations":[109120],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0010569"},{"annotations":[89945,91281,89548],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:2000815"},{"annotations":[88728,57879,68274,64774,60664,92894,89150,74019,99061],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0019430"},{"annotations":[74752,69467,71970,74947],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990414"},{"annotations":[72532,104477,96317,79896,118213],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034976"},{"annotations":[78791,75240],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030970"},{"annotations":[97898],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990516"},{"annotations":[93460,76656],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000012"},{"annotations":[116203,103761,92399,64666,93645,88733,89398,101899,112362,118252,63561,89012,118044,68322,112618],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032933"},{"annotations":[90918,90625,90010,71436,96504,87921,88106,69697,91734,109183,78598],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006283"},{"annotations":[98095],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0019985"},{"annotations":[93306,95469],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097466"},{"annotations":[75433,87758,93423,65413,69772,104018,105743,66074,112631,59958,64458,67214,95779,68349,96897],"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 the organism is under stress. The stress is usually, but not necessarily, exogenous (e.g. temperature, humidity, ionizing radiation).","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to stress","termid":"GO:0006950"},{"relation_name":"is_a","term_name":"cellular response to stimulus","termid":"GO:0051716"}],"gene_count":480,"genes_by_uniquename":{"SJAG_00027":null,"SJAG_00045":null,"SJAG_00054":null,"SJAG_00082":null,"SJAG_00111":null,"SJAG_00119":null,"SJAG_00126":null,"SJAG_00131":null,"SJAG_00141":null,"SJAG_00153":null,"SJAG_00169":null,"SJAG_00173":null,"SJAG_00177":null,"SJAG_00187":null,"SJAG_00198":null,"SJAG_00208":null,"SJAG_00209":null,"SJAG_00213":null,"SJAG_00219":null,"SJAG_00221":null,"SJAG_00226":null,"SJAG_00233":null,"SJAG_00250":null,"SJAG_00256":null,"SJAG_00270":null,"SJAG_00272":null,"SJAG_00288":null,"SJAG_00293":null,"SJAG_00302":null,"SJAG_00312":null,"SJAG_00327":null,"SJAG_00329":null,"SJAG_00335":null,"SJAG_00349":null,"SJAG_00364":null,"SJAG_00365":null,"SJAG_00369":null,"SJAG_00380":null,"SJAG_00403":null,"SJAG_00406":null,"SJAG_00409":null,"SJAG_00419":null,"SJAG_00424":null,"SJAG_00429":null,"SJAG_00436":null,"SJAG_00441":null,"SJAG_00457":null,"SJAG_00460":null,"SJAG_00475":null,"SJAG_00486":null,"SJAG_00500":null,"SJAG_00512":null,"SJAG_00530":null,"SJAG_00534":null,"SJAG_00552":null,"SJAG_00564":null,"SJAG_00573":null,"SJAG_00596":null,"SJAG_00610":null,"SJAG_00611":null,"SJAG_00618":null,"SJAG_00623":null,"SJAG_00627":null,"SJAG_00634":null,"SJAG_00640":null,"SJAG_00642":null,"SJAG_00661":null,"SJAG_00668":null,"SJAG_00681":null,"SJAG_00690":null,"SJAG_00696":null,"SJAG_00718":null,"SJAG_00727":null,"SJAG_00729":null,"SJAG_00757":null,"SJAG_00758":null,"SJAG_00766":null,"SJAG_00781":null,"SJAG_00783":null,"SJAG_00786":null,"SJAG_00790":null,"SJAG_00796":null,"SJAG_00805":null,"SJAG_00814":null,"SJAG_00819":null,"SJAG_00823":null,"SJAG_00845":null,"SJAG_00853":null,"SJAG_00857":null,"SJAG_00863":null,"SJAG_00884":null,"SJAG_00901":null,"SJAG_00931":null,"SJAG_00935":null,"SJAG_00941":null,"SJAG_00948":null,"SJAG_00980":null,"SJAG_00984":null,"SJAG_00995":null,"SJAG_00996":null,"SJAG_01010":null,"SJAG_01038":null,"SJAG_01044":null,"SJAG_01049":null,"SJAG_01051":null,"SJAG_01067":null,"SJAG_01076":null,"SJAG_01084":null,"SJAG_01114":null,"SJAG_01119":null,"SJAG_01134":null,"SJAG_01146":null,"SJAG_01150":null,"SJAG_01160":null,"SJAG_01162":null,"SJAG_01173":null,"SJAG_01181":null,"SJAG_01184":null,"SJAG_01186":null,"SJAG_01199":null,"SJAG_01204":null,"SJAG_01205":null,"SJAG_01207":null,"SJAG_01216":null,"SJAG_01221":null,"SJAG_01245":null,"SJAG_01253":null,"SJAG_01262":null,"SJAG_01292":null,"SJAG_01307":null,"SJAG_01332":null,"SJAG_01354":null,"SJAG_01385":null,"SJAG_01410":null,"SJAG_01419":null,"SJAG_01429":null,"SJAG_01480":null,"SJAG_01509":null,"SJAG_01516":null,"SJAG_01527":null,"SJAG_01528":null,"SJAG_01540":null,"SJAG_01556":null,"SJAG_01572":null,"SJAG_01573":null,"SJAG_01584":null,"SJAG_01585":null,"SJAG_01605":null,"SJAG_01611":null,"SJAG_01620":null,"SJAG_01624":null,"SJAG_01626":null,"SJAG_01644":null,"SJAG_01648":null,"SJAG_01652":null,"SJAG_01656":null,"SJAG_01657":null,"SJAG_01677":null,"SJAG_01680":null,"SJAG_01698":null,"SJAG_01708":null,"SJAG_01709":null,"SJAG_01734":null,"SJAG_01737":null,"SJAG_01762":null,"SJAG_01768":null,"SJAG_01776":null,"SJAG_01777":null,"SJAG_01787":null,"SJAG_01799":null,"SJAG_01807":null,"SJAG_01832":null,"SJAG_01854":null,"SJAG_01855":null,"SJAG_01858":null,"SJAG_01873":null,"SJAG_01878":null,"SJAG_01885":null,"SJAG_01887":null,"SJAG_01938":null,"SJAG_01942":null,"SJAG_01970":null,"SJAG_01971":null,"SJAG_01979":null,"SJAG_02026":null,"SJAG_02031":null,"SJAG_02039":null,"SJAG_02044":null,"SJAG_02069":null,"SJAG_02072":null,"SJAG_02079":null,"SJAG_02082":null,"SJAG_02091":null,"SJAG_02098":null,"SJAG_02104":null,"SJAG_02116":null,"SJAG_02135":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_02244":null,"SJAG_02249":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_02341":null,"SJAG_02342":null,"SJAG_02348":null,"SJAG_02380":null,"SJAG_02381":null,"SJAG_02385":null,"SJAG_02392":null,"SJAG_02416":null,"SJAG_02419":null,"SJAG_02424":null,"SJAG_02426":null,"SJAG_02433":null,"SJAG_02439":null,"SJAG_02460":null,"SJAG_02465":null,"SJAG_02474":null,"SJAG_02485":null,"SJAG_02495":null,"SJAG_02500":null,"SJAG_02503":null,"SJAG_02515":null,"SJAG_02521":null,"SJAG_02527":null,"SJAG_02528":null,"SJAG_02539":null,"SJAG_02542":null,"SJAG_02545":null,"SJAG_02556":null,"SJAG_02563":null,"SJAG_02573":null,"SJAG_02575":null,"SJAG_02576":null,"SJAG_02592":null,"SJAG_02601":null,"SJAG_02616":null,"SJAG_02667":null,"SJAG_02680":null,"SJAG_02685":null,"SJAG_02690":null,"SJAG_02694":null,"SJAG_02698":null,"SJAG_02699":null,"SJAG_02701":null,"SJAG_02703":null,"SJAG_02708":null,"SJAG_02724":null,"SJAG_02748":null,"SJAG_02771":null,"SJAG_02774":null,"SJAG_02785":null,"SJAG_02818":null,"SJAG_02822":null,"SJAG_02828":null,"SJAG_02837":null,"SJAG_02858":null,"SJAG_02866":null,"SJAG_02872":null,"SJAG_02878":null,"SJAG_02883":null,"SJAG_02908":null,"SJAG_02918":null,"SJAG_02945":null,"SJAG_02973":null,"SJAG_02990":null,"SJAG_03026":null,"SJAG_03032":null,"SJAG_03048":null,"SJAG_03051":null,"SJAG_03068":null,"SJAG_03092":null,"SJAG_03097":null,"SJAG_03145":null,"SJAG_03153":null,"SJAG_03160":null,"SJAG_03166":null,"SJAG_03185":null,"SJAG_03206":null,"SJAG_03221":null,"SJAG_03227":null,"SJAG_03230":null,"SJAG_03237":null,"SJAG_03256":null,"SJAG_03263":null,"SJAG_03288":null,"SJAG_03302":null,"SJAG_03303":null,"SJAG_03309":null,"SJAG_03319":null,"SJAG_03325":null,"SJAG_03330":null,"SJAG_03345":null,"SJAG_03371":null,"SJAG_03414":null,"SJAG_03417":null,"SJAG_03436":null,"SJAG_03454":null,"SJAG_03482":null,"SJAG_03486":null,"SJAG_03501":null,"SJAG_03519":null,"SJAG_03527":null,"SJAG_03529":null,"SJAG_03543":null,"SJAG_03579":null,"SJAG_03602":null,"SJAG_03611":null,"SJAG_03612":null,"SJAG_03613":null,"SJAG_03618":null,"SJAG_03628":null,"SJAG_03653":null,"SJAG_03657":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_03753":null,"SJAG_03780":null,"SJAG_03792":null,"SJAG_03797":null,"SJAG_03815":null,"SJAG_03828":null,"SJAG_03841":null,"SJAG_03855":null,"SJAG_03869":null,"SJAG_03886":null,"SJAG_03893":null,"SJAG_03896":null,"SJAG_03898":null,"SJAG_03903":null,"SJAG_03906":null,"SJAG_03924":null,"SJAG_03926":null,"SJAG_03941":null,"SJAG_03942":null,"SJAG_03949":null,"SJAG_03969":null,"SJAG_03994":null,"SJAG_04011":null,"SJAG_04018":null,"SJAG_04031":null,"SJAG_04032":null,"SJAG_04036":null,"SJAG_04039":null,"SJAG_04046":null,"SJAG_04055":null,"SJAG_04063":null,"SJAG_04067":null,"SJAG_04082":null,"SJAG_04089":null,"SJAG_04097":null,"SJAG_04103":null,"SJAG_04114":null,"SJAG_04118":null,"SJAG_04125":null,"SJAG_04140":null,"SJAG_04142":null,"SJAG_04147":null,"SJAG_04150":null,"SJAG_04151":null,"SJAG_04183":null,"SJAG_04187":null,"SJAG_04190":null,"SJAG_04199":null,"SJAG_04205":null,"SJAG_04210":null,"SJAG_04242":null,"SJAG_04262":null,"SJAG_04272":null,"SJAG_04280":null,"SJAG_04283":null,"SJAG_04287":null,"SJAG_04311":null,"SJAG_04332":null,"SJAG_04345":null,"SJAG_04353":null,"SJAG_04368":null,"SJAG_04372":null,"SJAG_04383":null,"SJAG_04384":null,"SJAG_04388":null,"SJAG_04399":null,"SJAG_04403":null,"SJAG_04410":null,"SJAG_04418":null,"SJAG_04429":null,"SJAG_04435":null,"SJAG_04457":null,"SJAG_04471":null,"SJAG_04508":null,"SJAG_04512":null,"SJAG_04522":null,"SJAG_04530":null,"SJAG_04540":null,"SJAG_04551":null,"SJAG_04567":null,"SJAG_04573":null,"SJAG_04583":null,"SJAG_04612":null,"SJAG_04613":null,"SJAG_04632":null,"SJAG_04666":null,"SJAG_04668":null,"SJAG_04671":null,"SJAG_04677":null,"SJAG_04725":null,"SJAG_04726":null,"SJAG_04743":null,"SJAG_04778":null,"SJAG_04788":null,"SJAG_04791":null,"SJAG_04793":null,"SJAG_04816":null,"SJAG_04823":null,"SJAG_04825":null,"SJAG_04843":null,"SJAG_04873":null,"SJAG_04877":null,"SJAG_04879":null,"SJAG_04904":null,"SJAG_04932":null,"SJAG_04953":null,"SJAG_04971":null,"SJAG_04989":null,"SJAG_04995":null,"SJAG_05000":null,"SJAG_05012":null,"SJAG_05014":null,"SJAG_05020":null,"SJAG_05022":null,"SJAG_05105":null,"SJAG_05173":null,"SJAG_05180":null,"SJAG_05181":null,"SJAG_05197":null,"SJAG_05232":null,"SJAG_05237":null,"SJAG_05239":null,"SJAG_05257":null,"SJAG_05274":null,"SJAG_05280":null,"SJAG_05282":null,"SJAG_05286":null,"SJAG_05295":null,"SJAG_05304":null,"SJAG_05323":null,"SJAG_05353":null,"SJAG_05372":null,"SJAG_05373":null,"SJAG_06597":null,"SJAG_06611":null,"SJAG_06621":null,"SJAG_06622":null,"SJAG_06642":null,"SJAG_07000":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":"cellular response to stress","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000108":null,"GO_REF:0000117":null},"secondary_identifiers":["Reactome:R-HSA-2262752"],"termid":"GO:0033554","terms_by_termid":{"GO:0000012":null,"GO:0000196":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: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:0009267":null,"GO:0010106":null,"GO:0010569":null,"GO:0010772":null,"GO:0016036":null,"GO:0019430":null,"GO:0019985":null,"GO:0030968":null,"GO:0030970":null,"GO:0031142":null,"GO:0031571":null,"GO:0031573":null,"GO:0031848":null,"GO:0031990":null,"GO:0032933":null,"GO:0034198":null,"GO:0034514":null,"GO:0034599":null,"GO:0034605":null,"GO:0034620":null,"GO:0034976":null,"GO:0036297":null,"GO:0036298":null,"GO:0036299":null,"GO:0036498":null,"GO:0036503":null,"GO:0042149":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:0061692":null,"GO:0070370":null,"GO:0070458":null,"GO:0070911":null,"GO:0070914":null,"GO:0070987":null,"GO:0071218":null,"GO:0071456":null,"GO:0071470":null,"GO:0071472":null,"GO:0071473":null,"GO:0071474":null,"GO:0071500":null,"GO:0071629":null,"GO:0071630":null,"GO:0097466":null,"GO:0097510":null,"GO:0097552":null,"GO:0097680":null,"GO:0106300":null,"GO:0140469":null,"GO:0140861":null,"GO:0180027":null,"GO:1900039":null,"GO:1901255":null,"GO:1901481":null,"GO:1901482":null,"GO:1902346":null,"GO:1903138":null,"GO:1903139":null,"GO:1904161":null,"GO:1904293":null,"GO:1904332":null,"GO:1904547":null,"GO:1905287":null,"GO:1990414":null,"GO:1990516":null,"GO:1990611":null,"GO:1990625":null,"GO:1990918":null,"GO:2000639":null,"GO:2000640":null,"GO:2000779":null,"GO:2000781":null,"GO:2000815":null,"GO:2001033":null,"GO:2001034":null}}


id: PBO:0076393
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptional adaptor 1","termid":"PBO:0076393"}


id: PBO:0046348
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 6","termid":"PBO:0046348"}


id: GO:0052241
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of a motile cell or organism towards a higher concentration of a specific chemical on or near a second organism, where the two organisms are in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete positive chemotaxis on or near other organism involved in symbiotic interaction (obsolete GO:0052241)","synonyms":[{"name":"positive chemotaxis on or near other organism during symbiotic interaction","type":"related"}],"termid":"GO:0052241"}


id: MOD:00480
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Isotopic label","definition_xrefs":["URL:http://www.appliedbiosystems.com/products/productdetail.cfm?prod_id=153","Unimod:105#C","OMSSA:129"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isotope tagged reagent derivatized residue","termid":"MOD:01426"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Applied Biosystems cleavable ICAT(TM) light","synonyms":[{"name":"Applied Biosystems cleavable ICAT(TM) light","type":"related"},{"name":"ICAT-C","type":"related"},{"name":"icatlight","type":"exact"}],"termid":"MOD:00480"}


id: PBO:0030177
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_3'-5'-exoribonuclease_activity","termid":"PBO:0030177"}


id: PBO:0062259
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 5 subfamily D member 15 pseudogene","termid":"PBO:0062259"}


id: MONDO:0003096
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hemangioma arising from the deep soft tissues.","definition_xrefs":["NCIT:C6555"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hemangioma","termid":"MONDO:0006500"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deep hemangioma","secondary_identifiers":["DOID:469","MEDGEN:232421","UMLS:C1333265"],"synonyms":[{"name":"deep angioma","type":"exact"},{"name":"deep hemangioma","type":"exact"}],"termid":"MONDO:0003096","xrefs":{"Monarch":{"xref_id":"0003096"}}}


id: GO:0018204
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The modification of peptidyl-leucine.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidyl-amino acid modification","termid":"GO:0018193"}],"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":"peptidyl-leucine modification","termid":"GO:0018204"}


id: GO:0090245
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The developmental growth that results in the elongation of the rostral-caudal axis that contributes to somitogenesis.","definition_xrefs":["GOC:dph","GOC:tb","GOC:ascb_2009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"axis elongation","termid":"GO:0003401"},{"relation_name":"part_of","term_name":"somitogenesis","termid":"GO:0001756"}],"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":"axis elongation involved in somitogenesis","termid":"GO:0090245"}


id: PBO:0045508
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"destrin, actin depolymerizing factor","termid":"PBO:0045508"}


id: PBO:0039395
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anaphase promoting complex subunit 1","termid":"PBO:0039395"}


id: GO:0060954
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process aimed at the progression of a neural crest-derived cardiac glial cell over time, from initial commitment of the cell to a specific fate, to the fully functional differentiated cell.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiac glial cell development","termid":"GO:0060952"},{"relation_name":"part_of","term_name":"neural crest-derived cardiac glial cell differentiation","termid":"GO:0060951"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"neural crest-derived cardiac glial cell development","termid":"GO:0060954"}


id: PATO:0001155
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001155 absolute concentration (obsolete PATO:0001155)","termid":"PATO:0001155"}


id: MONDO:0019636
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Unilateral renal agenesis (URA) is a form of renal agenesis characterized by the complete absence of development of one kidney accompanied by an absent ureter.","definition_xrefs":["Orphanet:93100"],"direct_ancestors":[{"relation_name":"is_a","term_name":"renal agenesis","termid":"MONDO:0018470"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"renal agenesis, unilateral","secondary_identifiers":["GARD:16804","MedDRA:10053624","icd11.foundation:760295498","ICD10CM:Q60.0","MEDGEN:75607","NCIT:C101220","UMLS:C0266294"],"synonyms":[{"name":"congenital single kidney","type":"exact"},{"name":"congenital solitary kidney","type":"exact"},{"name":"unilateral renal agenesis","type":"exact"}],"termid":"MONDO:0019636","xrefs":{"Monarch":{"xref_id":"0019636"}}}


id: FYPO:0008223
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed during the G2/M phase of the mitotic cell cycle in which trimethylation of lysine at position 20 of histone H4 is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PMID:27268234"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal histone H4-K20 monomethylation during vegetative growth","termid":"FYPO:0004220"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001312","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"normal histone H4-K20 trimethylation during mitotic G2/M phase","termid":"FYPO:0008223"}


id: PBO:0066534
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 1","termid":"PBO:0066534"}


id: PBO:0056109
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lysophospholipase 2","termid":"PBO:0056109"}


id: PBO:0066664
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RHO family interacting cell polarization regulator 1","termid":"PBO:0066664"}


id: PBO:0065505
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paraspeckle component 1 pseudogene 2","termid":"PBO:0065505"}


id: PBO:0063736
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PHB1 pseudogene 1","termid":"PBO:0063736"}


id: PBO:0064482
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA polymerase iota","termid":"PBO:0064482"}


id: PBO:0034414
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-regulates_process_that_acts_on_population_of","termid":"PBO:0034414"}


id: PBO:0039687
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"APC regulator of WNT signaling pathway","termid":"PBO:0039687"}


id: FYPO:0005040
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the phosphorylation of the serine residue at position 2 within one or more copies of the heptapeptide repeat (YSPTSPS) of the C-terminal domain of RNA polymerase II normal (i.e. indistinguishable from wild type) when the cell is subject to nitrogen starvation.","definition_xrefs":["GO:0071620","PMID:22144909","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein phosphorylation during nitrogen starvation","termid":"FYPO:0005035"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal phosphorylation of RNA polymerase II C-terminal domain serine 2 residues during nitrogen starvation","synonyms":[{"name":"normal phosphorylation of RNA polymerase II C-terminal domain serine 2 residues during nitrogen deprivation","type":"exact"},{"name":"normal phosphorylation of RNA polymerase II CTD serine 2 residues during nitrogen depletion","type":"exact"}],"termid":"FYPO:0005040"}


id: GO:1900347
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 methanethiol.","definition_xrefs":["GOC:TermGenie","GOC:mengo_curators"],"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 methanethiol","termid":"GO:1900345"},{"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 methanethiol","termid":"GO:2001133"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006790"},{"rel_name":"positively_regulates","termid":"GO:0006091"},{"rel_name":"regulates","termid":"GO:0006091"}],"interesting_parent_ids":["GO:0008150","GO:0006790","GO:0006091"],"is_obsolete":false,"name":"positive regulation of methane biosynthetic process from methanethiol","synonyms":[{"name":"activation of methane biosynthetic process from methanethiol","type":"narrow"},{"name":"up regulation of methane biosynthetic process from methanethiol","type":"exact"},{"name":"up-regulation of methane biosynthetic process from methanethiol","type":"exact"},{"name":"upregulation of methane biosynthetic process from methanethiol","type":"exact"}],"termid":"GO:1900347"}


id: MONDO:0017585
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"benign peripheral nerve sheath tumor","termid":"MONDO:0016752"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"painful orbital and systemic neurofibromas-marfanoid habitus syndrome","secondary_identifiers":["Orphanet:300501","MEDGEN:1650687","GARD:11006","UMLS:C4751109"],"synonyms":[{"name":"multiple orbital neurofibromas, painful peripheral nerve tumors, distinctive face and marfanoid habitus","type":"related"}],"termid":"MONDO:0017585","xrefs":{"Monarch":{"xref_id":"0017585"}}}


id: PBO:0073985
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 24 member 5","termid":"PBO:0073985"}


id: MONDO:0020807
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A sex cord-stromal tumor that arises from the ovary and is composed entirely of, or in various combinations of, Sertoli cells, Leydig cells, and fibroblast-like cells.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ovarian sex cord-stromal tumor","termid":"MONDO:0021657"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ovarian sertoli-stromal cell tumor","secondary_identifiers":["NCIT:C39966","MEDGEN:309515","UMLS:C1518732"],"synonyms":[{"name":"Ovarian Sertoli-Stromal Cell Tumor","type":"exact"},{"name":"Ovarian Sertoli-Stromal Cell Tumour","type":"exact"},{"name":"Ovarian Sertoli-Stromal Tumor","type":"exact"},{"name":"Ovarian Sertoli-Stromal Tumour","type":"exact"}],"termid":"MONDO:0020807","xrefs":{"Monarch":{"xref_id":"0020807"}}}


id: GO:1902415
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of mRNA binding.","definition_xrefs":["GOC:TermGenie","PMID:22890846","GOC:rb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of binding","termid":"GO:0051098"}],"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 mRNA binding","termid":"GO:1902415"}


id: GO:0030546
data:
  {"annotated_genes":["SJAG_05000"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[99240],"is_not":false,"summary":null,"term":"GO:0030546"}]},"cv_name":"molecular_function","definition":"The function of interacting (directly or indirectly) with receptors such that the proportion of receptors in the active form is increased.","definition_xrefs":["GOC:ceb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"signaling receptor regulator activity","termid":"GO:0030545"},{"relation_name":"is_a","term_name":"molecular function activator activity","termid":"GO:0140677"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05000":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0140677"}],"interesting_parent_ids":["GO:0098772","GO:0140677","GO:0003674"],"is_obsolete":false,"name":"signaling receptor activator activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"receptor activator activity","type":"broad"},{"name":"signalling receptor activator activity","type":"exact"}],"termid":"GO:0030546","terms_by_termid":{"GO:0030546":null}}


id: GO:0072288
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of a metanephric proximal tubule are generated and organized. The metanephric proximal tubule is a metanephric nephron tubule that connects Bowman's capsule to the descending thin limb of the loop of Henle in the metanephros. It has a brush border epithelial morphology.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proximal tubule morphogenesis","termid":"GO:0072158"},{"relation_name":"is_a","term_name":"metanephric nephron tubule morphogenesis","termid":"GO:0072282"},{"relation_name":"part_of","term_name":"metanephric proximal tubule development","termid":"GO:0072237"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"metanephric proximal tubule morphogenesis","termid":"GO:0072288"}


id: FYPO:0006206
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 is decreased during a cellular response to phosphate starvation.","definition_xrefs":["PMID:19933844","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein localization to chromatin during vegetative growth","termid":"FYPO:0002909"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000002","FYPO:0000138","FYPO:0001320"],"is_obsolete":false,"name":"decreased protein localization to chromatin during cellular response to phosphate starvation","synonyms":[{"name":"decreased protein localisation to chromatin during cellular response to phosphate starvation","type":"exact"},{"name":"decreased protein localization to chromatin during cellular response to phosphate ion starvation","type":"exact"},{"name":"decreased protein localization to chromatin during cellular response to phosphate starvation during mitotic cell cycle","type":"related"},{"name":"decreased protein localization to chromatin during cellular response to phosphate starvation during vegetative growth","type":"exact"},{"name":"reduced protein localization to chromatin during cellular response to phosphate starvation","type":"exact"}],"termid":"FYPO:0006206"}


id: PBO:0078886
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Gln (anticodon CTG) 1-3","termid":"PBO:0078886"}


id: GO:1905335
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of aggrephagy.","definition_xrefs":["GOC:pad","GOC:PARL","PMID:25686248","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of macroautophagy","termid":"GO:0016241"},{"relation_name":"regulates","term_name":"aggrephagy","termid":"GO:0035973"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006914"}],"interesting_parent_ids":["GO:0008150","GO:0006914"],"is_obsolete":false,"name":"regulation of aggrephagy","termid":"GO:1905335"}


id: PBO:0013477
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aldehyde dehydrogenase Atd3 (predicted)","termid":"PBO:0013477"}


id: PR:Q9P6I1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ubc16 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P6I1"],"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":"ubiquitin-conjugating enzyme E2 16 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1198.09","synonyms":[{"name":"E2 ubiquitin-conjugating enzyme 16 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-ubc16","type":"exact"},{"name":"ubiquitin carrier protein 16 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"ubiquitin-protein ligase 16 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9P6I1"}


id: MONDO:0009609
data:
  {"annotated_genes":["SJAG_04425"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85614],"is_not":false,"summary":null,"term":"MONDO:0009609"}]},"cv_name":"mondo","definition":"Methylcobalamin deficiency cbl G type is a rare condition that occurs when the body is unable to process certain amino acids (building blocks of protein) properly. In most cases, signs and symptoms develop during the first year of life; however, the age of onset can range from infancy to adulthood. Common features of the condition include feeding difficulties, lethargy, seizures, poor muscle tone (hypotonia), developmental delay, microcephaly (unusually small head size), and megaloblastic anemia. Methylcobalamin deficiency cbl G type is caused by changes (mutations) in the MTR gene and is inherited in an autosomal recessive manner. Treatment generally includes regular doses of hydroxycobalamin (vitamin B12). Some affected people may also require supplementation with folates and betaine.","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"kidney disorder","termid":"MONDO:0005240"},{"relation_name":"excluded_subClassOf","term_name":"thrombotic microangiopathy","termid":"MONDO:0019737"},{"relation_name":"is_a","term_name":"homocystinuria without methylmalonic aciduria","termid":"MONDO:0018964"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04425":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004736"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005066","MONDO:0004736","MONDO:0002280","MONDO:0005570"],"is_obsolete":false,"name":"methylcobalamin deficiency type cblG","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:250940","GARD:3577","MEDGEN:344426","DOID:0112256","UMLS:C1855128","DOID:0050733","NANDO:2201111","Orphanet:2170","SCTID:721187005"],"synonyms":[{"name":"HMAG","type":"related"},{"name":"cblG","type":"related"},{"name":"functional methionine synthase deficiency type cblG","type":"exact"},{"name":"homocystinuria due to defect in methylation Cbl g","type":"related"},{"name":"homocystinuria-megaloblastic Anaemia due to defect in cobalamin metabolism, cblG complementation type","type":"related"},{"name":"homocystinuria-megaloblastic Anemia due to defect in cobalamin metabolism, cblG complementation type","type":"related"},{"name":"homocystinuria-megaloblastic anemia, cblG complementation type","type":"related"},{"name":"methionine synthase deficiency","type":"related"},{"name":"methylcobalamin deficiency Cbl G type","type":"related"},{"name":"methylcobalamin deficiency type cblG","type":"exact"},{"name":"methylcobalamin deficiency, cblG type","type":"related"},{"name":"methylmalonic aciduria and homocystinuria type cblG","type":"related"}],"termid":"MONDO:0009609","terms_by_termid":{"MONDO:0009609":null},"xrefs":{"Monarch":{"xref_id":"0009609"}}}


id: PBO:0074654
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 41B","termid":"PBO:0074654"}


id: GO:0015364
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: dicarboxylate(out) + phosphate(in) = dicarboxylate(in) +  phosphate(out).","definition_xrefs":["TC:2.A.29.2.3"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dicarboxylic acid transmembrane transporter activity","termid":"GO:0005310"},{"relation_name":"is_a","term_name":"phosphate transmembrane transporter activity","termid":"GO:0005315"},{"relation_name":"is_a","term_name":"solute:inorganic anion antiporter activity","termid":"GO:0005452"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"dicarboxylate:phosphate antiporter activity","synonyms":[{"name":"dicarboxylate:inorganic phosphate antiporter activity","type":"exact"}],"termid":"GO:0015364"}


id: GO:1903343
data:
  {"annotated_genes":["SJAG_03048","SJAG_00100"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[108159,102166],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905263"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of meiotic DNA double-strand break formation.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:25103240"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of DNA metabolic process","termid":"GO:0051054"},{"relation_name":"is_a","term_name":"positive regulation of cell cycle process","termid":"GO:0090068"},{"relation_name":"is_a","term_name":"regulation of meiotic DNA double-strand break formation","termid":"GO:1903341"},{"relation_name":"is_a","term_name":"positive regulation of reproductive process","termid":"GO:2000243"},{"relation_name":"positively_regulates","term_name":"meiotic DNA double-strand break formation","termid":"GO:0042138"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00100":null,"SJAG_03048":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"positively_regulates","termid":"GO:0007049"},{"rel_name":"positively_regulates","termid":"GO:0006259"},{"rel_name":"regulates","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007049","GO:0008150","GO:0006259"],"is_obsolete":false,"name":"positive regulation of meiotic DNA double-strand break formation","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"activation of meiotic DNA double-strand break formation","type":"narrow"},{"name":"up regulation of meiotic DNA double-strand break formation","type":"exact"},{"name":"up-regulation of meiotic DNA double-strand break formation","type":"exact"},{"name":"upregulation of meiotic DNA double-strand break formation","type":"exact"}],"termid":"GO:1903343","terms_by_termid":{"GO:1905263":null}}


id: GO:0002078
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The fusion of the plasma membrane of the sperm with the outer acrosomal membrane.","definition_xrefs":["PMID:3886029","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular process involved in reproduction in multicellular organism","termid":"GO:0022412"},{"relation_name":"is_a","term_name":"membrane fusion","termid":"GO:0061025"},{"relation_name":"part_of","term_name":"acrosome reaction","termid":"GO:0007340"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0061024"],"is_obsolete":false,"name":"membrane fusion involved in acrosome reaction","synonyms":[{"name":"membrane fusion involved in the acrosomal reaction","type":"exact"}],"termid":"GO:0002078"}


id: GO:0160021
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of gene expression by which developmental control passes from the maternal genome to the zygotic genome.","definition_xrefs":["PMID:32558204","PMID:19204068"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of gene expression","termid":"GO:0010468"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"maternal-to-zygotic transition of gene expression","secondary_identifiers":["Reactome:R-HSA-9816359"],"synonyms":[{"name":"MZT","type":"related"}],"termid":"GO:0160021"}


id: GO:0047882
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: AH(2) + estradiol-17beta + O2 = 6beta-hydroxyestradiol-17beta + A + H2O.","definition_xrefs":["EC:1.14.99.11","RHEA:19137"],"direct_ancestors":[{"relation_name":"is_a","term_name":"steroid hydroxylase activity","termid":"GO:0008395"},{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen","termid":"GO:0016705"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"estradiol 6-beta-monooxygenase activity","secondary_identifiers":["MetaCyc:ESTRADIOL-6-BETA-MONOOXYGENASE-RXN","KEGG_REACTION:R03086"],"synonyms":[{"name":"estradiol 6-beta-hydroxylase activity","type":"related"},{"name":"estradiol 6b-hydroxylase activity","type":"exact"},{"name":"estradiol 6b-monooxygenase activity","type":"exact"},{"name":"estradiol 6beta-hydroxylase activity","type":"related"},{"name":"estradiol 6beta-monooxygenase activity","type":"related"},{"name":"estradiol-17beta,hydrogen-donor:oxygen oxidoreductase (6beta-hydroxylating)","type":"related"}],"termid":"GO:0047882"}


id: PBO:0072289
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S24 pseudogene 7","termid":"PBO:0072289"}


