# terms

id: GO:0070702
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The inner of two mucus layers secreted by epithelial cells in the colon; the inner mucus layer is firmly attached to the epithelium, is densely packed with a compact stratified appearance and is devoid of bacteria.","definition_xrefs":["PMID:18806221","PMID:19432394","GOC:mah","GOC:mm2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mucus layer","termid":"GO:0070701"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005576"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005576"],"is_obsolete":false,"name":"inner mucus layer","termid":"GO:0070702"}


id: GO:0051793
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of a medium-chain fatty acid. A medium-chain fatty acid has an aliphatic tail containing 6 to 12 carbons.","definition_xrefs":["Wikipedia:Fatty_acid_metabolism"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fatty acid catabolic process","termid":"GO:0009062"},{"relation_name":"is_a","term_name":"medium-chain fatty acid metabolic process","termid":"GO:0051791"}],"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:0008150","GO:0044281","GO:0006629"],"is_obsolete":false,"name":"medium-chain fatty acid catabolic process","synonyms":[{"name":"medium chain fatty acid catabolic process","type":"exact"},{"name":"medium chain fatty acid catabolism","type":"exact"},{"name":"medium-chain fatty acid breakdown","type":"exact"},{"name":"medium-chain fatty acid catabolism","type":"exact"},{"name":"medium-chain fatty acid degradation","type":"exact"}],"termid":"GO:0051793"}


id: GO:0001776
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of regulating the proliferation and elimination of cells of the immune system such that the total number of cells of a particular cell type within a whole or part of an organism is stable over time in the absence of an outside stimulus.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune system process","termid":"GO:0002376"},{"relation_name":"is_a","term_name":"homeostasis of number of cells","termid":"GO:0048872"}],"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":"leukocyte homeostasis","synonyms":[{"name":"immune cell homeostasis","type":"exact"},{"name":"leucocyte homeostasis","type":"exact"}],"termid":"GO:0001776"}


id: PBO:0045929
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EF-hand domain containing 2","termid":"PBO:0045929"}


id: PBO:0086624
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm and nucleus; YCR090C is not an essential gene","termid":"PBO:0086624"}


id: PBO:0042601
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDRT15 pseudogene 1","termid":"PBO:0042601"}


id: MONDO:0012015
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nystagmus","termid":"MONDO:0005712"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"nystagmus 3, congenital, autosomal dominant","secondary_identifiers":["OMIM:608345","UMLS:C1842186","MESH:C537855","MEDGEN:374873","DOID:0111793"],"synonyms":[{"name":"NYS3","type":"exact"},{"name":"NYSTAGMUS 3, congenital, autosomal dominant","type":"related"}],"termid":"MONDO:0012015","xrefs":{"Monarch":{"xref_id":"0012015"}}}


id: GO:0071610
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The appearance of chemokine (C-C motif) ligand 1 due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["GOC:rv","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chemokine production","termid":"GO:0032602"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"chemokine (C-C motif) ligand 1 production","synonyms":[{"name":"CCL1 production","type":"exact"},{"name":"T cell activation 3 production","type":"exact"},{"name":"TCA-3 production","type":"exact"}],"termid":"GO:0071610"}


id: PBO:0073992
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 25 member 2","termid":"PBO:0073992"}


id: PBO:0076174
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sulfotransferase family 1C member 5, pseudogene","termid":"PBO:0076174"}


id: PBO:0089891
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amino acid transmembrane transporter Dip5","termid":"PBO:0089891"}


id: GO:1901591
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of double-strand break repair via break-induced replication.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of double-strand break repair via homologous recombination","termid":"GO:0010569"},{"relation_name":"regulates","term_name":"double-strand break repair via break-induced replication","termid":"GO:0000727"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006281"},{"rel_name":"regulates","termid":"GO:0006310"},{"rel_name":"regulates","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006310","GO:0006281","GO:0006259"],"is_obsolete":false,"name":"regulation of double-strand break repair via break-induced replication","termid":"GO:1901591"}


id: FYPO:0007394
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which the structure of one or more RNA molecules differs from normal.","definition_xrefs":["PMID:24793650","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal phenotype","termid":"FYPO:0001985"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985"],"is_obsolete":false,"name":"abnormal RNA structure","synonyms":[{"name":"abnormal RNA secondary structure","type":"narrow"}],"termid":"FYPO:0007394"}


id: PBO:0028999
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_transcription_from_SRE_promoter","termid":"PBO:0028999"}


id: GO:0140065
data:
  {"annotated_genes":["SJAG_02990"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[99295],"is_not":false,"summary":null,"term":"GO:0140065"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: butyryl-CoA + lysine in peptide = CoA + N-butyryl-lysine-peptide.","definition_xrefs":["PMID:27105113"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-acyltransferase activity","termid":"GO:0016410"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02990":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016740","GO:0016746"],"is_obsolete":false,"name":"peptide butyryltransferase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["RHEA:53912"],"synonyms":[{"name":"protein butyryltransferase activity","type":"related"}],"termid":"GO:0140065","terms_by_termid":{"GO:0140065":null}}


id: GO:0006735
data:
  {"annotated_genes":["SJAG_02191","SJAG_02154"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[95444,95445],"is_not":false,"summary":null,"term":"GO:0006735"}]},"cv_name":"biological_process","definition":"A metabolic process that generates a pool of NADH by the reduction of NAD+.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"NADH metabolic process","termid":"GO:0006734"},{"relation_name":"is_a","term_name":"NAD metabolic process","termid":"GO:0019674"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02154":null,"SJAG_02191":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0055086","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"NADH regeneration","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"NAD (reduced) regeneration","type":"exact"},{"name":"reduced NAD regeneration","type":"exact"},{"name":"reduced nicotinamide adenine dinucleotide regeneration","type":"exact"}],"termid":"GO:0006735","terms_by_termid":{"GO:0006735":null}}


id: MONDO:0020423
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"coronary artery congenital malformation","termid":"MONDO:0015203"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"stenosis or atrophy of the coronary ostium","secondary_identifiers":["Orphanet:99087","UMLS:C5575847","MEDGEN:1842382","GARD:19643"],"synonyms":[{"name":"coronary ostial stenosis or atresia","type":"exact"},{"name":"stenosis or atresia of the coronary ostium","type":"related"}],"termid":"MONDO:0020423","xrefs":{"Monarch":{"xref_id":"0020423"}}}


id: FYPO:0007181
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the site of cell division is normal (i.e. indistinguishable from wild type) during anaphase of mitosis.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to cell division site","termid":"FYPO:0002442"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000138","FYPO:0001320","FYPO:0001312","FYPO:0000002"],"is_obsolete":false,"name":"normal protein localization to cell division site during mitotic anaphase","synonyms":[{"name":"normal protein localisation to cell division site during mitotic anaphase","type":"exact"},{"name":"normal protein localization to cell division site during anaphase of mitotic cell cycle","type":"exact"},{"name":"normal protein recruitment to cell division site during mitotic anaphase","type":"related"}],"termid":"FYPO:0007181"}


id: GO:0097613
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The part of a dinoflagellate cell above the cingulum; also referred to as the anterior portion of a dinoflagellate cell. It is separated from the hypocone by the cingulum.","definition_xrefs":["GOC:at","Wikipedia:Dinoflagellate#Morphology"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"dinoflagellate epicone","synonyms":[{"name":"epicone","type":"broad"},{"name":"episome","type":"related"},{"name":"epitheca","type":"related"}],"termid":"GO:0097613"}


id: GO:1903567
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of protein localization to ciliary membrane.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","GOC:krc","PMID:22072986","GOC:cilia"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein localization to cilium","termid":"GO:1903564"},{"relation_name":"is_a","term_name":"regulation of protein localization to cell periphery","termid":"GO:1904375"},{"relation_name":"is_a","term_name":"regulation of protein localization to membrane","termid":"GO:1905475"},{"relation_name":"regulates","term_name":"protein localization to ciliary membrane","termid":"GO:1903441"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of protein localization to ciliary membrane","synonyms":[{"name":"regulation of protein localisation in ciliary membrane","type":"exact"},{"name":"regulation of protein localisation to ciliary membrane","type":"exact"},{"name":"regulation of protein localization in ciliary membrane","type":"exact"}],"termid":"GO:1903567"}


id: MONDO:0016163
data:
  {"annotated_genes":["SJAG_00087"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86259],"is_not":false,"summary":null,"term":"MONDO:0016163"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant cerebellar ataxia","termid":"MONDO:0020380"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00087":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0002039"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0005559","MONDO:0002039"],"is_obsolete":false,"name":"autosomal dominant cerebellar ataxia type II","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:20405","Orphanet:94147","UMLS:C0752125","MEDGEN:156006","NCIT:C126562","OMIM:164500","SCTID:715726000","Orphanet:208508","DOID:0050958"],"synonyms":[{"name":"ADCA, type II","type":"related"},{"name":"ADCA2","type":"exact"},{"name":"ADCAII","type":"exact"},{"name":"ATXN7 autosomal dominant cerebellar ataxia type II","type":"exact"},{"name":"Adca, type 2","type":"related"},{"name":"OPCA 3","type":"related"},{"name":"OPCA III","type":"related"},{"name":"OPCA with macular Degeneration and external ophthalmoplegia","type":"related"},{"name":"OPCA with retinal Degeneration","type":"related"},{"name":"OPCA3","type":"related"},{"name":"SCA7","type":"exact"},{"name":"ataxia with pigmentary retinopathy","type":"exact"},{"name":"autosomal dominant cerebellar ataxia type 2","type":"exact"},{"name":"autosomal dominant cerebellar ataxia type II","type":"exact"},{"name":"autosomal dominant cerebellar ataxia type II caused by mutation in ATXN7","type":"exact"},{"name":"autosomal dominant cerebellar ataxia, type 2","type":"related"},{"name":"cerebellar syndrome-pigmentary maculopathy syndrome","type":"exact"},{"name":"olivopontocerebellar atrophy 3","type":"related"},{"name":"spinocerebellar ataxia 7","type":"related"},{"name":"spinocerebellar ataxia type 7","type":"exact"}],"termid":"MONDO:0016163","terms_by_termid":{"MONDO:0016163":null},"xrefs":{"Monarch":{"xref_id":"0016163"}}}


id: PBO:0057551
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 664b","termid":"PBO:0057551"}


id: GO:0002190
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process where translation initiation recruits the 40S ribosomal subunits in a Cap and 5' end independent fashion before an AUG codon is encountered in an appropriate sequence context to initiate mRNA or circRNA translation.","definition_xrefs":["PMID:17284590"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoplasmic translational initiation","termid":"GO:0002183"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0002181"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0002181","GO:0010467"],"is_obsolete":false,"name":"cap-independent translational initiation","termid":"GO:0002190"}


id: PBO:0004232
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ClC chloride channel (predicted)","termid":"PBO:0004232"}


id: PBO:0077971
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Ala (anticodon AGC) 23-1","termid":"PBO:0077971"}


id: GO:0004203
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete caspase-4 activity (obsolete GO:0004203)","synonyms":[{"name":"caspase-4 activity","type":"exact"}],"termid":"GO:0004203"}


id: MONDO:0012939
data:
  {"annotated_genes":["SJAG_02046"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87124],"is_not":false,"summary":null,"term":"MONDO:0012939"}]},"cv_name":"mondo","definition":"Any Diamond-Blackfan anemia in which the cause of the disease is a mutation in the RPS7 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Diamond-Blackfan anemia","termid":"MONDO:0015253"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02046":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0002280"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0002280"],"is_obsolete":false,"name":"Diamond-Blackfan anemia 8","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:390817","GARD:15570","MESH:C567253","DOID:0111881","NCIT:C176917","OMIM:612563","UMLS:C2675511"],"synonyms":[{"name":"DBA8","type":"related"},{"name":"Diamond-Blackfan Anaemia type 8","type":"exact"},{"name":"Diamond-Blackfan Anemia type 8","type":"exact"},{"name":"Diamond-Blackfan anaemia caused by mutation in RPS7","type":"exact"},{"name":"Diamond-Blackfan anemia 8","type":"exact"},{"name":"Diamond-Blackfan anemia caused by mutation in RPS7","type":"exact"},{"name":"RPS7 Diamond-Blackfan anaemia","type":"exact"},{"name":"RPS7 Diamond-Blackfan anemia","type":"exact"}],"termid":"MONDO:0012939","terms_by_termid":{"MONDO:0012939":null},"xrefs":{"Monarch":{"xref_id":"0012939"}}}


id: PBO:0083346
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; overlaps the verified gene DDR48/YML173W","termid":"PBO:0083346"}


id: MONDO:0033367
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"developmental and epileptic encephalopathy","termid":"MONDO:0100062"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"},{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0700092","MONDO:0005027"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy, 58","secondary_identifiers":["DOID:0080285","UMLS:C4693367","GARD:16259","OMIM:617830","MEDGEN:1646861"],"synonyms":[{"name":"DEE58","type":"exact"},{"name":"EIEE58","type":"exact"},{"name":"developmental and epileptic encephalopathy 58","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 58","type":"exact"},{"name":"infantile epileptic encephalopathy 58","type":"exact"}],"termid":"MONDO:0033367","xrefs":{"Monarch":{"xref_id":"0033367"}}}


id: MONDO:0700106
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Immune system disorder that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-human animal disease","termid":"MONDO:0005583"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immune system disorder, non-human animal","termid":"MONDO:0700106","xrefs":{"Monarch":{"xref_id":"0700106"}}}


id: GO:0022880
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the PEP-dependent, phosphoryl transfer-driven transport of substances across a membrane. The transport happens by catalysis of the reaction: protein N-phosphohistidine + N-acetylglucosamine(out) = protein histidine + N-acetylglucosamine phosphate(in). This differs from primary and secondary active transport in that the solute is modified during transport.","definition_xrefs":["GOC:mtg_transport","ISBN:0815340729"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-N(PI)-phosphohistidine-sugar phosphotransferase activity","termid":"GO:0008982"},{"relation_name":"is_a","term_name":"N-acetylglucosamine transmembrane transporter activity","termid":"GO:0015572"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"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:0022857"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0022857","GO:0016740","GO:0005215"],"is_obsolete":false,"name":"protein-N(PI)-phosphohistidine-N-acetylglucosamine phosphotransferase system transporter activity","synonyms":[{"name":"N-acetylglucosamine PTS transporter activity","type":"exact"}],"termid":"GO:0022880"}


id: PBO:0002886
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA replication factor C complex subunit Ctf8 (predicted)","termid":"PBO:0002886"}


id: PBO:0082003
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger SWIM-type containing 4","termid":"PBO:0082003"}


id: GO:0035827
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Enables the transfer of rubidium ions (Rb+) from one side of a membrane to the other.","definition_xrefs":["GOC:yaf"],"gene_count":0,"genotype_count":0,"name":"obsolete rubidium ion transmembrane transporter activity (obsolete GO:0035827)","synonyms":[{"name":"Rb+ transmembrane transporter activity","type":"exact"},{"name":"rubidium cation transmembrane transporter activity","type":"exact"},{"name":"rubidium transmembrane transporter activity","type":"related"}],"termid":"GO:0035827"}


id: GO:0001868
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the lectin pathway of complement activation.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of complement activation","termid":"GO:0030449"},{"relation_name":"is_a","term_name":"regulation of innate immune response","termid":"GO:0045088"},{"relation_name":"regulates","term_name":"complement activation, lectin pathway","termid":"GO:0001867"}],"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 complement activation, lectin pathway","synonyms":[{"name":"regulation of complement cascade, lectin pathway","type":"exact"}],"termid":"GO:0001868"}


id: MONDO:0008678
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare genetic multisystemic neurodevelopmental disorder characterized by a distinct facial appearance, cardiac anomalies (most frequently supravalvular aortic stenosis), cognitive and developmental abnormalities, and connective tissue abnormalities (such as joint laxity)","definition_xrefs":["Orphanet:904"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"excluded_subClassOf","term_name":"nervous system disorder","termid":"MONDO:0005071"},{"relation_name":"excluded_subClassOf","term_name":"heart disorder","termid":"MONDO:0005267"},{"relation_name":"excluded_subClassOf","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"excluded_subClassOf","term_name":"obsolete motor stereotypies (obsolete MONDO:0017656)","termid":"MONDO:0017656"},{"relation_name":"excluded_subClassOf","term_name":"obsolete syndromic epicanthus (obsolete MONDO:0020165)","termid":"MONDO:0020165"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"partial deletion of the long arm of chromosome 7","termid":"MONDO:0016906"},{"relation_name":"is_a","term_name":"neurodevelopmental disorder","termid":"MONDO:0700092"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"Williams syndrome","secondary_identifiers":["DECIPHER:3","NANDO:2200286","NCIT:C85232","NORD:1854","GARD:7891","ICD9:759.89","OMIM:194050","MedDRA:10049644","NANDO:1200664","DOID:1928","SCTID:63247009","UMLS:C0175702","MEDGEN:59799","MESH:D018980"],"synonyms":[{"name":"Fanconi Schlesinger syndrome","type":"exact"},{"name":"WBS","type":"related"},{"name":"WMS","type":"related"},{"name":"Williams syndrome","type":"exact"},{"name":"Williams-Beuren syndrome","type":"exact"},{"name":"Williams-Beuren syndrome (WBS)","type":"exact"},{"name":"chromosome 7Q11.23 deletion syndrome, 1.5- to 1.8-Mb","type":"related"},{"name":"deletion 7q11.23","type":"exact"},{"name":"monosomy 7q11.23","type":"exact"}],"termid":"MONDO:0008678","xrefs":{"Monarch":{"xref_id":"0008678"}}}


id: null:chado_properties:version
data:
  {"annotation_feature_type":"gene","cv_name":"chado_properties","definition":"Chado schema version","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"version","termid":"null:chado_properties:version"}


id: MONDO:1011015
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cerebellar degeneration that occurs in chicken.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bird disease","termid":"MONDO:0024905"},{"relation_name":"is_a","term_name":"cerebellar degeneration, non-human animal","termid":"MONDO:1010243"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cerebellar degeneration, chicken","secondary_identifiers":["OMIA:001221-9031"],"termid":"MONDO:1011015","xrefs":{"Monarch":{"xref_id":"1011015"}}}


id: PBO:0078698
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Leu (anticodon CAA) 1-1","termid":"PBO:0078698"}


id: MONDO:0019920
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Paternal uniparental disomy of chromosome 5 is an uniparental disomy of paternal origin that most likely does not have any phenotypic expression except from cases of homozygosity for a recessive disease mutation for which only father is a carrier.","definition_xrefs":["Orphanet:96190"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome 5 disorder","termid":"MONDO:0700012"},{"relation_name":"is_a","term_name":"uniparental disomy","termid":"MONDO:0700086"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paternal uniparental disomy of chromosome 5","secondary_identifiers":["UMLS:C4749377","GARD:19339","MEDGEN:1652849","icd11.foundation:1224981751"],"synonyms":[{"name":"UPD(5)pat","type":"exact"},{"name":"paternal uniparental disomy of chromosome type 5","type":"exact"}],"termid":"MONDO:0019920","xrefs":{"Monarch":{"xref_id":"0019920"}}}


id: MOD:01145
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-histidine residue to N-tau-(ADP-ribosyl)diphthamide.","definition_xrefs":["ChEBI:82697","DeltaMass:0"],"direct_ancestors":[{"relation_name":"derives_from","term_name":"2'-[3-carboxamido-3-(trimethylammonio)propyl]-L-histidine","termid":"MOD:00049"},{"relation_name":"is_a","term_name":"adenosine diphosphoribosyl (ADP-ribosyl) modified residue","termid":"MOD:00752"},{"relation_name":"is_a","term_name":"modified L-histidine residue","termid":"MOD:00909"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-tau-(ADP-ribosyl)diphthamide","synonyms":[{"name":"MOD_RES ADP-ribosyldiphthamide","type":"exact"}],"termid":"MOD:01145"}


id: MONDO:0024985
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Diseases of domestic and mountain sheep of the genus Ovis.","definition_xrefs":["MESH:D012757"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-human animal disease","termid":"MONDO:0005583"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sheep disease","synonyms":[{"name":"Ovine disease","type":"related"},{"name":"Ovine diseases","type":"related"},{"name":"disease, Ovine","type":"related"},{"name":"disease, sheep","type":"related"},{"name":"diseases, Ovine","type":"related"},{"name":"diseases, sheep","type":"related"},{"name":"sheep disease","type":"exact"}],"termid":"MONDO:0024985","xrefs":{"Monarch":{"xref_id":"0024985"}}}


id: PBO:0045183
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DnaJ heat shock protein family (Hsp40) member B4","termid":"PBO:0045183"}


id: MONDO:0013474
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the JPH2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial hypertrophic cardiomyopathy","termid":"MONDO:0024573"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"hypertrophic cardiomyopathy 17","secondary_identifiers":["MEDGEN:462614","OMIM:613873","UMLS:C3151264","DOID:0110323"],"synonyms":[{"name":"CMH17","type":"exact"},{"name":"JPH2 hypertrophic cardiomyopathy","type":"exact"},{"name":"cardiomyopathy familial hypertrophic 17","type":"exact"},{"name":"cardiomyopathy, familial hypertrophic, 17","type":"related"},{"name":"cardiomyopathy, familial hypertrophic, type 17","type":"exact"},{"name":"cardiomyopathy, hypertrophic, 17","type":"exact"},{"name":"hypertrophic cardiomyopathy caused by mutation in JPH2","type":"exact"},{"name":"hypertrophic cardiomyopathy type 17","type":"exact"}],"termid":"MONDO:0013474","xrefs":{"Monarch":{"xref_id":"0013474"}}}


id: GO:2000655
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of cellular response to testosterone stimulus.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cellular process","termid":"GO:0048523"},{"relation_name":"is_a","term_name":"negative regulation of response to stimulus","termid":"GO:0048585"},{"relation_name":"is_a","term_name":"regulation of cellular response to testosterone stimulus","termid":"GO:2000654"},{"relation_name":"negatively_regulates","term_name":"cellular response to testosterone stimulus","termid":"GO:0071394"}],"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 cellular response to testosterone stimulus","termid":"GO:2000655"}


id: GO:0035615
data:
  {"annotated_genes":["SJAG_00152","SJAG_00800","SJAG_04565","SJAG_01167","SJAG_02805","SJAG_04609","SJAG_02453","SJAG_03726","SJAG_04931","SJAG_00379","SJAG_00108","SJAG_00104","SJAG_01809"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[58324,62228,72399,74702,78096,78115,78454,89249,94527,96466,108653,111809,113094],"is_not":false,"summary":null,"term":"GO:0035615"}]},"cv_name":"molecular_function","definition":"Bringing together a cargo protein with clathrin, responsible for the formation of endocytic vesicles.","definition_xrefs":["GOC:BHF","PMID:15728179"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cargo adaptor activity","termid":"GO:0140312"}],"gene_count":13,"genes_by_uniquename":{"SJAG_00104":null,"SJAG_00108":null,"SJAG_00152":null,"SJAG_00379":null,"SJAG_00800":null,"SJAG_01167":null,"SJAG_01809":null,"SJAG_02453":null,"SJAG_02805":null,"SJAG_03726":null,"SJAG_04565":null,"SJAG_04609":null,"SJAG_04931":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0030674"},{"rel_name":"is_a","termid":"GO:0060090"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0030674","GO:0060090"],"is_obsolete":false,"name":"clathrin adaptor activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"clathrin-associated adaptor activity","type":"exact"}],"termid":"GO:0035615","terms_by_termid":{"GO:0035615":null}}


id: PBO:0083503
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the verified ORF APL2/YKL135C","termid":"PBO:0083503"}


id: MONDO:0016431
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal dominant Charcot-Marie-Tooth disease type 2M (CMT2M) is a form of axonal Charcot-Marie-Tooth disease, a peripheral motor and sensory neuropathy. CMT2M is characterized by congenital pstosis and early cataract associated to a mildly progressive peripheral neuropathy of variable onset from birth to the 6th decade, pes cavus, reduced to absent ankles tendon reflexes and sometimes neutropenia.","definition_xrefs":["Orphanet:228179"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Charcot-Marie-Tooth disease dominant intermediate B","termid":"MONDO:0011674"},{"relation_name":"is_a","term_name":"Charcot-Marie-Tooth disease type 2","termid":"MONDO:0018993"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0005244","MONDO:0000426"],"is_obsolete":false,"name":"autosomal dominant Charcot-Marie-Tooth disease type 2M","secondary_identifiers":["icd11.foundation:1601555981","UMLS:C4304672","GARD:17147","SCTID:719514002","MEDGEN:930341"],"synonyms":[{"name":"CMT2M","type":"exact"}],"termid":"MONDO:0016431","xrefs":{"Monarch":{"xref_id":"0016431"}}}


id: MONDO:0015540
data:
  {"annotated_genes":["SJAG_03536","SJAG_02453","SJAG_01697","SJAG_02572"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86654],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012146"},{"annotations":[86029],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011336"},{"annotations":[86975],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013135"},{"annotations":[86333],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011997"}]},"cv_name":"mondo","definition":"Hemophagocytic syndrome (HPS) is a rare immune disease and a potentially life-threatening disorder characterized by cytokine storm and overwhelming inflammation causing fever, hepatosplenomegaly, cytopenia, hypertriglyceridemia, hyperferritinemia, and hemophagocytosis in bone marrow, liver, spleen or lymph nodes. It can be either primary due to a genetic defect (primary hemophagocytic lymphohistiocytosis), or secondary to malignancies, to infections, most commonly with viruses such as Epstein-Barr virus or cytomegalovirus, human immunodeficiency virus, or to autoimmune disorders such as systemic lupus erythematosus or adult-onset Still disease (secondary hemophagocytic lymphohistiocytosis).","definition_xrefs":["Orphanet:158032"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"lymphatic system disorder","termid":"MONDO:0005833"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01697":null,"SJAG_02453":null,"SJAG_02572":null,"SJAG_03536":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"hemophagocytic syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NCIT:C35439","NANDO:2200032","ICD9:288.8","GARD:20024","MEDGEN:854411","DOID:0050120","NCIT:C34792","MedDRA:10058125","UMLS:C3887558","SCTID:234437005","NORD:1938"],"synonyms":[{"name":"FHL","type":"related"},{"name":"HLH","type":"exact"},{"name":"Hemophagocytic Lymphohistiocytosis","type":"exact"},{"name":"familial erythrophagocytic lymphohistiocytosis","type":"related"},{"name":"familial hemophagocytic lymphohistiocytosis","type":"related"},{"name":"familial histiocytic reticulosis","type":"related"},{"name":"haemophagocytic syndrome","type":"related"},{"name":"hemophagocytic disorder","type":"related"},{"name":"hemophagocytic lymphohistiocytosis","type":"exact"},{"name":"hemophagocytic syndrome","type":"exact"}],"termid":"MONDO:0015540","terms_by_termid":{"MONDO:0011336":null,"MONDO:0011997":null,"MONDO:0012146":null,"MONDO:0013135":null},"xrefs":{"Monarch":{"xref_id":"0015540"}}}


id: MONDO:0013782
data:
  {"annotated_genes":["SJAG_04335"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87027],"is_not":false,"summary":null,"term":"MONDO:0013782"}]},"cv_name":"mondo","definition":"Any pseudohypoaldosteronism type 2 in which the cause of the disease is a mutation in the CUL3 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pseudohypoaldosteronism type 2","termid":"MONDO:0019162"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04335":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"pseudohypoaldosteronism type 2E","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:483336","GARD:17373","OMIM:614496","UMLS:C3469606","Orphanet:300530","icd11.foundation:1263491925"],"synonyms":[{"name":"CUL3 pseudohypoaldosteronism type 2","type":"exact"},{"name":"Cul3 pseudohypoaldosteronism type 2","type":"exact"},{"name":"PHA2E","type":"exact"},{"name":"pseudohypoaldosteronism type 2 caused by mutation in CUL3","type":"exact"},{"name":"pseudohypoaldosteronism type 2 caused by mutation in Cul3","type":"exact"},{"name":"pseudohypoaldosteronism, type 2E","type":"related"},{"name":"pseudohypoaldosteronism, type IIE","type":"related"}],"termid":"MONDO:0013782","terms_by_termid":{"MONDO:0013782":null},"xrefs":{"Monarch":{"xref_id":"0013782"}}}


id: GO:0035905
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the ascending aorta over time, from its initial formation to the mature structure. The ascending aorta is the portion of the aorta in a two-pass circulatory system that lies between the heart and the arch of aorta. In a two-pass circulatory system blood passes twice through the heart to supply the body once.","definition_xrefs":["Wikipedia:Ascending_aorta","GOC:bf","MA:0002570","GOC:dgh","UBERON:0001496"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"aorta development","termid":"GO:0035904"}],"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":"ascending aorta development","termid":"GO:0035905"}


id: GO:0061156
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the pulmonary artery are generated and organized. The pulmonary artery is the artery that carries blood from the heart to the lungs.","definition_xrefs":["GOC:dph","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"artery morphogenesis","termid":"GO:0048844"}],"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":"pulmonary artery morphogenesis","termid":"GO:0061156"}


id: GO:0043371
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of CD4-positive, alpha-beta T cell differentiation.","definition_xrefs":["GOC:pr","ISBN:0781735149","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of CD4-positive, alpha-beta T cell differentiation","termid":"GO:0043370"},{"relation_name":"is_a","term_name":"negative regulation of alpha-beta T cell differentiation","termid":"GO:0046639"},{"relation_name":"is_a","term_name":"negative regulation of CD4-positive, alpha-beta T cell activation","termid":"GO:2000515"},{"relation_name":"negatively_regulates","term_name":"CD4-positive, alpha-beta T cell differentiation","termid":"GO:0043367"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007155"},{"rel_name":"negatively_regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"negative regulation of CD4-positive, alpha-beta T cell differentiation","synonyms":[{"name":"down regulation of CD4-positive, alpha beta T cell differentiation","type":"exact"},{"name":"down-regulation of CD4-positive, alpha beta T cell differentiation","type":"exact"},{"name":"downregulation of CD4-positive, alpha beta T cell differentiation","type":"exact"},{"name":"inhibition of CD4-positive, alpha beta T cell differentiation","type":"narrow"},{"name":"negative regulation of CD4-positive T-cell differentiation","type":"exact"},{"name":"negative regulation of CD4-positive T-lymphocyte differentiation","type":"exact"},{"name":"negative regulation of CD4-positive, alpha beta T cell development","type":"related"},{"name":"negative regulation of CD4-positive, alpha beta T lymphocyte differentiation","type":"exact"},{"name":"negative regulation of CD4-positive, alpha beta T-cell differentiation","type":"exact"},{"name":"negative regulation of CD4-positive, alpha beta T-lymphocyte differentiation","type":"exact"}],"termid":"GO:0043371"}


id: GO:0048897
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation of compact myelin sheaths around the axons of a lateral line nerve.","definition_xrefs":["PMID:12112375"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myelination","termid":"GO:0042552"},{"relation_name":"part_of","term_name":"lateral line nerve glial cell morphogenesis involved in differentiation","termid":"GO:0048938"}],"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":"myelination of lateral line nerve axons","termid":"GO:0048897"}


id: GO:0062123
data:
  {"annotated_genes":["SJAG_03048"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[102708],"is_not":false,"summary":null,"term":"GO:0062123"}]},"cv_name":"biological_process","definition":"Any process that modulates the rate, frequency or extent of linear element maturation.","definition_xrefs":["PMID:30640914"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of chromosome organization","termid":"GO:0033044"},{"relation_name":"is_a","term_name":"regulation of linear element assembly","termid":"GO:0090006"},{"relation_name":"regulates","term_name":"linear element maturation","termid":"GO:0062121"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03048":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0044085","GO:0007049"],"is_obsolete":false,"name":"regulation of linear element maturation","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0062123","terms_by_termid":{"GO:0062123":null}}


id: GO:0035847
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of an epithelium of the uterus over time from its initial formation to the mature structure. An epithelium is a tissue that covers the internal or external surfaces of an anatomical structure.","definition_xrefs":["GOC:yaf","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oviduct epithelium development","termid":"GO:0035846"},{"relation_name":"part_of","term_name":"uterus development","termid":"GO:0060065"}],"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":"uterine epithelium development","synonyms":[{"name":"uterus epithelial development","type":"exact"}],"termid":"GO:0035847"}


id: GO:0047544
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: biphenyl-2-ol + H+ + NADH + O2 = biphenyl-2,3-diol + H2O + NAD+. Also converts 2,2'-dihydroxybiphenyl into 2,2',3-trihydroxy-biphenyl.","definition_xrefs":["EC:1.14.13.44"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen","termid":"GO:0016709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"2-hydroxybiphenyl 3-monooxygenase (NADH) activity","secondary_identifiers":["UM-BBD_reactionID:r1423","KEGG_REACTION:R03964"],"synonyms":[{"name":"2-hydroxybiphenyl,NADH:oxygen oxidoreductase (3-hydroxylating)","type":"related"}],"termid":"GO:0047544"}


id: FYPO:0005220
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 protein oligomerization is abnormal.","definition_xrefs":["PomBase:mah","GO:0051259"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein-containing complex assembly","termid":"FYPO:0000447"}],"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":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"abnormal protein oligomerization","synonyms":[{"name":"abnormal protein oligomerisation","type":"exact"},{"name":"abnormal protein oligomerization during mitotic cell cycle","type":"related"},{"name":"abnormal protein oligomerization during vegetative growth","type":"exact"}],"termid":"FYPO:0005220"}


id: GO:0016891
data:
  {"annotated_genes":["SJAG_02156","SJAG_04582","SJAG_02039","SJAG_02790","SJAG_01433","SJAG_02621","SJAG_00955","SJAG_04527","SJAG_00400","SJAG_00306","SJAG_01884","SJAG_01463","SJAG_04885","SJAG_04916","SJAG_03796","SJAG_00997","SJAG_02374","SJAG_03689","SJAG_04019","SJAG_01623","SJAG_02553","SJAG_06613","SJAG_03234","SJAG_05212","SJAG_06022"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[76775],"is_not":false,"summary":null,"term":"GO:0016891"},{"annotations":[70472,80697],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042781"},{"annotations":[118398],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070551"},{"annotations":[92041],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990174"},{"annotations":[77047,59956,60593,68100,73961],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004525"},{"annotations":[95049,97123,104879,60630,71581,115612,63765,68706,102377],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004526"},{"annotations":[78109],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0061632"},{"annotations":[77323],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008419"},{"annotations":[76323,80582,103265,88644],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004523"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of ester linkages within ribonucleic acids by creating internal breaks to yield 5'-phosphomonoesters.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA endonuclease activity","termid":"GO:0004521"}],"gene_count":25,"genes_by_uniquename":{"SJAG_00306":null,"SJAG_00400":null,"SJAG_00955":null,"SJAG_00997":null,"SJAG_01433":null,"SJAG_01463":null,"SJAG_01623":null,"SJAG_01884":null,"SJAG_02039":null,"SJAG_02156":null,"SJAG_02374":null,"SJAG_02553":null,"SJAG_02621":null,"SJAG_02790":null,"SJAG_03234":null,"SJAG_03689":null,"SJAG_03796":null,"SJAG_04019":null,"SJAG_04527":null,"SJAG_04582":null,"SJAG_04885":null,"SJAG_04916":null,"SJAG_05212":null,"SJAG_06022":null,"SJAG_06613":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016788"}],"interesting_parent_ids":["GO:0140098","GO:0016787","GO:0016788","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"RNA endonuclease activity, producing 5'-phosphomonoesters","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000003":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["EC:3.1.26.-"],"synonyms":[{"name":"endoribonuclease activity, producing 5'-phosphomonoesters","type":"exact"}],"termid":"GO:0016891","terms_by_termid":{"GO:0004523":null,"GO:0004525":null,"GO:0004526":null,"GO:0008419":null,"GO:0016891":null,"GO:0042781":null,"GO:0061632":null,"GO:0070551":null,"GO:1990174":null}}


id: PBO:0004667
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit L34 (predicted)","termid":"PBO:0004667"}


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


id: PBO:0066758
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 56","termid":"PBO:0066758"}


id: PBO:0089755
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glucose-6-phosphate 1-dehydrogenase","termid":"PBO:0089755"}


id: MONDO:0020045
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete autosomal recessive cerebellar ataxia due to a DNA repair defect (obsolete MONDO:0020045)","secondary_identifiers":["Orphanet:98097"],"termid":"MONDO:0020045","xrefs":{"Monarch":{"xref_id":"0020045"}}}


id: GO:1901983
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of protein acetylation.","definition_xrefs":["GOC:TermGenie","PMID:22117195"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein modification process","termid":"GO:0031399"},{"relation_name":"regulates","term_name":"protein acetylation","termid":"GO:0006473"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of protein acetylation","synonyms":[{"name":"regulation of protein amino acid acetylation","type":"exact"}],"termid":"GO:1901983"}


id: GO:0071265
data:
  {"annotated_genes":["SJAG_00309","SJAG_00881","SJAG_03614","SJAG_00395","SJAG_03881","SJAG_02972","SJAG_02293","SJAG_03671","SJAG_02689","SJAG_01404"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[111401,106314,68742,65593],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071266"},{"annotations":[77263,78220,80460,79583,58760,78671],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019509"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of L-methionine, the L-enantiomer of (2S)-2-amino-4-(methylsulfanyl)butanoic acid.","definition_xrefs":["GOC:ecd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methionine biosynthetic process","termid":"GO:0009086"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00309":null,"SJAG_00395":null,"SJAG_00881":null,"SJAG_01404":null,"SJAG_02293":null,"SJAG_02689":null,"SJAG_02972":null,"SJAG_03614":null,"SJAG_03671":null,"SJAG_03881":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006520","GO:0008150","GO:0006790","GO:0044281"],"is_obsolete":false,"name":"L-methionine biosynthetic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000107":null,"GO_REF:0000108":null},"synonyms":[{"name":"L-methionine anabolism","type":"exact"},{"name":"L-methionine biosynthesis","type":"exact"},{"name":"L-methionine formation","type":"exact"},{"name":"L-methionine synthesis","type":"exact"}],"termid":"GO:0071265","terms_by_termid":{"GO:0019509":null,"GO:0071266":null}}


id: PBO:0065225
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proline rich 5 like","termid":"PBO:0065225"}


id: GO:0019639
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of 6-hydroxycineole (6-hydroxy-1,8-epoxy-p-menthane), a hydrocarbon with the formula C10H18O2.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monoterpenoid catabolic process","termid":"GO:0016100"},{"relation_name":"is_a","term_name":"6-hydroxycineole metabolic process","termid":"GO:0019638"},{"relation_name":"is_a","term_name":"xenobiotic catabolic process","termid":"GO:0042178"},{"relation_name":"is_a","term_name":"ether catabolic process","termid":"GO:1901502"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"6-hydroxycineole catabolic process","secondary_identifiers":["MetaCyc:6-HYDROXYCINEOLE-DEGRADATION-PWY"],"synonyms":[{"name":"6-endo-hydroxycineole catabolic process","type":"exact"},{"name":"6-endo-hydroxycineole catabolism","type":"exact"},{"name":"6-hydroxycineole breakdown","type":"exact"},{"name":"6-hydroxycineole catabolism","type":"exact"},{"name":"6-hydroxycineole degradation","type":"exact"},{"name":"hydroxycineol catabolic process","type":"exact"},{"name":"hydroxycineol catabolism","type":"exact"}],"termid":"GO:0019639"}


id: PBO:0030531
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_L-aminoadipate-semialdehyde_dehydrogenase_activity","termid":"PBO:0030531"}


id: GO:0015943
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of formate, also known as methanoate, the anion HCOO- derived from methanoic (formic) acid.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"formate metabolic process","termid":"GO:0015942"},{"relation_name":"is_a","term_name":"monocarboxylic acid biosynthetic process","termid":"GO:0072330"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"formate biosynthetic process","synonyms":[{"name":"formate anabolism","type":"exact"},{"name":"formate biosynthesis","type":"exact"},{"name":"formate formation","type":"exact"},{"name":"formate synthesis","type":"exact"},{"name":"formic acid biosynthesis","type":"exact"},{"name":"formic acid biosynthetic process","type":"exact"}],"termid":"GO:0015943"}


id: MONDO:0011563
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary gingival fibromatosis","termid":"MONDO:0016070"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibromatosis, gingival, 2","secondary_identifiers":["OMIM:605544","MEDGEN:344226","MESH:C565323","GARD:2474","UMLS:C1854181"],"synonyms":[{"name":"GGF2","type":"related"},{"name":"GINGF2","type":"exact"},{"name":"HGF2","type":"related"},{"name":"fibromatosis gingival, hereditary, 2","type":"related"},{"name":"fibromatosis, gingival, 2","type":"exact"},{"name":"fibromatosis, gingival, hereditary, 2","type":"related"},{"name":"gingival fibromatosis, 2","type":"related"},{"name":"hereditary gingival fibromatosis, 2","type":"related"}],"termid":"MONDO:0011563","xrefs":{"Monarch":{"xref_id":"0011563"}}}


id: PBO:0035848
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_protein_import_into_nucleus_during_vegetative_growth","termid":"PBO:0035848"}


id: GO:0004306
data:
  {"annotated_genes":["SJAG_04628"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[75731],"is_not":false,"summary":null,"term":"GO:0004306"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: CTP + ethanolamine phosphate = diphosphate + CDP-ethanolamine.","definition_xrefs":["EC:2.7.7.14"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytidylyltransferase activity","termid":"GO:0070567"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04628":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:0016779"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016779","GO:0016740","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"ethanolamine-phosphate cytidylyltransferase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["MetaCyc:2.7.7.14-RXN","Reactome:R-HSA-1483190","RHEA:24592"],"synonyms":[{"name":"CTP-phosphoethanolamine cytidylyltransferase activity","type":"related"},{"name":"CTP:ethanolamine-phosphate cytidylyltransferase activity","type":"exact"},{"name":"CTP:phosphoethanolamine cytidylyltransferase activity","type":"related"},{"name":"ET","type":"related"},{"name":"ethanolamine phosphate cytidylyltransferase activity","type":"related"},{"name":"phosphoethanolamine cytidylyltransferase activity","type":"exact"},{"name":"phosphorylethanolamine transferase activity","type":"broad"}],"termid":"GO:0004306","terms_by_termid":{"GO:0004306":null}}


id: PR:O59805
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC550.07 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O59805"],"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":"amidase C550.07 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC550.07","synonyms":[{"name":"Spom972h-SPCC550.07","type":"exact"}],"termid":"PR:O59805"}


id: PBO:0077061
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thrombospondin type 1 domain containing 7B","termid":"PBO:0077061"}


id: PR:Q9US27
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- vps66 gene.","definition_xrefs":["UniProtKB:Q9US27","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":"lysophosphatidic acid:oleoyl-CoA acyltransferase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1783.02c","synonyms":[{"name":"LPAAT (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-vps66","type":"exact"},{"name":"lysophosphatidic acid acyltransferase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"vacuolar protein sorting-associated protein 66 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9US27"}


id: GO:0022626
data:
  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ribosome located in the cytosol.","definition_xrefs":["GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ribosome","termid":"GO:0005840"},{"relation_name":"part_of","term_name":"cytosol","termid":"GO:0005829"}],"gene_count":142,"genes_by_uniquename":{"SJAG_00034":null,"SJAG_00069":null,"SJAG_00155":null,"SJAG_00166":null,"SJAG_00220":null,"SJAG_00384":null,"SJAG_00465":null,"SJAG_00468":null,"SJAG_00503":null,"SJAG_00523":null,"SJAG_00537":null,"SJAG_00541":null,"SJAG_00544":null,"SJAG_00629":null,"SJAG_00726":null,"SJAG_00733":null,"SJAG_00748":null,"SJAG_00749":null,"SJAG_00765":null,"SJAG_00921":null,"SJAG_00940":null,"SJAG_01087":null,"SJAG_01128":null,"SJAG_01132":null,"SJAG_01194":null,"SJAG_01202":null,"SJAG_01226":null,"SJAG_01287":null,"SJAG_01296":null,"SJAG_01322":null,"SJAG_01364":null,"SJAG_01365":null,"SJAG_01366":null,"SJAG_01387":null,"SJAG_01411":null,"SJAG_01512":null,"SJAG_01548":null,"SJAG_01551":null,"SJAG_01565":null,"SJAG_01568":null,"SJAG_01580":null,"SJAG_01588":null,"SJAG_01606":null,"SJAG_01608":null,"SJAG_01609":null,"SJAG_01632":null,"SJAG_01676":null,"SJAG_01721":null,"SJAG_01853":null,"SJAG_02020":null,"SJAG_02046":null,"SJAG_02081":null,"SJAG_02121":null,"SJAG_02184":null,"SJAG_02207":null,"SJAG_02224":null,"SJAG_02243":null,"SJAG_02253":null,"SJAG_02280":null,"SJAG_02283":null,"SJAG_02312":null,"SJAG_02335":null,"SJAG_02340":null,"SJAG_02477":null,"SJAG_02479":null,"SJAG_02510":null,"SJAG_02522":null,"SJAG_02531":null,"SJAG_02535":null,"SJAG_02546":null,"SJAG_02585":null,"SJAG_02597":null,"SJAG_02611":null,"SJAG_02682":null,"SJAG_02749":null,"SJAG_02755":null,"SJAG_02802":null,"SJAG_02803":null,"SJAG_02840":null,"SJAG_02861":null,"SJAG_02870":null,"SJAG_02871":null,"SJAG_02890":null,"SJAG_02891":null,"SJAG_02894":null,"SJAG_02904":null,"SJAG_03034":null,"SJAG_03043":null,"SJAG_03122":null,"SJAG_03127":null,"SJAG_03133":null,"SJAG_03159":null,"SJAG_03197":null,"SJAG_03254":null,"SJAG_03262":null,"SJAG_03326":null,"SJAG_03335":null,"SJAG_03364":null,"SJAG_03383":null,"SJAG_03422":null,"SJAG_03423":null,"SJAG_03424":null,"SJAG_03425":null,"SJAG_03568":null,"SJAG_03666":null,"SJAG_03762":null,"SJAG_03859":null,"SJAG_03919":null,"SJAG_03922":null,"SJAG_03971":null,"SJAG_04020":null,"SJAG_04029":null,"SJAG_04066":null,"SJAG_04160":null,"SJAG_04168":null,"SJAG_04174":null,"SJAG_04176":null,"SJAG_04188":null,"SJAG_04204":null,"SJAG_04256":null,"SJAG_04304":null,"SJAG_04324":null,"SJAG_04342":null,"SJAG_04414":null,"SJAG_04475":null,"SJAG_04476":null,"SJAG_04478":null,"SJAG_04534":null,"SJAG_04626":null,"SJAG_04663":null,"SJAG_04672":null,"SJAG_04695":null,"SJAG_04746":null,"SJAG_04814":null,"SJAG_04847":null,"SJAG_04897":null,"SJAG_04998":null,"SJAG_05216":null,"SJAG_05248":null,"SJAG_06612":null,"SJAG_07013":null,"SJAG_07014":null},"genotype_count":0,"in_subsets":["cc_goslim_japonicus"],"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005829"}],"interesting_parent_ids":["GO:0005829","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"cytosolic ribosome","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0005830","GO:0009281","GO:0030871"],"synonyms":[{"name":"70S ribosome","type":"narrow"},{"name":"80S ribosome","type":"narrow"}],"termid":"GO:0022626","terms_by_termid":{"GO:0022625":null,"GO:0022626":null,"GO:0022627":null}}


id: GO:0006904
data:
  {"annotated_genes":["SJAG_01697","SJAG_02587","SJAG_04966","SJAG_03499","SJAG_01772","SJAG_03005","SJAG_00280","SJAG_02320"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[60326,70126,75445,80162,80536,90918,92672,118515],"is_not":false,"summary":null,"term":"GO:0006904"}]},"cv_name":"biological_process","definition":"The initial attachment of a vesicle membrane to a target membrane, mediated by proteins protruding from the membrane of the vesicle and the target membrane, that contributes to exocytosis.","definition_xrefs":["GOC:aruk","GOC:bc","PMID:22438915","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle docking","termid":"GO:0048278"},{"relation_name":"is_a","term_name":"exocytic process","termid":"GO:0140029"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00280":null,"SJAG_01697":null,"SJAG_01772":null,"SJAG_02320":null,"SJAG_02587":null,"SJAG_03005":null,"SJAG_03499":null,"SJAG_04966":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0140056"},{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0140056","GO:0016192","GO:0008150","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"vesicle docking involved in exocytosis","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"vesicle docking during exocytosis","type":"related"}],"termid":"GO:0006904","terms_by_termid":{"GO:0006904":null}}


id: GO:0061400
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that increases the frequency, rate or extent of transcription from an RNA polymerase II promoter in response to a calcium ion stimulus.","definition_xrefs":["GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of transcription from RNA polymerase II promoter in response to calcium ion (obsolete GO:0061400)","termid":"GO:0061400"}


id: PBO:0072721
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribitol xylosyltransferase 1","termid":"PBO:0072721"}


id: PR:P87137
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A U3 small nucleolar RNA-associated protein 14 B that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C57A7.06 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC57A7.06","secondary_identifiers":["UniProtKB:P87137"],"synonyms":[{"name":"Spom972h-Utp14b","type":"exact"}],"termid":"PR:P87137"}


id: MONDO:0014569
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any lethal congenital contracture syndrome in which the cause of the disease is a mutation in the CNTNAP1 gene.","definition_xrefs":["MONDO:design_pattern"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lethal congenital contracture syndrome","termid":"MONDO:0017436"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lethal congenital contracture syndrome 7","secondary_identifiers":["MEDGEN:894160","UMLS:C4225386","OMIM:616286","GARD:18564"],"synonyms":[{"name":"CNTNAP1 lethal congenital contracture syndrome","type":"exact"},{"name":"LCCS7","type":"related"},{"name":"lethal congenital contracture syndrome 7","type":"exact"},{"name":"lethal congenital contracture syndrome caused by mutation in CNTNAP1","type":"exact"},{"name":"lethal congenital contracture syndrome type 7","type":"exact"}],"termid":"MONDO:0014569","xrefs":{"Monarch":{"xref_id":"0014569"}}}


id: PBO:0062155
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 4 subfamily G member 6 pseudogene","termid":"PBO:0062155"}


id: PR:O94329
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A DNA replication complex GINS protein PSF2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR12772:SF0","OMA:SCHPO02775","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":"DNA replication complex GINS protein psf2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC725.13c","secondary_identifiers":["UniProtKB:O94329"],"synonyms":[{"name":"Spom972h-GINS2","type":"exact"}],"termid":"PR:O94329"}


id: PBO:0090621
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cysteine transmembrane transporter","termid":"PBO:0090621"}


id: PBO:0084880
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial ribosome recycling factor; essential for mitochondrial protein synthesis and for the maintenance of the respiratory function of mitochondria","termid":"PBO:0084880"}


id: MOD:01188
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Isotopic label -","definition_xrefs":["PubMed:3155470","PubMed:12766232","PubMed:11710128","Unimod:212#Y","PubMed:957432"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-ethyl iodoacetamide-d5","termid":"MOD:00562"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-ethyl iodoacetamide-d5 - site Y","synonyms":[{"name":"N-ethyl iodoacetamide-d5","type":"related"},{"name":"NEIAA:2H(5)","type":"related"}],"termid":"MOD:01188"}


id: MONDO:1012554
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"atypical myopathy, non-human animal","termid":"MONDO:1011807"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"atypical myopathy, horse","secondary_identifiers":["OMIA:002480-9796"],"termid":"MONDO:1012554","xrefs":{"Monarch":{"xref_id":"1012554"}}}


id: MONDO:0032800
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Robinow syndrome","termid":"MONDO:0019978"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"robinow syndrome, autosomal recessive 2","secondary_identifiers":["UMLS:C5193143","DOID:0060974","MEDGEN:1676687","OMIM:618529"],"synonyms":[{"name":"ROBINOW SYNDROME, AUTOSOMAL RECESSIVE 2","type":"related"},{"name":"RRS2","type":"related"}],"termid":"MONDO:0032800","xrefs":{"Monarch":{"xref_id":"0032800"}}}


id: PBO:0060897
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NEURL1 antisense RNA 1","termid":"PBO:0060897"}


id: MONDO:0008796
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Aniridia - renal agenesis - psychomotor retardation is an extremely rare syndrome reported in two siblings of non consanguineous parents that is characterized by the association of ocular abnormalities (partial aniridia, congenital glaucoma, telecanthus) with frontal bossing, hypertelorism, unilateral renal agenesis and mild psychomotor delay. There have been no further descriptions in the literature since 1974.","definition_xrefs":["Orphanet:1064"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"disorder of visual system","termid":"MONDO:0024458"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aniridia-renal agenesis-psychomotor retardation syndrome","secondary_identifiers":["UMLS:C1859782","MEDGEN:347952","MESH:C000598722","GARD:690","SCTID:733116005","OMIM:206750"],"synonyms":[{"name":"Sommer Rathbun Battles syndrome","type":"related"},{"name":"Sommer-Rathbun-Battles syndrome","type":"exact"},{"name":"aniridia partial with unilateral renal agenesis and psychomotor retardation","type":"related"},{"name":"aniridia renal agenesis psychomotor retardation","type":"related"},{"name":"aniridia, partial, with unilateral renal agenesis and psychomotor retardation","type":"related"}],"termid":"MONDO:0008796","xrefs":{"Monarch":{"xref_id":"0008796"}}}


id: PBO:0052256
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KDEL endoplasmic reticulum protein retention receptor 3","termid":"PBO:0052256"}


id: MONDO:0800462
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A group of myopathies that includes Emery-Dreifuss muscular dystrophy (EDMD), and two allelic disorders characterized by the presence of reducing body on histopathology, namely reducing body myopathy (RBM) and scapuloperoneal myopathy.","direct_ancestors":[{"relation_name":"is_a","term_name":"myopathy","termid":"MONDO:0005336"},{"relation_name":"is_a","term_name":"hereditary skeletal muscle disorder","termid":"MONDO:0700223"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"FHL1-related myopathy","synonyms":[{"name":"FHL1-related myopathy","type":"exact"}],"termid":"MONDO:0800462","xrefs":{"Monarch":{"xref_id":"0800462"}}}


id: GO:0021921
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that modulates the frequency, rate or extent of cell proliferation in the dorsal spinal cord.","definition_xrefs":["GOC:dgh","GOC:dph","GO_REF:0000021","GOC:jid","GOC:cls"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of neural precursor cell proliferation","termid":"GO:2000177"},{"relation_name":"part_of","term_name":"dorsal spinal cord development","termid":"GO:0021516"},{"relation_name":"regulates","term_name":"cell proliferation in dorsal spinal cord","termid":"GO:0010456"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of cell proliferation in dorsal spinal cord","termid":"GO:0021921"}


id: GO:1904701
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a Wnt-Frizzled-LRP5/6 complex.","definition_xrefs":["GOC:bf","GO_REF:0000079","GOC:PARL","GOC:TermGenie","PMID:11448771"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex assembly","termid":"GO:0065003"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0065003","GO:0008150","GO:0044085"],"is_obsolete":false,"name":"Wnt-Frizzled-LRP5/6 complex assembly","synonyms":[{"name":"Frizzled-LRP5/6 complex assembly","type":"related"},{"name":"Frizzled-LRP5/6 complex formation","type":"related"},{"name":"WNT-FZD-LRP5 complex assembly","type":"narrow"},{"name":"WNT-FZD-LRP5 complex formation","type":"narrow"},{"name":"WNT-FZD-LRP6 complex assembly","type":"narrow"},{"name":"WNT-FZD-LRP6 complex formation","type":"narrow"},{"name":"Wnt receptor complex assembly","type":"broad"},{"name":"Wnt-FZD-LRP5/6 trimeric complex assembly","type":"exact"},{"name":"Wnt-FZD-LRP5/6 trimeric complex formation","type":"exact"},{"name":"Wnt-induced Frizzled-LRP5/6 complex assembly","type":"related"},{"name":"Wnt-induced Frizzled-LRP5/6 complex formation","type":"related"}],"termid":"GO:1904701"}


id: GO:0002079
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The acrosomal membrane region that underlies the acrosomal vesicle and is located toward the sperm nucleus. This region is responsible for molecular interactions allowing the sperm to penetrate the zona pellucida and fuses with the egg plasma membrane.","definition_xrefs":["GOC:dph","PMID:3899643","PMID:8936405"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoplasmic vesicle membrane","termid":"GO:0030659"},{"relation_name":"part_of","term_name":"acrosomal membrane","termid":"GO:0002080"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0031410"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0031410","GO:0005737"],"is_obsolete":false,"name":"inner acrosomal membrane","termid":"GO:0002079"}


id: FYPO:0006700
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 CDP measured in the cell is lower than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased cellular pentose phosphate level","termid":"FYPO:0006705"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"decreased cellular CDP level","synonyms":[{"name":"decreased cellular CDP level during mitotic cell cycle","type":"related"},{"name":"decreased cellular CDP level during vegetative growth","type":"exact"},{"name":"reduced cellular CDP level","type":"exact"}],"termid":"FYPO:0006700"}


id: PBO:0085320
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Phosphatidylinositol 4,5-bisphosphate 5-phosphatase; role in secretion; localizes to the endoplasmic reticulum via the C-terminal tail; lacks the Sac1 domain and proline-rich region found in the other 3 INP proteins","termid":"PBO:0085320"}


id: GO:0141040
data:
  {"annotated_genes":["SJAG_00630"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[69251],"is_not":false,"summary":null,"term":"GO:0141040"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: a very-long-chain (3R)-3-hydroxyacyl-CoA + NADP+ = a very-long-chain 3-oxoacyl-CoA + H+ + NADPH. This reaction is the second (reduction) step of the four-step fatty acid elongation cycle in the endoplasmic reticulum that extends fatty acids of C-16 or longer with an additional 2-C unit.","definition_xrefs":["PMID:16564093","PMID:19763486","RHEA:48680"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00630":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"very-long-chain 3-oxoacyl-CoA reductase activity","references_by_uniquename":{"GO_REF:0000003":null},"secondary_identifiers":["Reactome:R-HSA-548818","MetaCyc:RXN-7698","EC:1.1.1.330"],"termid":"GO:0141040","terms_by_termid":{"GO:0141040":null}}


id: GO:0000078
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A mitotic cell cycle checkpoint that detects whether chromosome segregation is complete and negatively regulates cytokinesis following mitosis.","definition_xrefs":["GOC:mtg_cell_cycle"],"gene_count":0,"genotype_count":0,"name":"obsolete cytokinesis after mitosis checkpoint (obsolete GO:0000078)","synonyms":[{"name":"cell morphogenesis checkpoint","type":"exact"},{"name":"cell shape checkpoint","type":"exact"}],"termid":"GO:0000078"}


id: SO:0002279
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The hAT terminal inverted repeat transposon superfamily elements were first found in maize (the Ac/Ds elements). Members of the hAT superfamily have TSDs of 8 bp, relatively short TIRs of 5–27 bp and overall lengths of less than 4 kb.","definition_xrefs":["PMID:11454746"],"direct_ancestors":[{"relation_name":"is_a","term_name":"terminal_inverted_repeat_element","termid":"SO:0000208"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hAT_TIR_transposon","synonyms":[{"name":"Ac transposon","type":"exact"},{"name":"Ac/Ds transposon","type":"exact"},{"name":"DTA transposon","type":"exact"},{"name":"Ds transposon","type":"exact"},{"name":"hAT TIR transposon","type":"exact"},{"name":"hAT transposon","type":"exact"},{"name":"hAT-Ac transposon","type":"exact"}],"termid":"SO:0002279"}


id: PBO:0109038
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CFAP69 pseudogene 1","termid":"PBO:0109038"}


id: PBO:0048897
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"golgin A6 family like 19","termid":"PBO:0048897"}


id: MONDO:0006368
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An extremely rare, benign or malignant mesenchymal tumor arising from the soft tissues or bones. It is a distinctive tumor, which usually displays the following morphologic characteristics: low cellularity, myxoid changes, presence of spindled cells and osteoclasts, hemangiopericytoma-like vessels, hemorrhage, and osteoid-like matrix. It is associated with the presence of a paraneoplastic syndrome called osteogenic osteomalacia. This syndrome usually precedes the appearance of the tumor, and it is characterized by phosphaturia, hypophosphatemia, normal serum calcium levels, and decreased levels of 1,25-dihydroxyvitamin D3. Patients present with bone and muscle pain, severe muscle weakness, fractures, gait disturbances, skeletal deformity, height loss, and slow growth. The metabolic disturbances improve or completely disappear after the complete resection of the tumor.","definition_xrefs":["NCIT:C67237"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neoplasm","termid":"MONDO:0005070"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphaturic mesenchymal tumor","secondary_identifiers":["UMLS:C1831619","MEDGEN:371179","EFO:1000473"],"synonyms":[{"name":"phosphaturic mesenchymal tumor","type":"exact"},{"name":"phosphaturic mesenchymal tumor, mixed connective tissue type","type":"exact"},{"name":"phosphaturic mesenchymal tumor, mixed connective tissue variant","type":"related"}],"termid":"MONDO:0006368","xrefs":{"Monarch":{"xref_id":"0006368"}}}


id: PBO:0003740
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA snR54 (predicted)","termid":"PBO:0003740"}


id: PBO:0071244
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23a pseudogene 85","termid":"PBO:0071244"}


id: GO:0061559
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structure of a cranial ganglion is generated and organized.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ganglion morphogenesis","termid":"GO:0061552"},{"relation_name":"part_of","term_name":"cranial nerve morphogenesis","termid":"GO:0021602"},{"relation_name":"part_of","term_name":"cranial ganglion development","termid":"GO:0061550"}],"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":"cranial ganglion morphogenesis","synonyms":[{"name":"cranial ganglia morphogenesis","type":"related"}],"termid":"GO:0061559"}


id: PATO:0000338
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000338 compatability value (obsolete PATO:0000338)","termid":"PATO:0000338"}


id: PBO:0051896
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"integrin subunit alpha 5","termid":"PBO:0051896"}


id: PBO:0052379
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kinesin family member 21B","termid":"PBO:0052379"}


id: PBO:0082481
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Carboxy-terminal domain (CTD) phosphatase; essential for dephosphorylation of the repeated C-terminal domain of the RNA polymerase II large subunit (Rpo21p); relocalizes to the cytosol in response to hypoxia","termid":"PBO:0082481"}


id: GO:0008009
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"The function of a family of small chemotactic cytokines; their name is derived from their ability to induce directed chemotaxis in nearby responsive cells. All chemokines possess a number of conserved cysteine residues involved in intramolecular disulfide bond formation. Some chemokines are considered pro-inflammatory and can be induced during an immune response to recruit cells of the immune system to a site of infection, while others are considered homeostatic and are involved in controlling the migration of cells during normal processes of tissue maintenance or development. Chemokines are found in all vertebrates, some viruses and some bacteria.","definition_xrefs":["PMID:12183377","GOC:BHF","Wikipedia:Chemokine","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine activity","termid":"GO:0005125"},{"relation_name":"is_a","term_name":"chemokine receptor binding","termid":"GO:0042379"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"positively_regulates","termid":"GO:0038023"},{"rel_name":"regulates","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0140677"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0038023","GO:0003674","GO:0098772","GO:0005488","GO:0005515","GO:0140677"],"is_obsolete":false,"name":"chemokine activity","termid":"GO:0008009"}


id: PBO:0064854
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase 1 regulatory inhibitor subunit 14B pseudogene 5","termid":"PBO:0064854"}


id: PBO:0001342
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-actin capping protein beta subunit (predicted)","termid":"PBO:0001342"}


id: GO:0003805
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the selective cleavage of Arg-Ala and Arg-Val bonds in factor IX to form factor IXa.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete coagulation factor XIa activity (obsolete GO:0003805)","synonyms":[{"name":"activated blood-coagulation factor XI","type":"related"},{"name":"activated plasma thromboplastin antecedent","type":"related"},{"name":"blood coagulation factor XI activity","type":"exact"},{"name":"blood-coagulation factor XIa","type":"related"},{"name":"coagulation factor XIa activity","type":"exact"},{"name":"plasma thromboplastin antecedent activity","type":"related"}],"termid":"GO:0003805"}


id: FYPO:0001649
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the import of glutamate into the cell occurs to a lower extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased amino acid import","termid":"FYPO:0001058"},{"relation_name":"is_a","term_name":"abnormal glutamate import","termid":"FYPO:0001646"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000138","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"decreased glutamate import","synonyms":[{"name":"decreased L-glutamate import","type":"exact"},{"name":"decreased glutamate import across plasma membrane","type":"exact"},{"name":"decreased glutamate import into cell","type":"exact"},{"name":"decreased glutamate uptake","type":"exact"},{"name":"reduced glutamate import","type":"exact"}],"termid":"FYPO:0001649"}


id: GO:0033407
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A triplet codon-amino acid adaptor activity that recognizes a UCA codon.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"triplet codon-amino acid adaptor activity","termid":"GO:0030533"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003723"},{"rel_name":"is_a","termid":"GO:0060090"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0003723","GO:0060090"],"is_obsolete":false,"name":"UCA codon-amino acid adaptor activity","synonyms":[{"name":"TCA codon-amino acid adaptor activity","type":"exact"},{"name":"serine tRNA","type":"related"}],"termid":"GO:0033407"}


id: PR:Q10065
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- trk2 gene.","definition_xrefs":["UniProtKB:Q10065","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":"potassium transport protein 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1639.02c","synonyms":[{"name":"Spom972h-trk2","type":"exact"}],"termid":"PR:Q10065"}


id: GO:1901235
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of (R)-carnitine from one side of a membrane to the other.","definition_xrefs":["PMID:20829798","GOC:TermGenie","PMID:16365042","PMID:20357772"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carnitine transmembrane transporter activity","termid":"GO:0015226"}],"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:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"(R)-carnitine transmembrane transporter activity","termid":"GO:1901235"}


id: PBO:0050239
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group nucleosomal binding domain 2 pseudogene 17","termid":"PBO:0050239"}


id: GO:0042084
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of a methyl group to an acceptor molecule; dependent on the presence of 5-methyltetrahydrofolate.","definition_xrefs":["GOC:ai"],"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:0016741","GO:0016740","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"5-methyltetrahydrofolate-dependent methyltransferase activity","termid":"GO:0042084"}


id: MONDO:0019549
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare axonal hereditary motor and sensory neuropathy characterized by early onset (<10 years) progressive distal muscle weakness and wasting of the lower limbs and later, to a lesser extent the upper limbs resulting in foot and wrist drop, areflexia, skeletal deformities (kyphoscoliosis, pes cavus with flattening, joint contractures), mild sensory impairment with vibration sense reduced to a greater extent than pain, optic atrophy and hearing loss. Wheelchair dependence by adolescence is usual and respiratory impairment with diaphragmatic paralysis may develop.","definition_xrefs":["Orphanet:90118"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary motor and sensory neuropathy","termid":"MONDO:0015358"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"severe early-onset axonal neuropathy due to MFN2 deficiency","secondary_identifiers":["SCTID:766977007","GARD:19123","MEDGEN:1641956","UMLS:C4707897"],"synonyms":[{"name":"AR-CMT2, Ouvrier type","type":"exact"},{"name":"SEOAN due to MFN2 deficiency","type":"exact"},{"name":"autosomal recessive Charcot-Marie-Tooth disease, Ouvrier type","type":"exact"}],"termid":"MONDO:0019549","xrefs":{"Monarch":{"xref_id":"0019549"}}}


id: PBO:0089517
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L20A","termid":"PBO:0089517"}


id: GO:0042117
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The change in morphology and behavior of a monocyte resulting from exposure to a cytokine, chemokine, cellular ligand, or soluble factor.","definition_xrefs":["ISBN:0781735149","GOC:mgi_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myeloid leukocyte activation","termid":"GO:0002274"}],"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":"monocyte activation","termid":"GO:0042117"}


id: PBO:0065352
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PTPN13 like Y-linked pseudogene 2","termid":"PBO:0065352"}


id: PBO:0029387
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_threonine_phosphorylation_at_Thr-Pro_site_during_cellular_response_to_hydrogen_peroxide","termid":"PBO:0029387"}


id: PBO:0081353
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 175","termid":"PBO:0081353"}


id: PBO:0034629
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_meiotic_centromere_clustering_with_centromeres_dissociated_from_spindle_pole_body","termid":"PBO:0034629"}


id: GO:0070210
data:
  {"annotated_genes":["SJAG_00581","SJAG_00868","SJAG_02439","SJAG_04389","SJAG_03627","SJAG_03230","SJAG_04576","SJAG_00441","SJAG_01926","SJAG_02981","SJAG_03441","SJAG_04758","SJAG_03867","SJAG_02846","SJAG_01230","SJAG_04396","SJAG_03255"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[75165,76075,77631,78519,79052,79376,80665,89448,93582,94977,103093,105038,105352,107065,110784,114447,114536],"is_not":false,"summary":null,"term":"GO:0070210"}]},"cv_name":"cellular_component","definition":"A protein complex that contains a histone deacetylase and is part of the chromatin remodeling machinery. In Saccharomyces cerevisiae this complex contains the Rpd3p, Sin3p, Ume1p, Pho23p, Sap30p, Sds3p, Cti6p, Rxt2p, Rxt3p, Dep1p, Ume6p, Ash1p, Dot6p, Snt1, Sif2p, Set3p, Hos2p, Tos4p and Tod6p proteins.","definition_xrefs":["PMID:19040720","GOC:rb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone deacetylase complex","termid":"GO:0000118"},{"relation_name":"part_of","term_name":"nuclear chromosome","termid":"GO:0000228"},{"relation_name":"part_of","term_name":"chromatin","termid":"GO:0000785"}],"gene_count":17,"genes_by_uniquename":{"SJAG_00441":null,"SJAG_00581":null,"SJAG_00868":null,"SJAG_01230":null,"SJAG_01926":null,"SJAG_02439":null,"SJAG_02846":null,"SJAG_02981":null,"SJAG_03230":null,"SJAG_03255":null,"SJAG_03441":null,"SJAG_03627":null,"SJAG_03867":null,"SJAG_04389":null,"SJAG_04396":null,"SJAG_04576":null,"SJAG_04758":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005654"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005654","GO:0005575","GO:0005694","GO:0005634","GO:0032991"],"is_obsolete":false,"name":"Rpd3L-Expanded complex","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"Clr6-LE complex","type":"exact"}],"termid":"GO:0070210","terms_by_termid":{"GO:0070210":null}}


id: PBO:0073338
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serpin family A member 15, pseudogene","termid":"PBO:0073338"}


id: GO:1900105
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of hyaluranon cable assembly.","definition_xrefs":["GOC:TermGenie","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cellular component organization","termid":"GO:0051129"},{"relation_name":"is_a","term_name":"regulation of hyaluranon cable assembly","termid":"GO:1900104"},{"relation_name":"negatively_regulates","term_name":"hyaluranon cable assembly","termid":"GO:0036118"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"negative regulation of hyaluranon cable assembly","synonyms":[{"name":"down regulation of HA cable assembly","type":"exact"},{"name":"down regulation of hyaluranon cable assembly","type":"exact"},{"name":"down-regulation of HA cable assembly","type":"exact"},{"name":"down-regulation of hyaluranon cable assembly","type":"exact"},{"name":"downregulation of HA cable assembly","type":"exact"},{"name":"downregulation of hyaluranon cable assembly","type":"exact"},{"name":"inhibition of HA cable assembly","type":"exact"},{"name":"inhibition of hyaluranon cable assembly","type":"narrow"},{"name":"negative regulation of HA cable assembly","type":"exact"}],"termid":"GO:1900105"}


id: GO:0006669
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation 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 biosynthetic process","termid":"GO:0008654"},{"relation_name":"is_a","term_name":"sphingolipid biosynthetic process","termid":"GO:0030148"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"sphinganine-1-phosphate biosynthetic process","synonyms":[{"name":"dihydrosphingosine-1-phosphate biosynthesis","type":"exact"},{"name":"dihydrosphingosine-1-phosphate biosynthetic process","type":"exact"},{"name":"sphinganine-1-phosphate anabolism","type":"exact"},{"name":"sphinganine-1-phosphate biosynthesis","type":"exact"},{"name":"sphinganine-1-phosphate formation","type":"exact"},{"name":"sphinganine-1-phosphate synthesis","type":"exact"}],"termid":"GO:0006669"}


id: GO:0048933
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of an afferent axon in the posterior lateral line nerve over time from its formation to the mature structure. This process includes axonogenesis and pathfinding of the afferent axons in the posterior lateral line nerve.","definition_xrefs":["PMID:15018940"],"direct_ancestors":[{"relation_name":"is_a","term_name":"afferent axon development in lateral line nerve","termid":"GO:0048893"},{"relation_name":"part_of","term_name":"posterior lateral line nerve development","termid":"GO:0048918"}],"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":"afferent axon development in posterior lateral line nerve","termid":"GO:0048933"}


id: GO:2000025
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of leaf formation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of plant organ formation","termid":"GO:1905428"},{"relation_name":"regulates","term_name":"leaf formation","termid":"GO:0010338"}],"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 leaf formation","termid":"GO:2000025"}


id: GO:0097615
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which an organism effects a change in the type IV pilus-dependent motility of a symbiont organism (i.e. the controlled movement of a bacterial cell which is dependent on the presence of type IV pili, and which includes social gliding motility and twitching motility). The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:12037568","GOC:als"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation by host of symbiont type IV pilus-dependent motility (obsolete GO:0097615)","synonyms":[{"name":"modulation by host of bacterial type IV pilus-dependent motility","type":"exact"}],"termid":"GO:0097615"}


id: PBO:0031747
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_mitotic_centromeric_sister_chromatid_cohesion","termid":"PBO:0031747"}


id: GO:0046272
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of stilbenes, a class of polyketide compounds formed from cinnamic acid and three molecules of malonyl CoA.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"stilbene metabolic process","termid":"GO:0009810"},{"relation_name":"is_a","term_name":"olefinic compound catabolic process","termid":"GO:0120256"}],"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":"stilbene catabolic process","synonyms":[{"name":"stilbene breakdown","type":"exact"},{"name":"stilbene catabolism","type":"exact"},{"name":"stilbene degradation","type":"exact"}],"termid":"GO:0046272"}


id: PBO:0027201
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-long_nuclear_microtubules_protruding_through_nuclear_envelope_during_interphase","termid":"PBO:0027201"}


id: PBO:0051635
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inner membrane mitochondrial protein","termid":"PBO:0051635"}


id: GO:1904272
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of L-tryptophan from outside of a cell, across the plasma membrane and into the cytosol.","definition_xrefs":["GOC:TermGenie","GO_REF:0000075","GOC:kmv","PMID:21097500"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid import across plasma membrane","termid":"GO:0089718"},{"relation_name":"is_a","term_name":"L-tryptophan transmembrane transport","termid":"GO:1904556"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0055085","GO:0051179"],"is_obsolete":false,"name":"L-tryptophan import across plasma membrane","termid":"GO:1904272"}


id: PBO:0041400
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 6 open reading frame 52","termid":"PBO:0041400"}


id: PBO:0075130
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nuclear ribonucleoprotein U11/U12 subunit 35","termid":"PBO:0075130"}


id: GO:0044354
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A membrane-bounded, uncoated intracellular vesicle formed by the process of macropinocytosis.","definition_xrefs":["PMID:14732047"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pinosome","termid":"GO:0044352"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0031410"},{"rel_name":"is_a","termid":"GO:0005768"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0031410","GO:0005768","GO:0005737","GO:0005575"],"is_obsolete":false,"name":"macropinosome","termid":"GO:0044354"}


id: GO:0003022
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which information about the levels of hydrogen ions are received and are converted to a molecular signal by chemoreceptors.","definition_xrefs":["ISBN:0323031951","GOC:mtg_cardio"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detection of hydrogen ion","termid":"GO:0003030"}],"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 pH by chemoreceptor signaling","synonyms":[{"name":"detection of pH by chemoreceptor signalling","type":"exact"}],"termid":"GO:0003022"}


id: GO:0045872
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of rhodopsin gene expression.","definition_xrefs":["GOC:tb","GOC:dph","GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of rhodopsin gene expression (obsolete GO:0045872)","synonyms":[{"name":"activation of rhodopsin gene activity","type":"narrow"},{"name":"positive regulation of rhodopsin gene activity","type":"exact"},{"name":"stimulation of rhodopsin gene activity","type":"narrow"},{"name":"up regulation of rhodopsin gene activity","type":"exact"},{"name":"up-regulation of rhodopsin gene activity","type":"exact"},{"name":"upregulation of rhodopsin gene activity","type":"exact"}],"termid":"GO:0045872"}


id: PBO:0001823
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homoisocitrate dehydrogenase","termid":"PBO:0001823"}


id: PBO:0088564
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Golgi alpha-1,2-mannosyltransferase Omh2","termid":"PBO:0088564"}


id: MONDO:0014744
data:
  {"annotated_genes":["SJAG_04622"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86241],"is_not":false,"summary":null,"term":"MONDO:0014744"}]},"cv_name":"mondo","definition":"An autosomal recessive cerebellar ataxia that has material basis in homozygous or compound heterozygous mutation in the SCYL1 gene on chromosome 11q13.","definition_xrefs":["DOID:0111155"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"autosomal recessive syndromic cerebellar ataxia","termid":"MONDO:0020047"},{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04622":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0006025"],"is_obsolete":false,"name":"acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:616719","Orphanet:466794","GARD:17833","MEDGEN:1800507","UMLS:C5569084"],"synonyms":[{"name":"SCAR21","type":"exact"},{"name":"acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome","type":"exact"},{"name":"autosomal recessive spinocerebellar ataxia 21","type":"related"},{"name":"autosomal recessive spinocerebellar ataxia 21 with hepatopathy","type":"exact"},{"name":"autosomal recessive spinocerebellar ataxia type 21","type":"exact"},{"name":"spinocerebellar ataxia, autosomal recessive 21","type":"exact"},{"name":"spinocerebellar ataxia, autosomal recessive 21, with hepatopathy","type":"related"},{"name":"spinocerebellar ataxia, autosomal recessive type 21","type":"exact"}],"termid":"MONDO:0014744","terms_by_termid":{"MONDO:0014744":null},"xrefs":{"Monarch":{"xref_id":"0014744"}}}


id: PBO:0064227
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phospholipase C gamma 1","termid":"PBO:0064227"}


id: MONDO:0011735
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A form of Hyper IgM syndrome characterized by mutations of the CD40 gene. In this type, Immature B cells cannot receive signal 2 from helper T cells which is necessary to mature into mature B cells.","definition_xrefs":["Wikipedia:Hyper-IgM_syndrome_type_3"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hyper-IgM syndrome","termid":"MONDO:0003947"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"hyper-IgM syndrome type 3","secondary_identifiers":["DOID:0060023","UMLS:C1720957","GARD:10579","OMIM:606843","Orphanet:101090","MEDGEN:328419"],"synonyms":[{"name":"CD40 deficiency","type":"related"},{"name":"CD40 hyper-IgM syndrome","type":"exact"},{"name":"HIGM3","type":"exact"},{"name":"hyper IgM syndrome 3","type":"related"},{"name":"hyper-IgM syndrome 3","type":"related"},{"name":"hyper-IgM syndrome caused by mutation in CD40","type":"exact"},{"name":"hyper-IgM syndrome due to CD40 deficiency","type":"exact"},{"name":"immunodeficiency with hyper IgM type 3","type":"related"},{"name":"immunodeficiency with hyper-IgM type 3","type":"exact"},{"name":"immunodeficiency with hyper-IgM, type 3","type":"related"},{"name":"type 3 hyper-IgM immunodeficiency","type":"exact"}],"termid":"MONDO:0011735","xrefs":{"Monarch":{"xref_id":"0011735"}}}


id: FYPO:0007526
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the phosphorylation of one or more specific proteins, or of specific protein sites, occurs to a greater extent than normal during a cellular response to salt stress.","definition_xrefs":["PMID:19625445","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein phosphorylation during vegetative growth","termid":"FYPO:0001038"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0002274","FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0002494"],"is_obsolete":false,"name":"increased protein phosphorylation during cellular response to salt stress","synonyms":[{"name":"increased protein phosphorylation during cellular response to salt stress during mitotic cell cycle","type":"related"},{"name":"increased protein phosphorylation during cellular response to salt stress during vegetative growth","type":"exact"}],"termid":"FYPO:0007526"}


id: MONDO:0970944
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":"Leigh syndrome, mitochondrial","secondary_identifiers":["OMIM:500017"],"termid":"MONDO:0970944","xrefs":{"Monarch":{"xref_id":"0970944"}}}


id: PBO:0033784
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_anaphase-promoting_complex-dependent_protein_catabolic_process","termid":"PBO:0033784"}


id: MONDO:0032714
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome","secondary_identifiers":["UMLS:C5193066","Orphanet:598603","MEDGEN:1679105","OMIM:618381","GARD:18019"],"synonyms":[{"name":"FACIAL DYSMORPHISM, HYPERTRICHOSIS, EPILEPSY, INTELLECTUAL/DEVELOPMENTAL DELAY, AND GINGIVAL OVERGROWTH SYNDROME","type":"related"},{"name":"FHEIG","type":"related"}],"termid":"MONDO:0032714","xrefs":{"Monarch":{"xref_id":"0032714"}}}


id: GO:0098888
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The component of the presynaptic membrane consisting of gene products and protein complexes that are loosely bound to one of its surfaces, but not integrated into the hydrophobic region.","definition_xrefs":["GOC:mf","GOC:autophagy"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extrinsic component of synaptic membrane","termid":"GO:0099243"},{"relation_name":"part_of","term_name":"presynaptic membrane","termid":"GO:0042734"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005886","GO:0005575"],"is_obsolete":false,"name":"extrinsic component of presynaptic membrane","synonyms":[{"name":"extrinsic component of presynaptic plasma membrane","type":"exact"}],"termid":"GO:0098888"}


id: PBO:0077662
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TNF receptor superfamily member 10c","termid":"PBO:0077662"}


id: PBO:0034134
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-in_paraxenology_relationship_with","termid":"PBO:0034134"}


id: PBO:0077650
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TNF alpha induced protein 8 like 2","termid":"PBO:0077650"}


id: PBO:0079674
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin conjugating enzyme E2 V2 pseudogene 4","termid":"PBO:0079674"}


id: MONDO:0021641
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Virus diseases caused by the bunyaviridae.","definition_xrefs":["MESH:D002044"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary viral infectious disease","termid":"MONDO:0100329"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Bunyaviridae infectious disease","secondary_identifiers":["EFO:0007188","SCTID:105632002"],"synonyms":[{"name":"Bunyaviridae caused disease or disorder","type":"exact"},{"name":"Bunyaviridae disease or disorder","type":"exact"},{"name":"Bunyaviridae infection","type":"related"},{"name":"Bunyaviridae infectious disease","type":"exact"},{"name":"Bunyavirus infection","type":"related"},{"name":"Bunyavirus infections","type":"related"},{"name":"disease caused by Bunyaviridae","type":"related"},{"name":"disease caused by Bunyavirus","type":"related"},{"name":"disease due to Bunyaviridae","type":"exact"},{"name":"disease due to Bunyavirus","type":"related"},{"name":"infections, Bunyaviridae","type":"related"},{"name":"infections, Bunyavirus","type":"related"}],"termid":"MONDO:0021641","xrefs":{"Monarch":{"xref_id":"0021641"}}}


id: GO:0140504
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Degradation of a lipid droplet by microautophagy.","definition_xrefs":["PMID:29601311","PMID:28838958","PMID:29293450","PMID:25070953","PMID:28394250"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microautophagy","termid":"GO:0016237"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006914"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006914","GO:0008150"],"is_obsolete":false,"name":"microlipophagy","synonyms":[{"name":"lipid droplet autophagy","type":"exact"}],"termid":"GO:0140504"}


id: GO:0000825
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 1D-myo-inositol 1,3,4,5-tetrakisphosphate + ATP = 1D-myo-inositol 1,3,4,5,6-pentakisphosphate + ADP + H+.","definition_xrefs":["MetaCyc:RXN-7184"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inositol tetrakisphosphate kinase activity","termid":"GO:0051765"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016301"}],"interesting_parent_ids":["GO:0016301","GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"inositol-1,3,4,5-tetrakisphosphate 6-kinase activity","secondary_identifiers":["Reactome:R-HSA-1855206","KEGG_REACTION:R10953"],"synonyms":[{"name":"1D-myo-inositol-tetrakisphosphate 6-kinase activity","type":"broad"},{"name":"inositol 1,3,4,5-tetrakisphosphate 6-kinase activity","type":"exact"},{"name":"inositol tetrakisphosphate 6-kinase activity","type":"broad"}],"termid":"GO:0000825"}


id: PBO:0090236
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotic Rho guanine nucleotide exchange factor","termid":"PBO:0090236"}


id: PBO:0060168
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MTSS I-BAR domain containing 2","termid":"PBO:0060168"}


id: GO:0120042
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of macrophage proliferation.","definition_xrefs":["GOC:BHF_miRNA","GOC:BHF","GOC:rph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of leukocyte proliferation","termid":"GO:0070664"},{"relation_name":"is_a","term_name":"regulation of macrophage proliferation","termid":"GO:0120040"},{"relation_name":"negatively_regulates","term_name":"macrophage proliferation","termid":"GO:0061517"}],"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 macrophage proliferation","termid":"GO:0120042"}


id: PBO:0113322
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein kinase; minor role relative to Kin4p in regulating peroxisomal transport and vacuolar inheritance; protects the peroxisomal Myo2p receptor Inp2p from degradation in mother cells along with Kin4p; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm; interacts with rRNA transcription and ribosome biogenesis factors and the long chain fatty acyl-CoA synthetase Faa3p; FRK1 has a paralog, KIN4, that arose from the whole genome duplication","termid":"PBO:0113322"}


id: MONDO:0022975
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":"diaphragmatic agenesis radial aplasia omphalocele","termid":"MONDO:0022975","xrefs":{"Monarch":{"xref_id":"0022975"}}}


id: PBO:0000120
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"antisense RNA (predicted)","termid":"PBO:0000120"}


id: MONDO:0006357
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma that arises from a pleomorphic adenoma in the parotid gland. Patients usually present with a history of a long-standing tumor mass which grew rapidly in the past few months. Patients with non-invasive or minimally invasive carcinoma have an excellent prognosis. In cases where there is invasion of the surrounding tissues, the clinical course is aggressive.","definition_xrefs":["NCIT:C5974"],"direct_ancestors":[{"relation_name":"is_a","term_name":"major salivary gland carcinoma ex pleomorphic adenoma","termid":"MONDO:0006285"},{"relation_name":"is_a","term_name":"carcinoma of parotid gland","termid":"MONDO:0021331"}],"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":"parotid gland carcinoma ex pleomorphic adenoma","secondary_identifiers":["EFO:1000461","MEDGEN:233311","SCTID:425127006","UMLS:C1335356"],"synonyms":[{"name":"carcinoma ex pleomorphic adenoma of parotid","type":"exact"},{"name":"carcinoma ex pleomorphic adenoma of parotid gland","type":"exact"},{"name":"carcinoma ex pleomorphic adenoma of the parotid","type":"exact"},{"name":"carcinoma ex pleomorphic adenoma of the parotid gland","type":"exact"},{"name":"parotid carcinoma ex pleomorphic adenoma","type":"exact"},{"name":"parotid gland carcinoma ex pleomorphic adenoma","type":"exact"}],"termid":"MONDO:0006357","xrefs":{"Monarch":{"xref_id":"0006357"}}}


id: FYPO:0009053
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A vegetative cell population growth phenotype in which cell growth is decreased relative to normal in a medium containing L-glutamate as the nitrogen source.","definition_xrefs":["PMID:34984977","PomBase:mlr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased vegetative cell population growth","termid":"FYPO:0001355"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002058"}],"interesting_parent_ids":["FYPO:0002058","FYPO:0000139","FYPO:0001985","FYPO:0000003","FYPO:0002057","FYPO:0002060","FYPO:0005447"],"is_obsolete":false,"name":"decreased cell population growth on glutamate nitrogen source","synonyms":[{"name":"decreased growth on glutamate nitrogen source","type":"broad"},{"name":"decreased vegetative cell growth on glutamate nitrogen source","type":"exact"},{"name":"growth defect, slow growth with glutamate nitrogen source","type":"related"},{"name":"reduced cell growth on glutamate nitrogen source","type":"related"},{"name":"slow cell growth on glutamate nitrogen source","type":"narrow"}],"termid":"FYPO:0009053"}


id: PBO:0048531
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gem nuclear organelle associated protein 7","termid":"PBO:0048531"}


id: GO:0006971
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 detection of, or exposure to, a hypotonic environment, i.e. an environment with a lower concentration of solutes than the organism or cell.","definition_xrefs":["GOC:jl","PMID:12598593"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to osmotic stress","termid":"GO:0006970"}],"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":"hypotonic response","synonyms":[{"name":"hypo-osmotic response","type":"exact"}],"termid":"GO:0006971"}


id: MONDO:0010811
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-cancerous nodular enlargement of the prostate gland. It is characterized by the presence of epithelial cell nodules, and stromal nodules containing fibrous and smooth muscle elements. It is the most common urologic disorder in men, causing blockage of urine flow.","definition_xrefs":["NCIT:C2897"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prostate disorder","termid":"MONDO:0003105"},{"relation_name":"is_a","term_name":"hyperplasia","termid":"MONDO:0005043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign prostatic hyperplasia","secondary_identifiers":["DOID:11132","OMIM:600082","HP:0008711","ICD9:600.0","ICD9:600","ICD9:600.20","MEDGEN:312369","SCTID:266569009","MESH:D011470","UMLS:C1704272","EFO:0000284"],"synonyms":[{"name":"BPH","type":"related"},{"name":"benign hyperplasia of prostate","type":"exact"},{"name":"benign hyperplasia of the prostate","type":"exact"},{"name":"benign prostate hyperplasia","type":"exact"},{"name":"benign prostatic Hypertrophy","type":"exact"},{"name":"benign prostatic hyperplasia","type":"exact"},{"name":"benign prostatic hyperplasia (disease)","type":"exact"},{"name":"benign prostatic hyperplasia - BPH","type":"exact"},{"name":"benign prostatic hypertrophy","type":"exact"},{"name":"prostate hypertrophy","type":"broad"},{"name":"prostatic hyperplasia, benign","type":"related"},{"name":"prostatic hypertrophy","type":"broad"}],"termid":"MONDO:0010811","xrefs":{"Monarch":{"xref_id":"0010811"}}}


id: GO:1904650
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of fat cell apoptotic process.","definition_xrefs":["GO_REF:0000058","PMID:17024416","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of apoptotic process","termid":"GO:0043066"},{"relation_name":"is_a","term_name":"regulation of fat cell apoptotic process","termid":"GO:1904649"},{"relation_name":"negatively_regulates","term_name":"fat cell apoptotic process","termid":"GO:1904606"}],"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 fat cell apoptotic process","synonyms":[{"name":"down regulation of adipocyte apoptosis","type":"narrow"},{"name":"down regulation of adipocyte apoptotic process","type":"exact"},{"name":"down regulation of adipose cell apoptosis","type":"narrow"},{"name":"down regulation of adipose cell apoptotic process","type":"exact"},{"name":"down regulation of fat cell apoptosis","type":"narrow"},{"name":"down regulation of fat cell apoptotic process","type":"exact"},{"name":"down-regulation of adipocyte apoptosis","type":"narrow"},{"name":"down-regulation of adipocyte apoptotic process","type":"exact"},{"name":"down-regulation of adipose cell apoptosis","type":"narrow"},{"name":"down-regulation of adipose cell apoptotic process","type":"exact"},{"name":"down-regulation of fat cell apoptosis","type":"narrow"},{"name":"down-regulation of fat cell apoptotic process","type":"exact"},{"name":"downregulation of adipocyte apoptosis","type":"narrow"},{"name":"downregulation of adipocyte apoptotic process","type":"exact"},{"name":"downregulation of adipose cell apoptosis","type":"narrow"},{"name":"downregulation of adipose cell apoptotic process","type":"exact"},{"name":"downregulation of fat cell apoptosis","type":"narrow"},{"name":"downregulation of fat cell apoptotic process","type":"exact"},{"name":"inhibition of adipocyte apoptosis","type":"narrow"},{"name":"inhibition of adipocyte apoptotic process","type":"narrow"},{"name":"inhibition of adipose cell apoptosis","type":"narrow"},{"name":"inhibition of adipose cell apoptotic process","type":"narrow"},{"name":"inhibition of fat cell apoptosis","type":"narrow"},{"name":"inhibition of fat cell apoptotic process","type":"narrow"},{"name":"negative regulation of adipocyte apoptosis","type":"narrow"},{"name":"negative regulation of adipocyte apoptotic process","type":"exact"},{"name":"negative regulation of adipose cell apoptosis","type":"narrow"},{"name":"negative regulation of adipose cell apoptotic process","type":"exact"},{"name":"negative regulation of fat cell apoptosis","type":"narrow"}],"termid":"GO:1904650"}


id: MONDO:0800182
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any primary hereditary glaucoma in which the cause of the disease is a mutation in the TEK gene.","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary glaucoma","termid":"MONDO:0018174"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"TEK-related primary glaucoma","termid":"MONDO:0800182","xrefs":{"Monarch":{"xref_id":"0800182"}}}


id: GO:0004377
data:
  {"annotated_genes":["SJAG_00747"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[77077],"is_not":false,"summary":null,"term":"GO:0004377"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: an alpha-D-Man-(1->3)-[alpha-D-Man-(1->6)]-beta-D-Man-(1->4)-beta-D-GlcNAc-(1->4)-D-GlcNAc-diphosphodolichol + 2 GDP-alpha-D-mannose = an alpha-D-Man-(1->2)-alpha-D-Man-(1->2)-alpha-D-Man-(1->3)-[alpha-D-Man-(1->6)]-beta-D-Man-(1->4)-beta-D-GlcNAc-(1->4)-D-GlcNAc-diphosphodolichol + 2 GDP + 2 H+. This reaction is the transfer of an alpha-D-mannosyl residue from GDP-mannose into lipid-linked oligosaccharide, forming an alpha-(1->2)-D-mannosyl-D-mannose linkage.","definition_xrefs":["EC:2.4.1.131"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alpha-1,2-mannosyltransferase activity","termid":"GO:0000026"},{"relation_name":"is_a","term_name":"glycolipid mannosyltransferase activity","termid":"GO:0004376"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00747":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016757"}],"interesting_parent_ids":["GO:0003824","GO:0016740","GO:0003674","GO:0016757"],"is_obsolete":false,"name":"GDP-Man:Man3GlcNAc2-PP-Dol alpha-1,2-mannosyltransferase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["MetaCyc:RXN-5464","RHEA:29523"],"synonyms":[{"name":"GDP-D-mannose:D-Man-alpha-(1->3)-[D-Man-alpha-(1->6)]-D-Man-beta-(1->4)-D-GlcNAc-beta-(1->4)-D-GlcNAc-diphosphodolichol alpha-1,2-mannosyltransferase activity","type":"related"},{"name":"GDP-mannose-oligosaccharide-lipid mannosyltransferase activity","type":"related"},{"name":"GDP-mannose:glycolipid 1,2-alpha-D-mannosyltransferase activity","type":"related"},{"name":"glycolipid 2-alpha-mannosyltransferase activity","type":"related"},{"name":"guanosine diphosphomannose-oligosaccharide-lipid mannosyltransferase activity","type":"related"},{"name":"oligosaccharide-lipid mannosyltransferase activity","type":"related"}],"termid":"GO:0004377","terms_by_termid":{"GO:0004377":null}}


id: PBO:0034193
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-ubiquitously_expressed_in","termid":"PBO:0034193"}


id: PR:O94370
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC1604.04 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94370"],"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 C1604.04 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1604.04","synonyms":[{"name":"Spom972h-SPBC1604.04","type":"exact"}],"termid":"PR:O94370"}


id: PBO:0087752
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the transmembrane ring of the nuclear pore complex (NPC); contributes to nucleocytoplasmic transport, NPC biogenesis and spindle pole body duplication; homologous to human NDC1","termid":"PBO:0087752"}


id: GO:0045513
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to interleukin-27.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"interleukin-17 binding","termid":"GO:0019975"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"interleukin-27 binding","synonyms":[{"name":"IL-27 binding","type":"exact"}],"termid":"GO:0045513"}


id: GO:0032488
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An intracellular signaling cassette in which a small monomeric GTPase of the Cdc42 subfamily relays a signal.","definition_xrefs":["PMID:18558478","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Rho protein signal transduction","termid":"GO:0007266"}],"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":"Cdc42 protein signal transduction","synonyms":[{"name":"Cdc42 signaling","type":"related"},{"name":"Cdc42 signaling pathway","type":"related"},{"name":"cdc42 signalling pathway","type":"related"}],"termid":"GO:0032488"}


id: GO:0033339
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the pectoral fin over time, from its formation to the mature structure.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fin development","termid":"GO:0033333"},{"relation_name":"is_a","term_name":"limb development","termid":"GO:0060173"}],"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":"pectoral fin development","termid":"GO:0033339"}


id: GO:0003037
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which information about the levels of hydrogen ions are received and are converted to a molecular signal by chemoreceptors in a carotid body.","definition_xrefs":["GOC:mtg_cardio"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detection of pH by chemoreceptor signaling","termid":"GO:0003022"},{"relation_name":"part_of","term_name":"detection of hypoxic conditions in blood by carotid body chemoreceptor signaling","termid":"GO:0003029"}],"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 pH by carotid body chemoreceptor signaling","synonyms":[{"name":"detection of pH by carotid body chemoreceptor signalling","type":"exact"}],"termid":"GO:0003037"}


id: MONDO:0018228
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Bipartite talus is a rare, genetic bone disorder characterized by the presence of two non-fused talar bone fragments, with the posterior fragment located at the level of the posterior talar process. Patients may present with foot and/or ankle pain (exercise-induced or not), repetitive ankle sprains, chronic ankle ligamentous laxity, restricted ankle motion (i.e. plantar flexion, eversion, and inversion), and mild swelling.","definition_xrefs":["Orphanet:364198"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"dysostosis","termid":"MONDO:0018234"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"bipartite talus","secondary_identifiers":["SCTID:763128009","MEDGEN:1631166","GARD:21566","UMLS:C4706298"],"termid":"MONDO:0018228","xrefs":{"Monarch":{"xref_id":"0018228"}}}


id: PBO:0004837
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER-localized ubiquitin ligase Doa10 (predicted)","termid":"PBO:0004837"}


id: PBO:0004146
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ric8 family guanine nulceotide exchange factor synembryn family","termid":"PBO:0004146"}


id: PBO:0083819
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential subunit of Sec63 complex; with Sec61 complex, Kar2p/BiP and Lhs1p forms a channel competent for SRP-dependent and post-translational SRP-independent protein targeting and import into the ER; other members are Sec62p, Sec66p, and Sec72p","termid":"PBO:0083819"}


id: GO:0008079
data:
  {"annotated_genes":["SJAG_02189","SJAG_01696","SJAG_02601","SJAG_01518","SJAG_02812","SJAG_04283","SJAG_03232","SJAG_05221","SJAG_00338","SJAG_00308"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[105027,109486,109487],"is_not":false,"summary":null,"term":"GO:0008079"},{"annotations":[72816,107494,69215,116336,66496],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003747"},{"annotations":[98979],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016150"},{"annotations":[74167],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016149"}]},"cv_name":"molecular_function","definition":"Functions in the termination of translation.","definition_xrefs":["GOC:ma"],"direct_ancestors":[{"relation_name":"is_a","term_name":"translation factor activity","termid":"GO:0180051"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00308":null,"SJAG_00338":null,"SJAG_01518":null,"SJAG_01696":null,"SJAG_02189":null,"SJAG_02601":null,"SJAG_02812":null,"SJAG_03232":null,"SJAG_04283":null,"SJAG_05221":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674"],"is_obsolete":false,"name":"translation termination factor activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0008079","terms_by_termid":{"GO:0003747":null,"GO:0008079":null,"GO:0016149":null,"GO:0016150":null}}


id: MONDO:0018932
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cirrhotic cardiomyopathy is the term used to describe a constellation of features indicative of abnormal heart structure and function in patients with cirrhosis. These include systolic and diastolic dysfunction, electrophysiological changes, and macroscopic and microscopic structural changes.","definition_xrefs":["Orphanet:57777"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-familial hypertrophic cardiomyopathy","termid":"MONDO:0016330"},{"relation_name":"is_a","term_name":"non-familial dilated cardiomyopathy","termid":"MONDO:0016338"}],"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":"cirrhotic cardiomyopathy","secondary_identifiers":["icd11.foundation:1268082489","SCTID:725416005","UMLS:C4511053","GARD:18852","MEDGEN:1391593"],"termid":"MONDO:0018932","xrefs":{"Monarch":{"xref_id":"0018932"}}}


id: PBO:0065661
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein tyrosine phosphatase receptor type K","termid":"PBO:0065661"}


id: PBO:0085657
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in modulation of Ime2p activity during meiosis; appears to act indirectly to promote Ime2p-mediated late meiotic functions; found in growing cells and degraded during sporulation","termid":"PBO:0085657"}


id: PBO:0053439
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 384","termid":"PBO:0053439"}


id: GO:0008746
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: NADPH + H+ + NAD+ = NADP+ + NADH + H+.","definition_xrefs":["EC:1.6.1.2"],"gene_count":0,"genotype_count":0,"name":"obsolete NAD(P)+ transhydrogenase activity (obsolete GO:0008746)","termid":"GO:0008746"}


id: MOD:00716
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-methionine residue to a methylated methionine, such as N-methyl-L-methionine.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methylated residue","termid":"MOD:00427"},{"relation_name":"is_a","term_name":"modified L-methionine residue","termid":"MOD:00913"}],"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":"methylated methionine","synonyms":[{"name":"MeMet","type":"exact"}],"termid":"MOD:00716"}


id: GO:0046230
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of 2-aminobenzenesulfonate, an aromatic sulfonate used in organic synthesis and in the manufacture of various dyes and medicines.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amine catabolic process","termid":"GO:0009310"},{"relation_name":"is_a","term_name":"organic acid catabolic process","termid":"GO:0016054"},{"relation_name":"is_a","term_name":"2-aminobenzenesulfonate metabolic process","termid":"GO:0018868"},{"relation_name":"is_a","term_name":"xenobiotic catabolic process","termid":"GO:0042178"},{"relation_name":"is_a","term_name":"sulfur compound catabolic process","termid":"GO:0044273"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006790","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"2-aminobenzenesulfonate catabolic process","synonyms":[{"name":"2-aminobenzenesulfonate breakdown","type":"exact"},{"name":"2-aminobenzenesulfonate catabolism","type":"exact"},{"name":"2-aminobenzenesulfonate degradation","type":"exact"},{"name":"2-aminobenzenesulphonate catabolic process","type":"exact"},{"name":"2-aminobenzenesulphonate catabolism","type":"exact"}],"termid":"GO:0046230"}


id: MONDO:0012433
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Senior-Loken syndrome in which the cause of the disease is a mutation in the CEP290 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Senior-Loken syndrome","termid":"MONDO:0017842"},{"relation_name":"is_a","term_name":"CEP290-related ciliopathy","termid":"MONDO:0100451"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005240"],"is_obsolete":false,"name":"Senior-Loken syndrome 6","secondary_identifiers":["UMLS:C1857779","MESH:C565708","MEDGEN:387907","GARD:15476","OMIM:610189"],"synonyms":[{"name":"CEP290 Senior-Loken syndrome","type":"exact"},{"name":"SENIOR-Loken syndrome 6","type":"related"},{"name":"SLSN6","type":"related"},{"name":"Senior-Loken syndrome 6","type":"exact"},{"name":"Senior-Loken syndrome caused by mutation in CEP290","type":"exact"},{"name":"Senior-Loken syndrome type 6","type":"exact"}],"termid":"MONDO:0012433","xrefs":{"Monarch":{"xref_id":"0012433"}}}


id: GO:0060861
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency, or extent of floral organ shedding, the controlled shedding of floral organs.","definition_xrefs":["GOC:sdb_2009","GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of developmental process","termid":"GO:0051094"},{"relation_name":"is_a","term_name":"regulation of floral organ abscission","termid":"GO:0060860"},{"relation_name":"is_a","term_name":"positive regulation of reproductive process","termid":"GO:2000243"},{"relation_name":"positively_regulates","term_name":"floral organ abscission","termid":"GO:0010227"}],"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 floral organ abscission","termid":"GO:0060861"}


id: MONDO:0001239
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A blood disorder characterized by low hemoglobin levels in premature neonates that usually spontaneously resolves within 3-6 months post birth. A combination of factors including the transition from the liver to the bone marrow for erythropoiesis in a neonate, blood loss experienced during delivery, the shortened life span of fetal blood cells, and an acclimation to a relatively hyperoxic environment outside the womb can predispose a neonate to this condition.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neonatal anemia","termid":"MONDO:0001240"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0002280"],"is_obsolete":false,"name":"anemia of prematurity","secondary_identifiers":["DOID:11243","MEDGEN:472907","ICD9:776.6","ICD10CM:P61.2","NCIT:C97167","SCTID:47100003","UMLS:C0158996"],"synonyms":[{"name":"AOP","type":"exact"}],"termid":"MONDO:0001239","xrefs":{"Monarch":{"xref_id":"0001239"}}}


id: MONDO:0006523
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inflammatory skin condition affecting children. It is often associated with Epstein-Barr virus infection, hepatitis B infection or cytomegalovirus infection. It is characterized by the presence of cutaneous rashes and patches on the palms and soles. The trunk is not affected.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dermatitis","termid":"MONDO:0002406"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"acrodermatitis","secondary_identifiers":["DOID:2722","UMLS:C0001197","MEDGEN:1301","ICD9:686.8","MESH:D000169","SCTID:8197001","CSP:4008-0032","NCIT:C84532","EFO:1000664"],"termid":"MONDO:0006523","xrefs":{"Monarch":{"xref_id":"0006523"}}}


id: PBO:0077346
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 87A","termid":"PBO:0077346"}


id: GO:1904554
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of chemotaxis to arachidonic acid.","definition_xrefs":["PMID:16382163","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of chemotaxis","termid":"GO:0050921"},{"relation_name":"is_a","term_name":"regulation of chemotaxis to arachidonate","termid":"GO:1904552"},{"relation_name":"positively_regulates","term_name":"chemotaxis to arachidonate","termid":"GO:0034670"}],"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 chemotaxis to arachidonate","synonyms":[{"name":"activation of chemotaxis to arachidonic acid","type":"narrow"},{"name":"positive regulation of chemotaxis to arachidonic acid","type":"exact"},{"name":"up regulation of chemotaxis to arachidonic acid","type":"exact"},{"name":"up-regulation of chemotaxis to arachidonic acid","type":"exact"},{"name":"upregulation of chemotaxis to arachidonic acid","type":"exact"}],"termid":"GO:1904554"}


id: PBO:0116753
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SWI/SNF related BAF chromatin remodeling complex subunit D3","termid":"PBO:0116753"}


id: GO:0031508
data:
  {"annotated_genes":["SJAG_01540","SJAG_03689","SJAG_04030","SJAG_02409","SJAG_03193","SJAG_03128","SJAG_04253","SJAG_04061","SJAG_04574","SJAG_03624","SJAG_04141","SJAG_03997","SJAG_00414","SJAG_01599","SJAG_00961","SJAG_01675","SJAG_01601","SJAG_04942","SJAG_02594","SJAG_01008","SJAG_02401","SJAG_03844","SJAG_01075","SJAG_00756","SJAG_03042","SJAG_02119","SJAG_02725","SJAG_00058","SJAG_02778","SJAG_04039","SJAG_00934","SJAG_00335","SJAG_00142","SJAG_03356","SJAG_00087","SJAG_03982","SJAG_03680","SJAG_03916","SJAG_02576","SJAG_00302","SJAG_01579","SJAG_02846","SJAG_03543","SJAG_02621"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[72555,90552,92412,93168,93789,94419,98580,103095,103542,104408,108472,111580,112414,112928,112929,112930,113600,114292,114724],"is_not":false,"summary":null,"term":"GO:0031508"},{"annotations":[91524],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0090053"},{"annotations":[100624,97516],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0090052"},{"annotations":[95673,106868,112518,89175,114609,91613,114873,118396,110799,117997,118282,119115,97062,116287,94432,99454,110965,115725,99892,89119,111519,113977],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140727"}]},"cv_name":"biological_process","definition":"The compaction of chromatin located adjacent to the CENP-A rich centromere 'central core' and characterized by methylation of histone H3K9, into heterochromatin, resulting in the repression of transcription at pericentric DNA.","definition_xrefs":["PMID:20206496","PMID:22729156","GOC:mah","PMID:14612388"],"direct_ancestors":[{"relation_name":"is_a","term_name":"constitutive heterochromatin formation","termid":"GO:0140719"}],"gene_count":44,"genes_by_uniquename":{"SJAG_00058":null,"SJAG_00087":null,"SJAG_00142":null,"SJAG_00302":null,"SJAG_00335":null,"SJAG_00414":null,"SJAG_00756":null,"SJAG_00934":null,"SJAG_00961":null,"SJAG_01008":null,"SJAG_01075":null,"SJAG_01540":null,"SJAG_01579":null,"SJAG_01599":null,"SJAG_01601":null,"SJAG_01675":null,"SJAG_02119":null,"SJAG_02401":null,"SJAG_02409":null,"SJAG_02576":null,"SJAG_02594":null,"SJAG_02621":null,"SJAG_02725":null,"SJAG_02778":null,"SJAG_02846":null,"SJAG_03042":null,"SJAG_03128":null,"SJAG_03193":null,"SJAG_03356":null,"SJAG_03543":null,"SJAG_03624":null,"SJAG_03680":null,"SJAG_03689":null,"SJAG_03844":null,"SJAG_03916":null,"SJAG_03982":null,"SJAG_03997":null,"SJAG_04030":null,"SJAG_04039":null,"SJAG_04061":null,"SJAG_04141":null,"SJAG_04253":null,"SJAG_04574":null,"SJAG_04942":null},"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":"is_a","termid":"GO:0006325"}],"interesting_parent_ids":["GO:0006325","GO:0008150","GO:0010467"],"is_obsolete":false,"name":"pericentric heterochromatin formation","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:1990141","GO:0030702"],"synonyms":[{"name":"centric heterochromatin formation","type":"related"},{"name":"centromere chromatin silencing","type":"exact"},{"name":"centromeric heterochromatin biosynthesis","type":"exact"},{"name":"centromeric heterochromatin formation","type":"exact"},{"name":"centromeric silencing","type":"exact"},{"name":"chromatin silencing at centromere","type":"exact"},{"name":"chromatin silencing at centromere outer repeat region","type":"narrow"},{"name":"chromatin silencing at pericentric region","type":"related"},{"name":"heterochromatic silencing at centromere","type":"exact"},{"name":"pericentric heterochromatin assembly","type":"exact"}],"termid":"GO:0031508","terms_by_termid":{"GO:0031508":null,"GO:0090052":null,"GO:0090053":null,"GO:0140727":null}}


id: MONDO:0014746
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"congenital disorder of glycosylation type II","termid":"MONDO:0005501"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"developmental anomaly of metabolic origin","termid":"MONDO:0015327"},{"relation_name":"is_a","term_name":"disorder of protein N-glycosylation","termid":"MONDO:0017740"},{"relation_name":"is_a","term_name":"central nervous system malformation","termid":"MONDO:0020022"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0020022"},{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0024322"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0020022","MONDO:0024322","MONDO:0005066"],"is_obsolete":false,"name":"SLC39A8-CDG","secondary_identifiers":["Orphanet:468699","DOID:0070266","GARD:17846","UMLS:C4225234","MEDGEN:899837","OMIM:616721"],"synonyms":[{"name":"CDG IIn","type":"related"},{"name":"CDG syndrome type IIn","type":"exact"},{"name":"CDG-IIn","type":"exact"},{"name":"CDG2N","type":"exact"},{"name":"SLC39A8 deficiency","type":"exact"},{"name":"carbohydrate deficient glycoprotein syndrome type IIn","type":"exact"},{"name":"congenital disorder of glycosylation type 2n","type":"exact"},{"name":"congenital disorder of glycosylation type IIn","type":"exact"},{"name":"congenital disorder of glycosylation, type IIn","type":"exact"}],"termid":"MONDO:0014746","xrefs":{"Monarch":{"xref_id":"0014746"}}}


id: PBO:0087114
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribosome-associated protein; proposed to act in protein synthesis, nuclear pore complex biogenesis and maintenance as well as protein folding and prion maintenance; ; has similarity to the mammalian BAG-1 protein","termid":"PBO:0087114"}


id: GO:1901438
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of toluene metabolic process.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of metabolic process","termid":"GO:0009892"},{"relation_name":"is_a","term_name":"regulation of toluene metabolic process","termid":"GO:1901437"},{"relation_name":"negatively_regulates","term_name":"toluene metabolic process","termid":"GO:0018970"}],"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 toluene metabolic process","synonyms":[{"name":"down regulation of methylbenzene metabolic process","type":"exact"},{"name":"down regulation of methylbenzene metabolism","type":"exact"},{"name":"down regulation of toluene metabolic process","type":"exact"},{"name":"down regulation of toluene metabolism","type":"exact"},{"name":"down-regulation of methylbenzene metabolic process","type":"exact"},{"name":"down-regulation of methylbenzene metabolism","type":"exact"},{"name":"down-regulation of toluene metabolic process","type":"exact"},{"name":"down-regulation of toluene metabolism","type":"exact"},{"name":"downregulation of methylbenzene metabolic process","type":"exact"},{"name":"downregulation of methylbenzene metabolism","type":"exact"},{"name":"downregulation of toluene metabolic process","type":"exact"},{"name":"downregulation of toluene metabolism","type":"exact"},{"name":"inhibition of methylbenzene metabolic process","type":"exact"},{"name":"inhibition of methylbenzene metabolism","type":"exact"},{"name":"inhibition of toluene metabolic process","type":"narrow"},{"name":"inhibition of toluene metabolism","type":"exact"},{"name":"negative regulation of methylbenzene metabolic process","type":"exact"},{"name":"negative regulation of methylbenzene metabolism","type":"exact"},{"name":"negative regulation of toluene metabolism","type":"exact"}],"termid":"GO:1901438"}


id: PBO:0085240
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Peptidyl-prolyl cis-trans isomerase (cyclophilin); catalyzes the cis-trans isomerization of peptide bonds N-terminal to proline residues; has a potential role in the secretory pathway; CPR4 has a paralog, CPR8, that arose from the whole genome duplication","termid":"PBO:0085240"}


id: PBO:0081333
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 133","termid":"PBO:0081333"}


id: GO:0002735
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of myeloid dendritic cell cytokine production.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of dendritic cell cytokine production","termid":"GO:0002732"},{"relation_name":"is_a","term_name":"regulation of myeloid dendritic cell cytokine production","termid":"GO:0002733"},{"relation_name":"is_a","term_name":"positive regulation of myeloid leukocyte mediated immunity","termid":"GO:0002888"},{"relation_name":"is_a","term_name":"positive regulation of myeloid leukocyte cytokine production involved in immune response","termid":"GO:0061081"},{"relation_name":"positively_regulates","term_name":"myeloid dendritic cell cytokine production","termid":"GO:0002372"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_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":"positive regulation of myeloid dendritic cell cytokine production","synonyms":[{"name":"activation of myeloid dendritic cell cytokine production","type":"narrow"},{"name":"stimulation of myeloid dendritic cell cytokine production","type":"narrow"},{"name":"up regulation of myeloid dendritic cell cytokine production","type":"exact"},{"name":"up-regulation of myeloid dendritic cell cytokine production","type":"exact"},{"name":"upregulation of myeloid dendritic cell cytokine production","type":"exact"}],"termid":"GO:0002735"}


id: PBO:0039740
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"apolipoprotein L2","termid":"PBO:0039740"}


id: MOD:00442
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"Covalent modification of a peptide or protein L-arginine residue to protonated omega-N,omega-N'-dimethylated L-arginine with secondary loss of an N,N'-carbodiimide molecular fragment.","definition_xrefs":["PubMed:18688235","PubMed:15835918"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified residue with a secondary neutral loss","termid":"MOD:00431"},{"relation_name":"is_a","term_name":"modified L-arginine residue","termid":"MOD:00902"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protonated omega-N,omega-N'-dimethylated L-arginine with secondary neutral loss of N,N'-carbodiimide","synonyms":[{"name":"dCDI-NNMe2+Arg","type":"exact"}],"termid":"MOD:00442"}


id: MONDO:0956967
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A medulloblastoma non-WNT/non-SHH that is characterized as a molecular subtype by the absence of MYC amplifications and TP53 mutations, while chromosome 17 abnormalities may be present.","definition_xrefs":["DOID:0080708"],"direct_ancestors":[{"relation_name":"is_a","term_name":"medulloblastoma non-WNT/non-SHH","termid":"MONDO:0850198"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"medulloblastoma non-WNT/non-SHH group 4","secondary_identifiers":["MEDGEN:1377534","UMLS:C4330666","NCIT:C129446"],"termid":"MONDO:0956967","xrefs":{"Monarch":{"xref_id":"0956967"}}}


id: PR:O94301
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- hfi1 gene.","definition_xrefs":["UniProtKB:O94301","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":"transcriptional coactivator hfi1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC887.18c","synonyms":[{"name":"Spom972h-hfi1","type":"exact"}],"termid":"PR:O94301"}


id: MONDO:1011857
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder, non-human animal","termid":"MONDO:1011336"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"progressive cerebellar abiotrophy, non-human animal","secondary_identifiers":["OMIA:000826"],"termid":"MONDO:1011857","xrefs":{"Monarch":{"xref_id":"1011857"}}}


id: GO:0008334
data:
  {"annotated_genes":["SJAG_03745"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[71244],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071044"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving an mRNA encoding a histone.","definition_xrefs":["PMID:17855393","GOC:mah","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mRNA metabolic process","termid":"GO:0016071"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03745":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016071"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0016071","GO:0008150"],"is_obsolete":false,"name":"histone mRNA metabolic process","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"histone mRNA metabolism","type":"exact"},{"name":"stem-loop-containing histone mRNA 3'-end processing","type":"narrow"}],"termid":"GO:0008334","terms_by_termid":{"GO:0071044":null}}


id: PBO:0036170
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_myxothiazol","termid":"PBO:0036170"}


id: GO:0006805
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving a xenobiotic compound, a compound foreign to the organism exposed to it. It may be synthesized by another organism (like ampicilin) or it can be a synthetic chemical.","definition_xrefs":["GOC:cab2","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metabolic process","termid":"GO:0008152"},{"relation_name":"part_of","term_name":"cellular response to xenobiotic stimulus","termid":"GO:0071466"}],"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":"xenobiotic metabolic process","secondary_identifiers":["Reactome:R-HSA-211859","Reactome:R-HSA-211981","Reactome:R-HSA-2161541","Reactome:R-HSA-9748784","GO:0017144","Wikipedia:Drug_metabolism","Wikipedia:Xenobiotic_metabolism"],"synonyms":[{"name":"drug metabolic process","type":"related"},{"name":"drug metabolism","type":"related"},{"name":"xenobiotic metabolism","type":"exact"}],"termid":"GO:0006805"}


id: GO:0009085
data:
  {"annotated_genes":["SJAG_01574","SJAG_00502","SJAG_03312","SJAG_01955","SJAG_04688","SJAG_02388","SJAG_01061","SJAG_00869","SJAG_01630"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[113755,76443,77016,77825,75413,70505,64435,65078,96691],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019878"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of lysine, 2,6-diaminohexanoic acid.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lysine metabolic process","termid":"GO:0006553"},{"relation_name":"is_a","term_name":"aspartate family amino acid biosynthetic process","termid":"GO:0009067"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00502":null,"SJAG_00869":null,"SJAG_01061":null,"SJAG_01574":null,"SJAG_01630":null,"SJAG_01955":null,"SJAG_02388":null,"SJAG_03312":null,"SJAG_04688":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006520"}],"interesting_parent_ids":["GO:0044281","GO:0006520","GO:0008150"],"is_obsolete":false,"name":"lysine biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:LYSINE-SYN"],"synonyms":[{"name":"lysine anabolism","type":"exact"},{"name":"lysine biosynthesis","type":"exact"},{"name":"lysine formation","type":"exact"},{"name":"lysine synthesis","type":"exact"}],"termid":"GO:0009085","terms_by_termid":{"GO:0019878":null}}


id: GO:0071153
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex formed by the association of the guanine nucleotide exchange factor synembrin with the alpha(o) subunit of a heterotrimeric G protein.","definition_xrefs":["GOC:mah","PMID:12509430"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular protein-containing complex","termid":"GO:0140535"},{"relation_name":"part_of","term_name":"intracellular anatomical structure","termid":"GO:0005622"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"G-protein alpha(o)-synembrin complex","synonyms":[{"name":"Ric-8A G(o) alpha-1 subunit complex","type":"narrow"},{"name":"Ric-8A G(o) alpha-2 subunit complex","type":"narrow"}],"termid":"GO:0071153"}


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


id: PBO:0050653
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock protein 90 alpha family class B member 3, pseudogene","termid":"PBO:0050653"}


id: GO:0120541
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification, often by sulfation, of sugars in the polysaccharide chain component of dermatan sulfate proteoglycans.","definition_xrefs":["PMID:38500384"],"gene_count":0,"genotype_count":0,"name":"obsolete dermatan sulfate proteoglycan biosynthetic process, enzymatic modification (obsolete GO:0120541)","termid":"GO:0120541"}


id: PBO:0085122
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nucleolar protein; forms a complex with Noc4p that mediates maturation and nuclear export of 40S ribosomal subunits; also present in the small subunit processome complex, which is required for processing of pre-18S rRNA","termid":"PBO:0085122"}


id: GO:0006974
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stress","type":"exact"}],"termid":"GO:0006974","terms_by_termid":{"GO:0000012":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:0010569":null,"GO:0010772":null,"GO:0019985":null,"GO:0031571":null,"GO:0031573":null,"GO:0031848":null,"GO:0036297":null,"GO:0036298":null,"GO:0036299":null,"GO:0042276":null,"GO:0043504":null,"GO:0044773":null,"GO:0045002":null,"GO:0045003":null,"GO:0045004":null,"GO:0045007":null,"GO:0045739":null,"GO:0061674":null,"GO:0070911":null,"GO:0070914":null,"GO:0070987":null,"GO:0097510":null,"GO:0097552":null,"GO:0097680":null,"GO:0106300":null,"GO:0140861":null,"GO:1901255":null,"GO:1902346":null,"GO:1904161":null,"GO:1904332":null,"GO:1990414":null,"GO:1990516":null,"GO:1990918":null,"GO:2000779":null,"GO:2000781":null,"GO:2001033":null,"GO:2001034":null}}


id: PBO:0071286
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L26 pseudogene 9","termid":"PBO:0071286"}


id: GO:0044349
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The removal of a section of DNA from a larger DNA molecule by the making of dual incisions that flank the section to be excised.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete DNA excision (obsolete GO:0044349)","termid":"GO:0044349"}


id: SO:0000647
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A primary transcript encoding a micro RNA.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"has_part","term_name":"pre_miRNA","termid":"SO:0001244"},{"relation_name":"is_a","term_name":"nc_primary_transcript","termid":"SO:0000483"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"miRNA_primary_transcript","secondary_identifiers":["SO:0000648"],"synonyms":[{"name":"miRNA primary transcript","type":"exact"},{"name":"micro RNA primary transcript","type":"exact"},{"name":"small temporal RNA primary transcript","type":"exact"},{"name":"stRNA primary transcript","type":"exact"},{"name":"stRNA_primary_transcript","type":"exact"}],"termid":"SO:0000647"}


id: PBO:0078461
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor gamma variable B (pseudogene)","termid":"PBO:0078461"}


id: PBO:0044213
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cathepsin Z","termid":"PBO:0044213"}


id: MONDO:0031021
data:
  {"annotated_genes":["SJAG_00516"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87198],"is_not":false,"summary":null,"term":"MONDO:0031021"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"developmental and epileptic encephalopathy","termid":"MONDO:0100062"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00516":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"},{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0700092","MONDO:0005027"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy 104","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0070390","MEDGEN:1823956","OMIM:619970","UMLS:C5774183"],"synonyms":[{"name":"DEE104","type":"exact"},{"name":"developmental and epileptic encephalopathy 104","type":"exact"}],"termid":"MONDO:0031021","terms_by_termid":{"MONDO:0031021":null},"xrefs":{"Monarch":{"xref_id":"0031021"}}}


id: GO:2000749
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of rDNA heterochromatin formation.","definition_xrefs":["PMID:10899127"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of heterochromatin formation","termid":"GO:0031453"},{"relation_name":"is_a","term_name":"regulation of rDNA heterochromatin formation","termid":"GO:0061187"},{"relation_name":"positively_regulates","term_name":"rDNA heterochromatin formation","termid":"GO:0000183"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006325"},{"rel_name":"positively_regulates","termid":"GO:0006325"},{"rel_name":"positively_regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0006325","GO:0010467","GO:0044085","GO:0008150"],"is_obsolete":false,"name":"positive regulation of rDNA heterochromatin formation","synonyms":[{"name":"positive regulation of chromatin silencing at rDNA","type":"broad"},{"name":"positive regulation of chromatin silencing at ribosomal DNA","type":"broad"},{"name":"positive regulation of heterochromatic silencing at rDNA","type":"broad"},{"name":"positive regulation of rDNA chromatin silencing","type":"broad"},{"name":"positive regulation of rDNA heterochromatin assembly","type":"exact"},{"name":"positive regulation of ribosomal DNA heterochromatin assembly","type":"exact"}],"termid":"GO:2000749"}


id: GO:0005109
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a frizzled (fz) receptor.","definition_xrefs":["GOC:ceb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor binding","termid":"GO:0001664"}],"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":"frizzled binding","secondary_identifiers":["GO:0005110"],"synonyms":[{"name":"frizzled ligand","type":"narrow"},{"name":"frizzled-2 binding","type":"narrow"},{"name":"frizzled-2 ligand","type":"narrow"},{"name":"fz binding","type":"exact"},{"name":"fz ligand","type":"narrow"},{"name":"fz2 binding","type":"narrow"},{"name":"fz2 ligand","type":"narrow"}],"termid":"GO:0005109"}


id: MONDO:0006305
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete mixed cell uveal melanoma (obsolete MONDO:0006305)","termid":"MONDO:0006305","xrefs":{"Monarch":{"xref_id":"0006305"}}}


id: MONDO:0002831
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A squamous cell carcinoma of the sinonasal tract characterized by a plexiform or ribbon-like growth pattern, cytological atypia, and lack of histological evidence of keratinization.","definition_xrefs":["NCIT:C54287"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"maxillary sinus carcinoma","termid":"MONDO:0001748"},{"relation_name":"is_a","term_name":"nasal cavity and paranasal sinus squamous cell carcinoma","termid":"MONDO:0044787"}],"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":"non-keratinizing sinonasal squamous cell carcinoma","secondary_identifiers":["MEDGEN:83119","DOID:4003","ONCOTREE:SNSC","ICDO:8121/3","UMLS:C0334270"],"synonyms":[{"name":"Ringertz carcinoma","type":"related"},{"name":"Schneiderian carcinoma","type":"related"},{"name":"Sinonasal Schneiderian carcinoma","type":"related"},{"name":"Sinonasal cylindrical cell carcinoma","type":"related"},{"name":"Sinonasal transitional cell carcinoma","type":"related"},{"name":"cylindrical cell carcinoma","type":"exact"},{"name":"non-keratinizing sinonasal squamous cell carcinoma","type":"exact"},{"name":"sinonasal squamous cell carcinoma","type":"related"}],"termid":"MONDO:0002831","xrefs":{"Monarch":{"xref_id":"0002831"}}}


id: MONDO:0010031
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neurocutaneous disorder caused by an inborn error of lipid metabolism and characterized by congenital ichthyosis, intellectual deficit, and spasticity.","definition_xrefs":["Orphanet:816"],"direct_ancestors":[{"relation_name":"is_a","term_name":"integumentary system disorder","termid":"MONDO:0002051"},{"relation_name":"is_a","term_name":"eye degenerative disorder","termid":"MONDO:0004884"},{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"syndromic dyslipidemia","termid":"MONDO:0015905"},{"relation_name":"is_a","term_name":"disorder of phospholipids, sphingolipids and fatty acids biosynthesis","termid":"MONDO:0018117"},{"relation_name":"is_a","term_name":"leukodystrophy","termid":"MONDO:0019046"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0002525","MONDO:0005559","MONDO:0006025","MONDO:0005066"],"is_obsolete":false,"name":"Sjogren-Larsson syndrome","secondary_identifiers":["GARD:7654","icd11.foundation:418359090","NCIT:C85070","NANDO:2200994","MEDGEN:11443","NORD:1377","SCTID:111303009","NANDO:1200620","OMIM:270200","UMLS:C0037231","DOID:14501","MedDRA:10048676","MESH:D016111"],"synonyms":[{"name":"FADH deficiency","type":"related"},{"name":"FALDH deficiency","type":"related"},{"name":"FAO deficiency","type":"related"},{"name":"SLS","type":"exact"},{"name":"Senior-Løken Syndrome","type":"exact"},{"name":"Sjogren Larsson syndrome","type":"exact"},{"name":"Sjogren-Larsson syndrome","type":"exact"},{"name":"Sjogren-Larsson's syndrome","type":"exact"},{"name":"Sjögren-Larsson syndrome","type":"related"},{"name":"fatty acid alcohol oxidoreductase deficiency","type":"exact"},{"name":"fatty alcohol:NAD+ oxidoreductase deficiency","type":"related"},{"name":"fatty aldehyde dehydrogenase deficiency","type":"related"},{"name":"ichthyosis, spastic neurologic disorder, and oligophrenia","type":"related"}],"termid":"MONDO:0010031","xrefs":{"Monarch":{"xref_id":"0010031"}}}


id: GO:1990695
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the Golgi trans cisterna membrane consisting of the gene products and protein complexes having either part of their peptide sequence embedded in the hydrophobic region of the membrane or some other covalently attached group such as a GPI anchor that is similarly embedded in the membrane.","definition_xrefs":["PMID:24119662","GOC:bhm","PMID:16038056"],"gene_count":0,"genotype_count":0,"name":"obsolete intrinsic component of Golgi trans cisterna membrane (obsolete GO:1990695)","synonyms":[{"name":"intrinsic component of trans-Golgi cisterna membrane","type":"exact"}],"termid":"GO:1990695"}


id: PBO:0018184
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leptomycin transmembrane transporter Pmd1","termid":"PBO:0018184"}


id: MONDO:0008300
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Prader-Willi syndrome is a rare genetic disorder characterized by hypothalamic-pituitary abnormalities with severe hypotonia during the neonatal period and first two years of life and the onset of hyperphagia with a risk of morbid obesity during infancy and adulthood, learning difficulties and behavioral problems or severe psychiatric problems.","definition_xrefs":["Orphanet:739"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome","termid":"MONDO:0015160"},{"relation_name":"is_a","term_name":"congenital hypogonadotropic hypogonadism","termid":"MONDO:0015770"},{"relation_name":"is_a","term_name":"chromosomal disorder","termid":"MONDO:0019040"},{"relation_name":"is_a","term_name":"complex neurodevelopmental disorder","termid":"MONDO:0100038"},{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092","MONDO:0002320"],"is_obsolete":false,"name":"Prader-Willi syndrome","secondary_identifiers":["MEDGEN:46057","NANDO:2200411","GARD:5575","NORD:1602","OMIM:176270","SCTID:89392001","DOID:11983","UMLS:C0032897","NANDO:1200678","NCIT:C75463","ICD9:759.81","MESH:D011218","icd11.foundation:393773440","MedDRA:10036476"],"synonyms":[{"name":"PWS","type":"related"},{"name":"Prader Willi syndrome","type":"exact"},{"name":"Prader-Labhart-Willi syndrome","type":"exact"},{"name":"Prader-Willi syndrome","type":"exact"},{"name":"Prader-Willi syndrome chromosome region","type":"related"},{"name":"Prader-Willi-Labhart syndrome","type":"exact"},{"name":"Prader-Willi-like syndrome associated with chromosome 6","type":"related"},{"name":"Willi-Prader syndrome","type":"exact"},{"name":"obesity, muscular hypotonia, intellectual disability, short stature, hypogonadotropic hypogonadism, and small hands and feet","type":"related"},{"name":"obesity, muscular hypotonia, mental retardation, short stature, hypogonadotropic hypogonadism, and small hands and feet","type":"related"}],"termid":"MONDO:0008300","xrefs":{"Monarch":{"xref_id":"0008300"}}}


id: FYPO:0003537
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the rate, or speed, of premeiotic DNA replication is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased rate of DNA replication","termid":"FYPO:0001981"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0000293"],"is_obsolete":false,"name":"decreased rate of premeiotic DNA replication","synonyms":[{"name":"reduced rate of premeiotic DNA replication","type":"exact"}],"termid":"FYPO:0003537"}


id: GO:0043472
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to an immunoglobulin of a D isotype.","definition_xrefs":["PMID:12886015"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immunoglobulin binding","termid":"GO:0019865"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"IgD binding","termid":"GO:0043472"}


id: PBO:0029058
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-vacuoles_present_in_decreased_numbers_during_vegetative_growth","termid":"PBO:0029058"}


id: PBO:0003380
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA damage response protein (predicted)","termid":"PBO:0003380"}


id: PBO:0028629
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_protein_threonine_phosphorylation_during_cellular_response_to_heat","termid":"PBO:0028629"}


id: GO:0051560
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process involved in the maintenance of an internal steady state of calcium ions within the cytoplasm of a cell or between mitochondria and their surroundings.","definition_xrefs":["GOC:mah","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular calcium ion homeostasis","termid":"GO:0006874"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098771"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0098771","GO:0008150"],"is_obsolete":false,"name":"mitochondrial calcium ion homeostasis","synonyms":[{"name":"calcium ion homeostasis in mitochondria","type":"exact"},{"name":"calcium ion homeostasis in mitochondrion","type":"exact"},{"name":"mitochondrial calcium ion concentration regulation","type":"exact"},{"name":"regulation of calcium ion concentration in mitochondria","type":"exact"},{"name":"regulation of calcium ion concentration in mitochondrion","type":"exact"},{"name":"regulation of mitochondrial calcium ion concentration","type":"exact"}],"termid":"GO:0051560"}


id: MONDO:0020091
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete male infertility due to obstructive azoospermia (obsolete MONDO:0020091)","secondary_identifiers":["Orphanet:98343"],"synonyms":[{"name":"Male infertility due to impaired sperm transport","type":"exact"}],"termid":"MONDO:0020091","xrefs":{"Monarch":{"xref_id":"0020091"}}}


id: PBO:0113395
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative pyridoxal kinase; a key enzyme involved in pyridoxal 5'-phosphate synthesis, the active form of vitamin B6; required for genome integrity; involved in bud-site selection; localizes to cytosol and peroxisomes; similarity to yeast BUD17 and human pyridoxal kinase (PDXK)","termid":"PBO:0113395"}


id: GO:0075248
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of aeciospore formation, a process in which a dikaryotic spore of typically a rust fungus is produced in an aecium.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of asexual sporulation resulting in formation of a cellular spore","termid":"GO:0043943"},{"relation_name":"regulates","term_name":"aeciospore formation","termid":"GO:0075247"}],"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 aeciospore formation","termid":"GO:0075248"}


id: GO:0098539
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The side (leaflet) of the transport vesicle membrane that faces the cytoplasm.","definition_xrefs":["GOC:ab"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoplasmic side of membrane","termid":"GO:0098562"},{"relation_name":"part_of","term_name":"transport vesicle membrane","termid":"GO:0030658"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0031410"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0031410","GO:0005737"],"is_obsolete":false,"name":"cytoplasmic side of transport vesicle membrane","synonyms":[{"name":"external side of transport vesicle membrane","type":"exact"}],"termid":"GO:0098539"}


id: MONDO:0001285
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"endometriosis","termid":"MONDO:0005133"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endometriosis of pelvic peritoneum","secondary_identifiers":["DOID:11429","ICD9:617.3","SCTID:198251001","ICD10CM:N80.3","MEDGEN:510249","UMLS:C0156345","icd11.foundation:1015401835"],"termid":"MONDO:0001285","xrefs":{"Monarch":{"xref_id":"0001285"}}}


id: PBO:0081969
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZRANB2 antisense RNA 1","termid":"PBO:0081969"}


id: GO:0140082
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Isoenergetic transfer of SUMO from one protein to an existing ubiquitin chain via the reaction X-ubiquitin + Y-ubiquitin = Y-ubiquitin-ubiquitin + X, where both the X-ubiquitin and Y-ubiquitin-ubiquitin linkages are thioester bonds between the C-terminal glycine of ubiquitin and a sulfhydryl side group of a cysteine residue.","definition_xrefs":["PMID:28552615"],"direct_ancestors":[{"relation_name":"is_a","term_name":"SUMO ligase activity","termid":"GO:0061665"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0019787"}],"interesting_parent_ids":["GO:0140096","GO:0016740","GO:0016746","GO:0003824","GO:0019787","GO:0003674"],"is_obsolete":false,"name":"SUMO-ubiquitin ligase activity","termid":"GO:0140082"}


id: PR:000036301
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A fungal-type cyclin-dependent kinase 1 that is encoded in the genome of Schizosaccharomyces pombe.","definition_xrefs":["PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein","termid":"PR:000000001"},{"relation_name":"is_a","term_name":"fungal-type cyclin-dependent kinase 1","termid":"PR:000037486"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclin-dependent kinase 1 (Schizosaccharomyces pombe)","pombase_gene_id":"SPBC11B10.09","synonyms":[{"name":"CDK1 (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-cdc2","type":"exact"},{"name":"cdk1","type":"related"},{"name":"cell division control protein 2 (Schizosaccharomyces pombe)","type":"exact"},{"name":"cell division protein kinase 1 (Schizosaccharomyces pombe)","type":"exact"},{"name":"p34 protein kinase (Schizosaccharomyces pombe)","type":"exact"},{"name":"pi002, SPBC11B10.09","type":"related"},{"name":"swo2","type":"related"}],"termid":"PR:000036301"}


id: MONDO:0014973
data:
  {"annotated_genes":["SJAG_02679","SJAG_01875"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87337,87338],"is_not":false,"summary":null,"term":"MONDO:0014973"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01875":null,"SJAG_02679":null},"genotype_count":0,"is_obsolete":false,"name":"sudden cardiac failure, infantile","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:934631","UMLS:C4310664","OMIM:617222"],"synonyms":[{"name":"PPA2 deficiency","type":"broad"},{"name":"PPA2-associated sudden cardiac death","type":"exact"},{"name":"SCFI","type":"exact"},{"name":"infantile sudden cardiac failure","type":"exact"},{"name":"sudden Cardiac failure, infantile","type":"exact"},{"name":"sudden cardiac failure, infantile; SCFI","type":"exact"}],"termid":"MONDO:0014973","terms_by_termid":{"MONDO:0014973":null},"xrefs":{"Monarch":{"xref_id":"0014973"}}}


id: GO:0150176
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of phosphatidylethanolamine metabolic process.","definition_xrefs":["GOC:aruk","GOC:bc","PMID:30074985"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of phosphatidylethanolamine metabolic process","termid":"GO:0150175"},{"relation_name":"is_a","term_name":"positive regulation of phospholipid metabolic process","termid":"GO:1903727"},{"relation_name":"positively_regulates","term_name":"phosphatidylethanolamine metabolic process","termid":"GO:0046337"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"positively_regulates","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"positive regulation of phosphatidylethanolamine metabolic process","termid":"GO:0150176"}


id: MONDO:0000030
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"frontal lobe epilepsy","termid":"MONDO:0002612"},{"relation_name":"is_a","term_name":"familial partial epilepsy","termid":"MONDO:0017704"},{"relation_name":"is_a","term_name":"variable-age onset focal epilepsy syndrome","termid":"MONDO:0800492"}],"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":"sleep-related hypermotor epilepsy","secondary_identifiers":["MEDGEN:937685","OMIMPS:600513","UMLS:C4313718"],"synonyms":[{"name":"SHE","type":"exact"},{"name":"epilepsy, nocturnal frontal lobe","type":"exact"},{"name":"sleep-related hyperkinetic epilepsy","type":"exact"},{"name":"sleep-related hypermotor epilepsy","type":"exact"}],"termid":"MONDO:0000030","xrefs":{"Monarch":{"xref_id":"0000030"}}}


id: PBO:0067329
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 420, pseudogene","termid":"PBO:0067329"}


id: MONDO:0017517
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"non-syndromic brachydactyly of toes","termid":"MONDO:0017452"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"brachydactyly of toes, unilateral","secondary_identifiers":["icd11.foundation:714196201","Orphanet:295132"],"synonyms":[{"name":"short toes, unilateral","type":"exact"}],"termid":"MONDO:0017517","xrefs":{"Monarch":{"xref_id":"0017517"}}}


id: GO:0008396
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 7-oxocholesterol + H+ + NADPH = 7alpha-hydroxycholesterol + NADP+.","definition_xrefs":["RHEA:68740"],"direct_ancestors":[{"relation_name":"is_a","term_name":"steroid 7-alpha-hydroxylase activity","termid":"GO:0008387"}],"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":"oxysterol 7-alpha-hydroxylase activity","secondary_identifiers":["Reactome:R-HSA-192178","Reactome:R-HSA-192065","Reactome:R-HSA-191972","Reactome:R-HSA-5602885"],"synonyms":[{"name":"cytochrome P450 CYP7B1","type":"narrow"}],"termid":"GO:0008396"}


id: PBO:0064160
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phospholipase A2 group IIE","termid":"PBO:0064160"}


id: PBO:0088848
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar transporter chaperone (VTC) complex subunit","termid":"PBO:0088848"}


id: PR:Q9P5N3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- alr2 gene.","definition_xrefs":["UniProtKB:Q9P5N3","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":"alanine racemase 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC359.02","synonyms":[{"name":"Spom972h-alr2","type":"exact"}],"termid":"PR:Q9P5N3"}


id: MONDO:0859570
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Braddock-Carey syndrome","termid":"MONDO:0031646"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"braddock-carey syndrome 2","secondary_identifiers":["OMIM:619981","MEDGEN:1823962","UMLS:C5774189"],"termid":"MONDO:0859570","xrefs":{"Monarch":{"xref_id":"0859570"}}}


id: PBO:0067150
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 200, pseudogene","termid":"PBO:0067150"}


id: PBO:0050554
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hemopexin","termid":"PBO:0050554"}


id: PBO:0043185
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chondrogenesis-associated transcript","termid":"PBO:0043185"}


id: GO:1990375
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The reproductive developmental process whose specific outcome is the progression of the baculum over time, from its formation to the mature structure.","definition_xrefs":["GOC:sl","PMID:21471296"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reproductive structure development","termid":"GO:0048608"}],"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":"baculum development","synonyms":[{"name":"os penis development","type":"exact"},{"name":"penile bone development","type":"exact"},{"name":"penis bone development","type":"exact"}],"termid":"GO:1990375"}


id: GO:0051641
data:
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id: GO:0000016
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: lactose + H2O = D-glucose + D-galactose.","definition_xrefs":["PMID:12023280"],"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:0003824"},{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016798","GO:0003674","GO:0016787","GO:0003824"],"is_obsolete":false,"name":"lactase activity","secondary_identifiers":["Reactome:R-HSA-5658001","RHEA:10076","Reactome:R-HSA-189062","MetaCyc:BETAGALACTOSID-RXN","EC:3.2.1.108"],"synonyms":[{"name":"lactose galactohydrolase activity","type":"exact"}],"termid":"GO:0000016"}


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":["PMID:1629949","VZ:857"],"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: MONDO:0002128
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A painful asymmetric asynchronous sensory and motor peripheral neuropathy involving isolated damage to at least 2 separate nerve areas; associated with (but not limited to) systemic disorders such as diabetes, vasculitis, amyloidosis, direct tumor involvement, polyarteritis nodosa, rheumatoid arthritis, systemic lupus erythematosus, and paraneoplastic syndromes. It also may be associated with Lyme disease, Wegener's granulomatosis, Sjogren syndrome, cryoglobulinemia, hypereosinophilia, temporal arteritis, scleroderma, sarcoidosis, leprosy, acute viral hepatitis A, and acquired immunodeficiency syndrome.","definition_xrefs":["NCIT:C70938"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuritis of upper limb","termid":"MONDO:0003607"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"mononeuritis multiplex","secondary_identifiers":["GARD:7056","ICD9:354.5","SCTID:30292005","UMLS:C0151295","DOID:1835","MEDGEN:101790","ICD10CM:G58.7","icd11.foundation:1838368265"],"synonyms":[{"name":"mononeuritis multiplex","type":"exact"}],"termid":"MONDO:0002128","xrefs":{"Monarch":{"xref_id":"0002128"}}}


id: GO:1902267
data:
  {"annotated_genes":["SJAG_04469"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[106710],"is_not":false,"summary":null,"term":"GO:1902267"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of polyamine transmembrane transport.","definition_xrefs":["GOC:TermGenie","PMID:23755272"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transmembrane transport","termid":"GO:0034762"},{"relation_name":"regulates","term_name":"polyamine transmembrane transport","termid":"GO:1902047"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04469":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0055085","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"regulation of polyamine transmembrane transport","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1902267","terms_by_termid":{"GO:1902267":null}}


id: MONDO:0012364
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A dilated cardiomyopathy that has material basis in variation in the chromosome region 7q22.3-q31.1.","definition_xrefs":["DOID:0110442","PMID:16228230"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial isolated dilated cardiomyopathy","termid":"MONDO:0700335"}],"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":"dilated cardiomyopathy 1Q","secondary_identifiers":["UMLS:C1835926","GARD:15470","MEDGEN:332088","MESH:C563688","OMIM:609915"],"synonyms":[{"name":"CMD1Q","type":"exact"},{"name":"cardiomyopathy, dilated, 1Q","type":"related"},{"name":"dilated cardiomyopathy type 1Q","type":"exact"}],"termid":"MONDO:0012364","xrefs":{"Monarch":{"xref_id":"0012364"}}}


id: GO:0001326
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Replication of circular DNA following excision from the chromosome; replication of extrachromosomal circular DNA generally occurs independently of chromosomal replication.","definition_xrefs":["GOC:jh","PMID:33867825"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA-templated DNA replication","termid":"GO:0006261"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006260"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006259","GO:0006260","GO:0008150"],"is_obsolete":false,"name":"replication of extrachromosomal circular DNA","termid":"GO:0001326"}


id: PBO:0077878
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thyroid peroxidase","termid":"PBO:0077878"}


id: MONDO:0800449
data:
  {"annotated_genes":["SJAG_00158","SJAG_04790","SJAG_02068"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85687,85688,85686],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0019149"},{"annotations":[85944,85946,85945],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0019148"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic dyslipidemia","termid":"MONDO:0015905"},{"relation_name":"is_a","term_name":"lysosomal lipid storage disorder","termid":"MONDO:0019245"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00158":null,"SJAG_02068":null,"SJAG_04790":null},"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:0002561"}],"interesting_parent_ids":["MONDO:0002525","MONDO:0002561","MONDO:0005066"],"is_obsolete":false,"name":"lysosomal acid lipase deficiency","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1807768","GARD:12097","UMLS:C5574740","icd11.foundation:381622932","OMIMPS:278000","MESH:C531854","Orphanet:275761","SCTID:715923003","DOID:0080217"],"synonyms":[{"name":"LAL deficiency","type":"exact"}],"termid":"MONDO:0800449","terms_by_termid":{"MONDO:0019148":null,"MONDO:0019149":null},"xrefs":{"Monarch":{"xref_id":"0800449"}}}


id: GO:0072040
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that reduces the occurrence or rate of mesenchymal stem cell death by apoptotic process that contributes to the shaping of the nephron.","definition_xrefs":["GOC:mtg_kidney_jan10","GOC:mtg_apoptosis"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mesenchymal cell apoptotic process involved in nephron morphogenesis","termid":"GO:0072039"},{"relation_name":"is_a","term_name":"negative regulation of apoptotic process involved in morphogenesis","termid":"GO:1902338"},{"relation_name":"is_a","term_name":"negative regulation of somatic stem cell population maintenance","termid":"GO:1904673"},{"relation_name":"is_a","term_name":"negative regulation of mesenchymal cell apoptotic process","termid":"GO:2001054"},{"relation_name":"negatively_regulates","term_name":"mesenchymal stem cell maintenance involved in nephron morphogenesis","termid":"GO:0072038"},{"relation_name":"negatively_regulates","term_name":"mesenchymal cell apoptotic process involved in nephron morphogenesis","termid":"GO:1901145"}],"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 mesenchymal cell apoptotic process involved in nephron morphogenesis","synonyms":[{"name":"negative regulation of mesenchymal stem cell apoptosis involved in nephron morphogenesis","type":"narrow"},{"name":"negative regulation of mesenchymal stem cell apoptotic process involved in nephron morphogenesis","type":"exact"}],"termid":"GO:0072040"}


id: PBO:0059542
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrially encoded tRNA-Ile (AUU/C)","termid":"PBO:0059542"}


id: GO:0005001
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with a signal and transmitting the signal from one side of the membrane to the other to initiate a change in cell activity by catalysis of the reaction: protein tyrosine phosphate + H2O = protein tyrosine + phosphate.","definition_xrefs":["PMID:34353440"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein tyrosine phosphatase activity","termid":"GO:0004725"},{"relation_name":"is_a","term_name":"transmembrane receptor protein phosphatase activity","termid":"GO:0019198"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0004721"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003674","GO:0038023","GO:0003824","GO:0004721","GO:0016787","GO:0140096","GO:0016788"],"is_obsolete":false,"name":"transmembrane receptor protein tyrosine phosphatase activity","termid":"GO:0005001"}


id: PBO:0055277
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 2704","termid":"PBO:0055277"}


id: FYPO:0001431
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An increased chemical resistance phenotype observed in the vegetative growth phase of the life cycle in which cells grow in the presence of a higher concentration of the antibiotic Dio-9 than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002682"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0002682","FYPO:0000139","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"resistance to Dio-9","synonyms":[{"name":"resistance to DIO 9","type":"exact"},{"name":"resistance to Dio-9 during mitotic cell cycle","type":"related"},{"name":"resistance to Dio-9 during vegetative growth","type":"exact"},{"name":"resistant to Dio-9","type":"exact"}],"termid":"FYPO:0001431"}


id: PBO:0044629
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deoxycytidine kinase","termid":"PBO:0044629"}


id: PBO:0077501
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 219","termid":"PBO:0077501"}


id: PR:Q92399
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A DNA-directed RNA polymerases I, II, and III subunit RPABC3 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","PANTHER:PTHR10917: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":"DNA-directed RNA polymerases I, II, and III subunit RPABC3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC14C8.12","secondary_identifiers":["UniProtKB:Q92399"],"synonyms":[{"name":"DNA-directed RNA polymerases I, II, and III 14.5 kDa polypeptide (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"RNA polymerases I, II, and III subunit ABC3 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"RPC14 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"SPBC14C8.12","type":"related"},{"name":"Spom972h-POLR2H","type":"exact"}],"termid":"PR:Q92399"}


id: GO:2000900
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving a cyclodextrin.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oligosaccharide metabolic process","termid":"GO:0009311"},{"relation_name":"is_a","term_name":"glucan metabolic process","termid":"GO:0044042"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0005975"],"is_obsolete":false,"name":"cyclodextrin metabolic process","synonyms":[{"name":"cyclodextrin metabolism","type":"exact"}],"termid":"GO:2000900"}


id: FYPO:0000345
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A transport phenotype observed in the vegetative growth phase of the life cycle in which the export of protein from the nucleus is abnormal. Export of all proteins or a specific protein may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal intracellular protein transport during vegetative growth","termid":"FYPO:0000215"},{"relation_name":"is_a","term_name":"abnormal nuclear export","termid":"FYPO:0000506"},{"relation_name":"is_a","term_name":"abnormal protein export from nucleus","termid":"FYPO:0005745"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0005447","FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"abnormal protein export from nucleus during vegetative growth","synonyms":[{"name":"abnormal protein export from nucleus during mitotic cell cycle","type":"related"}],"termid":"FYPO:0000345"}


id: PBO:0004948
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Translocase of the Inner Membrane","termid":"PBO:0004948"}


id: PBO:0113234
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Negative regulatory subunit of protein phosphatase 1 (Ppz1p); involved in coenzyme A biosynthesis; subunit of the phosphopantothenoylcysteine decarboxylase (PPCDC: Cab3p, Sis2p, Vhs3p) complex and the CoA-Synthesizing Protein Complex (CoA-SPC: Cab2p, Cab3p, Cab4p, Cab5p, Sis2p and Vhs3p); dose-dependent regulator of replicative lifespan; SIS2 has a paralog, VHS3, that arose from the whole genome duplication","termid":"PBO:0113234"}


id: PBO:0051584
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 18 binding protein","termid":"PBO:0051584"}


id: PBO:0087484
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of cleavage polyadenylation factor (CPF); interacts directly with poly(A) polymerase (Pap1p) to regulate its activity; bridging factor that links Pap1p and the CPF complex via Yth1p","termid":"PBO:0087484"}


id: MONDO:0008968
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":"cholestasis with gallstone, ataxia, and visual disturbance","secondary_identifiers":["OMIM:214980","MEDGEN:347812","UMLS:C1859161","MESH:C565856"],"synonyms":[{"name":"cholestasis with gallstone, ataxia, and visual disturbance","type":"exact"}],"termid":"MONDO:0008968","xrefs":{"Monarch":{"xref_id":"0008968"}}}


id: PBO:0090949
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-splicing endonuclease subunit Sen15","termid":"PBO:0090949"}


id: PBO:0070854
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L13 pseudogene 7","termid":"PBO:0070854"}


id: PBO:0060677
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NDNF antisense RNA 1","termid":"PBO:0060677"}


id: PBO:0004924
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved eukaryotic nuclear protein implicated in meiotic chromosome segregation","termid":"PBO:0004924"}


id: GO:1904740
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A transcription from RNA polymerase II promoter that results in positive regulation of filamentous growth of a population of unicellular organisms in response to starvation.","definition_xrefs":["GOC:TermGenie","PMID:26448198","GO_REF:0000063","GOC:rn"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of filamentous growth of a population of unicellular organisms in response to starvation by transcription from RNA polymerase II promoter (obsolete GO:1904740)","synonyms":[{"name":"positive regulation of filamentous growth of a population of unicellular organisms in response to starvation by RNA polymerase II transcription factor activity","type":"related"},{"name":"positive regulation of filamentous growth of a population of unicellular organisms in response to starvation by gene-specific transcription from RNA polymerase II promoter","type":"related"},{"name":"positive regulation of filamentous growth of a population of unicellular organisms in response to starvation by general transcription from RNA polymerase II promoter","type":"related"},{"name":"positive regulation of filamentous growth of a population of unicellular organisms in response to starvation by specific transcription from RNA polymerase II promoter","type":"related"},{"name":"positive regulation of filamentous growth of a population of unicellular organisms in response to starvation by transcription from Pol II promoter","type":"exact"}],"termid":"GO:1904740"}


id: GO:0070863
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of directed movement of proteins from the endoplasmic reticulum.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein exit from endoplasmic reticulum","termid":"GO:0070861"},{"relation_name":"is_a","term_name":"positive regulation of intracellular protein transport","termid":"GO:0090316"},{"relation_name":"positively_regulates","term_name":"protein exit from endoplasmic reticulum","termid":"GO:0032527"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"positive regulation of protein exit from endoplasmic reticulum","synonyms":[{"name":"activation of protein exit from endoplasmic reticulum","type":"narrow"},{"name":"positive regulation of protein exit from ER","type":"exact"},{"name":"positive regulation of protein export from ER","type":"exact"},{"name":"positive regulation of protein export from endoplasmic reticulum","type":"exact"},{"name":"stimulation of protein exit from endoplasmic reticulum","type":"narrow"},{"name":"up regulation of protein exit from endoplasmic reticulum","type":"exact"},{"name":"up-regulation of protein exit from endoplasmic reticulum","type":"exact"},{"name":"upregulation of protein exit from endoplasmic reticulum","type":"exact"}],"termid":"GO:0070863"}


id: GO:0060676
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The developmental process pertaining to the initial formation of the ureteric bud from the Wolffian duct. This process begins when the bud protrudes from the duct and ends when it is a recognizable bud.","definition_xrefs":["GOC:dph","PMID:16916378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mesonephric tubule formation","termid":"GO:0072172"},{"relation_name":"part_of","term_name":"ureteric bud morphogenesis","termid":"GO:0060675"}],"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":"ureteric bud formation","secondary_identifiers":["Reactome:R-HSA-9830674"],"termid":"GO:0060676"}


id: GO:0060133
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a somatotropin secreting cell over time, from its formation to the mature structure. A somatotropin secreting cell is an acidophilic cell of the anterior pituitary that produces growth hormone, somatotropin.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell development","termid":"GO:0048468"},{"relation_name":"part_of","term_name":"somatotropin secreting cell differentiation","termid":"GO:0060126"}],"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":"somatotropin secreting cell development","synonyms":[{"name":"growth hormone secreting cell development","type":"exact"},{"name":"somatotrope development","type":"related"},{"name":"somatotroph development","type":"related"},{"name":"somatotrophin secreting cell development","type":"exact"},{"name":"somatotropic cell development","type":"exact"},{"name":"somatrophic cell development","type":"related"}],"termid":"GO:0060133"}


id: GO:0061292
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of molecular signals initiated by binding of a Wnt protein to a frizzled family receptor on the surface of the target cell, followed by propagation of the signal via beta-catenin, and ending with a change in transcription of target genes that contributes to the progression of the mesonephros over time. In this pathway, the activated receptor signals via downstream effectors that result in the inhibition of beta-catenin phosphorylation, thereby preventing degradation of beta-catenin. Stabilized beta-catenin can then accumulate and travel to the nucleus to trigger changes in transcription of target genes.","definition_xrefs":["GOC:mtg_kidney_jan10"],"gene_count":0,"genotype_count":0,"name":"obsolete canonical Wnt signaling pathway involved in mesonephros development (obsolete GO:0061292)","synonyms":[{"name":"canonical Wnt receptor signaling pathway involved in mesonephros development","type":"exact"},{"name":"canonical Wnt receptor signalling pathway involved in mesonephros development","type":"exact"},{"name":"canonical Wnt-activated signaling pathway involved in mesonephros development","type":"exact"}],"termid":"GO:0061292"}


id: PBO:0090117
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L30","termid":"PBO:0090117"}


id: PBO:0085551
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein component of the small (40S) subunit; essential for control of translational accuracy; phosphorylation by C-terminal domain kinase I (CTDK-I) enhances translational accuracy; methylated on one or more arginine residues by Hmt1p; homologous to mammalian ribosomal protein S2 and bacterial S5","termid":"PBO:0085551"}


id: MONDO:0018584
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete placental insufficiency (obsolete MONDO:0018584)","termid":"MONDO:0018584","xrefs":{"Monarch":{"xref_id":"0018584"}}}


id: PBO:0017654
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"stationary phase-specific homeobox transcription factor Phx1","termid":"PBO:0017654"}


id: SO:1001188
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene that is alternately spliced, but encodes only one polypeptide.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"encodes_alternately_spliced_transcripts","termid":"SO:0000463"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"encodes_1_polypeptide","synonyms":[{"name":"encodes 1 polypeptide","type":"exact"}],"termid":"SO:1001188"}


id: MONDO:0009170
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id: GO:0048095
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id: GO:0004643
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id: PBO:0064974
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id: GO:0048546
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id: MONDO:0019052
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id: MOD:00680
data:
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id: GO:0014829
data:
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id: GO:0090410
data:
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id: GO:0046710
data:
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